ethiopian journal pediatric

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1 ETHIOPIAN JOURNAL OF PEDIATRICS AND CHILD HEALTH July 2009, Volume V, Number 5 Original articles The Prevalence of Nosocomial Infections and Associated Risk Factors in Pediatric Patients in Tikur Anbessa Hospital Mikyas Demissie ,M.D. , Sileshi Lulsesed, M.D. Clinical Predictors of Pneumonia Among Under-five Children At Tikur Anbesa Specilaized Hospital Kalid Asrat, MD, Amha Mekasha, MD, MSc Gullian Barre Syndrome in Children At Tikur Anbessa Specialized Hospital Tigist Bacha, MD Assessment of quality of care of sick under-five children in referral hospitals in Ethiopia. Sirak Hailu, MD, Solomon Emyu, MD/MPH, Fisseha Mamo, MPH, Tolawaq Kejela MD Management of severe acute malnutrition in children using community based therapeutic care approach: a review of three years data from southern Ethiopia. Efrem Teferi, MD Shiferaw Teklemariam, MD, MPH , Lopiso Erosie, BSC, MPH , Abel Hailu, MD, Tefera Belachew, MD, MSc, DLSHTM, Mohammed A Yassin, MD, MSc, PhD Review article Child Survival: Progress Towards meeting MDG4 Assaye Kassie, MD Case report A Case Report : Optic glioma in a child with NF1 Kalid Asrat, MD Notes for contributors Ethiopian Pediatric Society E-mail: [email protected] Telephone: 251-011-8602843 Addis Ababa, Ethiopia

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Page 1: Ethiopian Journal Pediatric

1

ETHIOPIAN JOURNAL OF PEDIATRICS AND CHILD HEALTH July 2009, Volume V, Number 5 Original articles The Prevalence of Nosocomial Infections and Associated Risk Factors in Pediatric Patients in Tikur Anbessa Hospital Mikyas Demissie ,M.D. , Sileshi Lulsesed, M.D. Clinical Predictors of Pneumonia Among Under-five Children At Tikur Anbesa Specilaized Hospital Kalid Asrat, MD, Amha Mekasha, MD, MSc Gullian Barre Syndrome in Children At Tikur Anbessa Specialized Hospital Tigist Bacha, MD

Assessment of quality of care of sick under-five children in referral hospitals in Ethiopia.

Sirak Hailu, MD, Solomon Emyu, MD/MPH, Fisseha Mamo, MPH, Tolawaq Kejela MD Management of severe acute malnutrition in children using community based therapeutic care approach: a review of three years data from southern Ethiopia. Efrem Teferi, MD Shiferaw Teklemariam, MD, MPH , Lopiso Erosie, BSC, MPH , Abel Hailu, MD, Tefera Belachew, MD, MSc, DLSHTM, Mohammed A Yassin, MD, MSc, PhD

Review article Child Survival: Progress Towards meeting MDG4 Assaye Kassie, MD

Case report A Case Report : Optic glioma in a child with NF1 Kalid Asrat, MD

Notes for contributors

Ethiopian Pediatric Society E-mail: [email protected] Telephone: 251-011-8602843

Addis Ababa, Ethiopia

Page 2: Ethiopian Journal Pediatric

2 Ethiopian Journal of Pediatrics and Child Health The official organ of Ethiopian Pediatric Society The Ethiopian Journal of Pediatrics and Child Health aims to contribute towards the improvement of child health in developing countries, particularly in Ethiopia. The journal publishes original articles, reviews, case reports pertaining to health problems of children. Editorial board Amha Mekasha, MD, Msc Editor-in-chief Assaye Kassie, MD Sirak Hialu, MD Tedbab Degife, MD

Page 3: Ethiopian Journal Pediatric

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Table of contents Original articles

The Prevalence of Nosocomial Infections and Associated Risk Factors in Pediatric Patients in Tikur

Anbessa Hospital

Mikyas Demissie ,M.D. , Sileshi Lulsesed, M.D.

Clinical Predictors of Pneumonia Among Under-five Children At Tikur Anbesa Specilaized Hospital Kalid Asrat, MD, Amha Mekasha, MD, MSc Gullian Barre Syndrome in Children At Tikur Anbessa Specialized Hospital

Tigist Bacha, MD

Assessment of quality of care of sick under-five children in referral hospitals in Ethiopia.

Sirak Hailu, MD, Solomon Emyu, MD/MPH, Fisseha Mamo, MPH, Tolawaq Kejela MD Management of severe acute malnutrition in children using community based therapeutic care approach: a review of three years data from southern Ethiopia. Efrem Teferi, MD Shiferaw Teklemariam, MD, MPH , Lopiso Erosie, BSC, MPH , Abel Hailu, MD, Tefera Belachew, MD, MSc, DLSHTM, Mohammed A Yassin, MD, MSc, PhD

Review article Child Survival: Progress Towards meeting MDG4 Assaye Kassie, MD

Case report A Case Report : Optic glioma in a child with NF1 Kalid Asrat, MD

Notes for contributors

Page 4: Ethiopian Journal Pediatric

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The Prevalence of Nosocomial Infections and Associated Risk Factors in Pediatric Patients in

Tikur Anbessa Hospital

Mikyas Demissie, MD, Sileshi Lulseged, MD, Msc

Abstract

Little is known about nosocomial infections and associated risk factors among children in Ethiopia.

The aim of the study is to generate data on nosocomial infection in children that will serve as a base for

further studies and to develop prevention interventions. A case control study was done on 111 cases and

222 controls from pediatrics wards of Tikur Anbessa Hospital, Aug 2002-Dec 2003. Nosocomial infection

rate was 5 per 100 discharges. A total of 143 nosocomial infections were detected in 111 cases. The

commonest infection was pneumonia 39.8%. Specimen for culture and sensitivity was taken from

63/143(44.1%) infections and organisms were isolated in 43 infections. And 14 different type of bacteria

were found. E coli, klebsiella pneumoniae and pseudomonas species were the most frequently isolated

organisms. The resistance to ampicillin was 91.9% , gentamycin 67.2%, , ceftriaxone 50%, norfloxacin

18.3%, and ciprofloxacin 15.4%. Age less than one year, malnutrition, admission to orthopedics unit,

peripheral intravenous line and prolonged hospitalization were significantly associated with nosocomial

infection. In conclusion surveillance for high risk patients, education of health personnel, proper isolation

technique, hand washing or use of glove and gowns, avoid prolonged hospitalization when possible and

reestablishment of infection control committee are needed for prevention of nosocomial infection. And

antimicrobial therapy should be guided based on drug susceptibility pattern of bacteria isolated from patients

with nosocomial infection in the hospital.

Page 5: Ethiopian Journal Pediatric

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Introduction

Nosocomial infections result in considerable

morbidity and mortality, prolongation of

hospitalization and increases patient care

expenditure (1).Published data about nosocomial

infection rate in Ethiopian pediatric patients are not

currently available. But there were two reports on

outbreak of klebsiella at the Etho-Swedish

Children's Hospital. The first report was on

outbreak of gentamycin-resistant klebsiella

bacteremia between February 1988 and February

1990, and infection control committee was

functioning at that time (2).The second report was

on outbreak of klebsiella oxytoca at Ethio-Swedish

hospital in 1992 and 1993(3).

Nosocomial infection rates in pediatric patients in

other countries range from 1.2 to 10.3 infections

per 100 discharges. In most studies the infection

rate varies by age and ward or service. The

highest infection rate was seen in infants younger

than one year of age (1,4-7).

The predominant site of infection differs by the

population studied and the type of surveillance

performed. Respiratory tract and gastrointestinal

tract infections were common in some studies

and surgical wound infection was common in

other studies. Gram negative bacteria, Gram

positive bacteria, and viruses were incriminated

as the predominant causes of nosocomial

infection in various places (1, 5, 7-9).

Determinants of infection include host factors,

prior invasive procedures, use of catheters, use

of antibiotics and exposure to other patients,

visitors or health care providers with contagious

diseases (10). Nosocomial infections can be

transmitted by contact, common source, air or

vectors. Most nosocomial infections in infants

and children result from contact transmission via

the hands of personnel (1,11-13). Malnutrition is

the most common cause of secondary

immunodeficiency (14-16). The cumulative

probability that an individual will experience at

least one nosocomial infection increases with

increasing exposure to the hospital (1,11).

Depressed level of consciousness increases the

likelihood of reflux of gastric contents and

aspiration into lower airway leading to

Pneumonia (11, 16-19). Antimicrobial therapy

reduces the concentration of normal flora and

Page 6: Ethiopian Journal Pediatric

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allowing antimicrobial resistant microorganisms

to gain a foothold. Any patient taking antibiotics

for prophylaxis or treatment may become a

source of highly resistant organisms.

Immunocompromised hosts are more likely to

have nosocomial infection(11,12,18,20,21).

Percutaneously inserted peripheral intravenous

catheters are associated with a low rate of local

infection in children and blood stream infections

are rare. Nosocomial infections also are caused

occasionally by contaminated intravenous fluids

or blood products (1,3,11,22,23) .

Surveillance for infection is the first step in

identifying nosocomial infection and suggesting

methods of prevention (10). Surveillance, by

itself, is an effective process to decrease the

frequency of hospital acquired infections (24).

Methods and Materials

A case control study was conducted reviewing

medical records of children who were discharged

from pediatric wards of Tikur Anbessa Hospital

from August 2002 to December 2003. Neonates

were excluded because the risk factors for

nosocomial infections for neonates are different

from others. Additionally the medical records of

the emergency ward were incomplete and those

who were discharged from the emergency ward

were excluded.

The sample size was calculated with assumption

of prevalence of malnutrition in hospitalized

children in Ethiopia to be 50% which makes

p2=0.5 and p1=0.66. Calculated sample size

was: total sample size=333, Cases=111 and

controls=222 with confidence interval (CI) =95%,

odds ratio (OR) =2 , Zα=1.96 and Zβ=0.84.

Cases are patients with nosocomial infection who

were discharged from pediatric wards excluding

neonates and those who were discharged from

the emergency ward. They were identified after

all charts of patients who were discharged from

August 2002 to December 2003 were reviewed.

For each case the next two discharged patients

without nosocomial infection were taken as

controls from registration book excluding

neonates and those discharged from emergency

ward.

Page 7: Ethiopian Journal Pediatric

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Data was collected from charts of cases and

controls using structured format that include age,

sex, primary diagnosis, weight, length,

community acquired infection, the ward and the

service the patient was admitted, procedure that

was done, nosocomial infection by site, culture

and sensitivity result, use of antibiotics, use of

chemotherapy, use of steroid, level of

consciousness, HIV status, duration of stay in

hospital, the status of admitted child at discharge.

Operational Definitions:

Nosocomial infections are infections acquired

during hospital care which are not present or

incubating at admission. Infections occurring

more than 48 hours after admission are usually

considered nosocomial. Infection that is acquired

in the hospital becomes evident after hospital

discharge is considered nosocomial. Definition to

identify nosocomial infections have been

developed for specific infection sites. These are

derived from those published by the Center for

Disease Control and Prevention(CDC) in the

United States of America or during international

conferences and are used for surviellance of

nosocomial infections (24,25).

Short duration nasotracheal or orotracheal

intubation is defined as intubation only during

general anaesthesia while Long duration

nasotracheal or orotracheal intubation is

intubation for respiratory failure(19). Orotracheal

or nasotracheal intubation is all episodes of

orotracheal or nasotracheal intubation with in the

period of one week prior to the onset of

nosocomial pneumonia will be considered.

Nasogastric intubation is the presence of a

nasogastric intubation will be accepted when it

was present for at least two days within the

period one week prior to the onset of nosocomial

infection (pneumonia) (19).

Wasting and stunting were based on calculating

weight as a percentage of reference median

weight for height and height as a percentage of

reference median height for age (26). Nutritional

status for under-five was according to the

welcome classification (27).

Data was entered into SPSS 10.4 statistical

software and it was analyzed using EPI info 6.

After analysis result was presented using

descriptive statistics, chi-square determination,

Page 8: Ethiopian Journal Pediatric

8

and p-value and odds ratio calculation. P-value

was considered as significant if it was less than

0.05. Multiple regression analysis was done

using SPSS to control the effect confounding

factors.

Results

A total of 1701 patients were discharge from

pediatric wards excluding neonatal ward and

emergency ward in 2003. Of these 85 patients

had acquired nosocomial infection at discharge.

Hence, nosocomial infection rate was 5 per 100

discharges in 2003 in these wards. Charts of 111

cases and 222 controls who were discharged

from pediatrics wards from August 2002 to

December 2003, excluding neonatal and

emergency wards were reviewed analyzed.

Among 111 cases 85 were discharged in 2003

and 26 were discharged in 2002.

Of all cases with nosocomial infection 86(77.5%)

had nosocomial infection once, 21(18.9%) twice,

2(1.8%) three times, and 2(1.8) four times. So,

143 nosocomial infections were detected in 111

cases. The majority of nosocomial infections

were detected in the 2nd week and after the 2nd

week . Out of 143 nosocomial infections 10(7%)

of them were detected in the first three days after

admission, 17(11.9%) between the 4th and 7th

day, 50(35%) between 8th and 14th day,

21(14.7%) between 15th and 21st day and

45(31.4%) nosocomial infections were detected

after 21 days of admission.

The commonest site of nosocomial infection was

pneumonia 39.8% followed by gastroenteritis

11.9% and primary blood stream infection

10.9%(Table 1).The predominant site of infection

was pneumonia in pediatrics, general surgery,

neurosurgery, plastic surgery, tumor therapy unit,

and ENT unit. In burn unit the predominant site of

infection was skin and soft tissue infection. And

in orthopedics upper respiratory tract infection

was the commonest nosocomial infection

detected followed by skin and soft tissue

infection. Surgical wound infection was the

second predominant site of nosocomial infection

in patients who were discharged from general

surgery.

Specimen for culture and sensitivity was taken

from 63/143(44.1%) nosocomial infections.

Among 63 nosocomial infections for which

specimen were collected for culture and

sensitivity test 30 (47.6%) were from blood,

11(17.5%) were from urine and 15(23.8%) were

Page 9: Ethiopian Journal Pediatric

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from pus and the remaining 7(11.1%) were from

other body fluids.

The result of culture and sensitivity test was

positive in 43/63(68.3%) of nosocomial

infections. A total of 62 different isolates were

found from those with positive culture result. A

single organism was isolated from each of 27

nosocomial infections and two or more bacteria

were isolated from 16 nosocomial infections.

When the isolates were classified by the type of

organism, 14 different types of bacteria were

isolated. Escherichia coli was the most frequently

isolated organism followed by klebsiella

pneumoniae, pseudomonas species, and

coagulase negative staphylococci as shown in

Table 3.

Drug susceptibility test for gentamycin was done

for 61 of isolates and 41/61(67.2%) were

resistant . And 11/60(18.3%)of isolates were

resistant to norfloxacin . In similar way

18/36(50%) were resistant to ceftriaxone. Drug

susceptibility for cloxacillin was done only for

three isolates. (Table 4)

Infants under one year of age (29days-11mo),

children with moderate wasting (Waterlow

classification), children admitted to orthopedics

unit, peripheral intravenous line, and prolonged

hospitalization were found to have significantly

increased nosocomial infection. And factors such

as sex, weight for age according Wellcome

classification, height for age according to

Waterlow classification, ward, infection at

admission, surgical intervention, urgency of

surgery, type of surgical wound, duration of

operative procedure, duration of stay before

surgical intervention, orothracheal intubation,

nasogastric intubation, urinary catheterization,

bronchoscopy, prior treatment with antibiotics,

chemotherapy or steroid, depressed level of

consciousness, and HIV status were not

significantly associated with the development of

nosocomial infection. Majority of children with

nosocomial infection (66.7%) stayed more than

21 days before discharge when compared to only

7.2% of controls stayed more than 21 days.

(Table 5)

Among 222 controls, 175(78.8%) were

discharged after improvement, 18(8.1%) were

discharged in the same or worse condition, and

29(13.1%) died. Of 111 cases, 77(69.4%) were

discharged after improvement, 13(11.7%) were

discharged in the same or worse condition, and

Page 10: Ethiopian Journal Pediatric

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21(18.9%) died. Children with nosocomial

infection had no significant increased risk of

death when compared to those without

nosocomial infection ( p value=0.157).

Discussion

Nosocomial infection rate in this study was with

in the range which was observed in other studies

(1, 4, 6, 7). The predominant site of nosocomial

infection was pneumonia followed by

gastroenteritis, and primary blood stream

infection. This was similar to the study done

Welliver and Mc Laughlin. (7).Though 49(44%) of

patients with nosocomial infection were admitted

to surgical service in this study, surgical wound

infection was not common. It accounted for only

5.6% of all nosocomial infections.

Specimen for culture and sensitivity was not

taken in 80(55.9%) of nosocomial infection and

they were treated empirically. But isolated

organisms are usually resistant to commonly

used antibiotics for nosocomial infection like

gentamycin and ceftriaxone. According to this

study, it does not seem rational to treat

nosocomial infection empirically with the above

mentioned antibiotics in Tikur Anbessa hospital.

Antimicrobial therapy should be guided based on

drug susceptibility pattern of organisms isolated.

The proportion of isolated bacteria resistant to

floroquinolones was less when compared to the

proportion of resistance to other antibiotics.

Changing or rotating standard group of antibiotics

used for empiric therapy has been efficacious in

limited studies. The role of floroquinolones in the

treatment of serious infections in children does

not appear to be compromised by safety

concerns since arthralgia and quenolone-induced

cartilage toxicity were low and episodes of

arthralgia were mostly reversible (12,28).

In this study Gram negative bacilli were

commonly isolated organisms which constituted

46/62(74.2%) of all isolated bacteria. In reports

from the 1960s and 1970s from USA Gram

negative bacteria accounted for more than 50%

of the infections which is similar to our study

(1,5,7-9). It is not possible to differentiate

whether the isolated coagulase negative

staphylococci were contaminant or etiologic

agent from this study since only one blood

culture sample was taken and details of blood

culture and clinical response to treatment was

not available. (10,25).

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Disruption of the physical barrier occurs in burn

patients and in those with degloving injury.

Admission to orthopedics unit was significantly

associated with nosocomial infection in this

study. But admission to burn unit in the hospital

was not significantly associated with nosocomial

infection. (10,12). Increased risk of nosocomial

infection in infants less than one year of age and

in nutritionally compromised patients was seen

in other studies as it was seen in this study (1, 5,

7, 14-17). Children admitted to tumor therapy

unit and those who took anti neoplastic

chemotherapy have no significantly increased

nosocomial infection unlike other studies (18).

The effect of peripheral intravenous line on the

occurrence of nosocomial infection needs further

prospective study since canula related

septicemia is considered when the same

organism is isolated from canula and blood.

Even though increased mortality is expected in

patients with nosocomial infection, mortality of

patients with nosocomial infection was not

increased in this study when compared to the

control group (1, 11, 23).

Effective targeted surveillance for high risk

patients, staff education, use of proper isolation

techniques and effective infection control practice

such as hand washing before and after patient

contact or use of glove and gowns are

recommended for the prevention of nosocomial

infection. Prolonged hospitalization should be

avoided as much as possible since it is

significantly associated with the development of

nosocomial infection. And reestablishment of

infection control committee is also required.

Page 12: Ethiopian Journal Pediatric

12Table 1. Distribution of nosocomial infection by site , Tikur Anbessa hospital, August 2002-December 2003.

.Site of nosocomial infection frequency %

Pneumonia 57 39.9

Gastroenteritis 17 11.9

Primary blood stream infection 15 10.9

Urinary tract infection 13 9.1

Skin and soft tissue infection 13 9.1

Upper respirator tract infection 9 6.3

Surgical wound infection 8 5.6

Central Nervous System infections 2 1.4

Others 7 4.9

Systemic infection 2 1.4

Total 143 100

Table 2. Site of nosocomial infections by the service in Tikur Anbessa hospital, August 2002-December 2003.

Service Site of nosocomial infection

Tot

al

SWI (%)

UTI (%)

URTI (%)

Pneumonia (%)

Skin & soft tissue (%)

primary blood stream infection(%) G

astr

o

Ent

eriti

s (%

)

CN

S(%

)

Oth

er(%

)

Sys

tem

ic

infe

ctio

(%)

(%)in

fect

ion

infe

ctio

m

Pediatrics 0 8 (18.2)

0 27 (61.4)

1 (2.3)

5 (11.4)

4 (9)

0 0 0 44

General surgery

5 (26.3)

2 (10.5)

0 7 (36.8)

1 (5.3)

0 2 (10.5)

1 (5.3)

1 (5.3)

0 19

Neuro surgery

0 0 1 (10)

3 (30)

2 (20)

0 1 (10)

1 (10)

1 (10)

0 10

Plastic surgery

1 (50)

0 0 1 (50)

0 0 0 0 0 0 2

Burn unit 1 (7.1)

1 (7.1)

0 3 (21.4)

4 (28.6)

2 (14.3)

1 (7.1)

0 0 1 (7.1)

14

Tumor therapy

0 1 (3.2)

1 (3.2)

11 (35.5)

1 (3.2)

8 (25.8)

6 (19.3)

0 3 (9.7)

0 31

ENT 0 0 1 (16.7)

3 (50)

0 0 1 (16.7)

0 1(16.7)

0 6

Orthopedics 1 (5.9)

1 (5.9)

6 (35.3)

2 (11.8)

4 (23.5)

0 2 (11.8)

0 0 1 (5.5)

17

Total 8 13 9 57 13 15 17 2 7 2 143

SWI=surgical wound infection UTI=urinary tract infection URTI= upper respiratory tract infection CNS= central nervous system

Page 13: Ethiopian Journal Pediatric

Table 3 Types of organism isolated from children with nosocomial infection in Tikur Anbessa hospital, August 2002-December 2003.

Organism isolated Frequency %

Escherichia coli 11 17.7

Klebsiella pneumoniae 9 14.5

Pseudomonas species 9 14.5

Coagulase negative staphylococci 6 9.7

Acinetobacter species 5 8.1

Klebsiella oxytoca 4 6.5

Salmonella species 4 6.5

Staphylococcus aureus 3 4.8

Proteus vulgaris 3 4.8

Citrobacter species 3 4.8

Shigella species 2 3.2

Group A streptococci 1 1.6

Morganella morgagne 1 1.6

Enterobacter cloaca 1 1.6

Total 62 100

Page 14: Ethiopian Journal Pediatric

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14

Table 4 Drug susceptibility pattern of bacteria isolated from children with nosocomial infections in Tikur Anbessa Hospital, August 2002- December 2003.

Antibiotics No. of isolates tested

sensitive Intermediate sensitive

Resistant

Ampicillin 62 4(6.5%) 1(1.6%) 57(91.9%)

Gentamycin 61 20(32.8%) 0 41(67.2%)

Norfloxacin 60 47(78.3%) 2(3.3%) 11(18.3%)

Trimethoprim-Sulfamethoxazole

58 10(17.2%) 2(3.5%) 46(79.3%)

Tetracycline 58 13(22.4%) 2(3.5%) 43(74.1%)

Chloramphenicol 55 8(14.5%) 0 47(85.5%)

Ceftriaxone 36 13(36.1%) 5(13.9%) 18(50%)

Augmentin 31 8(25.8%) 5(16.1%) 18(58.1%)

Doxycycline 25 5(20%) 1(4%) 19(76%)

Amoxicillin 24 2(8.3%) 1(4.2%) 21(87.5%)

Naldixic Acid 22 12(54.5%) 0 10(45.5%)

Nirofurantoin 19 6(31.6%) 1(5.3%) 12(63.1%)

Amikacin 14 11(78.6%) 1(7.1%) 2(14.3%)

Ciprofloxacin 13 9(69.2%) 2(15.4%) 2(15.4%)

Penicillin G 13 0 2(15.4%) 11(84.6%)

Erythromycin 13 4(30.8%) 3(10%) 6(46.2%)

Methicillin 11 2(18.2%) 3(27.3%) 6(54.5%)

Carbencillin 8 2(25%) 3(37.5%) 3(37.5%)

Kanamycin 4 0 2(50%) 2(50%)

Cephalotin 4 0 2(50%) 2(50%)

Cloxacillin 3 0 2(66.7%) 1(33.3%)

Lincomycin 3 1(33.3%) 2(66.7%) 0

Page 15: Ethiopian Journal Pediatric

15

15

Table 5 Risk factors associated with nosocomial infection in pediatric patients, Tikur Anbessa Hospital, August 2002-December 2003.

Variables Control Case OR P value Adjusted OR (95% CI)

Number % Number %

Age in month 1-11 35 15.8 31 27.9 2.21(1.03-4.79) 0.042 6.373(2.16-18.83)

12-59 85 38.3 33 29.7 0.97(0.48-1.97) 0.937 0.741(0.296-1.856)

60-119 52 23.4 27 24.3 1.30(0.61-2.76) 0.577 1.155(0.421-3.169)

120-180 50 22.5 20 18 1

Weight for height

>=90% 143 66.2 58 54.7 1

80-89% 44 20.4 21 19.8 1.18(0.62-2.24) 0.709 0.94(0.41-2.18)

70-79% 22 10.2 19 17.9 2.13(1.02-4.46) 0.0447 3.68(1.46-9.30)

<70% 7 3.2 8 7.6 2.82(0.88-9.13) 0.09 2.28(0.52-10.04)

Peripheral intravenous line

No 23 10.4 3 2.7 1

Yes 199 89.6 108 97.3 4.16(1.15-17.82) 0.025 7.566(1.009-56.708)

Use of antineoplastic chemotherapy

No 215 96.8 89 80.2 1

Yes 7 3.2 22 19.8 7.59(2.94-20.35) 0.000001 0.006(0.00-12)

Duration of stay before discharge

<7 days 74 33.3 2 1.8 1

8-14 days 62 27.9 19 17.1 11.34(2.4-73.44) 0.00032 13.43(2.65-68.08)

15-21days 40 18 16 14.4 14.8(3.02-98.38) 0.00005 9.29(1.74-48.64)

>21 days 46 7.2 74 66.7 59.52(13.41-368.48)

0.00000 70.15(13.96-352.46

Service General surgery 72 32.4 16 14.4 1

Pediatrics 90 40.5 38 34.2 1.9(0.94-3.89) 0.079 1.68(0.42-6.71)

Plastic surgery 10 4.5 2 1.8 0.90(0.0-5.09) 0.785 1.21(0.19-7.56)

ENT 14 6.3 4 3.6 1.29(o.31-5.001) 0.945 1.83(0.36-9.21)

Neurosurgery 6 2.7 5 4.5 3.75(o.85-16.41) 0.096 2.89(0.53-15.59)

Orthopedics 21 9.5 15 13.5 3.21(1.26-8.27) 0.012 4.86(1.31-18.01)

Burn unit 4 1.8 7 6.3 7.88(1.77-37.27) 0.003 4.89(0.93-25.83)

Tumor therapy unit

5 2.3 24 21.6 21.6(6.47-77.05) 0.000 1778.85(0.00-34)

Page 16: Ethiopian Journal Pediatric

16

16

References 1. Jarvis W.R : Epidemiology of nosocomial infections in pediatric patients. Pediatr. Infect. Dis. J. 1987; 6: 344-51 2. Moss W. An outbreak of getamycin-resistant klebsiella bacteremia at a children's hospital. Ethiop Med J. 1992;

30: 197-205 3. Worku B. Klebsiella oxytoca outbreak at Ethio-Swedish children’s hospital (ESCH). Ethiop Med J. 1997; 35:177-

83 4. Cooper R.G., Sumner C. Hospital infection data from a children’s hospital Med J. Aust. 1970; 2:1110-13 5. Gardner P, Carles D.G Infection acquired in a pediatric hospital. J. Pediatr. 1972; 81: 1205-1210 6. Wenzel R.P, Osterman C.A., Hunting K.J. Hospital acquired infection 11. Infection rates by site, service and

common procedures in a university hospital. Am. J. Epidemiol. 1976; 104: 645-51 7. Welliver R.C., Mc Laughlin S. Unique epidemiology of nosocomial infection in a children’s hospital. Am. J. Dis.

Child. 1984; 138: 131-5 8. Gaynes R.P., Edward J.R., Jarvis W.R., Culver D. H, Tolson J. S., Martone W. J. Nosocomial infection among

neonates in high- risk nurseries in the United States. Pediatrics. 1996; 98: 357-61 9. Sohn A. H., Garret D. O., Sinkovitz- Cochran R.L., Grohskopf L. A., Levine G. L., Stover B.H., Seigel J.D.,Jarvis

W.R. Prevalence of nosocomial infections in neonatal intensive care unit patients: Results from the first national point prevalence survey.J.Pediatr .2001;133:821-827.

10. Behrman R, Kleigman R, Jenson H. T lymphocyte, B lymphocyte and Natural Killer cells.-In: Buckley R., ed ; Infection control and prophylaxis.-In: Fisher, ed. Nelson, Text Book of pediatrics, 17th ed. New Delhi, Elsevier, 2004:683, 866, 1184.

11. Feigin, Cherry. Nosocomial infections.-In: Huskin W.C., Goldman D.A., eds., Textbook of pediatric infectious disease, 4th ed. Philadelphia, Elsevier, 1998; 2545-85.

12. Fleming C.A., Balaguera H.U., Craven D.E., Risk factors for nosocomial preumonia.Med chinics of north America 2001;85:1545-1563.

13. Knittle M.A., Eitzman D.V., Baer H, Role of hand contamination of personnel in the epidemiology of gram negative nosocomial infections: J.pediatr 1975; 86:433-437.

14. Chandra R.K: Nutrition, immunity, and infection: Present knowledge and future direction.Lancet.1983; 1:688-91. 15. Puri S, Chandra P.K: Nutritional regulation of host resistance and predictive value of immunlogic test in

assessement of outcome. Pediatric Clinics of North America.1985; 32:499-516. 16. Bhattacharyya N, Kosloske A.M., Macarlhia C.Nosocomial infection in pediatric surgical patients: a study of 608

infants and children: J.pediatr.Surg.1993; 28:338-343. 17. Bhattacharyya N, Koslosk A.M., postoperative wound infectious in pediatric surgical patients: A study of 676

infants and children. J.pediatr surg.1990; 25:125-129. 18. Haley R.W., Houton T.M., Culver D.H., Stanley R.C., Emori T.G., Hardisan C.D., Quade D, Schauchtman

R.H.Schaberg D.R., shah B.V., Schat, G.D., Nosocomial infections in U.S. Hospitals, 1975-1976 estimated frequency by selected characteristics of patients AM J Med 1981; 70: 947-959.

19. Calis R, Torres A, Gatell J.M., Almale M, Rodringuez-Roisin R.,Aqustin vidal A. Noscomial preumonia. A multivariate analysis of risk and prognosis. Chest 1988; 93:318-24.

20. Price D.J., Sleigh J.D., Control of infection due to klebsiella aerogenes in a neurosurgical unit by withdrawal of all antibiotics. Lancet 1970; 2:1213-1215.

21. Young L.S. Nosocomial infection in the immuocompromised adult. Am. J .Med 1981; 70:398-403.

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22. Garlsand I.S.,Nelson D.B., Cheah T.E., Hennes H.H., Johnson T.M. infectious complications during peripheral intravenous therapy with Teflon catheters: a prospective study.pediatr infect dis. J. 1987; 6: 918-921.

23. Tully J.L., Friedland F.H., Baldini L.M., Goldmann D.A., Complications of intravenous therapy with steel needles and Teflon catheters. Am. J Med 1981; 70:702-6.

24. Ducel.G, Fabry.J, Nicolle.L; Prevention of hospital acquired infections A Practical Guide 2nd edition.WHO/CDS/EPH/2002.12

25. Garner J.S., Jarvis W.R., Emori T. G., Horan T.C. , Hughes J .M.. CDC definition for nosocomial infections. Am J Infect Control 1988;16:128-140.

26. Waterlow. J.C. Note on the assessement and classification of protein energy malnutrition in children. Lancet 1973; 2:87-98.

27. Classification of infantile malnutrition. Lancet 1970; 2: 302-303. 28. Grady R., Safety profile of quinolone antibiotics in the pediatric population. Pediatr Infect Dis J 2003; 22: 1128-

32.

Acknowledgements I thank Dr Fithun Lulseged and staff at the statistics office who helped me collect data. I also extend my gratitude to Dr

Adamu Adissie and Dr Firew Mekonnen who helped me in the analysis of the data.

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Guillain Barre Syndrome in Children At Tikur Anbessa Specialized Hospital

Tigist Bacha, MD

Abstract This is a six years retrospective descriptive study conducted in the pediatric and child health department of Tikur Anbessa

Hospital from September, 2001 – September, 2006 G.C to assess the pattern of acute flaccid paralysis (AFP) and the

clinical and epidemiologic features of Guillain Barre syndrome (GBS).

Data was collected from medical records of all patients admitted with diagnosis of AFP, and analyzed using standard

statistical tests with SPSS version 14 software. Out of 70 admitted cases of AFP, forty six (65.7%) were males and 24

(34.3%) were females. Sixty seven cases (95.7%) were diagnosed to have GBS and the rest three were compatible with

poliomyelitis, transverse myelitis and post injection neuritis. Out of the 70 cases 66 (94.3%) have received at least one

dose of polio vaccination and the rest 4 (5.7%) were never vaccinated.

Out of the cases diagnosed to have GBS, 44 (65.7%) met NNCDS diagnostic criteria. History of antecedent event was

obtained in 31/67 (46.3%) patients. Majority of the patients 45 (67.17%) presented with ascending reflexes quadriparesis,

2 (2.98%) patients with descending areflexic quadriparesis, 19(28.35%) only with lower limb involvement and 1 (1.5%)

with typical miller-fisher type. Sensation was affected in 4 patients.

Cytoalbuminological dissociation was found in 27(40.3%). There were 11 deaths (16.4%) of whom five were admitted to

ICU the rest six didn’t. This study showed that the commonest cause of AFP is GBS which is associated with high

mortality. This high mortality rate 11/67 (16.42%) is attributed to absence of pediatrics ICU, late arrival to Hospital after

onset of illness, and poor supportive care.

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INTRODUCTION

Acute flaccid paralysis (AFP) is the clinical condition

diagnosed in any child under 15 years of age with

acute floppiness of one or more limbs or any age in

whom clinician suspect polio (1,2).It is caused by many

conditions including Guillain Barre syndrome (GBS) ,

poliomyelitis, transverse myelitis and metabolic

neuropathy like hypokalemia (3,4).The most common

cause of AFP is GBS followed by transverse myelitis

(2,5,6,7)

In Ethiopia, the polio eradication initiative (PEI) was

started in 1996. Surveillance for acute flaccid paralysis

(AFP) was initiated in May, 1997. AFP surveillance is

the detection of at least one AFP case per 100,000

children under 15 years of age. AFP surveillance

depends on immediate reporting, investigation of AFP

cases, routine monthly reporting of cases including zero

reporting (1, 9).

GBS is an acute inflammatory polyneuropathy. The

cause is unknown but autoimmunity is incriminated.

Unlike polio, GBS is usually symmetrical (asymmetrical

in 9%), and fever at presentation is not present.

Paralysis develops acutely over days, or at most weeks.

After brief plateau the patients’ improvement begins with

gradual resolution that lasts from weeks to months. 50%

has bulbar involvement, 33% of them require ICU

admission 25% required mechanical ventilation 5-10%

mortality rate (2-3% in best ICU) and 80% complete

recovery. Treatment is intensive care support; early

intravenous immunoglobulin (IVIg) therapy and plasma

exchange hasten early recovery. Corticosteroid alone

outcome is controversial (3,8,10).

The objectives of the study are to describe pattern of

AFP, determine the most common cause of AFP, and

determine the clinical and epidemiological feature of

GBS.

Material and method

Retrospective descriptive study was done in pediatric

and child health department of Tikur Anbessa Hospital,

Addis Ababa. Study groups were all children admitted

with the case definition of AFP from September 2001 –

September 2006. The medical report of Statistics Office

registered for AFP surveillance, Pediatric wards,

surgical and medical ICU and neurology clinic

registration books were reviewed to trace all cases. This

hospital is the only pediatric tertiary Hospital serving for

all the country.

In this study:

Antecedent triggering event was defined as the

presence of respiratory, gastrointestinal, febrile illness

or vaccination for the previous 4 weeks.

Polio-compatible case is defined as a case in which

one adequate stool specimen was not collected from a

probable case within 2 weeks of the onset of paralysis,

and there is either an acute paralytic illness with polio-

compatible residual paralysis at 60 days, or death takes

place within 60 days, or the case is lost to follow-up.

The diagnosis of GBS in this study is based on National

Institute of Neurological and Communicative Disorders

and stroke (NNCDS) diagnostic criteria. (11)

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1. Progressive weakness of more than one limb

due to neuropathy,

2. Areflexia or hyporeflexia

3. Duration of progress less than 4 weeks,

4. The absence of a sharp sensory level on the

trunk,

5. The absence of other causes of acute

neuropathy

6. Less than 50 mononuclear leukocytes per mm3

of CSF.

The data were transferred to a structured form which

was then entered into computer data base. SPSS

Version 14, 2005 was used to process the statistical

data.

Results

In this six year period 70 AFP cases (46 male and 24

female) were admitted and majority 67 (95.7%) were

GBS. Three cases were suspected to have a

compatible poliomyelitis, transverse myelitis and post

injection neuritis each accounting 1.4%. The mean age

of AFP is 5.82 year with a range of 1-12 year. Cases

were reported from different regions of Addis Ababa 44,

Oromia 12, Amhara 11 and South Nations Nationalities

and Peoples region (SNPPR) 3 (Fig 1). The distribution

over the years is shown in Fig 2 from 2001-06 (1993-

1998 Eth C). 1More cases were seen in 1996 Eth C.

Stool sample was taken for polio in 65 cases and was

not taken in 5 of them. Out of the 70 cases 66 (94.3%)

of the cases got at least one dose of polio vaccination

and the rest 4 (5.7%) never vaccinated (table 1). Prior

injection history is found in 7 (1%) of the patients.

Addis AbabaSNNPROromiyaAmhara

Region

50

40

30

20

10

0

NO

of

AF

P C

ases

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Fig. 1 AFP case Regional distributions Fig 2. AFP cases distribution per year

Table 1. Cranial nerve involvement

Cranial nerve involved Frequency Percentage

Facial nerve 3 27.2

Opthalmolopelgia 1 9.1

Glossopharyngeal nerve 5 45.4

Vagus nerve 1 9.1

Multiple cranial nerve 1 9.1

Total 11 100

199819971996199519941993

Admition Year

25.0%

20.0%

15.0%

10.0%

5.0%

0.0%

AF

P c

ases

in P

erce

nt

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Table 2: CSF analysis Result

Frequency Percent

CSF cell count >10/cumm and protein >45mg

3 4.5

CSF cell count >10/cumm and protein <45mg

7 10.4

CSF cell count <10/cumm and protein >45mg

27 40.3

CSF cell count <10/cumm and protein <45mg

21 31.3

Not Documented 9 13.4

Total 67 100.0

From those diagnosed as having GBS 44(62.8%) met

NNCDS diagnostic criteria. The mean age was 5.9 with

ranges of 15 months -12 years. Most of them were male.

History of antecedent event was obtained in 31(46.3%)

patients. Respiratory symptoms accounted 19(27.1%),

gastrointestinal symptoms 9 (11.4%), both gastrointestinal

and respiratory symptoms 1 (1.4%), 1 (1.4%) post

vaccine (Rabies), and 1 (1.4%) had prior malarial attack.

The pattern of progression of paralysis was ascending

areflexic quadriparesis in 45 (67.2%) patients, descending

areflexic quadriparesis in 2(3%), patients with only lower

limb involvement were 19 (28.3%) and one (1.4%) was

Miller - Fisher variant. The mean interval between onset

of symptoms to hospital admission was 6 days with a

range of 5 hrs-14days. Rapidity of the progression ranged

from 1 day to 14.0 days the mean being 3.44 days. The

mean duration of hospital stay is15.5days. Out of the 17

patients whose blood pressure was measured 12 patients

had normal measurement and 5 had transient

hypertension. Bladder and bowel dysfunction was

reported in 44 out of 64 documented cases. Cranial nerve

palsy was reported in 11 patients. As shown in table xxx

the commonest were cranial IX (45.4%) followed by facial

nerve (27.2%). Multiple cranial nerve involvement was

found in 1(9.1%) patient. Sensation was affected in 4

(6%) cases. Ataxia was documented in 8(11.9%) patients.

Cytoalbuminological dissociation was found in 27(40.3%)

patients. see table 5. EMG was done in 5 patients with

GBS out of which 2 were demyelinating, 2 axonal and 1

mixed axonal and demyelinating.

Fifteen15/67 (22.39%) patients required ICU care out of

which 6 didn’t get the service. There were 11(16.4%)

deaths. Five died in ICU and 6 patients died in the pediatric

ward. Four of them came within 4 days of onset of illness

and 7 of them after 4 days. Respiratory failure was

considered as a cause of death in 6, Respiratory failure and

infection were cause of death in 5 of them (3 had

pneumonia, 1 urosepsis). Specific treatment such as

plasmapheresis and Immunoglobulin was given to none of

the patients. Prednisolon was given only for 4 patients

(1.0%).HIV screening was done only for one patient and

the result was non reactive.

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Discussion

This is the first study done on pattern of AFP and clinical and

epidemiology of GBS in the pediatric age groups. The

predominance of male is similar to other studies (6-10). The

common AFP identified was GBS which also correlates with

other studies in Australia, Bangladesh, and Honduras (2,6-8).

Regarding GBS the antecedent events are lower in this study

than other studies done in Kenya, Tanzania, Nigeria and

including the study done in this hospital in adults (12-15).

Similar to other studies respiratory symptoms were the

commonest antecedent events (12). The cranial nerve

involvement are common findings similar to that of Kenya

and adult Ethiopian patient’s (12, 13).

In this study one patient gave history of antecedent malarial

attack the species not documented. From other studies the

development of Guillain–Barré syndrome was reported in 10

patients who had had acute P. falciparum malaria during its

seasonal exacerbation is reported (16).

The high mortality rate is higher to the report from other

studies done in Kenya (13) and Tanzania (9). Also a

higher mortality was observed in adult study done in the

same hospital (12). The main attributable cause is lack of

good pediatric ICU in this Hospital

which could be compounded by the late appearance of

patients to the hospital. In addition specific therapies such

as immunoglobulin and plasmapheresis are not available in

the setup.

This study showed a high need of having pediatric ICU. We

can see the mortality rate from GBS is high some of which

could have been prevented if there was a pediatric ICU.

The care of critical patients and universal precautions for

infection prevention should be encouraged. In addition the

use of specific treatments such as plasmaphereis and

immunoglobulin should be introduced.

For five cases stool sample for polio was not taken out of

whom four died. Taking specimen as soon as possible

especially on critical patients, including on weekend may

increase the surveillance. Improving the AFP surveillance

increased by case investigation reporting cases as early as

possible especially on critical patients should be

encouraged.

In addition care seeking behaviour should be improved so

that patients are brought to hospital as early as possible.

Finally a further large scale study with more investigation

modalities should be done in the near future.

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References

1. Acute Flacc

2. id paral

3. ysis surveillance: Ministry of Health and WHO Ethiopia June 2006: 5

4. Koul R, Chacko A, Javed H et al Acute flaccid paralysis in Australian children. . J Paediatr Child Health.

2003; 39 (1):22-6.

5. Hahn AF. Guillain-Barre syndrome. Lancet 1998; 352: 635-41.

6. Lovecchio F, Jacobson S. Approach to generalized weakness and peripheral neuromuscular disease.

Emerg Med clin N am 1997; 15(3):605-23

7. Rehman A, Idris M, Elahi M, Arif A. Guillain-Barre syndrome. The leading cause of Acute Flaccid Paralysis

in Hazara Division. J ayub Med Coll Abbottabad 2007;19:26-28.

8. Rasul CH, Das PL, Alam S, Ahmed S, Ahmed M. Clinical profile of acute flaccid paralysis. Med J Malaysia.

2002 ; 57 (1):61-5.

9. Molinero MR, Varon D, Holden KR, Sladky JT, Molina IB, Cleaves F. Epidemiology of childhood Guillain-

Barre syndrome as a cause of acute flaccid paralysis in Honduras: 1989-1999.

J Child Neurol. 2003; 18(11):741-7..

10. Kuwabara S. Guillain-Barre syndrome: epidemiology, pathophysiology and management. Drugs.

2004;64(6):597-610. .

11. Berhane Beyene, Ayele Gebremariam, Tilahun Teka et al. Laboratory and Epidemiology communications,

Regional Distribution of Acute Flaccid Paralysis Cases in Ethiopia in 2000 – 2002. Jpn.J.Infect. Dis., 2004;

52:. 72.

12. Harvey B.Sarnat. Neuromuscular Disorders. In: Richard E. Behrman, Robert M. Kliegman and Hal B.

Jenson, Editors. Nelson Text Book of Pediatrics, 17th Edition .Philadelphia Pennsylvania, 2004:2080-81.

13. Asbury Ak. Assessment of current diagnostic criteria for Guillian-Barre syndrome. Ann Neurol

1990:27(suppl):s21-4

14. Zenebe Melaku, Guta Zenebe, Abera Bekele .Guillaian barre syndrome in Ethiopian patients. Ethiop Med J

2005; 43( 1) :21

15. Bahemuka M. Guillain-Barre syndrome in Kenya: a clinical review of 54 patients.

J Neurol. 1988; 235(7):418-21.

16. Howlett WP, Vedeler CA, Nyland H, Aarli JA. Gullian-Barrre syndrome in Northern Tanzania: a comparison

of epidemiological and clinical findings with western Norway. Acta Neurol Scand 1987:75:95-100.

17. Osuntookun BO, Agebebi K. Prognosis of Guillain–Barre syndrome. Medicine in the African Region: The

Nigerian experience. Neurol Neurosurg Psychatry 1973:36:478-83.

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Acknowledgments:

I extend my thanks to Dr. Ahmed Bedru for his invaluable advice in the conduct of the research. Ato Tilahun

Zimita for his assistance in data entry and analysis.

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ASSESSMENT OF QUALITY OF CARE OF SICK UNDER-FIVE CHILDREN IN REFERRAL HOSPITALS IN ETHIOPIA

Sirak Hailu, MD1, Solomon Emyu, MD/MPH2, Fisseha Mamo, MPH3, Tolawaq Kejela MD4

ABSTRACT

Background: About 10-20% of sick children presenting to a primary care facility require referral to hospital for inpatient care. Improvement of the quality of pediatric referral care has a major contribution to the child survival efforts by ensuring the continuum of care and averting mortality. Objective: To assess the quality of care for children in selected referral hospitals based on the minimum standards derived from the “WHO Pocket book of Hospital Care for Children, 2005” and thereby to initiate pediatric referral care quality improvement process in the country. Methods: A qualitative assessment of pediatric referral care was conducted in 8 hospitals selected by convenient sampling, January – July 2008. A team composed of experienced pediatricians and health officer used an adapted WHO hospital assessment tool to assess the quality of triage, emergency care and case management practices & hospital infrastructure and support services. Results: None of these hospitals were practicing the standard triaging process by assessing children immediately on arrival for emergency and priority signs. All of them were not appropriately organized and fully equipped to handle pediatric emergencies effectively. Overall, the case management of common neonatal and childhood illnesses was not optimal. Generally, there was shortage of some essential drugs and lack of materials such as nasal prongs, infant and child size bag & masks, nebulizers, heaters and oxygen concentrators. Hygienic facilities were below the expected standard. Staff were not trained in ETAT (Emergency Triage Assessment and Treatment) and there were no protocols for pediatric referral care. There was no clearly designated high dependency area where very sick children receive highest attention and no special rooms for providing appropriate neonatal care in majority of the hospitals. The overall case fatality rate was 11% (10-16%) but first 24 hours mortality could not be determined due to problems with the recording system.

Conclusions: The quality of pediatric referral care needs serious attention and coordinated efforts utilizing the opportunity of the national hospital management initiative and the BPR (Business Process Re-engineering) to institutionalize ETAT and standards of hospital care for children. This has to be complemented with availing of appropriate job aids, essential supplies and equipments, and improvement of health worker skills through training, clinical mentoring and regular supportive supervision.

1 WHO/Ethiopia, 2 WHO/Ethiopia, 3 FMOH/Addis Ababa, 4 Medical Faculty/AAU,

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INTRODUCTION

The Ethiopian health service delivery system is organized as a four-tier system, characterized by a Primary Health Care Unit (PHCU) – 1st tier, then the district hospital – 2nd tier, zonal hospital – 3rd tier and specialized hospital- 4th tier. Services given at each level of these tiers have a crucial role in averting the morbidity and mortality burden of children and contributing a lot to the achievement of healthy society. In relation to this, Ethiopia has developed a comprehensive national child survival strategy, which is part of the national HSDP-3, and is implementing the IMNCI approach at a wide scale at health facility and community levels. Currently the national IMNCI coverage of the country at Health Center levels is about 60%. These interventions at a community and frontline health facilities (PHCU) levels are very important to address the majority of the health problems of children and also to make the services close and easily available to the society. The IMCI/IMNCI strategy seeks to strengthen prevention and care for children through appropriate community and household care, primary care, referral

practices, and care at the first-level hospital. On the basis of current guidelines, it has been estimated that 10% to 20% of sick children who present for primary care (i.e., the most severely ill) require referral to a first referral or district hospital. The quality of care provided in these hospitals is likely therefore to have a major impact on the health and lives of millions of children each year. It is estimated that 40-60% of deaths at the referral hospitals occurs in the first 24 hours of admission. Many of these deaths could be prevented if very sick children are identified soon after their arrival in the health facility, and treatment is started immediately. The Emergency Triage Assessment and Treatment (ETAT) tool is designed to enable health workers triage all sick children when they arrive at a health facility, into those with emergency signs, with priority signs, or non-urgent cases. It also enable them to provide emergency treatment for life-threatening conditions. The standards of care of the ETAT guidelines correspond to the minimum standards that should be maintained even in small hospitals and where resources are limited.

Early assessment and prioritization for management of sick children attending a health service are critical to achieving good health outcomes. Experience of Malawi in implementing ETAT showed a reduction of total inpatient mortality from 10-18% (median 12.4%) to 6-8% (median 5.7%) over a 2 year period (2001-

2003) and deaths within 24 hours of admission from 36% to 12.5%. This survey tries to assess the current situation of the quality of pediatric care in selected government hospitals.

OBJECTIVES & METHODOLOGY The objective of this study was to assess the quality of care for children in selected referral hospitals based on the minimum standards derived from the “WHO Pocket book of Hospital Care for Children, 2005” and to initiate pediatric referral care quality improvement process by identifying key areas that need immediate and long term action. Eight hospitals (Adama, Ambo, Bishoftu, Debre Birhan, Dessie, Yekatit 12, Yirgalem and Zewditu hospitals); one district, six zonal and one regional referral hospital, were included in the assessment using convenient sampling. The main criterion used for including a hospital was having functional pediatrics outpatient and inpatient services. WHO’s generic assessment tool, “Assessment of the quality of care for children in hospitals”, was

adapted and used for data collection. Adaptation of the tool was done by practicing pediatricians, general practitioners and nurses and it was pretested during a five days national orientation workshop on pediatric referral care. The assessment tool had 12 major sections: General hospital information, Hospital layout and structure, Hospital support systems (drugs, equipment and laboratory), Emergency care, Pediatric wards (layout, facilities, staff, supplies & equipments), Case management in the ward (Cough or difficult breathing, Diarrhoea, Fever conditions, Malnutrition, HIV/AIDS), Supportive care & nutrition, Monitoring of patients, Neonatal Care (layout and staff, Routine neonatal care and Sick newborn care), Paediatric surgery and rehabilitation, Hospital administration and Access to hospital.

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The adapted assessment tool was used to collect information from all hospitals, January to July 2008. Data was collected by two teams each composed of a pediatrician and a health officer who were trained and also involved in the adaptation of the data collection tool. Four different methods of data collection were used namely; hospital visit, case management observations, records review and interviews of caretakers and providers which took two full days for assessing each hospital. Hospital visit: Direct observation of the hospital layout and structure, OPD attendance, admission rates, availability of essential drugs, availability of diagnostic and therapeutic equipments were made. Areas of doubt were clarified

by interviews. Case observations: The care for admitted children to the hospital was observed without interference from the assessors. This is complemented by discussion of the cases with staff, review of the case records and monitoring charts, and interviewing the caretakers. Records review: Assessors obtain information on the quality of care for admitted and recently discharged patients by checking records. If there are not sufficient patients for direct case observations, assessors reviewed at least 3-5 records for each clinical problem. Interviews: Assessors conducted interviews with hospital staff and caretakers to gain some idea of their perception of care for children in the hospitals.

Each major assessment section consisted of a number of standards and each standard was qualified by several detailed criteria. Thus, each of the 12 sections of the assessment tool was scored based on the standards and the criteria to meet these standards. The standards are the minimum requirements for good quality of care for children as defined by the WHO “Pocket book of Hospital Care for Children, 2005”. The detailed criteria of each standard were rated/scored based on the need for improvement as “good” or “need to be improved”, where “Good” means the criteria is similar to the

standard, and “To be improved” means the component is below the expectation of the WHO standard and needs improvement. A summary score from 5 to 1 was awarded at the end of each section whereby 5 indicates “Good’’ practice complying with standards of care while scores from 4 to 1 indicate practices “To be improved” (4 = Little improvement, 3 = Some improvement, 2 = Considerable/Significant improvement is needed to reach standards of care, and 1 = Services not provided, totally inadequate care or potentially life-threatening practices).

Finally, a total summary evaluation score for complete assessment of all sections was marked in the summary evaluation sheet. The total summary score can assist in monitoring hospital improvements over time and to make also inter-hospital comparisons to some extent.

At the end of each hospital visit, assessors met with hospital administration and staff for a debriefing and to identify priority actions for improvement of the hospital services.

RESULTS

General hospital information All surveyed hospitals had isolated pediatrics OPD and ward except Bishoftu hospital whose pediatric inpatient room was part of the adult medical ward. Separate pediatric waiting area and archive rooms were found in only 3 and 2 hospitals respectively. Six of the 8 hospitals had separate room for admitting paediatric infectious cases while only 3 had separate

room for admitting newborns. In 6 hospitals, children with surgical conditions were admitted in the general pediatric ward. None of the hospitals had a clearly designated high dependency area or room where very sick children are cared for and receive closest attention.

Electricity and running water were available in all hospitals even though most of the hand washing and toilet facilities were non-functional in half of the

hospitals. Five hospitals had backup power supply. All hospitals had appropriate sharp disposal boxes.

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The pediatric service in these hospitals caters for children up to the age of 14 years. Based on available data for the period July 2006 to June 2007, there were on average 29 (range 12-66) children seen in the Paediatric OPD with about 5 admissions per day (range 1-9). The two commonest causes of OPD attendance and admission were severe pneumonia and diarrhoea with severe dehydration or dysentery. The mean bed capacity of the assessed hospitals was 39 (range 11-68) and the average bed occupancy rate was 58% (range 31% in Zewditu & 90% in Ambo). Children under 5 account for 64% of admissions to the pediatric wards. Based on available data from 5 hospitals, the average daily emergency patient load was 7 and the average all cause mortality in under fives was 11% (10-16%).

Hospital support systems (drugs, equipments and laboratory)

As shown in Tables 1 & 2, the availability of emergency drugs and equipments in the emergency area and the wards was inadequate. Drugs like parenteral Phenobarbitone (long acting anticonvulsant) were non-existent and those drugs that were available were often not immediately accessible. Only 3 hospitals had ambu bags (big mask) in the emergency area and the wards while infant size masks, nasal prongs and nebulizers were totally absent. Oxygen concentrator and heat sources were found in only one hospital. However, all hospitals had good laboratory facilities to perform the five basic laboratory tests for managing emergencies (RBS, blood film, HGB, CSF microscopy and blood group and cross match) even though results were delivered timely in half of the hospitals. Bilirubin and other chemistries were being done in 5 while culture facilities were available in only 2 hospitals.

Table 1: Availability of Essential Drugs

No Emergency area Ward Pharmacy/store

Drugs

1 Glucose 40% i.v. 5 (63%) 6 (75%) 7 (88%)

2 Glucose 5% i.v. 6 (75%) 7 (88%) 8 (100%)

3 Normal saline i.v. 6 (75%) 6 (75%) 7 (88%)

4 Ringer’s lactate i.v. 8 (100%) 7 (88%) 8 (100%)

5 Epinephrine (Adrenaline) s.c. 8 (100%) 7 (88%) 7 (88%)

6 Corticosteroids i.v. or p.o. 6 (75%) 5 (63%) 7 (88%)

7 Furosemide i.v. 5 (63%) 5 (63%) 5 (63%)

8 Diazepam i.m., i.v. 5 (63%) 5 (63%) 5 (63%)

9 Phenobarbital i.m., i.v. 0 (0%) 0 (0%) 0 (0%)

10 Paracetamol 6 (75%) 6 (75%) 8 (100%)

11 Ampicillin inj. 6 (75%) 4 (50%) 7 (88%)

12 Benzyl penicillin 5 (63%) 5 (63%) 7 (88%)

13 Cloxacillin 5 (63%) 5 (63%) 6 (75%)

14 3rd generation Cephalosporins 3 (38%) 4 (50%) 5 (63%)

15 Chloramphenicol 3 (38%) 3 (38%) 4 (50%)

16 Gentamicin 5 (63%) 5 (63%) 6 (75%)

17 *All anti-malaria drugs 4 (50%) 4 (50%) 8 (100%)

18 Digoxin 3 (50%) 4 (50%) 6 (75%)

19 F75 milk 2 (25%) 6 (75%) 6 (75%)

20 F100 milk 3 (50%) 7 (88%) 7 (88%)

21 Ready to Use Therapeutic Food 2 (25%) 5 (63%) 6 (75%)

22 Vitamin K i.m. injection 0 (0%) 0 (0%) 3 (38%)

23 ORS 6 (75%) 7 (88%) 8 (100%)

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Table 2: Availability of essential Equipments & supplies

No Equipments Emergency area Ward Pharmacy/ store

1 Resuscitation table/area 5 (63%) 2 (25%) 3 (38%)

2 Torch 4 (50%) 4 (50%) 4 (50%)

3 Otoscope 5 (63%) 6 (75%) 6 (75%)

4 Scales for children 7 (88%) 8 (100%) 7 (88%)

5 Stethoscopes 7 (88%) 7 (88%) 8 (100%)

6 Thermometers 8 (100%) 8 (100%) 7 (88%)

7 Heat source 1 (13%) 2 (25%) 0 (0%)

8 Lumbar puncture set 5 (63%) 6 (75%) 3 (38%)

9 Oxygen source: 7 (88%) 7 (88%) 4 (50%)

oxygen cylinder 7 (88%) 7 (88%) 4 (50%)

oxygen concentrator 1 (13%) 1 (13%) 0 (0%)

central supply 0 (0%) 0 (0%) 0 (0%)

10 Flow-meters for oxygen? 7 (88%) 7 (88%) 5 (63%)

11 Equipment for the administration of oxygen? 7 (88%) 7 (88%) 6 (75%)

nasal prongs 0 (0%) 0 (0%) 0 (0%)

catheters 7 (88%) 7 (88%) 6 (75%)

Masks 0 (0%) 1 (13%) 0 (0%)

12 Self inflating bags for resuscitation 3 (38%) 3 (38%) 2 (25%)

13 Masks

infant size 0 (0%) 0 (0%) 0 (0%)

child size 3 (38%) 4 (50%) 2 (25%)

adult size 1 (13%) 1 (13%) 0 (0%)

14 Butterflies and/or cannulas of paediatric size 7 (88%) 7 (88%) 7 (88%)

15 NG-tubes, paediatric size 4 (50%) 7 (88%) 7 (88%)

16 Suction equipment 5 (63%) 7 (88%) 6 (75%)

17 Nebulisers for administration of Salbutamol 0 (0%) 0 (0%) 0 (0%)

Emergency care Most of the surveyed hospitals (5/8) were not appropriately organized, fully staffed and equipped to handle pediatric emergencies effectively. Most of these hospitals were not practicing the standard triage process by assessing children immediately on arrival for emergency or priority signs before administrative procedures. However, three hospitals, two of them implementing the new hospital improvement initiative, had assigned qualified nurses

at the reception to facilitate smooth patient flow and prioritization of the management of emergency cases. Even in these three hospitals the triaging and management of emergency cases was not up to the expected standards of ETAT. None of the staff working in the OPD and emergency areas had been trained in ETAT and there was lack of job aids and standard protocol for pediatric referral care (Table 3).

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31 Table 3: Summary of grading of the emergency setup in the hospitals

No Standards and criteria Good To be

improved

1 Children are assessed for severity/ priority signs (triaged) immediately on arrival as per the ETAT standard

0 (0%) 8 (100%)

2 Patients do not have to wait for their turn, registration, payment etc. before a first assessment is done and action taken.

0 (0%) 8 (100%)

3 A wall chart or job aid for identifying children by severity of condition is located in the emergency admissions area.

0 (0%) 8 (100%)

Drugs, equipment and supplies

4 Essential drugs for emergency conditions (anticonvulsants, glucose, iv fluids) are always available and free of charge to the family

0 (0%) 8 (100%)

5 Essential lab tests (glucose, Hb or PCV) are available and results are obtained timely 4 (50%) 4 (50%)

6 Essential equipment (needles and syringes, naso-gastric tubes, oxygen equipment, self-inflating resuscitation bags with masks of different sizes, nebulisers or spacers) is available

0 (0%) 8 (100%)

Staffing

7 A qualified staff member is designated to carry out triage. 3 (38%) 5 (63%)

8 A health professional is available without delay to manage children determined to have an emergency condition.

3 (38%) 5 (63%)

Case management

9 Staff doing triage is trained in the ETAT guidelines and can implement them appropriately when the emergency room gets busy during peak hours

0 (0%) 8 (100%)

10 Staff is skilled in the management of common emergency conditions and starts treatment without delay: Management of convulsions, lethargy, severe respiratory distress, shock and severe dehydration.

0 (0%) 8 (100%)

Pediatrics ward

Table 4 summarizes the status of the 8 hospitals against the WHO standards and criteria for pediatric wards.

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33 Table 4: Standard's for children ward

No Standards and criteria Good To be improved

1 Children are seen in OPD only by the designated health professional in the designated room/area.

6/7 (86%) 1/7 (14%)

Closest attention for the most seriously ill

2 The most seriously ill children are cared for in a section where they receive closest attention.

0 (0%) 8 (100%)

Separate ward for children.

4 Children are kept in a separate ward or separate area of a ward. 7 (88%) 1 (13%)

5 Severely ill children are kept apart from adults in wards such as for infectious diseases or intensive care.

4 (50%) 4 (50%)

6 Children with surgical conditions are at least kept in a separate room, with staff aware of the special needs for children such as feeding and warmth.

3 (38%) 5 (63%)

7 Arrangements are made to meet these needs. 1 (13%) 7 (88%)

8 In cold climates, the ward has an efficient and safe heat source. 0 (0%) 8 (100%)

Separate room for sick neonates with mothers

9 Sick new-borns are kept separate from healthy babies. 3 (38%) 5 (63%)

10 Mothers of sick new-borns are rooming in with their babies, and have adequate facilities. 0 (0%) 8 (100%)

Hygiene and accident prevention

11 Staff has access to hand washing facilities The ward is kept clean and dangerous items are inaccessible for children

3 (38%) 5 (63%)

12 Sharps are disposed of in a special container preventing accidents 8 (100%) 0 (0%)

Hygienic and sufficient services facilitate the stay of mother and child

13 There are sufficient and adequate toilets which are easily accessible 0 (0%) 8 (100%)

14 Mothers have access to running water and to an appropriate space, near the ward, to wash themselves and their child.

0 (0%) 8 (100%)

15 Mothers have access to a washing facility, in order to wash her and her child’s clothes. 0 (0%) 8 (100%)

16 Patients are kept in a bed/cot with a clean mattress. 4 (50%) 4 (50%)

17 Patients receive bed sheets 6 (75%) 2 (25%)

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Case management practices Overall, the case management of common childhood problems including pneumonia, diarrhea, fever conditions and malnutrition was not optimal in almost all hospitals. Pneumonia was diagnosed and its severity correctly classified more or less based on diagnostic signs in 2 hospitals. Similarly, appropriate use of antibiotics and oxygen was observed in a third of the hospitals (3/8). Patient monitoring and supportive care were inadequate in all hospitals. None of the hospitals had nebulizers for inhalation therapy. Correct assessment of dehydration was documented in half of the hospitals and the monitoring and management of dehydration was inadequate in almost all hospitals. Inappropriate use of antibiotics for diarrhea was observed and supportive care especially feeding was inadequate.

In the majority of cases, differential diagnosis of fever was not considered exhaustively and investigations were incomplete. In some instances planned LP tests were not done and patients were treated empirically. Inappropriate choice and administration of antibiotics was observed and documentation of patient progress and treatment given was not up to the standard in almost all hospitals. Overall, patient records and monitoring charts were poorly recorded. Most of the hospitals had the dietary supplies needed for the management of severe malnutrition. Even though routine antibiotics were given for malnourished children as per the national guideline, feeding was not given according to the recommended schedule especially at night. Prevention and management of other complications like dehydration and hypothermia was inadequate. None of the surveyed hospitals had rooms with heaters for malnourished children. Monitoring of patients and recording of progress was poor in the majority of cases.

All the necessary guidelines and tools were in place for counseling, diagnosing and staging of paediatric HIV and for the treatment and monitoring of antiretroviral therapy. There were well trained staff who were regularly mentored and most of the HIV

services were conducted in line with the national standard especially at the outpatient level. However, inpatient management of some opportunistic infections and the supportive care of these patients need improvement.

Supportive care and nutrition Although breastfeeding was encouraged, none of the hospitals provide appropriate routine pediatric diet for children. Misuse of intravenous fluids was common including in children with severe acute malnutrition.

Multiple antibiotics were often prescribed some times for longer durations. Screened blood was used in all hospitals but the indications for its use and the administration procedure needs improvement.

Monitoring of patients All admitted children were assessed by a doctor at admission and majority of them were re-evaluated about once a day during working days and upon consultation during weekends. A qualified nurse was available 24 hours per day in the children's wards in all hospitals and a medical doctor in 6 of them. Nutritional status was assessed at admission using weight for age in most hospitals. All patients had individual charts, vital sign and medication sheets, but the case histories, progress notes and the other

monitoring charts were not properly and regularly recorded in the majority of cases both by physicians and nurses. There was no designated area where very ill children receive highest attention. Except for the Severe Acute Malnutrition Chart, there were no standardized monitoring charts consisting of all relevant parameters which could simplify patient monitoring.

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Neonatal care

Early and exclusive breastfeeding, skin to skin contact and proper thermal protection was not practiced adequately in almost all hospitals. Eye and Vitamin K prophylaxis and immunizations were given routinely in only 2 hospitals. Neonatal resuscitation flow chart was available in only one hospital. Overall, only three hospitals had a separate room for sick newborn babies with bed capacity ranging from 3 to 17. In the other 5 hospitals neonates were kept in the general pediatric ward or the maternity room. Only

one hospital was well staffed and equipped (heaters, oxygen sources, phototherapy and suction machines, resuscitation materials and other supplies) to closely monitor seriously ill newborns with 24 hour availability of skilled nursing staff. However, rooming-in and hygienic facilities for mothers were inadequate in all hospitals. As shown on Table 5, the case management of common neonatal problems is inadequate and needs strong effort to improve the situation.

Table 5: Sick newborn case management summary table

No Good To be improved

1 Neonatal sepsis is appropriately diagnosed. 2/6 (33%) 4/6 (67%)

2 Neonatal sepsis is appropriately treated. 1/6 (17%) 4/6 (67%)

3 Specific feeding needs of sick young infants and those with low birth weight, are met.

1/6 (17%) 5/6 (83%)

4 Jaundice is adequately recognized and managed. 1/6 (17%) 5/6 (83%)

Pediatric surgery & rehabilitation Of the 8 hospitals surveyed, one (Ambo Hospital) was not doing any major surgery for children. In 6 of the hospitals, children with surgical conditions were admitted in the general pediatric ward. Pre- and post-operative starving was kept to a minimum in the majority of the hospitals which perform major surgery. Overall, frequent post-operative monitoring of vital signs and the readiness for resuscitation was inadequate in nearly half of the hospitals. Only one hospital had basic rehabilitation facilities.

Hospital administration & access to hospital Nationally, there were no pediatric treatment guidelines for referral hospitals and none of the hospitals practice pediatric death audits. Availability of essential drugs and equipment that are basic for provision of quality pediatric emergency and inpatient services are inadequate in almost all of the hospitals surveyed. However, the handling of available drugs including the stock management was good and old drugs were used first.

Economic and transportation barriers were serious concerns for all the care takers interviewed and most of them had tried traditional medicine before seeking care from providers. Caretakers were not satisfied with the communication from providers regarding the problems of their sick children, explanations about ward procedures and the treatments and follow-up details. Almost all care takers indicated that the

condition of the toilet and washing facilities was very poor.

Summary The following table and figures 1 & 2 show the summarized score by major sections of the assessment and by facility. Table 6 is a summary sheet showing the details of the summary scores of the 8 hospitals in the different service areas.

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Table 6: Details of summary score of the 8 hospitals in the different service areas

No Summary score of different service areas Good To be improved

5 4 3 2 1

1 Essential drugs, supplies and equipment ** 5 3

2 Laboratory support 6 2

3 Emergency area and management 6 2

4 Children's ward and facilities 8

5 Cough or difficult breathing child management 2 1 5

6 Diarrhoea patient management 2 6

7 Febrile child management 2 5 1

8 Malnourished child management 1 7

9 Management of child with HIV/AIDS 3 5

10 Summary score of supportive care 6 2

11 Summary score in monitoring 4 4

12 Routine neonatal care service 1 6 1

13 Neonatal Care Unit facilities 1 1 6

14 Case management and sick newborn care 1 7

15 Paediatric surgery and rehabilitation 2 4 1 1

16 Summary score hospital administration 4 4

17 Summary score access to hospital 5 3

Total score = 405 30 84 222 68 1

Hospital summary score = total score / 8*17 2.98

NB: - ** = Five of 8 hospitals had a summary score of 3 out of 5, while 3 hospitals has a summary score of 2 out of 5 for emergency drugs, supplies and equipment section.

Similarly, Figure 1 shows average scoring of the quality of the different pediatric care services in the 8 hospitals out of a maximum score of 5. As it can be seen clearly from the figure, there are marked variations in quality of the different pediatric

care/services rendered. The quality of care given to children with HIV/AIDS is relatively in far better condition compared to services given to neonates, scores of 4.4 and 2.3 out of 5 respectively.

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Figure 1: Average summary score of the different pediatric care services out of a maximum score of 5

As shown in Figure 2 below, the hospitals’ quality of

care total summary score ranged from 2.6 to 3.44 out

of 5 with an average of 2.98 (~3.0) which indicates

that all hospitals need substantial actions for

improvement to reach defined standards. This figure

also shows the difference in the performance of the

eight hospitals.

4.4

3.8

3.6

3.3

3.3

3.1

3.0

3.0

2.9

2.8

2.8

2.6

2.6

2.5

2.5

2.4

2.3

0.0 1.0 2.0 3.0 4.0 5.0

HIV/AIDS mgt

Laboratory support

Cough mgt

Diarrhoea mgt

Malnutrition

Febrile child mgt

Ward and facilities

Routine neonatal care

Surgery and rehabilitation

Emergency area & mgt

Supportive care

Ess drugs & equipment

Access to hospital

Monitoring

Hospital administration

Neonatal Care Unit facilities

Sick newborn care

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Figure 2: Total summary score of the 8 hospitals, out of a total score of 5

CONCLUSIONS AND RECOMMENDATIONS

This assessment has the following limitations. First,

sampling of the hospitals was by convenience;

majority of them being zonal hospitals the results may

not fully reflect the situation in the more peripheral

district hospitals. Second, the study was largely

observational and assessments were in part based on

the judgments of the observers. Besides, the quality

of available hospital statistics was inadequate to

disaggregate patient load at OPD, emergency and

admission levels by appropriate age categories (0-28

days, 1-12 months, 1-5 years and > 5 years). The

statistics problem definitely under-estimates the

reported hospital mortality rate. Similarly, it was

impossible to determine the mortality rate within the

first 24 hours of admission which is a very sensitive

indicator of the quality of emergency care in any

hospital setting.

Despite the potential limitations, this study provides

some basic information about the status of pediatric

hospital care that could guide the national efforts in

improving the quality of referral care for children.

The overall case fatality rate of 11% (10-16%) in this

survey was comparable to that reported from Zambia

(12-15.8%) and Kenya (4-15%) but the possibility of

under-reporting is there.

All of the surveyed hospitals were not appropriately

organized and fully equipped to handle pediatric

emergencies effectively. None of these hospitals were

practicing the standard triaging process by assessing

children immediately on arrival for emergency and

priority signs & the overall management of emergency

cases was not up to the expected standards of ETAT.

In the majority of the surveyed hospitals (5/8), there

were no separate pediatric waiting areas which are

3.12.9 2.9

2.6

3.0

3.4

3.1 3.0

0.0

1.0

2.0

3.0

4.0

5.0

Adama Ambo Bishoftu Debre Birhan Dessie Yekatit 12 Yirgalem Zewditu

Hospitals

sco

re

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essential for the proper implementation of ETAT.

Even though the current quality improvement process

through the hospital BPR initiative is a very good

opportunity for the overall improvement of hospital

care for children, the centralized triaging mechanism

that keeps patients of all age groups together in one

waiting area is not conducive for the effective

implementation of the ETAT standards.

Generally, there was lack of some essential drugs

and materials such as nasal prongs, infant and child

size bag & masks, nebulizers, heaters and oxygen

concentrators. The total absence of long acting

parenteral anti-convulsants poses serious

shortcoming in the management of pediatric

neurologic emergencies.

In almost all hospitals, there was no clearly

designated and properly arranged/equipped high

dependency area where very sick children receive

highest attention. Majority of the hospitals (5/8) do not

have any special arrangement and facilities for

providing appropriate neonatal care.

Hygienic facilities were below the expected standard

in majority of the hospitals and none of the hospitals

provide appropriate routine pediatric diet for children.

Overall, the case management of common neonatal

and childhood illnesses was not optimal. None of the

hospital staff had been trained in ETAT and there

were no job aids or protocols for pediatric referral

care which could partly contribute to the problems

observed in the case management.

In summary, the quality of pediatric referral care needs serious attention and coordinated systematic improvement effort using the opportunity of the national hospital management initiative and the BPR process to institutionalize ETAT and standards of hospital care for children. This has to be complemented with availing of appropriate job aids, essential supplies and equipment, and improvement of health worker skills through training, clinical mentoring and regular supportive supervision.

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RECOMMENDATIONS

1. The ETAT standards should be incorporated into the Ethiopian Hospital Management Initiative blue print and the

BPR documents by the FMOH to ensure its systematic implementation.

2. National plan of action should be developed for systematic and phased implementation of ETAT in referral

hospitals.

3. Staff should be trained in ETAT through in-service courses & ETAT should also be introduced into the pre-service

teaching to ensure its sustainability.

4. National pediatric referral care protocol & job aids should be availed in all hospitals

5. Coordinated efforts and more resources needed for availing essential drugs, supplies and equipments in all

hospitals.

6. All hospitals should have arrangements/rooms for the care of sick neonates, high-dependency areas for critically

sick children and isolation rooms for infectious cases.

7. Efforts should be made to improve the hygienic facilities & the quality of routine hospital diet for children.

8. The recording and reporting system in the hospitals need to be improved and pediatric data should be

disaggregated by appropriate age categories.

9. Mechanisms for regular supportive supervision and mentoring needed to achieve sustained improvement in the

quality of pediatric referral care.

10. The Ethiopian Pediatric Society, the Medical teaching institutions, WHO, UNICEF and other partners should

support the quality improvement process.

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ACKNOWLEDGEMENTS

We would like to thank the FMOH especially the former Family Health and Health Services Departments, the Directors and staff of the surveyed hospitals for facilitating the whole process. We are very grateful to the World Health Organization for the financial and technical support provided for the assessment. Sincere gratitude is expressed to Dr Neghist Tesfaye (FMOH), Dr Teshome Desta (WHO/ICST-ESA), Dr Wilson Were (WHO/HQ) and Prof. Elizabeth Molyneux (Queen Elizabeth Central Hospital, College of Medicine, Blantyre/Malawi) for their valuable technical support.

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42Management of severe acute malnutrition in children using community based therapeutic care approach:

a review of three years data from southern Ethiopia.

Efrem Teferi, MD1, Shiferaw Teklemariam, MD, MPH1 , Lopiso Erosie, BSC, MPH1 , Abel Hailu, MD1

Tefera Belachew, MD, MSc, DLSHTM2, Mohammed A Yassin, MD, MSc, PhD1,3

Abstract

The objective of the study is to assess the outcome of community-based therapeutic care (CTC) for children with severe

malnutrition in Southern Ethiopia. Diagnosis of severe malnutrition was made based on anthropometric measurement and

all children received therapeutic food according to the protocol and were discharged from the feeding program when they

their weight for height was more than 80% of the reference for 2 consecutive weeks. Data on the number of admissions,

discharges, weight gain and length of stay in the program were recorded using standard formants and reports were sent to

the Regional Health Bureau monthly. The data was entered using EPI-Info proportions and means were compared using

chi-square test. This is a retrospective review of reports retained in the Bureau. A total of 12,316 patients with severe acute

malnutrition, 56.2% marasmic and 43.8% kwashiorkor cases were treated in CTC program from 2003 to 2005. The average

cure and death rates were 91% (9871) and 2.5% (217) and the average weight gain was 5.3 and 5.8 grams /kg/day and the

average length of stay was 49 and 42 days for cases of Marasmus and Kwashiorkor, respectively. Except for weight gain

and length of stay, our findings exceeded the minimum sphere standards for treatment outcome measures. In conclusion

the CTC approach has a comparable outcome to Therapeutic feeding centers and could be expanded quickly during

emergency situation. As majority of patients are treated at home, the workload for the health worker would be reduced, so it

is an alternative approach for management of severe malnutrition where human resource and space in health facilities are

limited.

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Introduction

Ethiopia has a long history of food insecurity and nutritional problems affecting a large proportion of the population. (1) Even during a relatively non-drought years, malnutrition in children in Ethiopia is extremely high exposing the survival of this group of the population at a great threat. An estimated 47% of Ethiopia’s under-five children are moderately or severely stunted contributing to an under five-mortality rate of 123/1000 live births. (2) Ethiopia stands 6th among countries with the highest number of under-five deaths in the world, with more than 472,000 under-five dying each year, (3) Malnutrition, even in its milder form, accounts directly or indirectly for 53% of all under-five deaths in Ethiopia (4). The Southern Nations, Nationalities and Peoples Regional State (SNNPR) is located in southwestern part of the country and has a population of about 14 million. The region is divided into 14 administrative Zones and 8

special Woredas (districts) with a total of 104 Woredas. There are 56 nationalities in the region , which gives it the unique feature in encompassing rich and diverse culture. According to the 2005 Regional Health Bureau annual report, there were 16 hospitals, 160 health centers, 1336 health posts with potential health service coverage of 50%. The regional ; DPT3 coverage was 90%, family planning 47%, antenatal care 60% and deliveries attended by health professionals of 18%. The major causes of mortality among children under five years of age are pneumonia, diarrhea and malaria. Malnutrition has become a common feature occurring in the region in recent years with large-scale famines reported in 2003 and cases continuing to be reported. Dependency on rainfall, poor resource management, uncontrolled population growth, poor farming planning and limited food reserves of households complemented with failure of rains in 2002 exacerbated the living condition of vulnerable communities leading to exhaustion of coping mechanisms.

In response to the recent famine, many international humanitarian agencies and the government opened Therapeutic Feeding Centers (TFC) to mitigate the crisis. A Decentralized therapeutic program was initiated with Concern, Save the Children US in collaboration with other international organizations. In 2004, the Ministry of health in cooperation with UNICEF initiated enhanced outreach strategy (EOS) for child survival. This involves screening for malnutrition, Vitamin A supplementation, strengthening immunization and health education for child survival and was started in 54 woredas of the region (17) and expanded to the entire region in 2006. Improvement in child survival is strongly associated with decrease in malnutrition in countries characterized by high rates of general malnutrition such as in Ethiopia (5-7). To reduce mortality due to severe acute malnutrition, TFCs were established in SNNPR in 2003, which provided a high quality individual inpatient care and

patients receive formula 75 (F75) and formula 100 (F100) milk with routine drugs (18). A high cure rate (87.2%) and a relatively low death rate (3.6%) was reported from 25 TFCs opened in the region in 2003-05 with an average length of stay of patients of 21-25 days (8). This high intensive care phase of treatment is very important for patients with complicated malnutrition associated with anorexia, septicemia, hypothermia, hypoglycemia and severe dehydration. However, management of children with malnutrition in TFC requires skilled staff, room for inpatient care, materials including bedding, cooking utensils and caretakers’ food (8-11). The centers were opened and ran by non-governmental organizations (NGO) and coordinated by the regional health bureau. When the activities were integrated into the routine health services and handed over to health facilities, it was difficult to continue with the limited work force, space and resource in the facilities.

-4- The traditional model of inpatient treatment of severe acute malnutrition (SAM) does not consider the social aspects of management of malnutrition and hence has high opportunistic costs to mothers/care givers (9). Mothers/care givers had to stay in centers for several weeks leaving their other children and family members at home and hindering them from their daily activities. Community therapeutic care (CTC) is a nutritional

intervention designed with the capacity to address SAM in both emergency and development contexts (9). Its underlying aims are to maximize coverage and access. In practice, this means giving priority to provision of care for acutely malnourished over inpatient care for a few extreme cases.

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44CTC was introduced in SNNPR in 2003 and expanded in 2004 and 2005. It integrates supplementary and therapeutic feeding with an emphasis on outreach and community based support. In out patient therapeutic program (OTP), the therapeutic product used is ready to use (plumpy nut and BP 100 biscuit) with outpatient drug treatment protocol. There were few referrals for inpatient treatment, which includes those with complication and who were admitted in stabilization centers (SC) and

treated for few days and referred to OTP like in phase one TFC (13). During emergency, CTC approach can quickly provide good coverage and treatment for a large number of severely malnourished people. This paper reviews reports of CTC to assess the outcome of malnourished children treated in community therapeutic care established in the southern Ethiopia and compared with the results of children treated in TFC.

Materials and methods

Children with severe acute malnutrition were admitted to therapeutic care established in response to the famine encountered in the region. Diagnosis of severe malnutrition was made based on anthropometric measurement and brief examination for bilateral pitting pedal edema. At admission, patients were assessed for hydration, anemia and signs of infection. Patients were given oral doses of Vitamin A, Folic acid, Amoxicillin (5-day course), Mebendazol, treated for dehydration with Resomal and given ready to use therapeutic food (RUTF) according to the protocol (18). Patients were discharged from the outpatient therapeutic feeding program when their weight for height was more than 80% of the reference for 2 consecutive weeks and if they did not have signs of infection. They were followed in supplementary feeding program until they reach 85% of the reference for 2 consecutive weeks. At each follow up visit, weight, extent of pitting edema, presence of infection and treatment were recorded. In CTC, plumpy

nut was used instead of F100. The main difference between F100 and plumpy nut is that part of dried skimmed milk in the F100 was replaced with peanut butter (with a 25% total weight). Plumpy nut has an energy density 5 times more than that of F100. Plumpy nut was used in all the centers except for few weeks when BP100 was used due to shortage of plumpy nut.Data on the number of monthly admissions, discharges, average weight gain and length of stay in the program were recorded in each therapeutic centre using standard formants and reports were compiled by the health facilities and NGOs supporting the programs and were sent to the Regional Health Bureau (RHB) monthly. The data was entered using EPI- Info programme(CDC Atlanta) and analyzed using descriptive statistics, proportions and means were compared using chi-squared test and p values value <0.05 was considered as significant.

This is a retrospective review of reports retained in the RHB. All reports from CTC sent to RHB were included in this paper, except reports of 243 cases from Kembata Tembaro zone and 44 admissions from Sidama Zone

because of incompleteness. Patients who were defaulters, referrals and non-respondents were excluded as their outcome was not known. Ethical approval was obtained from the SNNPR Health Bureau.

Results

A total of 12,316 patients with severe acute malnutrition, 56.2% marasmic and 43.8% kwashiorkor cases were treated in CTC program from 2003 to 2005. Of these, 1540 (12.5%) were treated in 2003, 1955 (16%) in 2004 and 8791(71%) in 2005. The majority (90%) of the cases were age between 6 months to 5 years old. The average cure and death rates for the region were 91% (9871) and 2.5% (217) respectively. The highest (99%) cure rate

was recorded in Boricha and Damot Gale districts (Woredas), while the lowest cure rate (80.6%) was observed in Malgano in Sidama zone. Death rate above minimum standard was not reported from any of the CTC, the highest death rate (8.4%) was reported from Bedessa and the lowest (0.4%) in Arbegona as shown in Table 1.

The number of admissions was not the same as the number of cases discharged, as some of the cases were on follow up when the report was compiled. There were also cases that defaulted from the program, referred to other places and non respondents making the total

number of cases discharged higher than the sum of deaths and cured cases. The average weight gain for the region was 5.3 and 5.8 grams /kg/day for cases with Marasmus and Kwashiorkor, respectively. The average length of stay was 49 and 42 days for marasmic and Kwashiorkor cases, respectively (p > 0.05 for both) as shown in Table

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452. The outcome of patients treated in CTC was comparable to those treated in TFC in the region during

the same period with cure rate of 91% vs. 87% (p>0.05) and death rates of 2.5% vs. 3.6% (p>0.05), respectively.

However, there was statistically significant difference in the mean length of stay which were 21 and 25 vs. 42 and 49 days for marasmus and kwashiorkor patients respectively and the average weight gain of 13.4 and14

vs. 5.3 and 5.8 g/kg/day for patients treated in TFC than in CTC (p<0.01 for both) (Table 3). A similar trend was observed when the outcome from the CTC program was compared to the sphere standard as shown in Table 4.

Discussion

Given the spatial arrangement of health service units and their limited capacity to handle a large number of cases of severe acute malnutrition during emergency and crisis in Ethiopia, seeking an alternative solution for management of such cases cannot be overlooked. Community base therapeutic care provides a promising alternative option to the TFCs and facility-based stabilization centers (9-12). Though CTC cannot totally replace an inpatient therapeutic care as some cases with complications, such as infections, may still need an inpatient care, it is complementary to therapeutic and supplementary feeding programs (9).

The experience in implementing therapeutic feeding programs in the region in the last few years enabled us to understand and expand CTC very quickly. The total number of cases treated in the region (12,316) was sizable enough to assess the outcome of the therapeutic feeding programs. Overall, the outcome of patients treated in the CTC approach were promising considering the minimum sphere standards for the outcome indictors of therapeutic feeding programs (9-11,15,). In addition, CTC handles the majority of cases by creating access and capacity which is very difficult to meet during emergency situation (9-11). The outcome of children treated by the CTC approach in the SNNPR exceeded the minimum standard for both cure and death rates although the average weight gain was low and the average length of stay was longer. The latter may be due to sharing of RUTF with siblings within the family as patients in CTC are treated at home. Our results are similar to the findings in study done in Badewacho in Hadiya in SNNPR, which reported a cure rate of 85% and death rate of 4%, mean weight gain of 4.8 g/kg/day with a mean length of stay of 42 days among 170 children treated in CTC (16). The results of our study were better compared to findings reported from other parts of

Ethiopia (Amhara, Oromia) and other African countries (Sudan, Malawi, and Niger) (13,17). The average length of stay was also shorter than results in other parts of Ethiopia, which reported 36-91 days with a similar average weight gain from studies in other parts of Ethiopia (3-6.5 g/kg/d) but less than those reported from other parts of Africa (4.2-10g/kg/day). (13, 17)

The cure and death rates of patients treated in CTC was comparable with those treated in TFC in SNNPR during a similar period. However, the duration of stay was shorter and the mean weight gain was much better for patients treated in TFC than those treated in CTC program. This could be due to the unavoidable sharing of RUTF with siblings and even adults where the bulk of the treatment period in CTC approach is based at home. The fact that most of the data from TFC were collected during emergency and data from the CTC were collected during non-emergency situation makes comparison difficult. However, according to reports (data not shown) from Boricha district from where data from TFC and CTC programs were collected during emergency situations in 2003 and 2005, the treatment outcome was similar confirming that CTC program was effective even during emergency situation. It was observed that inpatient treatment schemes had no additional advantage over CTC except the higher average weight gain obtained compared to the workload it incurs to health workers and the difficulty to admit all patients with the limited space and health professionals available in the health facilities.

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46The limitation of this study was the fact that it was based on a retrospective record review and there

was no information on the follow up of individual cases and suffers incompleteness and missing data.

In conclusion CTC as a new strategy for management of severe malnutrition was successfully implemented in SNNPR. It has a high coverage, low cost and could be expanded very quickly in emergency situations. The majority of patients can be treated in the outpatient program without disrupting caregivers from their daily activities and only very few patients who had infections and very severe malnutrition required inpatient care for few days. The product used in CTC was ready to use therapeutic food (plumpy nut, BP 100 biscuit) and could be implemented as an outreach and by Health Extension Workers.

CTC is an alternative approach for management of severe malnutrition where shortage of health professionals and limited space for admission are the major hurdles. However, problems including shortage of health professionals, drugs, therapeutic products, transportation, lack of space to admit complicated cases, misunderstanding among some who consider CTC as an NGO business, lack of training and high turnover of health workers should be anticipated during integration of CTC into the routine health system. As CTC is a community based approach, deployment of health extension workers in the region in the recent years would be a good opportunity for outreach activities including follow up and referral of cases in the villages.

For the CTC to be taken, scaled up and to be part of the routine service, continuous in-service training of health professionals, inclusion of CTC to the pre-service training, facilitation of transportation of materials required for CTC, local production of therapeutic food and integration of CTC into the routine health service is recommended. The program should be supported with proper nutrition behavioral change communication on infant and young children feeding so that to prevent malnutrition and its recurrence.

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47

-11-

Table 1: Outcome of cases of severe acute malnutrition treated in the CTC program from 2003-

2005, South Ethiopia

Zone Woredas

Number of cases Admitted

Treatment Outcomes

Cured Death Total Discharged N Percent N Percent

Silte Dalocha 762 631 92.79 19 2.8 680 Lanfuro 907 795 88.24 21 2.3 901

Sidama Malgano 1159 815 80.61 14 1.4 1011 Boricha 1255 1140 98.96 16 1.4 1152 Arbegona 248 215 93.48 1 0.4 230 Bensa 213 61 89.71 2 2.9 68 Bedessa 399 206 86.92 20 8.4 237 Shebedino 575 495 95.56 7 1.4 518 Awssa Zu. 748 479 89.53 11 2.1 535

Wolaita Boloso Sore 2593 2408 93.12 43 1.7 2586 Offa 801 641 86.50 20 2.7 741 Damot Gale 578 514 98.66 4 0.8 521 Humbo 159 142 95.30 5 3.4 149 Sodo Zurria 278 185 89.37 9 4.3 207

Kembata T. Modulla 313 141 86.50 6 3.7 163 Konso Karat 1328 1003 88.60 19 1.7 1132

Total 12316 9871 90.9 217 2.5 10831

CTC = Community based Therapeutic care, N = Number

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48

-12-

Table 2: Mean length of stay and average weight gain for cases of severe acute malnutrition

admitted to the Community based Therapeutic care program from 2003 to 2005, South Ethiopia.

Centers

Average length of stay in

days

Average weight gain in gram/kg/day

Marsmus Kwashiorkor Marasmus Kwashiorkor

Dalocha 63 47 5.2 4.0

Lanfuro 61 40 5.6 5.1

Malgano 37 32 7.8 10.0

Shebedino 40 32 4.6 5.0

Awassa Zu. 59 47 3.0 2.8

Arbegona 58 50 5.2 4.4

Boricha 45 32 6.0 5.5

Bedessa 70 66 3.0 18.0

Offa 62 52 3.9 3.1

Sodo Zur. 40 42 7.5 4.8

Boloso So. 58 52 5.0 4.2

Damot Ga. 36 33 5.4 4.4

Humbo 41 30 5.5 3.8

Modulla 32 30 5.3 6.3

Karat 39 37 6.0 5.6

Regional average 49.4 41.5 5.3 5.8

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49

-13-

Table 3: Comparison of outcome of patients treated in TFC and CTC

in the southern region treated during similar period (2003-2005)

CTC = Community based Therapeutic care, TFC = Therapeutic Feeding Centre

-14-

Table 4: Outcome of children treated by the Community based Therapeutic care e program from 2003- 2005 compared to the minimum sphere standard, South Ethiopia.

Indicator Sphere standard* Our Study findings

Cure rate >75% 90.9%

Death rate <10% 2.5%

Mean weight gain >8grams/kg/day 5.34-5.8 gram/ kg/ day

Mean duration of stay 30-40 days 42-49 days

Program Cure rate

Death rate

Average length of stay (day)

Average weight gain (g/kg/d)

Marasmus Kwashiorkor Marasmus Kwashiorkor

TFC 87.2 3.6 25 21 14 13.4

CTC 91 2.5 49 42 5.3 5.8

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*Guideline for management of severe acute malnutrition,FMOH,2007, Referrence.22

References

1. Birhane G. Running a national early warning system: the Ethiopian experience, Addis Ababa Relief

and Rehabilitation commission, 1991.

2. CSA & ORC Macro (Central Statistical Authority (Ethiopia) and OCR Macro), 2006, Ethiopia

Demographic and Health Survey 2005. Addis Ababa, Ethiopia and Calverton, Maryland, U.S.A:

Central Statistical Authority and OCR Macro.

3. Robert E Black, Saul S Morris, Jennifer Bryce. Where and why are 10 million children dying every

year? The Lancet 2003;28: 361,

4. BASICS II. Basic support for institutionalizing child survival. The Second Child Survival Revolution,

Summary of the Lancet Child Survival Series: BASICS II, 2003.

5. Pelletier, D., & E. Frongillo. 2002. Changes in Child Survival are Strongly Associated with

Changes in Malnutrition in Developing Countries. FANTA, Academy for Educational Development:

Washington DC, USA.

6. Federal Ministry of Health, Family Health Department. National strategy for child survival in

Ethiopia, Addis Ababa, July 2005.

7. WHO. Reducing severe and moderate malnutrition in Children. Bull WHO 1995, 73(4): 443-48.

8. Teferi E et al. Treatment Outcome of children admitted to Therapeutic Feeding centers in Southern

Region. (in press).

9. De Waal, A. Taffesse, L. Carruth . Child survival during the 2002–2003 droughts in Ethiopia,

Special Issue: Humanitarian Crises: The Emergency Rooms of Global Health, Taylor &

Francis,June 2006, 1(2).

10. Collins S, Dent N, Binns P etal. Management of Sever acute Malnutrition in children: Review,

online www.thelancet.com September 25, 2006.

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51

11. Collins, S. ‘Changing the Way we Address Severe Malnutrition during Famine’. The Lancet 2001,

358:498-501.

12. Collins, S. and Sadler, K. ‘The Outpatient care for severely malnourished children in emergency

relief programs: a retrospective cohort study’. The Lancet 2002, 360:1824-30.

13. Community based therapeutic care (CTC) in Ethiopia. Proceeding of workshop in Addis Ababa,

Ethiopia, 22- 23 June 2004.

14. Federal MoH/UNICEF/MOST. Guideline for enhanced outreach strategy (EOS) for child survival

interventions, revised version, Addis Ababa. July 2005.

15. EL HadjiIssakhaDiop, Nicolle Idohou, Marieb am Adeline Ndour, Andre Brined and Salimata Wade.

Comparison of

the efficacy of ready to use food and liquid milk Based diet for rehabilitation of severely

malnourished children. Am Clin Nutr 2003; 78: ; 302-7.

16. Steve Collins, Kate Sadler, Outpatient care for severely malnourished children in emergency relief

programmes; a retrospective Cohort study. The Lancet 2002;360;1824-30.

17. Community based approach to managing severe malnutrition, Proceedings of an interagency

workshop, Dublin October 2003.

18. Federal Ministry of Health . National guideline for the management of severe acute malnutrition for

Ethiopia. MoH, Addis Ababa, May 2004.

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Acknowledgments

We would like to thank members of Laboratory and Research Department for their valuable comments on

the draft. We also thank save the children USA, International Medical Corpus, Action Contra La Faim for

helping to implement the program and health workers in zones and woreda for working hard to save the

lives of patients. I t would have been difficult to implement the program with out the help of UNICEF (United

Nations Children’s Fund), who provided therapeutic products drugs, and conducted trainings in cooperation

with Regional Health Bureau.

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53

CHILD SURVIVAL: PROGRES TOWARDS MEETING MDG4

Assaye Kassie1

Abstract Few causes are responsible for the majority of under-five deaths in Ethiopia: pneumonia (28%), neonatal causes (25%), malaria (20%), diarrhea (20%), measles (4%) and AIDS (1%). To prevent these deaths, and to achieve Millennium Development Goal 4 (MDG4) (“to reduce by two thirds, between 1990 and 2015, the under 5 mortality rate”), it is necessary to ensure the implementation of cost-effective interventions that are listed in the National Child Survival Strategy. There are examples of remarkable achievements in coverage increase within short time periods, including training of 30,000 Health Extension Workers (HEWS) in the last 4 years, rapid increase, from 1% in 2005 to 42% in 2007, in percentage of children under the age of five years who slept under a Long Lasting Insecticide-treated Nets (LLINs), and increase in coverage of Vitamin A supplementation from 45 % in 2005 to 91% in 2007. These successes can serve as benchmarks to scaling up of other interventions. Among the major killers, the ones that are poorly addressed are childhood pneumonia and perinatal problems which are the leading causes of under-five mortality in Ethiopia. Realizing the continuum of care approach at delivery level and sustaining it over time, and searching for an alternative way of improving access to treatment of childhood pneumonia and essential newborn care, are crucial challenges for child survival in Ethiopia. Furthermore, there is growing consensus that a primary bottleneck to achieving MDGs in low-income countries is health systems that are too fragile and fragmented to deliver the volume and quality of services to those in need. Major shortfalls are identified in the health workforce, lack of donor coordination, and week information systems. It is for this reason that the Health Sector Development Programme (HSDP) in Ethiopia is focusing on cost-effective health interventions and on health systems strengthening in order to achieve the dual goals of improving population health and reducing health inequalities.

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1) Introduction: an historical perspective Following the success of the 1979 International Year of the Child, in the early 1980’s signs of hope were emerging for childrens’ causes. The evolution of Basic Service and Primary Health Care (PHC) approaches gave the practitioners of child health and human development a new sense of purpose and in 1982 an initiative known as the “Child Survival Revolution” (later including child development) was launched (19). The “Child Survival Revolution” was initiated to promote Growth monitoring, Oral rehydration therapy, Breast feeding, Immunization, the provision of Food and Family planning. These interventions have collectively come to be known as “GOBIFF” (19). Ethiopia was one of the first countries to implement these high-impact child survival interventions. The Ethiopian Expanded Programme on Immunization (EPI) was launched in 1980 but until recently coverage of all of the above key interventions, including EPI, remained very low. Regardless of the fact that so many lives could have been saved with the implementation of such simple, high-impact interventions, around the mid-nineties, it was noticed that child mortality was not yet receiving

1 UNICEF, Addis Ababa enough attention. This was mainly because the world’s attention had been, understandably, focused on the growing HIV pandemic and HIV associated opportunistic infections such as tuberculosis and the like. While progress in reducing under-five mortality has in many low income countries slowed, in others it has totally stopped declining and in some cases even regressed significantly (17;16). Following the Lancet Child Survival publications in 2003 (4), the second global “Child Survival Revolution” was launched. In 2004, the National Child Survival Conference was organised in Addis Ababa. The Federal Ministry of Health (FMOH) and its partners all participated and in 2005 the National Child Survival Strategy was developed (6). The overall objective of this strategy was to reduce under five mortality by two thirds between 1990 and 2015 to achieve the Millennium Development Goal 4 (MDG4). Primarily, the National Child Survival Strategy focuses on the health sector, but important distant determinants of child survival, like reducing poverty, improving household food security, raising levels of maternal education and providing safe water and sanitation, are also recognized in the document.

The National Child Survival Strategy has been instrumental in the scaling-up of child survival interventions through the active participation of partners, relevant sectors and the community at large (6). This has wide implications also in terms of poverty reduction. In fact, the focus on child (and maternal) care provides more of a poverty orientation than reliance on other services, since the disease burden at an early age or at childbirth is particularly important among the poor. In fact, not only are death rates higher among the poor, compared to the rich, but the highest poor-rich mortality ratio is observed

for complications of pregnancy and childhood infectious diseases (13).

2) Causes of mortality: what are Ethiopian Children dying from? The Child Survival Strategy identifies the direct causes that are responsible for under-five mortality (Figure 1): pneumonia (28%), neonatal causes (25%), malaria (20%), diarrhea (20%), measles (4%) and AIDS (1%). Underlying conditions are also identified, manly malnutrition and HIV/AIDS (6).

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Neonatal, 25%

Malaria, 20%

Pneumonia, 28%

Diarrhea, 20%

AIDS, 1%

Measles, 4%

Other, 2%

Figure 1. Causes of under-5 deaths in Ethiopia (1). In Ethiopia, neonatal mortality contributes to about one fourth of the overall under-five mortality. Newborns die mainly due to infections,

followed by perinatal asphyxia and prematurity/low birth weight (Figure 2).

Figure 2. Causes of neonatal deaths in Ethiopia (1).

Fortunately, for each target condition there are both preventive and curative interventions that can prevent around 72% of deaths in under five children. To prevent these deaths and to achieve

MDG4, it is necessary to ensure effective implementation of a limited number of interventions that are listed in the National Child Survival Strategy. In 2003, the Lancet child

Other7%

Diarrhoea3%

Congenital4%

Tetanus7%

Infection37%

Preterm birth17%

Asphyxia25%

Causes of neonatal

deaths

Infections and tetanus account for 47% of neonatal deaths in Ethiopia

Malnutrition

57%

HIV/AIDS

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survival series estimated that, with 99% coverage of the high impact interventions for which there is sufficient evidence for effect in prevention or treatment, it would be possible to prevent 65% of deaths due to pneumonia, 55% of deaths due to neonatal complications, 91% of deaths due to malaria, 88% of deaths from diarrhea, 100% of deaths from measles, and 48% of those due to AIDS (12).

3) Millennium Development Goal 4: where do we stand?

Achieving the MDG4 for child survival in Ethiopia demands focused and coordinated action to strengthen the health systems, improve nutrition and reduce inequities in access to effective interventions against all the diseases which kill under-five children (5; 20).

According to the Ethiopia Demographic and Health Survey carried out in 2005, there was an improvement in under 5 mortality rates, with a decrease from 165 to 123 per 1,000 live births between 1990 and 2005 (3). The plan is to decrease U5MR to 54 per 1,000 in the year 2015 to meet MDG4 (Figure 3).

165153

140

123109

95

165153

140

123

89

54

0

40

80

120

160

1990 1995 2000 2005 2010 2015

Years

Un

der

5 M

ort

alit

y R

ate

Current Trend MDG Trend

HSDP I II

Figure 3. Trend in under 5 Mortality Rate in the period 1990-2005 and projections until 2015 in Ethiopia.

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4) Opportunities to achieve MDG4: implementation of child survival interventions An integrated approach is in place in order to achieve MDG 4, with: Focus on the community: Ethiopia is investing a lot in the Health Extension Program (HEP) to reach the poorest of the poor with basic and essential life saving care by focusing mainly on the mothers, newborns and children of the rural population. HEP institutionalizes and standardizes the village health-care delivery system to empower care-takers, families and communities to take care of their own health. It

increases access and utilization of most of the high impact preventive and curative interventions which are listed in the National Child Survival Strategy. Accelerated Expansion of Primary health Care: within the context of HSDP III, the FMOH has initiated an accelerated expansion of PHC services. This new initiative aims to accelerate physical infrastructure expansion, a base for improving access to basic health care services in rural Ethiopia. Besides physical infrastructure expansion, the initiative also entails an increase in the number of health professionals mainly at primary health care unit level.

Child Survival Strategy: HSDP III is incorporated as the de facto health component of the Plan for Accelerated and Sustained Development to End Poverty (PASDEP) (15). Maternal and Child Health (MCH) are major focuses of HSDP III, with Child Survival Strategy being a major component of HSDP III. Availability of Experienced Programs: there are experienced programs relevant to child health in Ethiopia, including EPI, Integrated

Management of Neonatal and Childhood Illnesses (IMNCI), Nutrition, Safe Motherhood and Malaria control programs. Partnership for Maternal, Newborn and Child Health (PMNCH): there is a growing partnership between the Government, UN organizations, bilateral partners, Private institutions and Non-Governmental Organizations for Child Survival.

5) Benchmarks: scaling-up is possible Through proper and rational utilization of available opportunities in the country, it is possible to scale up the implementation of high impact child survival interventions. These are some examples of successes and remarkable achievements in coverage increase within short time periods that can serve as benchmarks to

scaling up of other interventions. These include training of 24,600 HEWs within a period of 3 years, and rapid increase in percentage of children under the age of five years who slept under Long Lasting Insecticide-treated Nets (LLINs) from 1% in 2005 (3) to 42% in 2007 (10). Furthermore, through the Enhanced Outreach Strategy, it has been possible to scale up bi-annual supplementation of Vitamin A from the 2005 baseline level of 45 % to 91% in 2007 (Figure 4).

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Figure 4. Coverage in Vitamin A supplementation among children aged 6-59 months in Ethiopia during the period 2004-07. To realize the continuum of care that starts from the household and continues up to the facility level, the Family Health Department (FHD) of the Federal Ministry of Health (FMOH) launched the case management IMCI training in 1996 and, following that, community IMCI was adopted by a national workshop in 2001. In 2004, 36 % of the Health Centers had at least one health worker trained in IMCI (5). Assessment, classification and management of early neonatal problems were incorporated into the formal IMCI training guideline in 2006 and since then IMCI was renamed as Integrated Management of Newborn and Childhood illnesses (IMNCI). According to the March 2008

IMNCI annual review meeting report of the FHD, 60% of the Health Centers have at least one person trained in IMNCI (11). On the other side, Community-integrated IMNCI (C-IMNCI) coverage has shown a significant increase from 2 woredas in 2004 to 180 woredas in 2008 (11). In the past five years, immunization coverage is also showing an increasing trend. In 2003, DPT3 coverage was 50 % and in 2007 the Pentavalent coverage reached 73% (8). Most importantly, the introduction of Haemophilus influenzae type b (Hib) vaccine in 2007 had brought a paramount benefit to prevent childhood pneumonia and meningitis in under five children (9).

6) Lessons learned and way forward: more of the same is not enough

Recent evidence suggests that, based on current trends, many low-income countries are unlikely to achieve the MDG health target by 2015 (21). This is despite the fact that there are a growing number of cost-effective interventions, as well as increasing international assistance for specific disease control programmes. There is growing consensus that a primary bottleneck to achieving MDGs in low-income countries is health systems that are too fragile and fragmented to deliver the

volume and quality of services to those in need (18). Major shortfalls are identified in the health workforce, lack of donor coordination, and week information systems as critical challenges to achieving MDGs. It is for this reason that HSDP in Ethiopia is focusing on cost-effective health interventions and on health systems strengthening in order to achieve the dual goals of improving population health and reducing health inequalities.

Child Survival: Children (6-59 months) supplemented with Vitamin AAchievements per round as of November 2007

11,423,171 11,926,235

1,389,4382,576,620

4,946,811

11,567,721

8,269,75310,154,375

0

2,000,000

4,000,000

6,000,000

8,000,000

10,000,000

12,000,000

2004 - 1stROUND

2004 - 2ndROUND

2005 - 1stROUND

2005 - 2ndROUND

2006 - 1stROUND

2006 - 2ndROUND

2007 - 1stROUND

2007 - 2ndROUND

Achievements: # of children covered with vitamin A

National target children in Child Survival

Child Survival: Children (6-59 months) supplemented with Vitamin AAchievements per round as of November 2007

11,423,171 11,926,235

1,389,4382,576,620

4,946,811

11,567,721

8,269,75310,154,375

0

2,000,000

4,000,000

6,000,000

8,000,000

10,000,000

12,000,000

2004 - 1stROUND

2004 - 2ndROUND

2005 - 1stROUND

2005 - 2ndROUND

2006 - 1stROUND

2006 - 2ndROUND

2007 - 1stROUND

2007 - 2ndROUND

Achievements: # of children covered with vitamin A

National target children in Child Survival

Child Survival: Children (6-59 months) supplemented with Vitamin AAchievements per round as of November 2007

11,926,23511,423,171

1,389,4382,576,620

4,946,811

11,567,721

8,269,753

10,154,375

0

2,000,000

4,000,000

6,000,000

8,000,000

10,000,000

12,000,000

2004 - 1stROUND

2004 - 2ndROUND

2005 - 1stROUND

2005 - 2ndROUND

2006 - 1stROUND

2006 - 2ndROUND

2007 - 1stROUND

2007 - 2ndROUND

Achievements: # of children covered with vitamin A

National target children in Child Survival

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Training a sufficient number of health professionals and construction of an adequate number of health facilities in a very short time are some of the grand achievements of the FMOH. However, the anatomy alone may not take us to the destination until and unless it is complimented with the physiology. The health

workers that we have trained until now must have the necessary knowledge and skills to fulfill their jobs, and, equally, health facilities should be equipped and supplied with essential items. Moreover, there should be regular and continuous supervision to achieve the ultimate goal of child survival.

Among the major killers, the ones that are poorly addressed are childhood pneumonia and perinatal problems which are the leading killers of under-five children in Ethiopia. According to the 2005 EDHS, only 4.9% of pneumonia cases have

had access to antibiotic therapy and, from the same source, skill delivery coverage was also alarmingly low, with only 6% of total deliveries being conducted by a skilled attendant (3).

The Child Survival Strategy identifies Health Extension Program as an important vehicle that carries most high impact child survival interventions to the community. At this juncture, the potential of HEWs to implementing most of the child survival interventions is not fully exploited. There are multiple reasons for this, including problems related to competency, shortage of supplies, lack of regular supportive supervision, and lack of community ownership. Therefore, the conclusion is that achieving MDG4 in Ethiopia is feasible, but demands addressing the following serious concerns:

• Mobilizing adequate amounts of resources to fully implement the Health Extension Program;

• Realizing the continuum of care approach at delivery level and sustaining it over time;

• Searching for an alternative way of improving access to treatment of childhood pneumonia and essential newborn care, which are the two major killers of the under five children: this may include provision of community-based pneumonia and neonatal infection treatment;

• Strengthening Monitoring and Evaluation, which is the life blood of the child survival strategy to track progress towards the goal and to ensure quality of service rendered to the community.

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References

1. Child health in Ethiopia. Background document for the National Child Survival Conference – April 22-22, 2004, Addis Ababa, Ethiopia. World Health Organization, Addis Ababa.

2. [http://www.afro.who.int/cah/documents/situational_analysis/et_final_cs_situation_analysis.pdf.

Accessed June 2008].

3. CSA, 2006. Ethiopia Demographic and Health Survey 2005. Central Statistic Agency, Addis Ababa and ORC Macro, Calverton.

4. Editorial, 2003. The world’s forgotten children. The Lancet, 361: 1.

5. FMOH, 2004. National review and planning meeting. Report of the Family Health Department of

the FMOH. Federal Ministry of Health, Addis Ababa.

6. FMOH, 2005a. National strategy for child survival. Family Health Department. Federal Ministry of Health, Addis Ababa.

7. FMOH, 2005b. HSDP III. Health Sector Strategic Plan 2005/06-2009/10. Federal Ministry of

Health, Addis Ababa.

8. FMOH, 2007a. Health and health related indicators2006/07. Federal Ministry of Health, Addis Ababa.

9. FMOH, 2007b. Annual performance report of HSDP III. EFY 1999 (2006/2007). Federal Ministry of

Health, Addis Ababa.

10. FMOH, 2008a. National Malaria Indicator Survey. Federal Ministry of Health, Addis Ababa.

11. FMOH, 2008b. IMNCI and C-IMNCI national review meeting. Report of the Family Health Department of the FMOH. Federal Ministry of Health, Addis Ababa.

12. Gareth, J., Steketee, R., W., Black, R., E., Bhutta, Z. A., Morris S. S., and the Bellagio Child

Survival Study Group, 2003. How many children deaths can we prevent this year? The Lancet, 362: 65-71.

13. Gwatkin, D.R., 2000. Health inequalities and the health of the poor: What do we know? What can

we do? Bull. World Health Organ. 78, 3-17.

14. Lawn J., Kerber, K., 2006. Opportunities for Africa’s newborns. Practical data, policy and programmatic support for newborn care in Africa. The partnership for maternal newborn and child health, Cape Town.

15. MOFED, 2007. Ethiopia: Building on progress. A Plan for Accelerated and Sustained Development

to End Poverty (PASDEP). Annual Progress Report 2006/07. Ministry of Finance and Economic Development, Addis Ababa.

16. Save The Children, 2006. New Report shows improvements in child survival in Africa , but more

than a million African babies die in the first month of life. Save The Children, US.

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17. Schuftan C., 1990. The child survival revolution: a critique. Family practice, 7(4):329-332.

18. Travis, P., Bennet, S., Haynes, A., Pang, T., Bhutta, Z., Hyder, A.A., Pielemeier, N.R., Mills, A.,

Evans, T., 2004. Overcoming health-systems constraints to achieve Millennium Development Goals. Lancet, 364: 900-906.

19. UNICEF, 1996. The state of the World Children 1996. The 1980s: Campaign for child survival.

page 1-5. United Nations Children’s Fund, New York.

20. UNICEF, 2006. Preliminary Report. Trends in Child Mortality in Eastern and Southern Africa 1990- 2005. United Nations Children’s Fund, New York.

21. World Bank, 2003. The Millennium Development Goals for Health: Rising to the Challenges (draft).

World Bank, Washington, DC.

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A CASE REPORT: Optic glioma in a child with NF1 Kalid Astrat, 1 MD

Abstract A 10 year old female patient presented with progressive right eye proptosis ( Fig 1) and skin rash of three years duration was seen at Tikur Anbessa Specialized Hospital, department of pediatrics hematology /oncology unit. Physical examination showed mildly decreased visual acuity and cafe au lait spot ( Fig 2) AND axillary freckling and Orbital CT ( Fig 3) showed right intraorbital mass with an assessment of right optic nerve glioma she is to be started on weekly vinblastine at a dose of 6mg/m2.

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INTRODUCTION Optic nerve glioma (also known as optic pathway glioma) is the most common primary neoplasm of the optic nerve. Along with reducing visual acuity in the affected eye, the tumor sometimes produces additional symptoms as it grows. A low-grade form of this neoplasm, benign optic glioma, occurs most often in pediatric patients. Another form, aggressive glioma, is most common in adults; it is frequently fatal, even with treatment.1

Optic-pathway glioma accounts for 1-5% of all brain tumors in children [1]. About half of these cases occur in children with neurofibromatosis type 1 [2]. The diagnosis is usually rendered before age 6 years, although there are some reports of older ages [3,4]. The vast majority of optic-pathway gliomas in children are pilocytic astrocytomas [2,5]. The tumor may arise anywhere along the optic pathway, from just behind the globe to the lateral geniculate body [5,6]. In patients with neurofibromatosis type 1, the tumor is usually smaller than in sporadic (non-neurofibromatosis type 1-associated) cases [5,7].

The clinical presentation is variable. In patients with neurofibromatosis type 1, 40-80% of optic-pathway gliomas are asymptomatic at diagnosis, whereas in sporadic cases, they are symptomatic [3,5,8-10]. The most common signs are vision-related: mainly visual loss, decreased visual acuity, and strabismus. Other findings include endocrine disturbances, signs of increased intracranial pressure, and hydrocephalus [2,5,8,9,10-13]. Ophthalmologic examination may reveal decreased visual acuity, pathologic visual fields, proptosis and more [9,10,13,14]. The generally young age of the children and high prevalence of neurofibromatosis type 1-associated attention deficit hyperactivity disorder render the ophthalmologic examination difficult, and decrease its sensitivity and specificity [2,15]. Early diagnosis is important so that the tumor can be carefully monitored and treatment can be administered early, before visual deterioration. The diagnosis can be made functionally by visual-evoked potentials, but as is

the case for eye examinations, their efficacy is limited, and specificity is low [2,16]. Modern neuroimaging modalities provide excellent characterization of optic-pathway gliomas, obviating the need for biopsy [17]. Magnetic resonance imaging was found to be superior to computed tomography for the detection and evaluation of extensive tumor involvement. It has a higher specificity, and can be used to assess disease progression [18,19]. The biological behavior of optic-pathway glioma varies. The tumor may progress rapidly, remain stable for years, or even shrink spontaneously or after biopsy, mostly with clinical improvement [2,5,7,20]. Regrowth after a stable period or after biopsy was also reported [2]. Tumor progression is apparently affected by the presence of neurofibromatosis type 1, patient age, and tumor location [21]. Less progression was evident in patients with neurofibromatosis type1 than in sporadic cases, and in children who were older at diagnosis [2,5,7,9,10,19,22]. Tumors situated at the optic nerve or chiasma tend to grow more slowly and less aggressively than chiasmatic/hypothalamic gliomas, with lower mortality [23,24]. Posterior involvement may also lead to significant morbidity and mortality [6,14,25].The natural 1 Department of Pediatrics and Child Health, Medical faculty, Addis

Ababa University. history of optic-pathway gliomas in neurofibromatosis type 1 is considered unpredictable [2,26]. Hence deciding whether, or when, to initiate treatment becomes difficult. The presence of an optic-pathway glioma in a patient without neurofibromatosis type 1 is considered an indication for treatment [5]. Although neurofibromatosis type 1 is thought to be relatively benign, given the risk of visual impairment, blindness, neurologic deficits, or death [27,28], patients affected by the tumor should be monitored routinely for its size and visual function, and an adverse change in either should be considered an indication for treatment [2]. If a glioma tends to remain stable, the

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intervals between magnetic resonance examinations can be gradually increased [10]. Nevertheless, the subjective timing of imaging scans and the lack of objective references to identify deviations from normality place patients at risk of either unnecessary or insufficient neuroimaging. An optic-pathway glioma tends to grow along the optic pathways by increasing its width, rather than as one ‘‘concentric’’ mass that grows in all directions [5]. As such, stereotypical patterns of growth as seen on imaging scans of children with optic-pathway glioma are often highly comparable, because the tumor tends to involve the same brain structure, and the manner of growth is very similar.

CASE REPORT

A 10 year old female patient presented with progressive right eye proptosis and skin rash of three years duration was seen at Tikur Anbessa Specialized Hospital, department of pediatrics hematology /oncology unit. Since the last 6 months the proptosis was more progressive to attain the current size. Family history is positive for paternal unilateral loss of vision unrelated to trauma. Physical examination showed mildly decreased visual acquity (OD =6/9, OS =6/6) and cafe au lait spot( Fig 2) and axillary freklings other wise no other findings on the musculoskletal and CNS. Orbital CT( Fig 3) showed right intraorbital mass with an assessment of right optic nerve glioma she was started on weekly vinblastine at a dose of 6mg/m2.

Fig 1

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Fig 2

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Fig 3 Discussion This is one of the rarely reported case of a 10 year old Ethiopian child with type 1 neurofibromatosis and right optic nerve glioma. In most young patients with optic glioma the presenting symptom is painless proptosis. Optic atrophy is common, as is reduced visual acuity, although the latter may be a late symptom. A large lesion may compress the optic chiasm, causing nystagmus or other symptoms. Hypothalamic symptoms, such as changes in appetite or sleep, also may occur. Massive lesions may compress the third ventricle, resulting in obstructive hydrocephalus accompanied by headache, nausea, and vomiting also may occur but these findings were not found in this patient. Historically, surgery and radiotherapy have played a primary role in management, however, in the last 15 years, chemotherapy has evolved into the first-line treatment of choice. The case presented was started on weekly Vinblastine at a dose of 6 mg/m2 for one year with regular

ophthalmologic and Orbital CT/MRI if feasible.

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References 1. Alshail E, Rutka JE, Becker LE, Hoffman HJ. Optic chiasmatic-hypothalamic glioma. Brain Pathol

1997;7:799-806. 2. Shuper A, Horev G, Kornreich L, et al. Visual pathway glioma: An erratic tumor with therapeutic

dilemmas. Arch Dis Child 1997;76: 259-63. 3. Thiagalingam S, Flaherty M, Billson F, North K. Neurofibromatosis type 1 and optic pathway

gliomas: Follow-up of 54 patients. Ophthalmology 2004;111:568-77. 4. Listernick R, Ferner RE, Piersall L, Sharif S, Gutmann DH, Charrow J. Late-onset optic pathway

tumors in children with neurofibromatosis1. Neurology 2004;63:1944-6. 5. Kornreich L, Blaser S, Schwarz M, et al. Optic pathway glioma: Correlation of imaging findings with

the presence of neurofibromatosis. AJNR 2001;22:1963-9. 6. Liu GT, Brodsky MC, Phillips PC, et al. Optic radiation involvement in optic pathway gliomas in

neurofibromatosis. Am J Ophthalmol 2004;137:407-14. 7. Astrup J. Natural history and clinical management of optic pathway glioma. Br J Neurosurg 2003;17:327-35. 8. Guillamo JS, Creange A, Kalifa C, et al. Prognostic factors of CNS tumors in neurofibromatosis 1

(NF1): A retrospective study of 104 patients. Brain 2003;126:152-60. 9. Czyzyk E, Jozwiak S, Roszkowski M, Schwartz RA. Optic pathway gliomas in children with and

without neurofibromatosis 1. J Child Neurol 2003;18:471-8. 10. Listernick R, Charrow J, Greenwald M, Mets M. Natural history of optic pathway tumors in children

with neurofibromatosis type 1: A longitudinal study. J Pediatr 1994;125:63-6. 11. Cnossen MH, Stam EN, Cooiman LC, et al. Endocrinologic disorders and optic pathway gliomas in

children with neurofibromatosis type1. Pediatrics 1997;100:667-70. 12. Shuper A, Kornreich L, Michowitz S, Schwartz M, Yaniv I,Cohen IJ. Visual pathway tumors and

hydrocephalus. Pediatr Hematol Oncol 2000;17:463-8. 13. Khafaga Y, Hassounah M, Kandil A, et al. Optic gliomas: A retrospective analysis of 50 cases. Int J

Radiat Oncol Biol Phys 2003;56:807-12. 14. Sigorini M, Zuccoli G, Ferrozzi F, et al. Magnetic resonance findings and ophthalmologic

abnormalities are correlated in patients with neurofibromatosis type 1(NF1). Am J Med Genet 2000;93:269-72.

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15. Wolsey DH, Larson SA, Creel D, Hoffman R. Can screening for optic nerve gliomas in patients with neurofibromatosis type I be performed with visual-evoked potential testing? J AAPOS 2006;10:307-11.

16. North K, Cochineas C, Tang E, Fagan E. Optic gliomas in neurofibromatosis type 1: Role of visual

evoked potentials. Pediatr Neurol 1994;10:117-23. 17. Pepin SM, Lessell S. Anterior visual pathway gliomas: The last 30 years. Semin Ophthal. 2006;21:117-24. 18. Van Es S, North KN, McHugh K, De Silva M. MRI findings in children with neurofibromatosis type

1: A prospective study. Pediatr Radiol 1996;26:478-87. 19. Chateil JF, Soussotte C, Pedespan JM, Brun M, Le Manh C, Diard F. MRI and clinical differences

between optic pathway tumours in children with and without neurofibromatosis. Br J Radiol 2001;74: 24-31.

20. Parsa CF, Hoyt CS, Lesser RL, et al. Spontaneous regression of optic gliomas: Thirteen cases

documented by serial neuroimaging. Arch Ophthalmol 2001;119:516-29. 21. Chan MY, Foong AP, Heisey DM, Harkness W, Hayward R, Michalski A. Potential prognostic

factors of relapse-free survival in childhood optic pathway glioma: A multivariate analysis. Pediatr Neurosurg 1998;29:23-8.

22. Grill J, Laithier V, Rodriguez D, Raquin MA, Pierre-Kahn A, Kalifa C. When do children with optic

pathway tumors need treatment? An oncological perspective in 106 patients treated in a single center. Eur J Pediatr 2000;159:692-6.

23. Schroder S, Baumann-Schroder U, Hazim W, Haase W, Mautner VF. Long-term outcome of

gliomas of the visual pathway in type 1 neurofibromatosis. Klin Monatsbl Augenheilkd 1999;215:349-54.

24. Tow SL, Chandela S, Miller NR, Avellino AM. Long-term outcome in children with gliomas of the

anterior visual pathway. Pediatr Neurol 2003;28:262-70. 25. Balcer LJ, Liu GT, Heller G, et al. Visual loss in children with neurofibromatosis type 1 and optic

pathway gliomas: Relation to tumor location by magnetic resonance imaging. Am J Ophthalmol 2001;131:442-5.

26. Serova NK, Lazareva LA, Gorelychev SK, Ozerova VI, Pronin IN. A follow-up of patients with

anterior optic tract glioma concurrent with type 1 neurofibromatosis. Vestn Oftalmol 2006;122:39-42.

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27. Luh GY, Bird CR. Imaging of brain tumors in the pediatric population. Neuroimag Clin North Am 1999;9:691-716.

28. Kosa E, Csakvary V. Neurofibromatosis type 1 in children—With special consideration of

ophthalmologic symptoms. Orv Hetil 2004;145:473-8. Acknowledgments I would like to thank Dr David N Korones pediatric oncologist at Rocester medical center , New York and Dr Ibrhaim Qaddumi , oncologist at St Jude Children’s Research hospital for their constructive ideas and providing me with important references.

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Clinical Predictors of Pneumonia Among Under-five Children At Tikur Anbesa Specilaized Hospital

Kalid Asrat1, MD, Amha Mekasha1, MD, MSc

Abstract

The aim of the study is to identify simple clinical signs and symptoms in under five children which are predictors of pneumonia at Tikur Anbesa Specialized Hospital (TASH), Department of Pediatrics and Child Health, emergency and regular out-patient units. The design of the study is a prospective cross-sectional study carried out during Aug 2004 – Sep 2005. All children between the age of 2-59 months who attended the regular and emergency pediatrics units at TASH during the study period who had either cough or difficulty of breathing or chest x-ray evidence of pneumonia were included in the study. A calculated sample of 164 was taken. Data analysis was done using SPSS and EPINFO version 1.1.2. Chi-square test was used to calculate the differences in distribution of clinical signs and symptoms between groups with and without chest x-ray (CXR) evidence of pneumonia. A total of 179 patients were studied of whom 102 were males and 77 females (M:F 1:0.75). Clinical symptoms and signs were related to CXR pneumonia. Tachypnea (94.5% with CXR pneumonia Vs 59.3% without CXR pneumonia) and retraction (86.3% CXR Vs 40.6% without CXR pneumonia) were the best clinical predictors of pneumonia. Tachypnea, flaring of alae nasi and retraction were also independently associated with CXR pneumonia. Vomiting, refusal to feed, history of rapid breathing , grunting and chest findings did not predict pneumonia. In conclusion pneumonia is a significant cause of morbidity and mortality in developing countries like

Ethiopia . Using simple clinical indicators pneumonia can be diagnosed by primary health workers and mortality can be

reduced significantly.

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INTRODUCTION Around 10.6 million children die every year before reaching their 5th birth day. Almost all of these deaths occur in low income and middle income countries mainly in Africa and south east Asia. Most deaths among under fives are still attributable to just a handful of conditions, acute respiratory infection(ARI) mostly pneumonia accounts for 19% of all deaths(1,2,3,). Age Specific mortality from lower respiratory infection( LRI) in young Gambian children has been estimated at 10 per 1000 each year(4 ) . In Ethiopia infant mortality rate is 77 per 1000, under five mortality is 120 per 1000 (5), ARI being one of the major cause of morbidity and mortality. Taking these into consideration WHO in 1981 initiated a programme for the control of ARI on a case management of pneumonia. One of the strategies is to improve case detection and patient management by primary health care workers (7) and so reduce mortality. The aim of this study is to evaluate the usefulness of simple clinical symptoms and signs in the diagnosis of LRI, mainly pneumonia, which can easily be used by primary health care workers. Despite LRI (mainly pneumonia) being a condition commonly encountered by clinicians, uncertainty remains over the

diagnosis, investigation and treatment of the condition. Infants and children may present with a number of different clinical symptoms and signs such as fever, cough and tachypnea. Minority of children may present with fever of unknown origin ( FUO) and may have no respiratory symptoms or signs.

WHO has developed algorithm (8) to aid medical and non-medical health care workers in diagnosis of LRI with out radiological confirmation. The WHO algorithm stresses the importance of tachypnea which has a 74% sensitivity and 67% specificity for radiologically defined pneumonia (8). However, in children who had diseases for less than three days (9), tachypnea had a lower sensitivity and specificity of illness. Clinicians must be aware that the absence of tachypnea does not necessarily mean the absence of pneumonia (10 ). Grunting and nasal flaring increase the chance of pneumonia, but their absence cannot be relied upon to rule out the chance of pneumonia (9). Other signs that relate to severity of pneumonia are chest indrawing, nasal flaring and cyanosis. High fever in young children (age up to 3 years) was found to be a sign of pneumonia (11,12).The British thoracic

1 Department of Pediatrics and Child Health, Medical faculty, Addis

Ababa University. society ( BTS) guidelines suggested that in children less than 3 years combination of fever > 38.5ºc,chest indrawing and RR >50/min indicate pneumonia, breathing difficulty is more reliable sign in older children (18). Chest x-ray (CXR) is still considered to be the gold standard for diagnosing pneumonia in the developed world. However, there is poor concordance between radiological changes which constitute pneumonia( inter and intra observer variation), consolidation on CXR was most commonly identified by the radiologist was generally agreed to represent pneumonic changes(12) . WHO has recognized the difficulties with CXR interpretation and developed a tool to standardize the reporting of CXR use in epidemiological studies of pneumonia (8) this system classifies CXR as: normal appearance, infiltrates and end stage consolidation defined

as significant amount of alveolar type of consolidation. So does a normal x-ray rule out pneumonia? There is anecdotal evidence for having pneumonia with a normal CXR. Fever and tachypnea may present before CXR changes are seen. Subjects and methods Study setting: The study was conducted at Tikur Anbessa Specialized Hospital (TASH), department of pediatrics and child health emergency and regular OPD which is one of the very few centers in the country which gives pediatric out patient and in patient services. Study design: a cross sectional survey was under-taken among children under five children in the period of (AUG 2004- SEP 2005) who have either cough or difficulty of breathing or CXR evidence of pneumonia

Study population: All children between the age of 2-59 months who attended the regular as well as the emergency pediatrics OPD at TASH during the study period(AUG 2004- SEP 2005) who have either cough or difficulty of breathing or CXR evidence of pneumonia were included. A calculated sample of 164 was taken. Data analysis: Data was entered and analysis was done using SPSS and EPINFO version 1.1.2 software. Chi-

square test was used to calculate the differences in distribution of clinical signs and symptoms between groups with and without CXR pneumonia. Signs and symptoms which were significant on univariate analysis were taken for multiple logistic regression analysis. Ethical consideration: Permission to undertake the study was obtained from the department of pediatrics and child health of TASH.

Results

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A total of 179 children among whom 102 (57%) males and 77 (43%) females who fulfilled the inclusion criteria’s were

included in this study. The age distribution is shown in table 1 where half of the patients were infants.

21 patients have severe PEM,13 patients have rickets,3 have sero-proven pediatrics HIV infection and one patient each have gastroenteritis, malaria, downs syndrome and meningitis (table 3). Table 2 shows clinical signs that best correlate with CXR

pneumonia, these are tachypnea, flaring and retraction ,the other clinical signs and symptoms like vomiting, refusal to feed, cough, fever and grunting and chest findings did not

correlate with CXR pneumonia. Table 4 shows the

sensitivity, specificity, 95% confidence intervals and prevalence of selected symptoms and signs and table 5

shows the frequency of clinical signs and symptoms. In children between the age of 2-59 months, tachypnea (94.5% with CXR pneumonia Vs 59.3% without) and retraction (86.3% Vs 40.6%) were the best predictors of CXR pneumonia. Tachypnea, flaring and retraction were independently associated with CXR pneumonia.

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Discussion In rural areas of developing countries the case fatality rate from LRI in children is most likely to be reduced if primary health care workers can identify the most serious forms of LRI and deal with them appropriately, accurate guidelines to detect LRI(pneumonia) who can be safely treated with antibiotics as outpatients from those who require immediate referral must be based on symptoms and signs that can be readily assessed. This study has attempted to look into clinical signs and symptoms predictors of pneumonia in less than 5 year children such as vomiting rapid breathing, tachypnea and chest retraction, age and sex distribution ,frequency of each clinical signs and symptoms at emergency and regular pediatric out-patient department of TASH over one year period. On a study done by Campbell, et al showed that in infants a fever of >38.5ºc, refusal to feed (breast feeding) or the presence of vomiting best correlated with CXR pneumonia. In children aged 1-4 year, a fever of > 38.5ºc, RR >60/min are best correlated with CXR pneumonia(11).Another study done by Cherian et al showed that RR >50/min in infants and RR >40/min in

children 12-35 months of age, as well as history of rapid breathing and the presence of chest retraction in both age groups were found to be sensitive and specific indicators of LRI. Increased RR and history of rapid breathing were also sensitive in diagnosing less severe LRI that did not necessitate admission to the wards, whereas chest retraction was not. All these clinical signs had a lower sensitivity in diagnosing LRI in children aged 36 months and over (19).Study done by Shan et al showed that chest indrawing was a reliable sign in children between the age of 0-4 years with cough for assessment of severe LRI (pneumonia) and among other children with cough a RR of >50/min is a reliable basis for diagnosing LRI (14). A multicentric study done by the WHO young infant study group indicated that the best threshold for predicting pneumonia in infants aged less than 2 months was RR > 60/min( 15).The best combination of sensitivity( 78-82%) and specificity (73-89%) was achieved by wing thresholds of 50 and 40 breaths/min for children aged 2-11 months and 1-4 years, respectively (16).

The Bangladesh study suggested that chest indrawing was more specific as a sign of severe pneumonia (17).Tachypnea has been exhaustively demonstrated to be an excellent predictor of radiologically defined pneumonia in a study done by Levantine J et al (10,14). In the present study tachypnea and retraction are very specific signs of CXR pneumonia, this is also consistent with other studies done on the subject(10,14,17,18) and their usefulness is further increased by their high sensitivity and are also easier to teach to non medical staff like primary health care workers. Vomiting, rapid breathing, fever, cough and grunting were not satisfactory predictors of CXR pneumonia.

Since our study is a hospital based study it should be interpreted with caution when community health workers (CHW) training and national guidelines are setup. Such programmes must adopt policies that take into consideration the health resource s available to implement them. In rural areas of many developing countries including Ethiopia the referral systems are poorly developed and much of the primary care must be developed to CHWs, this should come from community based studies. In conclusion pneumonia is still the significant cause of morbidity and mortality in developing countries like Ethiopia . If pneumonia is diagnosed earlier using simple clinical parameters which can also be used by non medical staff like community health workers and other health professional at each level mortality could be reduced significantly. Tachypnea (94.5%) and retraction(86.3%) were the best predictors of pneumonia as evidenced by

suggestive CXR (CXR pneumonia). Further studies should be conducted on the subject especially at the community level.

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References

1. World health report 2005 2. Demographic estimates of the annual number of infants and child defense in the

world.The pediatric health 1984. 3. Handbook of health information of India. Central Bureaus of health Intelligence, New

Delhi,1984. 4. Deaths in infancy and early childhood in well vaccinated rural west African population.

Ped 1994 ,91-99. 5. MOH. Health and health related indicators.1998. 6. Williams B et al estimate of world wide distribution of deaths from ARI. Lancet inf dis J

2002,2:25-32. 7. WHO. A programme for controlling ARI in children memorandum,WHO meeting. Bull

WHO 1994 ,62:45-58. 8. WHO ,management of ARI in children ,practical guidelines for outpatient care.

Geneva WHO 1995. 9. Plafox M etal diagnostic value of tachypnea in pneumonia defined radiologically. Arch

Dis child 2000,82:41-5 10. Leventhal J. clinical predictors of pneumonia as a guide to ordering chest X-ray.

Clinical pediatr 1982;21; 730-40 11. Campbell H et al .Assessment of clinical criteria for identification severe LRI in

children ,the lancet 1989,297-9 12. Campbell SM, Shann F, et al. The effect of panel membership and feedback in ratings

in a two round Delphi survey ,results of randomized controlled trial ,medicinal care 1999,37,964-8

13. Davies H et al. Reliability of chest X-ray of LRI in young children. pediatr inf dis 1996,16,600-4

14. Shann F et al. LRI in children, possible criteria for selection of patients for antibiotic therapy and hospital admission, bull of the WHO 1984,62,749-53

15. The WHO young infant study group, clinical prediction of serious bacterial infection in young infants in developing countries. Pediatr inf dis J 1999,18 suppl 8: 523-31

16. Mulholland EK et al. Standardized diagnosis of pneumonia in developing countries. Pediatr inf dis J 1992,11,77-81

17. Kalteer HD et al. Identifying sick children requiring referral to hospital in Bangladesh .Bull WHO 1997,75 supp1,65-75

18. BTS/SIGN ,British guideline on the management of Asthma Thorax 2003,58: supp 1 19. Cherian T et al evaluation of simple clinical signs for the diagnosis of LRI Lancet 1988 2:125-8

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Village, Tigray, Ethiop J HLth Dev 2000; 14:67-75

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