ijmrhs vol 3 issue 2
TRANSCRIPT
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Pallavi et al., Int J Med Res Health Sci. 2014;3(2):228-232
International Journal of Medical Research
&
Health Sciences
www.ijmrhs.com Volume 3 Issue 2 (April - Jun) Coden: IJMRHS Copyright @2014 ISSN: 2319-5886
Received: 10th
Oct 2013 Revised: 22nd
Dec 2013 Accepted: 4th
Jan 2014
Research Article
EFFECT OF AGE ON TEST PERFORMANCE IN COMMUNITY DWELLING ELDERLY PEOPLE:
6 MINUTES WALK TEST AND TEN STEPS TEST
*Mahajan Pallavi Janardhan1, Mistry Hetal M
2
Department of physiotherapy, Topiwala National Medical College, Mumbai, Maharashtra, India
*Corresponding author email: [email protected]
ABSTRACT
The data available in literature for test performance in elderly people are less and insufficient for use as a basis of
comparison. The aim of the study was to investigate age related changes in functional performance tests and to
determine criterion values depending on age in older adults who are functioning independently in the community.
Aim: To study the effect of age on test performance in 6 Minute Walk Test and Ten Step test in community
dwelling elderly people. Objectives: To assess 6 minute walk distance, time taken to perform ten step test and to
report data within age cohorts. Method: Total 90 subjects were included and divided into 3 groups according to
age group, A-(61-65), B-(66-70), and C-(71-75) in each 30 subjects. 6 Minute Walk Test and Ten Step Test were
performed on them. The data obtained was analyzed using one way ANOVA and post hoc test. Result: The mean
6 MWD in group A was 317.13 ± 35.44 mts, in group B was 297.10 ± 47.14 mts and in group C was 262.83 ±42.14 mts. The 10 Step Test time was found to be 11.36 ± 2.06 sec in group A, 13.24 ± 3.49 sec in group B and
14.74 ± 3.16 sec in group C. The results showed that there is a progressive decrease in the 6 MWD and
progressive increase in the time taken to complete TST with increasing age. Conclusion: From the results it can
be concluded that there is a progressive decrease in the test performance (6MWT & 10 Step test) with age in
community dwelling elderly people. The results of this study can be used as reference values while performing
performance tests for elderly people in the community.
Keywords: 6 minute walk test, 10 step test, Community dwelling
INTRODUCTION
In recent years there has been an increasing
international awareness of health issues relating to
aging populations.1There has been a sharp increase in
the number of older persons worldwide.2,3
According
to the Demographic Profile of Elderly, India carries
15% of world population. The fastest growing age
group by percentage is between 65 – 75 years of age.
With a decline in fertility and mortality rates,
compared with an improvement in child survival and
increased life expectancy, there is a progressive rise
in the number of elderly persons (accepting 60 years
of age as a practical demarcation for defining
elderly). Aging results in significant decline in
muscle power and exercise capacity. Therefore,
elderly often function at the limit of their capacity in
order to fulfill activities of daily living.
Determination of remaining physical capacity is
important in clinical decision making.4
Many
independent older adults often due to their sedentary
lifestyles, function dangerously close to their
maximum ability level during normal activities.
Climbing stairs or getting out of a chair requires the
use of near maximum efforts for many older
individuals. Early identification of physical decline
and appropriate interventions can help to prevent
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functional impairments such as in walking and stair
climbing that often results in fall and physical frailty.5
Quality of life in old age depends to a large extent on
‘being able to continue to do what you want without
pain as long as possible. Being able to perform
everyday activities like personal care, household
work requires the ability to perform functional
movements such as walking, stair climbing, and
standing. These functional movements in turn are
dependent on having sufficient physiological reserve
i.e. strength, balance, endurance, flexibility.
Functional fitness performance is ‘having the
physiological capacity to perform normal everyday
activities safely and independently without undue
fatigue.5
Many senior fitness instructors have been
frustrated with lack of tests available to assess the
functional fitness of older adults particularly tests that
have accompanying performance standards.
The ability to walk for a distance is a quick and
inexpensive measure of physical function and
important component of quality of life. It reflects the
capacity to undertake day to day activities. 6 Minute
Walk Test is used to measure the maximum distance
that a person can walk in 6 minutes. It is a sub
maximal test of aerobic capacity commonly used to
assess cardiovascular and pulmonary function.9
6
MWT can be performed by many elderly frail people
who cannot be tested with standard maximal cycle
ergometer or treadmill tests. 10 Step Test is a test that
measures the time taken by an individual to step up
10 times. It is a simple, reliable test and requires short
time.
However, there is little data available in literature
describing variation in test performance for older
adults who are functioning independently. The
available data are less and often difficult for
clinicians to use as a basis of comparison indocumentation because they are not presented in
terms of age and gender groupings. Hence a study is
needed which will give an accurate range of
measurements on these tests in different age groups.
Thus the aim of the study was to investigate aging
related changes in physical and functional,
performance and to determine criterion values
depending on age in community dwelling elderly
people.
METHOD
After the approval of the Institutional Ethics
committee TNMC, Mumbai, total 90 subjects were
included in the present study and they were divided
into 3 groups based on their age. Group A: age group
of 61-65 years, Group B: age group of 66-70 years
and Group C: age group of 71-75 years of age. N=30
in each group. Type of sampling was a convenience
sampling and the source was an urban population in
South Mumbai.
Inclusion criteria
1. Subjects between 60 to 75 years of age
2. Both male and female
3. Subjects who can tolerate standing, walking for at
least 6 minutes and stepping without any
complaints
4. Not dependent on assistance of another person or
supportive device for walking or stepping
Exclusion criteria
1. Use of any assistive device for walking or stair
climbing
2. Any acute illness in past 3 months
3. Subjects not willing to participate in the study
Outcome measures -1. 6 minute walk test, 2. 10 step
test
Subjects who fulfilled the inclusion criteria were
taken for the study. All procedure was adequately
explained to the patients and written consent was
taken from each one before starting the test.
Procedure: Case record form was filled and
demographic data collected from each subject.
Resting heart rate, respiratory rate, blood pressure
and rate of perceived exertion were taken.
The 6 minute walk test was conducted along a long
hallway. Standardized encouragement was given in
between at 1, 3, and 5 minutes interval. After
completion of test, heart rate, respiratory rate, blood
pressure and rate of perceived exertion were taken
immediately and after 1, 3 and 5 minutes to see the
recovery of subjects to baseline parametersThe 10 step test was conducted after the subject fully
recovered from previous test. The subject was asked
to step one foot onto a block of 10 cm height and then
quickly step down from the block. The same was
done with the opposite foot and was repeated 10
times. The subject was instructed to perform the
stepping sequence as quickly as possible. Similarly,
parameters were taken before and after the test to see
the recovery.
The 6 Minute Walk Test distance and Ten Step Testtime were statistically analyzed using one way
ANOVA with post hoc (Tukey) test.
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RESULTS
Table.1: Table showing 6MWD (mts) in the 3 study groups:
Mean± SD IQR Min Max
Upper
95% CI
Lower
95% CI
Group A 317.13± 35.44 54.0 254 385 330.37 303.9
Group B 297.10± 47.14 65.0 198 380 314.7 279.5Group C 262.83±42.14 64.0 176 332 278.57 247.1
Table.2: Table showing comparison in between the groups in 6MWD
All Pair wise Multiple Comparison Procedures (Tukey Test):
Groups P value
Group A vs. Group B >0.05
Group B vs. Group C
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complete TST with increasing age. The test also
showed high reliability as a test battery.10
Due to
age related changes, the aged are weaker, slower
and less powerful and hence, there is a reduction
in performances requiring the regulating and
coordinating functions of the nervous systems,i.e. balance, reaction time, agility and
coordination. Hence, older people cannot
perform well in almost any type of activity,
except for low intensity activities in which
energy demands are easily met.6
This might be
the reason for increase in TST distance.
Cardiopulmonary fitness and skeletal muscle
mass progressively decline in aged population
and both factors contribute to weakness andfunctional disability in elderly. These changes
might be responsible for the progressive decrease
in 6 MWT with increasing age in our study.
Cardiopulmonary exercise testing is a well
established procedure that provides peak oxygen
uptake as the gold standard in determining
exercise capacity but it is poorly accessible for a
large scale community based investigation.
Among the field tests, 6 MWT and TST are easy
to administer, inexpensive and safe tests that
provide a measure of sub maximal cardio
respiratory or endurance fitness.12
Steffen and Hacker in their study said that the
choice of measurement should be based on how
well the specific problems of a given patient
match the purpose of a given test.8
Rather than
selecting participants who were healthy (free
from any pathologies), older people were
selected who functioned independently withoutassistive devices in the community. People who
were independently functioning seemed to be a
more realistic standard of comparison for the
elderly subjects seen by physical therapists. It
was anticipated that the range of performance on
the tests by such participants would show
substantial variation. Hence, while interpreting
the findings, the characteristics of the subjects
were kept in mind.Thus, this study shows the age related changes in
functional performance in community dwelling
elderly people and provides a criterion related
reference values for functional performance tests
(6MWT and TST).
Clinical implications: To make a tailored
exercise program for elderly people, their
functional capacity should be known andaccordingly exercises should be prescribed. Most
of the Indian population is suffering from one or
the other pathology like osteoarthritis,
spondylosis, diabetes which is not taken into
consideration while planning an exercise
program. Such people seem to be a more realistic
standard of comparison for elderly subjects seen
by physical therapists. The reference values
available in litterateur are mainly for healthyelderly people. If we apply these standard values
to community dwelling elderly, their functional
capacity might be overestimated. In this study,
subjects taken were independently functioning in
community without the use of assistive devices.
Hence, the reference values obtained from this
study can be used as a basis of comparison while
planning an exercise program for community
dwelling elderly people. No research has been
done yet by using combinations of these two
tests (6MWT and TST) in Indian population. The
two tests used in this study are simple to
understand and perform and does not require the
use of any equipment. Walking and stair
climbing are two basic forms of ambulation
required in day to day life. By testing
performance in these activities, one can come to
know the functional capacity of an individual.
Limitations: 1. The sample size was small. 2.Comparison of test values between genders was
not analyzed. Females could have had a
confounding effect on the test results. 3. Subjects
were not compared with different age groups.
CONCLUSION
From the results it can be concluded that there is
a progressive decrease in the test performance
(6MWT & 10 Step test) with age in communitydwelling elderly people. The results of this study
can be used as reference values while performing
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performance tests on elderly people in the
community.
ACKNOWLEDGEMENT
I sincerely thank my H.O.D. and Guide for
inspiring me and guiding me throughout this
project. I thank our Dean whose permission for
the study did it occur. I also thank all subjects
who willingly participated in my study without
whom my study would not be completed. I
would also like to thank my statistician who
helped and guided me in preparing my tables and
graphs.
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elderly: Rationale for economic planning.
Cardiovascular Drugs Ther 2001; 15:359 –
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2. Hafez G, Bagchi K, Mahaini R. Caring for
the elderly: a report on the status of care for
the elderly in the Eastern Mediterranean
Region. EMHJ July 2000; 6 (4):636-43.
3. World Population Prospects: The 2002Revision, Highlights. New York: United
Nations Population Division; 2003.
(ESA/P/WP. 180).
4. Ivan Bautmanns , Margareta L, Tony M.
The six minute walk test in community
dwelling elderly: Influence of health status.
BMC Geriatrics. July 2004; 4:6
5. Jesse Jones, Roberta ER. Fitness of Older
Adults. Journal on Active Aging. 2002:24-
30
6. James Skinner. Exercise Testing and
Exercise Prescription for Special Cases. 2nd
Edition. USA: Williams and Wilkins; 2005
Pg no 85-98
7. Kenzo Miyamoto, Hideaki Takebayashi,
Koji Takimoto, Shoko Miyamoto, Shu
Morioka, Fumio Yagi. A New Simple
Performance Test Focused on Agility in
Elderly People: The Ten Step Test.Gerontology 2008;54:365-72
8. Teresa S, Timothy A H, Louise M. Age and
Gender Related Test Performance in
Community Dwelling Elderly People: Six
Minute Walk Test, Berg Balance Scale,
Timed Up & Go Test and Gait Speeds.
American Physical Therapy Journal. Feb2002;82(2):128-37.
9. Guidelines for Six Minute Walk Test.
American Journal of Respiratory and
Critical Care Medicine.2002;166:111-17.
10. Troosters T, Gosselink R, Decramer M.
Six minute walking distance in healthy
elderly subjects. Eur Respir J 1999;14:270-
74
11. Shin S, Demura S. Comparison and ageLevel differences among various step tests
for evaluating balance ability in the elderly.
Archives of Gerontology and Geriatrics.
May June 2010;50(3): 51-54
12. Chien MY, Hsu KK, Ying TW. Sarcopenia,
Cardiopulmonary Fitness And Physical
Disability In Community Dwelling Elderly
People. American Physical Therapy Ass.
2010;90(9):1277-87
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Doppler visually reflects the state of blood flow to the
tumor. It is based on Folkman’s theory of
neovascularization6
which states that tumor releases
the factor known as tumor angiogenesis factor which
stimulates rapid formation of new capillaries.
Neovascularisation occurs in malignant tumors and
results in lower pulsatile and resistance index.7
Resistance index is defined as the maximum systolic
velocity minus end diastolic velocity divided by
maximum systolic velocity. Pulsatility index is
defined as maximum systolic velocity minus end
diastolic velocity divided by mean systolic velocity.
Both indices increase with increasing distal vascular
resistance and the two indices have a high correlation.
A comparison of different studies shows that no
standard has been established concerning which
Doppler index to use or what cut off is most
appropriate. However the resistivity index less than
0.4-0.88
and pulsatility index less than 1 are generally
considered to be suspicious of malignancy.8,9
Doppler
ultrasound has yielded variable results in
distinguishing benign from malignant mass with a
sensitivity of 50-100% and specificity of 46-
100%10,11,12
. Different results are partly due to varying
threshold values and corresponding trade-offs between
specificity and sensitivity.
MATERIALS AND METHODS
This prospective study was conducted at Lalla Ded
Hospital, Government Medical College, Srinagar, over
a period of one and half year.100 patients (Women in
reproductive age group and postmenopausal women)
diagnosed with adnexal masses on pelvic examination,
conventional sonography and referred cases of
adnexal masses to our hospital were included in the
study. Prior to the study ethics committee permission
was obtained from our college. An inform consentform was obtained from all the participants.
Exclusion Criterion
Unilocular anechoic small cyst (less than 5
centimeters) which resolves on follow up ultrasound
examination, Tubal gestation, Masses that were found
to arise from uterus .
All the patients were evaluated by colour Dopplerultrasonography using a Philips IU-22 machine with
pulsed Doppler system and equipped with a colour
velocity imaging system for colour blood flow
codification. After characterizing masses by their
morphology, colour velocity imaging gate was
activated to identify blood flow. The resistance index
and Pulsatility index were calculated in each case. The
lowest pulsatility index and resistive index detected at
any point in the mass were considered for analysis.
The masses which were completely avascular with noblood flow were considered as benign.
The Doppler findings were considered suggestive of
malignancy when:
Resistive index (RI) < 0.4513
Pulsatility index (PI)
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Table 2: Mean RI and Mean PI in Benign and Malignant Adnexal Masses
n Mean95% Confidence Interval for Mean
p valueLower Bound Upper Bound
Doppler_RIMalignant 18 0.34 0.30 0.39
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was 84.2%, 96.3% , 84.2% and 96.3% respectively.
Our results are consistent with the studies of Fleischer
et al17
, Timor Tritsch et al18.
CONCLUSION
Colour Doppler sonography has added to theunderstanding and characterization of the adnexal
lesions, based on its depiction of the vascularity of the
masses. Doppler study is effective in the
differentiation of adnexal masses.
REFERENCES
1. Carter J, Saltzman A, Hartenbach E ,Fowler J,
Carson L, Twiggs LB. Flow characteristic in
benign and malignant gynaecological tumors
using transvaginal colour flow Doppler. Obstet
Gynecol 1994; 83(1): 125-30
2. ACOG. Practice Bulletin. Management of adnexal
masses. Obstet Gynecol 2007; 110(1): 201-14.
3. Drake J. Diagnosis and management of the
adnexal mass. Am Fam Physician. 1998; 57(10):
2471-76
4. Gallup DG, Talledo E. Management of the
adnexal mass in the 1990s. South Med J. 1997;
90(10): 972-81
5. EC Hill. Gynaecology in current surgical
diagnosis and treatment. East Norwalk, conn:
Appleton and Lange 1994: 1004-07
6. Folkman J, Watson K, Igber D, Hassahan D.
Induction of angiogensis during transition from
hyperplasia to neoplasia. Nature 1989; 339: 58-61.
7. Goldstein SR. Conservative management of small
postmenopausal cystic masses. Clin Obstet
Gynecol 1993; 36: 395-401
8. Hamper UM, Sheth S, Abbas FM, Rosenshein
NB, Aronson D, Kurman RJ. Transvaginal colour
Doppler sonography of adnexal masses:differences in blood flow impedance in benign
and malignant lesions. Am J Roentgenol 1993;
160: 1225-28
9. Stein SM, Laifer Narin S, Johnson MB, Roman
LD, Muderspach LI, Tyszka JM, Ralls PW.
Differentiation of benign and malignant adnexal
masses, relative value of gray scale colour
Doppler and spectral Doppler sonography. Am J
Roentgenol 1995; 164: 381-86
10. Salem S, White LM, Lai J. Dopler sonography of adnexal masses, the predictive value of the
pulsatility index in benign and malignant diseases.
Am J Roentgenol. 1994; 163: 1147-50
11. Hata K, Hata T, Manalse A, Sugimora K, Kiato
M. A critical evaluation of transvaginal colour
studies, transvaginal sonography, MRI and CA
125 in detecting ovarian cancer. Obstet Gynecol
1992; 80: 922-26
12. Lerner JP, Timor Treitsch TE, Federman A,
Abramouich G. Transvaginal ultrasonographic
characterization of ovarian masses with improved
weighted scoring system. Am J Obstet Gynecol
1994; 170: 81-85
13. JL Alcazar, T Errasti, A. Zornoza, JA Minguez, M
J Galan. Transvaginal colour doppler
ultrasonography, and CA 125 in suspicious
adnexal masses. Int J Gynecol and Obstet 1999;
66: 255-61
14. Curtin JP. Management of the adnexal mass.
Gynecol Oncol 1994; 55: 542-46
15. Luxman D, Bergamn A, Sagi J, David M. The
postmenopausal adnexal mass: correlation
between ultrasonic and pathological findings.
Obstet Gynecol. 1991; 77: 726
16. Tekay A, Jouppila P. Validity of pulsatility and
resistance indexes in classification of adnexal
tumors with transvaginal colour Doppler
ultrasound. Ultrasound Obstet Gynecol. 1992; 2:
338-44
17. AC Fleischer, JA Cullinan, HW Jones, W Peery,
RF Bluth, DM Keppler. Serial assessment of
adnexal masses with transvaginal colour Doppler
sonography. Ultrasound in Medicine Biology.
1995; 21(4): 435-41
18. Timor-Tritsch LE, Lerner JP, Monteagudo A,
Santos R. Transvaginal ultrasonographic
characterization of ovarian masses by means of
colour flow directed measurement andmorphologic scoring system. Am J Obstet
Gynecol 1993; 168: 909
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International Journal of Medical Research
&
Health Scienceswww.ijmrhs.com Volume 3 Issue 2 (April - Jun) Coden: IJMRHS Copyright @2014 ISSN: 2319-5886
Received: 11th Nov 2013 Revised: 24th Dec 2013 Accepted: 5th Jan 2014Research Article
GONIOSCOPIC CHANGES IN CONVENTIONAL ECCE VS MANUAL SICS: A COMPARATIVE
STUDY
Surya Joseph1, Sundararajan D
2, *Rajvin Samuel Ponraj
3, Srinivasan M
4, Veluchamy
5
1Senior Resident,
2Associate Professor,
3Postgraduate,
4Professor
, 5Senior resident Dept of Ophthalmology,
Meenakshi Medical College, Kanchipuram, Tamilnadu, India
*Corresponding author email: [email protected]
ABSTRACT
The aim of the study is to observe and compare the Gonioscopic changes in the angle of the anterior chamber of
the eye after surgeries namely; Conventional Extra capsular cataract extraction (ECCE) with Posterior chamber
Intraocular lens (PC IOL) implantation, Manual Small incision Cataract Surgery with PCIOL implantation. The
clinical study was undertaken after Institutional Ethical committee clearance, securing the inform consent, total
number of 100 patients were enrolled in the study. 50 ECCE; 50 SICS consisting of 57 Males and 43 Females
aged between 40 - 80yrs who were admitted and operated for Cataract at Meenakshi Medical college Hospital &
Research institute. The following parameters are studied: Gonioscopic changes in the angle, namely the PAS
formation in the quadrants, pigment dispersion in each of the methods. After this study, we arrive to a conclusion
that complications in the angle of anterior chamber occur mostly in Conventional with insignificant change inmanual SICS. So manual Small incision Cataract Surgery with PCIOL implantation is preferable over
Conventional ECCE with PCIOL implantation.
Keywords: Gonioscopy, Peripheral anterior synechiae, Scheie’s classification, Pigment dispersion,
Malpositioning of the Superior Haptics
INTRODUCTION
Cataract is the leading cause of Reversible Blindness
in our country. The ultimate goal of a cataract surgery
is to restore and preserve the pre cataract vision andto alleviate the other cataract related symptoms. In
the quest for perfection, the techniques and
approaches followed by cataract surgeons have
constantly changed over the years.
Hence the realistic portrayal of the trends in cataract
surgery can be best described as a wide spectrum,
ranging from Intra Capsular Cataract Extraction
(ICCE) to Phaco Emulsification. Such a diversity of
trend is governed by multiple factors, the most
pertinent of which are economical, patients'
awareness, surgeon’s caliber, availability of
equipments and the cataract backlog.
The current surgical trend for the majority of
surgeons in the developing world is towards
Conventional Extra capsular cataract extraction(ECCE) with PC IOL implantation. Small Incision
ECCE techniques are becoming quite popular for
those who have accepted the challenges of transition
towards a better technique. Perhaps about 5-10% of
the cataract surgeons in India routinely perform
Phaco. The advent of Phaco emulsification has
minimized the size of the incision and its related
complications, with an added benefit of early
stabilization of refraction.
The main objective of this study is to observe and to
compare the Gonioscopic changes in the angle after
conventional ECCE with PC IOL implantation and
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Surya et al.,
Small Incision Cataract Surgery
attempt has been made to note an
these changes and the possible
changes over the Intra Ocular Pre
Acuity.
Aim of the study: The main objecti
to observe and compare the Gonios
the angle after
Conventional ECCE with PC IOL i
Manual Small incision Cataract Sur
PC IOL implantation
An attempt has been made to note t
these changes and the possible
changes over the Intra Ocula
Postoperative Visual acuity.
MATERIALS AND METHOD
This clinical study was undertaken
ECCE; 50 SICS consisting of 5
Females aged between 40 - 80yrs w
and operated for Cataract at Me
college Hospital & Research institut
the inform consent, total number of
enrolled in the study.
Institutional Ethical clearance ha
before initiating the study. Patien
observing all proper inclusion and e
Inclusion criteria: No past history o
accidents, Diabetic patients with a
than 10 years, Non- Prolife
retinopathy, Best corrected visual ac
Exclusion criteria: Cataract, Gla
opacities or any evidence of optic at
nervous system disease, Prolif
retinopathy
Gonioscopic changes in the angle
chamber by Shaffer grading while dplane mirror gonioscopy. Based
posterior structure visible in the
Peripheral Anterior Synechiae f
quadrants, Pigment dispersion in
SICS.
Partial or complete closure Grade 0
≤10° angle of approach Grade I AC‡
20° angle of approach Grade II AC
20° – 35° angle of approach Grade III
35° – 45° angle of approach Grade IV
Int J Med Res Health
ith PCIOL. An
y progression of
effects of these
ssure and Visual
ve of this study is
copic changes in
plantation
gery (SICS) with
he progression of
effects of these
Pressure and
in 100 Eyes- 50
Males and 43
ho were admitted
enakshi Medical
. After Securing
100 patients were
s been obtained
ts were enrolled
clusion criteria.
f cerebrovascular
duration of less
rative Diabetic
uity at least 6/9
ucoma, Vitreous
rophy, Peripheral
erative diabetic
of the anterior
oing Goldmann 3 upon the most
ngle. Namely
rmation in the
CCE as well as
< 1/4 CT§
1/4 CT
AC = 1/2 CT
The Scheie’s method o
was followed. Larger n
amount of pigmentation.
Scheie classification
Grade 0 – Entire angle v
wide ciliary body band
Grade I - Last roll of iris
body
Grade II - Nothing poste
visible
Grade III - Posterior por
hidden
Grade IV - No structures
visible6.
RESULTS
Fig 1: Age-sex wise gro
Fig 2: Incidence of perip
ECCE
PAS formation was obse
which underwent conve
implantation. Superior a
Inferior angle PAS in 5
eyes that underwent SIC
238
ci. 2014;3(2):237-240
f grading TM pigmentation
umbers represent increasing
isible as far posterior as a
obscures part of the ciliary
rior to trabecular mesh-work
ion of trabecular mesh-work
posterior to Schwalbe’s line
p distribution graph
heral anterior synechiae in
rved in 28 eyes of 50 cases,
tional ECCE with PC IOL
ngle PAS noted in 23 eyes.
eyes. No PAS was seen in
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Fig 3: As overlying the lens haptics p
in angle structure
20 eyes showed PAS overlying th
IOL. Which accounts to 71.4%.
Haptics PAS were observed eaoperative period (3 Months) and rem
Fig 4: Incidence of pigment disper
DISCUSSION
The incidence of PAS in the presen
which is comparable to 54% observ
Liu.Y, et al in “Gonioscopic
posterior chamber IOL implantati
observed by Maden A, Gunenc U“Gonioscopic changes in eyes with
was seen in eyes in which SICS
(Capsular Bag Fixation of IOL)
Involvement of the Superior angle
suggested by 46% of PAS in the S
to malpositioning of the Sperior
ciliary Sulcus).
PAS were seen more frequently wit
vertical position than in Eyes
oriented Lens Haptics
3
.PAS overlying the Haptics of PC I
in 20 eyes (71.4%) in this study is c
Int J Med Res Health
igment dispersion
e Haptics of PC
ost of the lens
ly in the Post ain stable in size.
sion
t study was 56%,
d by Lis, Liao R,
bservation after
ion” and 41.8%
, Erkin E et al10
C IOL” No PAS
was performed a
is prominent as
perior angle due
Haptics (in the
h Lens Haptics at
ith horizontally
L was observed
mparable to 80%
observed by R Blair
Haptics of PC Lenses”
possessed a distinct m
marked anterior displace
broad iris apposition to t
more anterior angle struc
Most of the lens haptic
the Postoperative peri
progression in size was
rise in IOP attributable
changes in the postop
observed secondary to
Pigment dispersion is e
chafing effect of the len
aspect of iris and also d
Interestingly, it’s also no
limited clumping of pig
in 40 eyes (40%) compa
Maden A, Gunenc “Goni
PC IOL”. Inferior angl
due to gravitational settli
28 eyes with PAS had pa
related to the positio
compared to 88% of ey
Liu Y. Guoy & Pan H5
After three months, p
Cortex still existed in
PCIOL.
This study was under
suggestion that routine
should be performed afte
CONCLUSION
Conventional Extra Caps
PC IOL implantation si
alters the Gonio Anatom
to Small Incision CataracDecrease in the incision
cornea with a self- se
and a Corneal lip preven
the Bag fixation of IOL
pigment dispersion int
incidence of changes in t
Continuous Curvilinear
important for proper cap
(P
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Surya et al., Int J Med Res Health Sci. 2014;3(2):237-240
REFERENCE
1. Chen Weirong ,LIU Yizhi, Wang Ningli Guo
Yan, HE Mingguang , Comparison of the efftypes
of intraocular lens, Chinese Medical Journal
2001;114(12):1286-89
2. Maden A, Gunenc V, Erkin E. Doc. Ophthalmol,‘Gonioscopy changes in eye with posterior
chamber intraocular lens’ by. 1992, 82(3), 231-8.
3. Peripheral anterior synechiae overlying the
haptics of posterior chamber lenses’ Occurrence
and Natural history, Ophthalmology 1990, 97:
415-23.
4. Evans RB. Peripheral anterior synechiae
overlying the haptics of posterior chamber lenses.
Occurrence and natural history’,Ophthalmology
1990: 97(4), 415-23.5. LiaoR, LiS, LiuY, Guo Y, Pan H, Tao X. The
relation of the location of haptics of posterior
chamber intraocular lenses and peripheral
anterior synechiae’ by. Source: Medicine: PMID:
8575604, UI: 96148006.
6. Steven V. L Brown., Basic and Clinical Science
Cours e, Faculty, Section 10, Steven T. Simmons,
MD, Steven V. L. Brown, Consultants William
LH, Janis ER. Gonioscopy in the Management of
Glaucoma James A. Savage, MD , Focal PointsAmerican Academy of Ophthalmology.
2006;XXIV: (Section 3 of 3)
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International Journal of Medical Research
&
Health Sciences
www.ijmrhs.com Volume 3 Issue 2 (April - Jun) Coden: IJMRHS Copyright @2014 ISSN: 2319-5886Received: 13
thDec 2013 Revised: 8
thJan 2014 Accepted: 10
thJan 2014
Research Article
HISTOLOGICAL AND HISTOMETRIC STUDY OF TESTIS IN ALBINO RATS TREATED WITH
AMLODIPINE
*Karthick S, Harisudha R
Department of Anatomy, Melmaruvathur Adhiparasakthi Institute of Medical Science & Research,
Melmaruvathur, Tamil Nadu, India
*Corresponding author email: [email protected]
ABSTRACT
Amlodipine is the most common drug of choice to treat hypertension, one of its side effects is infertility and its
effect on the testis of male albino rats is not well documented. Aim: To observe the effect of amlodipine in testis
of male albino rats by the histological and histometric method. Materials& Method: we selected 12 adult male
albino rats divided into 2 groups, group 1 treated as control group 2 treated as experiment and amlodipine is
administered for 30 days. After 30 days testis were removed and analysed histologically and histometrically.
Result: Though there are no marked changes, but early degenerative changes and reduction in weight of testis of
experimental rats observed. Conclusion: Presence of vacuolated spermatogenic cells in some of the seminiferous
tubules indicates early degeneration and arrest of spermatogenesis.
Keywords: Hypertension, Infertility, Amlodipine Side Effects.
INTRODUCTION
Hypertension is one of the leading causes of the
global burden of disease. Approximately 7.6 million
deaths (13 – 15% of the total) and 92 million
disability-adjusted life years worldwide were
attributable to high blood pressure in 2001.1
Hypertension doubles the risk of cardiovasculardiseases, including coronary heart disease (CHD),
congestive heart failure (CHF), ischemic and
hemorrhagic stroke, renal failure, and peripheral
arterial disease.1The burden of hypertension increases
with age and among individuals aged ≥ 60, i ts
prevalence is 65.4%. Amlodipine has become the
second drug of choice for hypertension2, though its
side effect on infertility has been proved to some
extent.3,4
The exact mechanism of amlodipine causing
infertility in male remains to be completelyelucidated moreover, its effect on the microscopic
structure of the testis is not well documented
histometrically, and therefore it has been planned to
observe histological observation of testis, histometric
analysis of testis, determine the weight of testis.
MATERIALS AND METHODS
A total of 12 adult male albino rats was obtained from
the central animal house, Rajah Muthiah Medical
College, Annamalai University, which were
maintained under standard laboratory conditions at
28±2°C were provided with standard rat diet and
water ad libitum. After getting ethical committee
clearance, the animals were divided into 2 groups.
Group I comprised of 6 animals; Control: received
vehicle only (0.01% ethyl alcohol) and group II
comprised of 6 animals; Experimental (Test group):
received amlodipine orally (0.45mg/kg/day) given for30 days. All the animals were sacrificed after 30 days
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Karthick et al.,
of the experimental period, the testi
trimmed free of adipose tissue and
The weight of the testis was reco
were fixed in Bouin’s fluid for a t
hours. After fixation, the tissues w
light microscopy, the tissues w
Haematoxylin and Eosin and Mas
stain for connective tissue. The st
testis were examined in low power
power (x400). Qualitative evaluati
sections were supplemented by the
quantitative testicular biopsy score
Johnson (1970) to estimate the ex
alterations. For histometric assessm
emphasized by Hans Elias and Paul
as Weibel and Hans Elias (196
employed for estimating the volume
of various tissue components. Volu
and stroma were estimated by poin
eyepiece reticule with low ma
formula used for estimation of volu
Where Vi = volume of tissue co
volume of tissue, Pi = number of p
tissue component, PT = total numbe
reticule. The height of the secretor
the diameter of tubules was measur
micrometer with high magnification.
Statistical Analysis: Using latest HP
RESULTS
There is a decrease in weight of
experimental rats than the control
table 1. Histological observation
there was no testicular alteration a
was intact with normal sperm
experimental animals, when companimals. However, on closer exami
power revealed an interesting find
group animals.
Fig 1: Sections of testis Control and tes
Int J Med Res Healt
is were removed,
onnective tissue.
ded. The organs
otal period of 24
re processed for
re stained with
son’s Trichrome
ined sections of
(x 100) and high
ons of testicular
use of the semi
count (TSBC) of
tent of testicular
nt the principles
ly (1996) as well
7) were strictly
and surface area
e of parenchyma
t count using the
gnification. The
e (Vi = Pi / PT)
ponent per unit
ints touching the
r of points in the
y epithelium and
d using as ocular
SS software
the testis of the
rats presented in
f testis revealed
d the epithelium
atogenesis from
red with control ation under high
ing in these test
t rats (H &E 100X)
Fig 2: Testis control and te
100X)
Fig 3: Sections of testis fGieson’s stain 100X)
Fig 4: Sections of seminifer
(H& E 400X)
Arrow (test) shows early
spermatogenic cells
Fig 6: Seminiferous tubules
trichrome 400X)
Arrow (test) shows early
spermatogenic cells
Fig 7 : Seminiferous tubule
Gieson’s 400X)Arrow in (test) shows ea
spermatogenic cells
242
Sci. 2014;3(2):241-244
t (Masson’s trichrome stain
rom control and test (Van
ous tubules from control , test
fatty degeneration of
from control, test (Masson’s
fatty degeneration of
s from control, test (Van
ly fatty degeneration of
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Table 1 : Weight of testis, Volume of tissue components (values are expressed as Mean ± SEM)
Animal group Testis
(grams)
Volume of tissue components Diameter of
Seminiferous Tubules
(µm)Seminiferous
tubules (mm3 /mm
3)
Connective tissue
(mm3 /mm
3)
Leydig cell
(mm3 /mm
3)
Control 1.2595 0.7747 ± 0.0216 0.1309 ± 0.0245 0.0719 ± 0.0075 279.64 ± 10.922*
Test group 0.9109 0.6764 ± 0.0233 0.2342 ± 0.0233 0.0867 ± 0.0087 268.45 ± 16.19*
* - p < 0.05
There was the presence of vacuolated spermatogenic
cells interspersed among the seminiferous epithelium.
(Fig 2). Histometric data of testicular tissue
components are summarized in table 1. The
quantitative analysis of various tissue components of
the testis showed no significant change in any
component. But the diameter of seminiferous tubules
showed a significant increase in testis of experimental
(Test group) animals when compared to those of
control animals.
DISCUSSION
The anti-reproductive effect of amlodipine on male
reproductive organs varies from decrease in weight of
testis, epididymis, seminal vesicle and prostate,
decrease in hormone levels of testosterone, FSH andLH, and partial / complete arrest of spermatogenesis
by de-regulation of Ca2+ homeostasis, loss of libido
and erectile dysfunction. In our present study, we
observed that sacrificed rats after 30 days of
treatment with amlodipine showed a reduction in the
weight of testis. This finding is in agreement with the
findings of many investigators. Rabia et al. 5
showed a
significant drop in absolute testicular weight, gonado
– somatic index and serum testosterone levels in rats
after amlodipine treatment. Similar anti reproductiveeffects were described by Ayodele O et al., Benoffet
al.6,7
. They noticed altered serum parameters
(reduction in sperm count & motility) The drug may
not have a direct effect on Leydig cells, as the present
study shows that Leydig cells are not affected
histologically and histometrically in the treated
animals. It appears that, the mode of action of this
calcium channel blocker is through hypothalamo –
hypophyseal – testicular axis by altering either the
release of GnRH from hypothalamic neurons or the
release of gonadotrophins from the pituitary, this can
be augmented by the findings of Bourguignon JP, et
al.8
Who showed that in the presence of calcium
channel blockers, the release of GnRH was marked
and reversibly reduced. Lee JH et al9told nifidepine
causes male infertility by deregulation of Ca2+
homeostasis in testis of mice and arrest of
spermatogenesis. Juneja.R et al., Suresh C. Joshi et
al.10,11
also told calcium channel blocker causes
decrease in sperm density, sperm motility and cellular
energy content in guinea pigs. Histopathological
findings exhibited partial arrest of spermatogenesis in
experimental animals. With above findings, we
carried the present work i.e degenerative changes
occurring in the seminiferous epithelium indicate that
the amlodipine causes partial arrest of
spermatogenesis due to the deregulation of Ca2+
homeostasis. This partial arrest of spermatogenesis isdue to degeneration of spermatogenic cells observed
by us and is supported by reduction in weight of
testis. Although marked changes were not observed
in the histological structure of testis under low power,
early degenerative changes were noticed in the
seminiferous epithelium under high power this
indicates the beginning of the arrest of
spermatogenesis. Probably the complete arrest may
be noticed after long term treatment for more than 64
days as the spermatogonia takes 64 days to becomemature spermatozoa.
CONCLUSION
The following conclusions are arrived at from the
findings of our study on effect of amlodipine on testis
in albino rats. There is a marked decrease in weight
of testis, which may be correlated to decrease in
spermatogenesis as evidenced from the sparse content
of the spermatozoa presence of vacuolated
spermatogenic cells in some of the seminiferoustubules indicates early degeneration and arrest of
spermatogenesis. Further the mode of action of the
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drug is probably through hypothalamo – hypophyseal
– testicular axis as the Leydig cells parameters are not
disturbed in the experimental animals, and a long
term study is planned to identify the effects caused by
amlodipine.
ACKNOWLEDGEMENT
I will convey special thanks to my professor
Dr.J.P.GUNASEKARAN to given me an immense
support and valuable needy guidance for this work.
REFERENCES
1. Harrison. Principles of Internal Medicine. The
McGraw-Hill Companies, 2013;18th
edi; 247
2. http://www.nhs.uk/Conditions/Blood-pressure-
(high)/Pages/Treatment.aspx3. Almeida SA, Teofilo JM, AnselmoFranci JA,
Brentegani LG, Lamano TL. Antireproductive
effect of the calcium channel blocker amlodipine
in male rats. Exp Toxic Pathol 2000; 52: 353 – 56
4. Yoshida J. Amlodipine besylate. Eur J
Pharmacol. 2003;472:23 – 31
5. RabiaLatif, Ghulam Mustafa Lodhi, Muhammad
Aslam. ffects of amlodipine on serum
testosterome, testicular weight and gonado
somatic index in adult rats. J Ayub Med Coll
Abbottabad 2008;20(4):8-10
6. Ayodele O, Morakinyo, Bolanle O, Iranloye,
Olufeyisipe A, Adegoke.“Antireproductive effect
of calcium channel blockers on male rats. Reprod
med biol 2009;8(3): 97-102
7. Benoff S, Cooper GW, Hurley I, Mandel FS,
Rosenfeld DL, Scholl GM, Gilbert BR, Hershlag
A. “The effect of calcium ion channel blockers on
sperm fertilization potential. Fertility Sterility.
1994 ; 62(3):606-11
8. Jean-pierre bourguignon, Arlettegerard,
Georgette debougnoux, Joan rose and Paul
franchimont. Pulsatile release of GnRH from the
rat hypothalamus in vitro: calcium and glucose
dependency and inhibition by
superactiveGnRHanalogs. Endocrinology
1987;121: 993 – 99.
9. Lee JH, Kim H, Kim DH, GyeMC. Effects of
calcium channel blockers on the spermatogenesis
and gene expression in peripubertal mouse testis.
Arch Androl., 2006; 52(4):311-8.
10. Juneja.R, I. Gupta, A. Wall, S.N. Sanyal, R.N.
Chakravarti, S. Majumdar. “Effect of verapamil
on different spermatozoal functions in guinea
pigs — A preliminary study”. Contraception;
1990; 41 (2):179-87.
11. Suresh C. Joshi, Reena Mathur, Anita Gajraj,
Tripta Sharma. Influence of methyl parathion on
reproductive parameters in male rats.
Environmental Toxicology and Pharmacology ;
2003;14(3):91-98
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International Journal of Medical Research
&
Health Sciences
www.ijmrhs.com Volume 3 Issue 2 (April - Jun) Coden: IJMRHS Copyright @2014 ISSN: 2319-5886Received: 5
thDec 2013 Revised: 5
thJan 2014 Accepted: 11
thJan 2014
Research article
CLINICAL PROFILE AND ANTIBIOTIC SENSITIVITY PATTERN OF TYPHOID FEVER IN
PATIENTS ADMITTED TO PEDIATRIC WARD IN A RURAL TEACHING HOSPITAL
Sudharshan Raj C*
Dept. of Pediatrics MNR Medical College, MNR Nagar, Narsapur road, Sanga Reddy, Andhra Pradesh,
*Corresponding author email: [email protected]
ABSTRACT
Introduction: Typhoid is a major endemic health problem among children in India. The last two decades have
witnessed the emergence and spread of multidrug resistance against conventional anti typhoid drugs (Ampicillin,
chloramphenicol and trimethoprim – sulfamethoxazole) especially in the South and South-East Asia. Materials
and Methods: Children under twelve years of age with signs and symptoms suggestive of enteric fever were
included in this study. Blood cultures were carried by collecting aseptically 5ml of blood and inoculating into bile
broth and subcultured onto blood agar and Mac Conkey agar. Antimicrobial sensitivity performed according to
CLSI guidelines. Widal test was performed. Other investigations like haemoglobin, total count and differential
count of WBC, ESR were carried out. Results: The incidence of enteric fever in this study was 3%. The
maximum children were in age group more than 5 years. Maximum cases were admitted during June-September.
The most common symptoms were fever, anorexia, vomiting, and pain abdomen. The culture positivity of
Salmonella typhi (S.typhi) was 35.4%. The overall positivity of Widal test was 89.8%. Multidrug resistant isolates
in this study was 53.6%. Conclusion: Majority of the children were greater than 8 years old. Fever (intermittent
type), anorexia, vomiting were the three major symptoms. Among the signs spleenomegaly, hepatomegaly, coated
tongue and toxemia were common. Relative bradycardia was not seen. Widal test was found positive in the
majority of cases. Blood cultures were positive mainly in the first week of illness. The sensitivity pattern of
S.typhi revealed significant proportion of multidrug resistant strains and simultaneous presence of
chloramphenicol sensitive and resistant strains in the study.
Keywords: Typhoid, Salmonella typhi, multidrug resistant.
INTRODUCTION
Typhoid fever, also known as enteric fever is caused
by the Gram negative bacterium Salmonella enterica
serovar Typhi. The disease is mainly associated with
low socioeconomic status and poor hygiene, with
human beings the only natural host and reservoir of
infection.1
Estimates for the year 2000 suggest that
there are approximately 21.5 million infections and 2,
00,000 deaths from typhoid fever globally eachyear.
2-4
Typhoid is a major endemic health problem among
children in India. The last two decades have
witnessed the emergence and spread of multidrug
resistance against conventional antityphoid drugs
(Ampicillin, Chloramphenicol and Trimethoprim –
Sulfamethoxazole) among typhoid Salmonellae,
especially in South and Southeast Asia.5,6
Typhoid
fever caused by such multidrug-resistant (MDR)strains of Salmonella enterica serotype Typhi
presents a serious problem in many developing
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countries.7,6
It has left fluoroquinolones as the
antimicrobial agents of choice for the treatment of
typhoid fever.8
Fluoroquinolones, especially
ciprofloxacin, have been in use for more than 18
years and have remained an important weapon
against typhoid infections. Effective antimicrobial
therapy is required to control morbidity and prevent
death from typhoid.
This study aims to know the clinical profile of
pediatric enteric fever and the sensitivity of the
disease to drugs in this region.
MATERIALS AND METHODS
The prospective study was carried out in a rural
teaching hospital over a period of one year.
Data regarding admitted children below 12yrs of agewith signs and symptoms suggestive of enteric fever
and fulfilling any of the following criteria were
included in the study.
Inclusion criteria:
1. Positive culture for Salmonella typhi
2. Widal titre;TO and TH>=1:160
3. Fourfold or greater rise in Widal titres.
Thorough and detailed history, clinical examination
and laboratory investigations were done in all cases.
The following investigations were done:
Routine investigations: Haemoglobin estimation,
Total and differential count for white blood cells,
Erythrocyte sedimentation ratio, Urine and stool
examination, Other investigations such as a chest X
ray, liver function test, abdominal sonography were
done where ever required
Bacterial cultures: Blood cultures were carried out
by collecting aseptically 5ml of blood and added to
50ml of bile broth, incubated at 37°C for 24hrs.
Initial subculture was made after 24hrs and if found
negative, further sucultures were made after 48hrs,
4days and 7 days. Positive growths were subjected to
standard biochemical tests.9Species confirmation was
done by agglutination with high titre sera.
Stool specimens were plated directly onto
MacConkey and Salmonella, Shigella agar (SS), and
inoculated into Selenite F broth for enrichment. The
identity of isolates was confirmed by standard
biochemical tests9
and slide agglutination with
specific antisera.
Widal test: The Widal tube agglutination test was performed according to the manufacturer’s
instruction, using Tidal (Span diagnostics) containing
O and H antigens of S. typhi and S. paratyphi A and
S.paratyphi B. Positive and negative serum controls
were included, a titre of ≥1/160 to either antigen in a
single serum specimen (in addition to the
seroconversion) was taken to be indicative of typhoid
fever. The results were correlated with blood culture
results and interpreted in conjunction with the
patient’s history and recent clinical presentation on
admission.
Antimicrobial susceptibility testing: Susceptibility
to antimicrobial agents was performed using the
Kirby Bauers disc diffusion method as described by
the Clinical and Laboratory Standards Institute.10
Antimicrobial agents (discs) tested and reported were
obtained from Hi media and included: ampicillin
(10μg), trimethoprim – sulfamethoxazole
(25/23.75
μg), chloramphenicol (30
μg), ceftriaxone
(30μg) , ciprofloxacin (5μg), cefixime(30μg) and
cephalexin(30μg). MDR isolates of S. typhi were
those resistant to all three first line antityphoid drugs
(ampicillin, chloramphenicol and trimethoprim –
sulfamethoxazole).
RESULTS
In this study a total number of 79 cases of enteric
fever in children 12 years or less, admitted to the
pediatric ward were studied. Total number of
admissions in the pediatric ward during this period
was 2601 so the incidence was 3%.
The maximum children were in the age group of
more than 5 years (50, 63.3%). The youngest child in
this study was 13 months old.
Among the children affected 42 were males and 37
females. The male to female ratio was 1.1:1. Cases
were admitted throughout the year showing the
endemicity of the disease. Maximum cases were
admitted during June-September 36 (45.6%)
(Table1).
The most common presenting symptom was fever 79
(100%) followed by anorexia 43 (54.4%) and
vomiting 38 (48.1%), pain abdomen 21 (26.6%),
loose motions 10 (12.6%), altered sensorium 10
(12.6%). In this study maximum cases 35 (49.3%)
had fever for 8-14 days prior to admission. Almost
half the cases 39 (49.4%) showed intermittent type of
fever. The signs of enteric fever in this study were
(table2).
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Complications seen in this study were bronchitis 9
(11.3%), encephalopathy 7 (8.9%), cholecystitis 5
(6.3%), enteric hepatitis 3 (3.8%), shock 2 (2.53%)
and paralytic ileus 1 (1.26%).
Routine investigations: In this study haemoglobin <
10gm/dl was found in 41.8% of cases. Majority of the
children had WBC count in the range 5000-10000/cu
mm (70.9%).
Table 1: Month wise distribution of cases
Month No. of cases Percentage
January 05 6.3%
February 04 5.1%
March 04 5.1%
April 05 6.3%
May 07 8.8%
June 08 10.2%July 08 10.2%
August 12 15.2%
September 08 10.2%
October 05 6.3%
November 06 7.6%
December 07 8.8%
Total 79 100%
Table 2: Signs of enteric fever
Signs Number of
cases
Percentage
Tachycardia 64 81%
Spleenomegaly 54 68.4%
Hepatomegaly 44 55.7%
Coated tongue 41 51.9%
Pallor 41 51.9%
Table 3: Antibiotic resistance pattern of
salmonella typhi
Antibiotic Number n =
28
Percentage
Multi drug resistant 15 53.6%
Chloramphenicol 18 64.2%
Ampicillin 25 89.3%
Co-trimoxazole 27 96.4%
Ciprofloxacin 28 00%
Ceftriaxone 28 00%
Cefixime 28 00%
Cephalexin 13 46.4%
In this study S.typhi was isolated in 28 out of 79
cases (35.4%), 17 (53.1%) cases were Widal positive
in 1st
week showed TO & TH >1:160.The positivity
increased in 2nd
and subsequent weeks (91.4% &
100% ) respectively. Among 15 cases which were
widal negative in first week 9 cases (60%) showed
rise in titres. The overall positivity of Widal test was
89.8%. The sensitivity of the Widal test was 71.4%.
Antibiotic resistance pattern in this study was (table
3)
DISCUSSION
The incidence of enteric fever in this study was 3%,
which was in accordance with the studies conducted
by Pohawalla et al who also reported an incidence of
3%11
but Bavdekar etal reported 23%12
and Taneja
19%.13
The maximum children were in the age group
of more than 5years (63%) which is comparable to
that in Pandey K.K et al 86.5%14
and Subindra
73%.15
The male to female ratio in this study was1.1:1. Pandey etal reported 1.2:1.
14
In this study cases were admitted throughout the year
showing the endemicity of the disease. Maximum
cases were admitted during June-September (45.6%).
This period coincides with the onset of monsoon and
increase in housefly population, which facilitates
faeco-oral transmission. Pandey K.K et al reported
maximum incidence between May-July14
and Arora
et al reported 40.6% cases in the period of
September-October.
16
The most common symptoms were fever (100%),
anorexia (54.4%), vomiting (48.1%), pain abdomen
(26.6%), constipation (25.3%), loose motions
(12.6%) and altered sensorium (12.6%). These
symptoms were also seen in studies conducted by
Taneja Sood et al13
and Pandey KK et al.14
In the present study maximum cases (44.3%) had
fever for 8-14 days prior to admission which was
comparable to that of Kapoor JP et al (51.6%).16
Almost half the cases (49.4%) showed intermittent
type of fever. No case in this study had stepped
ladder type of fever and this finding is same as
reported by Pandey KK etal14
, Kapoor JP, et al.17
The
use of antipyretics and antibiotics were probably
responsible for this pattern.
The common signs seen were spleenomegaly
(68.4%), hepatomegaly (55.7%), coated tongue
(51.9%), pallor (51.9%) which was also reported by
Kapoor JP et al17
. The other signs tachycardias, toxic
look, dehydration seen in this study were not reported
by others.
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In this study haemoglobin 1 year were seen to be affected, majority
being >8 years old. Fever (intermittent type),
anorexia, vomiting were the three major symptoms.
Among the signs spleenomegaly, hepatomegaly,
coated tongue and toxemia were common. Relative
bradycardia was not seen. Bronchitis,encephalopathy, hepatitis, and cholecystitis were
common complications. Widal test was found
positive in majority of cases. Blood cultures were
positive mainly in the first week of illness. The
sensitivity pattern of S.typhi revealed significant
proportion of multidrug resistant strains and
simultaneous presence of chloramphenicol sensitive
and resistant strains in the study. Both ciprofloxacin
and ceftriaxone were effective in the treatment with
no major adverse effects.
REFERENCES
1. Evanson Mweu and Mike English. Typhoid fever
in children in Africa. Trop Med Int Health.
2008;13(4): 532 – 40
2. Crump J, Luby S, Mintz E. The global burden of
typhoid fever. Bulletin of the World Health
Organization. 2004;82:346 – 53
3. Bhan M, Bahl R, Bhatnagar S. Typhoid and
paratyphoid fever. Lancet. 2005;366:749 – 62
4. Bhutta Z. Current concepts in the diagnosis and
treatment of typhoid fever. British Medical
Journal. 2006;333:78 – 82.
5. Chandel DS, Chaudhry R, Dhawan B, Paudey A,
Dey AB. Drug-resistant Salmonella enterica
serotype Paratyphi A in India. Emerg Infect Dis
2000; 6: 420 – 21.
6. Rowe B, Ward LR, Threlfall EJ. Multidrug-
resistant Salmonella Typhi: a worldwide
epidemic. Clin Infect Dis 1997;24(1): S106 – 09.
7. Ivanoff B, Levine MM. Typhoid fever:
continuing challenges from a resilient bacterial
foe. Bull Inst Pasteur. 1997;95: 129 – 42
8. Parry CM, Hien TT, Dougan G, White NJ, Farrar
JJ. Typhoid fever. N Engl J Med.2002; 34:1770 –
82.
9. Colle JG, Miles RS, Watt B. Tests for
Identification of bacteria. Mackie and Mc
Cartney Practical Medical Microbiology,Churchill Livingstone 2008: 14
thedition : 131-
149.
10. Clinical and Laboratory Standards Institute.
Methods for Disk Susceptibility Tests for
Bacteria that Grow Aerobically. Wayne, PA:
Clinical and Laboratory Standards Institute.
2005;7th edn, document M2 – A8
11. Pohawalla JN, Bhandari NR. Some observations
on typhoid encephalopathy in chidren. I. J. of
child health 1960;9:375-80.
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12. Bavdekar A, Chaudhari M, Bhave S, Pandit
A.Ciprofloxacin in typhoid fever. Indian j pediatr
1991;58(3):335-39
13. Taneja PN, Sood SC. Typhoid fever :Clinical
picture and diagnosis .I.J. of child health
1961;69-76.
14. Pandey KK, Srinivasan S, Mahadevan S, Nalini
P, Rao RS. Typhoid fever below five years.
Indian pediatr 1990;27(2):153-6.
15. Sudhindra BK. Enteric fever in young children.
Indian pediatr 1995;32:1127
16. Arora RK, Gupta A, Joshi NM, Kataria VK, Lall
P, Anand AC. Multidrug resistant typhoid fever:
Study of outbreak in Calcutta. Indian pediatr
1992;29(1):61-65
17. Kapoor JP, Man Mohan, Vibha Talwar, Daral TS,
Bhargava SK. Typhoid fever in young children.
Indian pediatr 1985;22(11):811-13
18. Mishra AK, Patwari VK, Anand PK, Pillai S,
Aneja J, Chandra, Sharma D. A clinical profile of
multidrug resistant typhoid fever. Indian pediatr
1991;28(10):1171-74
19. Manchanda SS, Harjit Singh, Chitkara HL. A
Review of 270 cases of enteric fever in children.
Ind J Child Health 1959; 8 : 273-80
20. Garg K, Mangal N, Mathur HC. Clinical profile
of multi drug resistant typhoid fever in Jaipur
city. Indian pediatr 1994;31(2):191-93
21. Urmila Jhamb. Multidrug resistant typhoid in
children. NCPID – IAP 2001
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International Journal of Medical Research
&
Health Sciences
www.ijmrhs.com Volume 3 Issue 2 (April - Jun) Coden: IJMRHS Copyright @2014 ISSN: 2319-5886Received: 12
thDec 2013 Revised: 15
thJan 2014 Accepted: 16
thJan 2014
Research Article
ANTIBIOGRAM STUDY OF AEROBIC BACTERIAL ISOLATES FROM UROPATHOGENS
Mallikarjuna Reddy C1, Himabindu M
2, Maity Soumendranath
3, Kanta R.C
4, Kapur Indu
5
1Assistant Professor,
2Assistant Professor,
3Tutor,
4Professor,
5Professor & HOD Departments of Microbiology,
Mallareddy Institute of Medical Sciences, Hyderabad
*Corresponding author email: [email protected]
ABSTRACT
Background: Bacteria are capable of invading and infecting humans, leading to disease and sometimes death.
Systems and tissues in human body are vulnerable to different organisms. Infection pattern is likely to differ by
geographical regions. Aim: This study was aimed to isolate and identify the type of aerobic bacteria causing
Urinary Tract Infections (UTI) in different age groups and sexes, and also in some predisposing conditions. Their
antibiogram also was done. Materials and Methods: Midstream urine sample collected aseptically from 276
patients were subjected for isolation and identification of aerobic bacteria by standard technique and subsequently
antibiogram was done by Kirby – Bayer Method. Both sexes of patients with an age range of 10-70 years and
patients with diabetes (22), hypertension (8) and anemia (8) were also included in the study. Results: Escherichia
coli was the predominant organism(50%) among other isolates –
Klebsiella species (27.3%), Proteus
species(7.14%), Staphylococcus saprophyticus (5.95%), Staphylococcus aureus (3.57%), Enterococci (3.57%),
Pseudomonas species(2.38%). UTI was more common among patients of 60 and more years of age; however,
incidence was more in female patients (36.2 – 38.5%) compared with male patients (25-30%). Anemia, Diabetes
and Hypertension conditions were found to predispose UTI. Aminoglycosides and Quinolones were found to be
more effective against the isolates. Conclusion: The present study reveals in spite of the topographical diversity, the
infecting bacterial isolates from this area were found to be the same as from any other part of India.
Key words: UTI, Predisposing factors, Antibiogram.
INTRODUCTION
Urinary tract infection (UTI) is the commonest of all
infections seen in clinical practice. It is estimated that
10% of the patients visiting hospitals suffer from UTI.1
Both sexes of all age groups are vulnerable to UTI.
Women are especially prone to UTI. It is estimated
that 20% of women experience UTI in their life time.2
UTI is one major cause among hospital acquired
infections.2
Apart from socioeconomic reasons such as illiteracy,
ignorance and insanitation other factors are known to
predispose UTI which could be anatomical position of
the urethra, prostate hypotrophy, renal calculi, stricture
urethra, catheterization, and diabetes.3-5
UTI presents protein manifestations and may also be
asymptomatic.6
Reports indicates that different
spectrum of aerobic bacteria causes UTI. There seems
to be change in type of organisms in different areas.7
Hitherto study on isolation of aerobic bacteria and
their antibiogram associated with UTI has not been
done from this area. Hence this study was undertaken.
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MATERIALS & METHODS
This study was conducted in the department of
microbiology MNR Medical College and Hospital,
Sangareddy, Andhra Pradesh; from September 2008 to
August 2009. Two hundred and seventy six midstream
urine samples were collected in sterile container, frompatients from whom consent was obtained, with a
suggestive history of UTI. These patients were from
10 to 70 years of age; and of sex, 8 patients with
essential hypertension, 22 with diabetes mellitus and
36 with anemia. Pregnant women, women having
thyrotoxicosis, genitourinary procedure, carcinoma,
vaginitis, prostitis, recipient of renal transplant were
excluded from this study.
Midstream urine samples collected aseptically & with
all sterile precautions from the patients with symptomslike fever, chills, frequency, and urgency of urination,
dysuria and suprapubic pain were inoculated onto
MacConkey Agar, Blood Agar and Urichrome Agar,
and incubated at 370C for 18-24 hours for isolation.
Identification of the aerobic bacteria was performed by
various biochemical reactions.8
Antibiotic sensitivity
was done by disc diffusion method (Modified Kirby
Bayer) on Mueller-Hinton agar9
using Amoxycillin
(AMC) 20mcg, Cefepime (CPM) 30mcg, Cefotaxime
(CTX) 30mcg, Amikacin (AK) 30mcg, Gentamicin(G) 10mcg, Ofloxacin (OF) 5mcg, Ciprofloxacin (CIP)
5mcg, Norfloxacin (NR) 10mcg, Nalidixic Acid(NA)
30mcg, Nitrofurantoin (NIT) 300mcg and
Cotrimoxazole (COT) 1.25mcg discs from Himedia
Pvt Ltd.
Ethical clearance: Clearance from institutional ethical
committee was obtained prior to conducting this study
RESULTS & DISCUSSIONS
Total of 276 midstream urine samples, collected
aseptically were processed for isolation of aerobic
bacterial isolates, using standard methods.8
Out of 276
samples, 84 (30.43%) yielded aerobic bacterial isolates
(Table 1). The results indicate that out of 84 positive
aerobic isolates, 42 (50%) Escherichia coli followed
by Klebsiella spp. 23 (27.38%), Proteus spp.6 (7.14%),
Staphylococcus saprophyticus 5 (5.45%),
Staphylococcus aureus and Enterococci each 3
(3.57%) and the least isolate was Pseudomonas spp. 2
(2.33%).
Our findings 84 (30.43%) out of 276 were
considerably higher compared to the reports from Aziz
Marjan Khattak 8
which were 6.2%. Present findings of
the percentage of UTI which are noticeably high is
probably due to illiteracy, ignorance on the part of the
population and also that the study region comprises of
many poorly sanitated towns & villages. It was also
observed that the public &personal hygienic
conditions are poor.
Table: 1 Aerobic bacteria isolated from urine
Aerobic bacterial
isolates
No of isolates %
Escherichia coli 42 50%
Klebsiella Spp 23 27.38%
Proteus spp 6 7.14%
S. saprophyticus 5 5.95%
S. aureus 3 3.57%
Enterococci 3 3.57%
Pseudomonas spp 2 2.38%
*Total number of samples studied = 276, number of
positive samples = 84
The present study indicates that the predominant
isolate was Esch. coli (50%). Various studies7,11-13
(Table:2) on aerobic bacterial isolates from urine
samples including both sexes and all age groups show
a wide range of percent isolates from 30 – 53%.
Table 2: Aerobic isolates from other workers
References % of aerobic
isolates
Predominant
organism
Acharya et al 30% E. coli
Shobha Ram et al 45.5% E. coli
Mandal et al 53% E. coli
Ethel et al 53% E. coli
Incidence of aerobic bacterial isolates from UTI in
male and female patients with age ranging from 10 –
70 years is shown in Table: 3.
Table 3: Incidence of aerobic bacterial isolates from
UTI among male and female of different age groups
Age
(Years)
Male Female
Tota
l
+Ve % Total +Ve %
10 - 20 20 5 25 16 6 37.5
21 – 30 22 4 18.1 52 19 36.5
31 – 40 32 6 18.7 36 14 38.5
41 – 50 16 4 25 25 8 32
51 – 60 13 3 23 23 8 34.7
>61 10 3 30 11 4 36.3
Incidence was moderately higher in female patientsthan male patients and in the age group of 60 – 70
years in males, whereas prevalence is almost same in
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all age groups in female patients.Our findings are
almost consistent with the findings of Marie-vic O
etal.14
Women are prone to develop UTI and 20% of women
are known to develop UTI sometime during their
lifetime. More incidences in males could be due to
retention of urine due to prostate enlargement as it is
known that residual urine as minimal as 2-3ml is likely
to cause UTI.
Predisposing factors such as some metabolic diseases
might play some role in UTI17
. Hence the study was
done to know the role of diabetes, hypertension,
anemia,17
which are common ailments, nowadays.
Proven cases were considered for the study and the
results are depicted in Table: 4
The results indicate the association of these diseases
with UTI . However, more detailed study in this area
needs to be done. Studies conducted by Bahl et al
(1970)15
, Hansen RO (1964)16
on association of UTI
with diabetes and hypertension respectively throws
some message in this direction. Mandal et al. reported
64.3% diabetics having UTI.6
Table 4: Association of UTI with other conditions
Diseases No of cases
studied
No of +ve cases
Diabetes 22 6 (23.2%)Hypertension 8 2 (25%)
Anaemia 36 8 (22.2%)
Another important factor of the study was to evaluate
the antibiotic pattern of the bacterial isolates from the
UTI patients. The results are shown in Table 5.
Our study revealed that Esch. coli which was a
predominant isolate showing multidrug resistance,
particularly higher resistance to Nalidixic acid,
hitherto considered drug of choice for UTI. It
highlights the point that without confirming thesensitivity pattern of the organism, it is not advisable
to use the drug for treatment. Klebsiella showed
resistance to almost all antibiotics used. Proteus was
found to be less resistant to the antibiotics used
Table 5: Antibiotic sensitivity of the isolate
Organism Penicillin Cephalosporins Aminoglycosides Quinolones
COTAMC CPM CTX AK G OF CIP NR NA NIT
E.coli 19 16 15 24 33 18 15 22 8 26 14
Klebsiella 8 10 8 17 19 13 9 14 17 7 6
Proteus 3 4 4 5 5 3 3 4 4 2 1
Staph.
sapro
3 2 4 2 3 4 3 4 5 4 2
Enterococci - - - - - 2 1 2 - 3 -
The antibiotic pattern in this study correlates with the result of McFadyen et al18
. (AMC – Amoxyclav, CPM –
Cefepime, CTX – Cefotaxime, AK – Amikacin, G – Gentamicin, OF – Ofloxacin, CIP – Ciprofloxacin, NR –
Norfloxacin, NA - NAlidixic Acid, NIT - Nitrofurantoin, COT - Cotrimoxazole)
CONCLUSION
In spite of the topographical diversity the infecting
bacterial isolates from this area were found to be the
same as from any other part of India. Aerobic urinary
pathogens infectivity percentage is almost same as is
shown by other studies from different parts of our
country. Although incidence and infectivity pattern
match with other studies, antibiotic susceptibility
profile needs to be done for every isolate for proper
treatment.
ACKNOWLEDGEMENTS
We sincerely thank Dr. Chandrakanth Shirole, Dean,
Dr. Badhra Reddy and Dr. Preethi Reddy, Directors,
Mallareddy Institute of Medical Sciences, Mr. M. Ravi
Verma, Director, MNR Medical College for their
encouragement. We also thank Dr. Swarajya Lakshmi,Associate Professor and Mrs. Madhuri, Assistant
Professor and Mr. Amar Kumar, Department of
Microbiology, MNR Medical College for their
guidance.
REFERENCES
1 TaslimaTaher Lina, Sabitha Razwana Rahaman,
Donald James. Multiple antibiotic resistances
mediated by plasmids and integrons of
uropathogenic Escherichia coli and Klebsiellapneumoniae. Bangladesh J Microbiol.2007;24:19-
23.
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2 Ramprasad AV, Jayaram N, Nageshwara G. Urine
culture sensitivity pattern in a private laboratory
set up. Indian J path microbial. 1993;36(2):119-23
3 Ananthanarayan, Paniker. Text book of
microbiology. 9thed: Universities Press; 2013.
4 Ann pallett, Kieran Hand.Comlicated urinary tract
infections: practical solution for the treatment of
multiresistant Gram-negative bacteria. Journal of
antimicrobial chemotherapy 2010; 65(S3):25-33.
5 Thomas MH, Delia Scholes,James P . Hughes,
Carol Winter, Pachita L Roberts, Ann E
Stapneton, Andy Stergachis and Winter E Stamm.
A prospective study of risk factors for
symptomatic urinary tract infections in young
women. The New England Journal of
Medicine:1996;335:467-74.
6 Hanif S. Frequency and pattern of urinary
complaints among pregnant women .JCPSP.
2006; 16(8):514-17.
7 Mandal P, Kapil A, Goswami K, Das B, Dwivedi
SN. Uropathogenic Escherichia coli causing
urinary tract infections. Indian J Med
Resh.2001;114:207-11.
8 Collee JG, Fraser AG, Marmion BP Simmons -
Mackie and McCartney Practical Medical
Microbiology -14th
ed:Elsevier; 2013
9 Lisa PA. National committee for laboratory
standards-1984,performance standards for anti
microbiological susceptibility testing second
informational supplement M100-S2, nation
committee for clinical laboratory standards ,
villanova, Mackie & MacCartney: Practical
Medical Microbiology; 14 ed.
10 Aziz Marjan Khattak. Prevalence of asymptomatic
bacteriuria. Pak J Med Sci.2005;22(2):162-66
11 Acharya VN, JadavSK. Urinary tract infection -
current status. J Postgrad Med.1980; 26:95-9812 Ethel S. Bacterial adherence and humoral immune
response in women with symptomatic and
asymptomatic UTI. Indian J Med
Microbiol.2006;24(1):30-33
13 Ram S, Gupta R, Gaheer M. Emerging antibiotic
resistance among the uropathogens. Department of
Microbiology, Dayanand Medical College and
Hospital, Ludiana. Indian J Med Sci. 2000 Sep;
54(9):388-94
14 Marie-vic O. Rac. and Marie Yvette C. Barez.Profile of Community Acquired Urinary Tract
Infections in Davao City, Phil. J Microbiol Infect
Dis. 1998;27(2):62-66
15 Bhal AL , Chugh RN, Sharma KB, Asymptomatic
bacteriuria in diabetes attending a diabetic clinic.
Indian J of Med Sc. 1970; 24:1-6
16 Hansen RO. Bacteriuria in diabetic and non-
diabetic outpatients. Acta medica Scandinavia.
1964;176:721-30
17 Ghumman Surveen, Goel Neerja, Rajaram Shalini,
Harsha. Renal disease and pregnancy. J Obstet
Gynecol India.2006; 56(3): 219-23
18 McFadyen IR, Eykyn SJ. Suprapubic aspiration of
urine in pregnancy. Lancet.1968;1:1112-14.
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International Journal of Medical Research
&
Health Sciences
www.ijmrhs.com Volume 3 Issue 2 (April - Jun) Coden: IJMRHS Copyright @2014 ISSN: 2319-5886Received: 12
thDec 2013 Revised: 18
thJan 2014 Accepted: 20
thJan 2014
Research Article
A STUDY ON RADIAL ARTERY IN CADAVERS AND ITS CLINICALIMPORTANCE
*Prakash KG1, Saniya K
2
1Associate Professor,
2Assistant Professor, Department of Anatomy, Azeezia Medical College, Meeyyannoor, Kollam,
Kerala, India
*Corresponding author email: [email protected]
ABSTRACT
As the radial artery is the second most commonly used graft in coronary bypass (CABG)surgery(internal thoracic
artery first most common)and for transcatheter coronary interventions (angioplasty),cardiac surgeons should have
thorough knowledge about the normal anatomy and possible variations of it before these cardiac procedures.
Methods: 50 radial artery specimens(both right and left sided)were studied by dissection method in 25 cadavers
(20 male and 05 female). The data were tabulated in Microsoft excel and analysed by using Statistical Package for
Social Science (SPSS 17th
version). Mean, Proportion, Standard deviation and Unpaired‘t’ test were applied for
analysing the data obtained. Results& conclusion: Radial artery in all the specimens take origin from brachial
artery at or just below the elbow joint in the cubitalfossa, running superficially and laterally, giving radial recurrent,
manycollaterals, radial carpal and superficial palmar branches; total mean length of artery from origin to wrist jointis 20.63± 1.96cm; mean luminal diameter at its termination 2 cm proximal to styloid process just above the wrist
joint is 2.14± 0.28mm.This study revealed anomalies like tortuosity (30%)in distal 1/3rd
segment and radio-ulnar
loops were not found in any specimens.
Keywords: Radial artery, Coronary bypass graft, Transcathetercoronary interventions (Angioplasty), Internal
thoracic artery.
INTRODUCTION
Graft patency is a fundamental predictor of long term
survival after coronary bypass graft (CABG) surgery.
Given its proven survival benefit, left internal thoracic
artery to left anterior descending artery (LITA-LAD)
grafting has become a fundamental part of CABG.
This grafting also led to increased use of other arterial
conduits, of which radial artery is most popular(second
most common next to internal thoracic artery).1
In 1973, Carpentier suggested the use of radial artery
as a conduit for coronary bypass graft surgery.2
Eventhough radial artery had been abandoned in early
1970’s due to high rate of graft failure in post-
operative period,butdue to the latest concepts of total
arterial revascularisation in coronary bypass surgery in
1989, it has been proved thatradial artery is as good as
an internal thoracic artery in CABG due to histological
similarities.3
Radial artery is nowadays commonly used for
transcatheter coronary interventions (angioplasty)
compared to transfemoral or transbrachial technique
due to the lower risk access site related complications.
Lower risk is because of the radial artery being
superficial; haemostasis can be easily achieved just by
local compression.4Harvesting radial artery for
CABG5or during transcatheterisation does not cause
any damage as there are no large veins or nerves exist
nearby it and even does not cause ischemia in hand as
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Prakash et al.,
there exist collateral circulation
(ulnar artery).4
Normally, the radial artery is a small
of the brachial artery, arises at the
radius in the cubitalfossa. It runs su
to the ulnar artery, (another terminal
artery).During its course, at the begi
radial recurrent artery which takes p
around the elbow joint; it also giv
collateral or muscular branches whi
muscles and finally giving a palma
the lower part of the forearm. It lea
turning posteriorly and enters the an
Just before it leaves, gives a superfi
which completes the superficial p
with the ulnar artery.6
It is also