overview of neonatal surgery anne aspin 2010. gastroschisis defect lies to right of umbilicus...
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OVERVIEW OF NEONATAL
SURGERY
ANNE ASPIN2010
Gastroschisis
Defect lies to right of umbilicus
Central abdominal wall defect
No sac
Embryology
6TH Week intestine grows rapidly Rotates and inverts by 10th week
Liver, bladder, stomach
Can be caused by vascular accident.
Incidence
Omphalocele 1 :4000
Gastroschisis 1:6000 – 10,000
Increasing over last 30 years
Common in young mums, <20yrs.
Associated anomalies
Gastro-intestinal tract, atresia,stenosis
Duplication cysts.
Feeding problems
Gastro-oesophageal reflux Vomiting Poor weight gain Colic Fractious, fussy, crying Irregular bowel actions
NEC What is it?
Infection of the mucosal lining of the bowel
Lactobacilli Clostridium Unknown
Who does it effect? Maternal factors prematurity Hypoxic episodes Cardiac anomaly Exchange transfusion Umbilical line near mesenteric artery High osmolarity feeding Increasing feeds quickly
Signs and symptoms Change in behaviour Subtle signs Lethargy Increasing naso-gastric aspirates Labile temperature, labile blood sugars Vomiting, bile later Blood in stools Abdominal distension
Later Mottled, grey, capillary refill <4 secs Apnoeic Bradycardia Oxygen requirement Abdominal tenderness Oedema Dilated abdominal veins, dilated loops of
bowel Flare around umbilicus
Even later
Thrombocytopenia Raised CRP Pneumoperitoneum Collapse, ventilation Abdominal drain Surgery, stoma’s Short bowel
What to do
Large ng tube, aspirate and free drainage
Nil by mouth IVI, Antibiotics Blood sugar monitoring Sepsis screen. Blood gas, FBC, U/E’s,
Blood cultures Urine MC/S, CXR, AXR
Types of oesophageal atresia and fistula
86% 7%4%
Types continued
1%<1
<1
History
First case recorded Durston (1670) Gibson (1697) first recorded with
fistula Ladd (1939) first staged repair Height (1941) first successful
primary repair.
Survival
Survival rate of around 90% Incidence 1: 4500 Antenatal diagnosis –
polyhydramnios and absent stomach 56% predictive of OA.
After birth
Large NG tube CXR, AXR Replogle tube, 10 min suction to
pharynx
Associated anomalies
50% associated anomalies Cardiac 29%
Vertebral, Anorectal, Cardiac, Tracheo, Oesophageal, Renal, Limb
Table 1 Cardiovascular 29% Gastro intestinal (anorectal 14%)
27% Genito urinary 13% Vertebral and skeletal 10% Respiratory 6% Genetic 4%
Primary repair Paralyse and ventilate 5 days post
op Long gap – gastrostomy and
assessment of gap, may leave 6 – 12 weeks before primary closure.
Gap of more than 6-8 vertebrae, oesophageal replacement
Post operation- early complications
Anastomotic leak , 27%, 24 – 72hrs
Anastomotic stricture
Recurrent tracheo oesophageal fistula
Late complications
Tracheomalacia Gastro oesophageal reflux Respiratory problems Motility disorders Growth
Short Bowel Syndrome
Definition Rickham (1967) – an extensive resection to
maximum of 75cm
Kuffer (1972) – 15cm with ileocaecal valve - 38cm without ileocaecal valve
Dorney (1985) – 11cm with I/C valve or 25cm without I/C valve
Introduction Most common cause of intestinal
failure.
NEC, Congenital atresia, Gastroschisis and volvulus.
Promote adaptive response through enteral feeding and careful management of TPN.
What is SBS
Reduced bowel surface area for absorption of nutrients together with rapid transit of intestinal contents.
TPN reduced as enteral feeds are introduced.
Need to promote intestinal adaptation.
Motility
The IC valve and colon is important to slow intestinal transit.
Proteins, Fats and Carbohydrates are absorbed almost completely within first 150cm of small bowel.
After resection. Increase gastric emptying.
Ileal resection, increased transit time
An intact IC valve prolongs gut transit, loss of this causes an increase.
If colon resected transit increases.
How does the bowel adapt? Cellular hyperplasia Villous hypertrophy Intestinal
lengthening Altered motility Hormonal changes
Takes approx 2 years to reach max effect.
Central line complications
Infection Thrombosis Break in catheter Air embolus Tissue necrosis Malposition Cardiac tamponade
It takes approximately two years to achieve some normal diet
Gastroschisis NEC Bowel atresia, stenosis, web,
duplication cyst Meconium ileus Jejunostomy, ileostomy, colostomy.
Bowel atresia, stenosis, web, duplication cyst
Interruption in the bowel Effects motility Adhesive bowel obstruction Nil by mouth again
Meconium ileus
Thick, sticky meconium, secretions
Perforation or not (Ileum) Stoma
Absorption, enzymes, EBM
Jejunostomy
High stoma
Trophic feeding, EBM, Donor EBM
Electrolytes
Six weeks reversal
Ileostomy
High or low Milk Stomal diarrhoea Electrolytes Prolapse, inversion, sore, thrush Failure to thrive
Colostomy
Milk Prolapse, inversion, soreness, Diarrhoea Constipation Electrolytes
Important issues
Temperature Fluid and electrolytes Glucose Management of reflux Speech and language therapy family
Management of gastro- oesophageal reflux
Thick n easy, Thix od Gaviscon Erythromycin Domperidone Ranitidine Omeprazole