Paediatric Surgery Flashcards
(65 cards)
Biliary atresia - Jaundice in infants:
Colour of stools and urine…
Associated with…
> 14 days in term infants (>21 days in pre term infants)
Pale stool, yellow urine (colourless in babies)
Associated with cardiac malformations, polysplenia, situs inversus
Biliary atresia - Surgical Treatment with.
Jaundice > 14 days
Increased conjugated bilirubin
Roux-en-Y portojejunostomy (Kasai procedure).
If Kasai procedure fails or late recognition, a liver transplant becomes the only option.
Bilious vomiting in neonates ALL…
Few hours after birth - Duodenal atresia - Duoduodenostomy. Double bubble AXR
Around 24 hours of birth - Jejunal/ ileal atresia - Laparatomy + primrary resection/ Air -fluid level AXR.
Around 24-48 hours - Meconium ileus - surgical decompression, PR contrast or NG NAC. Fluid level AXR. Sweat test for CF.
Usually 3-7 days after birth - Malrotation with volvulus - Ladd’s procedure
The second week of life - Necrotising enterocolitis - Conservative and supportive for non perforated cases, laparotomy and resection in cases of perforation of ongoing clinical deterioration
Bronchogenic cysts
anomalous development of the ventral foregut
lie near the midline and most frequently occur in the region of the carina
maybe asymptomatic or present with respiratory symptoms early in the neonatal period.
maybe detected on conventional chest radiography as a midline spherical mass or cystic structure
Once the diagnosis is suspected a CT scan should be performed
Thoracoscopic resection is the ideal treatment. Very young babies can be operated on once they reach six weeks of age.
Cyanotic Congenital heart disease
Most Common…
TTTP
Tetralogy of Fallot
Transposition of the great arteries (TGA)
Tricuspid atresia
Pulmonary valve stenosis
Ayanotic Congenital heart disease
Most Common…
Ventricular septal defects (VSD) - most common, accounts for 30% Atrial septal defect (ASD) Patent ductus arteriosus (PDA) Coarctation of the aorta Aortic valve stenosis
Inguinal hernia in children
hernia sac is often a remnant of
ernia sac is often a remnant of the processus vaginalis and association with undescended testis is recognised
Inguinal hernia in children
Type and timing of presentation
Treatment..
Most common in the first few weeks of life. Nearly all will be indirect hernias. The treatment of which is inguinal herniotomy. Formal repair using meshes is not required because the posterior wall of the canal is usually intact.
BL tendency- offer BL exploration in females but not in males (risk of cord and testicular injury)
Fix on next available list!
Embryogenesis the intestine
4th week - into abdomen via umbilcus
270 degree clockwise twist
ligament of Treitz lies to the left of the spine and the caecum in the right lower quadrant.
Malrotation with volvulus - Ladd’s procedure
Usually 3-7 days after birth
Billous vomiting
an abdominal ultrasound scan to determine the relationship between the superior mesenteric artery and vein (normally SMA lies to the left of the SMV
Ladds procedure - division of adhesional bands - appendicectomy as caecum is replaced in upper left
Intraoperative fluid management
Neonates should receive
Other children should receive
Neonates should receive glucose 10% during surgery - at a rate of 60ml/Kg/day.
Other children should receive isotonic crystalloid.
Pyloric stenosis
2-6 weeks of life
30mins after feeding - Projectile non-bile stained vomitin, mass in RUQ
Treatment: Ramstedt pyloromyotomy (open or laparoscopic)
M>F
5-10% Family history in parents
Intussusception
6-9 months age - Telescoping bowel
Proximal to or at the level of, ileocaecal valve
Colicky pain, diarrhoea and vomiting, sausage shaped mass, red jelly stool.
Treatment: reduction with air insufflation
Hirschsprung’s disease
Absence of ganglion cells from myenteric and submucosal plexuses
Occurs in 1/5000 births
Full-thickness rectal biopsy for diagnosis
Delayed passage of meconium and abdominal distension
Treatment is with rectal washouts initially, thereafter an anorectal pull through procedure
Oesophageal atresia
Associated with tracheo-oesophageal fistula and polyhydramnios
May present with choking and cyanotic spells following aspiration
VACTERL associations
Cherry red rectile polyps
Juvenile polyps may occur as part of the familial polyposis coli syndromes. The lesions, which are hamartomas, are often cherry red if they protrude externally.
Umbilical vessels
The arteries are continuous with the internal iliac arteries (medial umbilical ligaments) and the vein is continuous with the falciform ligament (ductus venosus)
Omphalitis
infection of the umbilicus - Staphylococcus aureus is the commonest cause
cherry red lesions surrounding the umbilicus, they may bleed on contact and be a site of seropurulent discharge.
Umbilical granuloma - often respond favorably to chemical cautery with topically applied silver nitrate.
urinary discharge from the umbilicus
persistence of the urachus which attaches to the bladder. They are associated with other urogenital abnormalities.
umbilical discharge that discharges small bowel content
Persistent vitello-intestinal duct
Complete persistence of the duct is a rare condition. Much more common is the persistence of part of the duct (Meckels diverticulum). Persistent vitello-intestinal ducts are best imaged using a contrast study to delineate the anatomy and are managed by laparotomy and surgical closure.
dermatological condition in which scarring of the foreskin occurs leading to phimosis
Balanitis xerotica obliterans
This is a dermatological condition in which scarring of the foreskin occurs leading to phimosis. It is rare below the age of 5 years. Treatment is usually with circumcision.
Tetralogy of Fallot typically presents at around…
Most common CHD, typically presents at around 1-2 months, although may not be picked up until the baby is 6 months old.
ventricular septal defect (VSD)
right ventricular hypertrophy
right ventricular outflow tract obstruction, pulmonary stenosis
overriding aorta
Other features
causes a right-to-left shunt
ejection systolic murmur due to pulmonary stenosis (the VSD doesn’t usually cause a murmur)
a right-sided aortic arch is seen in 25% of patients
chest x-ray shows a ‘boot-shaped’ heart, ECG shows right ventricular hypertrophy
Management
surgical repair is often undertaken in two parts
cyanotic episodes may be helped by beta-blockers to reduce infundibular spasm
AT BIRTH, most common cyanotic heart disease presentation is…
at birth transposition of the great arteries is the more common lesion as patients with TOF generally present at around 1-2 months
