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Neonatal intestinal obstruction
HASHEM AL-MOMANI SENIOR CONSULTANT PEDIATRIC SURGEON JORDAN UNIVERSITY HOSPITAL
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Introduction Neonatal intestinal obstruction is one of the common pediatric emergencies. Neonatal intestinal obstruction has an incidence of in 2000 live births. A wide range of congenital anomalies may result in neonatal bowel obstruction.
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Causes of intestinal obstruction in the neonatal period
Congenital atresia and stenosis constitute the majority of cases. Other causes include Malrotation Volvulus Meconium ileus Hirschsprung disease Anorectal malformations
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Causes of intestinal obstruction in the neonatal period
Gastric Early pyloric stenosis Pyloric web or atresia Epidermolysis bullosa pyloric atresia syndrome Duodenum Stenosis Atresia Malrotation Annular pancreas Jejunum-Ileum Meconium ileus Vitello-intestinal duct remnant Intussusception Milk curd obstruction Colonic Stenosis Atresia Imperforate anus Poorly developed colon e.g. megacystis microcolon intestinal hypoperistalsis syndrome Global Duplication anomalies Internal hernia or inguinal hernia Volvulus with or without (e.g. about a Meckel’s band) malrotation Neoplasm
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Etiology 113 etiologies in 106 patients
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Presentation “A neonate with bilious vomiting or aspirate is considered to have intestinal obstruction until proved otherwise.” The presenting symptoms could be any combination of the following: Bilious vomiting Abdominal distension Delayed passage of meconium Sepsis
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Prenatal sonography Echogenic bowel Dilated bowel Polyhydramnios
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Bilious vomiting Bilious vomiting is synonymous with intestinal obstruction, be it functional or mechanical.
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Examination dehydration abdominal distension
Visible and palpable bowel loops Erythema and tenderness of abdominal wall The presence of a normal anus Associated anomaly
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A newborn with marked abdominal distension
suggesting distal obstruction necrotizing enterocolitis sepsis The more marked the abdominal distension, the more distal is the obstruction
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Perineal Examination Absent anus Rectal stimulation
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Vomiting Vomit produced by a neonate should be classified carefully into one of two groups: Non-bilious vomit: Colorless or milky if a feed has been taken. Bilious vomit: Dark green . Freshly produced bile of golden color has been acted upon by stomach acid to produce the green color. Neonatal bilious vomiting should be considered to be a surgical emergency until proved otherwise.
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Constipation A term neonate should pass meconium within 24 h of life.
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Passage of meconium is absent in complete duodenal and small intestinal obstruction meconium passage may be present in anomalies of rotation and fixation delayed in Hirschsprung’s disease Occurs by an abnormal route (by a fistula or micturition) or not at all in anorectal malformations
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Abdominal Radiology The simplest and most informative radiological procedure is the plain abdominal X-ray. confirmation of bowel obstruction with some information about the level of the obstruction.
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Imaging Studies Plain x-ray abdomen: supine film lateral decubitus
Invertogram or a prone cross-table lateral film for anorectal malformations
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Plain abdominal X-ray The extent and position of bowel gas
Presence or absence of gas in the rectum Degree and level of distended loops Air fluid levels Evidence of free gas would confirm perforation. “Football sign”, The rigler sign, also known as the double wall sign
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Intestinal air progression
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Abdominal x-ray showing dilatation of bowel loops with air–fluid level
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single air bubble
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Plain abdominal x-ray Dilated stomach with air distally suggesting partial duodenal obstruction
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Complete duodenal obstruction
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Triple bubbles
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Pneumo-peritoneum Free air due to perforation from any cause is suspected on supine film when “football sign” : a large pocket of air overlying liver and the ligamentum teres Rigler sign: the bowel wall is sharply delineated (pencil lining).
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Football sign
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Rigler sign
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Lateral decubitus Lateral decubitus film with the right side uppermost should be used to see air above the liver.
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Free air above the liver
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Ileal atresia with volvulus
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Calcification Calcification of meconium implies long-standing stasis and may be identifiable outside of the bowel loops, which would suggest previous perforation.
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Diffuse calcifications
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Contrast Studies The first enema a neonate receives should be a contrast enema. The contrast enema acts not just a diagnostic tool but works as a therapeutic measure in cases of: meconium plug meconium ileus Hirschsprung’s disease
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Lower contrast study showing small left colon syndrome
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Lower contrast study showing Hirschsprung’s disease
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Lower contrast study showing meconium plug syndrome
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A lower contrast study: small unused colon suggesting small bowel obstruction or total colonic hirschprung’s disease.
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Contrast upper gastrointestinal (GI) studies
If malrotation is suspected Sometimes to characterize the duodenal obstruction
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Malrotation
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Malrotation
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Volvulus neonatorum- spiral twist of the bowel
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Upper contrast study showing congenital duodenal obstruction.
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Remember While Doing the Contrast Study
Use water soluble contrast Make sure the baby is well hydrated Make sure the radiology suit temperature is warm enough for the baby. Avoid using Foley catheter with the baloon inflated. Perform the study using image intensifier.
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Ultrasound To look for other associated anomalies
Helps to diagnose free or loculated intra-abdominal fluid collection denoting perforation or a meconium cyst. In malrotation if the arrangement of the superior mesentric vessels is reversed, then malrotation should be suspected - operator-dependent and is not widely used.
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Transverse ultrasound scan through the upper abdomen
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“whirlpool” configuration of the superior mesenteric vessels
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Treatment The success of treatment of neonates with intestinal obstruction depends on several factors: Early diagnosis Proper preoperative stabilization The right choice of surgical procedure Good postoperative care
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Principles of Treatment
This is individualized according to the diagnosis but certain principals remain common. The baby is cared for in the NICU with regulation of temperature and adequate monitoring. The baby should receive broad spectrum antibiotic cover The baby should be transported in an incubator to and from the operating room (OR). The OR temperature should be kept high and measures should be taken to keep the baby warm during surgery. Warm saline is used during the procedure and all the fluids given to the baby are warmed appropriately.
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Preoperative care: Once the diagnosis of neonatal intestinal obstruction is made, the patient should be fully resuscitated. Fluid resuscitation. Gastric decompression via an orogastric or a nasogastric tube. The use of umbilical lines should be avoided because of the increased risk of infection and because they interfere with the incision for laparotomy. Vitamin K is given intramuscularly. Broad-spectrum antibiotics are given intravenously. Control of temperature to avoid hypothermia.
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Postoperative management:
The patient is admitted to the neonatal intensive care unit. Nothing by mouth (NPO). The baby should be kept warm. An orogastric tube should be placed for gastric decompression. TPN should be started shortly after surgery and continued until enteral feeds are tolerated.
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Outcome and Prognosis the overall survival rates of newborns with intestinal obstruction is 90 % The most common cause of death is infection related to pneumonia, peritonitis, or sepsis. The most important surgical complications are anastomotic leaks and functional intestinal obstruction at the level of the anastomosis
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Outcome in 106 patients at JUH
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THANK YOU
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