2 GASTROINTESTINAL EMERGENCIES Gastrointestinal emergencies are serious conditions that often develop suddenly and requires prompt and immediate treatment.Gastrointestinal emergencies can develop throughout the digestive system
3 GI TRACT EMERGENCIESEsophagus Stomach Small Intestines Large intestines Biliary system ( liver, pancreas, gallbladder, bile duct )
4 GASTROINTESTINAL EMERGENCIES IN Adults and Infants/Children Acute Abdominal PainGastrointestinal HemorrhageBiliary Tract ObstructionHepatic FailureHepatic Encephalopathy
5 GI TRACT EMERGENCIES UNIQUE TO THE PEDIATRIC PATIENT Two major categoriesIntestinal obstructionNeonatal cholestasis
6 INTESTINAL OBSTRUCTION Antral and Duodenal stenosis and webs Infantile hypertrophic pyloric stenosis Extrinsic Duodenal obstruction Duplications Malrotation with and without volvulus Hirschsprung’s disease Anorectal malformations or Imperforate anus Abdominal Wall Defect Hernias Thick Meconium syndromes Intussception Volvulus Other -Appendicitis - Meckel’s Diverticulum
8 GI EMERGENCIESyear old male presents with severe abdominal pain, and vomiting.There is no history of fever, weight loss , diarrhea , jaundice or joint pain.Based on above information, what additional history ,physical finding ,labs and/or radio imaging are needed tomake a diagnosis of :PancreatitisAppendicitisMalrotation with volvulusIncarcerated herniaIntussception
9 APPENDICITISMost common condition leading to emergency abdominal surgery in children/adultsIncidence : 140 in 100,000 people of all agesMost frequent between 15 and 24 years of age ( rare in preschool children and rarer in < 1 year of agePresentation : periumbilical abdominal pain, vomiting, fever1/3 of all presentation is with perforation of the appendix or lower abdominal massNote : 11 – 32 % false positive rate pre operatively> 50 % have nonsurgical abdominal
10 GI EMERGENCIES Pancreatitis Diagnosis : Key Points Symptoms :( age dependant )+ pancreatic isoenzymes( amylase and / or lipase) 2 to 3 timeselevated over normal reference level.Hydration very important especially in the early stages.Studies in animals indicate the CT contrast given early in the course of acute pancreatitis may further diminish blood flow to ischemic areas of the pancreas and increase the likelihood of necrosis------CT contrast should avoided in early stagesRx : NPO, IV FLUIDS, PAIN MEDS
12 GI EMERGENCIESA 12 month old infant presents with the history of increased irritability and inconsolable. Growth and development are normal . The physical examination was remarkable for abdominal distension, tenderness and bloody stools ( guiac positive for blood).Based on your working diagnosis, what labs or test would you request?
13 INTUSSCEPTION COMMON CAUSE OF INTESTINAL OBSTRUCTION IN CHILDREN Peak incidence is infancy50% < 1year of ageMale to female ratio is 3:2No lead point/ usually idiopathatic90 % proximal to the ileocecal valve –ileocolonic, ileoileal,colocolonic> 2 years of age associated with a lead pointDx/Rx : KUB features the target sign ( a mass in the RUQ ), cresent sign( intussceptum, intusscepting lead point, protruding into air filled pocket ), absent liver edge sign/absence of the subhepatic angle, and signs of obstruction ( smooth intestinal wall/dilation- hose or sausage- like due to loss of plication/haustration, air –fluid level –candy cane or upside down J, gas distribution, and orderliness)air or barium contrast enemaSurgery if lead point or > 48 hours10% recurrenceComplication – perforation ( greater in infants, < 6 months of age, and /or symptoms >3 days9
15 MALROTATION WITH OR WITHOUT VOLVULUS Malrotation occurs during normal formation of the bowel Its presence predisposes to volvulus Its incidence is 1 in 6,000 Male to female 3:1 Presentation : bilious vomiting, abdominal pain, blood in stool etc., but older children may have vague symptoms ( chronic abdominal pain and/or intermittent vomiting) Diff Dx : neonates – duodenal atresia and stenosis, annular pancreas, antral or duodenal web, small bowel atresia Older infant/children – pyloric stenosis, GER, formula intolerance, colic, lactose intolerance Associated anomalies : congenital diaphragmatic hernia, abdominal wall defect (30-60%), duodenal atresia (50%), CHD, Hirschsprung’s disease, mesenteric cysts Dx : Barium enema – cecum localized to the right or left quadrant UGI series – duodenum does not cross midline and the remainder of small bowel lies to the right of the midline U/S – clockwise rotation of the superior mesenteric vein around the mesenteric artery ( “ whirlpool” sign ) Rx : surgery
17 INFANTILE HYPERTROPHIC PYLORIC STENOSIS Hyper trophy and hyperplasia of the smooth muscle in the antral and pyloric regionsProposed etiology - ? Hypergastrinemia, ?increased prostaglandins E2 and F2alpha, ? Decreased NADPH diaphorase activity ( a lack of nitric oxide synthase in pyloric tissueSx : nonbilious vomiting < 5 months ( usually by 3 weeks )PE : visible gastric peristalic waveHypochloremic alkalosis( water loss and hydrochloric acid )Elevated unconjugated bilirubinDx : pathognomomic “ pyloric olive”+ clinical history + labsNo imaging is requiredPlain film “ caterpillar “shape ( hyperperistalsis and paucity of small and large bowel gas )Radio imaging with contrast – elongated , double channel ( railroad tract )-enlarged distal antrum muscle and duodenal bulbU/S : hypertrophied pyloric muscle ( anechoic mass )Rx : medical/surgery
18 DUPLICATIONS Esophageal – rare Gastric – incidence 10% -greater curvature-palpable abdominal mass+/- GI bleeding+/- chronic abdominal pain+/- pancreatitisDuodenal – incidence %-located in the mesenteric borderPresentation – abdominal mass , abdominal pain, jaundice ,GI bleeding , pancreatitisAssociated anomalies : Duplication cysts, vertebral anomalies, ectopic pancreasDx : UGI with contrast –beaklike projection from the duodenalCT scan or U/S – mass next to the duodenumEndoscopy – mass or extrinsic compressionERCP – duplication seen if the biliary or pancreatic duct is involvedRx : surgery
19 EXTRINSIC DUODENAL OBSTRUCTION Two most common causes Annular pancreas Congenital bands Associated anomalies : duodenal atresia or stenosis, cardiovascular defect, malrotation, Down’s , TEF Dx : plain film – double bubble
20 GI EMERGENCIESAs you are leaving the newborn nursery, your favorite nurse ask if you would see this 5 hour term infant because of feeding intolerance and mild abdominal distension. What two things performed that would aid in making a diagnosis? What was your differential diagnosis ? Give at least 3 associated anomalies .
21 INTESTINAL OBSTRUCTION Atresia – congenital absence or obstruction of the intestinal lumenTypesEsophageal - incidence 1 in 3000/4500Duodenal incidence 1 in 2000/40,00Jejunal and ileal -incidence 1 in 330/1500Colonic incidence 1 in 20,000
22 JEJUNAL AND ILEAL ATRESIA It is 30% of all neonatal intestinal obstructionMale = female30 % proximal jejunum70 % distal jejunum10 – 15 % proximal ileumPresentation – less than 24 hours of age – bilious vomiting, progressive abdominal distension ( ileal > jejunum ), failure to pass meconiumAssociated anomalies common – gastroschisis, meconium ileus, malrotation with and without volvulus, Hirschsprung’ disease*Microcolon is seen with all ileal atresiaDiff Dx : colonic atresia, Hirschsprung’s disease, meconium plug, meconium ileus, malrotation with volvulus, and bowel duplicationDx : Plain film –multiple dilated loops of bowel with air – fluid levelsRx : medical / surgery
23 DUODENAL ATRESIA Presentation : symptoms within hours of birth, abdominal distension, > 30 ml bilious gastric fluidNonbilious if obstruction is proximal tothe ampulla of vaterDiff Dx : webs, stenosis, duplication,annular pancreas, congenital bandsAssociated anomalies are common :esophageal atresia, malrotation,annular pancreas, imperforate anus,CHD, IUGRDx : plain film – “double bubble” signUGI with contrast ---confirms diagnosisBE with contrast –determine the presenceof malrotation and/or midgut volvulusRx : medical/surgery** 30 % Down’s syndrome
24 ESOPHAGEAL ATRESIAFive types 1. Proximal atresia with distal fistula ( 85 % ) 2. Proximal and distal blind pouch and no fistula (8 to 10 %) 3. H type , T E fistula and no atresia ( 3 to 4 % ) 4 and 5. variation of proximal fistula, etc. Presentation depends on the type Dx : Inability to pass NG tube into the stomach Plain film ----coiled NG tube Contrast study only to diagnose H type Diff Dx : choanal atresia, diaphragmatic hernia, CHD Associated anomalies : esophageal atresia (40-70%), cardiovascular(40%) VSD, TOF, COA,PDA,vascular rings 10% VACTERL ( vertebral defects, anal atresia, TEF, renal defect, radial limb dysplasia ) 10 – 15 % imperforated anus GI anomalies – malrotation, duodenal atresia
25 HERNIAS Location is along intestines diaphragm umbilical inguinal internal – rare/ seen at autopsy ( most common type mesocolon /paraduodenum )
26 INGUINAL HERNIAIts incidence is to 4.44 in children ( it is higher in premature infants )Male to female ratio is 6:1Right sided occurrence is 60 %Left sided occurrence is 30 %Bilateral occurrence is 10 %Associated anomalies : bladder exstrophy, Ehlers-Danlo’s syndrome, ascites, VPS, peritoneal dialysis, CF, congenital dislocation of the hip, undescended testicles,ambiguuous genitalia, congenital wall defectPresentation : bulge in the groin, scrotum, testiclesDx : clinicalTransillumination,UltrasoundDiff Dx : Testicle torsion, epididymis-orchitis, torsion of the appendix testis, hydrocele, inguinal or femoral lymph adenitisRx : surgery
27 INGUINAL HERNIAIt’s a sac containing abdominal contents and protrude into a patent processes virginals testis through the inguinal canalIT IS THE LEADING CAUSE OF INTESTINAL OBSTRUCTION IN INFANTS*Herniorraphies are the mostcommon surgical proceduresperformed in childrenTwo typesIndirect ( sac passes throughthe internal ring lateral tothe inferior epigastric vessels )Direct ( sac enters the canalthrough the posterior wallmedial to the inferior epigastric vessels )
28 GI EMERGENCIES KEY POINTS : Abdominal pain Clinical history Chronology – time of onsetLocation – epigastric, peri-umbilical, or hypogastricIntensity and characterization – type of pain : sharp dull, crampyPELABS/RADIOLOGY
29 MECKEL’S DIVERTICULUM Remnant of the embryonic proximal portion of the yolk stalk ( omphalomesenteric or vitelline duct in utero ) It usually disappears 5 the and 7th week of life It is located in the antimesenteric aspect of the ileum It is 40 to 100 cm from the ileocecal valve THE MOST COMMON congenital GI ANOMALY THE MOST COMMON CLINICAL PRESENTATION IS LOWER GASTROINTESTINAL HEMORRHAGE – “ currant jelly like “(painless ) Dx : Meckel’s (technetium 99m pertechnetate) scan Sensitivity can be increased by administration of cimetidine, glucagon or pentagastrin +/- angiography +/- Tagged RBC
32 GI EMERGENCIES Hemorrhage KEY POINTS : Bleeding from the gastrointestinal tract may be determinedby :Magnitude ( acute vs. chronic )Location of the bleeding site ( upper vs. lower )Pathogenesis mechanisms ( inflammatory vs. vascular)Mode of presentation (hematemesis vs. hematochezia)2. Management in GI HemorrhageFOUR SUCCESSIVE STEPS APPROACHAssessment of the severity of the bleed( HR, BP, and postural changes )Resuscitation and Empiric TherapyLocate the bleedDiagnostic testsBE ABLE TO DIFFERENTIATE BETWEEN UPPER AND LOWER BLEEDSDETERMINE IF PAINLESS VS. PAINFUL
33 GI EMERGENCIESA 28 day old infant has a history of jaundice in the first of life that resolved but has icteric sclera of recent onset. Growth and development are normal. On examination, the liver was enlarged ( span by percussion is 8 cm) but the spleen is nonpalpable. On rectal examination, soft pale yellow stool ( quaiac negative ) was obtained.Based on your working diagnosis, what test and / or treatment would you order ?
34 GI EMERGENCIESCholestasis – impairment of bile flow Causes – intrahepatic vs. extrahepatic Biliary atresia Choledocal cyst Alagille ‘s Neonatal hepatitis Metabolic causes
35 BILIARY ATRESIA INCIDENCE 1 IN 10,000 OR 25,000 FEMALE TO MALE RATIO IS 1.4:1PRESENTATION : JAUNDICE( CONJUGATED/DIRECT HYPERBILIRUBINEMIA) ONSET 2 TO 3 MONTHS OF AGE )ASSOCIATED ANOMALIES : ABSENT INFERIOR VENA CAVA, PREDUODENAL PORTAL VEIN, INTESTINAL MALROTATION, POLYSPENIASurgical intervention success is highly weighted on the time of surgery( greater success performed < 3months of age )
37 GI EMERGENCIESYou are asked to see a patient in the ER for elevated liver enzymes of unclear etiology. What tests/labs should be ordered to determine liver function?The clotting function tests were prolonged. What should be done next? What is the time above the normal PT level that is suggestive of the risk for bleeding.If mother describes her child as becoming more restless with wide mood changes, and confusion, what would the above suggest in regard to his present clinical status?
38 GI EMERGENCIESHepatic failure is defined as impairment/ loss of the liver to perform vital ( synthetic and biliary ) functions.Failure may be classified as acute, subacute /late – onset failure. It is time frame from the onset of hepatic failure to encephalopathy developmentFulminant hepatic failure: < 8 weeks after the beginning of acute hepatitisSubacute hepatic failure : encephalopathy develops 8 to 24 weeks after the onset of liver disease*Note : 1. The lack of preexisting liver disease is KEY to making this diagnosis.2. This strict definition may not be as applicable to all pediatrics disorders –Reye’s syndrome, several inborn errors and Wilson’s disease.
39 COAGULATION The liver has a role in the control of coagulation Almost exclusively all coagulation factors are produced in the liver except von Willbrand factorThe liver produces and breakdown factors integral to fibrinolysisIt clears activated clotting factors from the circulationVitamin K dependant factors : Factors ll, Vll, lX, and XNote : Vitamin K ( fat soluble vitamin) is stored in the liver in limited amountsFactor Vlll is made extensively in nonhepatic sites( vascular endothelium)
40 COAGULATION Clotting study PT – measures time to take factor ll, prothrombin, to be converted to thrombin then fibrinogen into fibrin.Factors activated are V, Vll, and X. This is the extrinsic pathway of coagulation. Normal 11.5 to 12.5Prolongation > 2 seconds is pathologicProlongation > 3 seconds is associated with risk for bleedingPTT – also measures the generation of thrombin. This is the intrinsic pathway of coagulation.All factors are involved except Factor Vll.Since all factors are exclusively made by the liver except Factor Vll, the clotting study can reasonably assess the live synthetic function. HOWEVER, Vitamin K deficiency must be ruled out as the cause for the prolonged coagulation.Give 1mg/year of age slowly IM OR IV with a minimum of 1 mg given to full term infantCan check PT 4 TO 6 HOURS AFTER Vit K administration.Other prognostic tests : Factor Vll levels > 8%Be cautious with interpreting prolonged PT or PTT ----? DIC ? ( Factor Vll level may be helpful, normal in liver disease but decreased in DIC )
41 GI EMERGENCIESHEPATIC ENCEPHALOPATHY (neuropsychiatric/ brain dysfunction resulting from acute hepatic dysfunction )
43 GI EMERGENCIESA term infant fails to pass meconium . If the exam is unremarkable , what is the possible etiology and evaluation to perform ?
44 THICK MECONIUM SYNDROMES Two typesMeconium ileusSimpleComplicatedMeconium plug syndromePresentation :Simple 24 – 48 hours after birthComplicated - less than 24 hours of ageNote : initial presentation for CFDx :Contrast study of the colonRx : contrast study of the colonSugery for the complicatedNote : polyhydraminious especially complicated“ soap bubbles” ( Neuhauser sign )
46 HIRSCHSPRUNG’S DISEASE * Most common cause of lower intestinal obstructionin the neonateIncidence is 1 in 5,000Male to female - 3.8:1 ( 2.2:1 for total aganglionosis)Rectum and sigmond colon are the most common sitesPositive family history – 3 to 7 %Etiology ? Ret proto-oncogene mapped to chromosome 10q11,2 ( gene has a critical role in oncgenesis and in the development of mammalian enteric neuron systemMEN 11a and MEN 11b syndromeAssociated anomalies : Down’s syndrome, Waardenburg’s syndrome, cerebral palsy, mental retardation or developmental delay, meconium plug syndrome, MEN 11a, MEN11bPresentation : failure to pass meconium < hours, or infrequent defecation from birthDiff Dx : meconium plug syndrome, microcolon, hypothyroidism, drugs that decrease intestinal transit, sepsis, neuronal intestinal dysplasia, functional constipation, anterior anus displacement, pseudo-obstructionDx :BE without prep- transition zone * negative after daily enemas in infants less than 2 weeks old and presence of total aganglionosisRectal suction biopsy (RSB) or full thicknessAnorectal manometry (ARM)RX : medical and surgery
50 CLINICAL STAGES OF HEPATIC ENCEPHALOPATHY 1 ( Prodrome ) altered mental alertness2 ( Impending coma) drowsiness, altered sleep pattern, confusion, mood swing, inappropriate behavior3 (Stupor) sleepy but arousable, unresponsive to verbal commands , hyperreflexia4( Coma) unconscious, decerebrate, decorticateResponse to pain present (4A) or absent (4B)ElectroencephalographicAsterixis /changes1 slight/minimal2 easily elicited/usually generalized slowing of rhythm3 present if patient cooperates / grossly abnormal slowing4 usually absent/appearance of delta waves, decreased amplitude
51 ABDOMINAL WALL DEFECT Gastroschisis Its incidence is 1 in 12,00 Its greater in prematurity or LBW INFANTS It results from mechanical insult ( early tear of the cord before the ring is complete. The abdominal wall is well developed It is associated with lower mortality than omphalocele as well as congenital anomalies NOTE : There is no change in mortality or morbidity with vaginal vs. C section. Also, there is no advantage to early delivery unless volvulus is highly suspected Dx : prenatal ultrasound Increased alpha fetoprotein (100 % ) Rx : medical/surgery
52 OMPHALOCELE Its incidence is 1 in 10,00 Associated anomalies are determined by the site of fusion failure ---cephalic, lateral, or cardiacPentalogy of Cantrell – combination of distal sternal, an omphalocele, an anterior diaphragmatic defect, and pericardial and intracardiac defectAssociated anomalies : cardiovascular, chromosomal abnormalities (trisomy D and E ), Beckwith- Wiedman syndrome, gigantismDx : prenatal ultrasoundIncreased alpha fetoprotein
53 UMBILICALIts an out pouching of the intestine through a defect of the fascia at the umbilical ringCommon in newbornsFive to ten times more common in Afro-American infantsIt’s a cosmetic problem
54 ANORECTAL MALFORMATION OR IMPERFORATION This results from abnormal development of the urorectal septum leading to an absent or abnormal anusClassification based on relationship of the rectal pouch to the pelvic musculature-high : rectal pouch lies above the levator muscles (male > female)Intermediate : rectum partially passes the levator muscles- Low : rectum tranverses the levator muscles completely ( male = female )Associated anomalies is common (50-70%)-genitourinary tract, skeletal, CNS, CVS, GI tract and esophageal atresiaDx : clinical/PEMRI AND / OR CT SCAN TO DISTINGUISH BETWEEN HIGH AND LOW
55 GI TRACT EMERGENCIES : Intestinal Obstruction Give an example of intestinal obstruction emergency include clinical presentation, differential diagnosis, diagnostic approach, associated anomalies and treatment approach. What is the most common cause of intestinal obstruction in the infant ? What is the most common cause in children?
56 GI TRACT EMERGENCIESWhat are the GI tract emergencies that are seen in both infants/children and adults ?What are the two categories that are seen in infants and children because of its unique presentation and/or more frequently seen in early in life ?