Gastrointestinal & Pain/Sedation Flashcards
Pain will be present with passive extension or flexion of the right lower extremity
Psoas Sign
Pain present with internal rotation of the right thigh
Obturator sign
Pain reported in the right lower quadrant with palpation of the left lower quadrant
Rovsing Sign
Antibiotic coverage targeted toward what bacterial flora in appendix
- E. coli
- Strep. milleri
- Anaerobes
- P. aeruginosa
Differential diagnoses for abdominal masses
- Organomegaly
- Constipation
- Umbilical hernia
- Benign cystic lesion (choledochal cyst, polycystic kidney disease, duplication cyst, cystic teratoma)
- Neuroblastoma
- Wilms tumor
- Hepatoblastoma
Most common extracranial tumor in children, age at presentation is 18 months, with the prevalence greatest in children <4 years
Neuroblastoma
Most common renal tumor and the 5th most common pediatric malignancy, with a common presentation age of 1-5 years
Wilms tumor
Most common malignant tumor of liver with a mean age at diagnosis 1 year, occurring in the right lobe of liver and associated with extreme prematurity, low birth weight, Beckwith-Wiedemann syndrome, Gardner syndrome, and familial adenomatous polyposis disease
Hepatoblastoma
Absence or obstruction (due to fibrosis) of the biliary tree, leading to intrahepatic bile duct obstruction and proliferation
Biliary Atresia
- Obstruction of bile flow from liver due to inflammatory process
- Fibrosis or scarring obliterates the ducts and prevent bile from being transported from liver to GI tract
- Resultant cirrhosis and eventual development of liver failure
Pathophysiology of biliary atresia
Physical exam findings of biliary atresia
Jaundice, acholic stool, dark urine
Management of Biliary Atresia
- Kasai procedure
- Nutrition (130-150% recommended daily allowance and 150kcal/kg/day)
- Treatment of cholestasis (actigal, questran, phenobarbital)
- Treatment of portal hypertension
- Liver transplantation
Most common indication for liver transplantation
Biliary Atresia
Pain on deep inspiration when the inflamed gallbladder is palpated
Murphy sign
Five Types of Esophageal Atresia
Type A: EA w/out fistula
Type B: EA w/ proximal fistula
Type C: EA with distal fistula; most common type
Type D: EA w/ proximal and distal fistula
Type E: Tracheoesophageal fistula w/out atresia
- Newborn with excessive oral secretions, drooling, accompanied by coughing, choking, or sneezing
- Feeding can cause cyanosis, choking, emesis
clinical presentation of EA
- Obstruction of proximal duodenum secondary to failure of recanalization
- Associated with T21
Duodenal Atresia
Bilious emesis in the first hours of life
clinical presentation of duodenal atresia
Abdominal radiograph with a double bubble sign representing the stomach and proximal duodenum
diagnostic evaluation of duodenal atresia
Antidiarrheal medications often contain aspirin, which contributes to Reye syndrome and show be avoided. True or False
True
Reasons for upper GI bleeding
- Ulcers (gastric or dodenal)
- Helicobacter pylori
- Esophageal varices
- Liver disease
Reasons for lower GI bleeding
- Infectious colitis
- Colonic polyps
- Allergic colitis/milk-protein enteropathy
- Anal fissure
- IBD (Crohn, UC)
- Ischemia (intussusception, obstruction)
- Meckel diverticulum
- Hematemesis/bright red blood from GT
- coffee-ground emesis/output from gastric tube
clinical presentations of upper GI bleeding
- Melena: hemoccult positive stool with black, tarry appearance
- Hematochezia (painful vs painless)
clinical presentations of lower GI bleeding
- metabolism of glucose, lipid, nitrogen, drugs, toxins
- synthesis of albumin and coagulation factors
- formation of bile and bile acids
Functions of the liver
Hepatitis A
fecal-oral; common in child care centers; contaminated food/water
Hepatitis B
blood, saliva, semen, transplacental; infants especially susceptible
Hepatitis C
mother to infant, blood, saliva, semen
Labs that can help distinguish if source is liver or other muscle/tissue etiology
- Fractionated alkaline phosphatase
- GGT
Rapid decrease in AST/ALT with increased coagulation and bilirubin suggests worsening hepatic failure. True or False.
True
Hepatitis Pearls
- Vaccination is available and part of the recommended immunization schedules for Hep A and B
- Diagnosis of Hep A does not lead to chronic infection
Unconjugated/indirect bilirubin levels suggest
hemolytic cause
- Physiologic (newborns): increased erythrocyte breakdown, enzyme deficiency, increased extrahepatic circulation
- Pathologic: infection, G6PD deficiency, ABO incompatibility, Gilbert syndrome
Conjugated/direct bilirubin levels suggest
hepatobiliary disease
- anatomic/obstruction: BA, choledochal cyst, gallstones/sludge, CF
- Infectious: sepsis, UTI, viral
- Metabolic/Genetic: Alagille syndrome, Down syndrome
Irreversible, bilirubin-induced brain dysfunction as a result of bilirubin deposition into gray matter of brain
Kernicterus
Hyperbilirubinemia Pearls
- Physiologic: total bilirubin e14mg/dL; resolves in 2 weeks
- Hyperbilirubinemia in children >2 weeks of age requires further investigation
- Direct bilirubin level e1.5mg/dL requires further evaluation
- nonmechanical obstruction of the intestines
- disruption of peristalsis that can be partial or complete, results in dilation of proximal intestines
Ileus
Management of Ileus
- bowel rest, NGT for decompression
- Postop pain management w/out narcotics
- Ambulation and time
inflammatory process that can affect any portion of the GI tract; most commonly affects the terminal ileum; inflammation is the entire lumen of the intestines
Crohn Disease
inflammatory process that affects the colon and rectum; inflammation is the mucosal layer of the intestinal wall
Ulcerative Colitis