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Gastrointestinal
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Function
1. Assists in maintaining F&E and acidacidbase balance 2. Processes and absorbs nutrients to maintain metabolism and support growth and development 3. Excrete waste products from digestive process
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Supplementary Feeding
Supplementary feeding 4-6 months Never wean an infant if in 1. Solid foods in order: - cereals rich in iron - fruits - vegetables - meat
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2. begin in small quantities 3. Finger foods offered at 6 months 4. Soft table foods 1 year 5. Dilute fruit juices 6 months; 1 is to 4 ounces of water 6. Never give half cooked eggs salmonelliosis/gastroenteritis 7. Don t give honey infant botulism
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8. Offer food one at a time interval of 4-7 days Total body fluids 65-85% of body 65weight Greater in extracellular dehydration
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Acid-Base Balance
1. Chemical buffers 2. Renal and respiratory system 3. Dilution of strong acids and bases in blood Respiratory acidosis carbonic acid excess - hypoventilation - RDS - COPD - Laryngotracheobronchitis
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carbonic acid
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Metabolic acidosis base HCO3 deficit etabolic - diarrhea - severe dehydration - malnutrition - ciliac crisis
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Metabolic alkalosis case HCO3 excess - uncontrolled vomiting - NGT insertion - gastric lavage
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Assess: Amount Frequency Force projectile Mgt: BRAT diet banana, rice, apply sauce, toast
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Diarrhea
Exaggerated excretion of intestinal contents Types: 1. Acute related to gastroenteritis, salmonellasis - dietary indescretion - antibiotic use (Ampicillin, tetracycline)
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2. Chronic non-specific non Cause: 1. food intolerance 2. Excessive fluid intake 3. carbohydrate and protein malabsorption Assess: Frequency, consistency, appearance Best criteria: consistency teret
Complication: Dehydration Mild 5% wt loss Moderate 10% wt loss Sever 15% wt loss
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Early signs and symptoms: Tachycardia, tachypnea, hypotension Increase temp, sunken fontanel and eyeballs, absence of tears Weight loss, scanty urine, dry skin Severe dehydration: marked oliguria, prolonged capillary refill
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Chronic: - thickened feeding with baby cereals - feed slowly, burp often (every 1 ounce)
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Hirschprungs s Disease
Congenital aganglionic megacolon Earliest sign: 1. failure to pass meconium after 24 hours 2. abdominal distention 3. vomitus of fecal material 4. foul smelling breath Early childhood ribbon-like stool ribbon
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Diagnosis
1. Barium enema reveals narrowed portion of bowel 2. Rectal biopsy reveals absence of aganglionic cells 3. Abdominal X-ray Xreveals dilated loops on intestine 4. Rectal manometry reveals failure of intestine sphincter to relax
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Management
1. NGT feeding 2. Surgery - Temporary colostomy - anastomosis and pull through porcedure Diet increase protein, increase calories, decrease residue pasta
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Management
Anticholinergic 1. Betanicol (Urecholine) increase esophageal tone and peristaltic activity 2. Metachlorpromide (Reglam) decrease esophageal pressure by relaxing pyloric duodenal segments - increase peristalsis without stimulating secretions
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3. H2 Receptor Antagonist decrease gastric acidity and pepsin secretion - Ranitidine (Zantac) Antacid neutralizes gastric acid between feedings - Maalox Surgery Nissen funduplication
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Esophageal Cancer
Assessment: 1. Chronic vomiting 2. Failure to thrive syndrome 4. Melena or hematemesis
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Diagnosis
1. Esophagoscopy 2. Esophageal manometry relveals lower esophageal sphincter pressure 3. Intra esophageal pH content reveals pH of distal esophagus
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Pyloric Stenosis
Hypertrophy of muscles of pylorus causing narrowing and obstruction Outstanding sign projectile vomiting - vomiting initial sign of upper GI obstruction - vomitus of upper GI blood tinged - vomitus of lower GI bile streaked; bilous
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- abdominal distention lower GI obstruction Metabolic alkalosis Failure to gain weight Olive shaped mass
major sign of
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Diagnosis
Increase Na and K, decrease Cl Ultrasound X-ray with barium swallow ABG
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Management
1. Pyloromyotomy incision of pyloric muscle 2. Fredt-Ramstedt procedure Fredtseparation of hyperthrophied muscle without incision
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Intussusception
Invagination or telescoping of position of bowel to another Common site: distal ileum and proximal colon Prone: eats fast Complication - peritonitis
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Sn/Sx: 1. persistent paroxysmal abdominal pain severe Frequency 1515-20 minutes 2. vomiting contains bile 3. currant jelly stool after 12 hours 4. sausage-shaped mass sausage
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Management
Hydrostatic reduction with barium enema Pneumatic insufflation air Surgery anastomosis and pull through
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Diagnosis
Guthrie test bacterial inhibition Pheric chloride green spots in the diaper as sign of PKU
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Diet
Low phenylalanine diet contraindicate high protein foods Lofenalac extremely-low extremelyphenylalanine formula
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Galactosemia
Carbohydrate metabolism disorder Deficient: galactose 1-phosphate 1uridyltransferase May die at 3 days of age Symptoms: Galactosemia Galactosuria
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Diagnosis
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Management
Diet galactose-free galactose Nutramigen milk substitute formula
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Celiac Disease
GlutenGluten-induced Enteropathy Intolerance to: B barley R rye O oat W wheat Inability to absorb fat
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Early sign: 1. Diarrhea 2. Constipation 3. Vomiting Late sign: 1. Abdominal pain abdomen 2. Steatorrhea
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protuberant
Diagnosis
1. history and clinical symptoms 2. Serum analysis IgA antigliadin antibodies
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Management
GlutenGluten-free diet lifetime Rice and corn OK Vitamin supplements Mineral supplements
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