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secondary pediatric hypertension
structural changes of kidneys/vessels, coarctation of the aorta
patent ductus arteriosus
duct does not close after birth, interventions with device closure, can develop LHF
atrial septal defect
hole between atria, atrial dilation leads to conductivity issues, A-fib and arrhythmia, can develop RHF, intervention with closure device
ventricular septal defect
opening between ventricular septum, most common congenital heart defect, causes mixing of oxygenated and deoxygenated blood, can lead to pulmonary hypertension causing localized vasoconstriction, eisenmenger syndrome if unrepaired
tetralogy of fallot
most common cyanotic heart defect, causes ventricular septal defect, shift of aorta, right ventricular hypertrophy, and narrowing of pulmonary valve
transposition of great arteries
arteries attached to ventricles, cyanotic, need surgery within first 2-3 weeks of life
coarctation of aorta
narrowing of aorta, increase in after load, hypertension, decreased pulses in lower extremities, intervention via ballooning
respiratory distress syndrome
decreased surfactant and smaller alveoli collapse, leads to atelectasis and hypoxia, can cause pulmonary hypertension, decreased perfusion, increased pulmonary capillary permeability, and pulmonary vascular constriction
day 1 RDS
breathing worsens and requires more support
day 2 RDS
remarkably stable on adequate support
day 3 RDS
resolution noted with diuresis
bronchopulmonary dysplasia
chronic lung disorder in preterm infants, lung function improves with growth, inflammatory and fibroproliferative stages, hypercapnia, rapid shallow breathing with chest retractions
croup
causes inflamed vocal cords and narrowed trachea leading to hoarseness, barking cough, SOB, cool air helps with swelling (misty shower)
acute epiglottis
inflamed epiglottis leading to narrowed airway, typically caused by strep throat, tripod position, inspiratory/expiratory stridor, nasal flaring, muscle retraction
acute bronchiolitis
lower airway infection due to RSV, produces inflammatory obstructions of small airways, rapid shallow breathing with retractions, nonproductive cough, diminished appetite
cystic fibrosis
autosomal recessive chromosome 7 mutation, affects chloride channels causing thick mucus secretions in respiratory, pancreatic, reproductive, and sweat gland systems, causes GI symptoms, sputum production, persistent cough, dyspnea, recurrent/severe pneumonia
osmoreceptors
stimulation causes thirst and ADH release
baroreceptors
sense stretch, stimulate sympathetic response and ADH release
diabetes insipidius
deficiency in ADH or decreased response to ADH, inability to concentrate urine, hypertonic dehydration, neurogenic and nephrogenic types
syndrome of inappropriate antidiuretic hormone
failure of negative feedback, ADH secretion continues despite decreased serum osmolality, fluid retention and dilution hyponatremia, caused by tumors, CNS disorders, and drugs
causes of edema formation
increased capillary permeability, lymph obstruction, increased capillary hydrostatic pressure, decreased capillary oncotic pressure
hyponatremia
hypotonic from dilution of bloodstream or hypertonic from osmotic shift from ICF to ECF with hyperglycemia, causes muscle cramps, weaknesses, confusion, lethargy, headache, increased risk for seizure activity
hypernatremia
hypertonicity of ECF and intracellular dehydration caused by disproportionate loss of water in relation to sodium, results in thirst, low urine output, high specific gravity, weak thready pulse, hypotension, dry sticky mucus membrane, muscle twitching, seizure activity
hypokalemia
caused by diets and EDs, symptoms don’t start until K is below 3, causes excitability, paraesthesia, no bowel sounds, vomitting, polyuria, treatment is to increase K intake
hyperkalemia
caused by acidosis, causes weakness, paraesthesia, peaked T waves, dyspnea, diarrhea, cramps, in severe cases causes muscle weakness, lethal arrhythmias and cardiac arrest, difficult to initiate muscle contraction
hypoparathyroidism
deficient PTH secretion that causes low serum and ionized calcium
hyperparathyroidism
increased PTH secretion, primary and secondary, causes high calcium levels and renal osteodystrophy
hypocalcemia
causes increased excitability, paraesthesia, muscle spasms, hyperactive reflexes, hypotension, chronic skeletal fractures
hypercalcemia
can occur in chronically ill bed bound patients, causes decreased neural excitability and muscle function, lethargy, behavioral changes, N/V, constipation, high output, renal calculi, treated with rehydration and drugs depending on cause
hypophosphatemia
characterized by musculoskeletal symptoms
hyperphosphatemia
characterized by cardiac arrhythmias
hypomagnesemia
same symptoms as hypocalcemia, increased neuromuscular excitability
hypermagnesemia
renal insufficiency of failure, causes lethargy, hyporeflexia, muscle weakness, confusion, hypotension, cardiac arrhythmias
acid
dissociate and release H ion, volatile and nonvolatile
base
accept H+ ion
metabolic acidosis
caused by production of metabolic acids, decreased renal function, increased bicarbonate losses, decreased perfusion, results in weakness, fatigue, peripheral vasodilation, N/V, compensate with increased respiration and acidic urine with increased ammonia in urine
metabolic alkalosis
caused by IV infusion excess, over ingestion of antacids, loss of fixed acid, fluid depletion, results in confusion, hyperactive reflexes, hypotension, arrhythmias, compensate with hypoventilation
respiratory acidosis
hypoventilation, increased carbon dioxide production, results in headache, confusion, stupor, compensate with acid in urine
respiratory alkalosis
hyperventilation, causes lightheadedness, panic, tingling, numbness, sweating, palpations, dyspnea, compensate with alkaline urine
achalasia
lower esophageal sphincter fails to relax, causes inflammation and aspiration
GERD
persistent reflex creating inflammatory response, can be caused by weak esophageal sphincter, lifestyle, causes mucosal injury, heartburn, hoarse voice, can develop ulcers and esophageal strictures
acute gastritis
injury to protective mucosal barrier, can cause vague abdominal discomfort, N/V, hematemenesis, self-limiting
chronic gastritis
H.pylori, chronic autoimmune, can lead to pernicious anemia, slow onset, antibodies to GI cells, chemical gastropathy
H. pylori gastritis
gram negative rods in stomach causing inflammation, secrete urease to make stomach more alkaline
peptic ulcer disease
ulcerative disorder of upper GI tract, caused bu increased acid and pectin production, healing periods and excaberations, pain, complications with hemorrhage, perforation, outlet obstruction
Crohn’s disease
characterized by skip lesions, cobblestone appearance, affect all bowel layers, granulomatous inflammatory response, periods of excaberations and remissions where lumen narrows and overtime bowel wall thickens and becomes inflexible, complications with fistulas
ulcerative colitis
lesions that work upwards from rectum, pseudo polyp formation, relapsing disorder, complications with toxic megacolon and increased risk of colon cancer
diverticulosis
diverticula/outpouchings of mucosa without inflammation, change in bowel habits
diverticulitis
inflammation of diverticula, pain and tenderness in LLQ, N/V, fever, complications with perforations, obstructions, abcess and fistula formation
acute intestinal obstruction
mechanical or nonmechanical, cause distention and edema, pain, fluid and electrolyte imbalance, diarrhea, constipation
peritonitis
inflammation of peritoneum, can be caused by bacterial invasion, true ulcer, perforated bowel, trauma, cause boardlike abdomen, hypoventilation causing atelectasis
gallbladder disease
impaired bile storage
cholelithiasis
gallstones
cholecystitis
inflammation from gallstones, cause colicky pain in RUQ, N/V, bile backup
chronic pancreatitis
progressive destruction with fibrotic replacement, usually from alcohol abuse but can be autoimmune or idiopathic, causes loss of endocrine and exocrine functions, fatty stools, weight loss, can develop diabetes
acute pancreatitis
auto digestion of pancreatic tissue, massive immune response, obstruction of bile duct, massive vasodilation, severe pain in epigastric region, N/V but do not feel better with vomiting, complications with breakdown of pancreatic tissue and abcesses
causes of liver failure
autoimmune hepatitis, intrahepatic, viral hepatitis, drug induced liver injury, cirrhosis
hepatitis a
fecal-oral, can be transmitted via anal sex, does not cause chronic hepatitis
hepatitis b
blood borne and sexual, usually asymptomatic, can lead to liver failure
hepatitis c
blood borne and sexual, usually asymptomatic, can lead to liver failure, large cause of hepatocellular cancer, no vaccine
acute fulminant hepatitis
acute hepatic insufficiency, sometimes viral caused, no history of liver injury and goes into liver failure, high mortality
liver failure symptoms
usually asymptomatic until far advanced, causes portal hypertension, weight loss, weakness, hepatomegaly, jaundice, pain in RUQ, fetter hepaticus, bleeding issues, sexual dysfunction
portal hypertension
nodules affecting flow cause backup, shunting of blood leads to development of collateral channels, cause varices, ascites
renal calculi
kidney stones, stones can be calcium, struvite, uric acid, or cystine, cause pain, N/V, hematuria, stones pass spontaneously, treatment via prevention
acute renal failure
rapid decline in kidney function, cause azotemia and decreased GFR
chronic renal failure
permanent loss of nephrons
dietary management in renal failure
decrease phosphorus, potassium required when GFR falls
azotemia
accumulation of nitrogenous waste
uremia
manifestation of kidney failure due to organic waste in blood
BUN
measures nitrogenous wastes from urea, protein byproduct
creatinine
waste product of muscle metabolism excreted by kidneys
hypervolemia
too much fluid in vascular space
ascites
fluid accumulation in peritoneal space