Exam 2 Flashcards
(272 cards)
Peritoneum
Layer of the digestive tract that constitutes the outer wall of the intestine and contains a serous fluid between its two layers.
Crohn Disease
Sharply demarcated, granulomatous lesions that are surrounded by normal-appearing mucosal tissue; cobblestone.
Manifestation: Fistula Formation
Submucosal layer
Layer of digestive tract that consists of nerves, blood vessels, and structures for secreting digestive juices
Treatment of Crohn disease with Sulfasalazine will focus on which aspect of this disease?
Inflammatory suppression
Duodenum
First section of small intestine, where bile from the liver and digestive enzymes from the pancreas aid in the digestion of fats, proteins, and carbohydrates.
Aldosterone
Regulates balance of sodium, potassium, and water in the body
Client diagnosed with Addisons disease will likely experience which abnormal lab result related to the absence of aldosterone?
Serum potassium levels elevated
Urinary Tract Infection (UTI)
Presence of bacteria in the urine (BACTERIURIA)
Creatinine
Waste product produced by muscles during muscle metabolism
Formed from the breakdown of creatine (creatine supplies energy to muscles)
Levels of creatine in the blood and urine is used as an indicator of kidney function because the kidneys filter it out of the blood and excrete it in urine
Disruption of which muscles contraction can lead to the inability to expel urine from the bladder?
Detrusor
What loss of function in the kidney results in anemia of end-stage kidney disease?
Produce erythropoietin
How to collect clean-catch urine specimen
Clean the external urethral opening and then collect the urine in the middle of the stream
Kidneys
Maintain blood volume and pressure, creates stable environment
Ensure balance of SODIUM, CHLORIDE, POTASSIUM, CALCIUM, HYDROGEN, PHOSPHATE & PH
Eliminate products of metabolism, such as urea, uric acid and creatinine
Nephrons
Functional unit of the kidney responsible for filtering blood and forming urine
Each nephron consists of a glomerulus and system of tools.
Glomerulus
High pressure mass of capillaries that filters the blood
Urine formation involves:
Filtration of blood by the glomerulus to form an ultrafiltrative urine
Tubular reabsoprtion of electrolytes and nutrients needed to maintain the constancy of the internal environment
Secretion of waste materials
Urinary Tract Obstruction: Classifying causes
Site:
-upper urinary tract
-lower urinary tract
-bilateral
-unilateral
Degree:
-Partial
-complete
Duration :
-acute
-chronic
Causes of Urinary Tract Obstructions
Calculi
Pregnancy
Tumors
Benign Prostatic hyperplasia (BPH)
Scar Tissue from infections and inflammation
Developmental defects
Neurogenic disorders (spinal cord injury)
Complications of Urinary tract obstructions:
Hydronephrosis, kidney failure, and infection
Renal damage process in Polycystic Kidney Disease
Decrease renal blood flow —> decreased glomerular blood flow —> decreased glomerular filtration rate (GFR)
Tubular cell damage —> increased NaCl delivery to macula densa (specialized group of cells in the kidney), or Tubular obstruction, or back leak of filtrate —> decreased glomerular filtration rate (GFR)
Glomerular damage —> decreased glomerular ultrafiltration —> decreased glomerular filtration rate (GFR)
Autosomal Dominant PKD (polycystic kidney disease)
Most common form
Inherited as an autosomal trait caused by a mutation in PKD1 gene and PKD2 gene, usually presenting in adulthood
Slow to develop & asymptomatic
Manifestations: pain, hematuria, hypertension, nephrolithiasis, hepatic cysts, and aneurysms (later stage)
Subarachnoid hemorrhage is a common cause of death
Kidney becomes enlarged with multiple round cysts in the kidney medulla, cysts may develop in other organs
Autosomal Recessive PKD (polycystic kidney disease)
Inherited disease caused by mutation in the PKHD1 gene.
Usually depend prenatally or within a few weeks after birth, can also appear in older children and adults
Potter fancies and defects associated with oligohydramnios may also be present
Manifestations: severe renal failure, impaired lung development, and liver fibrosis
ARPKD is characterized by the cystic dilation of cortical and medullary collection tubules and bilateral flank masses, causing an enlarged kidney
Nephronophthisis-Medullary Cystic Kidney Disease
Group of disorder that usually begin childhood
Damage occurs in distal tubules with disruption of basement membrane & chronic & progressive tubular atrophy
Manifestations (initial): polydipsia, polyuria, enuresis.
Additional manifestation: salt wasting, growth retardation, anemia, progressive renal insufficiency, ocular motor abnormalities, retinitis pigmentosa, liver fibrosis, cerebellar abnormalities, azotemia, and renal failure.
Kidneys are small and shrunken with cysts in the medullar or cortex, but usually at the corticomedullary junction
Azotemia
Elevated levels of nitrogen-containing compounds (urea and creatinine) in the blood.
These are substances normally removed by the kidneys, so if they are not being removed, that means that azotemia is the kidneys not functioning properly.