GFR 60-89 ml/min/1.73m2 is categorized as...
Stage G2
3500mg/24h
or a urine protein-creatinine ratio >3500mg/g
Calcium oxalate
Envelope; dumbbell; needle
Associated with hypercalciuria, hyperoxaluria, ethylene glycol poisoning.
This most common inherited kidney disorder can involve intracranial cerebral aneurysm, MVP, hepatic cysts, and diverticulosis
Autosomal dominant polycystic kidney disease
<115/75mmHg
(daytime average <120/80; nighttime average <100/65)
CKD is defined as abnormal kidney structure or function present for greater than _______ months.
3
__________ is the most common form of the nephrotic syndrome in black patients.
FSGS
The prevalence in the US is more than 20,000 patients, with a yearly incidence of approximately 5,000 newly diagnosed cases per year.
Uric acid
Rhomboid; needle; rosette; barrels; hexagonal plates
Associated with hyperuricemia; gout; diabetes mellitus; obesity; tumor lysis syndrome; urine pH <6.0
This noncystic kidney disorder is associated with conical deformation of the lens, as well as sensorineural hearing loss.
Hereditary nephritis (aka Alport syndrome)
This is a collagen type IV-related nephropathy
True or False
The live attenuated Influenza vaccine should be administered annually to patients with ESRD
False
Patients with ESRD should only receive the inactivated influenza vaccine due to risks associated with the live vaccines in immunocompromised patients.
GFR 30-44 ml/min/1.73m2
G3b
__________ is the most common cause of the nephrotic syndrome in children.
Minimal change glomerulonephropathy (aka minimal change disease).
Calcium phosphate
Prism; needle; star-like clumps
Associated with distal renal tubular acidosis; urine pH >6.5; tumor lysis syndrome; acute phosphate nephropathy.
This X-lined recessive disorder is caused by an inborn error of glycophospholipid metabolism caused by deficiency of alpha-galactosidase A.
Fabry Disease
Progressive kidney disease, premature CAD, severe neuropathic pain, telangiectasias, angiokeratomas.
IV potassium can safely be infused peripherally at a rate of...
20mEq/h
Infusion through a central vein can be increased to 40mEq/h with close monitoring.
GFR 15-29 ml/min/1.73m2
G4
The diagnosis of glomerulonephritis is traditionally made by...
Kidney biopsy.
Serologic testing can aid in the diagnosis.
Cystine
Hexagonal morphology
Associated with cystinuria.
This autosomal dominant kidney disorder is characterized by tumors in many organs, primarily in the brain, eyes, heart, kidney, skin, and lungs. Renal angiomyolipomas occur in 75% of patients with this.
Tuberous Sclerosis Complex
Initial ECG manifestations with hyperkalemia include...
peaked precordial T waves and a shortened QT interval.
(With further progression, will see lengthening of the PR interval, loss of the P wave, widening of the QRS complex, a sine wave pattern, and then possible asystole)
G3a has a GFR range of...
45-59ml/min/1.73
Kidney biopsy in ___________ disease shows a crescentic glomerulonephritis on light microscopy and pathognomonic linear staining for IgG along the glomerular capillaries.
anti-GBM
Serologic testing for anti-GBM Abies is performed at time of diagnosis
Struvite (magnesium ammonium phosphate)
Coffin-lid morphology
Associated with alkaline urine due to chronic UTI with urease-producing organisms
This primarily autosomal dominant disorder is associated with type IV collagen variants causing GBM thinning, which results in hematuria without significant proteinuria or ensuing glomerulosclerosis.
Thin glomerular basement membrane disease (benign familial hematuria).
Gadolinium contrast used in MRI is associated with risk for ____________ and must be avoided in patients with an eGFR < ____________.
Nephrogenic Systemic Fibrosis (NSF); 30 ml/min/1.73m2