What is the definition of oliguria?
Urine output of <400 mL/24 h.
What distinguishes Henoch-Schönlein purpura from IgA nephropathy?
Younger age (<20 years old), preceding infection, and abdominal complaints.
1/120
p.3
Acute Kidney Injury (AKI) Definitions and Causes

What is the definition of oliguria?

Urine output of <400 mL/24 h.

p.8
Glomerular Diseases and Their Characteristics

What distinguishes Henoch-Schönlein purpura from IgA nephropathy?

Younger age (<20 years old), preceding infection, and abdominal complaints.

p.4
Chronic Kidney Disease (CKD) Management and Complications

What is the definitive treatment for hepatorenal syndrome?

Liver transplantation.

p.6
Nephrotic vs. Nephritic Syndrome

What is the most common cause of nephrotic syndrome in the elderly?

Membranous Glomerulonephritis (MGN).

p.5
Glomerular Diseases and Their Characteristics

What is the most common cause of glomerulonephritis worldwide?

Malaria and schistosomiasis.

p.7
Chronic Kidney Disease (CKD) Management and Complications

What correlates best with renal disease in lupus?

Anti-dsDNA antibodies.

p.1
Renin-Angiotensin-Aldosterone System

What triggers the macula densa to detect decreased blood pressure or GFR?

Decreased blood pressure or decreased GFR.

p.1
Renin-Angiotensin-Aldosterone System

What do juxtaglomerular cells release in response to decreased blood pressure?

Renin.

p.10
Urinary Tract Infections (UTI) Risk Factors and Management

What is pathognomonic of vesicoureteral reflux?

Flank pain that occurs only with micturition.

p.2
Renal Replacement Therapy Options

What are the most common organisms in peritoneal dialysis-related peritonitis?

Gram-positive cocci, including Staphylococcus.

p.6
Nephrotic vs. Nephritic Syndrome

What is the mnemonic for signs and symptoms of nephrotic syndrome?

EPAL: Edema, Proteinuria >3.0g/day, HypoAlbuminemia, HyperLipidemia.

p.7
Glomerular Diseases and Their Characteristics

What is the main cause of Rapidly Progressive Glomerulonephritis (RPGN)?

Can be anti-GBM antibody-induced, immune complex-mediated, or pauci-immune.

p.2
Renal Replacement Therapy Options

What is the most common form of renal replacement therapy for AKI?

Hemodialysis.

p.8
Glomerular Diseases and Their Characteristics

What is the triad of Wegener's granulomatosis?

Necrotizing granulomas of the respiratory tract, necrotizing or granulomatous vasculitis, and focal necrotizing or crescentic glomerulonephritis.

p.4
Chronic Kidney Disease (CKD) Management and Complications

What is the leading cause of morbidity and mortality in patients at every stage of CKD?

Cardiovascular disease (CVD).

p.7
Glomerular Diseases and Their Characteristics

What is Post-Streptococcus Glomerulonephritis (PSGN) caused by?

Group A beta-hemolytic streptococcus (GABHS).

p.4
Chronic Kidney Disease (CKD) Management and Complications

What is a common cause of large kidneys observed in Chronic Kidney Disease (CKD)?

Diabetic nephropathy.

p.10
Urinary Tract Infections (UTI) Risk Factors and Management

What are common independent risk factors for acute cystitis?

Frequent sexual intercourse, history of UTI, and a new sexual partner.

p.8
Glomerular Diseases and Their Characteristics

What is the most common type of glomerulonephritis worldwide?

IgA nephropathy.

p.7
Glomerular Diseases and Their Characteristics

What is Alport Syndrome characterized by?

Hereditary structural defect in collagen IV leading to hematuria, hearing loss, and blindness.

p.3
Acute Kidney Injury (AKI) Definitions and Causes

What is the most common form of AKI?

Prerenal Azotemia.

p.6
Nephrotic vs. Nephritic Syndrome

What are the diseases presenting with nephritic syndrome?

Goodpasture syndrome, Alport syndrome, Lupus nephropathy.

p.1
Renin-Angiotensin-Aldosterone System

What is the role of angiotensin II?

Stimulates aldosterone release, increases Na+ reabsorption, K+ secretion, and H+ secretion.

p.7
Glomerular Diseases and Their Characteristics

What are the characteristic findings in PSGN on electron microscopy?

Hypercellular glomeruli, 'lumpy-bumpy' deposits of IgG and C3, subepithelial humps.

p.3
Acute Kidney Injury (AKI) Definitions and Causes

What is the definition of Acute Kidney Injury (AKI)?

A rise of at least 0.3 mg/dL within 48 hours or 50% higher than baseline within 1 week; or reduction in urine output to < 0.5 mL/kg/h for >6 hours.

p.5
Glomerular Diseases and Their Characteristics

What are RBC casts or dysmorphic RBCs indicative of?

Glomerulonephritis (GN).

p.10
Urinary Tract Infections (UTI) Risk Factors and Management

What are typical symptoms of cystitis?

Dysuria, urinary frequency, and urgency.

p.1
Renin-Angiotensin-Aldosterone System

What do principal cells of the late distal tubule absorb and secrete?

Absorb Na+ and H2O, and secrete K+.

p.6
Nephrotic vs. Nephritic Syndrome

What type of proteinuria is associated with Membranous Glomerulonephritis (MGN)?

Non-selective proteinuria.

p.2
Renal Replacement Therapy Options

What dialysis access has the highest long-term patency rate?

Fistula.

p.3
Acute Kidney Injury (AKI) Definitions and Causes

What are the most common clinical conditions associated with prerenal azotemia?

Hypovolemia and decreased cardiac output.

p.10
Urinary Tract Infections (UTI) Risk Factors and Management

What is the most common cause of bilateral hydronephrosis in boys?

Posterior urethral valves.

p.2
Renal Replacement Therapy Options

What are the most common additives to peritoneal dialysis solutions?

Heparin, antibiotics, and insulin.

p.2
Renal Replacement Therapy Options

What is an absolute indication for the urgent initiation of dialysis?

Uremic pericarditis.

p.9
Nephrolithiasis: Types and Management

What is the most common renal abnormality in Angiomyolipomas?

Tuberous sclerosis.

p.9
Nephrolithiasis: Types and Management

What is the most common type of urolithiasis?

Calcium oxalate stones.

p.8
Glomerular Diseases and Their Characteristics

What are the common presentations of IgA nephropathy?

Recurrent episodes of macroscopic hematuria often accompanied by proteinuria during or immediately following an upper respiratory infection, or persistent asymptomatic microscopic hematuria.

p.10
Urinary Tract Infections (UTI) Risk Factors and Management

What is the most common etiologic agent in acute uncomplicated UTIs?

E. coli, accounting for 75-90% of isolates.

p.2
Chronic Kidney Disease (CKD) Management and Complications

What are clear indications for initiation of renal replacement therapy in patients with CKD?

Uremic pericarditis, encephalopathy, intractable muscle cramping, evidence of malnutrition, and fluid & electrolyte abnormalities refractory to other measures.

p.8
Acute Kidney Injury (AKI) Definitions and Causes

What is the most common variant of Hemolytic Uremic Syndrome (HUS)?

D+ (diarrhea-associated) HUS, also known as enterohemorrhagic E. coli (EHEC) HUS.

p.8
Chronic Kidney Disease (CKD) Management and Complications

What is the most severe manifestation of scleroderma characterized by accelerated hypertension and rapid decline in renal function?

Scleroderma renal crisis (SRC).

p.5
Glomerular Diseases and Their Characteristics

What is a characteristic appearance of kidneys in endocarditis-associated GN?

Subcapsular hemorrhages with a 'flea-bitten' appearance.

p.6
Nephrotic vs. Nephritic Syndrome

What is the appearance of deposits in Membranous Glomerulonephritis?

Spike & dome appearance with subepithelial IgG and C3 deposits.

p.4
Chronic Kidney Disease (CKD) Management and Complications

What condition is seen almost exclusively in patients with advanced CKD?

Calciphylaxis.

p.2
Nephrolithiasis: Types and Management

What is the most useful renal imaging study?

Renal ultrasound.

p.10
Urinary Tract Infections (UTI) Risk Factors and Management

What factors are associated with pyelonephritis?

UTI in the previous 12 months, maternal history of UTI, diabetes, and incontinence.

p.6
Nephrotic vs. Nephritic Syndrome

What are the signs and symptoms of nephritic syndrome?

Oliguria, Hematuria, Hypertension, Azotemia.

p.4
Chronic Kidney Disease (CKD) Management and Complications

What is a major side effect of calcium-based phosphate binders?

Total-body calcium accumulation and hypercalcemia.

p.10
Urinary Tract Infections (UTI) Risk Factors and Management

What is a distinguishing feature of fever in pyelonephritis?

A high, spiking 'picket-fence' pattern that resolves over 72 hours of treatment.

p.10
Urinary Tract Infections (UTI) Risk Factors and Management

What drugs are considered relatively safe for UTI treatment in early pregnancy?

Nitrofurantoin, penicillin, and cephalosporins.

p.10
Urinary Tract Infections (UTI) Risk Factors and Management

What is the standard care for pregnant women with overt pyelonephritis?

Parenteral beta-lactam with or without aminoglycosides.

p.8
Chronic Kidney Disease (CKD) Management and Complications

What is the goal in treating scleroderma renal crisis?

Reduce SBP by 20 mmHg and DBP by 10 mmHg every 24 hours until BP normalized.

p.5
Glomerular Diseases and Their Characteristics

What characterizes Membranoproliferative GN (MPGN)?

Thickening of the GBM with mesangioproliferative changes.

p.3
Acute Kidney Injury (AKI) Definitions and Causes

What is the most common protein found in urine?

Uromodulin/Tamm-Horsfall Protein.

p.9
Chronic Kidney Disease (CKD) Management and Complications

What is the clinical syndrome that mimics chronic ingestion of loop diuretics?

Bartter's syndrome.

p.6
Nephrotic vs. Nephritic Syndrome

What is the most common cause of nephrotic syndrome in children?

Minimal Change Disease (MCD).

p.4
Chronic Kidney Disease (CKD) Management and Complications

What does ESRD refer to in the context of CKD?

Stage 5 CKD with a GFR of less than 15%.

p.1
Erythropoietin Production and Function

Where is erythropoietin (EPO) produced?

In the interstitial cells of the peritubular capillaries.

p.2
Renal Replacement Therapy Options

How many hours of hemodialysis do the majority of ESRD patients receive each week?

9 - 12 hours divided into 3 equal sessions.

p.2
Chronic Kidney Disease (CKD) Management and Complications

What is the leading cause of end-stage renal disease (ESRD)?

Diabetes mellitus.

p.8
Chronic Kidney Disease (CKD) Management and Complications

What is the first-line therapy in scleroderma renal crisis unless contraindicated?

Treatment with ACE inhibitor.

p.3
Acute Kidney Injury (AKI) Definitions and Causes

What are the most common causes of intrinsic AKI?

Sepsis, ischemia, and nephrotoxins.

p.6
Nephrotic vs. Nephritic Syndrome

What type of deposits are found in Renal Amyloidosis?

Subendothelial and mesangial amyloid deposits.

p.5
Glomerular Diseases and Their Characteristics

What is microalbuminuria a sensitive indicator of?

The presence of diabetes.

p.1
Chronic Kidney Disease (CKD) Management and Complications

What acid-base abnormality can acetazolamide cause?

Metabolic acidosis.

p.9
Nephrolithiasis: Types and Management

What type of stones are associated with Proteus mirabilis?

Struvite stones (magnesium ammonium phosphate stones).

p.4
Renal Replacement Therapy Options

In which situations is Continuous Renal Replacement Therapy often preferred?

Severe hemodynamic instability, cerebral edema, and significant volume overload.

p.3
Acute Kidney Injury (AKI) Definitions and Causes

What condition is associated with light chain cast nephropathy?

Multiple myeloma, commonly known as myeloma kidney.

p.6
Nephrotic vs. Nephritic Syndrome

What is the mnemonic for nephritic syndrome signs and symptoms?

OHHA: Oliguria, Hematuria, Hypertension, Azotemia.

p.5
Glomerular Diseases and Their Characteristics

When does PSGN typically develop after a skin infection?

2-6 weeks after skin infection.

p.5
Glomerular Diseases and Their Characteristics

Which M protein serotypes of Streptococcus pyogenes are associated with impetigo?

M types 47, 49, 55, 2, 60, and 57.

p.4
Chronic Kidney Disease (CKD) Management and Complications

What is the primary cause of anemia in CKD?

Insufficient production of erythropoietin (EPO) by the diseased kidneys.

p.6
Nephrotic vs. Nephritic Syndrome

What are Kimmelstiel-Wilson nodules associated with?

Diabetic Nephropathy.

p.1
ADH Mechanism and Triggers

What is the effect of ADH on the collecting ducts?

Inserts aquaporins (AQP-2) to increase water reabsorption.

p.1
Acute Kidney Injury (AKI) Definitions and Causes

What effect does vasoconstriction of the efferent arteriole have on filtration fraction?

It will decrease the filtration fraction.

p.9
Chronic Kidney Disease (CKD) Management and Complications

What distinguishes Gitelman's syndrome from most forms of Bartter's syndrome?

Severe hypomagnesemia and hypocalciuria.

p.9
Nephrolithiasis: Types and Management

What is the pathogenesis of struvite stones?

Bacterial urease production leading to urinary tract infections (UTIs).

p.7
Glomerular Diseases and Their Characteristics

What is the prognosis of Post-Streptococcus Glomerulonephritis?

Self-resolving.

p.2
Nephrolithiasis: Types and Management

What imaging test is used for the diagnosis of nephrolithiasis?

Helical computed tomography (CT) scanning without radiocontrast enhancement.

p.4
Chronic Kidney Disease (CKD) Management and Complications

What is microalbuminuria and its significance in early nephropathy?

It represents the presence of proteinuria increasing to 30-300 mg/24h, indicating renal disease.

p.10
Urinary Tract Infections (UTI) Risk Factors and Management

What indicates an invasive infection of the upper urinary tract?

Unilateral back or flank pain and fever.

p.3
Acute Kidney Injury (AKI) Definitions and Causes

What happens to renal autoregulation when systolic blood pressure falls below 80 mmHg?

Renal autoregulation usually fails.

p.3
Acute Kidney Injury (AKI) Definitions and Causes

What are the three broad categories of AKI?

Prerenal AKI, Intrinsic AKI, and Post-renal AKI.

p.4
Chronic Kidney Disease (CKD) Management and Complications

What is the target hemoglobin concentration in CKD?

100-115 g/L.

p.1
ADH Mechanism and Triggers

What are the main triggers for ADH secretion?

Decreased blood volume and decreased blood pressure.

p.5
Glomerular Diseases and Their Characteristics

What is the most common type of MPGN in children?

Type II MPGN.

p.1
Nephrolithiasis: Types and Management

What is the permeability of the descending limb of the Loop of Henle?

Permeable to water and impermeable to solutes.

p.9
Chronic Kidney Disease (CKD) Management and Complications

What is the triad of symptoms associated with heavy metal (lead) nephropathy?

Saturnine gout, hypertension, and renal insufficiency.

p.7
Nephritic vs. Nephritic Syndrome

What is a common pediatric cause of nephritic syndrome?

Post-Streptococcus Glomerulonephritis (PSGN).

p.10
Urinary Tract Infections (UTI) Risk Factors and Management

What recent activity is an independent risk factor for acute cystitis?

Recent use of a diaphragm with spermicide.

p.2
Chronic Kidney Disease (CKD) Management and Complications

What is the test for measurement of albuminuria?

Urinary albumin to creatinine ratio.

p.7
Glomerular Diseases and Their Characteristics

What is a key feature of Goodpasture Syndrome?

Presence of anti-GBM antibodies and hematuria with hemoptysis.

p.3
Acute Kidney Injury (AKI) Definitions and Causes

What is the hallmark of AKI?

Elevated BUN.

p.6
Nephrotic vs. Nephritic Syndrome

What is the characteristic feature of Minimal Change Disease (MCD)?

Effacement of foot processes.

p.2
Renal Replacement Therapy Options

What is the most important complication of arteriovenous grafts?

Thrombosis of the graft and graft failure.

p.2
Renal Replacement Therapy Options

What is the most common acute complication of hemodialysis?

Hypotension.

p.5
Glomerular Diseases and Their Characteristics

What is the most common cause of renal amyloidosis?

Fibrillar deposits of immunoglobulin light chains (AL).

p.1
Chronic Kidney Disease (CKD) Management and Complications

What acid-base abnormality can loop diuretics and thiazide diuretics cause?

Metabolic alkalosis.

p.9
Nephrolithiasis: Types and Management

What is the recommended target urine pH for uric acid stones?

At least 6.5.

p.8
Glomerular Diseases and Their Characteristics

What antibodies are more common in granulomatosis with polyangiitis?

Anti-PR3 antibodies.

p.5
Glomerular Diseases and Their Characteristics

What is Poststreptococcal GN (PSGN) prototypical for?

Acute endocapillary proliferative GN.

p.7
Chronic Kidney Disease (CKD) Management and Complications

What is the most severe type of lupus nephritis?

Class IV Nephritis, characterized by global, diffuse proliferative lesions.

p.7
Chronic Kidney Disease (CKD) Management and Complications

What is a significant complication for patients with crescents on biopsy in lupus nephritis?

Predisposition to renal-vein thrombosis and other thrombotic complications.

p.4
Chronic Kidney Disease (CKD) Management and Complications

What is the classic lesion of secondary hyperparathyroidism in CKD?

Osteitis fibrosa cystica.

p.1
ADH Mechanism and Triggers

What happens to free water clearance (CH20) when ADH is present?

Free water is reabsorbed and CH20 is negative.

p.5
Glomerular Diseases and Their Characteristics

Which schistosoma species is most commonly associated with clinical renal disease?

Schistosoma mansoni.

p.9
Chronic Kidney Disease (CKD) Management and Complications

What causes Bartter's syndrome?

Mutations affecting any of five ion transport proteins in the thick ascending limb (TAL).

p.4
Chronic Kidney Disease (CKD) Management and Complications

What stage of CKD is associated with normocytic, normochromic anemia?

As early as Stage 3 CKD, almost universal by Stage 4 CKD.

p.8
Acute Kidney Injury (AKI) Definitions and Causes

What is commonly involved in renal vein thrombosis?

Left renal vein.

p.5
Glomerular Diseases and Their Characteristics

What is a key feature of Type I MPGN?

Presence of subendothelial deposits and low C3.

p.9
Chronic Kidney Disease (CKD) Management and Complications

What is a hallmark feature of TIN associated with uveitis?

Painful anterior uveitis.

p.9
Nephrolithiasis: Types and Management

What is the treatment for struvite stones?

Complete removal by a urologist.

p.5
Glomerular Diseases and Their Characteristics

What is the primary treatment for endocarditis-associated GN?

Eradication of the infection with 4-6 weeks of antibiotics.

p.3
Acute Kidney Injury (AKI) Definitions and Causes

What is the most common clinical course of contrast nephropathy?

A rise in SCr beginning 24-48 hours following exposure, peaking within 3-5 days, and resolving within 1 week.

p.1
Acute Kidney Injury (AKI) Definitions and Causes

What is the normal value for the filtration fraction (FF)?

20%.

p.9
Chronic Kidney Disease (CKD) Management and Complications

What causes Analgesic nephropathy?

Long-term use of compound analgesic preparations containing phenacetin, aspirin, and caffeine.

p.1
Nephrolithiasis: Types and Management

What is the permeability of the ascending limb of the Loop of Henle?

Permeable to solutes and impermeable to water.

p.9
Chronic Kidney Disease (CKD) Management and Complications

What is the predominant pathology in chronic Tubulointerstitial Nephritis (TIN)?

Interstitial fibrosis.

p.9
Nephrolithiasis: Types and Management

What is the focus for cystine stone prevention?

Increasing cystine solubility through medications like tiopronin or penicillamine.

p.9
Chronic Kidney Disease (CKD) Management and Complications

What is Liddle's syndrome characterized by?

Early and severe hypertension, hypokalemia, and metabolic alkalosis with low plasma aldosterone and renin levels.

Study Smarter, Not Harder
Study Smarter, Not Harder