USMLE Nephrology Flashcards

(90 cards)

1
Q

5 oxoproline / pyroglutamic acid acidosis

A

Anion gap metabolic acidosis

Patients with Liver dz / Kidney failiure who ingest therapeutic amouts of acetaminophen can develop HAGMA due to 5 oxoproline accumulation.

No therapy currently / supportive care

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2
Q

Accomplish Trial finding with BP

A

Stage II HTN better results with ACEi and CCB then ACEi and HCTZ ( 20% better results

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3
Q

Acute Tubular Necrosis

A
  • associated with ischemia and/or nephrotoxins
  • < 500 mL/day or < 20 ml hr/ Diuretics do NOT change prognosis
  • Prototypically runs a 3-week course Acute Tubular Necrosis: Ischemic
  • FENa (fractional excretion of sodium) > 3%
  • U/A: muddy brown granular casts
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4
Q

Alport Syndrome

A
  • Type IV collagen defect / glomerulonephritis,
  • X linked
  • Kidney / EYE / EAR
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5
Q

Autosomal dominant polycystic kidney disease (ADPKD) infected Cysts

A

Ciprofloxacin

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6
Q

B/L Renal artery stenosis

Tx:

A
  • First treat with diuretic + ACEi or ARB since it is as efficacious as agioplasty or surgery.
  • Patients with inadequate blood pressure control or worsening renal function on medical therapy should considered for angiotplasty
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7
Q

Bartter syndrome

A
  • Hypokalemia
  • Normotensive
  • Hypercalciuria with Polydepsia / Polyuria
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8
Q

Behcet’s syndrome

A
  • Complex of recurrent oral aphthous ulcers, genital ulcers, and uveitis
  • Crescentic Glomerulonephritis
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9
Q

BP meds for Elderly

A

Choose HCTZ( complication in old frail elderly / hyponatremia)

ACEi ARBs Long acting CCB < 80 yr

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10
Q

Calcineurin inhibitors and Effect on Kidney

A

Cyclosporine and tacrolimus

  • Can cause acute and chronic nephrotoxic in renal transplant pt that at times my require bx to differentiate from other causes
  • Bx: Obliterative arteriopathy, tubular vacuolization and focal segmental glomerulosclerosis
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11
Q

Chronic kidney rejection

A
  • increasing proteinuria
  • worsening htn
  • biopsy looks like MPGN
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12
Q

Chronic respiratory alkalosis

A

Hepatopulmonary syndrome in cirrhosis

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13
Q

Causes of Urinary incontinance

  • Severe constipation
  • UTI
  • Atrophic vaginitis
  • Metabolic Conditions
  • Medications
  • Alcohol
  • Impared ability to reach tiolet
A
  • Severe constipation
    • laxitives
  • UTI
    • Abx
  • Atrophic vaginitis
    • Topical estrogen
  • Metabolic Conditions
    • Do your job and treat it
  • Medications
    • ID and DC
  • Alcohol
    • Blame it on the alcohol
  • Impared ability to reach tiolet
    • Bedside shitting arrangments
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14
Q

Cinacalcet

A

Calcimimietics decrease Ca/PO4/PTH levels

Increase the sensitivity of ca sensing receptors on parathyroid glands to ca.

Improve symptoms of secondary hyperparathyroidism (pruritus, bone pain, fx, calciphylaxis, avascular necrosis)

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15
Q

Colonic pseudo-obstruction

A

Up-regulation of potassium channels in the colon, resulting in secretory diarrhea, intestinal potassium loss, and hypokalemia.

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16
Q

CKD Phosphate

CKD III-V

  • Dietary restriciton
  • Non HD goal of 2.7-4.6
  • HD goal of 3.5-5.5
A
  • If Ca > 9.5
    • Sevalamer or Lanthanum
  • < 9.5 Adynamic bone dz, low PTH
    • if Yes - Sevelamer or lanthanum
    • if No Ca Acetate/ carbonate - if continues to be high > 5.5 then Sevelamer or lanthanum

IN CKD secondary hyperparathyroidism is due to hyperphosphatemia

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17
Q

Contraindications to Transplant

A
  • Active infection
  • Uncontrollable malignancy
  • Anti-GBM antibodies
  • ABO incompatibility
  • Antilymphocyte antibodies against donor
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18
Q

Cystinuria and cystine kidney stones *

A
  • Cystinuria: inherited disorder, excessive “COALCystine Ornithine Arginine, Lysine
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19
Q

Diuretic abuse and surreptitious vomiting vs Lasitavie abuse(diarrhea)

All cause hypokalemia

One losses H+ (vomit / piss)

One looses Bicarb( diarrhea)

A

Diuretic abuse and surreptitious vomiting can cause hypokalemic metabolic alkalosis

which is inconsistent with the hypokalemic metabolic acidosis observed in this patient.

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20
Q

Effects of Trimethoprime and Cimetidine on Creatnine

A

Increase serum creatnine without decreasing GFR

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21
Q

Epididymitis tx

A

Ceftriaxone and doxycyclin

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22
Q

Bladder issues

  • Anti Muscarinic agents
  • 5-alph reductase inhibitor
  • Alpha adrenergic blocking agent
A

Anti Muscarinic agents (tolterodin, oxybutynin, propiverine)

  • Work well with pateints with overactive bladders (will need post woid residual volume measurements before start of treatment.

5-alph reductase inhibitor

  • Improves lower urinary tract sx in men with bph - works best with alpha adrenergic blocking agents

Alpha adrenergic blocking agent

helps with bph as well

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23
Q

Features of tuberous sclerosis complex

A

Tuberous SC

  • Hypopigmneted macules, brown fibrous plaque on forehead, angiofibromas
  • Glioneuromas, subependymals nodules, seizures
  • Cognitive deficits
  • Renal angiomyolipomas -hematuria
  • Pulmonary LAM
  • _Retinal hamartomas -_grayish white

Neurofibromatosis (does not involve renal)

PCKD (not associated with antiomyolipomas)

Von Hippel-Lindau hemangioblastomas of the CNS, retinal angiomas, pheochromocytoma, pancreatic lesions, renal cyst, RCC

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24
Q

FSGS

  • Primary - nephrotic syndrome
  • Secondary (proteinuria 2-3 grams/day) non nephrotic syndrome
A

Primary:

  • Acute onset with edema, nephrotic syndrom, progresses to ESRD
  • Tx: Corticosteriods
  • Cyclosporine or tacrolimus
  • Mycophenolate

Secondary

  • Insidious onset without nephrotic syndrome
  • Slowly decrease GFR and increase protienuria
  • HIV / IV drug use / SLE nephritis / Atheroembolic dz, Vesicouretera reflux
  • Tx: ACEi and ARB
  • Non dihydropyridine ca antagonist
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25
FSGS / Focal segmental glomerulosclerosis / Nephrotic Syndrome
* Intravenous drug abuse * HIV infection * Malignancy * HTN\* * Obesity \* * African-American \*
26
Granulomatosis with polyangiitis (also known as Wegener granulomatosis) i
* Granulomatosis with polyangiitis (also known as Wegener granulomatosis) is a necrotizing vasculitis that typically affects the respiratory tract and the kidneys. More than 70% of patients present with upper airway symptoms, particularly sinusitis. * Kidney biopsy specimens reveal a pauci-immune crescentic glomerulonephritis; medium-sized artery aneurysms and stenosis are not found. * induction therapy for severe ANCA vasculitis includes plasmapheresis, cyclophosphamide, and corticosteroids.
27
Hemolytic-uremic syndrome
* Hemolytic anemia (anemia caused by destruction of red blood cells) microangiopathic hemolytic anemia (MAHA) * Acute kidney failure (uremia) * Low platelet count (thrombocytopenia) Clinical Dx / Supportive therapy HD
28
Henoch Schonlein purpura
Arthralgia and abd complaints IgA deposits * Skin: Ecchymosis, petechiea * Musculoskeletal: Arthritis 1-4 large joints * GI N/V, ABD pain * Renal: Hematuria, protienuria renal insufficiency
29
Henoch-Schb'nlein purpura
* "**_Classic Triad_**" Purpura, arthritis and abdominal pain * _Crescentic Glomerulonephritis_/RPGN * C3 and IgA
30
High serum or urine aldosterone + urinary K+loss of \> 30 mEq/day + HTN + low renin =
Aldosterone:renin ratio \> 20 is suggestive of primary hyperaldosteronism.
31
HTN + high renin + high urinary K+ loss =
Renovascular
32
HTN + low renin + low aldosterone + high urinary K+ loss + low K+ =
- Ingestion of exogenous mineralocorticoid or licorice
33
HUS Hemolytic Uremic Syndrome
Triad: * Microangiopathic hemolytic anemia (hb \< 8 negative coombs test, schistocytes) * thrombocytopenia (\< 140 000) * AKI LDH / billi high with low heptaglobin
34
Hypercalciuria to avoid ca in urine
Restrict: * Na and Animal protien Increase: * Ca, Citrate, Fluids and fruits
35
Hyperkalemia EKG changes Causes
EKG: * peaked Twaves * prolonged QT * widened QRS * absent P waves Causes * Metabolic acidosis * insulin deficiency * increased tissue catabolism * drugs * exercise
36
Hypocomplementemia in Renal Disease
* Membranoproliferative GN (includes **_SLE / Cryo_**) * Lupus * Cryoglobulinemia * Post-infectious GN * Atheroemboli
37
Hypokalemia and metabolic alkalosis
**_Vomiting / purging_** * Low urinary chloride **_Diuretic use _** * High urinary chloride
38
Idiopathic Postpartum Renal Failure
• Clinical Features: - Microangiopathic hemolytic anemia - Renal thrombotic microangiopathy - Acute renal failure - Malignant hypertension - Thrombocytopenia • Begins days to weeks following a normal pregnancy • Treatment: usually plasma exchange
39
IgA nephropathy
* Recurrent epidosdes of gross hematuria (glomerulonephritis) following an upper respiratory infection * Renal Bx: needed with protein excretion of \> 500 mg/day, elevated serum creatinin \> 1.5 and hypertension
40
Incontinence types * URGE * Stress * Overflow * Mixed
URGE * Involuntary leakage with urgency / sudden desire to pass * provoked by running water etc Stress * Sneezing, coughing, exertion * intraabdominal pressure overcomes urinary sphinter * younger population Overflow * Dribblind aor continous leakage with incomplete emptying * low stream high freq. usually outlet obstruction Mixed * Stress and urge together in women
41
Increased BUN
* Steroids * Gl bleeding * High protein intake (TPN) * Severe cardiomyopathy * Catabolic states (burns, sepsis, etc.)
42
Indications for Dialysis
* AEIOU * Acidosis * Electrolyte abn * Uremia * Intoxication * Overload * AEIOU * Unresponsive hypervolemia * Unresponsive hyperkalemia * Unresponsive acidosis * Uremic pericarditis or symptomatology * Undesirable poisonings * **_CAN NOT HD DIGOXIN_**
43
JC virus BK virus EBV virus
* PML **_progressive multifocal leukoencephalopahty_** when on NATALIZUMAB * BK tubulointersitial nephritis ureteral stenosis / renal trasnplant * EVB symptomatic mono associated with 2-3 fold increase of developing MS
44
Kidney stones ## Footnote Calcium oxalate Uric Acid Struvite Cystine
Calcium oxalate * **Envelope** shaped crystals * Hyperparathyroidism / Malabsorption / distal RTA Uric Acid * **Rhomboid** cyrstals / **_radiolucent_** stones * Gout / Myeloproliffrative DO Struvite * Staghorn calcula / **coffin lid /****ammonium phosphate** * Recurrent UTI Cystine * hexagonal green / larg branche calculi * Decreased reabsorption of cystine in kidney
45
Major Medical Complications Post-Transplant
1. Cardiovascular events 2. Malignancies: skin and lymphoma 3. Infections: CMV, EBV, hepatitis
46
Manage a patient with progressing mycosis fungoides/Sézary syndrome.
The most appropriate management of this patient is **_alemtuzumab_** monoclonal antibody therapy directed against CD52. Mycosis fungoides (which affects the skin) and Sézary syndrome (which affects the skin and blood) are the most common forms of _cutaneous T-cell non-Hodgkin lymphoma_.
47
Membranoproliferative Glomerulonephritis AKA crescentic glomerulonephritis
* Low complement * Hematuria / Tram traks * HTN * Tumors and CLL * Infections — endocarditis, hepatitis B and C * Cryo - Mixed essential cryoglobulinemia * Anti-GBM glomerulonephritis. * SLE - Systemic lupus erythematosus * HSP - Henoch-Schönlein purpura * IgA nephropathy * polyarteritis nodosa * ANCA-associated Wegener granulomatosis, microscopic polyangiitis and Churg-Strauss syndrome. Tx: Plasmapheresis, Corticosteroids, and Cytotoxic drugs
48
MPGN causes
.
49
Multiple Myeloma
CRAB * Ca * Rrenal insufficieny * Anemia * Bone mets
50
Myasthenia Gravis Crisi
Elective Intubation if **VC \< 20 ml/kg** or **MIF (Maximal inspiratory forsce is \< -30 cmH2O**
51
Name the Diuretics that work on these section of CT. * Proxima CT: * Loop: * Distal CT:
* Proxima CT: * Acetazolamide * AE:Metabolic acidosis * Loop: * furosemide Like "Bartter's" * AE: Hearing loss if \> 500 mg a day * Distal CT: * thiazides Like "Gittleman's" * A/E HypoNa, hypergly, hyperCa, bone marrow suppression
52
Nephrogenic DI Caused by which med: Test to do: Treatment:
* **_Lithium_** Test to do: * Water depervation untill urine osm 300 then give DDAVP * if \> 50% change then Central other wise renal Treatment: * Tx: amiloride or thiazides
53
Nephrolithiasis
75-80% contain calcium Indinavir causes Crystals Uric acid stones: typically not visible on x-ray Rx: alkalinization, allopurinol, increasing fluid intake, and a low purine diet
54
Liddle syndrome
autosomal dominant disorder that presents with early-onset hypertension and is often accompanied by **_metabolic alkalosis,_** hypokalemia, and suppressed renin and aldosterone levels.
55
Nephronolithisis-MCD Complex Medullary CYSTIC kidney vs MEDULLARY SPONGE KIDNEY
• Polyuria, polydipsia, anemia, FTT, retinitispigmentosa, \* NORMAL U/A • Medullary CYSTIC kidney - **_progressiveto ESRD_** MEDULLARY SPONGE KIDNEY \* - **_"Paintbrush" pattern_** / Nephrolithiasis, hematuria - Urinary tract infections / Decreased concentrating ability - \*\*\* _Good prognosis_
56
Non anion gap Acidosis Urinary Anion Gap Urine Na+ K - Chloride
**Negative** * Diarrhea * laxitive * Enteric fistula **Positive** * RTA * Carbonic anhydrase inhib * Low aldosteron state
57
Non anion gap metabolic acidosis Meds
Acetazolamide, topiramate Cisplatin Bactrim Ampho B
58
Pheochromocytoma
* The classic triad: headaches, sweating, and tachycardia * Orthostatic BP changes * Screen: 24-hour urine metanephrine measurement, could also measure a 24-hour urine VMA * Falsely elevated levels of urinary metanephrine due to Sympathetic drugs / Monoamine oxidase inhibitors / Labetalol * Localization: CT scan (MBIG is rarely used)
59
Hit \> 5 days \> 50% plt decrease stop what to use and why?
Bivalirudin is indicated for use only in patients with HIT or who are at risk for HIT and are undergoing acute cardiac interventions if they are unable to be delayed. Lepirudin is cleared through the kidneys and should be used with caution in patients with **_kidney impairment._** Argatroban is **_cleared through the liver_**, and dose adjustments are necessary in patients with elevated liver chemistry test values, including bilirubin level.
60
Prevent preeclampsia? * Low-dose aspirin * Methyldopa * Oral calcium supplement * Oral magnesium supplement * Reduce blood pressure to less than 120/80 mm Hg
Low-dose aspirin (75 to 150 mg/d) is associated with a 10% to 15% relative risk reduction in preventing preeclampsia and reducing adverse maternal and fetal outcomes.
61
Polyuria * Primary polydipsia * Central DI * Nephrogenic DI
**Primary polydipsia** * H2O depervation increase urin osmolality to \> 600 mOsm/Kg * Desmopressin no response **Central DI** * H2O depervatioin increase urine osmolality to \> 300 * Desmopressin increases Urine Osm 50-100% **Nephrogenic DI** * H2O Deperivation increase osmolality \< 300 * Desmopression no change in urine osmolality
62
Pregnancy and HTN
ACE inhibitors, angiotensin receptor blockers, and aldosterone antagonists should be avoided during pregnancy and in women planning to conceive. Labetalol and methyldopa
63
Pregnancy-Induced HTN: Preeclampsia
* HTN and proteinuria (Edema no longer part of the definition) * Typically **20 wks gestation/** If before 20 wks, suspect underlying **_chronic renal disease_** * Preeclampsia is typically associated with hyperuricemia * Pregnancy-induced HTN associated with low uteroplacental flow; avoid lasix Tx HTN & pregnancy methyldopa, hydralazine, and metoprolol (probably CBB)
64
Prerenal Azotemia
* Dx: volume depletion or decreased effective circulatory volume * U/A: hyaline casts * FENa \< 1 % / Na \< 20 / BUN/Cr \> 20 * SG \> 1.018 * Studies: Pul-Artery catheter, response to restoration of renal perfusion
65
Prostatitis Chronic Acute
Acute: Fever / Chills * Pyuria, tender prostate, UCx +ve * Tx: TPM-SMX / Fluoroquinolones Chronic: Dysuria and increase Freq * Recurrent UTI no symptoms of acute prostatitis * May have tender prostate * Tx: Fluoroquinolones
66
Pyroglutamic acidosis
Pyroglutamic acidosis usually occurs in critically ill patients receiving therapeutic doses of acetaminophen. Patients present with unexplained increased anion gap metabolic acidosis due to the accumulation of pyroglutamic acid (also known as 5-oxoproline) as a consequence of impaired glutathione regeneration. Lactic acidosis is not a feature of pyroglutamic acidosis.
67
Rasburicase
Rasburicase directly breaks down uric acid and minimizes xanthine accumulation
68
Renal Osteodystrophy
* Vitamin D and calcium * Phosphate control: binders and diet * Calcimimetics (cinacalcet) * Monitor secondary hyperparathyroidism(target iPTH 150-300)
69
Rhabdomyolysis / renal effects * Muscle enzymes * UA * Electrolytes * Renal Failure
Muscle enzymes * CPK \> 10000 UA * REd to brown urine with postive gross blood no RBCs Electrolytes * Hyperkalemia / Hyperphosphatemia / hyperuricemia * Hypocalcemia and dehydaraion Renal Failure * Tubular injury from myoglobinuria
70
Ringers lactete and cursh injuries
**_Contraindicated_** since it has potassium and can elevate K to life threatening levels
71
Severe Preeclampsia with HELLP Syndrome
• Haemolysis \ Abnormal peripheral smear \ Bilirubin \> 1.2 \ LDH \> 600 • Elevated LFT’s \ AST \> 70 • Low Platelets: \< 100,000
72
Sickle cell Trait Renal complications
* Impaired ability to concentrate the urine * Hematuria
73
SIDE EFFECTS ACEI / ARB / CCB / Clonidine / Beta-blockers / Diuretics / minoxidil, etc.
* ACEI: cough, hyperkalemia * ARB: hyperkalemia * CCB: constipation, pedal edema, AV block * Clonidine: sedation, dry mouth, rebound * Beta-blockers: fatigue, bronchospasm * Diuretics * Hydralazine, minoxidil, etc.
74
Staghorn calculi
- Uric acid stones (Coffin shape) - Struvite
75
Struvite stones Bacteria: When to expect? Tx:
* Proteus and Klebsiella / UA nitrite due to conversion to Urea to ammonia, PH elevated, * Expect when patient has multiple UTI with high ph, nitrite+ * **Nephrolithotomy** (percutaneouse first line. Open surgical for morbit obese, nephrectomy for patient how have over the years lost function of kidney due to stag horne
76
Superficical peroneal nerve Femoral nerve Sciatic notch Psterior tibial
Foot eversion / L5 S1 Acute thigh weakness and numbness / L4L3 S1
77
Testicular pain * Testicular torsion * Epididymitis * Fournier's Gangrene
Testicular torsion * No Cremasteric Reflex * Profound pain * U/S is the preferred test Epididymitis * Fever, Urinary frequency, posterior tenderness * Urine culture prefered test Fournier's Gangrene * Much pain to abd/scrotum/ penis * CT/MRI preferred + urgent surgical evaluation
78
Thrombotic thrombocytopenic purpura
* Microangiopathic hemolytic anemia (anemia, jaundice and a blood film featuring evidence of mechanical fragmentation of red blood cells) * Kidney failure * Thrombocytopenia (low platelet count), leading to bruising or purpura * Neurologic symptoms (fluctuating), such as hallucinations, bizarre behavior, altered mental status, stroke or headaches * Fever
79
TMP SMX * Side Effects * Skin * Hematologic * Renal
Skin * Stevens-Johnson syndrome * Toxic epidermal necrolysis * Exfoliative dermatitis Hematologic * Megaloblastic pancytopenia Renal * Hyperkalemia * Interstitial nephritis * Impairs tubular secretion of creat without effecting GFR * Crystalluria
80
Toxicity * Alcohol Ketoacidosis * Methanol injestion * Ethylene glycol ingestion * Isopropyl alcohol ingestion Serum osmolarity = 2\*Na + BUN/2.8 + glucose/18 Osmolar gap greater then 10
Alcohol Ketoacidosis * Slurred speech unsteady gait * **_High Osmolar gap_** / **_Anion gap Metabolic_** acidosis Methanol injestion * Visual blurring, central scotomata * **_High Osmolar gap_** / **_Anion gap Metabolic_** acidosis Ethylene glycol ingestion * Flank pain, hematuria, oliguria, tetany * **_High Osmolar gap_** / A**_nion gap Metabolic_** acidosis * UA Calcium _**oxalate crystals (**Envelope**)**_ Isopropyl alcohol ingestion * CNS depression, disonjugate gaze * **_High osmolar gap_** but **_no anion gap_** / no metabolic acidosis
81
Transverse myelitis vs Guillian barre syndrome
GBS: will not have bowel bladder symptoms or sensory loss below a spinal cord segment Sx of TM: paresthesias, b**_owel bladder and sphinctor dysfunction_** MRI show enhancing cord segments with surrounding edema Tx tM: Corticosteriods
82
Tumor Lysis Syndrome * LABS * Clinical
Labs * K \> 6 * Po4 \> 6.5 * Calcium \< 7 * Uric acid \> 8 * Or change of 25% in baseline of any Clinical * Labs + * Cr \> 1.5 times upper limit * cardiac arrhythmia * seizures TLS likelihood * Low: IVF * Intermediate: _allopurinal if Urica acid \< 8_ + IVF else Rasburicase + IVF * High: **_Rasburicase_** * Established: HD
83
Type B lactic acidosis Type A lactic acidosis
Type B lactic acidosis is often due to medication or toxin exposure and may also occur in patients with advanced malignancy, liver disease, or glucose-6-phosphate dehydrogenase deficiency. Type A lactic acidosis is associated with tissue hypoperfusion and hypoxia.
84
Types of GN * Focal segmental glumerulosclerosis * Membranoproliferative GN * Membranou GN * Minimal Change Disease
FSGS * Obesity * Herion * HIV * Reflux nerphropathy * AA MPGN * Autoimmune (SLE) * infection * Mixed cryoglobulinemia * Monoclonal gammopathies Membranous GN * SLE * Drugs * Infection (HBV, HCV) * Malignancy Minimal Change * Drugs * Lymphomas
85
Uremic Bleeding
* _Decreased Factor III_ * _Abnormal platelet aggregation_ * Increased **_prostacyclin_** * Abnormal _vWF-VIII complex production_ * Tx:- Desmopressin (DDAVP®) — acute / Cryoprecipitate & FFP / PRBCs - Estrogen — chronic therapy - Dialysis if uremic
86
Urinary casts * Granular casts * Fatty casts * Pigment casts * Crystal casts * Red blood cell casts * White blood cell casts * Bacterial casts * Epithelial cell casts
* Granular casts The "muddy brown cast" seen in acute tubular necrosis is a type of granular cast. * Fatty casts: Nephrotic syndrome * Pigment casts: rhabdomyolysis * Crystal casts: stones * Red blood cell casts:associated with nephritic syndromes or urinary tract injury * White blood cell casts: interstitial nephritis * Bacterial casts: pyelonephritis * Epithelial cell casts: acute tubular necrosis and toxic ingestion
87
von Hippel-Lindau (Cystic dz)
- AD - **_RCC_** (in 40-70%) \* - Retinal angiomas, _CNS hemangioblastomas_ (pancreatic and renal) cysts, **_pheo_**
88
What is Liddle syndrome?
- HTN, hypokalemia, metab alk. Rx amiloride/triamterene. Due to chronically open Na channels.
89
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