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Internal Medicine Resident Half-Day Ahsan Alam, MD. Acute Renal Failure. Internal Medicine Resident Half-Day Ahsan Alam, MD. Acute Kidney Injury. What is Acute Kidney Injury. Abrupt decline in GFR Increase in serum creatinine P UF = (P GC - P T ) - ( p GC - p T )
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Internal Medicine Resident Half-Day Ahsan Alam, MD Acute Renal Failure
Internal Medicine Resident Half-Day Ahsan Alam, MD AcuteKidneyInjury
What is Acute Kidney Injury Abrupt decline in GFR Increase in serum creatinine PUF = (PGC - PT) - (pGC - pT) Varying definitions (RIFLE, AKIN, etc)
Why do we care about AKI? Mortality with hospital-acquired AKI Mortality post cardiac surgery Nash K et al. Am J Kidney Dis 2002;39(5):930-936 Lassnigg, A. et al. J Am Soc Nephrol 2004;15:1597-1605
Case #1 A 76 yr old female presents to ED with abdominal pain and dyspnea Serum creatinine is 135 mmol Does she have AKI?
Diagnostic Approach Time of onset – prior serum creatinine Careful review of history and physical exam Comorbidities Medications Current illness (vomiting, diarrhea, blood loss, etc) BP, volume status, skin lesions, flank/abdominal signs
Case #1 DM2, HTN, CAD (CABG 2004), CVA 2000 (right CEA 2009), hypothyroidism Medications telmistartan 80 mg, ramipril 10 mg, furosemide 40/80 mg, metoprolol, clonidine, atorvastatin, clopidogrel, insulin, thyroxine If this is AKI, what are the most likely diagnoses?
Causes of Hospital-Acquired AKI and Mortality 4,622 consecutive patients 7.3% with AKI Nash K et al. Am J Kidney Dis 2002;39(5):930-936
Case #1 The patient undergoes investigations for her symptoms in hospital…
Case #1 *CI-AKI
Case #1 *CI-AKI *Stage 2-3 AKI
AKI Network (AKIN) Classification Lopes, J. A. et al. Crit Care 2008;12(4):R110
Risk Factors for AKI Lameire et al. NDT. 2008;6:392
Consistent Risk Factors • Age • Hypovolemia • Hypotension • Sepsis • CKD • Hepatic dysfunction • Cardiac dysfunction • DM • Exposure to nephrotoxins
Differential Diagnosis of AKI Pre-renal Renal Post-renal
Pre-renal Hypovolemia Diuretics, trauma, surgery, burns, hemorrhage, pancreatitis, GI loss, etc. Decreased effective circulating volume Nephrotic sydrome, cirrhosis, CHF, tamponade, massive PE, etc. Renovascular obstruction RAS/atherosclerosis/thrombosis/embolism, dissecting aneurysm, vasculitis, compression Impaired glomerular autoregulation NSAIDs, ACEi/ARB, calcineurin inhibitors
Intrinsic Renal Glomerular and small vessel diseases Rapidly progressive GN, endocarditis, post-strep GN, vasculitides, scleroderma/malignant HTN, HUS, PET, DIC Interstitial nephritis Infection-related, inlammation, drug-induced, infiltrative (lymphoma, leukemia, sarcoidosis) Tubular Lesions Post-ishemia, nephrotoxic (drugs, contrast, anesthetics, heavy metals), pigment nephropathy, light chain, hypercalcemia
Post-renal Bladder flow obstruction Urethral, bladder neck (BPH), neurogenic bladder Ureteral obstruction (bilateral or single kidney) Stones, clots, tumours, papillary necrosis, retroperitoneal fibrosis, surgical ligation
Urine Output and AKI Anuric < 50 cc / 24 hrs Oliguric < 500 cc / 24 hrs Non-olguric Normal urine output, but inadequate clearance GFR 2 ml/min will produce ~3L of urine/day if there is no tubular reabsorption
Diagnostic Approach Urine dipstick Urine microscopy Cellular elements RBC, WBC, Renal tubular epithelial cells Other (squamous, vaginal) Casts Hyaline, granular, waxy, RBC, WBC, tubular cell Organisms Bacteria, yeast Crystals Lipiduria Specific gravity pH Leukocytes Nitrites Protein Glucose Ketones Urobilinogen Bilirubin Blood
Urine Findings WBC casts - pyelonephritis WBC
Urine Findings Crystalluria – uric acid Crystalluria – calcium oxalate (ethylene glycol toxicity)
Urine Findings RBC casts - GN Dysmorphic RBC - GN
Urine Findings Muddy brown casts – acute tubular necrosis
Urine Findings 1.030 Specific gravity pH 5.0 Leukocytes Nitrites Protein Glucose Ketones + Urobilinogen Bilirubin Blood ++++ 80 yo female found on the floor of her apartment after 2 days, SCr 400 mol/L, K 6.8 mmol/L, CK 54,000
FeNa Limitations of FeNa Diuretic use Post-ischemic ATN who have less severe disease AKI on chronic pre-renal disease (cirrhosis, CHF) Contrast or pigment nephropathy Acute GN or vasculitis Alternatives FE of urea, lithium, uric acid FeNa = UNa/PNa x 100 UCr/PCr
Imaging Assess kidney size/morphology Hydronephrosis
Kidney Biopsy Intrinsic renal AKI Indications Isolated glomerular hematuria with proteinuria Nephrotic syndrome Acute nephritic syndrome Unexplained acute or rapidly progressive AKI
Kidney Biopsy Crescentic GN
Principles of AKI Management • Identify AKI • Avoid further nephrotoxic injury • Optimize renal hemodynamics • Treat complications • Fluid balance, electrolytes, uremia • Nutritional support • Renal Support (RRT) • Monitoring after AKI
Medications • Pre-renal • Calcineurin inhibitors, radiocontrast, ACEi/ ARB, NSAIDS, amphotericin B • Intra-renal • aminoglycosides, amphotericin B, cisplatin, cephalosporins, sulfa, rifampin, NSAIDS, interferon • Post-renal • acyclovir, MTX, indinavir, sulfadiazine • Review renal dosing of medications
Fluid Management • Correct fluid deficit • Will not guarantee AKI prevention • Studies of PA catheters did not reduce AKI • High urine flow in specific conditions • Myoglobinuria, tumour lysis, contrast media, etc. • Little evidence on fluid choice • Crystalloids • Hypooncotic colloids (4% albumin) • Hyperoncotic solutions (HES, dextrans) carry risk of renal dysfunction
Renal Perfusion and Vasoactive Agents • No support for • Loop diuretics • Dopamine • Selected use of • Mannitol (Rhabdomyolysis, post-cardiac surgery) • Unclear support for • Natriuretic peptides (ANP, BNP) • Fenoldopam (DA agonist) • Theophylline (adenosine antagonist)
Renal Perfusion • Vasopressors • Inotropes to improve low cardiac function • Target MAP needs to be individualized • Commonly 65 mmHg • Higher in elderly where autoregulation impaired
Nutrition in AKI • AKI is a catabolic state • Inadequate nutritional support can delay renal recovery • Cochrane review 2010: • “There is not enough evidence to support the effectiveness of nutritional support for AKI…” • Adequate calorie delivery in anuric patient will necessitate RRT
Treat Complications • Monitor and correct electrolytes, acidosis • Renal replacement therapy • If indicated, do not withhold until patient is anuric
Indications for Dialysis A E I O U Acidosis Electrolyte disturbance Ingestions Overload (volume) Uremia
New Paradigm for AKI CKD AKD AKI
Natural history of AKI Cerda et al. cJASN. 2008;
Case #1 *CI-AKI *Stage 2-3 AKI
Fluids – Isotonic vs. Hypotonic Isotonic saline (0.9%) more protective than half normal (0.45%) 1,620 pts undergoing cardiac catheterization Goal is to achieve ‘good’ urine flow Mueller C et al. Arch Intern Med. 162: 329-336, 2002
Fluids Optimal rate and duration is not clear IV rate >1-1.5 ml/kg/hr to achieve urine flow >150 ml/hr At least 1hr (3-12hr) prior and 3-6hr (6-12hr) after contrast
Bicarbonate vs Saline Zoungas S et al. Ann Intern Med 2009;151:631-638
Bicarbonate vs Saline Zoungas S et al. Ann Intern Med 2009;151:631-638