Chronic kidney disease: Difference between revisions
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*Dialysis access complications — thrombosed fistula/graft, access infection, dialysis catheter malfunction, steal syndrome | *Dialysis access complications — thrombosed fistula/graft, access infection, dialysis catheter malfunction, steal syndrome | ||
*Medication-related adverse effects — drug accumulation due to impaired clearance | *Medication-related adverse effects — drug accumulation due to impaired clearance | ||
==Differential Diagnosis== | ==Differential Diagnosis== | ||
Revision as of 19:01, 19 March 2026
Background
- Chronic kidney disease (CKD) is defined as abnormalities in kidney structure or function present for ≥3 months with implications for health[1]
- Affects ~37 million adults in the United States; the majority are unaware of their diagnosis[1]
- Most common causes: diabetes mellitus (~40%), hypertension (~30%), glomerulonephritis, polycystic kidney disease
- CKD is a major independent risk factor for cardiovascular disease — most patients with CKD die of cardiovascular events, not kidney failure
- CKD patients present to the ED frequently — often for complications of CKD rather than the kidney disease itself
KDIGO Staging
| Stage | eGFR (mL/min/1.73m²) | Description |
| G1 | ≥90 | Normal or high (CKD if other markers of kidney damage present) |
| G2 | 60-89 | Mildly decreased |
| G3a | 45-59 | Mildly to moderately decreased |
| G3b | 30-44 | Moderately to severely decreased |
| G4 | 15-29 | Severely decreased |
| G5 | <15 | Kidney failure (may require dialysis or transplant) |
- CKD also staged by albuminuria category: A1 (<30 mg/g), A2 (30-300 mg/g), A3 (>300 mg/g)
- Both eGFR and albuminuria predict risk of progression and cardiovascular events
- KDIGO 2024 update: Recommends creatinine-based eGFR (CKD-EPI 2021 equation without race); add cystatin C when eGFR creatinine may be inaccurate (extremes of muscle mass, amputation, cirrhosis)[1]
Clinical Features
- Volume overload / congestive heart failure — dyspnea, edema, hypertensive emergency
- Hyperkalemia — medication-related (ACEi, ARB, SGLT2i, spironolactone, trimethoprim), dietary, missed dialysis, metabolic acidosis
- Uremic symptoms — nausea, vomiting, anorexia, fatigue, pruritus, altered mental status, seizures, pericarditis
- Infections — CKD patients are immunocompromised; UTI, pneumonia, vascular access infections, peritonitis (peritoneal dialysis)
- Acute kidney injury (AKI on CKD) — dehydration, nephrotoxins, obstruction, sepsis
- Cardiovascular events — acute coronary syndrome, stroke, peripheral vascular disease (risk 2-10× higher than general population)
- Electrolyte disorders — hyperkalemia, hyperphosphatemia, hypocalcemia, metabolic acidosis
- Anemia exacerbation — GI bleeding, erythropoietin deficiency, iron deficiency
- Dialysis access complications — thrombosed fistula/graft, access infection, dialysis catheter malfunction, steal syndrome
- Medication-related adverse effects — drug accumulation due to impaired clearance
Differential Diagnosis
When evaluating a CKD patient with acute decompensation, consider:
- AKI on CKD — reversible causes should always be sought (dehydration, obstruction, nephrotoxins, sepsis)
- Volume overload: Congestive heart failure, nephrotic syndrome, cirrhosis, medication non-compliance
- Hyperkalemia: Medication-related, dietary, missed dialysis, tissue breakdown, metabolic acidosis
- Infection/sepsis: UTI, pneumonia, dialysis access infection, peritonitis (PD patients)
- Cardiovascular: Acute coronary syndrome (CKD patients may have atypical presentations), hypertensive emergency, uremic pericarditis/tamponade
- Uremic encephalopathy: Diagnosis of exclusion — rule out other causes of AMS (hypoglycemia, stroke, sepsis, drug toxicity, electrolyte abnormalities)
- Drug accumulation/toxicity: Medications not dose-adjusted for renal function (opioids, gabapentin, antibiotics, metformin, lithium, digoxin)
- GI bleeding: Platelet dysfunction + anticoagulant use + angiodysplasia (common in CKD)
Evaluation
Workup
- Standard Labs
- BMP — creatinine (compare to baseline), BUN, potassium, bicarbonate, calcium, glucose
- CBC — anemia (normocytic, from erythropoietin deficiency), platelet count
- Magnesium, phosphorus — hyperphosphatemia and hypomagnesemia are common
- VBG or ABG — assess for metabolic acidosis (non-anion gap from impaired H⁺ excretion ± anion gap from uremic toxins)
- Urinalysis — proteinuria, hematuria, casts (assess for active glomerulonephritis or UTI)
- Lactate — if concern for sepsis or tissue hypoperfusion
- Coagulation studies — if bleeding, uremic platelet dysfunction, or DIC suspected
- Troponin — chronic elevation is common in CKD (especially on dialysis); interpret in the context of symptoms and trending rather than a single value
- If AKI on CKD Suspected
- Renal ultrasound — assess kidney size (small echogenic kidneys = chronic disease), hydronephrosis (obstruction), renal vein thrombosis
- Bladder scan / post-void residual — if obstruction suspected
- Fractional excretion of sodium (FENa) or FEUrea (if on diuretics) — prerenal vs. intrinsic
- Urine electrolytes, urine protein-to-creatinine ratio
- Targeted
- ECG — mandatory in all CKD presentations — evaluate for hyperkalemia (peaked T waves, widened QRS, sine wave), ischemia, pericarditis (diffuse ST elevation)
- CXR — pulmonary edema, pleural effusion, pericardial effusion, pneumonia
- Blood cultures — if febrile (low threshold for blood cultures in dialysis patients and those with indwelling catheters)
Diagnosis
- CKD itself is usually an established diagnosis — the ED role is to identify acute complications and reversible causes of decompensation
- Always compare creatinine to baseline — a patient with baseline creatinine 3.0 who presents at 3.2 is very different from one presenting at 6.0
- Determine if the patient has a nephrology provider and whether they are on dialysis (and when their last session was)
- CKD is confirmed (not just diagnosed in the ED) when kidney damage or decreased function has been present for ≥3 months — a single elevated creatinine may represent AKI, not CKD[1]
Management
Life-Threatening Emergencies
- Hyperkalemia (K⁺ >5.5 mEq/L)
- ECG changes present or K⁺ >6.5:
- Calcium gluconate 10% 10 mL (or calcium chloride via central line) IV over 2-3 min — cardiac membrane stabilization (does not lower K⁺)
- Regular insulin 10 units IV + dextrose 25g (D50W) IV — shifts K⁺ intracellularly
- Albuterol 10-20 mg nebulized — additional K⁺ shift
- Sodium bicarbonate 50-100 mEq IV — if concurrent metabolic acidosis (effect on K⁺ is modest)
- Kayexalate (sodium polystyrene sulfonate) 15-30g PO or Patiromer or Sodium zirconium cyclosilicate (Lokelma) — true K⁺ elimination (delayed onset)
- Emergent dialysis — definitive treatment for severe/refractory hyperkalemia in CKD/ESRD
- See Hyperkalemia for full management
- Uremic Pericarditis
- Friction rub + chest pain + uremia = indication for emergent dialysis
- Avoid anticoagulation (risk of hemorrhagic pericardial effusion → tamponade)
- If hemodynamic compromise → evaluate for tamponade → pericardiocentesis if indicated
- Pulmonary Edema / Volume Overload
- NIV (BiPAP) for respiratory distress
- IV nitroglycerin for afterload reduction if hypertensive
- IV furosemide — CKD patients require higher doses (start 40-80mg IV for CKD G3-4; 80-200mg IV for G5/ESRD); may be ineffective in ESRD
- Emergent dialysis (ultrafiltration) if refractory to medical management or anuric
- See Congestive heart failure
- Severe Metabolic Acidosis
- Sodium bicarbonate IV if pH <7.1 or bicarbonate <8-10 mEq/L with hemodynamic instability
- Dialysis for severe refractory acidosis
- Caution: sodium bicarbonate can worsen volume overload and cause hypocalcemia (ionized calcium drops as pH rises)
Medication Safety in the ED
Critical drug dosing considerations in CKD:
- NSAIDs: Avoid in CKD G3-5 — worsen renal function, cause hyperkalemia, fluid retention, GI bleeding
- Metformin: Contraindicated when eGFR <30; hold when eGFR 30-45 if acutely ill; risk of lactic acidosis
- Opioids: Morphine — avoid (active metabolite accumulates → prolonged sedation/respiratory depression); use fentanyl or hydromorphone (safer in CKD). Meperidine — avoid (normeperidine accumulation → seizures)
- Gabapentin/pregabalin: Dose reduce; accumulation causes sedation, altered mental status, myoclonus
- Antibiotics: Many require dose adjustment — particularly vancomycin (dose by levels/AUC), aminoglycosides (avoid if possible), nitrofurantoin (ineffective and neurotoxic in CKD G4-5)
- Enoxaparin: If eGFR <30, use unfractionated heparin instead, or reduce enoxaparin dose (1 mg/kg daily instead of BID) with anti-Xa monitoring
- Contrast: IV iodinated contrast can be given when clinically indicated (e.g., CT angiography for PE, stroke) — do not withhold life-saving imaging for CKD; hydrate with IV crystalloid before and after; hold metformin for 48h after contrast if eGFR <30
- ACEi/ARB: Hold during acute illness, dehydration, or AKI ("sick day rules"); do not start or uptitrate in the ED during acute presentations
- Potassium-sparing medications: Review and hold spironolactone, amiloride, triamterene, trimethoprim if hyperkalemic
Dialysis-Specific Considerations
- Determine modality (hemodialysis vs. peritoneal dialysis), schedule, and when last session occurred
- Missed dialysis: Common ED presentation; check K⁺, bicarbonate, volume status; arrange urgent dialysis
- Dialysis access:
- Do not use an AV fistula or graft for blood draws, IV access, or blood pressure measurement
- Do not place a blood pressure cuff on the access arm
- Assess fistula/graft for thrill (palpable) and bruit (auscultate) — absence suggests thrombosis → vascular surgery or interventional radiology consultation
- Peritoneal dialysis peritonitis: Cloudy PD effluent + abdominal pain ± fever; send PD fluid for cell count (WBC >100/µL with >50% neutrophils), Gram stain, and culture; initiate empiric IP antibiotics (typically IP vancomycin + IP ceftazidime or gentamicin per local protocol) after consulting nephrology
- Dialysis catheter infection: Blood cultures from catheter AND peripheral site; empiric IV vancomycin + gram-negative coverage; consult nephrology regarding catheter removal vs. salvage
Disposition
Admit
- Hyperkalemia with ECG changes, K⁺ >6.5, or refractory to ED treatment
- Pulmonary edema/volume overload requiring dialysis or not responding to diuretics
- Uremic pericarditis or pericardial effusion with hemodynamic concern
- Uremic encephalopathy or severe uremic symptoms
- Severe metabolic acidosis (pH <7.2, bicarbonate <10)
- AKI on CKD with significant creatinine rise from baseline and no readily reversible cause
- Sepsis or serious infection (especially dialysis access infection, PD peritonitis)
- Need for emergent or urgent dialysis
- New diagnosis of ESRD requiring dialysis initiation
Discharge with Close Follow-Up
- Mild hyperkalemia (K⁺ 5.5-6.0, no ECG changes) corrected in ED with dietary counseling, medication adjustment, and follow-up within 24-48 hours
- Stable CKD with minor medication-related issue (dose adjustment made)
- Mild volume overload responsive to diuretic adjustment
- Ensure: Nephrology follow-up arranged, medication list reconciled, "sick day rules" reviewed (hold ACEi/ARB, metformin, NSAIDs, diuretics during acute illness/dehydration)
See Also
- Acute kidney injury
- Hyperkalemia
- Metabolic acidosis
- Congestive heart failure
- Dialysis complications
- Pericardial effusion and tamponade
- Hypertensive emergency
- Uremic encephalopathy
External Links
- KDIGO 2024 CKD Guideline (Full Text)
- MDCalc - Cockcroft-Gault Equation
- MDCalc - CKD-EPI eGFR Calculator
