Medication Management for Patient with GFR 22
Critical Immediate Actions Required
Your patient requires urgent medication adjustments: discontinue hydrochlorothiazide immediately and reduce lisinopril dose by 50%, as thiazide diuretics are contraindicated at GFR <30 mL/min and ACE inhibitors require dose reduction in stage 4 CKD. 1
Medications Requiring Immediate Changes
Hydrochlorothiazide - DISCONTINUE
- Thiazides are potentially inappropriate medications (PIMs) in elderly patients with CrCl <30 mL/min due to reduced diuretic response from impaired tubular secretion 1
- Loop diuretics have reduced efficacy below GFR 30 mL/min but thiazides become essentially ineffective 1
- If diuresis is still needed for volume management, switch to a loop diuretic (furosemide) with appropriate dose adjustment 1
Lisinopril - REDUCE DOSE BY 50%
- ACE inhibitors require dose reduction in stage 4 CKD (GFR 15-29 mL/min) 1, 2
- Monitor serum creatinine and potassium within 1-2 weeks after dose adjustment 2
- Accept a 10-25% increase in serum creatinine as this reflects hemodynamic effects on intraglomerular pressure 2
- Investigate if creatinine increases >30% for volume depletion, nephrotoxic agents, or renovascular disease 2
- Risk of hyperkalemia is significantly elevated with ACE inhibitors in elderly patients with CKD, particularly when combined with reduced renal potassium excretion 1, 3
Medications Requiring Enhanced Monitoring
Atorvastatin - CONTINUE with Caution
- Continue statin therapy in non-dialysis CKD as benefits outweigh risks for cardiovascular protection 1
- Myalgias may decrease physical activity and precipitate falls in oldest old patients 1
- Monitor for muscle symptoms and consider dose reduction if symptomatic 1
- Check lipid panel and creatinine kinase levels periodically 1
Cetirizine - REDUCE DOSE BY 50%
- Cetirizine is primarily renally cleared and requires dose adjustment at GFR <30 mL/min 1
- Reduce to 5 mg daily or every other day to prevent accumulation 1
- Monitor for excessive sedation, confusion, or dizziness which increase fall risk 1
Donepezil - CONTINUE with Monitoring
- No specific dose adjustment required for renal impairment 1
- Monitor for bradycardia and AV block, particularly in combination with other cardiac medications 1
- Assess ongoing benefit versus risk, as cognitive impairment medications should be periodically reassessed in advanced CKD 1
Medications Safe to Continue
Ferrous Sulfate - CONTINUE
- Use low-dose oral iron therapy in vulnerable elderly patients 1
- Monitor iron status to avoid iron overload 1
- Ensure anemia is attributed to iron deficiency before continuing 1
- Consider checking iron studies, as anemia of CKD may require erythropoiesis-stimulating agents rather than iron alone 4
Fluticasone Propionate - CONTINUE
- Topical/inhaled corticosteroids have minimal systemic absorption and no renal dose adjustment needed 1
- Continue for allergic rhinitis or asthma management 1
Vitamin D - CONTINUE and OPTIMIZE
- Vitamin D deficiency is extremely common in CKD and serum levels have an inverse correlation with kidney function 5
- Active vitamin D treatment can ameliorate renal injury by reducing fibrosis, apoptosis, and inflammation 5
- Consider checking 25-OH vitamin D levels and adjusting dose accordingly 5
- Monitor serum calcium and phosphorus to avoid hypercalcemia 4
Critical Monitoring Parameters
Within 1-2 Weeks of Medication Changes:
- Serum creatinine and potassium (most critical for lisinopril dose reduction) 2, 3
- Blood pressure (target <130/80 mmHg in CKD) 2
- Electrolytes including sodium and magnesium 1
Every 3-6 Months Ongoing:
- Complete metabolic panel including creatinine, potassium, bicarbonate 4
- Hemoglobin and iron studies 4
- Calcium, phosphorus, and PTH for CKD-mineral bone disorder 4
- Vitamin D levels 5
High-Risk Drug Interactions to Avoid
Hyperkalemia Risk - CRITICAL
- The combination of ACE inhibitor (lisinopril) with reduced renal function creates significant hyperkalemia risk 1, 3
- Avoid potassium supplements, potassium-sparing diuretics (spironolactone, amiloride, triamterene), and salt substitutes 1, 3
- NSAIDs are contraindicated as they worsen renal function and increase hyperkalemia risk in elderly patients on ACE inhibitors 3
Nephrotoxic Agents to Avoid:
- NSAIDs including COX-2 inhibitors can cause acute deterioration of renal function in elderly volume-depleted patients on ACE inhibitors 3
- Avoid aminoglycoside antibiotics, contrast dye without adequate hydration, and proton pump inhibitors if not clearly indicated 1
Polypharmacy Considerations
Current Pill Burden Assessment:
- This patient is on 8 medications, which places them in the polypharmacy category (≥5 medications) 1
- Polypharmacy in CKD patients is associated with increased risk for kidney failure, hospitalization, adverse drug reactions, and mortality 1
Deprescribing Opportunities:
- Hydrochlorothiazide should be discontinued as it provides no benefit at this GFR 1
- Consider whether all medications align with patient's goals of care and life expectancy 1, 6
- Medication reconciliation is paramount, especially during transitions of care 1
Common Pitfalls to Avoid
- Do not continue thiazide diuretics at GFR <30 mL/min - they are ineffective and potentially harmful 1
- Do not ignore the need for ACE inhibitor dose reduction - standard doses cause excessive drug accumulation 1, 2
- Do not add potassium supplements or potassium-sparing diuretics - hyperkalemia risk is already elevated 1, 3
- Do not prescribe NSAIDs for pain management - use acetaminophen instead 3
- Do not assume all medications need continuation - reassess benefit versus risk in context of advanced CKD 1, 6
Nephrology Referral Indicated
This patient meets criteria for prompt nephrology referral with GFR <30 mL/min 4
- Stage 4 CKD requires specialist co-management for complications including anemia, metabolic acidosis, hyperphosphatemia, and secondary hyperparathyroidism 4
- Nephrologist can guide decisions about renal replacement therapy planning versus conservative management 7
- In elderly patients with multiple comorbidities, an individualized patient-centered approach prioritizing quality of life may be more appropriate than aggressive disease-based management 6