Triamterene: Indications and Usage
Triamterene is indicated for treating edema associated with congestive heart failure, cirrhosis, nephrotic syndrome, steroid-induced edema, idiopathic edema, and secondary hyperaldosteronism, either alone or combined with other diuretics for its potassium-sparing properties. 1
Primary Indications
Edematous Conditions
- Congestive heart failure with fluid retention is a primary indication, where triamterene may be used alone or combined with thiazide or loop diuretics 1
- Cirrhosis of the liver with associated edema 1
- Nephrotic syndrome 1
- Steroid-induced edema and idiopathic edema 1
- Secondary hyperaldosteronism, particularly when patients prove resistant or only partially responsive to thiazides or other diuretics 1
Hypertension Management
- Combination therapy with hydrochlorothiazide to prevent hypokalemia while maintaining antihypertensive efficacy 2
- Add-on therapy in patients receiving other antihypertensive drug classes, with usual maintenance dosing of 1-2 mg/kg/day up to 300 mg/day 2
- Triamterene enhances blood pressure lowering beyond its potassium-sparing effect, reducing systolic BP by 1-4 mmHg when added to hydrochlorothiazide 3
Dosing Guidelines
Adult Dosing
- Initial dose: 100-200 mg daily in divided doses, typically combined with 50 mg hydrochlorothiazide 4
- Maximum dose: 300 mg/day 2
- Once-daily dosing is effective with optimally bioavailable formulations 5
Pediatric Dosing
Critical Contraindications and Precautions
Absolute Contraindications
- Significant renal dysfunction (GFR <45 mL/min) due to hyperkalemia risk 2
- Concurrent use with other potassium-sparing diuretics (amiloride, spironolactone) increases hyperkalemia risk 6, 2
Drug Interactions Requiring Monitoring
- ACE inhibitors or ARBs: Significantly increased hyperkalemia risk; close potassium monitoring mandatory 6, 2
- NSAIDs: Risk of acute renal failure, particularly concerning with over-the-counter availability 6, 7
- Potassium supplements or high-potassium salt substitutes: Avoid concurrent use 6
- Trimethoprim/trimethoprim-sulfamethoxazole: Additive hyperkalemia risk 6
Monitoring Requirements
Initial Phase
- Check potassium, creatinine, and electrolytes 1-2 weeks after initiation 6
- Recheck 1-2 weeks after each dose adjustment 6
Maintenance Phase
- Monitor blood chemistry every 4 months during stable therapy 6
- Stop triamterene if potassium rises >5.5 mmol/L 6
- Reduce or stop if creatinine increases >50% above baseline or reaches 266 μmol/L (3 mg/dL) 6
Clinical Considerations
Combination Therapy Advantages
- Synergistic effect with hydrochlorothiazide: Potentiates diuresis while minimizing potassium loss 8, 4
- Particularly valuable in digitalized patients: Prevents hypokalemia-related arrhythmias and digitalis toxicity 8
- Long-term management of chronic edema: Especially useful in diuretic-resistant patients 8
Pregnancy Considerations
- Not recommended for routine use in healthy pregnant women 1
- May be appropriate for pathologic edema (not physiologic pregnancy edema) after careful risk-benefit assessment 1
- Short courses only if extreme discomfort from edema unrelieved by rest 1
Common Pitfalls to Avoid
- Do not use triamterene alone as first-line heart failure therapy; always combine with ACE inhibitors and beta-blockers 6
- Avoid in elderly patients with creatinine clearance <30 mL/min due to impaired tubular secretion and hyperkalemia risk 6
- Do not combine with multiple potassium-retaining agents without intensive monitoring 6
- Warn patients about over-the-counter NSAIDs and potassium-containing salt substitutes 6