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Triamterene


Triamterene

Article Author:
Richard Niyazov
Article Editor:
Tariq Sharman
Updated:
10/1/2020 11:29:09 PM
For CME on this topic:
Triamterene CME
PubMed Link:
Triamterene

Indications

Triamterene is a potassium-sparing diuretic that has been in use since 1964. Triamterene is used by physicians who treat patients with fluid retention states secondary to conditions such as congestive heart failure, nephrotic kidney disease, liver cirrhosis, secondary hyperaldosteronism, or even merely idiopathic edema; all of which are FDA approved indications.[1] When giving triamterene in the combination dosage form with hydrochlorothiazide, other FDA approved indications of use include the management of hypertension or the treatment of edema in patients who develop hypokalemia secondary to hydrochlorothiazide monotherapy.[2] Of note, the use of triamterene can also be indicated for overcoming diuretic resistance in patients on only one full dose of a diuretic; by combining two types of diuretics such as triamterene with a loop diuretic, a diuretic synergism would successfully overcome the resistance and achieve the desired reduction in edema.[3]

Mechanism of Action

Among the potassium-sparing diuretics, triamterene was the second drug of this class to be FDA approved for use in the US following spironolactone. However, despite these two drugs being within the same class and achieving the same desired result, they have two distinct mechanisms of action. While spironolactone is an aldosterone receptor antagonist operating at the late distal tubule and collecting tubules of the nephron on the apical aspect of these sites, triamterene acts at the same region of the nephrons but specifically at the epithelial sodium channels (ENaC) which are on the luminal side. These channels are transmembrane channels that operate to increase sodium uptake in exchange for secreting potassium.[4] 

After the ENaC actively reabsorbs the sodium from the lumen of the nephron into the principal cells of the collecting tubule, the sodium is then transported out of the cell into the interstitium via a sodium-potassium exchange pump.[5] All this collective reabsorption of sodium out of the nephron and kidney back into the interstitium naturally causes water to passively follow suit in the pursuit of osmoregulation with sodium, creating a net gain of fluid retention. When triamterene is introduced to the ENaC, it inhibits this channel and thus exerts a strong diuretic and a limited natriuretic effect in the distal renal tubule and collecting tubule, decreasing the reabsorption of sodium for potassium and as a result effectively decreasing the passive reabsorption of water. Essentially, the action of triamterene is indirectly antagonistic to the role of aldosterone, an adrenal mineralocorticoid, but it is not a direct antagonist of aldosterone itself like the drug spironolactone is. 

Administration

Triamterene is administered only orally and can be administered either as a monotherapy or as a combination therapy depending on the indication. As a monotherapy, it is available as a capsule in either a 50 mg or 100 mg cap. In an adult patient with peripheral edema, 100 mg orally bid would be given with the max dose being 300 mg/day. In combination with hydrochlorothiazide, it is also available as a capsule; the dosage is 37.5 mg of triamterene with 25 mg of hydrochlorothiazide. For the treatment of a patient with hypertension or peripheral edema, 1 to 2 caps PO daily would be prescribed. For the treatment of a patient with hypertension or peripheral edema, one tab orally each day would be prescribed. 

Adverse Effects

The major side effects of triamterene include dizziness, fatigue, headache, dry mouth, hyperkalemia, and dehydration.[1] Other common side effects include nausea, vomiting, rash, diarrhea, muscle cramps, weakness, xerostomia, azotemia, and hyperuricemia. Serious adverse effects include anaphylaxis, ventricular arrhythmias, hyperkalemia, drug-induced interstitial nephritis, acute renal failure due to nephrotoxicity, thrombocytopenia, megaloblastic anemia, and hepatotoxicity. Triamterene can also cause triamterene nephrolithiasis in patients with a history of previous kidney stones; these patients should avoid this drug.[6] 

Urolithiasis may also occur as a result of triamterene use.[7] Drug hypersensitivity is a common side effect to be aware of; this can co-occur with acute hepatic injury, rash, drug fever, and jaundice.[8] There are also several patient populations to be cautious in the use of this drug, these populations include the use of this drug in patients 65 years and older, in patients with diabetes mellitus, congestive heart failure, gout, patients on sodium restriction, and women that are breastfeeding.[9] 

Contraindications

Triamterene is most often given in combination with hydrochlorothiazide, and thus more contraindications exist due to the combination of these drugs. Contraindications include hyperkalemia, pregnancy, severe hepatic impairment, severe renal impairment, metabolic or respiratory acidosis, acute myopia, and secondary angle-closure glaucoma. 

Monitoring

With the use of triamterene, it is essential to monitor specific labs and blood pressure of patients taking this drug in either its sole or combination form with HCTZ. BUN/creatinine, blood pressure, urine output, serum uric acid, CBC, and electrolytes in particular serum potassium should be monitored at a baseline when first placed on the drug. Once findings indicate the establishment of a stable tolerance of the drug, it can be periodically monitored, specifically when dose changes are made and during illnesses. 

Toxicity

Potassium-sparing diuretics overdose is relatively rare, and there are no reports of deaths. With mild to moderate toxicity, there can be the development of nausea, vomiting, diarrhea, mild dehydration, and hyperkalemia. If there is severe toxicity, there can be the development of severe dehydration coupled with hyperkalemia, which may lead to dysrhythmias, tachycardia, hypotension, hyperactive deep tendon reflexes, and possibly changes in mental status. Acute renal failure may also develop due to the deposition of triamterene in the renal tubules.[10] Should there be any signs of toxicity, the clinician should immediately discontinue the drug.

Enhancing Healthcare Team Outcomes

Patients taking triamterene or the combination form of triamterene/HCTZ should have close follow up with primary care physicians that are caring for them. Clinicians and other members of the interprofessional healthcare team should be educating patients on possible side effects or adverse effects that the patient could experience while beginning treatment or having a dose change, having the patient be on the lookout for potential issues with the use of the drug. In the in-patient setting, hospitalists should be prudent to contact the patient's primary care physicians or pharmacies to obtain a history of the patient's adherence and tolerance to the medication. Collaborative decision making between physicians, patients, pharmacists, and nurses are vital for creating the most effective outcomes and decreasing the likelihood of nonadherence.[11]


References

[1] Triamterene 2012;     [PubMed PMID: 31643196]
[2] Tu W,Decker BS,He Z,Erdel BL,Eckert GJ,Hellman RN,Murray MD,Oates JA,Pratt JH, Triamterene Enhances the Blood Pressure Lowering Effect of Hydrochlorothiazide in Patients with Hypertension. Journal of general internal medicine. 2016 Jan;     [PubMed PMID: 26194642]
[3] Hoorn EJ,Ellison DH, Diuretic Resistance. American journal of kidney diseases : the official journal of the National Kidney Foundation. 2017 Jan;     [PubMed PMID: 27814935]
[4] Knauf H,Wais U,Albiez G,Lübcke R, [Inhibition of the exchange of Na for K and and H by triamterene (in epithelia)(author's transl)]. Arzneimittel-Forschung. 1976 Apr;     [PubMed PMID: 133688]
[5] Horisberger JD,Giebisch G, Potassium-sparing diuretics. Renal physiology. 1987;     [PubMed PMID: 2455308]
[6] Ettinger B,Oldroyd NO,Sörgel F, Triamterene nephrolithiasis. JAMA. 1980 Nov 28;     [PubMed PMID: 7431573]
[7] Thürmann PA, [Influence of drugs on urological diseases]. Der Urologe. Ausg. A. 2016 Mar;     [PubMed PMID: 26908119]
[8] Nolan PJ,D'Arcy G, Triamterene drug fever and hepatitis. The Medical journal of Australia. 1987 Sep 7;     [PubMed PMID: 3670184]
[9] Triamterene 2006;     [PubMed PMID: 30000336]
[10] Nasr SH,Milliner DS,Wooldridge TD,Sethi S, Triamterene crystalline nephropathy. American journal of kidney diseases : the official journal of the National Kidney Foundation. 2014 Jan;     [PubMed PMID: 23958399]
[11] Corrêa NB,de Faria AP,Ritter AM,Sabbatini AR,Almeida A,Brunelli V,Calhoun DA,Moreno H,Modolo R, A practical approach for measurement of antihypertensive medication adherence in patients with resistant hypertension. Journal of the American Society of Hypertension : JASH. 2016 Jun;     [PubMed PMID: 27161936]