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DOI 10.1016/j.jchf.2024.08.003

Медицинская библиотека · JACC. Heart failure · 2024

Patiromer for Heart Failure Medication Optimization in Patients With Current or Past Hyperkalemia: DIAMOND Subanalysis.

Coats Andrew J S, Anker Stefan D, Lund Lars H, Filippatos Gerasimos, Rossignol Patrick, Pitt Bertram, Weir Matthew R, Kosiborod Mikhail N, Metra Marco, Böhm Michael, Ezekowitz Justin A, Bayes-Genis Antoni, Mentz Robert J, Ponikowski Piotr, Senni Michele, Cleland John G F, Goudev Assen, Khintibidze Irakli, Lindenfeld Joann, Merkely Bela, Waechter Sandra, Budden Jeffrey, Perrin Amandine, Butler Javed

СтатьяРандомизированное исследованиеКлиническое исследование III фазыПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

For heart failure with reduced ejection fraction (HFrEF), suboptimal use of renin-angiotensin-aldosterone system inhibitors (RAASis), including mineralocorticoid receptor antagonists (MRAs), due to hyperkalemia, may be improved by potassium binders.

OBJECTIVES

This prespecified analysis of the phase 3 DIAMOND (Patiromer for the Management of Hyperkalemia in Subjects Receiving RAASi Medications for the Treatment of Heart Failure) trial assessed the effect of patiromer in patients with HFrEF and either current or past hyperkalemia.

METHODS

Patients with HFrEF and current or past (within 1 year before enrollment) hyperkalemia (serum potassium [sK+] >5.0 mmol/L) entered a single-blind, run-in phase to optimize RAASis while receiving patiromer. They were subsequently randomized, double-blind, to continue patiromer or change to placebo.

RESULTS

Of the 1,038 patients who completed run-in, 354 (83.9%) of 422 with current hyperkalemia and 524 (85.1%) of 616 with past hyperkalemia achieved RAASi optimization and were randomized to treatment. During the double-blind phase, patiromer lowered sK+ levels compared with placebo in both the current and past hyperkalemia subgroups: difference in adjusted mean change from baseline: -0.12 (95% CI: -0.17 to -0.07) and -0.08 (95% CI: -0.12 to -0.05), respectively; Pinteraction = 0.166. Patiromer was more effective than placebo in maintaining MRA at target dose in patients with current vs past hyperkalemia (HR: 0.45 [95% CI: 0.26-0.76] vs HR: 0.85 [95% CI: 0.54-1.32]; Pinteraction = 0.031). Adverse events were similar between subgroups.

CONCLUSIONS

The use of patiromer facilitates achieving target doses of RAASis in patients with HFrEF with either current or past hyperkalemia. For those with current hyperkalemia before RAASi optimization, use of patiromer may be more beneficial in helping to maintain sK+ control and achieve MRA target dose. (Patiromer for the Management of Hyperkalemia in Subjects Receiving RAASi Medications for the Treatment of Heart Failure [DIAMOND]; NCT03888066).

Для цитирования: Coats Andrew J S, Anker Stefan D, Lund Lars H, Filippatos Gerasimos, Rossignol Patrick, Pitt Bertram, Weir Matthew R, Kosiborod Mikhail N, Metra Marco, Böhm Michael, Ezekowitz Justin A, Bayes-Genis Antoni, Mentz Robert J, Ponikowski Piotr, Senni Michele, Cleland John G F, Goudev Assen, Khintibidze Irakli, Lindenfeld Joann, Merkely Bela, Waechter Sandra, Budden Jeffrey, Perrin Amandine, Butler Javed. Patiromer for Heart Failure Medication Optimization in Patients With Current or Past Hyperkalemia: DIAMOND Subanalysis.. JACC. Heart failure. 2024. DOI: 10.1016/j.jchf.2024.08.003.

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