Patiromer Facilitates Angiotensin Inhibitor and Mineralocorticoid Antagonist Therapies in Patients With Heart Failure and Hyperkalemia
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu klinické zkoušky, fáze III, časopisecké články, multicentrická studie, randomizované kontrolované studie
PubMed
39322323
DOI
10.1016/j.jacc.2024.05.079
PII: S0735-1097(24)08033-1
Knihovny.cz E-zdroje
- Klíčová slova
- heart failure, hyperkalemia, mineralocorticoid receptor antagonists, patiromer, renin–angiotensin system inhibitors,
- MeSH
- antagonisté mineralokortikoidních receptorů * terapeutické užití MeSH
- antagonisté receptorů pro angiotenzin terapeutické užití MeSH
- hyperkalemie * farmakoterapie krev MeSH
- inhibitory ACE terapeutické užití MeSH
- lidé středního věku MeSH
- lidé MeSH
- polymery * terapeutické užití MeSH
- renin-angiotensin systém účinky léků MeSH
- senioři MeSH
- srdeční selhání * farmakoterapie MeSH
- tepový objem účinky léků MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze III MeSH
- multicentrická studie MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- antagonisté mineralokortikoidních receptorů * MeSH
- antagonisté receptorů pro angiotenzin MeSH
- inhibitory ACE MeSH
- patiromer MeSH Prohlížeč
- polymery * MeSH
BACKGROUND: Hyperkalemia (HK) is associated with suboptimal renin-angiotensin system (RAS) inhibitor and mineralocorticoid receptor antagonist (MRA) use in heart failure with reduced ejection fraction (HFrEF). OBJECTIVES: This study sought to assess characteristics and RAS inhibitor/MRA use in patients receiving patiromer during the DIAMOND (Patiromer for the Management of Hyperkalemia in Subjects Receiving RAASi Medications for the Treatment of Heart Failure) run-in phase. METHODS: Patients with HFrEF and HK or past HK entered a run-in phase of ≤12 weeks with patiromer-facilitated RAS inhibitor/MRA optimization to achieve ≥50% recommended RAS inhibitor dose, 50 mg/d MRA, and normokalemia. Patients achieving these criteria (randomized group) were compared with the run-in failure group (patients not meeting the randomization criteria). RESULTS: Of 1,038 patients completing the run-in, 878 (84.6%) were randomized and 160 (15.4%) were run-in failures. Overall, 422 (40.7%) had HK entering run-in with a similar frequency in the randomized and run-in failure groups (40.3% vs 42.5%; P = 0.605). From start to the end of run-in, in the randomized group, an increase was observed in target RAS inhibitor and MRA use in patients with HK (RAS inhibitor: 76.8% to 98.6%; MRA: 35.9% to 98.6%) and past HK (RAS inhibitor: 60.5% to 98.1%; MRA: 15.6% to 98.7%). Despite not meeting the randomization criteria, an increase after run-in was observed in the run-in failure group in target RAS inhibitor (52.5% to 70.6%) and MRA use (15.0% to 48.1%). This increase was observed in patients with HK (RAS inhibitor: 51.5% to 64.7%; MRA: 19.1% to 39.7%) and past HK (RAS inhibitor: 53.3% to 75.0%; MRA: 12.0% to 54.3%). CONCLUSIONS: In patients with HFrEF and HK or past HK receiving suboptimal RAS inhibitor/MRA therapy, RAS inhibitor/MRA optimization increased during patiromer-facilitated run-in.
Cardiology ASST Spedali Civili and University Brescia Italy
Central Michigan University College of Medicine Mount Pleasant Michigan USA
Clinic of Cardiology and Angiology General University Hospital Prague Prague Czech Republic
CSL Vifor Glattbrugg Switzerland
CSL Vifor Redwood City California USA
Department of Cardiology partner site Berlin Charité Universitätsmedizin Berlin Germany
Department of Cardiology University Medical Center Groningen Groningen the Netherlands
Department of Medicine Duke University School of Medicine Durham North Carolina USA
Department of Medicine University of Mississippi Jackson Mississippi USA
Division of Cardiology University of Michigan Ann Arbor Michigan USA
Erasmus MC University Medical Center Rotterdam the Netherlands
Faculty of Medicine and Dentistry University of Alberta Edmonton Alberta Canada
Heart Research Institute Sydney Australia
INECO Neurociencias Oroño Rosario Santa Fe Argentina
Institute of Heart Diseases Wroclaw Medical University Wroclaw Poland
Klinik für Innere Medizin 3 Saarland University Homburg Saar Germany
University of Milano Bicocca Cardiovascular Department Papa Giovanni XXIII Hospital Bergamo Italy
Citace poskytuje Crossref.org