Skip to content
DraconiticResearch
Search Sources API
203,234 studies31 sourcesUpdated 51 min ago
Peer-reviewedCC BY 4.0Journal of Clinical Medicine

Drug Therapies and Incident Heart Failure in Atrial Fibrillation: A Systematic Review

  1. 1School of Pharmacy and Pharmacology, University of Tasmania, Hobart, TAS 7005, Australia

Abstract

Background/Objectives: Atrial fibrillation (AF), the most common cardiac arrhythmia, significantly elevates the risk of new-onset heart failure (HF). We aimed to systematically map and appraise available evidence on drug therapies and incident HF in patients with AF. Methods: We searched Medline, Embase, Cochrane Central Register of Controlled Trials, and Scopus up to 16 September 2026 for relevant randomized controlled trials (RCTs), sub-analyses of RCTs, and observational/cohort studies. Results: Seventeen studies (397,991 participants) were included. The only randomized signal came from a prespecified subgroup of the ACTIVE-I trial, in which irbesartan was associated with fewer first HF hospitalizations than the placebo (HR 0.81, 95% CI 0.69–0.96; moderate certainty). Observational studies showed an association with lower first HF hospitalization for sodium-glucose cotransporter 2 (SGLT2) inhibitors in patients with type 2 diabetes (pooled HR 0.68, 95% CI 0.48–0.95; two studies; low certainty) and lower incident HF diagnosis in a larger cohort that included patients without diabetes (HR 0.86, 95% CI 0.82–0.89). The remaining cohort evidence largely reflected prescribing patterns rather than drug effects. Statins showed an inconsistent association. The higher HF incidence among users of diuretics, mineralocorticoid receptor antagonists, digoxin and renin-angiotensin system inhibitors was consistent with confounding by indication (very low certainty). Conclusions: Evidence on drug therapies to prevent HF in AF is limited to one randomized subgroup signal for irbesartan. The remaining findings were associations rather than demonstrated treatment effects. High-quality research, including RCTs in broader AF populations, is needed. PROSPERO Registration: CRD42024587926.

Related

  1. Non-alcoholic Fatty Liver Disease/Metabolic Dysfunction-Associated Steatotic Liver Disease and the Risk of Incident Atrial Fibrillation: An Updated Systematic Review and Meta-Analysis of Cohort Studies
    Disha Disha, Allah Rakhio Bhurgri, Deepak Verma +5
    CureusPeer-reviewedCC BYFull textCardiovascular medicineEurope PMCEurope PMCPMC
  2. Cardiometabolic Substrate Modification in Atrial Fibrillation: Obesity and Epicardial Adipose Tissue in the Era of Incretin-Based Therapies and Catheter Ablation
    Andrea Matteucci, Michela Bonanni, Luca Sgarra +7
    Journal of cardiovascular development and diseasePeer-reviewedCC BYFull textCardiovascular medicineEurope PMC
  3. Predictive Value of P-Wave Dispersion Combined with Left Atrial Reservoir Strain for Incident Atrial Fibrillation in Patients with Hypertrophic Cardiomyopathy: A Retrospective Cohort Study.
    Li Yu, Yan Zhang, Dandan Sun +2
    International journal of general medicinePeer-reviewedCC BY-NCFull textCardiovascular medicineEurope PMCPMC
  4. Moderate-to-Vigorous Intensity Physical Activity and Risk of Incident Atrial Fibrillation in Atrial Cardiomyopathy
    Min Kim, Pil-Sung Yang, Ho-Gi Chung +5
    JACC: AdvancesPeer-reviewedCC BY 4.0Full textCardiovascular medicinePMCDOAJ
  5. Trends in mortality involving atrial fibrillation/flutter and renal failure in the United States, 1999–2023 : A nationwide multiple-cause-of-death analysis
    Muhammad Shaheer Bin Faheem, Syed Tawassul Hassan, Huzaifa Sabir Nawaz +5
    MedicinePeer-reviewedCC BY-NCFull textGeneral medicineEurope PMC
BibTeX
@article{zobdeh2026drug,
  title = {{Drug Therapies and Incident Heart Failure in Atrial Fibrillation: A Systematic Review}},
  author = {Amirreza Zobdeh and Gregory M. Peterson and Woldesellassie M. Bezabhe and Pankti Shastri and Daniel J. Hoyle},
  journal = {Journal of Clinical Medicine},
  year = {2026},
  month = oct,
  doi = {10.3390/jcm15208118},
  url = {https://www.mdpi.com/2077-0383/15/20/8118},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Drug Therapies and Incident Heart Failure in Atrial Fibrillation: A Systematic Review
AU  - Amirreza Zobdeh
AU  - Gregory M. Peterson
AU  - Woldesellassie M. Bezabhe
AU  - Pankti Shastri
AU  - Daniel J. Hoyle
PY  - 2026
DA  - 2026/10/19
JO  - Journal of Clinical Medicine
DO  - 10.3390/jcm15208118
UR  - https://www.mdpi.com/2077-0383/15/20/8118
AB  - Background/Objectives: Atrial fibrillation (AF), the most common cardiac arrhythmia, significantly elevates the risk of new-onset heart failure (HF). We aimed to systematically map and appraise available evidence on drug therapies and incident HF in patients with AF. Methods: We searched Medline, Embase, Cochrane Central Register of Controlled Trials, and Scopus up to 16 September 2026 for relevant randomized controlled trials (RCTs), sub-analyses of RCTs, and observational/cohort studies. Results: Seventeen studies (397,991 participants) were included. The only randomized signal came from a prespecified subgroup of the ACTIVE-I trial, in which irbesartan was associated with fewer first HF hospitalizations than the placebo (HR 0.81, 95% CI 0.69–0.96; moderate certainty). Observational studies showed an association with lower first HF hospitalization for sodium-glucose cotransporter 2 (SGLT2) inhibitors in patients with type 2 diabetes (pooled HR 0.68, 95% CI 0.48–0.95; two studies; low certainty) and lower incident HF diagnosis in a larger cohort that included patients without diabetes (HR 0.86, 95% CI 0.82–0.89). The remaining cohort evidence largely reflected prescribing patterns rather than drug effects. Statins showed an inconsistent association. The higher HF incidence among users of diuretics, mineralocorticoid receptor antagonists, digoxin and renin-angiotensin system inhibitors was consistent with confounding by indication (very low certainty). Conclusions: Evidence on drug therapies to prevent HF in AF is limited to one randomized subgroup signal for irbesartan. The remaining findings were associations rather than demonstrated treatment effects. High-quality research, including RCTs in broader AF populations, is needed. PROSPERO Registration: CRD42024587926.
SN  - 2077-0383
ER  -