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Contemporary Use of Sodium-Glucose Cotransporter-2 Inhibitor Therapy Among Patients Hospitalized for Heart Failure With Reduced Ejection Fraction in the US: The Get With The Guidelines-Heart Failure Registry.
Pierce, Jacob B; Vaduganathan, Muthiah; Fonarow, Gregg C; Ikeaba, Uchechukwu; Chiswell, Karen; Butler, Javed; DeVore, Adam D; Heidenreich, Paul A; Huang, Joanna C; Kittleson, Michelle M; Joynt Maddox, Karen E; Linganathan, Karthik K; McDermott, James J; Owens, Anjali Tiku; Peterson, Pamela N; Solomon, Scott D; Vardeny, Orly; Yancy, Clyde W; Greene, Stephen J.
Afiliação
  • Pierce JB; Department of Medicine, Duke University School of Medicine, Durham, North Carolina.
  • Vaduganathan M; Division of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Fonarow GC; Ahmanson-UCLA Cardiomyopathy Center, University of California, Los Angeles.
  • Ikeaba U; Associate Editor for Health Care Quality and Guidelines, JAMA Cardiology.
  • Chiswell K; Duke Clinical Research Institute, Durham, North Carolina.
  • Butler J; Duke Clinical Research Institute, Durham, North Carolina.
  • DeVore AD; Department of Medicine, University of Mississippi Medical Center, Jackson.
  • Heidenreich PA; Baylor Scott and White Research Institute, Dallas, Texas.
  • Huang JC; Duke Clinical Research Institute, Durham, North Carolina.
  • Kittleson MM; Division of Cardiology, Duke University School of Medicine, Durham, North Carolina.
  • Joynt Maddox KE; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, California.
  • Linganathan KK; AstraZeneca, Wilmington, Delaware.
  • McDermott JJ; Department of Cardiology, Smidt Heart Institute, Cedars-Sinai, Los Angeles, California.
  • Owens AT; Cardiology Division, Department of Medicine, Washington University School of Medicine, St Louis, Missouri.
  • Peterson PN; AstraZeneca, Wilmington, Delaware.
  • Solomon SD; AstraZeneca, Wilmington, Delaware.
  • Vardeny O; Division of Cardiology, Department of Medicine University of Pennsylvania, Philadelphia.
  • Yancy CW; Department of Medicine, Denver Health Medical Center, Denver, Colorado.
  • Greene SJ; Department of Medicine, University of Colorado Anschutz Medical Center. Aurora.
JAMA Cardiol ; 8(7): 652-661, 2023 07 01.
Article em En | MEDLINE | ID: mdl-37212192
ABSTRACT
Importance Clinical guidelines for patients with heart failure with reduced ejection fraction (HFrEF) strongly recommend treatment with a sodium-glucose cotransporter-2 inhibitor (SGLT2i) to reduce cardiovascular mortality or HF hospitalization. Nationwide adoption of SGLT2i for HFrEF in the US is unknown.

Objective:

To characterize patterns of SGLT2i use among eligible US patients hospitalized for HFrEF. Design, Setting, and

Participants:

This retrospective cohort study analyzed 49 399 patients hospitalized for HFrEF across 489 sites in the Get With The Guidelines-Heart Failure (GWTG-HF) registry between July 1, 2021, and June 30, 2022. Patients with an estimated glomerular filtration rate less than 20 mL/min/1.73 m2, type 1 diabetes, and previous intolerance to SGLT2i were excluded. Main Outcomes and

Measures:

Patient-level and hospital-level prescription of SGLT2i at hospital discharge.

Results:

Of 49 399 included patients, 16 548 (33.5%) were female, and the median (IQR) age was 67 (56-78) years. Overall, 9988 patients (20.2%) were prescribed an SGLT2i. SGLT2i prescription was less likely among patients with chronic kidney disease (CKD; 4550 of 24 437 [18.6%] vs 5438 of 24 962 [21.8%]; P < .001) but more likely among patients with type 2 diabetes (T2D; 5721 of 21 830 [26.2%] vs 4262 of 27 545 [15.5%]; P < .001) and those with both T2D and CKD (2905 of 12 236 [23.7%] vs 7078 vs 37 139 [19.1%]; P < .001). Patients prescribed SGLT2i therapy were more likely to be prescribed background triple therapy with an angiotensin-converting enzyme inhibitor/angiotensin receptor blocker/angiotensin receptor-neprilysin inhibitor, ß-blocker, and mineralocorticoid receptor antagonist (4624 of 9988 [46.3%] vs 10 880 of 39 411 [27.6%]; P < .001), and 4624 of 49 399 total study patients (9.4%) were discharged with prescriptions for quadruple medical therapy including SGLT2i. Among 461 hospitals with 10 or more eligible discharges, 19 hospitals (4.1%) discharged 50% or more of patients with prescriptions for SGLT2i, whereas 344 hospitals (74.6%) discharged less than 25% of patients with prescriptions for SGLT2i (including 29 [6.3%] that discharged zero patients with SGLT2i prescriptions). There was high between-hospital variance in the rate of SGLT2i prescription in unadjusted models (median odds ratio, 2.53; 95% CI, 2.36-2.74) and after adjustment for patient and hospital characteristics (median odds ratio, 2.51; 95% CI, 2.34-2.71). Conclusions and Relevance In this study, prescription of SGLT2i at hospital discharge among eligible patients with HFrEF was low, including among patients with comorbid CKD and T2D who have multiple indications for therapy, with substantial variation among US hospitals. Further efforts are needed to overcome implementation barriers and improve use of SGLT2i among patients with HFrEF.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Disfunção Ventricular Esquerda / Diabetes Mellitus Tipo 2 / Insuficiência Renal Crônica / Inibidores do Transportador 2 de Sódio-Glicose / Insuficiência Cardíaca Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Disfunção Ventricular Esquerda / Diabetes Mellitus Tipo 2 / Insuficiência Renal Crônica / Inibidores do Transportador 2 de Sódio-Glicose / Insuficiência Cardíaca Idioma: En Ano de publicação: 2023 Tipo de documento: Article