TY - JOUR
T1 - Global disparities in prescription of guideline-recommended drugs for heart failure with reduced ejection fraction
AU - Tromp, Jasper
AU - Ouwerkerk, Wouter
AU - Teng, Tiew Hwa K.
AU - Cleland, John G.F.
AU - Bamadhaj, Sahiddah
AU - Angermann, Christiane E.
AU - Dahlstrom, Ulf
AU - Tay, Wan Ting
AU - Dickstein, Kenneth
AU - Ertl, Georg
AU - Hassanein, Mahmoud
AU - Perrone, Sergio V.
AU - Ghadanfar, Mathieu
AU - Schweizer, Anja
AU - Obergfell, Achim
AU - Collins, Sean P.
AU - Filippatos, Gerasimos
AU - Lam, Carolyn S.P.
N1 - Funding Information:
REPORT-HF: was funded by Novartis. C.S.P.L. is supported by a Clinician Scientist Award from the National Medical Research Council of Singapore; has received research support from AstraZeneca, Bayer, Boston Scientific and Roche Diagnostics; has served as consultant or on the Advisory Board/Steering Committee/Executive Committee for Actelion, Amgen, Applied Therapeutics, AstraZeneca, Bayer, Boehringer Ingelheim, Boston Scientific, Cytokinetics, Darma Inc., Janssen R&D, Medscape/WebMD Global, Merck, Novartis, Novo Nordisk, Roche Diagnostics, Sanofi, St Luke, Us2.ai; has received payment or honoraria from Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Medscape/WebMD Global, Novartis, Radcliffe, Roche Diagnostics; holds a patent (US patent no: 16/216,929) and has a patent pending unrelated to this work (no: 16/216,929); and serves as co-founder and non-executive director of Us2.ai; J.T. is supported by the National University of Singapore Start-up grant, the Tier 1 grant from the Ministry of Education and the CS-IRG New Investigator Grant from the National Medical Research Council; has received personal grants or speaker fees from Us2.ai, Daiichi-Sankyo, Boehringer Ingelheim, and Roche diagnostics and holds a patent (US patent no: 16/216,929) unrelated to this work. J.G.F.C. reports personal fees from Amgen, grants and personal fees from Bayer, grants and personal fees from Bristol Myers Squibb, personal fees from Novartis, personal fees from Medtronic, personal fees from Idorsia, grants and personal fees from Vifor, grants and personal fees from Pharmacosmos, grants and personal fees from Cytokinetics, personal fees from Servier, personal fees and non-financial support from Boehringer Ingelheim, personal fees from AstraZeneca, personal fees from Innolife, personal fees from Torrent, grants and personal fees from Johnson & Johsnon, grants and personal fees from Myokardia, personal fees from Respicardia, grants and personal fees from Stealth Biopharmaceuticals, grants and personal fees from Viscardia, personal fees from Abbott, outside the submitted work; U.D. reports research support from AstraZeneca, Pfizer, Boehringer Ingelheim, Vifor pharma, Roche Diagnostics, Boston Scientific and speaker’s honoraria, and consultancies from AstraZeneca. S.P.C. reports research grants from NIH, PCORI, and AstraZeneca and consulting fees from Bristol Myers Squibb, Boehringer Ingelheim, and Vixiar. M.G. and A.O. are former employees of Novartis and holds Novartis stocks. G.F. reports grants from the European Commission; payments or honoraria from Boehringer Ingelheim and Bayer; committee membership involving Medtronic, Vifor Pharma, Amgen and Servier. A.S. is employed by Novartis. The remaining authors have nothing to disclose.
Publisher Copyright:
© 2022 The Author(s) 2022
PY - 2022/6/14
Y1 - 2022/6/14
N2 - Background: Heart failure (HF) is a global challenge, with lower- and middle-income countries (LMICs) carrying a large share of the burden. Treatment for HF with reduced ejection fraction (HFrEF) improves survival but is often underused. Economic factors might have an important effect on the use of medicines. Methods and results: This analysis assessed prescription rates and doses of renin-angiotensin system (RAS) inhibitors, β-blockers, and mineralocorticoid receptor antagonists at discharge and 6-month follow-up in 8669 patients with HFrEF (1458 from low-, 3363 from middle-, and 3848 from high-income countries) hospitalized for acute HF in 44 countries in the prospective REPORT-HF study. We investigated determinants of guideline-recommended treatments and their association with 1-year mortality, correcting for treatment indication bias. Only 37% of patients at discharge and 34% of survivors at 6 months were on all three medication classes, with lower proportions in LMICs than high-income countries (19 vs. 41% at discharge and 15 vs. 37% at 6 months). Women and patients without health insurance, or from LMICs, or without a scheduled medical follow-up within 6 months of discharge were least likely to be on guideline-recommended medical therapy at target doses, independent of confounders. Being on ≥50% of guideline-recommended doses of RAS inhibitors, and β-blockers were independently associated with better 1-year survival, regardless of country income level. Conclusion: Patients with HFrEF in LMICs are less likely to receive guideline-recommended drugs at target doses. Improved access to medications and medical care could reduce international disparities in outcome.
AB - Background: Heart failure (HF) is a global challenge, with lower- and middle-income countries (LMICs) carrying a large share of the burden. Treatment for HF with reduced ejection fraction (HFrEF) improves survival but is often underused. Economic factors might have an important effect on the use of medicines. Methods and results: This analysis assessed prescription rates and doses of renin-angiotensin system (RAS) inhibitors, β-blockers, and mineralocorticoid receptor antagonists at discharge and 6-month follow-up in 8669 patients with HFrEF (1458 from low-, 3363 from middle-, and 3848 from high-income countries) hospitalized for acute HF in 44 countries in the prospective REPORT-HF study. We investigated determinants of guideline-recommended treatments and their association with 1-year mortality, correcting for treatment indication bias. Only 37% of patients at discharge and 34% of survivors at 6 months were on all three medication classes, with lower proportions in LMICs than high-income countries (19 vs. 41% at discharge and 15 vs. 37% at 6 months). Women and patients without health insurance, or from LMICs, or without a scheduled medical follow-up within 6 months of discharge were least likely to be on guideline-recommended medical therapy at target doses, independent of confounders. Being on ≥50% of guideline-recommended doses of RAS inhibitors, and β-blockers were independently associated with better 1-year survival, regardless of country income level. Conclusion: Patients with HFrEF in LMICs are less likely to receive guideline-recommended drugs at target doses. Improved access to medications and medical care could reduce international disparities in outcome.
KW - Global differences
KW - Heart failure
KW - Medication
UR - http://www.scopus.com/inward/record.url?scp=85131903297&partnerID=8YFLogxK
U2 - 10.1093/eurheartj/ehac103
DO - 10.1093/eurheartj/ehac103
M3 - Article
C2 - 35393622
AN - SCOPUS:85131903297
VL - 43
SP - 2224
EP - 2234
JO - European Heart Journal
JF - European Heart Journal
SN - 0195-668X
IS - 23
ER -