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Multicenter Study
. 2023 May 16;329(19):1650-1661.
doi: 10.1001/jama.2023.5942.

Global Variations in Heart Failure Etiology, Management, and Outcomes

Collaborators, Affiliations
Multicenter Study

Global Variations in Heart Failure Etiology, Management, and Outcomes

G-CHF Investigators et al. JAMA. .

Erratum in

Abstract

Importance: Most epidemiological studies of heart failure (HF) have been conducted in high-income countries with limited comparable data from middle- or low-income countries.

Objective: To examine differences in HF etiology, treatment, and outcomes between groups of countries at different levels of economic development.

Design, setting, and participants: Multinational HF registry of 23 341 participants in 40 high-income, upper-middle-income, lower-middle-income, and low-income countries, followed up for a median period of 2.0 years.

Main outcomes and measures: HF cause, HF medication use, hospitalization, and death.

Results: Mean (SD) age of participants was 63.1 (14.9) years, and 9119 (39.1%) were female. The most common cause of HF was ischemic heart disease (38.1%) followed by hypertension (20.2%). The proportion of participants with HF with reduced ejection fraction taking the combination of a β-blocker, renin-angiotensin system inhibitor, and mineralocorticoid receptor antagonist was highest in upper-middle-income (61.9%) and high-income countries (51.1%), and it was lowest in low-income (45.7%) and lower-middle-income countries (39.5%) (P < .001). The age- and sex- standardized mortality rate per 100 person-years was lowest in high-income countries (7.8 [95% CI, 7.5-8.2]), 9.3 (95% CI, 8.8-9.9) in upper-middle-income countries, 15.7 (95% CI, 15.0-16.4) in lower-middle-income countries, and it was highest in low-income countries (19.1 [95% CI, 17.6-20.7]). Hospitalization rates were more frequent than death rates in high-income countries (ratio = 3.8) and in upper-middle-income countries (ratio = 2.4), similar in lower-middle-income countries (ratio = 1.1), and less frequent in low-income countries (ratio = 0.6). The 30-day case-fatality rate after first hospital admission was lowest in high-income countries (6.7%), followed by upper-middle-income countries (9.7%), then lower-middle-income countries (21.1%), and highest in low-income countries (31.6%). The proportional risk of death within 30 days of a first hospital admission was 3- to 5-fold higher in lower-middle-income countries and low-income countries compared with high-income countries after adjusting for patient characteristics and use of long-term HF therapies.

Conclusions and relevance: This study of HF patients from 40 different countries and derived from 4 different economic levels demonstrated differences in HF etiologies, management, and outcomes. These data may be useful in planning approaches to improve HF prevention and treatment globally.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Joseph reported grants from Bayer AG during the conduct of the study. Dr Lonn reports grants or contracts from Novartis, Bayer, Amgen, Boehringer Ingelheim, the Population Health Research Institute (PHRI), and the Canadian Institute of Health Research; personal fees (consulting) from Alnylam, Amgen, Bayer, HLS Therapeutics, NovoNordisk, Sanofi, Servier, and Takeda; personal fees (presentation honoraria) from Amgen, Bayer, HLS Therapeutics, and Servier; and serving on the data safety monitoring board or advisory board for Novartis, Resvirologix, and LIB Therapeutics. Dr Störk reported grants from the Federal Ministry of Education and Research during the conduct of the study; personal fees (advisory board) from Boehringer Ingelheinm, Bayer, Novartis, Pfizer, and Pharmacosoms; other (case payment in trials) from Boehringer Ingelheinm, Bayer, Novartis, and Pfizer outside the submitted work. Dr Mielniczuk reported other (speaker consulting fees) from Astra Zeneca and Merck, and speaker fees from Janssen and Servier outside the submitted work. Dr Rouleau reported personal fees (data monitoring committee membership) from Novartis, AstraZeneca, Bristol Myers Squibb, and Bayer outside the submitted work. Dr Zhu reported grants from PHRI during the conduct of the study; personal fees (speaker honoraria) from Boehringer Ingelheim, Bayer, Sanofi, and Novartis outside the submitted work. Dr Branch reported research grants from Bayer, Sanofi, Eli Lilly, Kestra, and Medic One Foundation; and consulting fees from Bayer, Janssen, Amgen, Sana, Kestra, and Hanmi. Dr Budaj reported personal fees (investigator fees, honoraria for lectures, advisory board, travel, and accommodations) from Bayer, AstraZeneca, and Pfizer; personal fees (investigator fees, honoraria for lectures, advisory board) from Novartis, and personal fees (investigator fees) from Amgen and NovoNordisk outside the submitted work. Dr Ertl reported grants or contracts and consulting fees from Novartis; and advisory board membership with the General Secretary of the German Society of Internal Medicine. Dr Mondo reports travel funding from Bayer AG. Dr Pogosova reports grants or contracts from Bristol Myers Squibb (AXIOMATIC-SSP); presentation honoraria from Bayer; and serving as a board member of the Russian National Society of Preventive Cardiology. Dr Maggioni reported personal fees (participation in study committees) from AstraZeneca, Bayer, and Novartis outside the submitted work. Dr Orlandini reported grants from PHRI during the conduct of the study. Dr Parkhomenko reported grants from PHRI; and personal fees (lectures and consulting) from Astra Zeneka and Boehringer Ingelheim outside the submitted work. Mr Grinvalds reported grants from Bayer AG awarded to Hamilton Health Sciences during the conduct of the study. Dr Hage reported personal fees (consulting) from AnaCardio AB and Roche Diagnostics; and serving on the data safety monitoring board, advisory board, or committee board for Roche Diagnostics, AnaCardio AB, and the Swedish National HF registry outside the submitted work. Dr Lund reports grants or contracts from AstraZeneca, Vifor Pharma, Novartis, Boston Scientific, and Boerhinger Ingelheim; personal fees (consulting) from Merck, Vifor Pharma, AstraZeneca, Bayer, Pharmacosmos, MedScape, Sanofi, Lexicon, Myokardia, Boehringer Ingelheim, and Servier; personal fees (presentation honoraria) from Abbott, MedScape, Radcliffe, AstraZeneca, Novartis, Bayer, TMA Academy, Boehringer Ingelheim, and Orion Pharma; serving as an advisory board member of the European Society of Cardiology Heart Failure Association, the European Society of Cardiology, the Swedish Society of Cardiology, and the Heart Failure Working Group; and holding stock in AnaCardio. Dr Fox reported grants from AstraZeneca and personal fees from Bayer outside the submitted work. Dr McMurray reported other (to his institution: investigator fees, executive committee membership, and advisory board membership for various trials) from AstraZeneca; fees for travel and accommodations from AstraZeneca associated with these meetings; other (fees to his institution for steering committee membership) from Bayer, Amgen, Servier, Theracos, Dalcor, Glaxo Smith Kline, and Bristol Myers Squibb; other (fees to his institution for advisory board participation) from Alnylam and Cardurion; other (fees to his institution for executive committee membership) from Novartis; other (fees to his institution for consultancy services) from Ionis Pharmaceuticals and Boehringer Ingelheim; and personal fees (for lectures) from Abbott, Alkem Metabolics, Eris Lifesciences, Hikma, Lupin, Sun Pharmaceuticals, Medscape/Heart.Org, ProAdWise Communications, Radcliffe Cardiology, Servier, and the Corpus outside the submitted work. Dr Al Mulla reported nonfinancial support from PHRI and grants from Bayer during the conduct of the study. Dr Bayés-Genís reported personal fees (lectures and advisory board) from Abbott Lecture, AstraZeneca, Boehringer Ingelheim, and Roche Diagnostics; personal fees Vifor (lecture fees); and grants from Boehringer Ingelheim outside the submitted work. Dr McCready reported grants from Bayer AG to Hamilton Health Sciences during the conduct of the study. Dr Yusef reported personal fees (honoraria and travel expenses) from Bayer, Astra Zeneca and Boehringer Ingelheim. No other disclosures were reported.

Figures

Figure 1.
Figure 1.. Countries Included in the Registry
The countries are sorted by income level then listed by continent from west to east, north to south. Türkiye is the new spelling, approved by the United Nations in June 2022 and also by the US Board on Geographic Names, for the country formerly known as Turkey. The basis for this figure was created with MapChart.
Figure 2.
Figure 2.. Variation in the Causes of Heart Failure and the Use of Treatments for Heart Failure With Reduced Ejection Fraction by Country Income Level in a Registry Study of 40 Countries
A, See eTable 3 in Supplement 1 for an expanded list of heart failure causes by income level. B, See eTable 4 in Supplement 1 for an expanded list of heart failure treatments by country income level. Data report on the proportion of participants with an left ventricular ejection fraction of less than or equal to 40% taking a specific class of medication or combination of medications. Implantable cardioverter-defibrillator use is reported in participants with a left ventricular ejection fraction of less than or equal to 35%. RAS inhibitor refers to angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, or an angiotensin receptor–neprilysin inhibitor. MRA indicates mineralocorticoid receptor antagonist; RAS, renin-angiotensin system.
Figure 3.
Figure 3.. Rate of Hospitalization, Rate of Death, and Proportional Risk of Death From Any Cause by Country Income Level
Events were captured at a median follow-up period of 2.0 years. HR indicates hazard ratio. aData reflect the first hospitalization after enrollment. Observation hospitalizations are common in the US but uncommon in many of the other countries participating in the registry; therefore, observation vs inpatient hospitalizations were not specifically delineated in the registry. bModel was adjusted for age and sex. cModel was adjusted for variables in model 1 plus clinical characteristics (body mass index, systolic blood pressure, diabetes, chronic obstructive pulmonary disease, current tobacco use, stage 4-5 kidney dysfunction, left ventricular ejection fraction [>50%, 41%-49%, ≤40%], having no echocardiography performed within the previous year, New York Heart Association functional class, heart failure duration >12 months), heart failure etiology (ischemic, hypertension, dilated, rheumatic valvular, nonrheumatic valvular, other), inpatient recruitment, patient education level, chronic heart failure treatments (β-blocker, renin-angiotensin system inhibitor, mineralocorticoid receptor antagonist, implantable cardioverter-defibrillator).
Figure 4.
Figure 4.. Risk of Death Within 30 Days of the First Hospital Admission by Country Income Level
HR indicates hazard ratio. aData reflect the first hospitalization after enrollment. Observation hospitalizations are common in the US but uncommon in many of the other countries participating in the registry; therefore, observation vs inpatient hospitalizations were not specifically delineated in the registry. bModel was adjusted for age and sex. cModel was adjusted for variables in model 1 plus clinical characteristics (body mass index, systolic blood pressure, diabetes, chronic obstructive pulmonary disease, current tobacco use, stage 4-5 kidney dysfunction, left ventricular ejection fraction [>50%, 41%-49%, ≤40%], having no echocardiography performed within the previous year, New York Heart Association functional class, heart failure duration >12 months), heart failure etiology (ischemic, hypertension, dilated, rheumatic valvular, nonrheumatic valvular, other), inpatient recruitment, patient education level, chronic heart failure treatments (β-blocker, renin-angiotensin system inhibitor, mineralocorticoid receptor antagonist, implantable cardioverter-defibrillator).

Comment in

References

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