TY - JOUR
T1 - Global mortality variations in patients with heart failure
T2 - results from the International Congestive Heart Failure (INTER-CHF) prospective cohort study
AU - INTER-CHF Investigators
AU - INTER-CHF Investigators
AU - Dokainish, Hisham
AU - Teo, Koon
AU - Zhu, Jun
AU - Roy, Ambuj
AU - AlHabib, Khalid F.
AU - ElSayed, Ahmed
AU - Palileo-Villaneuva, Lia
AU - Lopez-Jaramillo, Patricio
AU - Karaye, Kamilu
AU - Yusoff, Khalid
AU - Orlandini, Andres
AU - Sliwa, Karen
AU - Mondo, Charles
AU - Lanas, Fernando
AU - Prabhakaran, Dorairaj
AU - Badr, Amr
AU - Elmaghawry, Mohamed
AU - Damasceno, Albertino
AU - Tibazarwa, Kemi
AU - Belley-Cote, Emilie
AU - Balasubramanian, Kumar
AU - Islam, Shofiqul
AU - Yacoub, Magdi H.
AU - Huffman, Mark D.
AU - Harkness, Karen
AU - Grinvalds, Alex
AU - McKelvie, Robert
AU - Bangdiwala, Shrikant I.
AU - Yusuf, Salim
AU - Campos, R.
AU - Chacón, C.
AU - Cursack, G.
AU - Diez, F.
AU - Escobar, C.
AU - Garcia, C.
AU - Vilamajo, O. Gomez
AU - Hominal, M.
AU - Ingaramo, A.
AU - Kucharczuk, G.
AU - Pelliza, M.
AU - Rojas, A.
AU - Villani, A.
AU - Zapata, G.
AU - Bourke, P.
AU - Lanas, F.
AU - Nahuelpan, L.
AU - Olivares, C.
AU - Riquelme, R.
AU - Ai, F.
AU - Bai, X.
N1 - Publisher Copyright:
© 2017 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY-NC-ND 4.0 license
PY - 2017/7
Y1 - 2017/7
N2 - Background Most data on mortality and prognostic factors in patients with heart failure come from North America and Europe, with little information from other regions. Here, in the International Congestive Heart Failure (INTER-CHF) study, we aimed to measure mortality at 1 year in patients with heart failure in Africa, China, India, the Middle East, southeast Asia and South America; we also explored demographic, clinical, and socioeconomic variables associated with mortality. Methods We enrolled consecutive patients with heart failure (3695 [66%] clinic outpatients, 2105 [34%] hospital in patients) from 108 centres in six geographical regions. We recorded baseline demographic and clinical characteristics and followed up patients at 6 months and 1 year from enrolment to record symptoms, medications, and outcomes. Time to death was studied with Cox proportional hazards models adjusted for demographic and clinical variables, medications, socioeconomic variables, and region. We used the explained risk statistic to calculate the relative contribution of each level of adjustment to the risk of death. Findings We enrolled 5823 patients within 1 year (with 98% follow-up). Overall mortality was 16·5%: highest in Africa (34%) and India (23%), intermediate in southeast Asia (15%), and lowest in China (7%), South America (9%), and the Middle East (9%). Regional differences persisted after multivariable adjustment. Independent predictors of mortality included cardiac variables (New York Heart Association Functional Class III or IV, previous admission for heart failure, and valve disease) and non-cardiac variables (body-mass index, chronic kidney disease, and chronic obstructive pulmonary disease). 46% of mortality risk was explained by multivariable modelling with these variables; however, the remainder was unexplained. Interpretation Marked regional differences in mortality in patients with heart failure persisted after multivariable adjustment for cardiac and non-cardiac factors. Therefore, variations in mortality between regions could be the result of health-care infrastructure, quality and access, or environmental and genetic factors. Further studies in large, global cohorts are needed. Funding The study was supported by Novartis.
AB - Background Most data on mortality and prognostic factors in patients with heart failure come from North America and Europe, with little information from other regions. Here, in the International Congestive Heart Failure (INTER-CHF) study, we aimed to measure mortality at 1 year in patients with heart failure in Africa, China, India, the Middle East, southeast Asia and South America; we also explored demographic, clinical, and socioeconomic variables associated with mortality. Methods We enrolled consecutive patients with heart failure (3695 [66%] clinic outpatients, 2105 [34%] hospital in patients) from 108 centres in six geographical regions. We recorded baseline demographic and clinical characteristics and followed up patients at 6 months and 1 year from enrolment to record symptoms, medications, and outcomes. Time to death was studied with Cox proportional hazards models adjusted for demographic and clinical variables, medications, socioeconomic variables, and region. We used the explained risk statistic to calculate the relative contribution of each level of adjustment to the risk of death. Findings We enrolled 5823 patients within 1 year (with 98% follow-up). Overall mortality was 16·5%: highest in Africa (34%) and India (23%), intermediate in southeast Asia (15%), and lowest in China (7%), South America (9%), and the Middle East (9%). Regional differences persisted after multivariable adjustment. Independent predictors of mortality included cardiac variables (New York Heart Association Functional Class III or IV, previous admission for heart failure, and valve disease) and non-cardiac variables (body-mass index, chronic kidney disease, and chronic obstructive pulmonary disease). 46% of mortality risk was explained by multivariable modelling with these variables; however, the remainder was unexplained. Interpretation Marked regional differences in mortality in patients with heart failure persisted after multivariable adjustment for cardiac and non-cardiac factors. Therefore, variations in mortality between regions could be the result of health-care infrastructure, quality and access, or environmental and genetic factors. Further studies in large, global cohorts are needed. Funding The study was supported by Novartis.
UR - http://www.scopus.com/inward/record.url?scp=85018958747&partnerID=8YFLogxK
U2 - 10.1016/S2214-109X(17)30196-1
DO - 10.1016/S2214-109X(17)30196-1
M3 - Artículo Científico
C2 - 28476564
AN - SCOPUS:85018958747
SN - 2214-109X
VL - 5
SP - e665-e672
JO - The Lancet Global Health
JF - The Lancet Global Health
IS - 7
ER -