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Causes of cardiovascular and noncardiovascular death in the ISCHEMIA trial.
Sidhu, Mandeep S; Alexander, Karen P; Huang, Zhen; O'Brien, Sean M; Chaitman, Bernard R; Stone, Gregg W; Newman, Jonathan D; Boden, William E; Maggioni, Aldo P; Steg, Philippe Gabriel; Ferguson, Thomas B; Demkow, Marcin; Peteiro, Jesus; Wander, Gurpreet S; Phaneuf, Denis C; De Belder, Mark A; Doerr, Rolf; Alexanderson-Rosas, Erick; Polanczyk, Carisi A; Henriksen, Peter A; Conway, Dwayne S G; Miro, Vicente; Sharir, Tali; Lopes, Renato D; Min, James K; Berman, Daniel S; Rockhold, Frank W; Balter, Stephen; Borrego, David; Rosenberg, Yves D; Bangalore, Sripal; Reynolds, Harmony R; Hochman, Judith S; Maron, David J.
Afiliação
  • Sidhu MS; Albany Medical College, Albany, NY. Electronic address: sidhum@amc.edu.
  • Alexander KP; Duke Clinical Research Institute - Duke University Medical Center, Durham, NC.
  • Huang Z; Duke Clinical Research Institute - Duke University Medical Center, Durham, NC.
  • O'Brien SM; Duke Clinical Research Institute - Duke University Medical Center, Durham, NC.
  • Chaitman BR; St Louis University School of Medicine Center for Comprehensive Cardiovascular Care, St. Louis, MO.
  • Stone GW; Icahn School of Medicine at Mount Sinai, Cardiovascular Research Foundation, New York, NY.
  • Newman JD; NYU Grossman School of Medicine, New York, NY.
  • Boden WE; VA New England Healthcare System, Boston University School of Medicine, Boston, MA.
  • Maggioni AP; ANMCO Research Center, Florence, Italy.
  • Steg PG; Université de Paris, Assistance Publique-Hôpitaux de Paris, INSERM-1148, Paris, France.
  • Ferguson TB; Brody School of Medicine, East Carolina University, Greenville, NC, USA.
  • Demkow M; Dept of Coronary and Structural Heart Diseases, National Institute of Cardiology, Warsaw, Poland.
  • Peteiro J; CHUAC, Universidad de A Coruña, CIBER-CV, A Coruña, Spain.
  • Wander GS; Dayanand Medical College & Hospital, Ludhiana, Punjab, India.
  • Phaneuf DC; Hôpital Pierre-Le Gardeur, Quebec, Terrebonne, Canada.
  • De Belder MA; Barts Health NHS Trust, London, United Kingdom.
  • Doerr R; Praxisklinik Herz und Gefaesse, Dresden, Germany.
  • Alexanderson-Rosas E; Instituto Nacional de Cardiología "Ignacio Chávez", Mexico City, Mexico.
  • Polanczyk CA; Federal University of Rio Grande do Sul, Hospital Clínicas de Porto Alegre, Porto Alegre, Brazil.
  • Henriksen PA; Edinburgh Heart Centre, Royal Infirmary of Edinburgh, Edinburgh, United Kingdom.
  • Conway DSG; Northern General Hospital, Sheffield, United Kingdom.
  • Miro V; Hospital universitario y politecnico La Fe, Valencia, Spain.
  • Sharir T; Assuta Medical Center and Ben Gurion University of the Negev, Tel Aviv, Israel.
  • Lopes RD; Duke Clinical Research Institute - Duke University Medical Center, Durham, NC.
  • Min JK; Cleerly, Inc. New York, NY.
  • Berman DS; Cedars-Sinai Medical Center, Los Angeles, CA.
  • Rockhold FW; Duke Clinical Research Institute - Duke University Medical Center, Durham, NC.
  • Balter S; Columbia University, New York, NY.
  • Borrego D; Radiation Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
  • Rosenberg YD; National Institute of Health- NHLBI, Bethesda, MD.
  • Bangalore S; NYU Grossman School of Medicine, New York, NY.
  • Reynolds HR; NYU Grossman School of Medicine, New York, NY.
  • Hochman JS; NYU Grossman School of Medicine, New York, NY.
  • Maron DJ; Department of Medicine, Stanford University School of Medicine, Stanford, CA.
Am Heart J ; 248: 72-83, 2022 06.
Article em En | MEDLINE | ID: mdl-35149037
ABSTRACT

BACKGROUND:

The International Study of Comparative Health Effectiveness with Medical and Invasive Approaches trial demonstrated no overall difference in the composite primary endpoint and the secondary endpoints of cardiovascular (CV) death/myocardial infarction or all-cause mortality between an initial invasive or conservative strategy among participants with chronic coronary disease and moderate or severe myocardial ischemia. Detailed cause-specific death analyses have not been reported.

METHODS:

We compared overall and cause-specific death rates by treatment group using Cox models with adjustment for pre-specified baseline covariates. Cause of death was adjudicated by an independent Clinical Events Committee as CV, non-CV, and undetermined. We evaluated the association of risk factors and treatment strategy with cause of death.

RESULTS:

Four-year cumulative incidence rates for CV death were similar between invasive and conservative strategies (2.6% vs 3.0%; hazard ratio [HR] 0.98; 95% CI [0.70-1.38]), but non-CV death rates were higher in the invasive strategy (3.3% vs 2.1%; HR 1.45 [1.00-2.09]). Overall, 13% of deaths were attributed to undetermined causes (38/289). Fewer undetermined deaths (0.6% vs 1.3%; HR 0.48 [0.24-0.95]) and more malignancy deaths (2.0% vs 0.8%; HR 2.11 [1.23-3.60]) occurred in the invasive strategy than in the conservative strategy.

CONCLUSIONS:

In International Study of Comparative Health Effectiveness with Medical and Invasive Approaches, all-cause and CV death rates were similar between treatment strategies. The observation of fewer undetermined deaths and more malignancy deaths in the invasive strategy remains unexplained. These findings should be interpreted with caution in the context of prior studies and the overall trial results.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article