Dose of Cardiac Rehabilitation to Reduce Mortality and Morbidity: A Population-Based Study
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
R21 AG058738
NIA NIH HHS - United States
R33 AG058738
NIA NIH HHS - United States
UL1 TR000135
NCATS NIH HHS - United States
PubMed
34612055
PubMed Central
PMC8751887
DOI
10.1161/jaha.120.021356
Knihovny.cz E-resources
- Keywords
- cardiac rehabilitation, major adverse cardiovascular events, mortality,
- MeSH
- Myocardial Infarction * epidemiology MeSH
- Cardiac Rehabilitation * MeSH
- Cohort Studies MeSH
- Humans MeSH
- Morbidity MeSH
- Coronary Artery Disease * MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
Background There is wide variability in cardiac rehabilitation (CR) dose (ie, number of sessions) delivered, and no evidence-based recommendations regarding what dose to prescribe. We aimed to test what CR dose impacts major adverse cardiovascular events (MACEs). Methods and Results This is an historical cohort study of all patients who had coronary artery disease and who initiated supervised CR between 2002 and 2012 from a single major CR center. CR dose was defined as number of visits including exercise and patient education. Follow-up was performed using record linkage from the Rochester Epidemiology Project. MACEs included acute myocardial infarction, unstable angina, ventricular arrhythmias, stroke, revascularization, or all-cause mortality. Dose was analyzed in several ways, including tertiles, categories, and as a continuous variable. Cox models were adjusted for factors associated with dose and MACE. The cohort consisted of 2345 patients, who attended a mean of 12.5±11.1 of 36 prescribed sessions. After a mean follow-up of 6 years, 695 (29.65%) patients had a MACE, including 231 who died. CR dose was inversely associated with MACE (hazard ratio, 0.66 [95% CI]; 0.55-0.91) in those completing ≥20 sessions, when compared with those not exposed to formal exercise sessions (≤1 session; log-rank P=0.007). We did not find evidence of nonlinearity (P≥0.050), suggesting no minimal threshold nor ceiling. Each additional session was associated with a lower rate of MACE (fully adjusted hazard ratio, 0.98 [95% CI, 0.97-0.99]). Greater session frequency was also associated with lower MACE risk (fully adjusted hazard ratio, 0.74 [95% CI, 0.58-0.94]). Conclusions CR reduces MACEs, but the benefit appears to be linear, with greater risk reduction with higher doses, and no upper threshold.
Division of Epidemiology Department of Quantitative Health SciencesMayo Clinic Rochester MN
Division of Preventive Cardiology Department of Cardiovascular Medicine Mayo Clinic MN
Faculty of Health York University Toronto Ontario Canada
Gregorio Marañón Health Research InstituteGregorio Marañón General University Hospital Madrid Spain
International Clinical Research Center St Anne University Hospital Brno Czech Republic
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