| Literature DB >> 33557486 |
Chul Kim1, Insun Choi2, Songhee Cho2, Ae Ryoung Kim3, Wonseok Kim4, Sungju Jee5,6,7.
Abstract
OBJECTIVE: We conducted a systematic review and meta-analysis to analyze the effects of cardiac rehabilitation (CR) on post-discharge prognoses of patients with acute myocardial infarction (AMI).Entities:
Keywords: Cardiac rehabilitation; Mortality; Myocardial infarction; Readmission; Recurrence
Year: 2021 PMID: 33557486 PMCID: PMC7960955 DOI: 10.5535/arm.20080
Source DB: PubMed Journal: Ann Rehabil Med ISSN: 2234-0645
Strategy for study inclusion
| Contents | |
|---|---|
| Population | Acute myocardial infarction |
| Intervention/comparator | Cardiac rehabilitation/usual care |
| Outcomes | Recurrence, readmission, re-intervention, death |
| Time | Publication: after 2000 |
| Duration of study and follow-up: no limitation | |
| Setting | - |
| Study design | RCT |
| Non-RCT (quasi-RCT, case-control study, cohort study) |
RCT, randomized controlled trial.
Category and parameters for subgroup analysis
| Category | Parameters |
|---|---|
| Patient characteristics | Age, sex, country |
| Study design | Number of subjects |
| Prospective or retrospective | |
| Publication year | |
| Follow-up length | Above/below 1 year |
| Risk of bias | RCT |
| - Blindness for intervention: low/high/not known | |
| - Blindness for evaluation: low/high/not known | |
| Non-RCT | |
| - Study population selection: low/high/not known | |
| - Blindness for evaluation: low/high/not known |
RCT, randomized controlled trial.
Fig. 1.Summary of study selection process.
Summary of included trials and characteristics (14 studies)
| No. | RCT/non-RCT | Study | Publication year | Country | Population | Intervention | Control | Follow-up duration | Outcome variables | Remark | ||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Characteristics | n | Characteristics | n | |||||||||
| 1 | RCT | West et al. [ | 2012 | England | AMI | Sessions: 1 or 2 times/week CR participation | 903 | Usual care | 910 | 1 yr | All-cause mortality | 1–9 years followup for allcause mortality |
| Duration: 6–8 weeks | Combined endpoint (death, non-fatal MI, stroke or revascularization) | |||||||||||
| Contents: exercise, counselling, education | ||||||||||||
| Setting: centrebase | Hospitalization | |||||||||||
| 2 | RCT | Maroto Montero et al. [ | 2005 | Spain | AMI | Session: 1 hour, 3 times/week, CR | 90 | Usual care | 90 | 10 yr | All-cause mortality | |
| 3 | Non-RCT, prospective cohort study | Kureshi et al. [ | 2016 | USA | AMI | CR participants | 2,015 | Non-participants | 2,914 | 7 yr | All-cause mortality | |
| 4 | Non-RCT, prospective cohort study | Pouche et al. [ | 2016 | France | AMI | CR participants | 639 | Non-participants | 2,255 | 5 yr | All-cause mortality | |
| 5 | Non-RCT, prospective cohort study | Meurs et al. [ | 2015 | Netherland | AMI | Supervised complex intervention, CR participants | 878 | Non-participants | 824 | 1 yr | All-cause mortality | |
| Readmission | ||||||||||||
| 6 | Non-RCT, prospective cohort study | Coll-Fernandez et al. [ | 2014 | Spain | AMI | Centre-base CR participants | 521 | Non-participants | 522 | 18 mo | All-cause mortality | Follow-up until 36 months for ischemic events |
| Ischemic events (MI, ischemic stroke, limb amputation) | ||||||||||||
| 7 | Non-RCT, prospective cohort study | Lewinter et al. [ | 2014 | England | AMI | CR participants | EM-MACE-1: 986 | Non-participants | EM-MACE-1: 338 | 1 yr | All-cause mortality | Follow-up until 80 months for survival |
| EM-MACE-2: 1,256 | EM-MACE-2: 719 | Proportion of survivor | ||||||||||
| 8 | Non-RCT, prospective cohort study | Rauch et al. [ | 2014 | Germany | AMI | Centre-base CR participants | 2513 | Non-participants | 1047 | 4-12 mo | All-cause mortality | |
| Cardiac mortality | ||||||||||||
| Readmission | ||||||||||||
| Re-intervention (PCI/CABG) | ||||||||||||
| MACCE | ||||||||||||
| 9 | Non-RCT, prospective cohort study | Kim et al. [ | 2011 | South Korea | AMI | Comprehensive CR participants about 6–8 weeks | 69 | Usual care (risk factor management and counselling) | 72 | 1 yr | All-cause mortality | |
| Cardiac mortality | ||||||||||||
| Recurrence | ||||||||||||
| Re-intervention | ||||||||||||
| Readmission | ||||||||||||
| 10 | Non-RCT, prospective cohort study | Junger et al. [ | 2010 | Germany | AMI | Centre-base comprehensive CR participants | STEMI: 1,649 | Non-participants | STEMI: 783 | 1 yr | All-cause mortality | |
| NSTEMI: 1,107 | NSTEMI: 1,008 | MACE | ||||||||||
| MACCE | ||||||||||||
| 11 | Non-RCT, retrospective cohort study | Beauchamp et al. [ | 2013 | Australia | Acute coronary syndrome | Group-based comprehensive CR participants (>1 session) | 154 | Non-participants | 143 | 14 yr | All-cause mortality | |
| 12 | Non-RCT, retrospective cohort study | Suaya et al. [ | 2009 | USA | Acute coronary syndrome | CR participants | 25,966 | Non-participants | 25,966 | 5 yr | All-cause mortality | |
| 13 | Non-RCT, retrospective cohort study | Nielsen et al. [ | 2008 | Denmark | AMI | Centre-base comprehensive CR participants | 145 | Non-participants | 55 | 1 yr | All-cause mortality | Follow-up during 2 years for allcause mortality |
| Readmission | ||||||||||||
| Re-intervention | ||||||||||||
| 14 | Non-RCT, retrospective cohort study | Boulay and Prud'homme [ | 2004 | Canada | AMI | Centre-base comprehensive CR participants | Shortterm: 37 | Usual care (risk factor management and counselling) | 54 | 1 yr | Emergency room visit | |
| Longterm: 37 | Readmission | |||||||||||
| Recurrence | ||||||||||||
RCT, randomized controlled trial; CR, cardiac rehabilitation; AMI, acute myocardial infarction; MACE, major adverse cardiac events; MACCE, major adverse cardiac and cerebrovascular events; STEMI, ST elevation myocardial infarction; NSTEMI, non-ST elevation myocardial infarction.
Outcome variables according to study designs
| Outcomes variable | Study design | ||
|---|---|---|---|
| Randomized controlled trial | Prospective cohort | Retrospective cohort | |
| Cardiac mortality | O | ||
| All-cause mortality | O | O | O |
| Re-intervention | O | O | |
| Recurrence | O | ||
| Readmission | O | O | O |
| Ischemic event | O | ||
| Major adverse cardiac events | O | ||
| Major adverse cardiac and cerebrovascular events | O | ||
| Emergency room visit | O | ||
Fig. 2.Summary of risk of bias of the randomized controlled study.
Fig. 3.Summary of risk of bias according to the study design. (A) Prospective cohort study. (B) Retrospective cohort study.
Fig. 4.Forest plot of all-cause mortality in two randomized controlled trials (RCTs). There was a decreased tendency on all-cause mortality in the cardiac rehabilitation (CR) group.
Summary of study outcomes
| RCT/non-RCT | Outcome variable | Authors, year | Follow-up duration | Results | Statistical significance |
|---|---|---|---|---|---|
| RCT | All-cause mortality | Maroto Montero et al. [ | 10 yr | Intervention: 7.7% (7/90) | Yes |
| Control: 17.7% (16/90) | |||||
| West et al. [ | 9 yr | RR=0.99 (95% CI, 0.85–1.15) | No | ||
| Readmission | West et al. [ | 1 yr | Intervention: 25% (222/903) | No | |
| Control: 26% (239/910) | |||||
| Non-RCT, prospective cohort | Cardiac mortality | Rauch et al. [ | 4–12 mo | OR=0.43 (95% CI, 0.23–0.79) | Yes |
| All-cause mortality | Kureshi et al. [ | 7 yr | HR=0.59 (95% CI, 0.46–0.75) | Yes | |
| Pouche et al. [ | 5 yr | HR=0.76 (95% CI, 0.60–0.96) | Yes | ||
| Meurs et al. [ | 1 yr | HR=0.83 (95% CI, 0.54–1.30) | No | ||
| Coll-Fernandez et al. [ | 18 mo (mean) | RR=0.03 (95% CI, 0.00–0.10) | Yes | ||
| Lewinter et al. [ | 1 yr | Cohort 1: OR=0.34 (95% CI, 0.24–0.46) | Yes | ||
| Cohort 2: OR=0.19 (95% CI, 0.15–0.23) | Yes | ||||
| Rauch et al. [ | 4–12 mo | OR=0.46 (95% CI, 0.27–0.77) | Yes | ||
| Kim et al. [ | 1 yr | Intervention: 1.4% (1/69) | No | ||
| Control: 1.4% (1/72) | |||||
| Junger et al. [ | 1 yr | STEMI: OR=0.41 (95% CI, 0.28–0.60) | Yes | ||
| NSTEMI: OR=0.53 (95% CI, 0.38–0.76) | Yes | ||||
| Non-RCT, retrospective cohort | All-cause mortality | Beauchamp et al. [ | 14 yr | HR=1.58 (95% CI, 1.16–2.15) | Yes |
| reference: CR attenders | |||||
| Suaya et al. [ | 5 yr | Intervention: 18.9% | - | ||
| Control: 30.9% | |||||
| Nielsen et al. [ | 1 yr | Intervention: 2.1% (3/145) | - | ||
| Control: 14.5% (8/55) | |||||
| 2 yr | Intervention: 2.8% (4/145) | - | |||
| Control: 21.8% (12/55) |
RR, relative risk; CI, confidence interval; OR, odds ratio; HR, hazard ratio; STEMI, ST elevation myocardial infarction; NSTEMI, non-ST elevation myocardial infarction; CR, cardiac rehabilitation.
Fig. 5.Forest plot for re-intervention among non-randomized controlled trials (non-RCTs).
Fig. 6.Forest plot on recurrence after acute myocardial infarction among non-randomized controlled trials (non-RCTs). Cardiac rehabilitation (CR) group showed a significant decrease in recurrence.
Fig. 7.Forest plot on readmission after acute myocardial infarction among non-randomized controlled trials (non-RCTs). CR, cardiac rehabilitation.
Fig. 8.Forest plot on major adverse cardiac and cerebrovascular events after acute myocardial infarction