n or mean±SD (range) | |
Study parameters (n=121)* | |
Total patients | 13 220 |
Patient group parameters (n=196)† | |
Age, years | 58.4±4.9 (45.3–75.0) |
EF, % | 53.7±5.6 (42.4–67.0) |
Sex | |
Male | 41 |
Female | 3 |
Mixed (%F) | 116 (17.1±7.2) |
Did not report | 36 |
Primary diagnosis | |
Post-MI | 81 |
CABG only | 32 |
PCI only | 12 |
CABG/PCI | 5 |
VR | 8 |
Mix | 55 |
Rehabilitation programme parameters (n=150)‡ | |
Intensity | |
Light | 2 |
Moderate | 18 |
Moderate-to-vigorous | 52 |
Vigorous | 68 |
Unable to categorise | 10 |
Length, weeks | 11.0±6.4 |
<6 | 24 |
6 | 21 |
6–11 | 26 |
12 | 58 |
>12 | 21 |
Frequency, sessions/week | 3.3±1.8 |
1–2 | 22 |
3–4 | 106 |
5–7 | 15 |
>7 | 5 |
Supervision | |
Clinic | 133 |
Home | 8 |
Mixed | 8 |
Intervention type | |
Comprehensive | 33 |
Exercise only | 117 |
Training type | |
Continuous | 133 |
Interval | 14 |
Mixed | 3 |
Exercise modality | |
Aerobic only | 124 |
Aerobic and resistance | 26 |
*Number of participants.
†Number of patient groups.
‡Number of rehabilitation programmes.
%F, percent female; CABG, coronary artery bypass graft; EF, ejection fraction; MI, myocardial infarction; PCI, percutaneous coronary intervention; VR, valve repair/replacement.