Table 17: Study characteristics of prognostic studies.
Author, Year | Study Design & No. Patients | Patient Population | Mean Follow-up | Technique (tracer) | Outcomes | Viability Criteria |
---|---|---|---|---|---|---|
Desideri et al., 2005 (52) | Prospective cohort n=261 |
|
2.1y (median) | 13N- ammonia / FDG |
|
|
Feola et al., 2008 (53) | Prospective cohort n=93* |
|
342 ± 78 days Range: 110- 434 |
13N-ammonia / FDG |
|
|
Sawada et al., 2005 (54) | Prospective cohort n=61 |
|
4.3 ± 8.8 years | 13N-ammonia / FDG |
|
|
Rohatgi et al., 2001 (55) | Retrospective cohort n=99† |
|
25±9 months Range: 9-50 |
13N-ammonia / FDG |
|
|
Zhang et al., 2001 (56) | Cohort‡ n=123 |
|
26±10 months Range: 1-36 Median: 28 |
Tc-MIBI SPECT / FDG PET |
|
|
Di Carli et al., 1998 (57) | Cohort‡ n=93 |
|
3.8 years Range: 0-6.2 |
13N-ammonia / FDG |
|
|
vom Dahl et al., 1997 (58) | Prospective cohort n=161* |
|
29±6 months Range: 22-44 |
99Tc-MIBI SPECT / FDG PET |
|
|
Lee et al., 1994 (59) | Retrospective cohort n=129§ |
|
17±9 months | Rb-82 / FDG |
|
|
Eitzman et al., 1992 (60) | Retrospective cohort n=82║ |
|
12 months | 13N-ammonia / FDG or Rb-82 / FDG |
|
|
CAD refers to coronary artery disease; CCS, Canadian Cardiovascular Society; d, days; FDG, F-18-flurodeoxyglucose; LV, left ventricular; LVEF, left ventricular ejection fraction; mo, months; MI, myocardial infarction; NR, not reported; NYHA, New York Heart Association; revasc, revascularization; Rb-82, rubidium-82; yr, years
Consecutive patients
144 patients were eligible for inclusion, but only 99 were included as 46 were lost to follow-up.
Prospective or retrospective not reported in paper.
137 patients were enrolled in the study, but the analysis only includes 129 patients. Reasons for exclusion were: technically inadequate studies (2 patients); cardiac transplantation (4 patients); loss to follow-up (2 patients).
110 patients were eligible for the study, but complete data acquisition was not possible in 23 patients, 3 received heart transplants, and 2 had poor quality PET scans which provided inadequate data for inclusion in the study.