From: Prosthetic heart valves in pregnancy: a systematic review and meta-analysis protocol
Criteria | Star allocated (maximum 9 stars)a |
---|---|
Selection | |
1) Representativeness of the exposed cohort | |
a) Population truly representative of pregnant women with prosthetic heart valves | ★ |
b) Somewhat representative of the population of pregnant women with prosthetic heart valves | ★ |
c) Selected group of users (for example, referral hospital patients) | - |
d) No description of the derivation of the cohort | - |
2) Selection of the non-exposed cohortb | |
a) Drawn from the same community as the exposed cohort | ★ |
b) Drawn from a different source | - |
c) No description of the derivation of the non-exposed cohort | - |
d) Not applicable | - |
3) Ascertainment of exposure | |
a) Secure record (for example, medical records) | ★ |
b) Structured interview | ★ |
c) Written self-report | - |
d) No description | - |
4) Demonstration that outcome of interest was not present at start of studyc | |
a) Yes | ★ |
b) No | - |
c) Not applicable | - |
Comparability | |
Comparability of cohorts on the basis of the design or analysis | |
a) Study controls for maternal age (select the most important factor) | ★ |
b) Study controls for any additional factor (type of valve, valve location, anticoagulation regimen) | ★ |
c) Not applicable | - |
Outcome | |
1) Assessment of outcome | |
a) Independent blind assessment | ★ |
b) Record linkage | ★ |
c) Self-report | - |
d) No description | - |
2) Was follow-up long enough for outcomes (as defined by study) to occur? | |
a) Yes | ★ |
b) No | - |
3) Adequacy of follow up of cohorts | |
a) Complete follow up (all subjects accounted for and no missing data) | ★ |
b) Subjects lost to follow-up unlikely to introduce bias - small number lost - ≥ 80% | ★ |
c) Follow-up rate < 80% | - |
d) No statement | - |