Table 2.
First author, publication year | Representativeness of the exposed cohort | Selection of the unexposed cohort | Ascertainment of exposure | Outcome of interest not present at start of study | Control for important factor or additional factor† | Assessment of outcome | Follow-up long enough for outcomes to occur‡ | Adequacy of follow-up of cohorts§ | Quality |
---|---|---|---|---|---|---|---|---|---|
McBane et al. (2016) | ☆ | ☆ | ☆ | ☆ | ☆ | ☆ | ☆ | ☆ | Low risk of bias |
Angelini et al. (2018) | ☆ | ☆ | ☆ | ☆ | ☆ | ☆ | — | ☆ | Moderate risk of bias |
Ageno et al. (2016) | ☆ | ☆ | ☆ | ☆ | ☆☆ | — | ☆ | ☆ | Low risk of bias |
*A study could be awarded a maximum of one star for each item except for the item control for important factor or additional factor. The definition/explanation of each column of the Newcastle–Ottawa scale is available from http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp.
†A maximum of two stars could be awarded for this item. Studies that controlled for anticoagulation treatment for at least 3 months received one star, whereas studies that controlled for other important confounders received an additional star.
‡A cohort study with a follow-up time >6 months was assigned one star.
§A cohort study with a follow-up rate >75% was assigned one star.