Table 9.
—[Section 4.1.1] Optimal Therapeutic INR Range: Higher Target vs 2 to 3119
Outcomes | No. of Participants, (Studies) Follow-up | Quality of the Evidence (GRADE) | Relative Effect (95% CI) | Anticipated Absolute Effectsa |
|
Risk With INR 2-3 | Risk Difference With INR 3-5 (95% CI) | ||||
Major hemorrhage per 100 patient-y, various definitions | 76,646 (17 studiesb), 1.8 y | Lowc,d due to risk of bias, dose-response gradient | RR 2.7 (1.8-3.9) | 6 per 1,000 | 10 more per 1,000 (from 5 more to 17 more) |
| |||||
Thromboembolism per 100 patient-y, various definitions | 835 (10 studiese) | Very lowf,g due to risk of bias, inconsistency | RR 0.9 (0.6-1.3) | Study population | |
|
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46 per 1,000 | 5 fewer per 1,000 (from 18 fewer to 14 more) | ||||
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Moderate | |||||
|
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50 per 1,000 | 5 fewer per 1,000 (from 20 fewer to 15 more) |
Time frame in days to months.
Six studies had a randomized controlled trial design.
The majority of studies (eight) were retrospective cohorts.
It is biologically plausible that with increased intensity there will be more bleeding.
One study had a randomized control design.
Three of four studies had a retrospective cohort design.
Thromboembolic events were more frequent with an INR of 2 to 3 in two studies, less frequent in one study, and similar in one study.