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. 2012 Jan 23;141(2 Suppl):e152S–e184S. doi: 10.1378/chest.11-2295

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

46 per 1,000 5 fewer per 1,000 (from 18 fewer to 14 more)

Moderate

50 per 1,000 5 fewer per 1,000 (from 20 fewer to 15 more)

See Table 1-3 legends for expansion of abbreviations.

a

Time frame in days to months.

b

Six studies had a randomized controlled trial design.

c

The majority of studies (eight) were retrospective cohorts.

d

It is biologically plausible that with increased intensity there will be more bleeding.

e

One study had a randomized control design.

f

Three of four studies had a retrospective cohort design.

g

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.