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The new england journal of medicine

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Dabigatran in Atrial Fibrillation<br />

1.0<br />

0.05<br />

Cumulative Hazard Rate<br />

0.8<br />

0.6<br />

0.4<br />

0.2<br />

0.04<br />

0.03<br />

0.02<br />

0.01<br />

Dabigatran,<br />

110 mg<br />

Warfarin<br />

Dabigatran,<br />

150 mg<br />

0.00<br />

0 6 12 18 24 30<br />

No. at Risk<br />

Warfarin<br />

Dabigatran, 110 mg<br />

Dabigatran, 150 mg<br />

0.0<br />

0 6 12 18 24 30<br />

6022<br />

6015<br />

6076<br />

5862<br />

5862<br />

5939<br />

5718<br />

5710<br />

5779<br />

Months<br />

4593<br />

4593<br />

4682<br />

2890<br />

2945<br />

3044<br />

1322<br />

1385<br />

1429<br />

Figure 1. Cumulative Hazard Rates for the AUTHOR: Primary Connolly Outcome <strong>of</strong> Stroke or RETAKE Systemic 1st Embolism, According to Treatment<br />

Group.<br />

ICM<br />

REG F FIGURE: 1 <strong>of</strong> 2<br />

2nd<br />

3rd<br />

CASE<br />

Revised<br />

EMail<br />

Line 4-C<br />

SIZE<br />

H/T<br />

Combo<br />

AUTHOR, PLEASE NOTE:<br />

Figure has been redrawn and type has been reset.<br />

Please check carefully.<br />

was associated with a trend toward ARTIST: an increased ts<br />

Enon<br />

risk <strong>of</strong> major bleeding (P = 0.052) and also with<br />

increased risks <strong>of</strong> gastrointestinal, minor, and any<br />

bleeding. <strong>The</strong> net clinical benefit was almost identical<br />

for the two doses.<br />

JOB: 36112 ISSUE: 09-17-09<br />

Adverse Events and Liver Function<br />

<strong>The</strong> only adverse effect that was significantly more<br />

common with dabigatran than with warfarin was<br />

dyspepsia (Table 4). Dyspepsia occurred in 348<br />

patients (5.8%) in the warfarin group and in 707<br />

patients (11.8%) and 688 patients (11.3%) in the<br />

110-mg and 150-mg dabigatran groups, respectively<br />

(P

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