Authors [ref.] | Country | Design | Number of patients | Study patients | IM (%) | Bleeding rate (%) | Comments |
---|---|---|---|---|---|---|---|
Armbruster et al. [12] | USA | R | 458 | I | 16.6 | 14.4 | - |
Simon et al. [13] | USA | R | 395 | A | 2 | 16 | No serum creatinine levels were available within 1 week before and after the time of dabigatran initiation in 37% of patients. |
Kimmons et al. [14] | USA | R | 160 | I | 9a, 10b | 3.8 | aIndication and bdose. Only 61% of patients were newly initiated on dabigatran during the study period. |
McDonald et al. [15] | USA, Canada and Australia | R | 16,000 | A | 34.1–51.1 | 27.3–43.7 | PIM was judged solely by co-administration of medicines potentially increase bleeding riskc |
Larock et al. [16] | Belgium | P | 69 | I/A | 49 | 14.7 | MAI was used for assessing PIM |
Basaran et al. [17] | Turkey | P | 148 | A | 47 | NA | MAI was used for assessing PIM |
Chowdhry et al. [18] | Canada | R | 109 | I | 31.2 | NA | - |
The present study | Japan | R | 228 | I/A | I (11) vs. A (33) | 7.7 | Inappropriate prescription was judged according to the descriptions in prescribing information |