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Table 4 Summary of previous and present studies investigating inappropriate prescriptions of dabigatran

From: Impact of Pharmacists’ audit on improving the quality of prescription of dabigatran etexilate methanesulfonate: a retrospective study

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

  1. R retrospective chart review, P prospective study, I inpatients, A ambulant patients, MAI medication appropriate index, MAI is a tool designed to measure appropriateness of prescribing for people aged 65 years and older using 10 criteria comprising indication, choice, dosage, modalities and practicability of administration, drug-drug interaction and cost-effectiveness. [16, 17], IM inappropriate medication PIM potentially inappropriate medication, NA not available
  2. cselective serotonin reuptake inhibitor, non-steroidal anti-inflammatory drug, oral corticosteroids, systemic azole antifungals, macrolide antibiotics, HIV protease inhibitors, cyclosporine, dronedarone, tacrolimus, verapamil, amiodarone and quinidine