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Table 1 Selected tracts of the 804 cases of upper gastrointestinal complications and 12,787 controls

From: Oral bisphosphonates do not increase the risk of severe upper gastrointestinal complications: a nested case–control study

 

Case patients

Controls

p-value*

BPs exposure

   

  No use

709 (88.2%)

11,345 (88.7%)

0.6029

  Current use

38 (4.7%)

643 (5.0%)

 

  Past use

57 (7.1%)

799 (6.2%)

 

  Type prescribed during the current period

  

  Alendronate

30 (79.0%)

412 (64.1%)

0.0620

  Risedronate

8 (21.0%)

231 (35.9%)

 

  Regimen prescribed during the current period

  

  Weekly

37 (97.4%)

631 (98.1%)

0.7376

  Daily

1 (2.6%)

12 (1.9%)

 

Use of other medicaments

   

  Antidepressants

139 (17.3%)

1,841 (14.4%)

0.0242

  Antithrombotic

240 (29.9%)

3,174 (24.8%)

0.0014

  Gastroprotective agents

211 (26.2%)

1,993 (15.6%)

<0.0001

  Corticosteroids

65 (8.1%)

533 (4.2%)

<0.0001

  Statins

41 (5.1%)

724 (5.7%)

0.5021

  Calcium channel blockers

105 (13.1%)

1,548 (12.1%)

0.4223

  Other antihypertensive drugs

371 (46.1%)

5,294 (41.4%)

0.0082

  Nonsteroidal antiinflammatory drugs

170 (21.1%)

1,529 (12.0%)

<0.0001

Co-morbidity #

   

  0

629 (78.2%)

11,531 (90.2%)

<0.0001

  ≥1

175 (21.8%)

1,256 (9.8%)

  1. BPs: Bisphosphonates.
  2. A patient was defined current user if at least one prescription of BPs was refilled within 30 days or less prior the index date. A patient was defined past user if at least one prescription of BPs was refilled later than 31 days prior the index date. No users were patients who during the entire observational period did not experience BPs dispensation.
  3. Measured over the 60-day period prior the index date.
  4. #Charlson comorbidity index score measured in the six months prior the entry into the cohort and during the entire observational period.
  5. *According to chi-square test.