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Table 4 Effects of BZD and Z-drug properties, half-life, and polypharmacy on the elderly patients hospitalised for fall injuries

From: Association of benzodiazepine and Z-drug use with the risk of hospitalisation for fall-related injuries among older people: a nationwide nested case–control study in Taiwan

 

Cases

Controls

Unadjusted

Adjustedab

n = 2238

%

n = 8645

%

OR

95% CI

OR

95% CI

Elimination half-life of BZD

 Only long-acting BZD

160

7.2

502

5.8

1.35

1.12–1.62

1.41

1.16–1.71

 Only short-acting BZD

213

9.5

692

8.0

1.29

1.10–1.52

1.42

1.20–1.69

 Long- + short- acting BZD

299

13.4

950

11.0

1.33

1.15–1.53

1.61

1.37–1.89

 Non-users

1566

70.0

6501

75.2

1

 

1

 

Polypharmacy of BZD and Z-drugs

 Only one kind of BZD

238

10.6

781

9.0

1.30

1.11–1.52

1.40

1.19–1.65

 Two or more kinds of BZD

309

13.8

979

11.3

1.35

1.17–1.55

1.61

1.38–1.89

 Only Z-drugs

99

4.4

337

3.9

1.26

1.00–1.59

1.33

1.04–1.69

 One kind of BZD + Z-drugs

34

1.5

89

1.0

1.61

1.08–2.40

1.65

1.08–2.50

 Two or more kinds of BZD + Z-drugs

91

4.1

295

3.4

1.33

1.04–1.70

1.58

1.21–2.07

 Non-users

1467

65.6

6164

71.3

1

 

1

 
  1. aAdjusted for dementia, Parkinson’s disease, cerebrovascular disease, diabetes, hypertension, ischemia heart disease, antipsychotics, antidepressants, anticonvulsants, thiazide diuretics, opioids, Charlson comorbidity index, and number of outpatient services in the 180 days before the index date
  2. bSignificant results (p<0.05) are in italicize