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. 2017 Apr 10;189(14):E519-E529.
doi: 10.1503/cmaj.160126.

Risk of pneumonia associated with incident benzodiazepine use among community-dwelling adults with Alzheimer disease

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Risk of pneumonia associated with incident benzodiazepine use among community-dwelling adults with Alzheimer disease

Heidi Taipale et al. CMAJ. .

Abstract

Background: Knowledge regarding whether benzodiazepines and similarly acting non-benzodiazepines (Z-drugs) are associated with an increased risk of pneumonia among older adults is lacking. We sought to investigate this association among community-dwelling adults with Alzheimer disease, a condition in which both sedative/hypnotic use and pneumonia are common.

Methods: We obtained data on all community-dwelling adults with a recent diagnosis of Alzheimer disease in Finland (2005-2011) from the Medication use and Alzheimer disease (MEDALZ) cohort, which incorporates national registry data on prescriptions, reimbursement, hospital discharges and causes of death. Incident users of benzodiazepines and Z-drugs were identified using a 1-year washout period and matched with nonusers using propensity scores. The association with hospital admission or death due to pneumonia was analyzed with the Cox proportional hazards model and adjusted for use of other psychotropic drugs in a time-dependent manner.

Results: Among 49 484 eligible participants with Alzheimer disease, 5232 taking benzodiazepines and 3269 taking Z-drugs were matched 1:1 with those not taking these drugs. Collectively, use of benzodiazepines and Z-drugs was associated with an increased risk of pneumonia (adjusted hazard ratio [HR] 1.22, 95% confidence interval [CI] 1.05-1.42). When analyzed separately, benzodiazepine use was significantly associated with an increased risk of pneumonia (adjusted HR 1.28, 95% CI 1.07-1.54), whereas Z-drug use was not (adjusted HR 1.10, 95% CI 0.84-1.44). The risk of pneumonia was greatest within the first 30 days of benzodiazepine use (HR 2.09, 95% CI 1.26-3.48).

Interpretation: Benzodiazepine use was associated with an increased risk of pneumonia among patients with Alzheimer disease. Risk of pneumonia should be considered when weighing the benefits and risks of benzodiazepines in this population.

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Conflict of interest statement

Competing interests: Heidi Taipale, Antti Tanskanen and Jari Tiihonen have participated in research projects funded by Janssen with grants paid to the institution where they were employed. Jari Tiihonen received consultant fees from Lundbeck, Organon, Janssen-Cilag, Eli Lilly, AstraZeneca, F. Hoffman-La Roche and Bristol-Myers Squibb. He also received fees for expert opinions from Bristol-Myers Squibb and GlaxoSmithKline; lecture fees from Janssen-Cilag, Bristol-Myers Squibb, Eli Lilly, Pfizer, Lundbeck, GlaxoSmithKline, AstraZeneca and Novartis; and a grant from the Stanley Foundation. He is a member of advisory board in AstraZeneca, Janssen-Cilag, and Otsuka. Marjaana Koponen has received personal research grants from Oy H. Lundbeck Ab foundation. No other conflicts of interest were declared.

Figures

Figure 1:
Figure 1:
Flow chart showing selection of participants for the study. AD = Alzheimer disease, BZD = benzodiazepine, Z-drug = non-benzodiazepine similar in activity to benzodiazepine, BZDR = benzodiazepine and/or Z-drug.
Figure 2:
Figure 2:
Process of propensity score matching for participants using benzodiazepines (BZDs) to those not using them and particpants using Z-drugs (non-benzodiazepines similar in activity to benzodiazepines) to those not using them, by time-since-diagnosis of Alzheimer disease (AD). PS = propensity score.

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