The Use of Benzodiazepine Receptor Agonists and the Risk of Hospitalization for Pneumonia A Nationwide Population-Based Nested Case-Control Study

被引:34
作者
Chen, Tien-Yu [1 ,2 ]
Winkelman, John W. [9 ,10 ,11 ]
Mao, Wei-Chung [1 ,2 ,3 ]
Liu, Chia-Lin [6 ]
Hsu, Chung-Yao [7 ,8 ]
Wu, Chi-Shin [4 ,5 ]
机构
[1] Triserv Gen Hosp, Dept Psychiat, Taipei, Taiwan
[2] Natl Def Med Ctr, Sch Med, Taipei, Taiwan
[3] Natl Yang Ming Univ, Inst Brain Sci, Taipei, Taiwan
[4] Natl Taiwan Univ Hosp, Dept Psychiat, 7 Chung Shan South Rd, Taipei 10002, Taiwan
[5] Natl Taiwan Univ, Coll Med, 7 Chung Shan South Rd, Taipei 10002, Taiwan
[6] En Chu Kong Hosp, Dept Family Med, New Taipei, Taiwan
[7] Kaohsiung Med Univ Hosp, Dept Neurol, Kaohsiung, Taiwan
[8] Kaohsiung Med Univ, Coll Med, Kaohsiung, Taiwan
[9] Massachusetts Gen Hosp, Dept Psychiat, Boston, MA 02114 USA
[10] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[11] Harvard Med Sch, Boston, MA USA
关键词
benzodiazepine-receptor agonist; midazolam; pneumonia; PULMONARY-DISEASE; SURVIVAL ANALYSIS; OLDER-ADULTS; MORTALITY; COPD; METAANALYSIS; DIAZEPAM; ZOLPIDEM; TAIWAN; SCORES;
D O I
10.1016/j.chest.2017.07.030
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
BACKGROUND: The relationship between the use of benzodiazepine-receptor agonists (BZRAs) and the risk of hospitalization for pneumonia remains inconclusive. This study aimed to explore the association between BZRA use and hospitalization for pneumonia in a general population. METHODS: This population-based nested case-control study used Taiwan's National Health Insurance Research Database between 2002 and 2012. We included only new users who did not have any BZRA prescriptions on record in the preceding 2 years and identified 12,002 subjects who were hospitalized for pneumonia (International Classification of Diseases, Ninth Revision codes 480-486, and 507) and 12,002 disease risk score-matched control subjects. A logistic regression model was used to determine the association of BZRA use and hospitalization for pneumonia. The exposure date, dose-response relationship, and class of BZRAs were comprehensively assessed. RESULTS: Current BZRA exposure was associated with hospitalization for pneumonia (adjusted OR [aOR], 1.86; 95% CI, 1.75-1.97). Benzodiazepine hypnotic agents (aOR, 2.42; 95% CI, 2.16-2.71) had a higher risk of pneumonia than did benzodiazepine anxiolytic agents (aOR, 1.53; 95% CI, 1.44-1.63) or nonbenzodiazepine hypnotic agents (aOR, 1.60; 95% CI, 1.46-1.76). The pneumonia risk was increased with ultrashort-acting and short-to intermediate-acting agents, a higher defined daily dose, and the number of BZRAs used. Among individual BZRAs examined, midazolam had a higher risk (aOR, 5.77; 95% CI, 4.31-7.73) of hospitalization for pneumonia than did the others. CONCLUSIONS: This study suggests that there is a dose-response relationship between current BZRA use and the risk of hospitalization for pneumonia. In addition, benzodiazepine hypnotic agents, especially midazolam, present a greater risk of hospitalization for pneumonia. These findings reinforce the importance of a careful analysis of the benefits vs the risks of BZRA use.
引用
收藏
页码:161 / 171
页数:11
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