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

被引:36
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
相关论文
共 32 条
[1]   New evidence of risk factors for community-acquired pneumonia:: a population-based study [J].
Almirall, J. ;
Bolibar, I. ;
Serra-Prat, M. ;
Roig, J. ;
Hospital, I. ;
Carandell, E. ;
Agusti, M. ;
Ayuso, P. ;
Estela, A. ;
Torres, A. .
EUROPEAN RESPIRATORY JOURNAL, 2008, 31 (06) :1274-1284
[2]  
[Anonymous], 2013, Guidelines for ATC Classification and DDD assignment 2014, V17th
[3]   Use of disease risk scores in pharmacoepidemiologic studies [J].
Arbogast, Patrick G. ;
Ray, Wayne A. .
STATISTICAL METHODS IN MEDICAL RESEARCH, 2009, 18 (01) :67-80
[4]   Basic pharmacologic mechanisms involved in benzodiazepine tolerance and withdrawal [J].
Bateson, AN .
CURRENT PHARMACEUTICAL DESIGN, 2002, 8 (01) :5-21
[5]   RESPIRATORY CENTER OUTPUT FOLLOWING ZOPICLONE OR DIAZEPAM ADMINISTRATION IN PATIENTS WITH PULMONARY-DISEASE [J].
BEAUPRE, A ;
SOUCY, R ;
PHILLIPS, R ;
BOURGOUIN, J .
RESPIRATION, 1988, 54 (04) :235-240
[6]   Bias in Observational Studies of Prevalent Users: Lessons for Comparative Effectiveness Research From a Meta-Analysis of Statins [J].
Danaei, Goodarz ;
Tavakkoli, Mohammad ;
Hernan, Miguel A. .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2012, 175 (04) :250-262
[7]   Benzodiazepine use and risk of Alzheimer's disease: case-control study [J].
de Gage, Sophie Billioti ;
Moride, Yola ;
Ducruet, Thierry ;
Kurth, Tobias ;
Verdoux, Helene ;
Tournier, Marie ;
Pariente, Antoine ;
Begaud, Bernard .
BMJ-BRITISH MEDICAL JOURNAL, 2014, 349
[8]   Usage of benzodiazepines: A review [J].
Donoghue, John ;
Lader, Malcolm .
INTERNATIONAL JOURNAL OF PSYCHIATRY IN CLINICAL PRACTICE, 2010, 14 (02) :78-87
[9]   Use of Opioids or Benzodiazepines and Risk of Pneumonia in Older Adults: A Population-Based Case-Control Study [J].
Dublin, Sascha ;
Walker, Rod L. ;
Jackson, Michael L. ;
Nelson, Jennifer C. ;
Weiss, Noel S. ;
Von Korff, Michael ;
Jackson, Lisa A. .
JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2011, 59 (10) :1899-1907
[10]   Effects of repeated administration of zolpidem on sleep, diurnal and nocturnal respiratory function, vigilance, and physical performance in patients with COPD [J].
Girault, C ;
Muir, JF ;
Mihaltan, F ;
Borderies, P ;
DeLaGiclais, B ;
Verdure, A ;
SamsonDollfus, D .
CHEST, 1996, 110 (05) :1203-1211