Suppr超能文献

苯二氮䓬类药物和Z类药物的使用与慢性肾脏病患者肺炎风险:一项基于人群的巢式病例对照研究。

Benzodiazepine and Z-drug use and risk of pneumonia in patients with chronic kidney disease: A population-based nested case-control study.

作者信息

Wang Meng-Ting, Wang Yun-Han, Chang Hsin-An, Tsai Chen-Liang, Yang Ya-Sung, Lin Chen Wei, Kuo Cheng-Chin, Hsu Yu-Juei

机构信息

School of Pharmacy, National Defense Medical Center, Taipei, Taiwan, Republic of China.

Department of Psychiatry, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, Republic of China.

出版信息

PLoS One. 2017 Jul 10;12(7):e0179472. doi: 10.1371/journal.pone.0179472. eCollection 2017.

Abstract

BACKGROUND

Concerns were raised about pneumonia development from benzodiazepines (BZDs) and Z-drugs, but direct evidence is limited, conflicting and without examining the highly susceptible patients with chronic kidney disease (CKD) nor specifying the risk for different drug utilizations. This study aimed to investigate whether use of BZDs and Z-drugs was each associated with an increased risk of pneumonia in a CKD population.

METHODS

We performed a nested case-control study of 36,880 CKD patients analyzing the Taiwan National Health Insurance Database between 01/1/2000 and 12/31/2011. Among the study cohort, we identified 4,533 cases of pneumonia based on validated disease codes, chest x-ray examination, and prescriptions of respiratory antibiotics, and randomly selected 16,388 controls from risk sets, matched by sex, age, and number of CKD-related hospitalizations. All prescription filling records of BZDs and Z-drugs in the year before the event/index date were analyzed for cases and controls. Conditional logistic regressions were performed to estimate the odds ratios (ORs).

RESULTS

Current use of BZDs was associated with a 1.31-fold (95% CI, 1.18-1.26) increased risk of pneumonia compared to nonuse, but not for recent and past use. The risk from current BZD use was confined to new initiation (adjusted OR, 2.47; 95% CI, 2.02-3.03) or use for ≤ 30 days, and elevated to 2.88-fold (95% CI, 1.87-4.42) with parenteral administration. New initiation and current short-term use of Z-drugs was associated with a 2.94-fold (95% CI, 1.65-5.26) and 1.75-fold (95% CI, 1.13-2.72) increased risk of pneumonia, respectively. The findings were robust to adoption of a case-crossover study that analyzed cases only.

CONCLUSIONS

Use of BZRAs is associated with an increased risk of pneumonia in CKD patients, especially for patients newly initiating BZDs or Z-drugs or those injected with BZDs. Physicians should exercise cautions for signs of pneumonia when prescribing BZDs or Z-drugs to CKD patients.

摘要

背景

人们对苯二氮䓬类药物(BZDs)和Z类药物引发肺炎表示担忧,但直接证据有限且相互矛盾,同时未对慢性肾脏病(CKD)的高危患者进行研究,也未明确不同药物使用情况的风险。本研究旨在调查在CKD人群中,使用BZDs和Z类药物是否各自与肺炎风险增加相关。

方法

我们对36880例CKD患者进行了一项巢式病例对照研究,分析了2000年1月1日至2011年12月31日期间的台湾全民健康保险数据库。在研究队列中,我们根据经过验证的疾病编码、胸部X光检查和呼吸抗生素处方确定了4533例肺炎病例,并从风险集合中随机选取16388例对照,按照性别、年龄和CKD相关住院次数进行匹配。对病例和对照在事件/索引日期前一年的所有BZDs和Z类药物处方记录进行分析。进行条件逻辑回归以估计比值比(ORs)。

结果

与未使用相比,当前使用BZDs与肺炎风险增加1.31倍(95%CI,1.18 - 1.26)相关,但近期和过去使用则不然。当前使用BZDs的风险仅限于新开始使用(调整后的OR,2.47;95%CI,2.02 - 3.03)或使用≤30天,且经肠胃外给药时风险升高至2.88倍(95%CI,1.87 - 4.42)。新开始使用和当前短期使用Z类药物分别与肺炎风险增加2.94倍(95%CI,1.65 - 5.26)和1.75倍(95%CI,1.13 - 2.72)相关。这些发现对于仅分析病例的病例交叉研究而言是可靠的。

结论

使用苯二氮䓬类受体激动剂(BZRAs)与CKD患者肺炎风险增加相关,尤其是新开始使用BZDs或Z类药物的患者或接受BZDs注射的患者。医生在给CKD患者开具BZDs或Z类药物时应警惕肺炎迹象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a9/5503235/e606f8b92cd7/pone.0179472.g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验