Isbister Geoffrey K, Downes Fiona, Sibbritt David, Dawson Andrew H, Whyte Ian M
Discipline of Clinical Pharmacology, University of Newcastle, Australia.
Crit Care Med. 2004 Jan;32(1):88-93. doi: 10.1097/01.CCM.0000104207.42729.E4.
To characterize the frequency of aspiration pneumonitis in an unselected population of overdose patients and, further, to identify factors that predispose to aspiration pneumonitis and the outcomes of patients with aspiration pneumonitis compared with those without.
Retrospective cohort study.
Toxicology unit of a tertiary referral hospital.
All poisoning admissions.
A total of 71 of 4,562 poisoning admissions to the Hunter Area Toxicology Service between January 1997 and October 2002 had definite aspiration pneumonitis (1.6%; 95% confidence interval, 1.2-2.0). Older age, Glasgow Coma Score of <15, spontaneous emesis, seizures, delayed presentation to hospital, and ingestion of tricyclic antidepressants were associated with an increased risk of aspiration pneumonitis. Paracetamol poisoning and female sex were associated with a decreased risk of aspiration pneumonitis with univariate analysis. Ingestion of alcohol, benzodiazepines, antipsychotics, and administration of activated charcoal were not associated with aspiration pneumonitis. A logistic regression model for predicting aspiration pneumonitis contained seven predictors: age, sex, Glasgow Coma Score of <15 (odds ratio, 3.14; 95% confidence interval, 1.87-5.27), emesis (odds ratio, 4.17; 95% confidence interval, 2.44-7.13), seizure, tricyclic antidepressant ingestion, and time from ingestion to presentation (delay of >24 hrs [odds ratio, 4.42; 95% confidence interval, 2.42-8.10]). The mortality for patients with aspiration pneumonitis was 8.5% compared with 0.4% for those without (odds ratio, 23; 95% confidence interval, 9-60; p <.0001), and they had a significantly higher intensive care unit admission rate. The median length of stay of patients with aspiration pneumonitis was 126 hrs (interquartile range, 62-210 hrs) compared with 14.7 hrs (interquartile range, 7-23 hrs) in patients without (p <.0001).
Our study has shown a number of risk factors in overdose patients that are associated with aspiration pneumonitis that may allow the early identification of these patients for appropriate observation and management. Patients with aspiration pneumonitis have a significantly increased mortality and length of stay in the hospital.
描述未经过筛选的过量用药患者群体中吸入性肺炎的发生率,并进一步确定易患吸入性肺炎的因素,以及比较发生吸入性肺炎患者与未发生者的预后情况。
回顾性队列研究。
一家三级转诊医院的毒理学科室。
所有中毒入院患者。
1997年1月至2002年10月期间,亨特地区毒理学服务中心收治的4562例中毒患者中,共有71例确诊为吸入性肺炎(1.6%;95%置信区间为1.2 - 2.0)。年龄较大、格拉斯哥昏迷评分<15分、自发呕吐、癫痫发作、延迟就医以及摄入三环类抗抑郁药与吸入性肺炎风险增加相关。单因素分析显示,对乙酰氨基酚中毒和女性与吸入性肺炎风险降低相关。饮酒、服用苯二氮䓬类药物、抗精神病药物以及使用活性炭与吸入性肺炎无关。预测吸入性肺炎的逻辑回归模型包含七个预测因素:年龄、性别、格拉斯哥昏迷评分<15分(比值比为3.14;95%置信区间为1.87 - 5.27)、呕吐(比值比为4.17;95%置信区间为2.44 - 7.13)、癫痫发作、摄入三环类抗抑郁药以及从摄入到就医的时间(延迟>24小时[比值比为4.42;95%置信区间为2.42 - 8.10])。发生吸入性肺炎患者的死亡率为8.5%,未发生者为0.4%(比值比为23;95%置信区间为9 - 60;p<.0001),且前者重症监护病房收治率显著更高。发生吸入性肺炎患者的中位住院时间为126小时(四分位间距为62 - 210小时),未发生者为14.7小时(四分位间距为7 - 23小时)(p<.0001)。
我们的研究显示,过量用药患者中存在一些与吸入性肺炎相关的危险因素,这可能有助于早期识别这些患者以便进行适当的观察和管理。发生吸入性肺炎的患者死亡率和住院时间显著增加。