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电子烟对急性呼吸窘迫综合征患者住院结局的影响。

Impact of Vaping on Hospital Outcomes in Patients With Acute Respiratory Distress Syndrome.

作者信息

Tran Danny V, Sheets Nicholas W, Limas Jocelyn

机构信息

Internal Medicine, HCA Florida Trinity Hospital, Trinity, USA.

Trauma and Acute Care Surgery, Riverside Community Hospital, Riverside, USA.

出版信息

Cureus. 2025 Jul 31;17(7):e89138. doi: 10.7759/cureus.89138. eCollection 2025 Jul.

DOI:10.7759/cureus.89138
PMID:40896029
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12398337/
Abstract

Objective Introduced in the early 2000s, e-cigarettes and vaping have risen in popularity, leading to a notable increase in acute lung injury and the coining of electronic cigarette or vaping-associated lung injury (EVALI). Current studies have examined outcomes in EVALI specifically; however, data on the impact of vaping in acute respiratory distress syndrome (ARDS) is lacking. Thus, the objective of this study is to investigate the impact of vaping on hospital outcomes in patients with ARDS. Materials and methods This study is a retrospective chart review utilizing the Hospital Corporation of America (HCA) Healthcare Far West Division database. Unique patient encounters between January 1, 2016, and July 31, 2022, were included if they were associated with a diagnosis of acute respiratory distress syndrome (ARDS) and had documented vaping status. Pediatric patients under the age of 18 years were excluded. Due to the retrospective nature of the study, no interventions were performed. Outcomes were stratified and compared based on vaping status. Demographics and comorbidities were controlled for in the analysis. Measurements Patient demographics and medical comorbidities were extracted and analyzed. Key hospital outcomes of interest include use of non-invasive positive pressure ventilation (NIPPV), use of mechanical ventilation, hospital and intensive care unit (ICU) length of stay (LOS), and mortality. Statistical analysis of comorbidities was performed using chi-square analyses and Fisher's exact test between the two groups. Multinomial logistic regression was used to analyze the type of respiratory support required, while negative binomial regression was used to analyze hospital and ICU length of stay. Binary logistical regression with Firth correction was used to analyze differences in mortality. Statistical significance for all analyses was defined as a p-value of less than 0.05. Odds ratios were calculated with a 95% confidence interval. All analyses controlled for age, BMI, sex, medical comorbidities, and smoking status. Results A total of 269 patients were identified, of whom 42 vaped. Statistical analysis revealed no significant differences in demographics between those who vaped and those who did not. Fifty-seven patients required NIPPV, of whom 12 vaped. Eighty patients required mechanical ventilation, of whom seven vaped. Binary logistic regression with a Firth correction revealed a statistically significant decrease in odds (odds ratio {OR}: 0.377; 95% CI: 0.145, 0.979; p=0.045) of requiring mechanical ventilation in patients who vaped compared to those who did not. There were 15 mortalities, of whom four vaped. Binary logistic regression did not reveal statistical significance in mortality. The average hospital length of stay was 8.94 days, and the average length of stay (ICU LOS) was 5.48 days. Negative binomial regression revealed no statistically significant difference in both hospital and ICU LOS between patients who vaped and those who did not. Conclusion While statistical analysis did reveal a significantly decreased odds ratio of requiring mechanical ventilation in patients who vaped, the power of this and other findings was low, given a sample size of 42 who vaped. Despite its limitations, the study shares some preliminary insight into vaping and ARDS for future studies.

摘要

目的

电子烟和雾化产品于21世纪初问世,其受欢迎程度不断上升,导致急性肺损伤显著增加,并催生了“电子烟或雾化相关肺损伤(EVALI)”这一术语。目前的研究专门考察了EVALI的相关结果;然而,关于雾化对急性呼吸窘迫综合征(ARDS)影响的数据却很缺乏。因此,本研究的目的是调查雾化对ARDS患者医院治疗结果的影响。

材料与方法

本研究是一项回顾性图表审查,利用美国医院公司(HCA)医疗保健远西部部门数据库。纳入2016年1月1日至2022年7月31日期间与急性呼吸窘迫综合征(ARDS)诊断相关且有记录的雾化状态的独特患者病例。排除18岁以下的儿科患者。由于本研究的回顾性性质,未进行任何干预。根据雾化状态对结果进行分层和比较。分析中对人口统计学和合并症进行了控制。

测量

提取并分析患者人口统计学和医疗合并症信息。感兴趣的关键医院治疗结果包括无创正压通气(NIPPV)的使用、机械通气的使用、住院时间和重症监护病房(ICU)住院时间以及死亡率。使用卡方分析和两组间的Fisher精确检验对合并症进行统计分析。使用多项逻辑回归分析所需的呼吸支持类型,而使用负二项回归分析住院时间和ICU住院时间。使用经Firth校正的二元逻辑回归分析死亡率差异。所有分析的统计学显著性定义为p值小于0.05。计算比值比并给出95%置信区间。所有分析均对年龄、体重指数、性别、医疗合并症和吸烟状态进行了控制。

结果

共识别出269例患者,其中42例使用雾化产品。统计分析显示,使用雾化产品的患者和未使用雾化产品的患者在人口统计学上无显著差异。57例患者需要NIPPV,其中12例使用雾化产品。80例患者需要机械通气,其中7例使用雾化产品。经Firth校正的二元逻辑回归显示,与未使用雾化产品的患者相比,使用雾化产品的患者需要机械通气的几率在统计学上显著降低(比值比{OR}:0.377;95%置信区间:0.145,0.979;p = 0.045)。有15例死亡病例,其中4例使用雾化产品。二元逻辑回归未显示死亡率有统计学显著性差异。平均住院时间为8.94天,平均住院时间(ICU住院时间)为5.48天。负二项回归显示,使用雾化产品的患者和未使用雾化产品的患者在住院时间和ICU住院时间方面均无统计学显著性差异。

结论

虽然统计分析确实显示使用雾化产品的患者需要机械通气的几率显著降低,但鉴于使用雾化产品的样本量为42例,本研究及其他研究结果的效力较低。尽管存在局限性,但该研究为未来研究提供了一些关于雾化与ARDS的初步见解。

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