Association between Dexamethasone and Delirium in Critically Ill Patients: A Retrospective Cohort Study of a Large Clinical Database.

Zehao Wu, Huili Li, Kaihua Liao, Yun Wang
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引用次数: 4

Abstract

BACKGROUND Delirium is a common complication in intensive care unit (ICU) patients, and it can significantly increase the length of hospital stay and cost. Dexamethasone is widely used in various inflammatory diseases and must be used with caution in critically ill patients. Previous studies have shown that the effect of corticosteroid use on the development of delirium in critically ill patients is still controversial, and there is inconclusive conclusion about the effect of dexamethasone on delirium in such patients. Therefore, this study aimed to confirm the effect of dexamethasone use and the dose on the incidence of delirium and patient prognosis in critically ill patients through a large cohort study. METHODS A retrospective cohort study was conducted using data extracted from the Medical Information Mart for Intensive Care III database, which is a large and freely available database of all 46,476 patients who visited Beth Israel Deaconess Medical Center in Boston, Massachusetts, USA and were admitted to the ICU between 2001 and 2012. The primary outcome was the development of delirium, using multivariate logistic regression analysis to reveal the relationship between dexamethasone and delirium. Secondary endpoints were in-hospital mortality, ICU mortality, total length of stay, and length of ICU stay, and the relationship between dexamethasone and prognosis was assessed with Cox proportional hazards models. Propensity score matching with 1:1 grouping was used to eliminate the effect of confounders on both cohorts. The locally weighted scatter plot smoothing technique was used to investigate the dose correlation between dexamethasone and outcomes, subgroup analysis was used to account for heterogeneity, and different correction models and propensity matching analysis were used to eliminate potential confounders. RESULTS Finally, 38,509 patients were included, and 2204 (5.7%) used dexamethasone. No significant statistical difference was observed in basic demographic information after propensity score matching between the two study groups. A significantly higher incidence of delirium (5.0% versus 3.4%, P < 0.001), increased in-hospital mortality (14.9% versus 10.3%, P < 0.001), ICU mortality (9.0% versus 7.5%, P = 0.008), and longer length of stay and ICU stay were observed in patients taking dexamethasone compared with those not taking dexamethasone. Multivariate logistic and Cox regression analyses confirmed that dexamethasone was significantly associated with delirium (adjusted odds ratio = 1.48, 95% confidence interval [CI] = 1.09-2.00, P = 0.012), in-hospital mortality (adjusted hazard ratio = 1.19, 95% CI = 1.02-1.40, P = 0.032), and ICU mortality (adjusted hazard ratio = 1.62, 95% CI = 1.22-2.15, P = 0.001). Compared with critically ill patients using high-dose dexamethasone, the risk of delirium was lower in the dose less than the 10 mg group, and patients using 10-14 mg may be associated with a lower risk of in-hospital death and the least ICU mortality, length of hospital stay, and ICU stay. CONCLUSIONS This study demonstrated that the use of dexamethasone in critically ill patients exacerbated the occurrence of delirium while increasing the risk of in-hospital death, ICU death, and length of hospital stay, with a lower risk of delirium and a shorter total length of hospital stay with low-dose dexamethasone than with larger doses.
地塞米松与危重患者谵妄的关系:大型临床数据库的回顾性队列研究。
背景:谵妄是重症监护病房(ICU)患者的常见并发症,可显著增加住院时间和费用。地塞米松广泛用于各种炎症性疾病,危重患者必须谨慎使用。既往研究表明,皮质类固醇对危重患者谵妄发展的影响仍存在争议,地塞米松对危重患者谵妄的影响尚无定论。因此,本研究旨在通过大队列研究,证实地塞米松的使用及剂量对危重患者谵妄发生率及患者预后的影响。方法采用回顾性队列研究,数据取自美国马萨诸塞州波士顿Beth Israel Deaconess医疗中心2001 - 2012年ICU收治的46,476例重症监护医学信息市场III数据库,该数据库是一个大型免费数据库。主要结局为谵妄的发生,采用多因素logistic回归分析揭示地塞米松与谵妄的关系。次要终点为住院死亡率、ICU死亡率、总住院时间和ICU住院时间,采用Cox比例风险模型评估地塞米松与预后的关系。采用倾向评分匹配1:1分组来消除混杂因素对两个队列的影响。采用局部加权散点图平滑技术研究地塞米松剂量与预后之间的相关性,采用亚组分析解释异质性,采用不同的校正模型和倾向匹配分析消除潜在的混杂因素。结果最终纳入38509例患者,2204例(5.7%)使用地塞米松。倾向评分匹配后,两组基本人口学信息无统计学差异。与未服用地塞米松的患者相比,服用地塞米松的患者谵妄发生率(5.0%比3.4%,P < 0.001)、住院死亡率(14.9%比10.3%,P < 0.001)、ICU死亡率(9.0%比7.5%,P = 0.008)、住院时间和ICU住院时间均显著增加。多因素logistic和Cox回归分析证实,地塞米松与谵妄(校正优势比= 1.48,95%可信区间[CI] = 1.09-2.00, P = 0.012)、住院死亡率(校正风险比= 1.19,95% CI = 1.02-1.40, P = 0.032)和ICU死亡率(校正风险比= 1.62,95% CI = 1.22-2.15, P = 0.001)显著相关。与使用高剂量地塞米松的危重患者相比,剂量小于10 mg组谵妄风险较低,使用10-14 mg的患者院内死亡风险较低,ICU死亡率、住院时间和ICU住院时间最短。结论:地塞米松加重危重患者谵妄的发生,增加院内死亡、ICU死亡风险和住院时间,低剂量地塞米松比大剂量地塞米松谵妄发生风险低,总住院时间短。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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