Time-Varying Effects of Glucocorticoid Treatment in Critically III Patients with Severe Fever with Thrombocytopenia Syndrome: An Inverse Probability of Treatment Weighting Analysis.

IF 4.2 2区 医学 Q2 IMMUNOLOGY
Journal of Inflammation Research Pub Date : 2025-04-18 eCollection Date: 2025-01-01 DOI:10.2147/JIR.S505421
Peng Xia, Yun Liu, Jun Wang, Haopeng Li, Yu Zhai, Baoyan Wang, Hanwen Tong, Weihong Ge, Chenxiao Jiang
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引用次数: 0

Abstract

Purpose: To evaluate the efficacy of glucocorticoid treatment in critically ill patients with severe fever with thrombocytopenia syndrome (SFTS) and to assess whether glucocorticoid use increases the risk of fungal infections.

Patients and methods: A retrospective cohort study was conducted involving confirmed SFTS patients from a tertiary hospital. After applying the Inverse Probability of Treatment Weights (IPTW), multivariable Cox regression and logistic regression analyses were utilized to assess the impact of glucocorticoids on the 28-day mortality rate and the risk of fungal infections. Additionally, landmark analysis and time-varying Cox regression were employed to evaluate the effects of glucocorticoids on mortality across different time intervals.

Results: The study included 112 patients with severe SFTS, comprising 67 patients in the glucocorticoid (GC) group and 45 in the non-glucocorticoid (non-GC) group. While glucocorticoid treatment did not significantly alter the overall 28-day mortality in severe SFTS (aHR 0.92, 95% CI 0.44-1.93, P = 0.828), it was associated with a notable reduction in mortality within the first 7 days of hospitalization (aHR 0.35, 95% CI 0.15-0.82, P = 0.016) and an increased mortality risk between days 7 and 28 (aHR 4.92, 95% CI 1.30-18.67, P = 0.019). Furthermore, glucocorticoid use was linked to a significantly higher risk of developing fungal infections (aOR 15.22, 95% CI 4.04-57.38, P < 0.001).

Conclusion: The effects of glucocorticoid treatment in severe SFTS patients vary depending on the disease stage, suggesting that the timing of glucocorticoid administration is crucial. Additionally, the increased risk of fungal infections warrants careful consideration when prescribing glucocorticoids in this population.

糖皮质激素治疗对重症发热伴血小板减少综合征的时变效果:治疗加权逆概率分析。
目的:评价糖皮质激素治疗重症发热伴血小板减少综合征(SFTS)的疗效,并评估糖皮质激素的使用是否会增加真菌感染的风险。患者和方法:对某三级医院确诊的SFTS患者进行回顾性队列研究。应用治疗权重逆概率(IPTW),采用多变量Cox回归和logistic回归分析评估糖皮质激素对28天死亡率和真菌感染风险的影响。此外,采用里程碑分析和时变Cox回归来评估糖皮质激素对不同时间间隔死亡率的影响。结果:纳入112例重度SFTS患者,其中糖皮质激素(GC)组67例,非糖皮质激素(non-GC)组45例。虽然糖皮质激素治疗没有显著改变严重SFTS患者28天的总死亡率(aHR 0.92, 95% CI 0.44-1.93, P = 0.828),但与住院前7天死亡率的显著降低(aHR 0.35, 95% CI 0.15-0.82, P = 0.016)和第7天至28天死亡风险的增加(aHR 4.92, 95% CI 1.30-18.67, P = 0.019)相关。此外,糖皮质激素的使用与发生真菌感染的风险显著增加有关(aOR 15.22, 95% CI 4.04-57.38, P < 0.001)。结论:糖皮质激素治疗重症SFTS患者的效果因疾病分期而异,提示糖皮质激素的给药时机至关重要。此外,真菌感染的风险增加值得仔细考虑,当处方糖皮质激素在这一人群。
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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来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
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