类固醇是卡波西肉瘤-免疫重建炎症综合征和HIV感染死亡率的危险因素

M. Fernández-Sánchez, M. Iglesias, Y. Ablanedo-Terrazas, C. Ormsby, C. Alvarado-de la Barrera, G. Reyes-Terán
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引用次数: 24

摘要

目的:探讨hiv感染者卡波西肉瘤相关免疫重建炎症综合征(KS-IRIS)和死亡率与糖皮质激素使用的关系。设计:病例对照研究。方法:我们回顾了145例接受抗逆转录病毒治疗的hiv相关卡波西肉瘤患者的医疗记录。通过单因素和多因素分析探讨不同变量与KS-IRIS和卡波西肉瘤相关死亡率的关系。主要的暴露是糖皮质激素的使用。我们还比较了接受糖皮质激素治疗的患者与未接受糖皮质激素治疗的患者到KS-IRIS的时间和死亡时间,以及接受KS-IRIS治疗的患者与未接受KS-IRIS治疗的患者的死亡时间。结果:145例患者中有60例(41.4%)接受糖皮质激素治疗或怀疑为乙氏肺囊虫肺炎。50人有KS-IRIS(37%)。有KS-IRIS的患者使用糖皮质激素的频率高于无KS-IRIS的患者(54.9% vs. 36.47%, P = 0.047)。卡波西氏肉瘤相关死亡17例(11.7%),该组糖皮质激素使用频率更高(76.47比36.7%,P = 0.003)。糖皮质激素的使用是死亡率的危险因素(调整后的优势比= 4.719,95%可信区间= 1.383-16.103,P = 0.0132),并且与较短的KS-IRIS周期(P = 0.03)和死亡(P = 0.0073)相关。KS-IRIS是死亡率的危险因素(P = 0.049)。结论:在hiv感染者中,糖皮质激素的使用是KS-IRIS和卡波西氏肉瘤相关死亡率的危险因素。此外,KS-IRIS是死亡的危险因素。因此,在这一人群中使用糖皮质激素需要根据个体化的风险-收益分析进行仔细考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Steroids are a risk factor for Kaposi's sarcoma-immune reconstitution inflammatory syndrome and mortality in HIV infection
Objectives:To investigate the association between Kaposi's sarcoma-associated immune reconstitution inflammatory syndrome (KS-IRIS) and mortality, with the use of glucocorticoids in HIV-infected individuals. Design:Case–control study. Methods:We reviewed the medical records of 145 individuals with HIV-associated Kaposi's sarcoma receiving antiretroviral therapy. The association of different variables with KS-IRIS and Kaposi's sarcoma-related mortality was explored by univariate and multivariate analyses. The main exposure of interest was the use of glucocorticoids. We also compared the time to KS-IRIS and the time to death of individuals treated with glucocorticoids vs. those nontreated with glucocorticoids, and the time to death of individuals with KS-IRIS vs. those without KS-IRIS by hazards regression. Results:Sixty of 145 individuals received glucocorticoids (41.4%) for the management or suspicion of Pneumocystis jirovecii pneumonia. Fifty individuals had KS-IRIS (37%). The use of glucocorticoids was more frequent in individuals with KS-IRIS than in those without KS-IRIS (54.9 vs. 36.47%, P = 0.047). Kaposi's sarcoma-related mortality occurred in 17 cases (11.7%), and glucocorticoid use was more frequent in this group (76.47 vs. 36.7%, P = 0.003). Glucocorticoid use was a risk factor for mortality (adjusted odds ratio = 4.719, 95% confidence interval = 1.383–16.103, P = 0.0132), and was associated with shorter periods to KS-IRIS (P = 0.03) and death (P = 0.0073). KS-IRIS was a risk factor for mortality (P = 0.049). Conclusion:In HIV-infected individuals, the use of glucocorticoids is a risk factor for KS-IRIS and Kaposi's sarcoma-associated mortality. In addition, KS-IRIS is a risk factor for mortality. Therefore, glucocorticoid administration in this population requires careful consideration based on individualized risk–benefit analysis.
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