S F Xue, J H Ren, L J Chen, X Q Zhao, T Yang, J D Hu
{"title":"[Therapeutic effects of glucocorticoids in patients with hematologic diseases with neutropenia and severe pneumonia classified by the PSI scores].","authors":"S F Xue, J H Ren, L J Chen, X Q Zhao, T Yang, J D Hu","doi":"10.3760/cma.j.cn121090-20240624-00234","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objective:</b> This study aimed to investigate the clinical value of glucocorticoids in patients with neutropenic severe pneumonia at moderate to high risk according to the Pneumonia Severity Index (PSI) in patients with hematologic diseases. <b>Methods:</b> Clinical data were collected from 534 patients at the Fujian Medical University Union Hospital from October 2016 to December 2018. We evaluated the changes in inflammatory cytokines, treatment failure, in-hospital mortality, and other outcomes, adjusting for potential confounders through propensity score matching. <b>Results:</b> Patients were categorized into glucocorticoids (<i>n</i>=176) and control (<i>n</i>=358) groups. The glucocorticoid group demonstrated higher levels of C-reactive protein, procalcitonin, and interleukin-6, alongside higher PSI scores. The differences in comorbidities diminished, except for inflammatory cytokine levels, with a notable reduction in inflammatory cytokines observed in the glucocorticoid group, after matching 125 pairs based on propensity scores. Late treatment failure was more prevalent in the glucocorticoid group (39.2% <i>vs</i> 24.8%, <i>P</i>=0.015), but this was primarily caused by radiographic progression. The incidences of respiratory failure, mechanical ventilation, and septic shock were similar between the groups. Logistic regression analyses revealed that glucocorticoids reduced the risk of treatment failure (<i>OR</i>=0.367, 95% <i>CI</i> 0.165-0.818, <i>P</i>=0.014). The 30-day in-hospital mortality rates were comparable (8.0% in glucocorticoids <i>vs</i> 7.2% in controls, <i>P</i>=0.811), with indications that glucocorticoids may exert a protective effect on mortality. The PSI score was determined as the sole independent risk factor for 30-day in-hospital mortality (<i>OR</i>=1.077, 95% <i>CI</i> 1.032-1.123, <i>P</i>=0.001). No evidence indicated that glucocorticoids increased the incidence of hyperglycemia, gastrointestinal bleeding, or 30-day infection recurrence. <b>Conclusion:</b> Glucocorticoids reduce inflammatory cytokine levels and are potentially related to decreased treatment failure and mortality in patients with neutropenic pneumonia classified as PSI Ⅳ and Ⅴ among hematological patients.</p>","PeriodicalId":24016,"journal":{"name":"Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi","volume":"45 11","pages":"1035-1042"},"PeriodicalIF":0.0000,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3760/cma.j.cn121090-20240624-00234","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: This study aimed to investigate the clinical value of glucocorticoids in patients with neutropenic severe pneumonia at moderate to high risk according to the Pneumonia Severity Index (PSI) in patients with hematologic diseases. Methods: Clinical data were collected from 534 patients at the Fujian Medical University Union Hospital from October 2016 to December 2018. We evaluated the changes in inflammatory cytokines, treatment failure, in-hospital mortality, and other outcomes, adjusting for potential confounders through propensity score matching. Results: Patients were categorized into glucocorticoids (n=176) and control (n=358) groups. The glucocorticoid group demonstrated higher levels of C-reactive protein, procalcitonin, and interleukin-6, alongside higher PSI scores. The differences in comorbidities diminished, except for inflammatory cytokine levels, with a notable reduction in inflammatory cytokines observed in the glucocorticoid group, after matching 125 pairs based on propensity scores. Late treatment failure was more prevalent in the glucocorticoid group (39.2% vs 24.8%, P=0.015), but this was primarily caused by radiographic progression. The incidences of respiratory failure, mechanical ventilation, and septic shock were similar between the groups. Logistic regression analyses revealed that glucocorticoids reduced the risk of treatment failure (OR=0.367, 95% CI 0.165-0.818, P=0.014). The 30-day in-hospital mortality rates were comparable (8.0% in glucocorticoids vs 7.2% in controls, P=0.811), with indications that glucocorticoids may exert a protective effect on mortality. The PSI score was determined as the sole independent risk factor for 30-day in-hospital mortality (OR=1.077, 95% CI 1.032-1.123, P=0.001). No evidence indicated that glucocorticoids increased the incidence of hyperglycemia, gastrointestinal bleeding, or 30-day infection recurrence. Conclusion: Glucocorticoids reduce inflammatory cytokine levels and are potentially related to decreased treatment failure and mortality in patients with neutropenic pneumonia classified as PSI Ⅳ and Ⅴ among hematological patients.
目的:根据血液病患者肺炎严重程度指数(PSI),探讨糖皮质激素在中性粒细胞减少型中高危重症肺炎患者中的临床应用价值。方法:收集2016年10月至2018年12月福建医科大学协和医院534例患者的临床资料。我们评估了炎症细胞因子、治疗失败、住院死亡率和其他结果的变化,并通过倾向评分匹配调整了潜在的混杂因素。结果:患者分为糖皮质激素组(176例)和对照组(358例)。糖皮质激素组显示出更高水平的c反应蛋白、降钙素原和白细胞介素-6,以及更高的PSI分数。在基于倾向评分匹配125对后,除了炎症细胞因子水平外,合并症的差异减少了,糖皮质激素组的炎症细胞因子显著减少。晚期治疗失败在糖皮质激素组更为普遍(39.2% vs 24.8%, P=0.015),但这主要是由影像学进展引起的。两组间呼吸衰竭、机械通气和感染性休克的发生率相似。Logistic回归分析显示,糖皮质激素降低了治疗失败的风险(OR=0.367, 95% CI 0.165-0.818, P=0.014)。住院30天死亡率具有可比性(糖皮质激素组为8.0%,对照组为7.2%,P=0.811),有迹象表明糖皮质激素可能对死亡率起保护作用。PSI评分被确定为30天住院死亡率的唯一独立危险因素(OR=1.077, 95% CI 1.032-1.123, P=0.001)。没有证据表明糖皮质激素会增加高血糖、胃肠道出血或30天感染复发的发生率。结论:糖皮质激素降低炎症细胞因子水平,并可能与血液患者中PSI(Ⅳ和Ⅴ)分类的中性粒细胞减少性肺炎患者的治疗失败和死亡率降低有关。