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血液恶性肿瘤合并肺毛霉菌病患者早期死亡的危险因素。

Risk factors for early mortality in haematological malignancy patients with pulmonary mucormycosis.

机构信息

Department of Infectious Diseases, Infection Control and Employee Health, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

出版信息

Mycoses. 2014 Jan;57(1):49-55. doi: 10.1111/myc.12101. Epub 2013 Jun 12.

Abstract

Pulmonary mucormycosis (PM) is a life-threatening opportunistic mycosis with a variable clinical evolution and few prognostic markers for outcome assessment. Several clinical risk factors for poor outcome present at the diagnosis of PM were analyzed in 75 consecutive hematology patients from 2000-2012. Significant variables (P < 0.1) were entered into a multivariate Cox-proportional hazard regression model adjusting for baseline APACHE II to identify independent risk factors for mortality within 28 days. Twenty-eight of 75 patients died within 4-week follow up. A lymphocyte count < 100/mm³ at the time of diagnosis (adjusted hazard ratio 4.0, 1.7-9.4, P = 0.01) and high level of lactate dehydrogenase (AHR 3.7, 1.3-10.2, P = 0.015) were independent predictors along with APACHE II score for 28-day mortality. A weighted risk score based on these 3 baseline variables accurately identified non-surviving patients at 28 days (area under the receiver-operator curve of 0.87, 0.77-0.93, P < 0.001). A risk score > 22 was associated with 8-fold high rates of mortality (P < 0.0001) within 28 days of diagnosis and median survival of 7 days versus ≥28 days in patients with risk scores ≤22. We found that APACHE II score, severe lymphocytopenia and high LDH levels at the time of PM diagnosis were independent markers for rapid disease progression and death.

摘要

肺毛霉菌病(PM)是一种危及生命的机会性真菌感染,其临床演变具有多变性,预后评估的标志物较少。本研究分析了 2000 年至 2012 年期间 75 例连续血液科患者在确诊 PM 时的多个与预后不良相关的临床危险因素。对有统计学意义的变量(P < 0.1)进行单因素分析,再通过多因素 Cox 比例风险回归模型进行分析,校正基线急性生理与慢性健康评分(APACHE II),以明确 28 天内死亡的独立危险因素。75 例患者中有 28 例在 4 周随访内死亡。诊断时淋巴细胞计数 < 100/mm³(校正风险比 4.0,1.7-9.4,P = 0.01)和乳酸脱氢酶水平较高(AHR 3.7,1.3-10.2,P = 0.015),与 APACHE II 评分一起是 28 天死亡率的独立预测因素。基于这 3 个基线变量的加权风险评分可准确识别 28 天内死亡的患者(受试者工作特征曲线下面积为 0.87,0.77-0.93,P < 0.001)。风险评分 > 22 与 28 天内死亡率增加 8 倍相关(P < 0.0001),而风险评分≤22 的患者的中位生存时间为 7 天,而不是≥28 天。我们发现,APACHE II 评分、PM 诊断时严重的淋巴细胞减少症和高乳酸脱氢酶水平是疾病快速进展和死亡的独立标志物。

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