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Outcomes in Invasive Pulmonary Aspergillosis Infections Complicated by Respiratory Viral Infections in Patients With Hematologic Malignancies: A Case-Control Study

机译:血液恶性肿瘤患者侵袭性肺曲霉菌感染并发呼吸道病毒感染的结果:病例对照研究

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BackgroundData regarding invasive pulmonary aspergillosis (IPA) following respiratory viral infections (RVIs) in patients with leukemia and/or hematopoietic stem cell transplantation (LHSCT) are limited.MethodsWe conducted a retrospective case-control study of post-RVI IPA (2006–2016). Cases were patients who underwent LHSCT and had RVI due to respiratory syncytial virus (RSV), influenza virus (INF), or parainfluenza virus (PIV) followed by culture-documented IPA within 6 weeks. Controls had IPA only.ResultsWe identified 54 cases and 142 controls. Among cases, 29 (54%) had PIV infection, 14 (26%) had INF infection, and 11 (20%) had RSV infection. The median time to IPA after RVI was 7 days. A greater percentage of cases (37 [69%]) than controls (52 [37%]) underwent allogeneic HSCT (P .0001). Cases were more likely to be nonneutropenic (33 [61%] vs 56 [39%]; P = .009) and in hematologic remission (27 [50%] vs 39 [27%]; P = .003) before IPA. Cases were more likely to have monocytopenia (45 [83%] vs 99 [70%]; P = .05) and less likely to have severe neutropenia (21 [39%] vs 86 [61%]; P = .007) at IPA diagnosis. Prior use of an Aspergillus-active triazole was more common in cases (27 of 28 [96%] vs 50 of 74 [68%]; P = .0017). Median time to empirical antifungal therapy initiation was 2 days in both groups. Crude 42-day mortality rates did not differ between cases (22%) and controls (27%), but the 42-day mortality rate was higher among cases with IPA after RSV infection (45%) than among those with IPA following INF or PIV infection (13%; P = .05).ConclusionsIPA had comparable outcomes when it followed RVI in patients who underwent LHSCT, and post-RVI IPA occurred more frequently in patients with prior allogeneic HSCT and was associated with leukemia relapse and neutropenia.
机译:背景关于白血病和/或造血干细胞移植(LHSCT)患者呼吸道病毒感染(RVI)后的侵袭性肺曲霉病(IPA)的数据有限。方法我们对RVI IPA后(2006-2016年)进行了病例回顾性研究。 。病例为在6周内因呼吸道合胞病毒(RSV),流感病毒(INF)或副流感病毒(PIV)接受LHSCT并接受RVI治疗的患者。对照仅具有IPA。结果我们确定了54例病例和142个对照。其中29例(54%)感染PIV,14例(26%)感染INF,11例(20%)感染RSV。 RVI后达到IPA的中位时间为7天。接受异基因HSCT的病例(37 [69%])比对照组(52 [37%])高(P <.0001)。在IPA之前,病例更有可能是非中性粒细胞减少症(33 [61%]比56 [39%]; P = .009)和血液学缓解(27 [50%]比39 [27%]; P = .003)。病例更有可能出现单核细胞减少症(45 [83%] vs 99 [70%]; P = .05),而发生严重中性粒细胞减少症的可能性较小(21 [39%] vs 86 [61%]; P = .007)在IPA诊断中。在这种情况下,更常见的是使用曲霉活性三唑(28例中有27例[96%],而50例中有74例[68%]; P = 0.0017)。两组中经验性抗真菌治疗开始的中位时间为2天。病例(22%)和对照组(27%)的42天粗死亡率没有差异,但RSV感染后IPA病例的42天死亡率更高(45%),而INF或IPV后IPA病例的42天死亡率更高。 PIV感染(13%; P = 0.05)。

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