首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Overall survival and fungal infection-related mortality in patients with invasive fungal infection and neutropenia after myelosuppressive chemotherapy in a tertiary care centre from 1995 to 2006.
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Overall survival and fungal infection-related mortality in patients with invasive fungal infection and neutropenia after myelosuppressive chemotherapy in a tertiary care centre from 1995 to 2006.

机译:1995年至2006年,三级护理中心骨髓抑制化疗后浸润性真菌感染和中性粒细胞减少的患者的总生存率和与真菌感染相关的死亡率。

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OBJECTIVES: Invasive fungal infections (IFIs) contribute significantly to mortality and morbidity in patients receiving myelosuppressive chemotherapy for haematological malignancies. The present study investigates the overall survival (OS), infection-related mortality and changes in treatment of IFIs in our department from 1995 until 2006. METHODS: Outcomes of all chemotherapy courses were retrospectively evaluated using a standard questionnaire. Modified EORTC/MSG criteria for IFIs were applied: a positive PCR result for Aspergillus spp. in bronchoalveolar lavage was also defined as probable IFI. RESULTS: In total, 1693 chemotherapy courses in 592 patients were evaluated. Sixty-three percent of chemotherapy courses were given to treat acute myeloid leukaemia, with the rest for acute lymphoblastic leukaemia or aggressive lymphoma. IFIs were observed in 139/592 patients [23.5%, 95% confidence interval (CI) 20%-27%] and in 149/1693 courses (8.8%, 95% CI 8%-10%). IFI-related mortality was 56.9% in 1995-2001 and 28.6% in 2002-06, P < 0.001. Accordingly, median OS in patients with IFI increased: 54 days (95% CI 26-82 days) in 1995-2001 versus 229 days (95% CI 35-423 days) in 2002-06, P = 0.001. By multivariate analysis, factors predictive for better OS were controlled disease after chemotherapy [hazard ratio (HR) 0.228, P < 0.001], possible IFI (in contrast to proven/probable IFI, HR 0.537, P = 0.005), age <60 years (HR 0.583, P = 0.008), time period 2002-06 (HR 0.612, P = 0.021) and use of novel antifungals (HR 0.589, P = 0.033). CONCLUSIONS: Compared with 1995-2001, IFI-related mortality decreased and OS in patients with IFI increased significantly in recent years. Improved OS was associated with controlled haematological disease, certainty of IFI diagnosis (possible), younger age, time period 2002-06 and the use of novel antifungals.
机译:目的:侵袭性真菌感染(IFIs)对接受血液系统恶性肿瘤骨髓抑制化疗的患者的死亡率和发病率有显着贡献。本研究调查了我科1995年至2006年的总生存期(OS),与感染有关的死亡率以及IFI治疗的变化。方法:使用标准调查表对所有化疗课程的结果进行回顾性评估。应用了针对IFI的改良EORTC / MSG标准:曲霉属菌种PCR阳性。支气管肺泡灌洗中的IFI也被定义为可能的IFI。结果:总共评估了592例患者的1693疗程。进行了63%的化学疗法疗程来治疗急性髓细胞性白血病,其余的则用于急性淋巴细胞白血病或侵袭性淋巴瘤。在139/592例患者中观察到IFI [23.5%,95%置信区间(CI)20%-27%],在149/1693疗程中观察到(8.8%,95%CI 8%-10%)。 IFI相关死亡率在1995-2001年为56.9%,在2002-06年为28.6%,P <0.001。因此,IFI患者的中位OS增加:1995-2001年为54天(95%CI 26-82天),而2002-06年为229天(95%CI 35-423天),P = 0.001。通过多变量分析,预测OS改善的因素是化疗后控制的疾病[危险比(HR)0.228,P <0.001],可能的IFI(与已证实/可能的IFI相对,HR 0.537,P = 0.005),年龄<60岁(HR 0.583,P = 0.008),2002-06年期间(HR 0.612,P = 0.021)和使用新型抗真菌药(HR 0.589,P = 0.033)。结论:与1995-2001年相比,近年来IFI患者的IFI相关死亡率降低,OS显着增加。 OS改善与血液系统疾病的控制,IFI诊断的确定性(可能),年龄较小,2002-06年期间以及使用新型抗真菌药有关。

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