pulmonary Mucormycosis

  • 文章类型: Journal Article
    肺毛霉菌病是一种罕见但快速进展的致命疾病。关于肺毛霉菌病预后不良的结果和相关因素的数据有限。这项研究的目的是评估临床特征,与死亡率相关的因素,以及巴基斯坦三级医院的肺毛霉菌病结果。
    这是一项在卡拉奇三级医院进行的回顾性观察研究,巴基斯坦。回顾了2018年1月至2022年12月期间诊断为已证实或可能的肺毛霉菌病的住院患者的医疗记录。进行单因素和回归分析以确定与死亡率相关的因素。
    包括53例肺毛霉菌病患者(69.8%为男性),平均年龄51.19±21.65岁。糖尿病是最常见的合并症[n=26(49.1%)]。慢性肺部疾病出现在[n=5(9.4%)],[n=16(30.2%)]患有2019年冠状病毒病(COVID-19)肺炎。主要分离的毛霉是根霉[n=32(60.3%)]和毛霉[n=9(17%)]。主要放射学发现包括巩固[n=39(73.6%)]和结节[n=14(26.4%)]。[n=38(71.7%)]中开了两性霉素B脱氧胆酸盐,[n=14(26.4%)]的患者接受了内科和外科综合治疗。中位[四分位距(IQR)]住院时间为15.0(10.0-21.5)天。[n=30(56.6%)]患者需要重症监护病房(ICU)护理,26人(49.1%)需要机械通气。29例(54.7%)患者出现总死亡率。在需要机械通气20/29的患者中发现了更高的死亡率(69%,p=0.002)。免疫抑制(p=0.042),血小板减少症(p=0.004),和机械通气(p=0.018)在多变量分析中被确定为死亡的危险因素.
    这项研究提供了对临床特征的基本见解,结果,和与肺毛霉菌病相关的死亡因素。死亡率高(54.7%),特别是在免疫抑制患者中,血小板减少症,和那些需要机械通气的人。
    UNASSIGNED: Pulmonary mucormycosis is a rare but rapidly progressive fatal disease. Limited data exist on the outcomes and factors associated with poor prognosis of pulmonary mucormycosis. The objective of this study was to evaluate clinical characteristics, factors associated with mortality, and outcomes of pulmonary mucormycosis at a tertiary care hospital in Pakistan.
    UNASSIGNED: This was a retrospective observational study conducted at a tertiary care hospital in Karachi, Pakistan. Medical records of hospitalized patients diagnosed with proven or probable pulmonary mucormycosis between January 2018 and December 2022 were reviewed. Univariate and regression analyses were performed to identify factors associated with mortality.
    UNASSIGNED: Fifty-three pulmonary mucormycosis patients (69.8% male) were included, with mean age of 51.19 ± 21.65 years. Diabetes mellitus was the most common comorbidity [n = 26 (49.1%)]. Chronic lung diseases were present in [n = 5 (9.4%)], and [n = 16 (30.2%)] had concurrent coronavirus disease 2019 (COVID-19) pneumonia. The predominant isolated Mucorales were Rhizopus [n = 32 (60.3%)] and Mucor species [n = 9 (17%)]. Main radiological findings included consolidation [n = 39 (73.6%)] and nodules [n = 14 (26.4%)]. Amphotericin B deoxycholate was prescribed in [n = 38 (71.7%)], and [n = 14 (26.4%)] of patients received combined medical and surgical treatment. The median [interquartile range (IQR)] hospital stay was 15.0 (10.0-21.5) days. Intensive care unit (ICU) care was required in [n = 30 (56.6%)] patients, with 26 (49.1%) needing mechanical ventilation. Overall mortality was seen in 29 (54.7%) patients. Significantly higher mortality was found among patients requiring mechanical ventilation 20/29 (69%, p = 0.002). Immunosuppression (p = 0.042), thrombocytopenia (p = 0.004), and mechanical ventilation (p = 0.018) were identified as risk factors for mortality on multivariable analysis.
    UNASSIGNED: This study provides essential insights into the clinical characteristics, outcomes, and mortality factors associated with pulmonary mucormycosis. The mortality rate was high (54.7%), particularly in patients with immunosuppression, thrombocytopenia, and those who required mechanical ventilation.
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  • 文章类型: Journal Article
    背景:肺毛霉菌病(PM)是一种危及生命的侵袭性霉菌感染。毛霉菌病的诊断具有挑战性,并且经常延迟,导致更高的死亡率。
    目的:PM的疾病表现和诊断工具的贡献是否受患者潜在病情的影响?
    方法:回顾性分析了2008年至2019年法国六家教学医院的所有PM病例。根据更新的欧洲癌症/真菌病研究和治疗组织研究组标准定义病例,增加糖尿病和创伤作为宿主因素,血清或组织PCR阳性作为真菌学证据。集中检查胸部CT扫描。
    结果:共记录了114例PM,包括40%的传播形式。主要疾病为恶性血液病(49%),异基因造血干细胞移植(21%),和实体器官移植(17%)。传播时,主要传播部位是肝脏(48%),脾脏(48%),大脑(44%),和肾脏(37%)。放射学表现包括巩固(58%),胸腔积液(52%),反晕符号(26%),光环(24%),血管异常(26%),和空腔(23%)。53例患者中有42例(79%)血清定量聚合酶链反应(qPCR)阳性,96例患者中有46例(50%)BAL阳性。11例无贡献BAL患者中,有8例(73%)的经胸肺活检结果被诊断。总体90天死亡率为59%。中性粒细胞减少症患者更频繁地表现出血管侵袭性表现,包括逆转晕征和播散性疾病(P<0.05)。血清qPCR对中性粒细胞减少症患者的贡献更大(91%vs62%;P=0.02),非中性粒细胞减少症患者的BAL贡献更大(69%vs41%;P=0.02)。血清qPCR在>3cm主要病变的患者中更常见(91%vs62%;P=0.02)。总的来说,qPCR阳性与早期诊断(P=0.03)和治疗开始(P=0.01)相关。
    结论:中性粒细胞减少症和放射学发现影响PM期间的疾病表现和诊断工具的贡献。血清qPCR对中性粒细胞减少症患者和非中性粒细胞减少症患者的BAL检查更有贡献。在无贡献BAL的情况下,肺活检的结果具有很高的贡献。
    Pulmonary mucormycosis (PM) is a life-threatening invasive mold infection. Diagnosis of mucormycosis is challenging and often delayed, resulting in higher mortality.
    Are the disease presentation of PM and contribution of diagnosis tools influenced by the patient\'s underlying condition?
    All PM cases from six French teaching hospitals between 2008 and 2019 were retrospectively reviewed. Cases were defined according to updated European Organization for Research and Treatment of Cancer/Mycoses Study Group criteria with the addition of diabetes and trauma as host factors and positive serum or tissue PCR as mycologic evidence. Thoracic CT scans were reviewed centrally.
    A total of 114 cases of PM were recorded, including 40% with disseminated forms. Main underlying conditions were hematologic malignancy (49%), allogeneic hematopoietic stem cell transplantation (21%), and solid organ transplantation (17%). When disseminated, main dissemination sites were the liver (48%), spleen (48%), brain (44%), and kidneys (37%). Radiologic presentation included consolidation (58%), pleural effusion (52%), reversed halo sign (26%), halo sign (24%), vascular abnormalities (26%), and cavity (23%). Serum quantitative polymerase chain reaction (qPCR) was positive in 42 (79%) of 53 patients and BAL in 46 (50%) of 96 patients. Results of transthoracic lung biopsy were diagnostic in 8 (73%) of 11 patients with noncontributive BAL. Overall 90-day mortality was 59%. Patients with neutropenia more frequently displayed an angioinvasive presentation, including reversed halo sign and disseminated disease (P < .05). Serum qPCR was more contributive in patients with neutropenia (91% vs 62%; P = .02), and BAL was more contributive in patients without neutropenia (69% vs 41%; P = .02). Serum qPCR was more frequently positive in patients with a > 3 cm main lesion (91% vs 62%; P = .02). Overall, positive qPCR was associated with an early diagnosis (P = .03) and treatment onset (P = .01).
    Neutropenia and radiologic findings influence disease presentation and contribution of diagnostic tools during PM. Serum qPCR is more contributive in patients with neutropenia and BAL examination in patients without neutropenia. Results of lung biopsies are highly contributive in cases of noncontributive BAL.
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  • 文章类型: Multicenter Study
    目的:COVID-19的临床过程并发继发感染,包括细菌和真菌感染。这些患者中侵袭性毛霉菌病的发病率迅速上升非常令人担忧。在印度第二波COVID-19大流行期间,大量发现了COVID-19相关的毛霉菌病,在其发病机理中发现了几种诱发因素。本研究旨在评估流行病学,诱发因素,冠状病毒疾病COVID-19相关毛霉菌病(CAM)的累积死亡率和影响预后的因素。
    方法:在2021年4月至6月期间,对印度南部的三个三级医疗保健中心进行了一项多中心回顾性研究。
    结果:在217例CAM中,影响鼻窦的毛霉菌病是最常见的,影响95(44%)的患者,在84(38%)中看到的轨道扩展,肺(n=25,12%),胃肠(n=6,3%),孤立的大脑(n=2)和播散的毛霉菌病(n=2)。糖尿病,大剂量全身性类固醇是CAM患者中最常见的基础疾病.6周毛霉菌病相关病死率为14%,大脑或胃肠道或播散性毛霉菌病的死亡风险比其他地区高9倍.广泛的手术清创术以及序贯抗真菌药物治疗改善了毛霉菌病患者的生存率。
    结论:对与CAM相关的诱发因素和影响死亡率的因素进行明智和适当的管理,采用多学科的方法和及时的手术和医疗管理,对取得成功的结果非常有帮助。
    OBJECTIVE: The clinical course of COVID-19 has been complicated by secondary infections, including bacterial and fungal infections. The rapid rise in the incidence of invasive mucormycosis in these patients is very much concerning. COVID-19-associated mucormycosis was detected in huge numbers during the second wave of the COVID-19 pandemic in India, with several predisposing factors indicated in its pathogenesis. This study aimed to evaluate the epidemiology, predisposing factor, cumulative mortality and factors affecting outcomes among the coronavirus disease COVID-19-associated mucormycosis (CAM).
    METHODS: A multicenter retrospective study across three tertiary health care centers in Southern part of India was conducted during April-June 2021.
    RESULTS: Among the 217 cases of CAM, mucormycosis affecting the nasal sinuses was the commonest, affecting 95 (44%) of the patients, orbital extension seen in 84 (38%), pulmonary (n = 25, 12%), gastrointestinal (n = 6, 3%), isolated cerebral (n = 2) and disseminated mucormycosis (n = 2). Diabetes mellitus, high-dose systemic steroids were the most common underlying disease among CAM patients. The mucormycosis-associated case-fatality at 6 weeks was 14%, cerebral or GI or disseminated mucormycosis had 9 times higher risk of death compared to other locations. Extensive surgical debridement along with sequential antifungal drug treatment improved the survival in mucormycosis patients.
    CONCLUSIONS: Judicious and appropriate management of the predisposing factor and factors affecting mortality associated with CAM with multi-disciplinary approach and timely surgical and medical management can be much helpful in achieving a successful outcome.
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  • 文章类型: Journal Article
    BACKGROUND: In acute leukaemia (AL), the occurrence of pulmonary mucormycosis (PM), the incidence of which is increasing, as a result of chemotherapy induced marrow aplasia, remains a life threatening complication.
    METHODS: Analysis of clinical, biological and thoracic CT characteristics of patients with PM developing during the treatment of AL between 2000 and 2015. Day 0 (D0) was defined as the day with first CT evidence of PM.
    RESULTS: Among 1193 patients, 25 cases of PM were recorded during 2099 episodes of bone marrow aplasia. At time of diagnosis of PM, 24/25 patients had been neutropenic for a median of 12 days. None of the patients had diabetes mellitus. On initial CT (D0), the lesion was solitary in 20/25 cases and a reversed halo sign (RHS) was observed in 23/25 cases. From D1 to D7, D8 to D15 and after D15, RHS was seen in 100 %, 75 % and 27 % of cases, respectively. A tissue biopsy was positive in 17/18 cases. The detection of circulating Mucorales DNA in serum was positive in 23/24 patients and in 97/188 serum specimens between D-9 and D9. Bronchoalveolar lavage contributed to diagnosis in only 3/21 cases. The antifungal treatment was mainly based on liposomal amphotericin B combined with, or followed by, posaconazole. A pulmonary surgical resection was performed in 9/25 cases. At 3 months, 76 % of patients were alive and median overall survival was 14 months.
    CONCLUSIONS: In AL, early use of CT could improve the prognosis of PM. The presence of a RHS on CT suggests PM and is an indication for prompt antifungal treatment.
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  • 文章类型: Comparative Study
    Pulmonary mucormycosis (PM) is a life-threatening infection and the diagnosis can be challenging. The objective was to retrospectively explore the value of the RHS in our cohort of 27 patients with mucormycosis and its relation to neutropenia. This was a retrospective study including all patients with a diagnosis of probable or proven invasive PM according to the 2008 EORTC/MSG criteria between September 2003 to April 2016. Fisher\'s exact test and Mann-Whitney test, with a P-value statistically significant under .05 (P<.05), were used to compare neutropenic and non-neutropenic groups. 27 patients were eligible. The RHS could be identified in 78% of cases in the neutropenic group, and was less common in the non-neutropenic group (31%) (P<.05). Reticulations inside ground-glass opacity in case of RHS were present in 13 out of 15 patients (87%). Mucorales DNA detection by PCR on serum provided, a median time to the first PCR-positive sample of 3 days (-33 to +60 days) before diagnosis was confirmed. Six patients had IPA co-infection. In conclusion, RHS is more frequent in case of PM in neutropenic patients compare to non-neutropenic patients. Its presence in immunocompromised patients should be sufficient to promptly start Mucorales-active antifungal treatment, while its absence especially in non-neutropenic cases should not be sufficient to exclude the diagnosis.
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  • 文章类型: Case Reports
    我们在2004-2013年期间对圣彼得堡9家医院的36例毛霉菌病患者进行了前瞻性观察。最常见的基础疾病是急性白血病(64%),主要危险因素是中性粒细胞减少(92%)和淋巴细胞减少(86%)。在50%的患者中,侵袭性曲霉病1-65天后诊断为毛霉菌病。毛霉菌病的主要临床形式是肺部(64%),而在50%的病例中发现了两个或两个以上的器官受累。毛霉菌病最常见的病因是根霉病。(48%)。12周生存率为50%。联合治疗(棘白菌素两性霉素B形式)和从潜在疾病中恢复可显着提高生存率。
    We prospectively observed 36 haematological patients with mucormycosis from nine hospitals of St. Petersburg during 2004-2013. The most frequent underlying diseases were acute leukaemia (64%), and main risk factors were prolonged neutropenia (92%) and lymphocytopenia (86%). In 50% of the patients, mucormycosis was diagnosed 1-65 days after invasive aspergillosis. Main clinical form of mucormycosis was pulmonary (64%), while two or more organ involvement was noted in 50% of the cases. The most frequent aetiological agents of mucormycosis were Rhizopus spp. (48%). Twelve-week survival rate was 50%. Combination therapy (echinocandins + amphotericin B forms) and recovery from the underlying disease significantly improved the survival rate.
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