Management, outcomes and predictors of mortality of Cryptococcus infection in patients without HIV: a multicentre study in 46 hospitals from Australia and New Zealand.

IF 8.2 1区 医学 Q1 IMMUNOLOGY Clinical Infectious Diseases Pub Date : 2024-12-18 DOI:10.1093/cid/ciae630
Julien Coussement, Christopher H Heath, Matthew B Roberts, Rebekah J Lane, Tim Spelman, Olivia C Smibert, Anthony Longhitano, C Orla Morrissey, Blake Nield, Monica Tripathy, Joshua S Davis, Karina J Kennedy, Sarah A Lynar, Lucy C Crawford, Simeon J Crawford, Benjamin J Smith, Andrew P Gador-Whyte, Rose Haywood, Andrew A Mahony, Julia C Howard, Genevieve B Walls, Gabrielle M O'Kane, Matthew T Broom, Caitlin L Keighley, Olivia Bupha-Intr, Louise Cooley, Jennifer A O'Hern, Justin D Jackson, Arthur J Morris, Caroline Bartolo, Adrian R Tramontana, Katherine C Grimwade, Victor Au Yeung, Roy Chean, Emily Woolnough, Benjamin W Teh, Monica A Slavin, Sharon C-A Chen
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引用次数: 0

Abstract

Background: Limited data exist regarding outcomes of cryptococcosis in patients without HIV with few studies having compared outcomes of Cryptococcus gattii, versus C. neoformans, infection.

Methods: We conducted a retrospective study in 46 Australian and New Zealand hospitals to determine the outcomes of cryptococcosis in patients without HIV diagnosed between 2015 and 2019, and compared outcomes of C. gattii versus C. neoformans infections. Multivariable analysis identified predictors of mortality within one year.

Results: Of 426 patients, one-year all-cause mortality was 21%. C. gattii infection was associated with a lower mortality than C. neoformans (adjusted odds ratio [OR]: 0.47, 95% confidence interval [CI]: 0.23-0.95), whilst severe neurological symptoms at presentation was the strongest predictor of death (adjusted OR: 8.46, 95% CI: 2.99-23.98). Almost all (99.5%) patients with central nervous system (CNS) infection received induction antifungal therapy versus 27.7% of isolated pulmonary cryptococcosis. The commonest regimen in CNS disease was liposomal amphotericin B with flucytosine (93.8%, mean duration 31 ± 13 days). Among patients with CNS cryptococcosis, C. gattii infection was associated with higher risk of immune reconstitution inflammatory response (C-IRIS) than C. neoformans (21% versus 3%, p<0.001). Nineteen patients received amphotericin B-based re-induction therapy for suspected relapse but none had microbiological relapse. Serum cryptococcal antigen positivity and lung imaging abnormalities resolved slowly (resolution at one year in 25% and 34% of patients, respectively).

Conclusion: Compared with C. neoformans, C. gattii infection demonstrated lower mortality but higher C-IRIS risk in CNS infection. Severe neurological symptoms were the strongest predictor of mortality.

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无艾滋病毒患者隐球菌感染的管理、结果和死亡率预测因素:澳大利亚和新西兰46家医院的多中心研究
背景:关于非HIV患者隐球菌感染的结果的数据有限,很少有研究比较了加蒂隐球菌与新生隐球菌感染的结果。方法:我们在澳大利亚和新西兰的46家医院进行了回顾性研究,以确定2015年至2019年期间未诊断出HIV的患者隐球菌病的结局,并比较了C. gati和C. neoformans感染的结局。多变量分析确定了一年内死亡率的预测因素。结果:426例患者一年全因死亡率为21%。加蒂梭菌感染的死亡率低于新生梭菌(校正优势比[OR]: 0.47, 95%可信区间[CI]: 0.23-0.95),而发病时出现的严重神经系统症状是死亡的最强预测因子(校正优势比:8.46,95% CI: 2.99-23.98)。几乎所有(99.5%)中枢神经系统(CNS)感染患者接受了诱导抗真菌治疗,而孤立性肺隐球菌感染患者接受了27.7%的诱导抗真菌治疗。在中枢神经系统疾病中最常见的方案是两性霉素B脂质体联合氟胞嘧啶(93.8%,平均持续时间31±13天)。在中枢神经系统隐球菌感染患者中,C. gatii感染与免疫重建炎症反应(C-IRIS)的风险相关(21%比3%)。结论:与C. nefortes相比,C. gatii感染在中枢神经系统感染中表现出更低的死亡率,但更高的C-IRIS风险。严重的神经系统症状是死亡率的最强预测因子。
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来源期刊
Clinical Infectious Diseases
Clinical Infectious Diseases 医学-传染病学
CiteScore
25.00
自引率
2.50%
发文量
900
审稿时长
3 months
期刊介绍: Clinical Infectious Diseases (CID) is dedicated to publishing original research, reviews, guidelines, and perspectives with the potential to reshape clinical practice, providing clinicians with valuable insights for patient care. CID comprehensively addresses the clinical presentation, diagnosis, treatment, and prevention of a wide spectrum of infectious diseases. The journal places a high priority on the assessment of current and innovative treatments, microbiology, immunology, and policies, ensuring relevance to patient care in its commitment to advancing the field of infectious diseases.
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