El Zein Said, Challener Doug W, Ranganath Nischal, Khodadadi Ryan B, Theel Elitza S, Abu Saleh Omar M
Division of Public Health, Infectious Diseases and Occupational Medicine, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
Open Forum Infect Dis. 2024 May 10;11(6):ofae277. doi: 10.1093/ofid/ofae277. eCollection 2024 Jun.
Identifying and treating patients with acute Q fever who are at an increased risk of progressing to persistent disease is crucial for preventing future complications. In this study, we share our decade-long clinical experience with acute Q fever, highlighting the challenges that clinicians encounter from making an initial diagnosis and performing risk stratification to determining the appropriate prophylaxis regimen and duration.
We retrieved records of adult Mayo Clinic patients (≥18 years) with positive serology results between 1 January 2012 and 31 March 2022. Patients with Q fever anti-phase II immunoglobulin G ≥1:256 by indirect immunofluorescence were further analyzed.
Thirty-one patients were included. Their median age was 58 years (IQR, 50-64), and the majority were men (84%). Acute hepatitis (29%), flu-like illness (25.8%), and pneumonia (16%) were the most common presentations. Thirteen patients (42%) received antibiotic prophylaxis to prevent disease progression, with significant variation in the indications and duration across physicians. The combination of doxycycline and hydroxychloroquine was the preferred regimen. Prophylaxis was administered for a median 333 days (IQR, 168-414). Four patients (13%) progressed to Q fever native valve infective endocarditis, with elevated anticardiolipin immunoglobulin G levels being the sole risk factor in 2 cases. The small sample size precluded drawing conclusions on the impact of prophylaxis in preventing disease progression.
Management of acute Q fever is complicated by the lack of comprehensive clinical guidelines leading to varied clinical practices. There is a critical need for randomized trials to establish robust evidence-based protocols for management.
识别和治疗有进展为持续性疾病风险增加的急性Q热患者对于预防未来并发症至关重要。在本研究中,我们分享了我们在急性Q热方面长达十年的临床经验,强调了临床医生从初步诊断、进行风险分层到确定合适的预防方案和疗程所面临的挑战。
我们检索了2012年1月1日至2022年3月31日期间梅奥诊所血清学结果呈阳性的成年患者(≥18岁)的记录。对间接免疫荧光法检测Q热抗II期免疫球蛋白G≥1:256的患者进行进一步分析。
共纳入31例患者。他们的中位年龄为58岁(四分位间距,50 - 64岁),大多数为男性(84%)。急性肝炎(29%)、流感样疾病(25.8%)和肺炎(16%)是最常见的表现形式。13例患者(42%)接受了抗生素预防以防止疾病进展,不同医生在适应证和疗程方面存在显著差异。多西环素和羟氯喹的联合用药是首选方案。预防用药中位时间为333天(四分位间距,168 - 414天)。4例患者(13%)进展为Q热天然瓣膜感染性心内膜炎,2例患者中抗心磷脂免疫球蛋白G水平升高是唯一危险因素。样本量小妨碍了就预防措施对预防疾病进展的影响得出结论。
急性Q热的管理因缺乏全面的临床指南而变得复杂,导致临床实践各不相同。迫切需要进行随机试验以建立强有力的基于证据的管理方案。