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Treatment of persistent focalized Q fever: time has come for an international randomized controlled trial

羟基氯喹 医学 贝氏柯克西拉菌 强力霉素 随机对照试验 内科学 重症监护医学 养生 儿科 抗生素 病毒学 生物 微生物学 传染病(医学专业) 疾病 2019年冠状病毒病(COVID-19)
作者
Audrey Delahaye,Carole Eldin,Alexandre Bleibtreu,Félix Djossou,Thomas J. Marrie,Nesrin Ghanem‐Zoubi,Sonja E. van Roeden,L. Epelboin
出处
期刊:Journal of Antimicrobial Chemotherapy [Oxford University Press]
卷期号:79 (8): 1725-1747
标识
DOI:10.1093/jac/dkae145
摘要

Q fever is a worldwide zoonosis due to Coxiella burnetii, responsible for endocarditis and endovascular infections. Since the 1990s, the combination hydroxychloroquine + doxycycline has constituted the curative and prophylactic treatment in persistent focalized Q fever. This combination appears to have significantly reduced the treatment's duration (from 60 to 26 months), yet substantial evidence of effectiveness remains lacking. Data are mostly based on in vitro and observational studies. We conducted a literature review to assess the effectiveness of this therapy, along with potential alternatives. The proposed in vitro mechanism of action describes the inhibition of Coxiella replication by doxycycline through the restoration of its bactericidal activity (inhibited in acidic environment) by alkalinization of phagolysosome-like vacuoles with hydroxychloroquine. So far, the rarity and heterogeneous presentation of cases have made it challenging to design prospective studies with statistical power. The main studies supporting this treatment are retrospective cohorts, dating back to the 1990s-2000s. Retrospective studies from the large Dutch outbreak of Q fever (>4000 cases between 2007 and 2010) did not corroborate a clear benefit of this combination, notably in comparison with other regimens. Thus, there is still no consensus among the medical community on this issue. However insufficient the evidence, today the doxycycline + hydroxychloroquine combination remains the regimen with the largest clinical experience in the treatment of 'chronic' Q fever. Reinforcing the guidelines' level of evidence is critical. We herein propose the creation of an extensive international registry, followed by a prospective cohort or ideally a randomized controlled trial.

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