Mpox 临床表现、诊断方法和治疗策略:综述。

JAMA Pub Date : 2024-10-14 DOI:10.1001/jama.2024.21091
Boghuma K Titanji,Aniruddha Hazra,Jason Zucker
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引用次数: 0

摘要

重要意义 2022 年 7 月至 2023 年 5 月,全球爆发 IIb 支猴痘病毒(MPXV)感染疫情,疫情迅速蔓延至至少 118 个国家,导致出现国际关注的突发公共卫生事件(PHEIC)。这次疫情影响到全球 99 000 多人,在美国造成 33 000 多人感染和 60 人死亡。2024 年,美国每月新增感染病例约 200 例。2024 年 8 月 14 日,世界卫生组织第二次宣布天花为公共卫生紧急信息通报项目,原因是在中非感染 I 型 MPXV 的人数迅速增加。对于 IIb 支 MPXV,最常见的感染与同性恋、双性恋和其他男男性行为者的性行为有关。中位潜伏期为 7-10 天,前驱症状包括发热(62%-72%)、淋巴结病(56%-86%)、肌痛(31%-55%)、乏力(23%-57%)和头痛(25%-55%)。皮损在 2 至 4 周内经历 4 个明确的阶段(斑丘疹、丘疹、水泡和脓疱)。支原体 IIb 型 MPXV 通常是一种自限性疾病,死亡率较低(在美国小于 0.2%);但免疫力低下的人,尤其是晚期艾滋病毒感染者(CD4 细胞计数小于 200 cells/μL)可能会出现重症和死亡。对于可能接触过 MPXV 并出现皮损的患者,应怀疑其感染了 Mpox,并通过对皮损进行聚合酶链反应检测来确诊。治疗方法是支持性的,重点是皮肤护理和使用止痛药缓解症状。虽然美国食品和药物管理局目前还没有批准针对麻疹的抗病毒治疗,但有几种治疗方法,如替考病毒、布林昔多韦和疫苗免疫球蛋白静脉注射,可通过扩大使用计划或临床试验获得。建议高发人群接种两剂改良型安卡拉-巴伐利亚-北欧疫苗,其有效率为 66% 至 86%。天花是一种主要通过皮肤密切接触传播的病毒感染,通常会引起自愈性疾病,但在免疫力低下的人群中可导致重症和死亡。一线治疗是支持性护理,但严重感染天花的患者可能需要接受先进的治疗。接种麻痘疫苗是有效的,如果有条件,应为有接触麻痘风险的人接种。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mpox Clinical Presentation, Diagnostic Approaches, and Treatment Strategies: A Review.
Importance A global outbreak of clade IIb Monkeypox virus (MPXV) infections spread rapidly across at least 118 countries resulting in a Public Health Emergency of International Concern (PHEIC) from July 2022 to May 2023. This outbreak affected more than 99 000 persons worldwide and caused more than 33 000 infections and 60 deaths in the US. In 2024, there have been approximately 200 new infections per month in the US. On August 14, 2024, the World Health Organization declared mpox a PHEIC for a second time due to a rapid increase in infections with clade I MPXV in Central Africa. Observations Mpox is primarily acquired through direct skin to skin contact with MPXV. With clade IIb MPXV, infections are most commonly associated with sexual activity among individuals who are gay, bisexual, and other men who have sex with men. After a median incubation period of 7 to 10 days, prodromal symptoms include fever (62%-72%), lymphadenopathy (56%-86%), myalgias (31%-55%), malaise (23%-57%), and headache (25%-55%). Skin lesions progress through 4 well-defined stages (macules, papules, vesicles, and pustules) over 2 to 4 weeks. Clade IIb MPXV is typically a self-limited illness with a low mortality rate (<0.2% in the US); however, severe illness and death may occur in immunocompromised individuals, especially those with advanced HIV (CD4 count <200 cells/μL). Mpox should be suspected in patients with potential exposure to MPXV who have skin lesions, and the diagnosis is confirmed with polymerase chain reaction testing of lesions. Management is supportive and focuses on skin care and symptom relief with analgesics. While no antiviral treatments are currently approved for mpox by the US Food and Drug Administration, several therapeutics, such as tecovirimat, brincidofovir, and vaccinia immune globulin intravenous, are available through expanded access programs or clinical trials. Vaccination with the 2-dose Modified Vaccinia Ankara-Bavarian Nordic vaccine is recommended for high-incidence populations and has an efficacy of 66% to 86%. Conclusions and Relevance Mpox is a viral infection transmitted primarily through close skin to skin contact that typically causes a self-resolving illness but can result in severe illness and death in immunocompromised individuals. First-line therapy is supportive care, although patients with severe mpox infection may be treated with advanced therapeutics. Mpox vaccination is effective and, if available, should be offered to individuals at risk of exposure to mpox.
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