Dionne Jodie A, Zhu Chunming, Mejia-Galvis Jorge, Workowski Kimberly, Batteiger Teresa A, Dombrowski Julia C, Mayer Kenneth H, McNeil Candice J, Seña Arlene C, Taylor Stephanie, Wiesenfeld Harold C, Hamill Matthew M, Perlowski Charlotte, Hook Edward W
Division of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham.
Emmes Company LLC, Rockville, Maryland.
JAMA Netw Open. 2025 Feb 3;8(2):e2459490. doi: 10.1001/jamanetworkopen.2024.59490.
Syphilis rates have been increasing in the US for the past decade. The incidence of the Jarisch-Herxheimer reaction (JHR) after penicillin treatment for early syphilis is reported to range from 8% to 56%.
To prospectively assess the incidence of JHR signs and symptoms among adults with early syphilis treated with benzathine penicillin G and to document factors associated with JHR and benzathine penicillin G treatment response outcomes.
DESIGN, SETTING, AND PARTICIPANTS: The main study was designed as a phase 4 randomized clinical trial to compare the treatment efficacy of 1 vs 3 doses of benzathine penicillin G in adults with early syphilis, measured as serologic response at 6 months. A total of 249 adults with or without HIV were screened and enrolled between October 31, 2018, and March 3, 2020. Participants were screened and enrolled at 10 US study sites in the Sexually Transmitted Infections Clinical Trials Group. Statistical analysis for this secondary analysis took place between March 2023 and August 2024.
Participants received a first dose of benzathine penicillin G, 2.4 million units intramuscularly, at the enrollment visit. The JHR assessment window was day 1 to day 7 after the first dose of benzathine penicillin G.
Primary outcomes in this study were the incidence of symptoms consistent with JHR within 7 days after benzathine penicillin G treatment. Unelicited and elicited symptoms were assessed by participant self-report using a standardized checklist during contact made by a study clinician. Factors associated with JHR were collected at baseline, and serologic treatment response was assessed at 6 months. Posttreatment incident JHR symptoms were captured as safety outcomes for this trial. Analysis was performed on an intention-to-treat basis.
Of 249 participants, the median age was 32 years (IQR, 27-41 years), 242 (97.2%) were men, and 153 (61.4%) were living with HIV. One or more JHR symptoms occurred in 59 participants (23.7%) treated for early syphilis, with a median symptom onset at 4.9 hours (IQR, 3.0-9.2 hours) and a median duration of 12.8 hours (IQR, 5.0-24.0 hours). Symptom onset was within 12 hours of treatment for 49 of 57 participants (86.0%). Among 59 symptomatic participants, myalgias (30 [50.8%]), chills (27 [45.8%]), weakness (23 [39.0%]), and feverishness (21 [35.6%]) were most common. In adjusted models, JHR was associated with secondary syphilis (adjusted odds ratio [AOR], 2.91 [95% CI, 1.51-5.61]) and the absence of HIV (AOR for living with HIV, 0.49 [95% CI, 0.26-0.94]). The proportion of participants with a serologic treatment response to benzathine penicillin G at 6 months was higher among participants with JHR (84.7% [50 of 59] vs 68.9% [131 of 190] without JHR).
In this prespecified secondary analysis of a randomized clinical trial of early syphilis treatment wtih benzathine penicillin G in adults, approximately 1 in 4 participants experienced short-lived JHR symptoms, which were associated with secondary syphilis stage, lack of HIV, and successful treatment outcomes at 6 months. These messages could be used in patient counseling.
ClinicalTrials.gov Identifier: NCT03637660.
在过去十年中,美国梅毒发病率一直在上升。据报道,早期梅毒患者接受青霉素治疗后发生雅-赫反应(JHR)的发生率在8%至56%之间。
前瞻性评估接受苄星青霉素G治疗的早期梅毒成年患者中JHR体征和症状的发生率,并记录与JHR及苄星青霉素G治疗反应结果相关的因素。
设计、地点和参与者:主要研究设计为一项4期随机临床试验,比较1剂与3剂苄星青霉素G在早期梅毒成年患者中的治疗效果,以6个月时的血清学反应作为衡量指标。2018年10月31日至2020年3月3日期间,共筛选并招募了249名有或无HIV的成年人。参与者在美国性传播感染临床试验组的10个研究地点进行筛选和招募。本次二次分析的统计分析于2023年3月至2024年8月进行。
参与者在入组访视时接受第一剂苄星青霉素G,240万单位肌肉注射。JHR评估窗口为第一剂苄星青霉素G后的第1天至第7天。
本研究的主要结局是苄星青霉素G治疗后7天内符合JHR的症状发生率。未引出和引出的症状由研究临床医生在接触过程中使用标准化检查表通过参与者自我报告进行评估。在基线时收集与JHR相关的因素,并在6个月时评估血清学治疗反应。治疗后发生的JHR症状作为该试验的安全性结局进行记录。分析采用意向性分析。
249名参与者中,中位年龄为32岁(四分位间距,27 - 41岁),242名(97.2%)为男性,153名(61.4%)感染HIV。59名(23.7%)接受早期梅毒治疗的参与者出现了一种或多种JHR症状,症状发作的中位时间为4.9小时(四分位间距,3.0 - 9.2小时),中位持续时间为12.8小时(四分位间距,5.0 - 24.0小时)。57名参与者中有49名(86.0%)症状发作在治疗后12小时内。在59名有症状的参与者中,肌痛(30名[50.8%])、寒战(27名[45.8%])、虚弱(23名[39.0%])和发热(21名[35.6%])最为常见。在调整模型中,JHR与二期梅毒相关(调整比值比[AOR],2.91[95%置信区间,1.51 - 5.61])以及未感染HIV相关(感染HIV者的AOR,0.49[95%置信区间,0.26 - 0.94])。在6个月时对苄星青霉素G有血清学治疗反应的参与者比例,有JHR的参与者中更高(84.7%[59名中的50名]对比无JHR的参与者中68.9%[190名中的131名])。
在这项对成人早期梅毒用苄星青霉素G治疗的随机临床试验的预先设定的二次分析中,约四分之一的参与者经历了短暂的JHR症状,这些症状与二期梅毒阶段、未感染HIV以及6个月时的成功治疗结果相关。这些信息可用于患者咨询。
ClinicalTrials.gov标识符:NCT03637660。