Department of Medicine, Division of Allergy and Infectious Diseases, University of Washington, Seattle, Washington, USA
Public Health-Seattle & King County, HIV/STD Program, Seattle, Washington, USA.
Antimicrob Agents Chemother. 2020 Dec 16;65(1). doi: 10.1128/AAC.01739-20.
The threat of ceftriaxone-resistant necessitates new gonorrhea treatment regimens. Repurposing older antibiotics not routinely used for may expeditiously identify new therapies. Ideally, all recommended therapies should eradicate gonorrhea at the pharynx. Between April and September 2019, we enrolled men in an open-label, one-arm clinical trial of single-dose intramuscular aztreonam (2 g). Enrollment criterion included (i) nucleic acid amplification test (NAAT)-positive pharyngeal gonorrhea for ≤14 days or (ii) Gram stain-positive gonococcal urethritis plus report of performing oral sex in ≤2 months. At enrollment, we collected cultures from NAAT-positive or screening sites, and men returned 3 to 8 days following treatment for a test of cure (TOC) by culture. The per-protocol analysis required men to be culture positive at enrollment and to return for TOC. We calculated efficacy as the number of subjects with negative culture at TOC divided by the number culture positive at enrollment by anatomic site. Thirty-two men enrolled in the study; 21 were pharyngeal NAAT positive, and 11 had gonococcal urethritis. The per-protocol analysis included 17 men, 6 with pharyngeal, 9 with urethral, and 4 with rectal gonococcal infections. Aztreonam cured 2 of 6 pharyngeal infections (33%; 95% confidence interval [CI], 4.3% to 78%) and 3 of 4 rectal infections (75%; 95% CI, 19% to 99%). All 11 men with urethritis were cured (100%; 95% CI, 66% to 100%). The aztreonam MIC was 0.5 μg/ml (range, 0.06 to 2.0 μg/ml). All treatment failures occurred at a MIC of ≥0.25 μg/ml. Single-dose aztreonam is not a reliable treatment for gonorrhea at the pharynx but may be useful for men with gonococcal urethritis and beta-lactam allergy. (This study has been registered at ClinicalTrials.gov under identifier NCT03867734.).
头孢曲松耐药的威胁需要新的淋病治疗方案。重新利用不常用于淋病治疗的旧抗生素可能会迅速确定新的治疗方法。理想情况下,所有推荐的治疗方法都应能彻底治愈咽部淋病。2019 年 4 月至 9 月,我们招募了一名接受单剂量肌内注射氨曲南(2 g)的开放性、单臂临床试验的男性参与者。纳入标准包括:(i)核酸扩增试验(NAAT)阳性的咽部淋病不超过 14 天,或(ii)革兰氏染色阳性的淋球菌性尿道炎,加上报告在不超过 2 个月内进行过口交。在入组时,我们从 NAAT 阳性或筛查部位采集培养物,男性在治疗后 3 至 8 天返回进行治疗后检测(TOC)培养。按方案分析要求男性在入组时培养阳性,并返回进行 TOC。我们将疗效定义为 TOC 时培养阴性的受试者数量除以按解剖部位培养阳性的受试者数量。32 名男性参与了这项研究;21 名是咽 NAAT 阳性,11 名患有淋球菌性尿道炎。按方案分析包括 17 名男性,6 名患有咽淋病,9 名患有尿道淋病,4 名患有直肠淋病。氨曲南治愈了 6 例咽感染中的 2 例(33%;95%置信区间 [CI],4.3%至 78%)和 4 例直肠感染中的 3 例(75%;95%CI,19%至 99%)。所有 11 名患有尿道炎的男性均治愈(100%;95%CI,66%至 100%)。氨曲南的 MIC 为 0.5 μg/ml(范围,0.06 至 2.0 μg/ml)。所有治疗失败均发生在 MIC 为≥0.25 μg/ml 时。单剂量氨曲南不能可靠治疗咽部淋病,但对患有淋球菌性尿道炎和β-内酰胺类过敏的男性可能有用。(这项研究已在 ClinicalTrials.gov 上注册,标识符为 NCT03867734。)