Division of Foodborne, Waterborne, and Environmental Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Epidemic Intelligence Service, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Clin Infect Dis. 2022 Feb 11;74(3):455-460. doi: 10.1093/cid/ciab450.
In 2018, the Centers for Disease Control and Prevention and the Vermont Department of Health investigated an outbreak of multidrug-resistant Shigella sonnei infections in a retirement community that offered a continuum of care from independent living through skilled nursing care. The investigation identified 24 culture-confirmed cases. Isolates were resistant to trimethoprim-sulfamethoxazole, ampicillin, and ceftriaxone, and had decreased susceptibility to azithromycin and ciprofloxacin.
To evaluate clinical and microbiologic response, we reviewed inpatient and outpatient medical records for treatment outcomes among the 24 patients with culture-confirmed S. sonnei infection. We defined clinical failure as diarrhea (≥3 loose stools per day) for ≥1 day after treatment finished, and microbiologic failure as a stool culture that yielded S. sonnei after treatment finished. We used broth microdilution to perform antimicrobial susceptibility testing, and whole genome sequencing to identify resistance mechanisms.
Isolates contained macrolide resistance genes mph(A) and erm(B) and had azithromycin minimum inhibitory concentrations above the Clinical and Laboratory Standards Institute epidemiological cutoff value of ≤16 µg/mL. Among 24 patients with culture-confirmed Shigella infection, 4 were treated with azithromycin; all had clinical treatment failure and 2 also had microbiologic treatment failure. Isolates were susceptible to ciprofloxacin but contained a gyrA mutation; 2 patients failed treatment with ciprofloxacin.
These azithromycin treatment failures demonstrate the importance of clinical breakpoints to aid clinicians in identifying alternative treatment options for resistant strains. Additionally, these treatment failures highlight a need for comprehensive susceptibility testing and systematic outcome studies, particularly given the emergence of multidrug-resistant Shigella among an expanding range of patient populations.
2018 年,疾病控制与预防中心和佛蒙特州卫生部调查了一家提供从独立生活到熟练护理连续性护理的退休社区中多重耐药性宋内志贺菌感染的暴发。该调查确定了 24 例经培养确认的病例。分离株对复方磺胺甲噁唑、氨苄西林和头孢曲松耐药,对阿奇霉素和环丙沙星的敏感性降低。
为了评估临床和微生物学反应,我们回顾了 24 例经培养确认的宋内志贺菌感染患者的住院和门诊病历,以评估治疗结果。我们将临床治疗失败定义为治疗结束后至少 1 天仍有≥3 次稀便,微生物学治疗失败定义为治疗结束后粪便培养仍有宋内志贺菌。我们使用肉汤微量稀释法进行抗菌药物敏感性试验,使用全基因组测序确定耐药机制。
分离株含有大环内酯类耐药基因 mph(A)和 erm(B),且阿奇霉素最小抑菌浓度超过临床和实验室标准协会的流行病学折点>16μg/ml。在 24 例经培养确认的志贺菌感染患者中,有 4 例接受了阿奇霉素治疗;所有患者均出现临床治疗失败,其中 2 例还出现了微生物学治疗失败。分离株对环丙沙星敏感,但含有 gyrA 突变;2 例患者环丙沙星治疗失败。
这些阿奇霉素治疗失败表明,临床折点对于帮助临床医生识别耐药菌株的替代治疗方案非常重要。此外,这些治疗失败凸显了全面药敏试验和系统结局研究的必要性,特别是考虑到多药耐药性志贺菌在不断扩大的患者群体中的出现。