Clarke Emily J, Vodstrcil Lenka A, Plummer Erica L, Aguirre Ivette, Samra Ranjit S, Fairley Christopher K, Chow Eric P F, Bradshaw Catriona S
Melbourne Sexual Health Centre, Alfred Health, Carlton, Victoria, Australia.
Central Clinical School, Monash University, Melbourne, Victoria, Australia.
Open Forum Infect Dis. 2023 Aug 11;10(8):ofad427. doi: 10.1093/ofid/ofad427. eCollection 2023 Aug.
High levels of macrolide resistance and increasing fluoroquinolone resistance are making increasingly difficult to treat. Minocycline is an alternative treatment for patients with macrolide-resistant infections that have failed moxifloxacin, or for those with fluoroquinolone contraindications or resistance. Published efficacy data for minocycline for are limited.
We evaluated minocycline 100 mg twice daily for 14 days at Melbourne Sexual Health Centre (MSHC). Microbial cure was defined as a negative test of cure within 14-90 days after completing minocycline. The proportion cured and 95% confidence intervals (CIs) were calculated, and logistic regression was used to explore factors associated with treatment failure. We pooled data from the current study with a prior adjacent case series of patients with who had received minocycline 100 mg twice daily for 14 days at MSHC.
Minocycline cured 60 of 90 (67% [95% CI, 56%-76%]) infections. Adherence was high (96%) and side effects were mild and self-limiting. No demographic or clinical characteristics were associated with minocycline failure in regression analyses. In the pooled analyses of 123 patients, 83 (68% [95% CI, 58%-76%]) were cured following minocycline.
Minocycline cured 68% of macrolide-resistant infections. These data provide tighter precision around the efficacy of minocycline for macrolide-resistant and show that it is a well-tolerated regimen. With high levels of macrolide resistance, increasing fluoroquinolone resistance, and the high cost of moxifloxacin, access to nonquinolone options such as minocycline is increasingly important for the clinical management of .
大环内酯类药物的高耐药率以及氟喹诺酮类药物耐药率的不断上升,使得[疾病名称]的治疗愈发困难。米诺环素可作为对莫西沙星治疗失败的大环内酯类耐药感染患者,或有氟喹诺酮类药物禁忌证或耐药的患者的替代治疗方案。关于米诺环素治疗[疾病名称]的已发表疗效数据有限。
我们在墨尔本性健康中心(MSHC)评估了每日两次、每次100毫克米诺环素,疗程为14天的治疗方案。微生物学治愈定义为在完成米诺环素治疗后的14 - 90天内治愈检测呈阴性。计算治愈比例及95%置信区间(CIs),并采用逻辑回归分析探索与治疗失败相关的因素。我们将本研究的数据与之前在MSHC接受每日两次、每次100毫克米诺环素、疗程为14天的相邻病例系列研究的数据进行了汇总。
90例感染患者中,60例(67%[95%CI,56% - 76%])经米诺环素治疗后治愈。依从性高(96%),且副作用轻微且为自限性。回归分析中,未发现任何人口统计学或临床特征与米诺环素治疗失败相关。在对123例患者的汇总分析中,83例(68%[95%CI,58% - 76%])经米诺环素治疗后治愈。
米诺环素治愈了68%的大环内酯类耐药[疾病名称]感染。这些数据更精确地显示了米诺环素对大环内酯类耐药[疾病名称]的疗效,并表明它是一种耐受性良好的治疗方案。鉴于大环内酯类药物的高耐药率、氟喹诺酮类药物耐药率的不断上升以及莫西沙星的高昂成本,对于[疾病名称]的临床管理而言,获得米诺环素等非喹诺酮类治疗选择变得越来越重要。