Department of Health Research Methods, Evidence and Impact, McMaster University, Hamilton, Ontario, Canada.
Faculty of Medicine, University of Toronto, Ontario, Canada.
J Pediatric Infect Dis Soc. 2018 Aug 17;7(3):e107-e115. doi: 10.1093/jpids/piy060.
With the continued high prevalence of chlamydia worldwide and high risk of transfer from mothers to their infant during delivery, a need for safe and effective therapies for infants who acquire a chlamydial infection remains. We conducted a systematic review and meta-analysis of antibiotic treatments, including oral erythromycin, azithromycin, and trimethoprim, for neonatal chlamydial conjunctivitis.
We searched Medline, Embase, and the Cochrane Central Register of Controlled Trials (CENTRAL) from their inception to July 14, 2017. We included randomized and nonrandomized studies that evaluated the effects of erythromycin, azithromycin, or trimethoprim in neonates with chlamydial conjunctivitis. A meta-analysis using a random-effects generic inverse-variance method was performed, and the certainty of evidence was assessed using the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) approach.
We found 12 studies (n = 292 neonates) and were able to meta-analyze 7 studies that used erythromycin at a dose of 50 mg/kg body weight per day for 14 days. The clinical and microbiological cure were 96% (95% confidence interval [CI], 94%-100%) and 97% (95% CI, 95%-99%), respectively, and adverse gastrointestinal effects occurred in 14% (95% CI, 1%-28%) of the neonates. The microbiological cure in the study that assessed azithromycin at 20 mg/kg per day were 60% (95% CI, 27%-93%) when it was given in a single dose and 86% (95% CI, 61%-100%) when given in a 3-day course. Two studies reported compliance with treatments, and 1 study reported no pyloric stenosis events. Because of the risk of bias and the few neonates included across the studies, the certainty of evidence is low to very low. No studies assessed trimethoprim.
Although evidence suggests that erythromycin at 50 mg/kg per day for 14 days results in higher numbers of cure than does azithromycin, compliance and risk of pyloric stenosis related to their use for other infections in neonates will factor into treatment recommendations. More data are needed to compare these treatments directly.
由于全世界衣原体的高流行率以及分娩过程中母亲向婴儿传播的高风险,对于感染衣原体的婴儿,仍需要安全有效的治疗方法。我们对治疗新生儿衣原体结膜炎的抗生素治疗(包括口服红霉素、阿奇霉素和甲氧苄啶)进行了系统评价和荟萃分析。
我们检索了 Medline、Embase 和 Cochrane 中央对照试验注册库(CENTRAL),从建库至 2017 年 7 月 14 日。我们纳入了评估红霉素、阿奇霉素或甲氧苄啶治疗衣原体结膜炎新生儿的随机和非随机研究。采用随机效应通用倒数方差法进行荟萃分析,并使用推荐评估、制定与评价分级(GRADE)方法评估证据质量。
我们发现了 12 项研究(n = 292 名新生儿),并能够对 7 项使用 50mg/kg/天红霉素治疗 14 天的研究进行荟萃分析。临床和微生物学治愈率分别为 96%(95%置信区间[CI],94%-100%)和 97%(95%CI,95%-99%),不良反应发生率为 14%(95%CI,1%-28%)。评估阿奇霉素 20mg/kg/天时,单次剂量和 3 天疗程的微生物学治愈率分别为 60%(95%CI,27%-93%)和 86%(95%CI,61%-100%)。两项研究报告了治疗的依从性,一项研究报告无幽门狭窄事件。由于偏倚风险和研究中纳入的新生儿数量较少,证据质量为低到极低。没有研究评估甲氧苄啶。
尽管有证据表明,50mg/kg/天红霉素治疗 14 天比阿奇霉素的治愈率更高,但由于新生儿其他感染的使用会涉及到依从性和幽门狭窄的风险,这些因素将影响治疗建议。需要更多的数据来直接比较这些治疗方法。