Medical Centre Haaglanden-Bronovo, The Hague, The Netherlands.
Laboratory of Medical Microbiology and Immunology, St Elisabeth Hospital, Tilburg, The Netherlands.
Clin Microbiol Infect. 2017 Jun;23(6):355-362. doi: 10.1016/j.cmi.2016.08.003. Epub 2016 Aug 17.
Nitrofurantoin has been used for the prevention of urinary tract infection (UTI) for over 60 years. We conducted a systematic review and meta-analysis to assess its efficacy and safety in the prophylaxis of UTI.
We performed a systematic review of all controlled trials in humans assessing nitrofurantoin for UTI prophylaxis published from 1946 to 2015. We further reviewed population-level cohort studies evaluating nitrofurantoin's toxicity. Meta-analyses assessing efficacy and adverse events were conducted on controlled trials.
Twenty-six controlled trials including 3052 patients fulfilled entry criteria for the systematic review and meta-analysis on efficacy and toxicity, and 16 population-level cohort studies were identified for review of toxicity. Overall quality was poor, with all studies at increased risk for various biases. When compared with no prophylaxis, nitrofurantoin is effective in the prevention of UTI (risk ratio 0.38 in favour of nitrofurantoin, 95% CI 0.30-0.48). Its prophylactic efficacy is superior to that of methenamine hippurate and comparable to that of other antibacterials. Compared with patients receiving other antibacterials, those receiving nitrofurantoin had an increased risk of 2.24 (95% CI 1.77-2.83) for a non-severe adverse effect. In all controlled trials, only one patient experienced a severe adverse effect (interstitial pneumonia). Cohort studies reported severe adverse effect frequencies of 0.02-1.5 per 1000 nitrofurantoin users.
Nitrofurantoin is effective in the prevention of UTI. Its use may be associated with increased non-severe adverse effects; severe adverse effects occur infrequently. The risk of severe toxicity seems to increase with the duration of nitrofurantoin prophylaxis.
呋喃妥因用于预防尿路感染(UTI)已有超过 60 年的历史。我们进行了系统评价和荟萃分析,以评估其在预防 UTI 中的疗效和安全性。
我们对 1946 年至 2015 年期间发表的所有评估呋喃妥因用于 UTI 预防的人类对照试验进行了系统评价。我们还对评估呋喃妥因毒性的人群队列研究进行了回顾。对对照试验进行了评估疗效和不良事件的荟萃分析。
26 项对照试验(共 3052 名患者)符合系统评价和荟萃分析疗效和毒性的标准,16 项人群队列研究被确定为毒性评价。总体质量较差,所有研究均存在各种偏倚的风险增加。与无预防措施相比,呋喃妥因在预防 UTI 方面有效(风险比 0.38,有利于呋喃妥因,95%置信区间 0.30-0.48)。其预防效果优于三聚氰胺尿酸盐,与其他抗菌药物相当。与接受其他抗菌药物的患者相比,接受呋喃妥因治疗的患者发生非严重不良事件的风险增加 2.24 倍(95%置信区间 1.77-2.83)。在所有对照试验中,只有 1 名患者出现严重不良事件(间质性肺炎)。队列研究报告呋喃妥因使用者的严重不良事件发生率为每 1000 名患者 0.02-1.5 例。
呋喃妥因可有效预防 UTI。其使用可能与增加的非严重不良事件相关;严重不良事件发生频率较低。严重毒性的风险似乎随着呋喃妥因预防的持续时间而增加。