The Antibiotic Centre for Primary Care, Department of General Practice, Institute of Health and Society, University of Oslo, Oslo, Norway.
Infect Dis (Lond). 2020 Jun;52(6):405-412. doi: 10.1080/23744235.2020.1736329. Epub 2020 Mar 14.
There is a lack of evidence on treatment of urinary tract infections (UTIs) in male patients in a primary care setting, and whether narrow-spectrum antibiotics are safe and effective. To explore antibiotic switch rates after treatment with UTI antibiotics in men over the last 11 years. We analysed data from the Norwegian Prescription Database (NorPD). Men ≥16 years receiving cefalexin, ciprofloxacin, cotrimoxazole, nitrofurantoin, ofloxacin, pivmecillinam or trimethoprim during the period 2008-2018 were included. Antibiotic switch was defined as being prescribed a different antibiotic drug appropriate for UTI within 14 days after initial treatment. We calculated rates of antibiotic switch and corresponding odds ratios for each antibiotic drug. Seven hundred twenty-six thousand and ninety-six (726,096) prescriptions to 429,807 men were defined as possible UTI episodes. Fluoroquinolones, pivmecillinam and cotrimoxazole were most frequently prescribed. Forty-nine thousand five hundred and thirty-one (49,531) (6.8%) of the treatments resulted in antibiotic switch. Compared to cotrimoxazole, the risk of antibiotic switch was higher for pivmecillinam (OR: 2.46; 95% CI, 2.39-2.53) and trimethoprim (OR: 2.12; 95% CI, 2.04-2.20), and lower for fluoroquinolones (OR: 0.40; 95% CI, 0.39-0.42) and cefalexin (OR: 0.28; 95% CI, 0.26-0.30). Treatment duration of ≥7 days and age of ≥50 years were associated with an increased risk of antibiotic switch. Fluoroquinolones and cefalexin were associated with lower antibiotic switch rates than the recommended UTI antibiotics (pivmecillinam, nitrofurantoin and trimethoprim). However, the rates of antibiotic switch following treatment of male patients with first-line empirical UTI antibiotics are relatively low, indicating that the current guidelines are safe.
在初级保健环境中,针对男性患者的尿路感染 (UTI) 治疗缺乏证据,并且不清楚窄谱抗生素是否安全有效。本研究旨在探究过去 11 年中男性 UTI 抗生素治疗后的抗生素转换率。我们分析了挪威处方数据库 (NorPD) 的数据。纳入年龄≥16 岁、2008 年至 2018 年期间接受头孢氨苄、环丙沙星、复方磺胺甲噁唑、呋喃妥因、氧氟沙星、匹美西林或甲氧苄啶治疗的男性患者。抗生素转换定义为初始治疗后 14 天内开处方另一种治疗 UTI 的抗生素药物。我们计算了每种抗生素药物的抗生素转换率和相应的比值比 (OR)。726096 份处方治疗 429807 名男性患者被定义为可能的 UTI 发作。氟喹诺酮类药物、匹美西林和复方磺胺甲噁唑是最常开的药物。49531 (6.8%)的治疗方案需要抗生素转换。与复方磺胺甲噁唑相比,匹美西林(OR:2.46;95%CI,2.39-2.53)和甲氧苄啶(OR:2.12;95%CI,2.04-2.20)的抗生素转换风险更高,而氟喹诺酮类药物(OR:0.40;95%CI,0.39-0.42)和头孢氨苄(OR:0.28;95%CI,0.26-0.30)的抗生素转换风险更低。治疗持续时间≥7 天和年龄≥50 岁与抗生素转换风险增加相关。氟喹诺酮类药物和头孢氨苄的抗生素转换率低于推荐的 UTI 抗生素(匹美西林、呋喃妥因和甲氧苄啶)。然而,一线经验性 UTI 抗生素治疗男性患者后的抗生素转换率相对较低,这表明当前的指南是安全的。