Department of Epidemiology, Gillings School of Global Public Health,
Division of Pharmaceutical Outcomes and Policy, School of Pharmacy.
Pediatrics. 2021 Jun;147(6). doi: 10.1542/peds.2020-033316. Epub 2021 May 14.
To estimate the association between fluoroquinolone use and tendon injury in adolescents.
We conducted an active-comparator, new-user cohort study using population-based claims data from 2000 to 2018. We included adolescents (aged 12-18 years) with an outpatient prescription fill for an oral fluoroquinolone or comparator broad-spectrum antibiotic. The primary outcome was Achilles, quadricep, patellar, or tibial tendon rupture identified by diagnosis and procedure codes. Tendinitis was a secondary outcome. We used weighting to adjust for measured confounding and a negative control outcome to assess residual confounding.
The cohort included 4.4 million adolescents with 7.6 million fills for fluoroquinolone (275 767 fills) or comparator (7 365 684) antibiotics. In the 90 days after the index antibiotic prescription, there were 842 tendon ruptures and 16 750 tendinitis diagnoses (crude rates 0.47 and 9.34 per 1000 person-years, respectively). The weighted 90-day tendon rupture risks were 13.6 per 100 000 fluoroquinolone-treated adolescents and 11.6 per 100 000 comparator-treated adolescents (fluoroquinolone-associated excess risk: 1.9 per 100 000 adolescents; 95% confidence interval -2.6 to 6.4); the corresponding number needed to treat to harm was 52 632. For tendinitis, the weighted 90-day risks were 200.8 per 100 000 fluoroquinolone-treated adolescents and 178.1 per 100 000 comparator-treated adolescents (excess risk: 22.7 per 100 000; 95% confidence interval 4.1 to 41.3); the number needed to treat to harm was 4405.
The excess risk of tendon rupture associated with fluoroquinolone treatment was extremely small, and these events were rare. The excess risk of tendinitis associated with fluoroquinolone treatment was also small. Other more common potential adverse drug effects may be more important to consider for treatment decision-making, particularly in adolescents without other risk factors for tendon injury.
评估氟喹诺酮类药物使用与青少年肌腱损伤之间的关联。
我们开展了一项基于人群的回顾性队列研究,利用 2000 年至 2018 年的基于人群的理赔数据,纳入接受门诊氟喹诺酮类或广谱抗生素(作为对照)处方的 12-18 岁青少年。主要结局为通过诊断和手术代码确定的跟腱、股四头肌肌腱、髌腱或胫骨肌腱断裂。肌腱炎为次要结局。我们使用加权法调整了已测量的混杂因素,并使用负对照结局评估残余混杂因素。
该队列纳入了 440 万青少年,处方氟喹诺酮(275767 例)或对照抗生素(7365684 例)共 7600 万例。在索引抗生素处方后的 90 天内,共有 842 例肌腱断裂和 16750 例肌腱炎诊断(粗率分别为每 1000 人年 0.47 例和 9.34 例)。氟喹诺酮治疗青少年的 90 天肌腱断裂风险为 13.6/10 万,对照治疗青少年为 11.6/10 万(氟喹诺酮相关的超额风险为 1.9/10 万;95%置信区间-2.6 至 6.4);相应的危害需治疗人数为 52632 人。对于肌腱炎,氟喹诺酮治疗青少年的 90 天风险为 200.8/10 万,对照治疗青少年为 178.1/10 万(超额风险为 22.7/10 万;95%置信区间 4.1 至 41.3);相应的危害需治疗人数为 4405 人。
氟喹诺酮类药物治疗相关的肌腱断裂风险的超额风险极小,且此类事件极为罕见。氟喹诺酮类药物治疗相关的肌腱炎风险的超额风险也较小。对于治疗决策,可能需要考虑其他更常见的潜在药物不良反应,特别是在无肌腱损伤其他风险因素的青少年中。