Faghihi Toktam, Tekmehdash Leila Yavari, Radfar Mania, Gholami Kheirollah
Department of Clinical Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
J Res Pharm Pract. 2017 Oct-Dec;6(4):193-198. doi: 10.4103/jrpp.JRPP_17_27.
Fluoroquinolones are not routinely used as the first-line antimicrobial therapy in pediatrics. The American Academy of Pediatrics (AAP) and the United States Food and Drug Administration (FDA) approved fluoroquinolones on certain indications in children. The aim of this study was to evaluate to what extent and how ciprofloxacin is used on approved indication or as off-label. Besides, dose adequacy and treatment duration were assessed.
In a 10-month observational study, all children receiving systemic ciprofloxacin were assessed. We classified ciprofloxacin prescription to an AAP/FDA or off-label indication. The off-label prescriptions were further categorized to justified and unjustified therapy subgroups. The AAP/FDA category and the justified subgroup constituted the appropriate prescriptions.
During the study period, 32 patients were prescribed ciprofloxacin. In general, 37% (12) of prescriptions determined to be appropriate. Of the appropriate prescriptions, 7 were AAP/FDA-approved indications. Children with Crohn's disease with abdominal abscess and children with infectious bloody diarrhea constituted the off-label; justified therapy subgroup. Unjustified prescriptions mainly occurred in the presence of a suitable alternative antibiotic for ciprofloxacin. Mean ± SD of ciprofloxacin dose (mg/kg/day) and duration (days) were 21.25 ± 6.35 and 13.56 ± 8.48, respectively. Of the appropriate prescriptions, 41% were underdosed. Underdosing was more encountered in patients with cystic fibrosis. Duration of treatment of the appropriate prescriptions was determined to be appropriate.
The majority of children were receiving ciprofloxacin off-label and in an inappropriate manner. This issue emphasizes that antimicrobial stewardship program on ciprofloxacin use in pediatric hospitals should be implemented. Further studies evaluating clinical and microbiological outcomes of these programs in children are needed.
氟喹诺酮类药物在儿科并非常规用作一线抗菌治疗药物。美国儿科学会(AAP)和美国食品药品监督管理局(FDA)已批准氟喹诺酮类药物用于儿童的某些适应证。本研究的目的是评估环丙沙星在批准适应证或超说明书用药方面的使用程度及方式。此外,还评估了剂量充足性和治疗持续时间。
在一项为期10个月的观察性研究中,对所有接受全身性环丙沙星治疗的儿童进行了评估。我们将环丙沙星处方分类为AAP/FDA适应证或超说明书用药适应证。超说明书处方进一步分为合理和不合理治疗亚组。AAP/FDA类别和合理亚组构成适当处方。
在研究期间,32例患者被开具了环丙沙星处方。总体而言,37%(12例)的处方被确定为适当。在适当的处方中,7例为AAP/FDA批准的适应证。患有腹部脓肿的克罗恩病儿童和感染性血性腹泻儿童构成了超说明书用药的合理治疗亚组。不合理处方主要出现在有适合替代环丙沙星的抗生素的情况下。环丙沙星剂量(mg/kg/天)和疗程(天)的平均值±标准差分别为21.25±6.35和13.56±8.48。在适当的处方中,41%剂量不足。囊性纤维化患者中剂量不足的情况更为常见。适当处方的治疗持续时间被确定为合适。
大多数儿童接受的是超说明书且不适当的环丙沙星治疗。这个问题强调应在儿科医院实施关于环丙沙星使用的抗菌药物管理计划。需要进一步研究评估这些计划在儿童中的临床和微生物学结果。