Canintika Anissa Feby, Dilogo Ismail Hadisoebroto
Department of Orthopaedics and Traumatology, Faculty of Medicine-Universitas Indonesia, Cipto Mangunkusumo Hospital, Jakarta, Indonesia.
J Clin Orthop Trauma. 2020 Feb;11(Suppl 1):S107-S112. doi: 10.1016/j.jcot.2019.10.009. Epub 2019 Nov 5.
Fracture nonunion remains a great challenge for orthopaedic surgeons. Approximately 5-10% of bone fractures do not heal promptly, and require another surgical procedure. Previously, several small studies have found that teriparatide, a parathyroid hormone (PTH) analogue, has been found to induce union in those with delayed union and nonunion. However, to date, no systematic reviews regarding the use of teriparatide for delayed union and nonunion are available. The present review aims to investigate the safety and efficacy of teriparatide in delayed union and nonunion.
Systematic literature search was performed in PubMed, ScienceDirect, and Google Scholar until September 26, 2019. We included studies involving adult patients (age >16 years) diagnosed with delayed union or nonunion fracture regardless of location (long bone, short bone, flat bone or irregular bone). The language was restricted to English and Indonesian. Outcomes that were recorded were fracture union and adverse events.
Initial search found 5416 abstract and titles. Of these, 20 articles consisting of 64 subjects were retrieved. Of these, 15 case reports, 4 case series, and one prospective study were included. All of the studies administered subcutaneous injection of teriparatide 20 μg/day with mean duration of 7.3 ± 1.5 weeks to 9.7 months. Sixty-one (95.3%) of 64 subjects developed complete union. The follow-up ranged from 3 to 24 months. No side effects occurred during the follow-up period.
Limited evidence demonstrates that daily subcutaneous injection of teriparatide 20 μg is a potential new safe treatment for delayed union and nonunion with no side effects. We highly suggest the use of such drug, as it is highly effective and safe. However, further clinical studies are required to investigate its safety and efficacy.
骨折不愈合仍然是骨科医生面临的巨大挑战。大约5%-10%的骨折不能及时愈合,需要再次进行外科手术。此前,几项小型研究发现,甲状旁腺激素(PTH)类似物特立帕肽可促使延迟愈合和不愈合患者实现骨折愈合。然而,迄今为止,尚无关于特立帕肽用于延迟愈合和不愈合的系统评价。本综述旨在研究特立帕肽治疗延迟愈合和不愈合的安全性和有效性。
在PubMed、ScienceDirect和谷歌学术上进行系统的文献检索,直至2019年9月26日。我们纳入了涉及诊断为延迟愈合或不愈合骨折的成年患者(年龄>16岁)的研究,骨折部位不限(长骨、短骨、扁骨或不规则骨)。语言限于英语和印尼语。记录的结果为骨折愈合情况和不良事件。
初步检索发现5416篇摘要和标题。其中,检索到20篇文章,共64例受试者。其中包括15篇病例报告、4篇病例系列研究和1篇前瞻性研究。所有研究均皮下注射特立帕肽20μg/天,平均疗程为7.3±1.5周至9.7个月。64例受试者中有61例(95.3%)实现了完全愈合。随访时间为3至24个月。随访期间未出现副作用。
有限的证据表明,每日皮下注射20μg特立帕肽是一种治疗延迟愈合和不愈合的潜在新的安全疗法,且无副作用。我们强烈建议使用这种药物,因为它高效且安全。然而,需要进一步的临床研究来调查其安全性和有效性。