Department of Neurosurgery, University Medical Centre Ljubljana.
Department for rehabilitation, University Rehabilitation Institute of Republic Slovenia - Soča.
Int J Rehabil Res. 2023 Sep 1;46(3):209-215. doi: 10.1097/MRR.0000000000000586. Epub 2023 Jun 22.
Since the first implantation in July 2001, the intrathecal baclofen (ITB) therapy for patients with generalized spasticity has been used in Slovenia for 20 years. The aim of this retrospective study was to evaluate the rates of different complications, especially if catheter-related complications were less frequent after the introduction of the coated catheter type in February 2013, and the potential correlation between higher baclofen doses and the incidence of complications. We retrospectively collected data from all patients in the registry during the period from 3 July 2001 to 31 December 2021. Among 138 patients (48 females), 120 patients had the first ITB system implanted at the University Medical Centre Ljubljana. Forty-three complications were reported in 38 patients (27%), with a total complication rate of 0.203/1000 days or 0.074/pump year. The most frequent was catheter-related (0.083/1000 days or 0.030/pump year), followed by skin-related (0.063/1000 days or 0.023/pump year) and pump-related complication (0.026/1000 days or 0.009/pump year). The incidence of catheter-related complications decreased significantly since the use of Ascenda type catheter: 14/7 complications per 88/147 implantations ( P = 0.008). Patients with complications had a statistically significantly higher dose of baclofen: median 400 µg/24h vs. median 300 µg/24h ( P = 0.016). Our retrospective analysis confirmed a significant decrease of catheter-related complications after the implementation of Ascenda type catheter in February 2013. Patients with a higher ITB dose had a statistically significantly higher incidence of complications. The total complication rate was a bit higher as previously reported in other studies, which is consistent with a long follow-up time.
自 2001 年 7 月首例植入以来,鞘内巴氯芬(ITB)治疗全身性痉挛已在斯洛文尼亚使用了 20 年。本回顾性研究的目的是评估不同并发症的发生率,特别是在 2013 年 2 月引入涂层导管类型后,导管相关并发症是否减少,以及较高巴氯芬剂量与并发症发生率之间的潜在相关性。我们回顾性地从注册中心的所有患者中收集了 2001 年 7 月 3 日至 2021 年 12 月 31 日期间的数据。在 138 名患者(48 名女性)中,有 120 名患者在卢布尔雅那大学医学中心植入了第一个 ITB 系统。38 名患者(27%)报告了 43 种并发症,总并发症发生率为 0.203/1000 天或 0.074/泵年。最常见的是导管相关(0.083/1000 天或 0.030/泵年),其次是皮肤相关(0.063/1000 天或 0.023/泵年)和泵相关并发症(0.026/1000 天或 0.009/泵年)。自使用 Ascenda 型导管以来,导管相关并发症的发生率显著下降:88/147 例植入中有 14/7 例并发症( P = 0.008)。有并发症的患者巴氯芬剂量明显较高:中位数 400μg/24h 与中位数 300μg/24h( P = 0.016)。我们的回顾性分析证实,自 2013 年 2 月实施 Ascenda 型导管以来,导管相关并发症显著减少。巴氯芬剂量较高的患者并发症发生率显著较高。总的并发症发生率略高于之前其他研究报道的结果,这与较长的随访时间一致。