NeuroPain Care Center, Lake Success, NY 11042, USA.
NYU Langone Health, New York, NY 10017, USA.
Toxins (Basel). 2024 Sep 29;16(10):420. doi: 10.3390/toxins16100420.
OnabotulinumtoxinA (onabotA) is approved in the US for 12 therapeutic indications. Real-world data on onabotA multi-indication use are limited, often leading to delayed or reduced treatment. This study provides real-world evidence on the safety of onabotA when treating multiple indications concomitantly. SYNCHRONIZE was a multicenter, retrospective, chart-review study evaluating onabotA's safety for adults treated for ≥2 therapeutic indications within a 3-month period. The primary outcome was treatment-emergent adverse events (TEAEs) within 6 months post-treatment. A total of 279 patients were included. The most common concomitant indications treated were cervical dystonia and chronic migraine (43.4%). The average 3-month cumulative dose for multiple indications was 282.2 U. The treatment interval for multiple indications was ≤24 h for most patients (62.4%). Overall, 28.7% of patients reported ≥1 TEAE with no apparent trends in TEAEs and dose interval or cumulative dose. Reported TEAEs included UTI (5.7%), neck pain (5.0%), and headache (4.3%). No patient had a lack of effect according to clinical objective measurements. SYNCHRONIZE described the real-world safety of onabotA for patients treated concomitantly for ≥2 indications within a 3-month period. TEAEs were generally consistent with the known safety profiles of individual indications. No new safety signals were identified).
肉毒杆菌毒素 A(onabotA)在美国获准用于 12 种治疗适应症。关于同时治疗多种适应症的 onabotA 多适应症使用的真实世界数据有限,这通常导致治疗延迟或减少。本研究提供了同时治疗多种适应症时 onabotA 安全性的真实世界证据。SYNCHRONIZE 是一项多中心、回顾性、图表审查研究,评估了成人在 3 个月内接受≥2 种治疗适应症的 onabotA 的安全性。主要结局是治疗后 6 个月内出现的治疗中出现的不良事件(TEAEs)。共纳入 279 例患者。同时治疗的最常见的伴随适应症是颈部肌张力障碍和慢性偏头痛(43.4%)。多种适应症的平均 3 个月累积剂量为 282.2U。大多数患者的多适应症治疗间隔时间≤24 小时(62.4%)。总体而言,28.7%的患者报告了≥1 次 TEAEs,但 TEAEs 、剂量间隔或累积剂量无明显趋势。报告的 TEAEs 包括尿路感染(5.7%)、颈部疼痛(5.0%)和头痛(4.3%)。根据临床客观测量,没有患者出现疗效缺失。SYNCHRONIZE 描述了在 3 个月内同时治疗≥2 种适应症的患者中,onabotA 的真实世界安全性。TEAEs 通常与个别适应症的已知安全性特征一致。未发现新的安全性信号)。