Kassam Farris, Saeidiborojeni Sepehr, Finlayson Heather, Winston Paul, Reebye Rajiv
Canadian Advances in Neuro-Orthopedics for Spasticity Congress, Kingston, Ontario, Canada.
Division of Physical Medicine and Rehabilitation, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Arch Rehabil Res Clin Transl. 2021 Oct 8;3(4):100158. doi: 10.1016/j.arrct.2021.100158. eCollection 2021 Dec.
To investigate the practice patterns of Canadian physicians who use perioperative botulinum toxin (BoNT) injections to improve surgical outcomes on spastic limbs.
A cross-sectional national survey composed of an invitation email and an 18-item questionnaire was disseminated by a national physical medicine and rehabilitation (PMR) society to 138 physician members involved in spasticity management.
Not applicable.
Twenty-five percent of the participants (N=34) fully completed the survey.
Not applicable.
Participants completed an online questionnaire that examined the practice patterns and surgical outcomes associated with perioperative BoNT injections.
The majority (n=21; 84%) of Canadian physicians who inject BoNT perioperatively to improve outcomes of surgeries performed on spastic limbs are specialists in PMR practicing in academic settings. Most respondents (74%) used BoNT injections for perioperative treatment for patients with limb spasticity undergoing surgery. Of those surveyed, 65% of physicians used BoNT preoperatively, 21% used BoNT intraoperatively, and 24% used BoNT postoperatively.Of the physicians who performed BoNT injections preoperatively, 6% performed BoNT injections 7 to 12 weeks preoperatively, 32% performed BoNT injections 4 to 6 weeks preoperatively, 47% performed BoNT injections 2 to 3 weeks preoperatively, and 15% performed BoNT injections 0 to 1 week preoperatively. The majority of physicians (85%) responded that injecting BoNT perioperatively may improve a patient's surgical outcome and all of the participants (100%) stated that BoNT did not contribute to any perioperative complications or adverse effects. Qualitative responses emphasized that successful outcomes from the perioperative BoNT were linked to enhanced collaboration with surgeons and that more research is needed to determine the optimal timing of perioperative BoNT.
Canadian physicians, mostly PMR specialists, administer perioperative BoNT to improve outcomes of surgeries performed on spastic limbs. The optimal timing for perioperative BoNT was suggested to be 2 to 3 weeks before the surgery by 47% of survey respondents. All participating physicians responded that perioperative BoNT did not contribute to any known perioperative complications or adverse events. This study highlights the importance of conducting more robust research to better understand optimal timing for perioperative BoNT injection, enhancing collaboration between physicians and surgeons, and increasing awareness of perioperative BoNT when planning for surgeries on spastic limbs.
调查使用围手术期肉毒杆菌毒素(BoNT)注射以改善痉挛肢体手术效果的加拿大医生的实践模式。
一项横断面全国性调查,由一封邀请电子邮件和一份包含18个条目的问卷组成,由一个全国性物理医学与康复(PMR)协会分发给138名参与痉挛管理的医生成员。
不适用。
25%的参与者(N = 34)完全完成了调查。
不适用。
参与者完成了一份在线问卷,该问卷调查了与围手术期BoNT注射相关的实践模式和手术效果。
大多数(n = 21;84%)在围手术期注射BoNT以改善痉挛肢体手术效果的加拿大医生是在学术环境中执业的PMR专科医生。大多数受访者(74%)将BoNT注射用于接受手术的肢体痉挛患者的围手术期治疗。在接受调查的医生中,65%的医生在术前使用BoNT,21%的医生在术中使用BoNT,24%的医生在术后使用BoNT。在术前进行BoNT注射的医生中,6%在术前7至12周进行BoNT注射,32%在术前4至6周进行BoNT注射,47%在术前2至3周进行BoNT注射,15%在术前0至1周进行BoNT注射。大多数医生(85%)回答说围手术期注射BoNT可能会改善患者的手术效果,所有参与者(100%)表示BoNT不会导致任何围手术期并发症或不良反应。定性回答强调围手术期BoNT的成功效果与加强与外科医生的合作有关,并且需要更多研究来确定围手术期BoNT的最佳时机。
加拿大医生,大多是PMR专科医生会在围手术期使用BoNT以改善痉挛肢体的手术效果。47%的调查受访者建议围手术期BoNT的最佳时机是手术前2至3周。所有参与的医生都回答说围手术期BoNT不会导致任何已知的围手术期并发症或不良事件。本研究强调了进行更有力的研究以更好地了解围手术期BoNT注射的最佳时机、加强医生与外科医生之间的合作以及在计划对痉挛肢体进行手术时提高对围手术期BoNT的认识的重要性。