Holzer S E, Ludlow C L
Voice and Speech Section, National Institute on Deafness and Other Communication Disorders, Bethesda, MD 20892, USA.
Laryngoscope. 1996 Jan;106(1 Pt 1):86-92. doi: 10.1097/00005537-199601000-00017.
Botulinum toxin type A (BOTOX) injection of the thyroarytenoid muscle is used to control speech symptoms in patients with adductor spasmodic dysphonia. Transient difficulty in swallowing liquids is a common treatment side effect. Laryngeal movement durations were measured during swallowing in 13 adductor spasmodic dysphonia patients undergoing treatment and in 6 normal control subjects in order to determine the following: 1. whether, prior to the injection, laryngeal movement durations were longer in the spasmodic dysphonia patients than in the control subjects; 2. whether movement durations increased following the injections; 3. whether preinjection swallowing difficulties related to postinjection swallowing measurements and postinjection patient reports of swallowing problems. A piezoelectric movement transducer was shown to be accurate for noninvasive measurement of laryngeal movement duration in relation to muscle onset and offset for hyoid elevation and relaxation. Before botulinum toxin type A injection, no significant differences in swallowing duration were found between the patient and control groups. Four patients with swallowing complaints prior to injection had longer laryngeal movement durations than the other spasmodic dysphonia patients and the control subjects. Following injection, laryngeal movement durations increased in the patients with spasmodic dysphonia, and eight patients reported dysphagia for an average of 2 weeks. Relationships were found between the patients' initial reports of swallowing problems and increased laryngeal movement durations before and after botulinum toxin type A injection. Those patients initially reporting swallowing difficulties had severe dysphagia for 2 weeks after the injection. Patient reports of dysphagia prior to injection may indicate a greater likelihood of significant dysphagia following thyroarytenoid injection with botulinum toxin type A.
A型肉毒杆菌毒素(保妥适)注射甲状杓肌用于控制内收型痉挛性发声障碍患者的言语症状。吞咽液体时出现短暂困难是常见的治疗副作用。为了确定以下几点,对13名接受治疗的内收型痉挛性发声障碍患者和6名正常对照受试者在吞咽过程中的喉部运动持续时间进行了测量:1. 在注射前,痉挛性发声障碍患者的喉部运动持续时间是否比对照受试者更长;2. 注射后运动持续时间是否增加;3. 注射前的吞咽困难是否与注射后的吞咽测量结果以及患者注射后吞咽问题的报告相关。结果表明,压电运动传感器可准确无创测量与舌骨抬高和放松的肌肉起始和偏移相关的喉部运动持续时间。在注射A型肉毒杆菌毒素之前,患者组和对照组之间的吞咽持续时间没有显著差异。4名注射前有吞咽主诉的患者的喉部运动持续时间比其他痉挛性发声障碍患者和对照受试者更长。注射后,痉挛性发声障碍患者的喉部运动持续时间增加,8名患者报告吞咽困难,平均持续2周。在患者最初报告的吞咽问题与A型肉毒杆菌毒素注射前后喉部运动持续时间增加之间发现了相关性。那些最初报告吞咽困难的患者在注射后出现了2周的严重吞咽困难。患者注射前报告的吞咽困难可能表明在注射A型肉毒杆菌毒素到甲状杓肌后出现明显吞咽困难的可能性更大。