Crawley Brianna K, Dehom Salem, Kutzner Emily, Murry Thomas, Krishna Priya, Hata Justin
Department of Otolaryngology-Head and Neck Surgery, Loma Linda University Health, Loma Linda, California, U.S.A.
Voice and Swallowing Center, School of Public Health, Loma Linda University Health, Loma Linda, California, U.S.A.
Laryngoscope. 2018 Apr;128(4):929-934. doi: 10.1002/lary.27061. Epub 2018 Jan 22.
OBJECTIVES/HYPOTHESIS: In-office laryngology procedures are important in the treatment of voice and swallowing disorders. Patient tolerance determines which procedures can be performed without sedation or formal anesthesia. This study examines pain perception during and after in-office vocal fold injection augmentation.
Prospective cohort study.
Patients scheduled for office-based vocal fold injection augmentation were prospectively enrolled at an academic voice center. The short-form McGill Pain Questionnaire was administered before, during, and after the procedure and on postprocedure days 1, 3, and 7. Pre- and postprocedure vital signs were recorded and heart rate was continuously monitored. Telephone questionnaires were completed on postprocedure days 1 and 3.
Forty-five patients consented to participate in our study (24 males, mean age 61 years). Most patients experienced mild to moderate pain with increasing heart rate during the procedure. Pain remained or increased 20 minutes after the procedure and improved but persisted for 1 day. Sensory and affective discomfort was endorsed by the majority. A minority of patients experienced bruising and changes in swallowing with diet modification for 3 days after the procedure. Sixteen percent had discomfort after 1 week.
This is the first prospective study examining patient perception of pain during and after in-office injection augmentation using a validated scale and pain descriptors with extended follow-up. The results may offer guidance for patient counseling, consent, and treatment to improve tolerance and success.
目的/假设:门诊喉科手术在嗓音和吞咽障碍治疗中很重要。患者的耐受性决定了哪些手术可以在无镇静或正规麻醉的情况下进行。本研究考察门诊声带注射填充术期间及术后的疼痛感知。
前瞻性队列研究。
在一家学术性嗓音中心前瞻性纳入计划接受门诊声带注射填充术的患者。在手术前、手术期间、手术后以及术后第1、3和7天进行简短麦吉尔疼痛问卷评估。记录术前和术后的生命体征并持续监测心率。在术后第1和3天完成电话问卷调查。
45名患者同意参与我们的研究(24名男性,平均年龄61岁)。大多数患者在手术过程中经历了轻度至中度疼痛,且心率增加。术后20分钟疼痛持续或加重,随后有所改善但持续了1天。大多数患者认可感觉和情感上的不适。少数患者在术后3天出现瘀斑以及因饮食调整导致吞咽改变。16%的患者在1周后仍有不适。
这是第一项使用经过验证的量表和疼痛描述词并进行延长随访来考察患者对门诊注射填充术期间及术后疼痛感知的前瞻性研究。研究结果可为患者咨询、同意和治疗提供指导,以提高耐受性并取得更好疗效。
4。《喉镜》,2018年,第128卷,第929 - 934页。