Division of Pediatric Otolaryngology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.
Department of Otolaryngology: Head & Neck Surgery, Perelman School of Medicine, The University of Pennsylvania, Philadelphia, Pennsylvania, U.S.A.
Laryngoscope. 2021 Nov;131(11):2550-2557. doi: 10.1002/lary.29592. Epub 2021 May 6.
OBJECTIVES/HYPOTHESIS: We report a posterior laryngeal rating system and measures of voice disability in pediatric patients undergoing phonosurgery for vocal fold paralysis. Posterior glottic deficiency may account for persistent voice disability.
Retrospective Study.
Retrospective analyses of 66 subjects with primary unilateral vocal fold paralysis were reviewed for the status of posterior glottis and voice disability (Pediatric Voice Handicap Index [pVHI]). Gestation age (GA), weight, and medical/surgical history were reviewed. The width, length, and depth of the larynx were analyzed to create a reproducible rating scale.
Mean GA was 29 weeks, with an intubation history for all subjects, with 90% having a left vocal fold immobility. Cardiac surgery was performed in 92% of subjects. A progressive rating (type 0-3) Benjamin Defect Severity Scale (BDSS) was developed to rate the absence or presence of a posterior abnormality. BDSS-2 and BDSS-3 subjects were more likely to have low birth weight. Extremely preterm GA was more likely to be associated with BDSS-1 (mild) or BDSS-2. History of multiple and prolonged intubations were seen more frequently in BDSS-2 or BDSS-3. Post-op pVHI reduced an average of 15 points for BDSS-0 to BDSS-2, but only 3 points for BDSS-3. Post-op pVHI matched normal values for preintervention dysphonic children.
The presence of a persistent breathy voice after intervention for unilateral vocal fold immobility is potentially associated with posterior glottic defects. Low birth weight with multiple/prolonged intubation is more likely to be present with higher-grade BDs, whereas low GA is more likely to be associated with BDSS-1 to BDSS-2.
4 Laryngoscope, 131:2550-2557, 2021.
目的/假设:我们报告了一种用于评估儿童声带麻痹行嗓音外科手术后声门下后区的嗓音障碍的评估系统和评估指标。声门下后区的缺失可能是持续性嗓音障碍的原因。
回顾性研究。
回顾性分析了 66 例原发性单侧声带麻痹患者的资料,评估了声门下后区的状态和嗓音障碍(儿童嗓音障碍指数[pVHI])。回顾了胎龄(GA)、体重和医疗/手术史。分析了喉的宽度、长度和深度,以创建一个可重复的评分系统。
平均 GA 为 29 周,所有患者均有插管史,90%的患者左侧声带固定不动。92%的患者接受了心脏手术。我们开发了一种渐进性评分(0-3 型)的 Benjamin 缺陷严重程度评分(BDSS),以评估是否存在或不存在后区异常。BDSS-2 和 BDSS-3 患者更有可能体重低。极早产 GA 更可能与 BDSS-1(轻度)或 BDSS-2 相关。BDSS-2 或 BDSS-3 患者中,多次和长时间插管的病史更为常见。BDSS-0 到 BDSS-2 的术后 pVHI 平均降低了 15 分,但 BDSS-3 仅降低了 3 分。术后 pVHI 与术前发声障碍儿童的正常值相匹配。
单侧声带固定术干预后持续性声音嘶哑可能与声门下后区缺陷有关。低出生体重合并多次/长时间插管更有可能出现高级别 BD,而低 GA 更可能与 BDSS-1 到 BDSS-2 相关。
4 级喉镜,131:2550-2557,2021。