Hospices Civils de Lyon, Hopital Edouard Herriot, Service d'ORL et de chirurgie cervico-faciale, Lyon cedex, F-69003, France.
Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, Service d'ORL, d'otoneurochirurgie et de chirurgie cervico-faciale, Pierre Bénite cedex, F-69495, France; Université de Lyon, Université Lyon 1, F-69003, Lyon, France; Université Paris Est Creteil, INSERM, IMRB, F-94010, Créteil, France; CNRS ERL 7000, F-94010, Créteil, France.
Int J Pediatr Otorhinolaryngol. 2022 Jul;158:111142. doi: 10.1016/j.ijporl.2022.111142. Epub 2022 May 13.
Laryngeal mobility disorder after a pediatric heart surgery is common (between 5 and 10% of cases), and has important consequences on swallowing, breathing and speaking. After reviewing the literature, the recovery rate is variable and the postoperative follow-up is often done on a short time frame. The primary objective of the study is to describe the recovery from laryngeal mobility disorder with a follow-up time of at least 5 years. The secondary objective is to describe of the quality of life of the child in terms of phonation and swallowing, and to identify potential risk factors for a lasting laryngeal mobility disorder.
We collected data (morphological characteristics and details of the procedures and medical care) on children who had undergone a heart surgery with risks of complications, between 2010 and 2015, and with a laryngeal mobility disorder detected after the surgery through nasal flexible laryngoscopy. During a follow-up consultation, carried at least 5 years after the surgery, we performed a nasal flexible laryngoscopy to assess whether or not the patient had recovered a full mobility of the larynx. Two questionnaires were also given to the patients, the pVHI and the PEDI EAT-10, to assess respectively the quality of their speech and of their swallowing function.
The recovery rate for a laryngeal mobility disorder more than 5 years after surgery was found to be 65% (9 children out of the 14 included in the study). We identified a risk factor for the persistence of a laryngeal mobility disorder after surgery: the presence of an associated genetic syndrome, p = 0.025. Children with persistent laryngeal mobility disorder have an impaired quality of life score, using the pVHI scale, which correlates well with the flexible laryngoscopy findings, p = 0.033.
Children with a lasting laryngeal mobility disorder have disabling respiratory and vocal symptoms in their daily lives. Nasal flexible laryngoscopy should therefore be systematically performed postoperatively after a surgery carrying risks. For improved patient management, early detection of these disorders by pharyngolaryngeal nasal flexible laryngoscopy in the aftermath of high-risk cardiac surgery is strongly advised, with prolonged follow-up.
小儿心脏手术后出现喉运动障碍较为常见(占 5%至 10%),对吞咽、呼吸和言语功能有重要影响。通过文献回顾,其恢复率存在差异,术后随访时间通常较短。本研究的主要目的是描述至少 5 年随访时间的喉运动障碍恢复情况。次要目标是描述患儿的发音和吞咽生活质量,并确定持续性喉运动障碍的潜在危险因素。
我们收集了 2010 年至 2015 年期间因心脏手术风险而出现并发症的患儿数据(形态学特征以及手术和医疗护理的详细信息),术后通过鼻软式喉镜检查发现患儿存在喉运动障碍。术后至少 5 年进行随访时,我们通过鼻软式喉镜检查评估患者的喉运动是否完全恢复。同时还向患儿发放了两个问卷,即 pVHI 和 PEDI EAT-10,以分别评估他们的言语质量和吞咽功能。
术后 5 年以上喉运动障碍的恢复率为 65%(14 例患儿中有 9 例)。我们发现了一个与术后持续性喉运动障碍相关的风险因素:存在伴发的遗传综合征,p=0.025。持续性喉运动障碍患儿的生活质量评分较低,使用 pVHI 量表评估时与软式喉镜检查结果相关,p=0.033。
持续性喉运动障碍患儿在日常生活中存在呼吸和发声功能障碍。因此,手术后应系统地进行鼻软式喉镜检查。为了改善患者的管理,强烈建议在高危心脏手术后,通过软式喉镜检查早期发现这些障碍,并进行长期随访。