Department of Pediatric Pulmonology, Armand Trousseau University Hospital, Paris, France.
I-Motion, Hôpital Armand Trousseau, Paris, France.
Pediatr Pulmonol. 2022 Jun;57(6):1505-1512. doi: 10.1002/ppul.25899. Epub 2022 Mar 28.
The recent development of disease-modifying treatments in spinal muscular atrophy (SMA) type 1 shifted these patients' management from palliative to proactive. The aim of this study was to assess patients' nocturnal gas exchanges before noninvasive ventilation (NIV) initiation and their clinical evolution to determine if capnia is a good criterion to decide when to introduce respiratory support.
This multicentric retrospective study reports the respiratory management and evolution of 17 SMA type 1 children (10 females) for whom treatment with Nusinersen was initiated between 2016 and 2018.
Median [interquartile range-IQR] age at diagnosis and at first Nusinersen injection was of 4 [3;8] and 4 [3;9] months, respectively. Patients were followed during 38 [24;44] months. Thirteen (76%) patients were started on NIV at a median [IQR] age of 12 [9;18] months. Repeated hospitalizations and intensive care unit admissions were needed for 11 of them. Blood gas and nocturnal gas exchange recordings performed before NIV initiation were always normal. 9/13 X-ray performed before NIV showed atelectasis and/or acute lower respiratory tract infections. There was a significant decrease in the total number of hospital admissions between the first and second year of treatment (p = 0.04).
This study shows that patients do not present with nocturnal hypoventilation before respiratory decompensations and NIV initiation, and suggests that a delay in NIV initiation might result in respiratory complications. There is a need for disease-centered guidelines for the respiratory management of these patients, including NIV indications.
脊髓性肌萎缩症(SMA)1 型的新型治疗方法的出现,使得这些患者的治疗从姑息性转变为主动治疗。本研究旨在评估患者在开始无创通气(NIV)之前的夜间气体交换情况,并评估其临床演变,以确定碳酸血症是否是决定何时引入呼吸支持的良好标准。
本多中心回顾性研究报告了 17 例 SMA 1 型患儿(10 例女性)的呼吸管理和演变情况,他们均在 2016 年至 2018 年间接受了 Nusinersen 治疗。
诊断时和首次接受 Nusinersen 注射时的中位年龄[四分位距(IQR)]分别为 4[3;8]和 4[3;9]个月。患者的中位随访时间为 38[24;44]个月。13 例(76%)患者在中位年龄为 12[9;18]个月时开始使用 NIV。其中 11 例需要反复住院和入住重症监护病房。在开始使用 NIV 之前进行的血气和夜间气体交换记录始终正常。在开始使用 NIV 之前进行的 9/13 例 X 光检查显示肺不张和/或急性下呼吸道感染。在治疗的第一年和第二年之间,总住院人数显著减少(p=0.04)。
本研究表明,患者在呼吸失代偿和开始使用 NIV 之前没有出现夜间通气不足的情况,这提示延迟开始 NIV 可能导致呼吸并发症。需要制定以疾病为中心的指南来管理这些患者的呼吸,包括 NIV 的适应证。