Pediatric Pulmonary Unit, The National Center for Cystic Fibrosis, The Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Department of Physical Therapy, Faculty of Social Welfare and Health Sciences, University of Haifa, Haifa, Israel.
Pediatr Pulmonol. 2020 Nov;55(11):3046-3052. doi: 10.1002/ppul.25020. Epub 2020 Aug 24.
Autogenic drainage (AD) is used for airway clearance in individuals with cystic fibrosis (CF). The mechanical insufflator-exsufflator (MI-E) device is commonly used in patients with neuromuscular diseases for airway clearance by increasing inspiratory volume and expiratory flow. MI-E use has not been studied extensively in CF patients.
To examine whether there are advantages to using the MI-E device in patients with CF.
Fourteen males and eight females from the national center for CF, with an average FEV of 54% were recruited DESIGN: Prospective cross-over trial (IRB 3009-16-SMC).
Subjects received either AD or MI-E in a random order. Sputum was collected and weighed immediately after treatment. Subjects performed lung function tests at baseline, 20 minutes after and 1 hour after treatment; additionally, a 2-minute walk test was performed at the end of all lung function tests. Saturation, dyspnea scores while resting and after a 2-minute walk and subjective fatigue were recorded.
Thirty-six percent more sputum was collected following MI-E than AD treatment (P < .0001). A significant difference in saturation in response to the 2MWT was noted in both treatments significantly less desaturation was recorded after the 2MWT in the MI-E treatment (P < .01).
Treatment with the MI-E was more effective for clearing sputum in CF subjects, initial evidence suggests that the MI-E may be successfully incorporated into treatment protocols. Further studies are needed to assess the long-term benefits of MI-E in patients with CF.
自主引流 (AD) 用于清除囊性纤维化 (CF) 患者的气道。机械性吹气-呼气装置 (MI-E) 常用于神经肌肉疾病患者,通过增加吸气量和呼气流量来清除气道。MI-E 在 CF 患者中的应用尚未得到广泛研究。
研究 MI-E 装置在 CF 患者中的使用是否具有优势。
来自国家 CF 中心的 14 名男性和 8 名女性,平均 FEV 为 54%,采用前瞻性交叉试验设计(IRB 3009-16-SMC)。
受试者随机接受 AD 或 MI-E 治疗。治疗后立即收集并称重痰液。受试者在基线、治疗后 20 分钟和 1 小时进行肺功能测试;此外,在所有肺功能测试结束时进行 2 分钟步行测试。记录饱和度、休息时和 2 分钟步行后呼吸困难评分以及主观疲劳。
MI-E 治疗后收集的痰液比 AD 治疗多 36%(P<0.0001)。两种治疗方法在 2MWT 后的饱和度均有显著差异,MI-E 治疗后的饱和度下降明显较少(P<0.01)。
MI-E 治疗 CF 患者的痰液清除效果更好,初步证据表明 MI-E 可能成功纳入治疗方案。需要进一步研究来评估 MI-E 在 CF 患者中的长期益处。