Saddi Vishal, Teng Arthur, Thambipillay Ganesh, Allen Hugh, Pithers Sonia, Sullivan Colin
Department of Sleep Medicine Sydney Children's Hospital Sydney New South Wales Australia.
School of Women and Children's Health, Faculty of Medicine University of New South Wales Sydney New South Wales Australia.
Respirol Case Rep. 2019 Jun 22;7(6):e00448. doi: 10.1002/rcr2.448. eCollection 2019 Aug.
Congenital central hypoventilation syndrome (CCHS) is a rare disorder characterized by alveolar hypoventilation and autonomic dysregulation secondary to mutations of the genes. Treatment consists of assisted ventilation using positive pressure ventilators via tracheostomy, bi-level positive airway pressure (BPAP), negative pressure ventilators, or diaphragm pacing. Previous case reports have highlighted early use of nasal non-invasive BPAP use in infants with CCHS. We present a case of a 10-month-old infant who was successfully managed on a new feature of non-invasive ventilation called average volume assured pressure support (AVAPS) without the need for tracheostomy. The AVAPS feature enables the machine to automatically adjust the inspiratory pressures to deliver a constant targeted tidal volume. This feature enabled a better control of ventilation as indicated by a more stable transcutaneous carbon dioxide profile compared to conventional nasal non-invasive BPAP, making non-invasive ventilation a more accessible method of managing sleep hypoventilation in CCHS.
先天性中枢性低通气综合征(CCHS)是一种罕见的疾病,其特征为肺泡低通气以及继发于基因突变的自主神经调节异常。治疗方法包括通过气管造口术使用正压通气机进行辅助通气、双水平气道正压通气(BPAP)、负压通气机或膈肌起搏。既往病例报告强调了在患有CCHS的婴儿中早期使用经鼻无创BPAP。我们报告一例10个月大的婴儿,该婴儿通过一种名为平均容量保证压力支持(AVAPS)的无创通气新功能成功得到治疗,无需气管造口术。AVAPS功能使机器能够自动调整吸气压力以输送恒定的目标潮气量。与传统经鼻无创BPAP相比,该功能能够更好地控制通气,表现为经皮二氧化碳曲线更稳定,使得无创通气成为管理CCHS睡眠低通气更易获得的方法。