Sekioka Akinori, Fukumoto Koji, Miyake Hiromu, Nakaya Kengo, Nomura Akiyoshi, Yamada Susumu, Kanai Risa, Urushihara Naoto
Department of Pediatric Surgery, Shizuoka Children's Hospital, Shizuoka, Japan.
Department of Pediatric Surgery, Shizuoka Children's Hospital, Shizuoka, Japan.
J Surg Res. 2020 Nov;255:216-223. doi: 10.1016/j.jss.2020.05.061. Epub 2020 Jun 19.
Although pediatric tracheostomy has been a widely performed, life-saving procedure, its long-term outcomes have remained unclear. This study aimed to review outcomes after tracheostomy at a Japanese tertiary hospital and clarify candidates for and timing of decannulation.
Hospital records of critically ill children who underwent tracheostomy from 2001 to 2014 were retrospectively reviewed, subsequently analyzing outcomes according to demographics, complications, and decannulation. After excluding those who were lost to follow-up or had irreversible neuromuscular impairment, the remaining patients were divided into the decannulation (D group) and nondecannulation (ND group) groups and compared.
In total, 184 patients who underwent tracheostomy were analyzed (median age at operation: 0.5 y). The major indication for tracheostomy was irreversible neuromuscular impairment (46%). Surgery-related and overall mortality rates were 1% and 25%, respectively, while the successful decannulation rate was 21%. No significant difference in surgical indications or comorbidities was observed between the D (n = 39) and ND (n = 50) groups, except for infection (7 in D group versus 0 in ND group; P = 0.002) and chromosome-gene disorder (15% versus 34%; P = 0.04). The ND group had a significantly higher mortality rate than the D group (46% versus 3%; P < 0.0001). The median time to decannulation was 3.6 years, while that for infection was 0.7 y.
Patients who underwent tracheostomy at our institution due to temporary infections achieved more successful and earlier decannulation compared to other indications. Chromosome-gene disorder as a comorbidity can negatively affect decannulation.
尽管小儿气管切开术是一种广泛开展的挽救生命的手术,但其长期预后仍不明确。本研究旨在回顾一家日本三级医院气管切开术后的预后情况,并明确拔管的适应证和时机。
对2001年至2014年期间接受气管切开术的危重症患儿的医院记录进行回顾性分析,随后根据人口统计学、并发症和拔管情况分析预后。在排除失访或有不可逆神经肌肉损伤的患者后,将其余患者分为拔管组(D组)和未拔管组(ND组)并进行比较。
共分析了184例接受气管切开术的患者(手术时的中位年龄:0.5岁)。气管切开术的主要适应证是不可逆神经肌肉损伤(46%)。手术相关死亡率和总死亡率分别为1%和25%,而成功拔管率为21%。D组(n = 39)和ND组(n = 50)在手术适应证或合并症方面未观察到显著差异,但感染情况除外(D组7例,ND组0例;P = 0.002)以及染色体 - 基因疾病(15%对34%;P = 0.04)。ND组的死亡率显著高于D组(46%对3%;P < 0.0001)。拔管的中位时间为3.6年,而感染的中位时间为0.7年。
与其他适应证相比,因临时感染在我院接受气管切开术的患者实现了更成功、更早的拔管。染色体 - 基因疾病作为合并症会对拔管产生负面影响。