Funamura Jamie L, Yuen Sonia, Kawai Kosuke, Gergin Ozgul, Adil Eelam, Rahbar Reza, Watters Karen
Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital, Boston, Massachusetts, U.S.A.
Department of Otology and Laryngology, Harvard Medical School, Boston, Massachusetts, U.S.A.
Laryngoscope. 2017 Jul;127(7):1701-1706. doi: 10.1002/lary.26361. Epub 2016 Nov 3.
OBJECTIVES/HYPOTHESIS: To assess the longitudinal risk of death following tracheostomy in the pediatric age group.
Retrospective cohort study.
Hospital records of 513 children (≤18 years) at a tertiary care children's hospital who underwent tracheostomy between 1984 and 2015 were reviewed. The primary outcome measure was time from tracheostomy to death. Secondary patient demographic and clinical characteristics were assessed, with likelihood of death using χ tests and the Cox proportional hazards model.
Median age at time of tracheostomy was 0.8 years (interquartile range, 0.3-5.2 years).The highest mortality rate (27.8%) was observed in patients in the 13- to 18-year-old age category; their mortality rate was significantly higher when compared to the lowest mortality risk group patients (age 1-4 years, P = .031). Timing of death was evenly distributed: <90 days (37.6%), 90 days to 1 year (27.1%), and >1 year after tracheostomy (35.3%). Patients who underwent tracheostomy for cardiopulmonary disease had an increased risk of mortality compared with airway obstruction (adjusted hazard ratio: 3.53, 95% confidence interval: 1.72-7.24, P < .001) and other indications. Adjusted hazard ratios for bronchopulmonary dysplasia (BPD) and congenital heart disease (CHD) were 2.63 and a 2.61, respectively (P < .001).
Pediatric patients with tracheostomy have a high mortality rate, with an increased risk of death associated with a cardiopulmonary indication for undergoing tracheostomy. The majority of deaths occur after the index hospitalization during which the tracheostomy was performed. BPD and CHD are independent predictors of mortality in pediatric tracheostomy patients.
4 Laryngoscope, 127:1701-1706, 2017.
目的/假设:评估儿科年龄组气管切开术后的纵向死亡风险。
回顾性队列研究。
回顾了一家三级医疗儿童医院1984年至2015年间接受气管切开术的513名儿童(≤18岁)的医院记录。主要结局指标是从气管切开术到死亡的时间。评估了次要的患者人口统计学和临床特征,使用χ检验和Cox比例风险模型评估死亡可能性。
气管切开术时的中位年龄为0.8岁(四分位间距,0.3 - 5.2岁)。在13至18岁年龄组的患者中观察到最高死亡率(27.8%);与最低死亡风险组患者(1 - 4岁,P = 0.031)相比,他们的死亡率显著更高。死亡时间分布均匀:气管切开术后<90天(37.6%)、90天至1年(27.1%)和>1年(35.3%)。因心肺疾病接受气管切开术的患者与气道阻塞患者相比,死亡风险增加(调整后的风险比:3.53,95%置信区间:1.72 - 7.24,P < 0.001)以及其他指征。支气管肺发育不良(BPD)和先天性心脏病(CHD)的调整后风险比分别为2.63和2.61(P < 0.001)。
儿科气管切开术患者死亡率高,因心肺指征接受气管切开术与死亡风险增加相关。大多数死亡发生在进行气管切开术的首次住院之后。BPD和CHD是儿科气管切开术患者死亡的独立预测因素。
4《喉镜》,127:1701 - 1706,2017年。