Department of Otolaryngology-Head & Neck Surgery, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Department of Otolaryngology-Head & Neck Surgery, Weill Cornell Medicine, New York, New York.
Laryngoscope. 2020 Jan;130(1):217-224. doi: 10.1002/lary.27765. Epub 2019 Jan 10.
Tracheo-innominate fistula (TIF) is a rare but fatal complication of tracheotomy. To date, there is a paucity of literature regarding pediatric TIFs. The objectives of this study were to conduct a systematic review of literature on pediatric TIF following tracheotomy and describe three demonstrative cases from our institutional experience.
We conducted a systematic review using MEDLINE, Embase, Cochrane Database of Systematic Reviews, Web of Science, and CINAHL. All studies with pediatric patients (under 18 years of age) who developed TIF following tracheotomy were included.
Fifty-four publications met inclusion criteria, reporting on 77 cases. The most common indication for tracheotomy was prolonged intubation and the need for ventilatory support (38.6%), with neurological comorbidities being the most common indication (72.7%). The mean time to TIF was 395.7 days (95% confidence interval, 225.9-565.5). Fifty-four patients (70.1%) presented with massive hemorrhage, whereas 18 patients (23.3%) presented with a sentinel bleeding event. The most common diagnostic interventions were computed tomography scan with or without contrast and bronchoscopy (55.8%). A substantial number of patients did not have any investigations (41.6%). Surgical management occurred in 70.1% of patients. Mortality was 38.6% in reported cases with variable follow-up periods.
TIF may occur in long-term tracheostomy-dependent children, contrary to the conventionally described 3-week postoperative period. The mortality may not be as high as previously reported with timely intervention. Our results are limited by inherent risks of bias. Further research including well-designed cohort studies are needed to guide an evidence-based approach to TIF.
NA Laryngoscope, 130:217-224, 2020.
气管-无名动脉瘘(TIF)是气管切开术后罕见但致命的并发症。迄今为止,关于儿科 TIF 的文献相对较少。本研究的目的是对气管切开术后小儿 TIF 的文献进行系统回顾,并描述我们机构经验中的三个示范病例。
我们使用 MEDLINE、Embase、Cochrane 系统评价数据库、Web of Science 和 CINAHL 进行了系统回顾。所有纳入研究均为气管切开术后发生 TIF 的儿科患者(年龄<18 岁)。
54 篇文献符合纳入标准,共报道 77 例病例。气管切开最常见的适应证是长时间插管和通气支持的需要(38.6%),最常见的合并症是神经系统疾病(72.7%)。TIF 的平均发生时间为 395.7 天(95%置信区间,225.9-565.5)。54 例患者(70.1%)表现为大出血,18 例患者(23.3%)表现为首发出血事件。最常见的诊断干预措施是计算机断层扫描(CT)扫描伴或不伴造影剂和支气管镜检查(55.8%)。相当一部分患者没有进行任何检查(41.6%)。手术治疗发生在 70.1%的患者中。报道病例的死亡率为 38.6%,随访时间不一。
TIF 可能发生在长期依赖气管切开的儿童中,与传统描述的术后 3 周不同。及时干预,死亡率可能没有之前报道的那么高。我们的结果受到固有偏倚风险的限制。需要进一步包括精心设计的队列研究在内的研究,以指导基于证据的 TIF 处理方法。
临床研究
NA
喉镜,130:217-224,2020。