Department of Pediatrics, Hanoi Medical University, Hanoi, Vietnam.
Department of Cardiology, Heart Center, Vietnam National Children's Hospital, Hanoi, Vietnam.
Eur J Cardiothorac Surg. 2024 Jun 3;65(6). doi: 10.1093/ejcts/ezae227.
Children with congenital tracheal stenosis born in the developing world face a high risk of mortality due to limited access to proper treatment. Patients who required preoperative respiratory support were suspected to have poor survival after slide tracheoplasty; however, this was not clearly demonstrated in the previous studies. This study aims to investigate the impact of preoperative respiratory conditions on outcomes of slide tracheoplasty.
From 2016 to 2022, children who underwent slide tracheoplasty were retrospectively reviewed. Patients with respiratory distress requiring emergency operations (group A) were compared with patients in stable condition who were scheduled for surgery (group B).
Perioperative results revealed that group A (n = 43) had a longer bypass time (P < 0.001), operation time (P = 0.01), postoperative ventilation time (P < 0.001) and length of intensive care unit stay (P = 0.00125) than group B (n = 60). The early mortality rate was 7.8%, and the actuarial 5-year survival rate was 85.3%. The cumulative incidence test revealed that group A was highly significant for overall mortality [sudistribution (SHR) 4.5; 95% confidence interval (CI) 1.23-16.4; P = 0.023]. Risk factors for overall mortality were prolonged postoperative ventilation time (hazard ratio 3.86; 95% CI 1.20-12.48; P = 0.024), bronchial stenosis (hazard ratio 5.77; 95% CI 1.72-19.31; P = 0.004), and preoperative tracheal mucositis (hazard ratio 5.67; 95% CI 1.51-21.31; P = 0.01). Four patients needed reintervention during a follow-up of 28.4 months (interquartile range 15.3-47.3).
Preoperative respiratory distress negatively affected the outcomes of patients who required slide tracheoplasty. Therefore, early detection of congenital tracheal stenosis and aggressive slide tracheoplasty are crucial and obligatory to enhance long-term survival in this lethal congenital airway disease.
发展中国家出生的先天性气管狭窄患儿因无法获得适当的治疗而面临高死亡率。需要术前呼吸支持的患者在进行滑式气管成形术后被怀疑存活率低,但这在以前的研究中并未得到明确证明。本研究旨在探讨术前呼吸状况对滑式气管成形术结果的影响。
回顾性分析 2016 年至 2022 年期间接受滑式气管成形术的患儿。将需要紧急手术的呼吸窘迫患儿(A 组)与择期手术的稳定患儿(B 组)进行比较。
围手术期结果显示,A 组(n=43)的体外循环时间(P<0.001)、手术时间(P=0.01)、术后通气时间(P<0.001)和重症监护病房住院时间(P=0.00125)均长于 B 组(n=60)。早期死亡率为 7.8%,5 年生存率为 85.3%。累积发病率检验显示,A 组的总死亡率显著升高[分布(SHR)4.5;95%置信区间(CI)1.23-16.4;P=0.023]。总死亡率的危险因素包括术后通气时间延长(风险比 3.86;95%CI 1.20-12.48;P=0.024)、支气管狭窄(风险比 5.77;95%CI 1.72-19.31;P=0.004)和术前气管黏膜炎(风险比 5.67;95%CI 1.51-21.31;P=0.01)。4 例患者在 28.4 个月的随访中需要再次干预(四分位间距 15.3-47.3)。
术前呼吸窘迫对需要滑式气管成形术的患者的结果产生负面影响。因此,早期发现先天性气管狭窄并积极进行滑式气管成形术对于提高这种致命性先天性气道疾病的长期生存率至关重要。