Yonkov Alexander S, Yazova Iliana K, Chatalbashev Dimitar N
Clinic of Pediatric Surgery, University Hospital "St. George", Medical University, Plovdiv, Bulgaria.
Folia Med (Plovdiv). 2006;48(2):44-9.
The PURPOSE of the present study was to establish the treatment results of the applied approach for preoperative stabilization through mechanical ventilation and delayed surgical intervention as opposed to emergency surgical treatment in children with congenital diaphragmatic hernia.
Twenty-seven children have been treated (nine girls and 18 boys, twenty-four of them--newborns) over a ten-year period. The criteria for successful stabilization are arterial saturation of SaO2 90%, PaO2 = 90-100 mm Hg, PaCO2 40 mm Hg, pH 7.35.
Twenty-five of the children were with left-sided hernia (92.59%) and only two (7.41%) with right-sided hernia. The stabilization period ranged from 1 to 4 days, mean 1.48 +/- 0.18 (Sx = 0.81). Preoperatively, in eighteen newborns we used conventional mechanical ventilation; in one child only we used high frequency oscillating ventilation. In three children we failed to achieve stabilization and after worsening of their condition they died before they could be operated. In all children, postoperative mechanical ventilation was applied from 3 to 16 days, mean 7 +/- 0.65 (Sx = 3.16). The mortality was 59.26%.
The approach used for delayed surgical treatment has significant advantages compared to the urgent correction of the congenital diaphragmatic hernia. It provides opportunities for stabilization of the gas exchange and pulmonary circulation but still mortality remains high. New therapeutic techniques such as antenatal intervention or pulmonary transplantation are probably needed to save the lives of such patients.
本研究的目的是确定与先天性膈疝患儿的急诊手术治疗相反,通过机械通气进行术前稳定和延迟手术干预的应用方法的治疗效果。
在十年期间对27名儿童进行了治疗(9名女孩和18名男孩,其中24名是新生儿)。成功稳定的标准是动脉血氧饱和度SaO₂≥90%,动脉血氧分压PaO₂ = 90 - 100 mmHg,动脉血二氧化碳分压PaCO₂≤40 mmHg,pH值为7.35。
25名儿童为左侧疝(92.59%),仅2名(7.41%)为右侧疝。稳定期为1至4天,平均1.48 ± 0.18(标准误Sx = 0.81)。术前,18名新生儿使用传统机械通气;仅1名儿童使用高频振荡通气。3名儿童未能实现稳定,病情恶化后在手术前死亡。所有儿童术后机械通气时间为3至16天,平均7 ± 0.65(标准误Sx = 3.16)。死亡率为59.26%。
与先天性膈疝的紧急矫正相比,延迟手术治疗所采用的方法具有显著优势。它为气体交换和肺循环的稳定提供了机会,但死亡率仍然很高。可能需要新的治疗技术,如产前干预或肺移植,以挽救此类患者的生命。