Reid I S, Hutcherson R J
J Pediatr Surg. 1976 Dec;11(6):939-42. doi: 10.1016/s0022-3468(76)80070-x.
A long-term follow-up was carried out on 30 patients who had congenital diaphragmatic hernias operated on over a 21-yr period. The review took the form of clinical examination, chest x-rays, pulmonary function tests, and lung scans. Lungs that were hypoplastic at birth remained underdeveloped as judged by pulmonary function tests and hypoperfusion on lung scan; however, children who survived birth6 and operative repair went on to live normal lives through the period studied. There was some suggestion from pulmonary function tests and lung scans that in the older group a preemphysematous state may exist but this was asymptomatic. There was no evidence of increased susceptibility to respiratory infection in the group. Ten per cent of the children were mentally retarded, evidently from hypoxia after birth.
对30例在21年期间接受先天性膈疝手术的患者进行了长期随访。随访形式包括临床检查、胸部X光、肺功能测试和肺部扫描。根据肺功能测试和肺部扫描显示的灌注不足判断,出生时发育不全的肺仍未发育成熟;然而,出生并接受手术修复后存活下来的儿童在研究期间继续过着正常生活。肺功能测试和肺部扫描显示,年龄较大的一组可能存在肺气肿前期状态,但无症状。该组没有证据表明对呼吸道感染的易感性增加。10%的儿童智力迟钝,显然是出生后缺氧所致。