Normand J, Joffre B, André M, Jocteur-Monrozier D, Bozio A, Champsaur G
Arch Mal Coeur Vaiss. 1981 May;74(5):593-7.
A review of 122 cases of symptomatic coarctation of the aorta in neonates and infants confirmed the need for early corrective surgery in the majority of cases, in relation to the usual coexistence of associated cardiovascular malformations. The operative risk in the newborn up to one month of age was very high (42 %) but fell very sharply thereafter (5%). Restenosis was the principal late complication (36 %), persistent hypertension being rare in this age group. The risk of restenosis (not a significant vital risk during secondary surgery) should not weigh in the balance against life saving surgery where clinical deterioration is observed despite medical therapy or due to associated malformations.
对122例新生儿和婴儿症状性主动脉缩窄病例的回顾证实,鉴于通常并存相关心血管畸形,大多数病例需要早期进行矫正手术。1个月龄以内新生儿的手术风险非常高(42%),但此后急剧下降(5%)。再狭窄是主要的晚期并发症(36%),该年龄组持续性高血压罕见。再狭窄风险(二次手术时并非重大生命风险)不应与挽救生命的手术相权衡,即便尽管进行了药物治疗或由于相关畸形而出现临床恶化的情况。