Perron J, Moran A M, Gauvreau K, del Nido P J, Mayer J E, Jonas R A
Department of Cardiology, Children's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Ann Thorac Surg. 1999 Aug;68(2):542-8. doi: 10.1016/s0003-4975(99)00614-1.
Valved homograft conduit repair in neonates and young infants creates a physiologically normal biventricular circulation, and unlike shunts, avoids surgery on the branch pulmonary.
Retrospective chart review was used for 84 patients operated on between 1990 and 1995 (mean age 26+/-28 days, mean weight 3.3+/-0.8 kg) undergoing homograft conduit repair in the first 3 months of life. Cases were divided into simple and complex, eg, absent pulmonary valve syndrome or associated interrupted arch. Mean homograft size was 9.0+/-2 mm.
Early mortality was 4.7% (simple) and 30% (complex). Mean hospital stay was 18 days. Mean follow-up was 34 months. Thirty-seven (47%) patients underwent conduit replacement. Median time to reoperation was 3.1 years. Mean size of replacement homograft was 17+/-2 mm. There were no deaths at reoperation. Mean hospital stay at conduit change was 6.3 days. Probability of survival at 5 years is 75%.
Biventricular repair employing a conduit can be performed safely in noncomplex anomalies in the first 3 months of life. Time interval until repeat surgery is relatively short but equal or greater than that with most palliative procedures.
新生儿和小婴儿的带瓣同种异体管道修复可建立生理上正常的双心室循环,并且与分流术不同,避免了对肺分支进行手术。
对1990年至1995年间接受手术的84例患者(平均年龄26±28天,平均体重3.3±0.8千克)进行回顾性病历审查,这些患者在生命的前3个月接受了同种异体管道修复。病例分为简单型和复杂型,例如肺动脉瓣缺如综合征或合并主动脉弓中断。同种异体管道的平均尺寸为9.0±2毫米。
早期死亡率为4.7%(简单型)和30%(复杂型)。平均住院时间为18天。平均随访时间为34个月。37例(47%)患者进行了管道置换。再次手术的中位时间为3.1年。置换同种异体管道的平均尺寸为17±2毫米。再次手术时无死亡病例。更换管道时的平均住院时间为6.3天。5年生存率为75%。
在生命的前3个月,对于非复杂性畸形,采用管道进行双心室修复可以安全进行。直到再次手术的时间间隔相对较短,但与大多数姑息性手术相当或更长。