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右心室双出口或大动脉转位合并骑跨房室瓣的手术入路

Surgical approaches for double-outlet right ventricle or transposition of the great arteries associated with straddling atrioventricular valves.

作者信息

Serraf A, Nakamura T, Lacour-Gayet F, Piot D, Bruniaux J, Touchot A, Sousa-Uva M, Houyel L, Planche C

机构信息

Department of Pediatric Cardiac Surgery, Marie-Lannelongue Hospital, Le Plessis-Robinson, France.

出版信息

J Thorac Cardiovasc Surg. 1996 Mar;111(3):527-35. doi: 10.1016/s0022-5223(96)70304-5.

DOI:10.1016/s0022-5223(96)70304-5
PMID:8601966
Abstract

The surgical management of patients with double-outlet right ventricle or transposition of the great arteries and straddling atrioventricular valves remains a subject of controversy. Biventricular repair has theoretic advantages because it establishes normal anatomy and physiology. In some instances, however, it seems to carry too high operative risk, and a univentricular heart repair is preferred. Since 1984, we have operated on 34 patients with double-outlet right ventricle (n = 15) or transposition of the great arteries (n = 19) with isolated straddling tricuspid valve (n = 17), isolated straddling mitral valve (n = 9), both mitral and tricuspid straddling (n = 2), or abnormal insertion of tricuspid (n = 7) or mitral (n = 2) chordae in the left ventricular outlet, precluding an adequate tunnel construction. Straddling was categorized according to the location of the papillary muscle insertion in the opposite ventricular chamber: type A, on the edge of the ventricular septal defect (n = 14); type B, on the opposite side of the ventricular septum away from the edge of the defect (n = 8); type C, on the free wall of the opposite ventricular chamber (n = 8). Abnormal chordal insertions were classified according to the location of their attachments around the edges of the defect. Three types of chordal distribution were identified: on the aortic conus, on the pulmonary conus crossing the ventricular septal defect, or around the defect closing it like a curtain. All but three patients had two ventricles of adequate size. Sixteen patients underwent palliation. Median age at the definitive operation was 6.5 months (range 1 to 130 months). Thirty patients underwent a biventricular repair and four had a univentricular repair. Biventricular repair was achieved by an arterial switch operation in 18 patients and by tunnel construction from the left ventricle to the aorta in 12. In isolated straddling of types A and B, the ventricular septal defect was closed by adjusting the septal patch on the ventricular side above the straddled papillary muscle. In type C, the patch was sewn over the papillary muscle by applying it on the septum. In double straddling, the ventricular septum was incised between the two papillary muscles, and an ellipsoid patch was used to reconstruct the septal defect, directing each subvalvular apparatus into its own ventricular chamber. When the abnormal chordae in the left outflow tract inserted on the aortic or pulmonary conus, the conus was incised and tailored to make a flap, leaving an unobstructed left ventricular outflow tract. In two patients the subvalvular apparatus was resected and reattached to the patch. Curtainlike chordae were a contraindication to biventricular repair in double-outlet right ventricle but not in transposition. There were four early deaths and one late death, all occurring in the group having biventricular repair. Death was due to myocardial ischemia (n = 1), right ventricular hypoplasia (n = 1), pulmonary hypertension (n = 1), and residual subaortic stenosis (n = 1). Two patients had moderate to severe postoperative atrioventricular valve incompetence, caused by a cleft in the mitral valve in one patient. Three patients were reoperated on for subaortic stenosis (n = 1), pulmonary stenosis (n = 1), and mitral regurgitation (n = 1). Mean follow-up of 30.7 +/- 19.4 months was achieved in the survivors. All but one patient (univentricular repair) were in New York Heart Association class I, without atrioventricular valve incompetence. Actuarial survival at 4 years was 85.3% +/- 3%. We conclude that straddling or abnormal distribution of chordae tendineae of the atrioventricular valves does not preclude biventricular repair in double-outlet right ventricle or transposition of the great arteries provided that the ventricles are of adequate size. Curtainlike abnormal tricuspid chordae remain a contraindication to biventricular repair in double-outlet right ventricle.

摘要

右心室双出口或大动脉转位合并跨立房室瓣患者的外科治疗仍是一个有争议的话题。双心室修复具有理论上的优势,因为它能建立正常的解剖结构和生理功能。然而,在某些情况下,其手术风险似乎过高,因此更倾向于单心室心脏修复。自1984年以来,我们对34例右心室双出口(n = 15)或大动脉转位(n = 19)患者进行了手术,这些患者合并孤立性三尖瓣跨立(n = 17)、孤立性二尖瓣跨立(n = 9)、二尖瓣和三尖瓣均跨立(n = 2),或三尖瓣(n = 7)或二尖瓣(n = 2)腱索在左心室流出道异常附着,妨碍了合适的隧道构建。跨立根据乳头肌插入对侧心室腔的位置进行分类:A型,位于室间隔缺损边缘(n = 14);B型,位于室间隔对侧远离缺损边缘(n = 8);C型,位于对侧心室腔的游离壁(n = 8)。异常腱索附着根据其围绕缺损边缘的附着位置进行分类。确定了三种腱索分布类型:在主动脉圆锥上、穿过室间隔缺损的肺动脉圆锥上,或像帘子一样围绕缺损闭合处。除3例患者外,其余患者的两个心室大小均足够。16例患者接受了姑息治疗。确定性手术的中位年龄为6.5个月(范围1至130个月)。30例患者接受了双心室修复,4例接受了单心室修复。18例患者通过动脉调转术实现双心室修复,12例通过从左心室到主动脉构建隧道实现。在孤立性A型和B型跨立中,通过在跨立乳头肌上方的心室侧调整间隔补片来闭合室间隔缺损。在C型中,将补片应用于间隔并缝在乳头肌上。在双跨立中,在两个乳头肌之间切开室间隔,使用椭圆形补片重建室间隔缺损,将每个瓣下结构引导至其各自的心室腔。当左流出道的异常腱索插入主动脉或肺动脉圆锥时,切开并修整圆锥以形成一个瓣叶,使左心室流出道通畅。2例患者切除了瓣下结构并重新附着于补片上。帘子状腱索是右心室双出口双心室修复的禁忌证,但在大动脉转位中不是。有4例早期死亡和1例晚期死亡,均发生在接受双心室修复的患者组中。死亡原因分别为心肌缺血(n = 1)、右心室发育不全(n = 1)、肺动脉高压(n = 1)和残余主动脉下狭窄(n = 1)。2例患者术后出现中度至重度房室瓣关闭不全,其中1例是由于二尖瓣裂缺所致。3例患者因主动脉下狭窄(n = 1)、肺动脉狭窄(n = 1)和二尖瓣反流(n = 1)接受了再次手术。幸存者的平均随访时间为30.7±19.4个月。除1例患者(单心室修复)外,所有患者均为纽约心脏协会I级,无房室瓣关闭不全。4年的精算生存率为85.3%±3%。我们得出结论,只要心室大小足够,房室瓣的跨立或腱索异常分布并不妨碍右心室双出口或大动脉转位的双心室修复。帘子状异常三尖瓣腱索仍是右心室双出口双心室修复的禁忌证。

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