Anagnostopoulos Petros V, Alphonso Nelson, Nölke Lars, Hornberger Lisa K, Raff Gary W, Azakie Anthony, Karl Tom R
Pediatric Heart Center, University of California San Francisco Children's Hospital, San Francisco, California 94143, USA.
Ann Thorac Surg. 2007 Apr;83(4):1458-62. doi: 10.1016/j.athoracsur.2006.10.077.
Papillary muscle rupture in the fetus and neonate is a rare event that leads to severe mitral or tricuspid insufficiency and is associated with high perinatal mortality. We undertook surgical repair of this lesion in the neonatal period and report on our midterm results.
Three neonates with tricuspid insufficiency and 1 infant with mitral insufficiency, all due to papillary muscle or chordal rupture, underwent surgical repair with artificial chordal replacement and a modification of the de Vega annuloplasty technique that allowed external adjustment of the annulus size under transesophageal echocardiographic guidance after separation from cardiopulmonary bypass.
All patients recovered well from the operation. There have been no late deaths and no valve-related complications. On discharge, all 3 patients had evidence of trace to mild atrioventricular valve regurgitation. At a median follow-up of 33 months (range, 7 to 50; 123 patient-months), all 4 patients are growing normally. Three patients have had no change in the degree of tricuspid or mitral regurgitation. One patient required reoperation at 54 months postoperatively for acute mitral insufficiency secondary to separation of an artificial chorda from the ventricular wall.
Surgical repair of critical neonatal tricuspid and mitral insufficiency associated with papillary muscle or chordal rupture is feasible and can result in good early and midterm results. Our modification of the De Vega annuloplasty technique with the ability to externally adjust the size of the annulus under echocardiographic guidance may improve the accuracy of the repair in the neonate.
胎儿和新生儿乳头肌破裂是一种罕见事件,可导致严重的二尖瓣或三尖瓣关闭不全,并伴有高围产期死亡率。我们在新生儿期对该病变进行了手术修复,并报告中期结果。
3例三尖瓣关闭不全的新生儿和1例二尖瓣关闭不全的婴儿,均因乳头肌或腱索破裂,接受了人工腱索置换手术,并对德维加瓣环成形术进行了改良,使其在体外循环脱离后能在经食管超声心动图引导下对外侧瓣环大小进行调整。
所有患者术后恢复良好。无晚期死亡病例,也无瓣膜相关并发症。出院时,所有3例患者均有微量至轻度房室瓣反流。中位随访33个月(范围7至50个月;123患者-月),所有4例患者生长发育正常。3例患者三尖瓣或二尖瓣反流程度无变化。1例患者术后54个月因人工腱索与心室壁分离继发急性二尖瓣关闭不全而需再次手术。
对与乳头肌或腱索破裂相关的严重新生儿三尖瓣和二尖瓣关闭不全进行手术修复是可行的,且可取得良好的早期和中期效果。我们对德维加瓣环成形术的改良,使其能够在超声心动图引导下对外侧瓣环大小进行调整,可能会提高新生儿修复手术的准确性。