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孤立性多发性室间隔缺损的外科治疗。130例的合理治疗方法。

Surgical management of isolated multiple ventricular septal defects. Logical approach in 130 cases.

作者信息

Serraf A, Lacour-Gayet F, Bruniaux J, Ouaknine R, Losay J, Petit J, Binet J P, Planché C

机构信息

Department of Pediatric Cardiac Surgery, Marie-Lannelongue Hospital, Université Paris-Sud, France.

出版信息

J Thorac Cardiovasc Surg. 1992 Mar;103(3):437-42; discussion 443.

PMID:1545542
Abstract

From January 1980 through September 1990, 130 children underwent surgical closure of isolated multiple ventricular septal defects (mean age 14 +/- 18 months, mean weight 7.0 +/- 4.4 kg). Sixty-one were less than 1 year of age. Sixty-one children had pulmonary protection, 51 had pulmonary artery banding, and 10 had pulmonary valve stenosis. All other patients had severe pulmonary hypertension (mean systolic pressure 75.7 +/- 20.5 mm Hg and already disabling heart failure (New York Heart Association classes III and IV). The surgical management was based on the location of the defects and the ventricular dominance that were assessed preoperatively and intraoperatively. Midtrabecular ventricular septal defects were always centered by the moderator band and were therefore divided into low trabecular, midtrabecular, and high trabecular defects. The perimembranous septum was involved in 102 patients, the trabecular in 121, the inlet septum in 12, and the infundibular septum in 9. Fifty patients had the "Swiss cheese" form of the lesion. Closure of the ventricular septal defects included Dacron patch and mattress sutures. They were always first approached through a right atriotomy, which was sufficient for complete repair in 82 patients. In midtrabecular ventricular septal defects, section of the moderator band (n = 24) allowed closure of all the defects with a single Dacron patch. In 48 patients a right atriotomy and a right (n = 32) or left (n = 14) (particularly for low trabecular ventricular septal defects) or both right and left (n = 2) ventriculotomies were necessary to secure the repair. The hospital mortality rate was 7.7% (10 patients). The causes of deaths were residual ventricular septal defect (n = 5), pulmonary hypertension (n = 2), hypoplastic right ventricle (n = 1) and left ventricle (n = 1), and myocardial infarction (n = 1). Among eighteen survivors with residual ventricular septal defect, six were reoperated on; there were two deaths. A permanent pacemaker was necessary in four patients. Low trabecular ventricular septal defects and left ventriculotomy were significant risk factors for morbidity (death, residual ventricular septal defect), p less than 0.01. At 7 years of follow-up, 90% of survivors were in New York Heart Association class I. Actuarial survival and freedom from reoperation at 7 years were 89.6% and 87.5%, respectively.

摘要

从1980年1月至1990年9月,130例儿童接受了孤立性多发性室间隔缺损的手术闭合治疗(平均年龄14±18个月,平均体重7.0±4.4千克)。61例年龄小于1岁。61例儿童采用了肺保护措施,51例行肺动脉环扎术,10例有肺动脉瓣狭窄。所有其他患者均有严重肺动脉高压(平均收缩压75.7±20.5毫米汞柱)且已出现致残性心力衰竭(纽约心脏协会III级和IV级)。手术治疗方案基于术前和术中评估的缺损位置及心室优势情况。小梁部室间隔缺损总是以节制索为中心,因此分为低位小梁部、中位小梁部和高位小梁部缺损。102例患者累及膜周部间隔,121例累及小梁部,12例累及流入道间隔,9例累及漏斗部间隔。50例患者有“瑞士奶酪”样病变形式。室间隔缺损的闭合采用涤纶补片和褥式缝线。总是首先经右心房切口入路,82例患者经此入路足以完成完全修复。对于中位小梁部室间隔缺损,切断节制索(n = 24)可使用单个涤纶补片闭合所有缺损。48例患者需要右心房切口及右心室(n = 32)或左心室(n = 14)(特别是对于低位小梁部室间隔缺损)或左右心室(n = 2)切开术以确保修复。医院死亡率为7.7%(10例患者)。死亡原因包括残余室间隔缺损(n = 5)、肺动脉高压(n = 2)、右心室发育不全(n = 1)和左心室发育不全(n = 1)以及心肌梗死(n = 1)。在有残余室间隔缺损的18例存活者中,6例再次手术;其中2例死亡。4例患者需要植入永久性起搏器。低位小梁部室间隔缺损和左心室切开术是发病(死亡、残余室间隔缺损)的显著危险因素,P<0.01。随访7年时,90%的存活者为纽约心脏协会I级。7年时的精算生存率和免于再次手术率分别为89.6%和87.5%。

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