Hawkins J A, Minich L L, Tani L Y, Day R W, Judd V E, Shaddy R E, McGough E C
Department of Surgery, Primary Children's Medical Center and the University of Utah, Salt Lake City 84113, USA.
Ann Thorac Surg. 1998 Jun;65(6):1758-62; discussion 1763. doi: 10.1016/s0003-4975(98)00268-9.
Many centers have adopted balloon valvuloplasty for treatment of infants with critical aortic stenosis because of historically poor early results and a lack of long-term results with surgical valvotomy. We evaluated our results with open aortic valvotomy over the past decade, specifically examining factors influencing survival and reintervention in the current era.
From 1986 to 1996, 37 infants in the first 3 months of life underwent open aortic valvotomy for critical aortic stenosis. All patients underwent cardiopulmonary bypass, valvotomy, and valve debridement under direct vision with standard techniques.
Early mortality was 11% (4 of 37, 70% confidence limit 7% to 20%) and all early deaths were in neonates less than 2 weeks of age. Late death occurred in 6 patients a mean of 10 +/- 12 months (range, 2 to 36 months) after valvotomy. Actuarial survival, including operative deaths was 92% +/- 6% at 1 month, 78% +/- 9% at 1 year, and 73.4% +/- 10% at 10 years. In a multifactorial regression analysis, the best predictors of death were the presence of endocardial fibroelastosis and small body surface area and the best predictor of the need for late reintervention was preoperative aortic annular size. Thirteen patients required reintervention: repeat operation in 7 patients, balloon valvuloplasty in 3 patients, and both balloon valvuloplasty and reoperation in 3 patients. Actuarial freedom from reintervention postoperatively is 97% +/- 3% at 1 month, 73% +/- 9% at 1 year, and 55% +/- 11% at 10 years. Reintervention was for recurrent left ventricular outflow obstruction in 9 patients and mixed aortic stenosis and aortic insufficiency in 4. Echocardiography 4.3 +/- 2.5 years after aortic valvotomy in survivors who have not required reintervention (n = 20) revealed a Doppler peak instantaneous systolic gradient of 37 +/- 14 mm Hg and mild or less aortic regurgitation in 16 patients and moderate aortic regurgitation in 4 patients.
Current surgical results with critical aortic stenosis in the neonate and young infant are acceptable in terms of both late survival, reintervention, and functional results in the majority of patients. Newer interventions, such as balloon valvuloplasty, should be carefully evaluated for long-term results and should be compared more appropriately to current surgical results to determine the best treatment modality for the neonate and infant with critical aortic stenosis.
由于历史上早期结果不佳且缺乏手术瓣膜切开术的长期结果,许多中心已采用球囊瓣膜成形术治疗重症主动脉狭窄婴儿。我们评估了过去十年开放主动脉瓣膜切开术的结果,特别研究了影响当前时代生存和再次干预的因素。
1986年至1996年,37例出生后前3个月的婴儿因重症主动脉狭窄接受了开放主动脉瓣膜切开术。所有患者均采用标准技术在直视下进行体外循环、瓣膜切开术和瓣膜清创术。
早期死亡率为11%(37例中的4例,70%置信区间为7%至20%),所有早期死亡均发生在年龄小于2周的新生儿中。6例患者在瓣膜切开术后平均10±12个月(范围2至36个月)发生晚期死亡。包括手术死亡在内的精算生存率在1个月时为92%±6%,1年时为78%±9%,10年时为73.4%±10%。在多因素回归分析中,死亡的最佳预测因素是心内膜弹力纤维增生症的存在和小体表面积,晚期再次干预需求的最佳预测因素是术前主动脉环大小。13例患者需要再次干预:7例患者再次手术,3例患者进行球囊瓣膜成形术,3例患者同时进行球囊瓣膜成形术和再次手术。术后无再次干预的精算自由度在1个月时为97%±3%,1年时为73%±9%,10年时为55%±11%。再次干预的原因是9例患者出现复发性左心室流出道梗阻,4例患者出现混合性主动脉狭窄和主动脉瓣关闭不全。在未需要再次干预的幸存者(n = 20)中,主动脉瓣膜切开术后4.3±2.5年的超声心动图显示多普勒峰值瞬时收缩压梯度为37±14 mmHg,16例患者有轻度或以下主动脉瓣反流,4例患者有中度主动脉瓣反流。
就大多数患者的晚期生存、再次干预和功能结果而言,目前新生儿和幼儿重症主动脉狭窄的手术结果是可以接受的。对于较新的干预措施,如球囊瓣膜成形术,应仔细评估其长期结果,并应与当前手术结果进行更恰当的比较,以确定治疗新生儿和婴儿重症主动脉狭窄的最佳治疗方式。