Georgiev Stanimir G, Lazarov Stojan D, Mitev Ivajlo D, Latcheva Alexandra Z, Christov Georgi A, Velkovski Ivan G, Mitev Plamen D
Department for Pediatric Cardiology, National Heart Hospital, Sofia, Bulgaria.
World J Pediatr Congenit Heart Surg. 2012 Jul 1;3(3):321-7. doi: 10.1177/2150135111431844.
The study evaluates the long-term results of surgery for anomalous left coronary artery from the pulmonary artery (ALCAPA) with special attention on the left ventricular (LV) function and mitral regurgitation.
Twenty-one children underwent surgery for ALCAPA over 23 years (1987-2010). All patients underwent establishment of a two-coronary system, by direct reimplantation (n = 13) or by intrapulmonary tunnel technique (n = 8), with concomitant mitral valve repair in one. The follow-up echocardiograms were evaluated to assess LV function and mitral regurgitation.
Five patients died. The age of the nonsurvivors was lower, 4.2 ± 1.3 versus 22.7 ± 29.4 months, P = .04. All nonsurvivors had moderate or severe mitral regurgitation preoperatively and higher LV diameter z score than the survivors: 11.8 (9-14.6) versus 4.6 (1.9-13.1), P = .01. At last follow-up, all survivors were asymptomatic; the diastolic LV diameter was normal, with z scores: 0.3 (0.1-1.9) versus 7 (1.9-14.6) preoperatively, P = .001, as was the LV ejection fraction: 66% (61%-78%) versus 38% (16%-70%) preoperatively, P = .001. Fifteen patients had moderate or severe mitral regurgitation at initial presentation and it eventually regressed to insignificant in all survivors (P = .001). No subsequent interventions on the coronary arteries or the mitral valve were needed. Four patients with intrapulmonary tunnel had mild suprapulmonary obstruction with Doppler peak gradients between 20 and 30 mm Hg.
In our experience, establishment of a two-coronary circulation without mitral valve repair leads to normalization of LV dimension and systolic function and to improvement of mitral regurgitation in the surviving patients. Mortality is related to low age and to the associated higher degree of LV dysfunction.
本研究评估了肺动脉起源异常左冠状动脉(ALCAPA)手术的长期结果,特别关注左心室(LV)功能和二尖瓣反流。
21例儿童在23年期间(1987 - 2010年)接受了ALCAPA手术。所有患者均通过直接再植入(n = 13)或肺内隧道技术(n = 8)建立双冠状动脉系统,其中1例同时进行了二尖瓣修复。对随访超声心动图进行评估以评估左心室功能和二尖瓣反流。
5例患者死亡。非存活者年龄较小,分别为4.2±1.3个月和22.7±29.4个月,P = 0.04。所有非存活者术前均有中度或重度二尖瓣反流,且左心室直径z评分高于存活者:11.8(9 - 14.6)对4.6(1.9 - 13.1),P = 0.01。在最后一次随访时,所有存活者均无症状;舒张期左心室直径正常,z评分为0.3(0.1 - 1.9),术前为7(1.9 - 14.6),P = 0.001,左心室射血分数也是如此:66%(61% - 78%),术前为38%(16% - 70%),P = 0.001。15例患者初诊时有中度或重度二尖瓣反流,最终在所有存活者中均消退至无明显反流(P = 0.001)。无需对冠状动脉或二尖瓣进行后续干预。4例采用肺内隧道技术的患者有轻度肺上梗阻,多普勒峰值压差在20至30 mmHg之间。
根据我们的经验,在不进行二尖瓣修复的情况下建立双冠状动脉循环可使存活患者的左心室大小和收缩功能恢复正常,并改善二尖瓣反流。死亡率与低年龄和相关的较高程度的左心室功能障碍有关。