Mater Kathryn, Ayer Julian, Nicholson Ian, Winlaw David, Chard Richard, Orr Yishay
1 Faculty of Medicine, The University of New South Wales, Sydney, New South Wales, Australia.
2 Heart Centre for Children, Children's Hospital at Westmead, Westmead, New South Wales, Australia.
World J Pediatr Congenit Heart Surg. 2019 May;10(3):304-312. doi: 10.1177/2150135119837200.
Mitral valve replacement (MVR) is the only option for infants with severe mitral valve disease that is not reparable; however, previously reported outcomes are not always favorable. Our institution has followed a tailored approach to sizing and positioning of mechanical valve prostheses in infants requiring MVR in order to obtain optimal outcomes.
Outcomes for 22 infants ≤10 kg who have undergone MVR in Sydney, Australia, from 1998 to 2016, were analyzed. Patients were at a mean age of 6.8 ± 4.1 months (range: 0.8-13.2 months) and a mean weight of 5.4 ± 1.8 kg at the time of MVR. Most patients (81.8%) had undergone at least one previous cardiac surgical procedure prior to MVR, and 36.4% had undergone two previous procedures. Several surgical techniques were used to implant mechanical bileaflet prostheses.
All patients received bileaflet mechanical prostheses, with 12 receiving mitral prostheses and 10 receiving inverted aortic prostheses. Surgical technique varied between patients with valves implanted intra-annularly (n = 6), supra-annularly (n = 11), or supra-annularly with a tilt (n = 5). After a mean follow-up period of 6.2 ± 4.4 years, the survival rate was 100%. Six (27.3%) patients underwent redo MVR a mean of 102.2 ± 10.7 months after initial MVR. Four (18.2%) patients required surgical reintervention for development of left ventricular outflow tract obstruction and three (13.6%) patients required permanent pacemaker placement during long-term follow-up.
The tailored surgical strategy utilized for MVR in infants at our institution has resulted in reliable valve function and excellent survival. Although redo is inevitable due to somatic growth, the bileaflet mechanical prostheses used displayed appropriate durability.
二尖瓣置换术(MVR)是患有不可修复的严重二尖瓣疾病的婴儿的唯一选择;然而,先前报道的结果并不总是令人满意。我们机构采用了一种定制方法来确定需要进行MVR的婴儿机械瓣膜假体的尺寸和位置,以获得最佳结果。
分析了1998年至2016年在澳大利亚悉尼接受MVR的22例体重≤10 kg的婴儿的结果。患者在MVR时的平均年龄为6.8±4.1个月(范围:0.8 - 13.2个月),平均体重为5.4±1.8 kg。大多数患者(81.8%)在MVR之前至少接受过一次心脏外科手术,36.4%的患者接受过两次先前的手术。采用了几种手术技术来植入双叶机械假体。
所有患者均接受双叶机械假体,其中12例接受二尖瓣假体,10例接受倒置主动脉假体。瓣膜植入方式在瓣环内(n = 6)、瓣环上(n = 11)或瓣环上倾斜(n = 5)的患者之间有所不同。平均随访6.2±4.4年后,生存率为100%。6例(27.3%)患者在首次MVR后平均102.2±10.7个月接受了再次MVR。4例(18.2%)患者因左心室流出道梗阻需要手术再次干预,3例(13.6%)患者在长期随访期间需要植入永久起搏器。
我们机构用于婴儿MVR的定制手术策略导致了可靠的瓣膜功能和出色的生存率。尽管由于身体生长再次手术不可避免,但所使用的双叶机械假体显示出适当的耐用性。