Department of Cardiology, The Royal Children's Hospital Melbourne, Victoria, Australia; Heart Research Group, Murdoch Childrens Research Institute, Victoria, Australia; Department of Pediatrics, University of Melbourne, Victoria, Australia.
Department of Cardiac Surgery, The Royal Children's Hospital Melbourne, Victoria, Australia; Heart Research Group, Murdoch Childrens Research Institute, Victoria, Australia; Department of Pediatrics, University of Melbourne, Victoria, Australia.
Semin Thorac Cardiovasc Surg. 2021;33(2):483-489. doi: 10.1053/j.semtcvs.2020.09.007. Epub 2020 Sep 23.
Stenosis or diffuse hypoplasia of central pulmonary arteries (PA) is common in patients with single ventricle physiology, often requiring surgical patching. Such repairs are prone to failure, particularly with low pressure venous flow (bidirectional cavopulmonary connection or Fontan). We describe our experience of disconnection of central PA and selective systemic-PA shunt to the hypoplastic vessel. Single ventricle patients (n = 12) with diffuse left pulmonary artery (LPA) hypoplasia (LPA:right pulmonary artery diameter <0.7) underwent PA disconnection (ligation clip) and selective arterial shunt to the LPA. Patients with ≤mild atrioventricular valve regurgitation, and no more than mild systolic dysfunction on echocardiogram were considered. Following systemic-LPA shunt, patients were reassessed by cardiac catheterization prior to further surgery, with follow-up catheterization later performed and description of changes observed. Increased volume loading was well tolerated with no greater than mild atrioventricular valve regurgitation and preserved systolic function (normal or mildly reduced). Selective arterial shunting increased the caliber of the LPA from 4.1 mm (1.2-5.6) to 6.5 mm (1.7-11.9) and this increase was preserved post-Fontan (6.7 mm [1.3-8.0]) (median [range]). Ventricular end diastolic pressure increased with arterial shunting but resolved after shunt takedown and Fontan completion (median +3 and -4 mm Hg respectively). Post-Fontan hospital length of stay was not prolonged (median 11 days, range 7-14). No deaths occurred. In univentricular hearts and PA hypoplasia, selective systemic-PA shunting physiologically increases the caliber of the distal vessels. In selected patients this can be done safely with maintenance of PA growth and resolution of the elevated end diastolic pressure with Fontan completion.
中心性肺动脉(PA)狭窄或弥漫性发育不良在单心室生理患者中很常见,通常需要手术修补。这些修复容易失败,特别是在低压力静脉血流(双向腔肺连接或 Fontan)的情况下。我们描述了我们对中心性 PA 离断和向发育不良血管选择性体肺动脉分流的经验。12 例弥漫性左肺动脉(LPA)发育不良(LPA:右肺动脉直径<0.7)的单心室患者接受了 PA 离断(结扎夹)和向 LPA 选择性动脉分流。考虑到患者具有≤轻度房室瓣反流,且超声心动图显示无明显收缩功能障碍。在进一步手术前,通过心导管术对体肺动脉分流患者进行了评估,随后进行了随访心导管术,并描述了观察到的变化。增加的容量负荷耐受良好,无大于轻度房室瓣反流和保留的收缩功能(正常或轻度降低)。选择性动脉分流使 LPA 的直径从 4.1 毫米(1.2-5.6)增加到 6.5 毫米(1.7-11.9),这种增加在 Fontan 后保持(6.7 毫米[1.3-8.0])(中位数[范围])。动脉分流使心室舒张末期压力增加,但在分流拆除和 Fontan 完成后恢复正常(中位数分别增加+3 和-4 毫米汞柱)。Fontan 后住院时间未延长(中位数 11 天,范围 7-14 天)。无死亡病例。在单心室心脏和 PA 发育不良中,选择性体肺动脉分流可使远端血管的口径生理性增加。在选择的患者中,通过 Fontan 完成,PA 生长的维持和舒张末期压力的升高可以安全地进行。