Gorbachevsky Sergey V, Shmalts Anton A, Barishnikova Irina Y, Zaets Sergey B
Department of Pulmonary Hypertension, Bakoulev Center for Cardiovascular Surgery, Moscow, Russia.
Interact Cardiovasc Thorac Surg. 2017 Oct 1;25(4):595-599. doi: 10.1093/icvts/ivx209.
Since 2004, different techniques for the Potts shunt have been used in patients with incurable pulmonary arterial hypertension. However, the experience with these interventions in a single institution is limited. We present our series of Potts shunts in children with pulmonary arterial hypertension.
Eight patients with suprasystemic pulmonary arterial hypertension (pulmonary artery-to-aorta mean pressure ratio of 1.39 ± 0.30) had a Potts shunt at the median age of 13.5 months. Six patients were followed up for 2-32 (median 17) months after the operation.
In all cases, the Potts shunt caused a decrease in arterial blood oxygen saturation at the lower extremities and was the genesis of the arterial blood oxygen saturation gradient between the upper and lower extremities (10.5 ± 1.8% at discharge). Postoperative echocardiography revealed flattening of the ventricular septum as well as a decrease in the right ventricle-to-left ventricle end-diastolic diameter ratio from 1.36 ± 0.14 preoperatively to 0.99 ± 0.22 at discharge (P = 0.010). The 2 patients with the highest preoperative pulmonary artery-to-aorta mean pressure ratio (1.79-1.86) died during the early postoperative period from repeated pulmonary hypertension crises and uncontrolled hypoxaemia. There were no deaths during the follow-up period. The paediatric functional class of the patients improved from IIIb-IV to I-II, syncopal episodes no longer persisted and the weight deficit decreased from 21.8 ± 7.5% preoperatively to 11.5 ± 5.9% at the latest follow-up examination (P = 0.004). The arterial blood oxygen saturation gradient between the upper and lower extremities and the right ventricle-to-left ventricle end-diastolic diameter ratio were the same as they were while the patients were in the hospital.
Our limited experience demonstrates that the Potts shunt lowers suprasystemic pulmonary hypertension to the systemic level, limits manifestations of right-sided heart failure and improves the overall functional status of the patients.
自2004年以来,不同的波茨分流术已应用于无法治愈的肺动脉高压患者。然而,单一机构开展这些干预措施的经验有限。我们展示了我们对患有肺动脉高压儿童进行波茨分流术的系列病例。
8例患有系统性肺动脉高压(肺动脉与主动脉平均压力比为1.39±0.30)的患者在13.5个月的中位年龄时接受了波茨分流术。6例患者术后随访2至32个月(中位时间17个月)。
在所有病例中,波茨分流术导致下肢动脉血氧饱和度下降,并且是上下肢动脉血氧饱和度梯度的成因(出院时为10.5±1.8%)。术后超声心动图显示室间隔变平,右心室与左心室舒张末期内径比从术前的1.36±0.14降至出院时的0.99±0.22(P = 0.010)。术前肺动脉与主动脉平均压力比最高的2例患者(1.79 - 1.86)在术后早期因反复的肺动脉高压危象和无法控制的低氧血症死亡。随访期间无死亡病例。患者的儿科功能分级从IIIb - IV级改善为I - II级,晕厥发作不再持续,体重不足从术前的21.8±7.5%降至最近一次随访检查时的11.5±5.9%(P = 0.004)。上下肢动脉血氧饱和度梯度和右心室与左心室舒张末期内径比与患者住院时相同。
我们有限的经验表明,波茨分流术可将系统性肺动脉高压降至体循环水平,限制右心衰竭的表现,并改善患者的整体功能状态。