Bautista-Hernandez Victor, Scheurer Mark, Thiagarajan Ravi, Salvin Joshua, Pigula Frank A, Emani Sitaram, Fynn-Thompson Francis, Loyola Hugo, Schiff Jared, del Nido Pedro J, Bacha Emile A
Department of Cardiac Surgery, Children's Hospital Boston, 300 Longwood Avenue Bader 273, Boston, MA 02115, USA.
Pediatr Cardiol. 2011 Feb;32(2):160-6. doi: 10.1007/s00246-010-9835-1. Epub 2010 Nov 24.
This study aimed to evaluate clinical outcomes including hemodynamics, right ventricle (RV) function, and tricuspid valve (TV) function in patients with hypoplastic left heart syndrome (HLHS) at midterm after completion of staged palliation based on the source of pulmonary blood flow provided at stage 1. The records of all patients with HLHS who completed Fontan palliation between 2001 and 2007 were retrospectively reviewed. The outcome variables were RV dysfunction, TV, and neo-atrioventricular (neo-AV) regurgitation (from latest echocardiogram), cardiac index (CI), pulmonary vascular resistance (PVR), pulmonary artery pressure (PAp), and right ventricular end-diastolic pressure (RVEDp) (from latest catheterization). Clinical status was obtained from medical records and by contact with the referring cardiologist if necessary. Of 118 patients undergoing a Fontan for HLHS, 116 had a fenestrated lateral tunnel and 2 had an extracardiac conduit. At the time of stage 1 palliation, 36 patients had a right ventricle-to-pulmonary artery (RV-PA) conduit, and 82 patients had a modified Blalock-Taussig shunt (mBTS). All the patients except one who died of sepsis on extracorporeal membrane oxygenation (ECMO) survived the Fontan operation and were discharged home. At a mean follow-up post-Fontan period of 28.4 months (range, 0.16-95.3 months), three patients had died (2 on the transplantation list and 1 from pulmonary vein stenosis), and one patient had the Fontan circulation taken down. No patient had a heart transplantation. A follow-up echocardiogram was performed for 115 patients (after a mean of 15.6 months for RV-PA and 32.1 months for BTS), and 66 patients underwent a post-Fontan catheterization (after a mean of 15.8 months for RV-PA and 29.3 months for BTS). The hemodynamic results for RV-PA conduit versus BTS were a CI of 3.4 ± 0.8 versus 3.4 ± 1.2, a PVR of 1.8 ± 0.7 versus 1.7 ± 0.8, a PAp of 14.3 ± 3.1 versus 14.2 ± 4.5, and an RVEDp of 7.1 ± 3.3 versus 8.9 ± 5.3. No statistically significant differences were found between shunt types regarding survival or degree of RV dysfunction or in terms of neo-AV regurgitation, CI, PVR, PAp, RVEDp, or rhythm problems. Patients in the BTS group required more tricuspid valvuloplasties and had more tricuspid regurgitation at follow-up evaluation. The patients in the RV-PA group had more PA interventions. In conclusion, the contemporary results after Fontan palliation for HLHS were excellent. At the midterm follow-up evaluation, outcomes and hemodynamic data were similar between shunt types. However, the patients in the BTS group exhibited more tricuspid regurgitation, and the patients in the RV-PA group had increased pulmonary artery interventions.
本研究旨在根据一期提供的肺血流来源,评估左心发育不全综合征(HLHS)患者在分期姑息治疗完成中期的临床结局,包括血流动力学、右心室(RV)功能和三尖瓣(TV)功能。对2001年至2007年间完成Fontan姑息治疗的所有HLHS患者的记录进行了回顾性分析。结局变量包括RV功能障碍、TV和新房室(neo-AV)反流(来自最新超声心动图)、心脏指数(CI)、肺血管阻力(PVR)、肺动脉压(PAp)和右心室舒张末期压力(RVEDp)(来自最新心导管检查)。临床状况通过病历获取,必要时与转诊心脏病专家联系。在118例接受HLHS的Fontan手术患者中,116例采用开窗侧隧道Fontan,2例采用心外管道Fontan。在一期姑息治疗时,36例患者采用右心室至肺动脉(RV-PA)管道,82例患者采用改良Blalock-Taussig分流术(mBTS)。除1例在体外膜肺氧合(ECMO)上死于败血症的患者外,所有患者均存活至Fontan手术并出院回家。在Fontan术后平均随访28.4个月(范围0.16 - 95.3个月)时,3例患者死亡(2例在等待移植名单上,1例死于肺静脉狭窄),1例患者拆除了Fontan循环。无患者接受心脏移植。对115例患者进行了随访超声心动图检查(RV-PA组平均15.6个月,BTS组平均32.1个月),66例患者进行了Fontan术后心导管检查(RV-PA组平均15.8个月,BTS组平均29.3个月)。RV-PA管道与BTS的血流动力学结果为:CI分别为3.4±0.8与3.4±1.2,PVR分别为1.8±0.7与1.7±0.8,PAp分别为14.3±3.1与14.2±4.5,RVEDp分别为7.1±3.3与8.9±5.3。在生存、RV功能障碍程度、neo-AV反流、CI、PVR、PAp、RVEDp或节律问题方面,分流类型之间未发现统计学显著差异。BTS组患者在随访评估时需要更多的三尖瓣成形术且三尖瓣反流更多。RV-PA组患者有更多的肺动脉干预。总之,HLHS患者Fontan姑息治疗的当代结果良好。在中期随访评估中,分流类型之间的结局和血流动力学数据相似。然而,BTS组患者三尖瓣反流更多,RV-PA组患者肺动脉干预增加。