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用于左心发育不全综合征及其变异型的混合治疗方法:肺动脉的转归

Hybrid approach for hypoplastic left heart syndrome and its variants: the fate of the pulmonary arteries.

作者信息

Dave Hitendu, Rosser Barbara, Knirsch Walter, Hübler Michael, Prêtre René, Kretschmar Oliver

机构信息

Division of Congenital Cardiovascular Surgery, University Children's Hospital Zurich, Switzerland Children's Research Centre, University of Zurich, Switzerland

Division of Congenital Cardiovascular Surgery, University Children's Hospital Zurich, Switzerland Children's Research Centre, University of Zurich, Switzerland.

出版信息

Eur J Cardiothorac Surg. 2014 Jul;46(1):14-9. doi: 10.1093/ejcts/ezt604. Epub 2014 Jan 12.

Abstract

OBJECTIVES

To analyse the results of hybrid palliation of hypoplastic left heart syndrome (HLHS) patients and its variants with an emphasis on the long-term fate of the pulmonary arteries.

METHODS

We analysed 28 neonates (2006-11) with HLHS and its variants, who underwent bilateral pulmonary artery banding, patent ductus arteriosus (PDA) stenting and balloon atrial septostomy using a true hybrid approach. Median age and weight were 4 (0-36) days and 3 (1.9-3.7) kg respectively. Diagnoses included 23 HLHS and 5 variants. The fate of all surviving branch pulmonary arteries (PA) after a hybrid approach were compared with their counterparts in 29 Norwood I survivors (2002-11).

RESULTS

Four of 28 hybrid procedures needed to be converted to a Norwood procedure. Mortality after stage I hybrid palliation was 3/24 (12.5%). All 21 acute survivors underwent a comprehensive stage II at a median age of 4 (2.3-5.7) months, without any mortality (0%). Eleven of 21 comprehensive stage II survivors have undergone extracardiac Fontan; including 1 who underwent a rescue Fontan at 7 months of age and died (1/11: 9%). While 18/21 (86%) needed branch PA intervention in the hybrid group during the median follow-up duration of 39 (10-81) months, 9/29 (31%) needed the same in the Norwood group during a median follow-up duration of 58 (16-128) months (P < 0.001). Eight of 21 (38%) needed stenting [all on the left pulmonary artery (LPA)] in the hybrid group vs 5/29 (17%) in the Norwood group (P = 0.097). Ten of 21 (48%) patients had surgical/catheter intervention on both branch PA in the hybrid group vs 2/29 (7%) in the Norwood group (P = 0.001). Pre-Fontan Nakata index was significantly better in the Norwood group 206 (118-406) compared with the hybrid group 153 (56-230) mm(2)/m(2) (P = 0.01). The comparable lower lobe indices were 149 (103-333) and 137 (45-178) mm(2)/m(2) (P = 0.04), respectively.

CONCLUSIONS

Hybrid approach can be pursued with a low mortality. However, the high frequency of catheter and/or surgical interventions, and the sluggish growth of the branch PA pre-Fontan need innovative solutions. A comparison of the neurodevelopmental outcome for the hybrid vs the Norwood cohort would define the role of the hybrid strategy in the treatment of HLHS and its variants.

摘要

目的

分析采用以肺动脉长期转归为重点的杂交姑息治疗方法治疗左心发育不全综合征(HLHS)患者及其变异型的结果。

方法

我们分析了28例(2006 - 2011年)HLHS患者及其变异型,这些患者采用真正的杂交方法接受了双侧肺动脉环扎术、动脉导管未闭(PDA)支架置入术和球囊房间隔造口术。中位年龄和体重分别为4(0 - 36)天和3(1.9 - 3.7)kg。诊断包括23例HLHS和5例变异型。将所有杂交治疗后存活的分支肺动脉(PA)的转归与29例Norwood I手术幸存者(2002 - 2011年)的相应情况进行比较。

结果

28例杂交手术中有4例需要转为Norwood手术。I期杂交姑息治疗后的死亡率为3/24(12.5%)。所有21例急性期幸存者在中位年龄4(2.3 - 5.7)个月时接受了全面的II期治疗,无死亡(0%)。21例全面II期治疗幸存者中有11例接受了心外Fontan手术;其中1例在7个月时接受了挽救性Fontan手术并死亡(1/11:9%)。在杂交组中位随访时间39(10 - 81)个月期间,18/21(86%)需要分支PA干预,而在Norwood组中位随访时间58(16 - 128)个月期间,9/29(31%)需要同样的干预(P < 0.001)。杂交组21例中有8例(38%)需要支架置入[均在左肺动脉(LPA)],而Norwood组为5/29(17%)(P = 0.097)。杂交组21例中有10例(48%)患者对双侧分支PA进行了手术/导管干预,而Norwood组为2/29(7%)(P = 0.001)。Fontan手术前的Nakata指数在Norwood组为206(118 - 406)mm²/m²,显著优于杂交组的153(56 - 230)mm²/m²(P = 0.01)。相应的下叶指数分别为149(103 - 333)和137(45 - 178)mm²/m²(P = 0.04)。

结论

杂交方法可实现低死亡率。然而,导管和/或手术干预的高频率以及Fontan手术前分支PA的缓慢生长需要创新解决方案。对杂交组与Norwood组队列的神经发育结局进行比较将明确杂交策略在HLHS及其变异型治疗中的作用。

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