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专利动脉导管支架与改良 Blalock-Taussig 分流术在依赖动脉导管的肺血流婴儿中的姑息治疗比较:来自先天性导管插入术研究协作组的见解。

Comparison Between Patent Ductus Arteriosus Stent and Modified Blalock-Taussig Shunt as Palliation for Infants With Ductal-Dependent Pulmonary Blood Flow: Insights From the Congenital Catheterization Research Collaborative.

机构信息

Cardiac Center at the Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine (A.C.G., A.M., T.B., C.E.M.)

Children's Healthcare of Atlanta, Emory University School of Medicine, GA (C.J.P., M.S.K., C.E.M., S.S., R.A.L., J.A.).

出版信息

Circulation. 2018 Feb 6;137(6):589-601. doi: 10.1161/CIRCULATIONAHA.117.029987. Epub 2017 Oct 17.

Abstract

BACKGROUND

Infants with ductal-dependent pulmonary blood flow may undergo palliation with either a patent ductus arteriosus (PDA) stent or a modified Blalock-Taussig (BT) shunt. A balanced multicenter comparison of these 2 approaches is lacking.

METHODS

Infants with ductal-dependent pulmonary blood flow palliated with either a PDA stent or a BT shunt from January 2008 to November 2015 were reviewed from the 4 member centers of the Congenital Catheterization Research Collaborative. Outcomes were compared by use of propensity score adjustment to account for baseline differences between groups.

RESULTS

One hundred six patients with a PDA stent and 251 patients with a BT shunt were included. The groups differed in underlying anatomy (expected 2-ventricle circulation in 60% of PDA stents versus 45% of BT shunts; =0.001) and presence of antegrade pulmonary blood flow (61% of PDA stents versus 38% of BT shunts; <0.001). After propensity score adjustment, there was no difference in the hazard of the primary composite outcome of death or unplanned reintervention to treat cyanosis (hazard ratio, 0.8; 95% confidence interval [CI], 0.52-1.23; =0.31). Other reinterventions were more common in the PDA stent group (hazard ratio, 29.8; 95% CI, 9.8-91.1; <0.001). However, the PDA stent group had a lower adjusted intensive care unit length of stay (5.3 days [95% CI, 4.2-6.7] versus 9.19 days [95% CI, 7.9-10.6]; <0.001), a lower risk of diuretic use at discharge (odds ratio, 0.4; 95% CI, 0.25-0.64; <0.001) and procedural complications (odds ratio, 0.4; 95% CI, 0.2-0.77; =0.006), and larger (152 mm/m [95% CI, 132-176] versus 125 mm/m [95% CI, 113-138]; =0.029) and more symmetrical (symmetry index, 0.84 [95% CI, 0.8-0.89] versus 0.77 [95% CI, 0.75-0.8]; =0.008] pulmonary arteries at the time of subsequent surgical repair or last follow-up.

CONCLUSIONS

In this multicenter comparison of palliative PDA stent and BT shunt for infants with ductal-dependent pulmonary blood flow adjusted for differences in patient factors, there was no difference in the primary end point, death or unplanned reintervention to treat cyanosis. However, other markers of morbidity and pulmonary artery size favored the PDA stent group, supporting PDA stent as a reasonable alternative to BT shunt in select patients.

摘要

背景

依赖动脉导管的肺血流的婴儿可能通过动脉导管未闭(PDA)支架或改良的 Blalock-Taussig(BT)分流术进行姑息治疗。目前缺乏这两种方法的平衡多中心比较。

方法

从 2008 年 1 月至 2015 年 11 月,回顾了来自先天性导管插入术研究协作组的 4 个成员中心接受 PDA 支架或 BT 分流术姑息治疗的依赖动脉导管的肺血流婴儿。通过使用倾向评分调整来考虑组间基线差异,比较了结局。

结果

纳入了 106 例接受 PDA 支架治疗和 251 例接受 BT 分流术的患者。两组的基础解剖结构存在差异(预计 2 心室循环在 PDA 支架中占 60%,而 BT 分流术占 45%;=0.001),且存在顺行肺血流(PDA 支架中占 61%,BT 分流术占 38%;<0.001)。在倾向评分调整后,死亡或计划外再干预以治疗发绀的主要复合结局的风险无差异(危险比,0.8;95%置信区间[CI],0.52-1.23;=0.31)。PDA 支架组的其他再干预更为常见(危险比,29.8;95%CI,9.8-91.1;<0.001)。然而,PDA 支架组的 ICU 住院时间更短(5.3 天[95%CI,4.2-6.7] vs 9.19 天[95%CI,7.9-10.6];<0.001),出院时利尿剂使用率较低(比值比,0.4;95%CI,0.25-0.64;<0.001),且手术并发症较少(比值比,0.4;95%CI,0.2-0.77;=0.006),且随后的手术修复或最后一次随访时肺动脉较大(152mm/m[95%CI,132-176] vs 125mm/m[95%CI,113-138];=0.029)且更对称(对称性指数,0.84[95%CI,0.8-0.89] vs 0.77[95%CI,0.75-0.8];=0.008)。

结论

在这项针对依赖动脉导管的肺血流的婴儿的姑息性 PDA 支架和 BT 分流术的多中心比较中,调整了患者因素的差异后,主要终点(死亡或计划外再干预以治疗发绀)没有差异。然而,其他发病率和肺动脉大小的标志物支持 PDA 支架组,支持在某些患者中选择 PDA 支架作为 BT 分流术的合理替代方案。

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