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肺动脉支架:长期随访。

Pulmonary artery stents: long-term follow-up.

机构信息

Department of Pediatric Cardiology, University of Alabama at Birmingham, Birmingham, Alabama, USA.

出版信息

Catheter Cardiovasc Interv. 2010 Apr 1;75(5):757-64. doi: 10.1002/ccd.22356.

Abstract

OBJECTIVES

Determine the long-term outcomes of branch pulmonary artery (PA) stents.

BACKGROUND

PA stents in congenital heart disease effectively relieve stenoses in the short-term. Published long-term data are limited.

METHODS

Patients enrolled in an FDA IDE protocol from 1989-92 were included. Clinical follow-up and catheterization data were evaluated. Patients were included if >5 year follow-up data was available or if mortality occurred following the initial procedure.

RESULTS

There were five deaths: four due to progression of their underlying heart disease, and one from a complication during a follow-up catheterization. Clinical data for 43 surviving patients demonstrated 39 patients (91%) are in NYHA class I or II. Seven patients underwent surgical intervention during the follow-up period (five RV-PA conduit, two Fontan revisions), but none addressed PA stenosis. Final repeat catheterizations were performed in 36 patients (55 stents) 7.2 +/- 4.3 years post stent insertion with 1.2 +/- 0.9 further procedures with stent dilations. In this subgroup, the minimum vessel diameter increased from 4.7 +/- 1.8 to 13.4 +/- 2.4 mm (P < 0.001), and the pressure gradient improved from 41 +/- 25 to 9 +/- 11 mm Hg (P < 0.001). Higher initial gradient and smaller balloons were associated with a final stent diameter of <14 mm (P = 0.030 and 0.046). Jailed vessels occurred in 49% of stents with abnormal angiographic flow in 18/55. Six repeat catheterizations resulted in complications, including the one procedural death.

CONCLUSION

Stents implants for PA stenoses provide effective improvement in vessel caliber in the long-term. Although repeat interventions are necessary, this procedure reduces RV pressure and provides an important alternative to surgery for residual PA obstruction.

摘要

目的

确定肺分支动脉(PA)支架的长期结果。

背景

PA 支架在先天性心脏病中可在短期内有效缓解狭窄。目前已发表的长期数据有限。

方法

纳入了 1989 年至 1992 年期间参加 FDA IDE 方案的患者。评估了临床随访和导管插入术数据。如果有超过 5 年的随访数据,或在初始手术之后发生死亡,则将患者纳入研究。

结果

共有 5 例死亡:4 例死于基础心脏病的进展,1 例死于随访导管插入术中的并发症。43 例存活患者的临床数据显示,39 例(91%)患者处于纽约心脏协会(NYHA)心功能 I 级或 II 级。在随访期间,7 例患者接受了手术干预(5 例 RV-PA 导管,2 例 Fontan 修订),但都没有解决 PA 狭窄。在支架置入后 7.2 ± 4.3 年对 36 例患者(55 个支架)进行了最终重复导管插入术,其中 1.2 ± 0.9 例进行了支架扩张术。在该亚组中,最小血管直径从 4.7 ± 1.8 增加到 13.4 ± 2.4 mm(P < 0.001),压力梯度从 41 ± 25 改善至 9 ± 11 mm Hg(P < 0.001)。较高的初始梯度和较小的球囊与最终支架直径<14 mm 相关(P = 0.030 和 0.046)。49%的支架出现嵌顿血管,其中 18/55 个支架的血管造影血流异常。6 次重复导管插入术导致并发症,包括 1 例手术死亡。

结论

PA 狭窄支架植入术可长期有效改善血管口径。尽管需要重复介入,但该手术可降低 RV 压力,并为残留 PA 阻塞提供一种重要的手术替代方案。

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