Suppr超能文献

3个月以下婴儿的严重主动脉缩窄:经皮球囊血管成形术成功缓解

Severe aortic coarctation in infants less than 3 months: successful palliation by balloon angioplasty.

作者信息

Rao P Syamasundar, Jureidini Saadeh B, Balfour Ian C, Singh Gautam K, Chen Su-Chiung

机构信息

Division of Pediatric Cardiology, UT-Houston Medical School, 6431 Fannin, Suite 3.132, Houston, TX 77030, USA.

出版信息

J Invasive Cardiol. 2003 Apr;15(4):202-8.

Abstract

The optimal management strategy of the neonate and young infant with native aortic coarctation (AC) is controversial. We reviewed our experience with balloon angioplasty (BA) in neonates and infants 3 months to test our thesis that BA provides successful palliation, defined as avoidance of surgery for 4 weeks along with control of presenting symptoms. We also compared the results of the transumbilical arterial (UA), transfemoral arterial (FA) and transfemoral venous anterograde (FVA) approaches we have used to accomplish BA. During a 6.5-year period ending June 2001, fifty-one neonates and infants 3 months presenting with heart failure, hypertension or both underwent UA (n = 16), FA (n = 26) and FVA (n = 9) balloon coarctation angioplasty. Immediate and follow-up results were evaluated. Acute reduction of peak-to-peak gradients across the coarctation (40 17 mmHg vs. 5 6 mmHg; p < 0.001), increase in diameter of the coarcted segment (2.2 0.5 mm vs. 5.6 0.8 mm; p < 0.001) and improvement in symptomatology occurred following BA. Surgical relief of aortic obstruction was required in 4 infants at 5, 21, 24 and 28 days after the procedure. Effective palliation was thus achieved in the remaining 47 infants (92%). During intermediate-term follow-up, twenty-two infants (50%) developed recoarctation requiring repeat balloon (n = 14) or surgical (n = 8) intervention 2 10 months (median, 3 months) after initial BA. The indication for reintervention was hypertension in all patients. At a median follow-up of 3 years (range, 0.5 5.5 years), blood pressures remained low (98 11 mmHg) with an arm/leg blood pressure gradient of 4 6 mmHg. Comparison of the groups revealed similar effectiveness both immediately and at follow-up. However, femoral artery complications were seen in only the FA group. Based on these data, we conclude that effective palliation is achieved with BA in all 3 groups, femoral artery complications are seen only in the FA group and BA is an excellent alternative to surgical intervention in the management of native AC in neonates and young infants.

摘要

患有先天性主动脉缩窄(AC)的新生儿和小婴儿的最佳管理策略存在争议。我们回顾了我们在3个月以下新生儿和婴儿中进行球囊血管成形术(BA)的经验,以检验我们的论点,即BA可提供成功的姑息治疗,定义为避免手术4周并控制现有症状。我们还比较了我们用于完成BA的经脐动脉(UA)、经股动脉(FA)和经股静脉顺行(FVA)方法的结果。在截至2001年6月的6.5年期间,51例3个月以下出现心力衰竭、高血压或两者兼有的新生儿和婴儿接受了UA(n = 16)、FA(n = 26)和FVA(n = 9)球囊缩窄血管成形术。评估了即刻和随访结果。球囊血管成形术后,缩窄部位的峰峰压差急性降低(40±17 mmHg对5±6 mmHg;p < 0.001),缩窄段直径增加(2.2±0.5 mm对5.6±0.8 mm;p < 0.001),症状改善。4例婴儿在术后5、21、24和28天需要手术解除主动脉梗阻。其余47例婴儿(92%)因此实现了有效的姑息治疗。在中期随访期间,22例婴儿(50%)出现再缩窄,需要在初次球囊血管成形术后2至10个月(中位时间3个月)进行重复球囊扩张(n = 14)或手术(n = 8)干预。所有患者再次干预的指征均为高血压。在中位随访3年(范围0.5至5.5年)时,血压仍较低(98±11 mmHg),臂/腿血压梯度为4±6 mmHg。各组比较显示,即刻和随访时的效果相似。然而,仅在FA组中观察到股动脉并发症。基于这些数据,我们得出结论,所有3组中球囊血管成形术均实现了有效的姑息治疗,仅在FA组中观察到股动脉并发症,并且在新生儿和小婴儿先天性AC的管理中,球囊血管成形术是手术干预的极佳替代方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验