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大动脉转位心房调转术后经直接心室入路杂交支架置入治疗肺静脉挡板严重狭窄:一例报告

Hybrid stenting through direct ventricular access for severe stenosis of the pulmonary venous baffle after atrial switch operation for transposition of the great arteries: a case report.

作者信息

Van Kerrebroeck Margaretha, Budts Werner, Pasquet Agnès, De Meester Pieter

机构信息

Division of Congenital and Structural Cardiology, UZ Leuven, Herestraat 49, 3000 Leuven, Belgium.

Department of Cardiovascular Sciences, KU Leuven, Herestraat 49 - box 911, 3000 Leuven, Belgium.

出版信息

Eur Heart J Case Rep. 2024 Nov 20;8(12):ytae616. doi: 10.1093/ehjcr/ytae616. eCollection 2024 Dec.

Abstract

BACKGROUND

Atrial switch repair was the first surgical intervention to result in long-term survival in patients with ventriculo-arterial discordance or transposition of the great arteries. However, the natural history after atrial switch is not uneventful with frequent atrial arrhythmia, development of baffle stenosis, and eventually heart failure. For this, new interventions might be necessary but are often associated with increased risk.

CASE SUMMARY

We present the case of a 49-year-old woman born with ventriculo-arterial discordance or dextro-transposition of the great arteries who underwent atrial switch repair according to Mustard at the age of 1 year. She presented with shortness of breath and reduced exercise capacity. The echocardiography revealed prominent turbulent flow at the level of the pulmonary venous baffle (PVB). This was confirmed on cardiac computed tomography. After multidisciplinary discussion, a hybrid approach was considered as the preferred strategy. In this, the cardiac surgeon provided apical access by left lateral thoracotomy. The PVB was accessed retrograde through right ventricular apical access, and stenting with a covered stent with subsequent balloon dilatation up to 13 mm was performed. This reduced the peak gradient on echocardiography from 18 to 11 mmHg. Clinical follow-up was uneventful with improved functional capacity 6 months after discharge.

DISCUSSION

This case provides an alternative access to the PVB by left lateral mini-thoracotomy and apical ventricular access. Furthermore, we highlight the challenges in decision-making and the importance of the multidisciplinary collaboration between adult congenital cardiologist, the echocardiographer, and cardiac surgeon as well as the flexibility in interventional techniques to individualize the management of such cases.

摘要

背景

心房调转术是使心室动脉不一致或大动脉转位患者获得长期生存的首例外科干预措施。然而,心房调转术后的自然病程并非一帆风顺,常出现频繁的房性心律失常、挡板狭窄的进展,最终导致心力衰竭。因此,可能需要新的干预措施,但这些措施往往伴随着风险增加。

病例摘要

我们报告一例49岁女性患者,出生时患有心室动脉不一致或大动脉右位转位,1岁时根据马斯塔德手术进行了心房调转术。她出现呼吸急促和运动能力下降。超声心动图显示肺静脉挡板(PVB)水平有明显的湍流。心脏计算机断层扫描证实了这一点。经过多学科讨论,混合方法被认为是首选策略。在此方法中,心脏外科医生通过左侧胸廓切开术提供心尖入路。通过右心室心尖入路逆行进入PVB,并使用覆膜支架进行支架置入,随后进行球囊扩张至13毫米。这使超声心动图上的峰值梯度从18毫米汞柱降至11毫米汞柱。出院6个月后临床随访情况良好,功能能力有所改善。

讨论

本病例提供了一种通过左侧小切口胸廓切开术和心尖心室入路进入PVB的替代方法。此外,我们强调了决策中的挑战以及成人先天性心脏病专家、超声心动图专家和心脏外科医生之间多学科合作的重要性,以及介入技术的灵活性,以便对此类病例进行个体化管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/490f/11630560/a3a5822ac849/ytae616il2.jpg

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