First experience of staged treatment of an infant with heterotaxy syndrome with total anomalous pulmonary vein drainage combined with a single ventricular heart and pulmonary atresia

K. Kuatbekov, A. Mishin, A. Sepbayeva, G. Nigay, D. Kanzhigalin
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Abstract

The combination of monoventricular congenital heart disease with total anomalous pulmonary vein drainage and pulmonary atresia, is a rare pathology and characterized by an extremely severe course with the highest mortality. In the presented work we described a clinical case of the first and successful experience of two-stage treatment of an infant with total anomalous pulmonary vein drainage combined with single ventricular heart disease and pulmonary atresia in the Republic of Kazakhstan. For total anomalous pulmonary vein drainage correction we used a sutureless technique — primary sutureless repair, which is used in our center as a primary one. Due to severe anatomy of the defect, we used unusual area of the distal end of the central systemic-pulmonary artery anastomoses during primary surgery at the mouth of the severed patent ductus arteriosus in the area of pulmonary artery bifurcation, where it is associated with high surgical risks. Taking into account the presence of an additional obstacle to pulmonary blood flow in the form of left branch pulmonary artery orifice stenosis, we performed one-stage dilatation plasty of the pulmonary artery branch bifurcation with autopericardium. During the repeated surgery we faced such a serious complication as aortic damage for the first time, thanks to emergency actions it did not turn out to be fatal. We also managed to perform the most preferable dilation of hypoplastic branches of the pulmonary artery by plasty with the own tissues of the superior vena cava during the formation of Glenn-anastomosis.Received 29 November 2021. Revised 21 December 2021. Accepted 22 December 2021.Informed consent: Informed consent was obtained from the patient's mother for the publication and use of the patient's medical data for scientific purposes.Funding: The study did not have sponsorship.Conflict of interest: Authors declare no conflict of interest.Contribution of the authorsLiterature review: A.V. MishinDrafting the article: A.V. MishinCritical revision of the article: K.N. Kuatbekov, A.D. SepbayevaSurgical treatment: K.N. Kuatbekov, A.V. Mishin, A.D. Sepbayeva, G.S. Nigay, D.M. KanzhigalinFinal approval of the version to be published: K.N. Kuatbekov, A.V. Mishin, A.D. Sepbayeva, G.S. Nigay, D.M. Kanzhigalin
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分阶段治疗婴儿异位综合征伴肺静脉完全异常引流合并单心室心脏和肺闭锁的首次经验
单室先天性心脏病合并肺静脉完全异常引流和肺闭锁是一种罕见的病理,其特点是病程极其严重,死亡率最高。在提出的工作中,我们描述了一个临床病例的第一个和成功的经验两阶段治疗的婴儿完全异常肺静脉引流合并单室心脏病和肺闭锁在哈萨克斯坦共和国。对于完全异常肺静脉引流矫正,我们使用无缝线技术-初级无缝线修复,这是我们中心使用的主要技术。由于严重的解剖缺陷,我们在原发性手术中在肺动脉分叉区切断的动脉导管未闭口处使用了中央系统-肺动脉吻合处远端不寻常的区域,该区域手术风险高。考虑到肺动脉左分支口狭窄对肺血流的额外障碍,我们对肺动脉分支进行了一期心包自闭扩张成形术。在反复的手术过程中,我们第一次遇到了严重的并发症,如主动脉损伤,幸亏采取了紧急措施,没有致命的危险。在格伦吻合形成的过程中,我们还利用上腔静脉自身组织进行了最理想的肺动脉发育不全分支扩张。收到2021年11月29日。2021年12月21日修订。2021年12月22日接受。知情同意:为科学目的出版和使用患者的医疗数据已获得患者母亲的知情同意。经费来源:本研究未获得赞助。利益冲突:作者声明无利益冲突。作者贡献文献综述:A.V. Mishin文章起草:A.V. Mishin文章关键性修改:K.N. Kuatbekov, A.D. Sepbayeva手术治疗:K.N. Kuatbekov, A.V. Mishin, A.D. Sepbayeva, G.S. Nigay, D.M. Kanzhigalin最终审定版本:K.N. Kuatbekov, A.V. Mishin, A.D. Sepbayeva, G.S. Nigay, D.M. Kanzhigalin
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来源期刊
Patologiya krovoobrashcheniya i kardiokhirurgiya
Patologiya krovoobrashcheniya i kardiokhirurgiya Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.00
自引率
0.00%
发文量
42
审稿时长
12 weeks
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