索引超出了数组界限。 文章摘要
|本期目录/Table of Contents|

[1]万泽浩,比拉力·排祖拉,芦梓楠,等.补片加宽左房室瓣环在完全性房室通道手术中的应用[J].国际心血管病杂志,2024,03:190-192.
点击复制

补片加宽左房室瓣环在完全性房室通道手术中的应用(PDF)

《国际心血管病杂志》[ISSN:1006-6977/CN:61-1281/TN]

期数:
2024年03期
页码:
190-192
栏目:
经验交流
出版日期:
2024-05-20

文章信息/Info

Title:
-
作者:
万泽浩; 比拉力·排祖拉; 芦梓楠; 马松峰
830011 乌鲁木齐，新疆医科大学第一附属医院小儿心胸外科（万泽浩，比拉力·排祖拉，马松峰）；830000 乌鲁木齐，新疆医科大学附属肿瘤医院 新疆肿瘤学重点实验室（芦梓楠）
Author(s):
-
关键词:
完全性房室通道; 先天性心脏病; 房室瓣狭窄; 房室瓣反流
Keywords:
-
分类号:
-
DOI:
10.3969/j.issn.1673-6583.2024.03.016
文献标识码:
-
摘要:
目的：探讨采用自体心包片进行修补瓣叶、加宽左房室瓣环技术在完全性房室通道（CAVC）合并左房室瓣狭窄患儿手术中的应用。 方法：回顾性分析2015 年1 月至2021 年2 月于新疆医科大学第一附属医院小儿心胸外科行手术治疗的36 例合并左房室瓣狭窄CAVC 患儿的临床资料，均采用自体心包片进行修补瓣叶、加宽瓣环后行CAVC 根治术。 结果：35 例患儿痊愈出院，1 例患儿术后因肺部感染死亡。35 例患儿随访至1 年。术后7 d 复查心电图均无明显异常。术后1 年超声心动图检查提示二尖瓣轻度反流2
Abstract:
-

参考文献/References

[1] Kwon MH, Schultz AH, Lee M, et al. Complete atrioventricularseptal defect with absent or diminutive primum component:incidence, anatomic characteristics, and outcomes[J]. J ThoracCardiovasc Surg, 2022, 163(3):1156-1162.
[2] Doi H, Muneuchi J, Watanabe M, et al. Characteristics of thepulmonary circulation in infants with complete atrioventricularseptal defect[J]. Cardiol Young, 2021, 31(4):556-561.
[3] Basgoze S, Yildiz O, Ozturk E, et al. Repair of completeatrioventricular canal defects: early and midterm results andcomparison of the left anterior leaflet augmentation techniquewith traditional technics[J]. J Card Surg, 2021, 36(8):2658-2668.
[4] Ijsselhof R, Gauvreau K, Nido PD, et al. Atrioventricular valvefunction predicts reintervention in complete atrioventricularseptal defect[J]. World J Pediatr Congenit Heart Surg, 2020,11(2):247-248.
[5] Dranseika V, Pretre R, Kretschmar O, et al. Melody valve toreplace the mitral valve in small children: lessons learned[J]. AnnPediatr Cardiol, 2021, 14(1):35-41.
[6] Olariu IC, Popoiu A, Ardelean AM, et al. Challenges in thesurgical treatment of atrioventricular septal defect in childrenwith and without Down syndrome in Romania—a developingcountry[J]. Front Pediatr, 2021, 9:612644.
[7] Fong LS, Betts K, Ayer J, et al. Predictors of reoperation andmortality after complete atrioventricular septal defect repair[J].Eur J Cardiothorac Surg, 2021, 61(1):45-53.
[8] Aziz S, Ayub M, Masood L, et al. Major septal defects:comparative study of Down syndrome and non-Down syndromeinfants, before and after surgery[J]. Pak J Med Sci, 2020,36(5):925-929.
[9] Alhuzaimi AN, Alotaibi NM, Alsuhaibani GI, et al. Congenitalheart defect and pulmonary hypertension in children with Downsyndrome: clinical profile over two decades[J]. Cureus, 2021,13(2):e13212.
[10] Reynen S, H?vels-Gürich HH, Vazquez-Jimenez JF, et al. Longtermoutcome up to 40 years after single patch repair of completeatrioventricular septal defect in infancy or childhood[J]. ThoracCardiovasc Surg, 2021, 69(S 03):e68-e75.
[11] Pierre Louis ME, Bhutta A, Holloway A, et al. Postoperativecourse of pulmonary artery pressure after completeatrioventricular canal defect repair[J]. Cardiol Young, 2022,32(3):398-404.
[12] Nathan M, Levine JC, Van Rompay MI, et al. Impact of majorresidual lesions on outcomes after surgery for congenital heartdisease[J]. J Am Coll Cardiol, 2021, 77(19):2382-2394.
[13] Ramgren JJ, Nozohoor S, Zindovic I, et al. Reoperations afterrepair for atrioventricular septal defects: ＞25 years experienceat a single center[J]. Semin Thorac Cardiovasc Surg, 2023,35(3):530-538.

备注/Memo

备注/Memo:
通信作者：马松峰，E-mail：masongfeng2@163.com
更新日期/Last Update: 2024-05-20