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首页> 外文期刊>Heart rhythm: the official journal of the Heart Rhythm Society >The cardiac veins in congenitally corrected transposition of the great arteries: delivery options for cardiac devices.
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The cardiac veins in congenitally corrected transposition of the great arteries: delivery options for cardiac devices.

机译:先天性纠正大动脉移位的心脏静脉:心脏设备的递送选择。

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BACKGROUND: Device implantation is sometimes required in congenitally corrected transposition of the great arteries (ccTGA) because of morphologic right ventricular (RV) dysfunction and complete heart block. The anatomical course of the veins remains unknown, despite well-described coronary arterial anatomy. Knowledge of the venous anatomy may facilitate planning of percutaneous cardiac procedures in these patients. OBJECTIVE: This study sought to characterize the venous anatomy in ccTGA. METHODS: Pathologic cardiac specimens from patients with ccTGA were identified from the Mayo Clinic pathology database. Coronary sinus (CS) anatomy and distances from the CS ostium to the major cardiac veins were evaluated. Thebesian veins with ostial openings >1 mm, epicardial veins, and venous collaterals were also quantified. RESULTS: There were 56 hearts with a diagnosis of ccTGA identified. The CS was unidentifiable in 5 hearts due to slicing, and assessment of the Thebesian veins was not possible in 16. Seven hearts had an abnormal CS, 2 of which had atretic ostia and the other 5 of which either had an abnormal ostial location or multiple ostia. There were 28 hearts with at least 1 Thebesian vein with an ostial opening >1 mm. All 12 hearts with unidentifiable Thebesian veins had venous collaterals from the right ventricle (RV) to the major cardiac veins. Epicardial veins extended to the proximal, middle, and distal thirds of the RV in 71%, 23%, and 6%, respectively. CONCLUSION: In ccTGA, the ventricular venous anatomy is abnormal and follows the morphologic RV. However, large interventricular and Thebesian veins may offer options for percutaneous lead or catheter placement when approaching the systemic RV.
机译:背景:先天性大动脉移位(ccTGA)有时需要植入器械,这是由于形态右室(RV)功能障碍和完全的心脏传导阻滞。尽管已对冠状动脉进行了详尽的描述,但静脉的解剖过程仍是未知的。静脉解剖学知识可能有助于这些患者的经皮心脏手术计划。目的:本研究旨在表征ccTGA中的静脉解剖结构。方法:从Mayo Clinic病理数据库中鉴定出ccTGA患者的病理心脏标本。评价了冠状窦(CS)解剖结构以及从CS口到主要心脏静脉的距离。贝比斯静脉开口> 1 mm,心外膜静脉和静脉侧支也被定量。结果:共有56例心脏被诊断出患有ccTGA。由于切片原因,无法在5颗心脏中发现CS,在16颗中无法对Thebesian静脉进行评估。7颗心脏的CS异常,其中2颗存在闭孔造口,另外5颗的眼口位置异常或多发奥斯蒂亚。有28颗心脏,至少有1枚Thebesian静脉,其眼孔> 1 mm。所有12例无法识别的底比斯静脉的心脏均具有从右心室(RV)到主要心脏静脉的静脉侧支。心外膜静脉分别延伸至RV的近端,中间和远端三分之一,分别占71%,23%和6%。结论:在ccTGA中,心室静脉解剖结构异常并且遵循形态RV。但是,当接近全身性RV时,较大的室间隔和Thebesian静脉可能为经皮导联或导管置入提供选择。

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