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使用 Carpentier-Edwards Physio II 瓣环成形环进行二尖瓣修复的初步经验。

Initial experience of mitral valve repair using the Carpentier-Edwards Physio II annuloplasty ring.

机构信息

Wessex Cardiothoracic Centre, Southampton University Hospitals NHS Trust, Southampton, United Kingdom.

出版信息

Eur J Cardiothorac Surg. 2011 Jun;39(6):881-5. doi: 10.1016/j.ejcts.2010.10.004. Epub 2010 Nov 23.

Abstract

OBJECTIVE

The Carpentier-Edwards (CE) Physio II ring is a new prosthetic ring designed to accommodate the changing pathology seen in the spectrum of degenerative valve disease, particularly the larger anterior leaflet in repair of the Barlow valve. The aim of our study was to assess the safety and efficacy of mitral valve (MV) repair with the CE Physio II ring.

METHODS

Between April 2009 and March 2010, 100 patients underwent MV repair using the Physio II ring. Median age of patients was 70 years (54-85 years). The left ventricle (LV) was moderately (30-50%; n=21) or severely (<30%; n=6) impaired in 27 patients preoperatively. Mitral regurgitation (MR) was due to degenerative disease in 87 patients (bileaflet prolapse: 34 patients). Mean logistic EuroSCORE was 10.07 ± 8.9 and mean follow-up was 6.3 ± 2.4 months.

RESULTS

Seventeen patients were non-elective (eight emergencies), five were re-do operations and 23 Maze ± pulmonary vein isolations, and 14 tricuspid annuloplasties were performed. Neo-chordae were inserted in 50 patients (50%), whereas sliding annuloplasty was performed only in three patients. The median ring size was 32 mm (range 26-40 mm). On-table trans-oesophageal echocardiography (TOE) showed trivial/no MR in 87 patients, and mild in 13 patients, and there were no cases of systolic anterior motion (SAM). There were two re-explorations for bleeding and two patients required haemofiltration. There were no strokes or deep sternal wound infections (DSWIs). There was one hospital death (1%). At discharge, mean left ventricular end-diastolic (LVEDD) was 4.8 ± 0.7 cm compared with 5.5 ± 0.8 cm preoperatively (p=0.03) and mean left ventricular end-systolic (LVESD) was 3.3 ± 0.5 cm as compared with 3.6 ± 0.8 preoperatively (p=0.4). There was no MR in 87 patients and mild MR in 13 patients. The mean mitral valve area (MVA) was 2.8 ± 0.7 cm(2). The mean systolic pulmonary artery pressure (SPAP) was 26.6 ± 7.3 mmHg as compared with 50.9 ± 17.2 mmHg preoperatively (p=0.02). During follow-up, there were no thrombo-embolic complications, re-operation, endocarditis or deaths.

CONCLUSIONS

MV repair with the Physio II ring has excellent short-term results, including subgroups with large anterior mitral valve leaflet (AMVL). Moreover, the dimensional ratios of the ring may allow it to be used for MV repair for degenerative MV disease, irrespective of anterior leaflet size.

摘要

目的

卡彭蒂尔-爱德华兹(CE)生理 II 环是一种新的假体环,旨在适应退行性瓣膜病谱中所见的不断变化的病理学,特别是在巴洛瓣膜修复中较大的前瓣叶。我们研究的目的是评估二尖瓣(MV)修复使用 CE 生理 II 环的安全性和有效性。

方法

2009 年 4 月至 2010 年 3 月,100 例患者接受了使用 Physio II 环的 MV 修复。患者的中位年龄为 70 岁(54-85 岁)。27 例患者术前左心室(LV)中度(30-50%;n=21)或重度(<30%;n=6)受损。87 例患者的二尖瓣反流(MR)归因于退行性疾病(双叶瓣脱垂:34 例)。平均逻辑欧洲心脏手术风险评分(EuroSCORE)为 10.07±8.9,平均随访时间为 6.3±2.4 个月。

结果

17 例为非急诊(8 例为紧急情况),5 例为再手术,23 例行迷宫术+肺静脉隔离术,14 例行三尖瓣环成形术。50 例患者(50%)插入新腱索,仅 3 例患者行滑动瓣环成形术。中位环大小为 32mm(范围 26-40mm)。术中经食管超声心动图(TOE)显示 87 例患者无或微量 MR,13 例患者轻度 MR,无收缩期前向运动(SAM)。有 2 例再次探查出血,2 例患者需要血液滤过。无中风或深部胸骨伤口感染(DSWI)。有 1 例院内死亡(1%)。出院时,左心室舒张末期(LVEDD)平均为 4.8±0.7cm,与术前的 5.5±0.8cm 相比(p=0.03),左心室收缩末期(LVESD)平均为 3.3±0.5cm,与术前的 3.6±0.8cm 相比(p=0.4)。87 例患者无 MR,13 例患者轻度 MR。平均二尖瓣瓣口面积(MVA)为 2.8±0.7cm(2)。平均肺动脉收缩压(SPAP)为 26.6±7.3mmHg,与术前的 50.9±17.2mmHg 相比(p=0.02)。随访期间,无血栓栓塞并发症、再次手术、心内膜炎或死亡。

结论

使用生理 II 环进行 MV 修复具有极好的短期结果,包括前瓣叶较大(AMVL)的亚组。此外,环的尺寸比可能允许其用于退行性 MV 疾病的 MV 修复,而与前瓣叶大小无关。

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