Flores Flores Jesús, Ledesma Velasco Mariano, Palomo Villada José Antonio, Montoya Guerrero Silvestre, Estrada Gallegos Joel, Astudillo Sandoval Raúl, Abundes Velasco Arturo, González Díaz Belinda, Argüero Sánchez Rubén, Farell Campa Javier
Servicio de Hemodinamia, Hospital de Cardiología del Centro Médico Nacional Siglo XXI, Institute Mexicano del Seguro Social, México, DF.
Arch Cardiol Mex. 2006 Jan-Mar;76(1):28-36.
Since the last decade, percutaneous balloon mitral valvuloplasty with Inoue catheter is considered the treatment of choice for selected patients (mobile valve, no calcification and minimal subvalvular disease) with rheumatic mitral stenosis.
We present the seven-year follow-up experience of 456 patients treated with this technique in the catheter laboratory of the Cardiology Hospital in National Medical Center SXXI.
It is a retrospective, transversal and observational study performed with data obtained from January 1994 and December 2000, with a follow-up of 58.5 +/- 26.6 months (range 12-96 mean 22).
We achieve an initial success of 82.8%, improvement of initial mitral valve area from 0.9 +/- 0.1 to 1.8 +/- 0.3 cm2, with a gain area from 88 to 106% (p < or = 0.001). At the end of the follow-up, the mean valvular area was maintained in 1.7 +/- 0.3 cm2 in 69.8% of the cases. We found a significant reduction of transmitral gradient and of the pulmonary artery systolic pressure immediately after the procedure; 93.1% of patients were in NYHA functional class II at the end of the follow-up, 11.6% presented complications (mitral regurgitation as the most important), in 15.9% of them, due to leaflet rupture, but only 9.1% corresponded to severe grade Ill-IV.
Only one patient died due to septal perforation; 93.8% of the patients remained free of major cardiac events at the end of the study. Only 6.1% of the patients required surgery at the end of the follow-up; 5.5% were in functional class NYHA Ill-IV and restenosis occurred in 14.6%.
Percutaneous balloon mitral valvuloplasty with Inoue balloon catheter is a safe and effective technique for treating rheumatic mitral stenosis with Wilkins score < 10, with minimal risk and complications and offers good life expectancy with absence of major cardiac events in > 90%. From these patients, 93.1% remained in NYHA-II or -I functional class and the incidence of restenosis decreased.
自上世纪九十年代以来,使用Inoue导管进行经皮球囊二尖瓣成形术被认为是对特定风湿性二尖瓣狭窄患者(瓣膜活动度好、无钙化且瓣下病变轻微)的首选治疗方法。
我们展示了在国立医学中心SXXI心脏病医院导管室接受该技术治疗的456例患者的七年随访经验。
这是一项回顾性、横向观察性研究,数据来源于1994年1月至2000年12月,随访时间为58.5±26.6个月(范围12 - 96个月,平均22个月)。
我们取得了82.8%的初始成功率,二尖瓣初始面积从0.9±0.1改善至1.8±0.3平方厘米,面积增加了88%至106%(p≤0.001)。随访结束时,69.8%的病例平均瓣膜面积维持在1.7±0.3平方厘米。术后即刻二尖瓣跨瓣压差和肺动脉收缩压显著降低;随访结束时93.1%的患者心功能分级为纽约心脏协会(NYHA)II级,11.6%出现并发症(以二尖瓣反流最为重要),其中15.9%是由于瓣叶破裂,但只有9.1%为严重的III - IV级。
仅1例患者因间隔穿孔死亡;研究结束时93.8%的患者无重大心脏事件。随访结束时仅6.1%的患者需要手术治疗;5.5%的心功能分级为NYHA III - IV级,再狭窄发生率为14.6%。
使用Inoue球囊导管进行经皮球囊二尖瓣成形术是治疗威尔金斯评分<10的风湿性二尖瓣狭窄的一种安全有效的技术,风险和并发症极小,90%以上患者无重大心脏事件,预期寿命良好。这些患者中93.1%的心功能维持在NYHA - II或 - I级,再狭窄发生率降低。