King Faisal Heart Institute, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Eur J Cardiothorac Surg. 2011 Sep;40(3):543-51. doi: 10.1016/j.ejcts.2010.12.060. Epub 2011 Feb 25.
We aim to report time-related outcomes following mitral valve replacement (MVR) in children and to identify factors affecting outcomes.
Clinical records from 307 children who underwent MVR between 1985 and 2004 were reviewed. Competing-risks methodology determined time-related prevalence of three mutually exclusive end-states: death, mitral reoperation and survival without subsequent MVR, and their associated risk factors.
Mean age was 11.4 ± 5.6 years including 36 (12%) patients < 2 years old. There were 154 (50%) males. Underlying pathology was rheumatic fever (n = 195, 64%), congenital (n = 83, 27%) and other (n = 29, 9%) with congenital pathology predominant in younger children while rheumatic fever predominant in older children. Hemodynamic manifestation was regurgitation (83%), stenosis (5%), or mixed disease (12%). One hundred and twenty-six patients (41%) had undergone a prior cardiac surgery including mitral surgery (n = 96, 31%). Initial mitral prosthesis was mechanical (n = 229, 75%), tissue (n = 71, 23%), or homograft (n = 7, 2%). Concomitant cardiac surgery was required in 141 patients (46%). Competing-risks analysis predicted that 20 years following MVR, approximately 17% of patients have died, 51% have undergone mitral reoperation and only 33% were alive and free from mitral reoperation. Risk factors for death without mitral reoperation included younger age < 3 years [PE (parameter estimates): +1.66 ± 0.31, p < 0.001], longer cross-clamp time (PE: +0.11 ± 0.04/10 min, p = 0.005), postoperative complications (PE: +1.5 8 ± 0.31, p < 0.001), and higher prosthesis size/body surface area (BSA)-predicted mitral annulus ratio (PE: + 0.48 ± 0.10, p < 0.001). Risk factors for mitral reoperation included implantation of homograft or tissue prosthesis (PE: +1.12 ± 0.23, p < 0.001) and smaller prosthesis size (PE: +0.06 ± 0.03/1 mm, p = 0.05). Fifteen-year freedom from pacemaker implantation, endocarditis, bleeding, and thromboembolism was 92%, 96%, 82%, and 92%, respectively.
Mortality and mitral reoperation are common after MVR in children and outcomes can be predicted based on patient's age, prosthesis size, and other associated factors. Some modifiable factors such as avoiding oversized prostheses may improve outcomes especially in the smallest children.
报告儿童二尖瓣置换术(MVR)后的时间相关结果,并确定影响结果的因素。
回顾了 1985 年至 2004 年间接受 MVR 的 307 名儿童的临床记录。竞争风险方法确定了三个相互排斥的终末状态的时间相关流行率:死亡、二尖瓣再次手术和无后续 MVR 的存活,以及它们相关的危险因素。
平均年龄为 11.4 ± 5.6 岁,其中 36 名(12%)患者<2 岁。有 154 名(50%)男性。基础病理为风湿热(n=195,64%)、先天性(n=83,27%)和其他(n=29,9%),先天性病理在年龄较小的儿童中更为常见,而风湿热在年龄较大的儿童中更为常见。血流动力学表现为反流(83%)、狭窄(5%)或混合病变(12%)。126 名患者(41%)曾接受过心脏手术,包括二尖瓣手术(n=96,31%)。初始二尖瓣假体为机械(n=229,75%)、组织(n=71,23%)或同种异体(n=7,2%)。141 名患者(46%)需要同时进行其他心脏手术。竞争风险分析预测,在 MVR 后 20 年,约有 17%的患者死亡,51%的患者进行了二尖瓣再次手术,只有 33%的患者存活且无需二尖瓣再次手术。无二尖瓣再次手术死亡的危险因素包括年龄<3 岁(PE:+1.66±0.31,p<0.001)、体外循环时间较长(PE:+0.11±0.04/10min,p=0.005)、术后并发症(PE:+1.58±0.31,p<0.001)和更大的假体尺寸/体表面积(BSA)预测二尖瓣瓣环比值(PE:+0.48±0.10,p<0.001)。二尖瓣再次手术的危险因素包括同种异体或组织假体的植入(PE:+1.12±0.23,p<0.001)和较小的假体尺寸(PE:+0.06±0.03/1mm,p=0.05)。15 年免于起搏器植入、心内膜炎、出血和血栓栓塞的几率分别为 92%、96%、82%和 92%。
儿童二尖瓣置换术后死亡率和二尖瓣再次手术率较高,可根据患者年龄、假体尺寸和其他相关因素进行预测。一些可改变的因素,如避免过大的假体,可能会改善结果,特别是在最小的儿童中。