Namboodiri Narayanan, Remash Krishnan, Tharakan Jaganmohan A, Shajeem Othayoth, Nair Krishnakumar, Titus Thomas, Ajitkumar Valaparambil K, Sivasankaran Sivasubramonian, Krishnamoorthy Kavassery M, Harikrishnan Sivadasan P, Harikrishnan Madhavankutty S, Bijulal Sasidharan
Department of Cardiology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, Kerala, India.
J Heart Valve Dis. 2009 Jan;18(1):61-7.
A significant proportion of patients who require interventions for rheumatic mitral valve (MV) disease have coexisting aortic valve (AV) disease. To date, little is known of the natural history of AV disease in these patients.
The details of a cohort of 200 patients (146 females, 54 males; mean age at MV intervention 30.3 +/- 9.9 years) with rheumatic heart disease were retrospectively reviewed. The patients had undergone an index MV intervention (either closed or balloon mitral valvotomy) or MV replacement between 1994 and 1996, and received long-term regular follow up examinations. The clinical and echocardiographic data at entry and at follow up were noted. Patients were allocated to two groups, based on whether the AV disease was absent (group I, n=98) or present (group II, n=102) at baseline. The AV disease was categorized as thickening only (group IIA), isolated aortic regurgitation (AR) (group IIB), or combined aortic stenosis (AS) and AR (group IIC). No patient had isolated AS at baseline.
The mean follow up period was 9.3 +/- 1.07 years; during which 10 patients in group I developed new AV disease, which included AV thickening only (n=2), trivial-mild AR (n=7) and mild AS with trivial AR (n=1). Of 16 patients in group IIA, 11 developed isolated AR, and one patient progressed to have mild AS and AR. Among 69 patients in group IIB, 22 (31.9%) developed AS, and all had either mild (n=8) or moderate (n=14) AR with mild AS. Group IIC included 17 patients with mild combined AV disease at baseline, except for moderate AS and moderate AR in one patient each. Among 16 patients with mild AS in group IIC, six progressed to moderate AS and two to severe AS. AR became moderate in 10 patients and severe in one patient. The two patients who progressed to severe AS requiring AV replacement had mild AS at baseline. No patient who developed new combined AV disease had lesions with severity more than mild AS or moderate AR. On logistic regression analysis of the variables predisposing to progression of AV disease, such as age, gender, history of rheumatic fever (RF) and recurrence, and interval from RF episode to symptom onset, only the initial AV gradient was identified as being statistically significant (beta coefficient 0.528, SE = 0.17, p < 0.0001).
Patients with no or mild AV disease at the time of MV intervention rarely develop severe AV disease, and seldom require AV surgery over the long-term follow up. The presence of mild AS at baseline is predictive in the minority of cases where AV disease will progress relatively more rapidly.
相当一部分需要接受风湿性二尖瓣(MV)疾病干预的患者同时存在主动脉瓣(AV)疾病。迄今为止,对于这些患者中AV疾病的自然病史知之甚少。
回顾性分析了200例风湿性心脏病患者(146例女性,54例男性;MV干预时的平均年龄为30.3±9.9岁)的详细情况。这些患者在1994年至1996年间接受了首次MV干预(闭式或球囊二尖瓣切开术)或MV置换,并接受了长期定期随访检查。记录了入组时和随访时的临床及超声心动图数据。根据基线时是否存在AV疾病,将患者分为两组,无AV疾病的为I组(n = 98),存在AV疾病的为II组(n = 102)。AV疾病分为仅增厚(IIA组)、单纯主动脉瓣反流(AR)(IIB组)或合并主动脉瓣狭窄(AS)和AR(IIC组)。基线时无患者存在单纯AS。
平均随访期为9.3±1.07年;在此期间,I组有10例患者出现了新的AV疾病,包括仅AV增厚(n = 2)、轻度至中度AR(n = 7)和轻度AS合并轻度AR(n = 1)。IIA组的16例患者中,11例出现了单纯AR,1例进展为轻度AS和AR。IIB组的69例患者中,22例(31.9%)出现了AS,且均伴有轻度(n = 8)或中度(n = 14)AR及轻度AS。IIC组基线时有17例轻度联合AV疾病患者,其中各有1例为中度AS和中度AR。IIC组16例轻度AS患者中,6例进展为中度AS,2例进展为重度AS。10例患者的AR变为中度,1例变为重度。进展为需要AV置换的重度AS的2例患者基线时为轻度AS。新出现联合AV疾病的患者中,病变严重程度均未超过轻度AS或中度AR。对易导致AV疾病进展的变量进行逻辑回归分析,如年龄、性别、风湿热(RF)病史及复发情况,以及从RF发作到症状出现的间隔时间,仅初始AV梯度具有统计学意义(β系数0.528,标准误 = 0.17,p < 0.0001)。
MV干预时无或轻度AV疾病的患者很少发展为重度AV疾病,在长期随访中很少需要AV手术。基线时存在轻度AS可预测少数情况下AV疾病进展相对较快。