Setty H S Natraj, Rao Murali, Srinivas K H, Srinivas B C, Usha M K, Jayaranganath M, Patil Shivanand S, Manjunath C N
Sri Jayadeva Institute of Cardiovascular Sciences and Research, Bengaluru, Karnataka, India.
Sri Jayadeva Institute of Cardiovascular Sciences and Research, Bengaluru, Karnataka, India.
Int J Cardiol. 2016 Oct 1;220:924-8. doi: 10.1016/j.ijcard.2016.06.194. Epub 2016 Jun 26.
Aim of the study was to evaluate clinical, angiographic profile and percutaneous endovascular management of Takayasu's arteritis.
Takayasu's arteritis is a chronic inflammatory vasculitis affecting the aorta and its major branches. Although it is more prevalent in Asia, the distribution of the disease is worldwide with different vascular involvement patterns and clinical manifestations.
In this prospective study a total of 50 consecutive patients who were reported as having Takayasu's arteritis between January 2010 and April 2016 were evaluated. Detailed clinical presentation and angiograms of all patients were analysed.
50 patients were analysed during study period. Among 50 patients, 43(86%) were female and 7 (14%) were male. Average age of presentation was 26.92years. Most common clinical presentation was claudication (74%) followed by, musculoskeletal symptoms (48%), fatigue (46%), weight loss (22%), headache (22%), visual disturbances (16%), syncope (10%), dyspnoea (20%). Most common features were absent/diminished pulses (80%), difference in blood pressure (80%), followed by bruit (70%)hypertension (64%), cerebrovascular accident (8%),heart failure (8%) and aortic regurgitation (4%). According to the new angiographic classification, angiographic type I (40%) was encountered most frequently, followed by type III (30%), type V (16%), type IIb (8%), type IIa (2%), and type IV is (4%). Angioplasty was the main stay of treatment in 66% of the patients, remaining 34% of them were treated medically either with corticosteroids or methotrexate.
Takayasu's arteritis is a rare disease, affects mainly women, manifestations range from asymptomatic disease, found as a result of impalpable pulses or bruits, to catastrophic neurological impairment. Takayasu's arteritis is the common cause of renovascular hypertension. Angiography remains the gold standard for diagnosis. Angiographic evaluation and percutaneous transluminal angioplasty with stenting is useful in selected cases.
本研究旨在评估高安动脉炎的临床、血管造影特征及经皮血管腔内治疗。
高安动脉炎是一种累及主动脉及其主要分支的慢性炎症性血管炎。尽管该病在亚洲更为常见,但在全球范围内均有分布,且具有不同的血管受累模式和临床表现。
在这项前瞻性研究中,对2010年1月至2016年4月期间报告患有高安动脉炎的50例连续患者进行了评估。分析了所有患者的详细临床表现和血管造影。
研究期间分析了50例患者。在50例患者中,43例(86%)为女性,7例(14%)为男性。平均发病年龄为26.92岁。最常见的临床表现是跛行(74%),其次是肌肉骨骼症状(48%)、疲劳(46%)、体重减轻(22%)、头痛(22%)、视觉障碍(16%)、晕厥(10%)、呼吸困难(20%)。最常见的体征是脉搏减弱或消失(80%)、血压差异(80%),其次是血管杂音(70%)、高血压(64%)、脑血管意外(8%)、心力衰竭(8%)和主动脉瓣关闭不全(4%)。根据新的血管造影分类,血管造影I型(40%)最为常见,其次是III型(30%)、V型(16%)、IIb型(8%)、IIa型(2%)和IV型(4%)。血管成形术是66%患者的主要治疗方法,其余34%患者接受了皮质类固醇或甲氨蝶呤的药物治疗。
高安动脉炎是一种罕见疾病,主要影响女性,其表现范围从因脉搏触诊不到或血管杂音而发现的无症状疾病到灾难性的神经功能损害。高安动脉炎是肾血管性高血压的常见原因。血管造影仍然是诊断的金标准。血管造影评估和经皮腔内血管成形术加支架置入术在某些病例中是有用的。