Lucarini A R, Picano E, Bongiorni M G, Lattanzi F, Marini C, Paperini L, L'Abbate A, Salvetti A
Institute of Clinical Physiology Consiglio Nazionale delle Richerche CNR, Pisa, Italy.
J Hypertens. 1991 Sep;9(9):839-44. doi: 10.1097/00004872-199109000-00011.
Essential hypertensives are at greater risk for ventricular arrhythmias than normotensive controls. A reduction in coronary flow reserve may be one of the mechanisms underlying this increased prevalence of ventricular dysrhythmias in hypertensives. It has previously been shown that dipyridamole infusion may provoke ischemic-like S-T segment depression in essential hypertensives with angiographically normal coronary arteries and reduced flow reserve. The aim of the present study was to assess whether electrocardiographic positivity (S-T segment depression greater than 0.1 mV from baseline) during dipyridamole testing (12-lead electrocardiogram and two-dimensional echomonitoring, with the infusion of 0.84 mg/kg dipyridamole over 10 min) might identify hypertensives at greater risk for ventricular dysrhythmias. We therefore studied 51 mild-to-moderate essential hypertensives by dipyridamole testing and 48-h Holter monitoring. All patients were off therapy for at least 2 weeks before testing and Holter evaluation. Left ventricular mass (by Penn convention) and ejection fraction (by Teichholtz rule) were evaluated by two-dimensional echocardiography. Lown classes 0-1 were found in 31 patients (Group 1) and Lown classes II-IV in 20 (Group 2). The two groups overlapped for mean blood pressure (121 +/- 9 versus 124 +/- 8 mmHg), left ventricular mass index (120 +/- 27 versus 141 +/- 42 g/m2) and left ventricular ejection fraction (54 +/- 6 versus 52 +/- 6). An electrocardiographically-positive dipyridamole test was found in seven of Group I and 16 of Group II patients (23 versus 80%, P less than 0.01). No patient showed a transient, either regional or global, systolic dysfunction during dipyridamole testing.(ABSTRACT TRUNCATED AT 250 WORDS)
原发性高血压患者比血压正常的对照组发生室性心律失常的风险更高。冠状动脉血流储备的降低可能是高血压患者室性心律失常患病率增加的潜在机制之一。此前有研究表明,双嘧达莫输注可能会在冠状动脉造影正常但血流储备降低的原发性高血压患者中诱发缺血样S-T段压低。本研究的目的是评估在双嘧达莫试验(12导联心电图和二维超声心动图监测,在10分钟内输注0.84mg/kg双嘧达莫)期间心电图阳性(S-T段压低超过基线0.1mV)是否能识别出发生室性心律失常风险更高的高血压患者。因此,我们通过双嘧达莫试验和48小时动态心电图监测研究了51例轻至中度原发性高血压患者。所有患者在试验和动态心电图评估前至少停药2周。通过二维超声心动图评估左心室质量(按照Penn标准)和射血分数(按照Teichholtz规则)。31例患者(第1组)的Lown分级为0-1级,20例患者(第2组)的Lown分级为II-IV级。两组患者的平均血压(121±9与124±8mmHg)、左心室质量指数(120±27与141±42g/m²)和左心室射血分数(54±6与52±6)存在重叠。第1组7例患者和第2组16例患者的双嘧达莫试验心电图呈阳性(23%与80%,P<0.01)。在双嘧达莫试验期间,没有患者出现短暂的局部或整体收缩功能障碍。(摘要截短至250字)