Chinese Journal of Stroke ›› 2020, Vol. 15 ›› Issue (06): 637-643.DOI: 10.3969/j.issn.1673-5765.2020.06.012

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Application Value of 0.25 mg Low-dose Nitroglycerin-stimulated Head-up Tilt Test for the Diagnosis of Vasovagal Syncope

  

  • Received:2020-04-20 Online:2020-06-20 Published:2020-06-20

0.25 mg低剂量硝酸甘油激发直立倾斜试验在血管迷走性晕厥诊断中的应用

刘杰昕*,杜嵩*,王跃,金泽宁,黄泽民,宋柯,樊志奇,陈章煌,吴斌(*第一作者)   

  1. 1100070 北京首都医科大学附属北京天坛医院心脏中心
    2中国航天员科研训练中心
    3深圳市绿航星际太空科技研究院
  • 通讯作者: 吴斌wubinacc@sina.com

Abstract:

Objective To evaluate the feasibility of 0.25 mg low-dose nitroglycerin-stimulated head-up tilt testing (HUTT) for the diagnosis of vasovagal syncope (VVS) . Methods Patients with suspected VVS were selected in this study for a HUTT provoked by 0.25 mg low-dose sublingual nitroglycerin. Noninvasive beat to beat blood pressure was monitored continuously, then the positive rate and the time from tilt to presyncope were compared with that in previous studies. Results A total of 343 patients were included, of whom 241 patients (70.3%) were elicited a positive result by the low-dose nitroglycerin-stimulated HUTT. Of the positive HUTT patients, 83 (34.4%) were mixed syncope, 2 (0.8%) were cardioinhibitory syncope and 156 (64.7%) were vasodepressor syncope. No significant differences in the drug provoked positive rate and overall positive rate were found between this study and previous international studies, while the overall positive rate in this study was higher than that in previous domestic studies (70.3% vs 64%, P =0.016). The time from tilt to presyncope in this study was shorter, compared to that in the study using 0.3 mg sublingual nitroglycerin (5.0±2.2 min vs 7±8 min, P =0.001), while had no statistical difference with that in the study using 0.4 mg sublingual nitroglycerin (spray) (P >0.99).

Conclusions Due to an acceptable positive result, the drug stimulated HUTT by 0.25 mg low-dose nitroglycerin are feasible in the clinical practice.

Key words: Head-up tilt testing; Nitroglycerin; Vasovagal syncope

摘要:

目的 评价0.25 mg低剂量硝酸甘油激发直立倾斜试验(head-up tilt testing,HUTT)诊断血管迷走 性晕厥(vasovagal syncope,VVS)的临床可行性。 方法 入选疑似VVS患者进行0.25 mg低剂量硝酸甘油激发HUTT检查,通过无创连续逐搏血压监测 数据的脱机分析,获取阳性率和达到阳性反应时间,并与既往国内外研究相比较。 结果 共入组疑似VVS患者343例,241例(70.3%)在HUTT过程中出现了阳性结果,其中混合型83例 (34.4%),心脏抑制型2例(0.8%),血管减压型156例(64.7%)。低剂量硝酸甘油药物激发阶段阳性 率与国外既往研究差异无统计学意义,整体阳性率与国外既往研究差异无统计学意义,但高于国内 既往研究(70.3% vs 64%,P =0.016)。低剂量硝酸甘油激发阶段出现阳性反应的时间低于国外既往 使用0.3 mg片剂舌下含服激发的研究(5.0±2.2 min vs 7±8 mi n,P =0.001),与使用0.4 mg硝酸甘油舌 下喷雾研究结果的差异无统计学意义(P>0.99)。 结论 0.25 mg低剂量硝酸甘油激发HUTT的阳性率和达到阳性反应时间与国外0.4 mg硝酸甘油激发 HUTT的结果无差异,具有临床应用的可行性。

关键词: 直立倾斜试验; 硝酸甘油; 血管迷走性晕厥