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窦房结对腺苷的反应与窦房结功能障碍的严重程度有关。

Sinus nodal response to adenosine relates to the severity of sinus node dysfunction.

机构信息

3rd Cardiology Department, Hippokration Hospital, Aristotle University Medical School, 49 Konstantinoupoleos Street, 54642 Thessaloniki, Greece.

出版信息

Europace. 2012 Jun;14(6):859-64. doi: 10.1093/europace/eur399. Epub 2011 Dec 26.

Abstract

AIMS

It is unknown as to whether the result of adenosine testing for the diagnosis of sinus node dysfunction (SND) depends on the clinical presentation. We investigated whether syncope or presyncope are associated with a more pronounced sinus nodal inhibition by adenosine in SND.

METHODS AND RESULTS

We studied 46 patients with SND, 33 with syncope or presyncope and 13 without such history. Controls were 30 subjects undergoing electrophysiological studies for supraventricular tachycardia or unexplained syncope. We calculated the corrected sinus node recovery time after intravenous adenosine 0.15 mg/kg (ADSNRT) as well as after atrial pacing (CSNRT). Corrected sinus node recovery time values >525 ms were considered abnormal. Corrected sinus node recovery time after adenosine injection was more prolonged in SND patients with syncope or presyncope as compared with those without such history [median: 4900 inter-quartile range (IQR): 920-8560 ms vs. median: 280 IQR: 5-908 ms; P< 0.005]. In SND patients with syncope or presyncope ADSNRT was more prolonged than CSNRT (median: 4900 IQR: 920-8560 ms vs. median: 680 IQR: 359-1650 ms, P< 0.01). In SND patients without syncope or presyncope no statistical difference was noted between ADSNRT and CSNRT (median: 280 IQR: 5-908 ms vs. median: 396 IQR: 270-600 ms, P = 0.80). The sensitivity of CSNRT for SND diagnosis was 57% and the specificity was 100%. A cut-off of 1029 ms for ADSRNT yields the same sensitivity with a specificity of 96.6%.

CONCLUSION

In patients with SND syncope or presyncope relate to an exaggerated sinus nodal suppression by adenosine. Prolonged ADSNRT can diagnose cases with severe underlying SND where a more aggressive management strategy is probably warranted.

摘要

目的

腺苷试验用于诊断窦房结功能障碍(SND)的结果是否取决于临床特征尚不清楚。我们研究了晕厥或先兆晕厥是否与 SND 中由腺苷引起的更明显的窦房结抑制有关。

方法和结果

我们研究了 46 例 SND 患者,其中 33 例有晕厥或先兆晕厥,13 例无此病史。对照组为 30 例因室上性心动过速或不明原因晕厥行电生理研究的患者。我们计算了静脉注射腺苷 0.15mg/kg 后的校正窦房结恢复时间(ADSNRT)和心房起搏后的校正窦房结恢复时间(CSNRT)。校正窦房结恢复时间值>525ms 被认为异常。与无此病史的患者相比,有晕厥或先兆晕厥的 SND 患者腺苷注射后的校正窦房结恢复时间明显延长[中位数:4900 四分位距(IQR):920-8560ms 与中位数:280 IQR:5-908ms;P<0.005]。在有晕厥或先兆晕厥的 SND 患者中,ADSNRT 比 CSNRT 更长(中位数:4900 IQR:920-8560ms 与中位数:680 IQR:359-1650ms,P<0.01)。在无晕厥或先兆晕厥的 SND 患者中,ADSNRT 与 CSNRT 之间无统计学差异(中位数:280 IQR:5-908ms 与中位数:396 IQR:270-600ms,P=0.80)。CSNRT 对 SND 诊断的敏感性为 57%,特异性为 100%。ADSRNT 的截断值为 1029ms 时,其敏感性为 57%,特异性为 96.6%。

结论

在 SND 患者中,晕厥或先兆晕厥与由腺苷引起的窦房结抑制过度有关。延长的 ADSNRT 可诊断出严重的潜在 SND 病例,可能需要更积极的治疗策略。

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