Somani Riyaz, Krahn Andrew D, Healey Jeffrey S, Chauhan Vijay S, Birnie David H, Champagne Jean, Sanatani Shubhayan, Angaran Paul, Gow Robert M, Chakrabarti Santabhanu, Gerull Brenda, Yee Raymond, Skanes Allan C, Gula Lorne J, Leong-Sit Peter, Klein George J, Gollob Michael H, Talajic Mario, Gardner Martin, Simpson Christopher S
Queen׳s University, Kingston, Ontario, Canada.
University of British Columbia, Vancouver, British Columbia, Canada.
Heart Rhythm. 2014 Jun;11(6):1047-54. doi: 10.1016/j.hrthm.2014.03.022. Epub 2014 Mar 18.
Provocative testing with sodium channel blockers is advocated for the evaluation of unexplained cardiac arrest (UCA) with the primary purpose of unmasking the typical ECG features of Brugada syndrome. The Cardiac Arrest Survivors with Preserved Ejection Fraction Registry (CASPER) systematically assesses subjects with UCA or a family history of sudden death (FHSD).
The purpose of this study was to determine the clinical yield of procainamide infusion in a national registry of subjects with either UCA or a FHSD.
Subjects with either UCA or a FHSD without evidence of a Brugada pattern at baseline underwent procainamide testing (15 mg/kg to a maximum of 1 g at 50 mg/min). A test was considered positive for Brugada pattern if there was an increase in ST elevation >1 mm or if there was >1 mm of new ST elevation in leads V1 and/or V2. Genetic testing was performed on the basis of phenotype detection.
Procainamide testing was performed in 174 subjects (age 46.8 ± 15.4 years, 47% female). Testing provoked a Brugada pattern in 12 subjects (6.9%), 5 of whom had no ST abnormalities at baseline. No subjects with a negative procainamide challenge were subsequently diagnosed with Brugada syndrome. Genetic testing was conducted in 10 of the 12 subjects with a provoked Brugada pattern and was positive for a mutation in the SCN5A gene in 1.
Irrespective of the baseline ECG, procainamide testing provoked a Brugada pattern in a significant proportion of subjects with UCA or a FHSD, thereby facilitating a diagnosis of Brugada syndrome, and is recommended in the workup of UCA.
对于不明原因心脏骤停(UCA)的评估,提倡使用钠通道阻滞剂进行激发试验,其主要目的是揭示 Brugada 综合征的典型心电图特征。心脏骤停幸存者射血分数保留注册研究(CASPER)系统地评估了患有 UCA 或有猝死家族史(FHSD)的受试者。
本研究的目的是确定在一个全国性的 UCA 或 FHSD 受试者注册研究中普鲁卡因胺输注的临床诊断价值。
基线时无 Brugada 图形证据的 UCA 或 FHSD 受试者接受普鲁卡因胺试验(15mg/kg,以 50mg/min 的速度输注,最大剂量为 1g)。如果 ST 段抬高增加>1mm 或 V1 和/或 V2 导联出现>1mm 的新 ST 段抬高,则试验被认为 Brugada 图形阳性。根据表型检测进行基因检测。
174 名受试者(年龄 46.8±15.4 岁,47%为女性)接受了普鲁卡因胺试验。试验诱发 12 名受试者(6.9%)出现 Brugada 图形,其中 5 名受试者基线时无 ST 段异常。普鲁卡因胺激发试验阴性的受试者随后均未被诊断为 Brugada 综合征。12 名诱发 Brugada 图形的受试者中有 10 名进行了基因检测,其中 1 名 SCN5A 基因突变检测呈阳性。
无论基线心电图如何,普鲁卡因胺试验在相当比例的 UCA 或 FHSD 受试者中诱发了 Brugada 图形,从而有助于 Brugada 综合征的诊断,因此在 UCA 的检查中推荐使用。