Yamashita Yusuke, Takasusuki Toshifumi, Kimura Yoshiyuki, Komatsuzaki Makoto, Yamaguchi Shigeki
Department of Anesthesiology, Dokkyo Medical University, School of Medicine, Mibu, Tochigi, Japan.
Cardiol Ther. 2018 Dec;7(2):163-172. doi: 10.1007/s40119-018-0119-9. Epub 2018 Sep 14.
Reversal of non-depolarizing neuromuscular blocking agent neostigmine is associated with QT prolongation under general anesthesia. To clarify the effects of neostigmine and sugammadex on hemodynamic status, the QT interval and QT dispersion after reversal of neuromuscular blockade were evaluated with a 12-lead electrocardiogram. To exclude QT prolongation due to sevoflurane, the present study was performed under propofol anesthesia.
After receiving approval from the ethics committee of Dokkyo Medical University Hospital, 40 patients with American Society of Anesthesiologists physical status I or II were randomly allocated to group N (n = 20) or group S (n = 20). Group N was administered neostigmine (40 μg/kg) and atropine (20 μg/kg), while Group S was administered sugammadex (4 mg/kg) for reversal of neuromuscular blockade after surgery. The changes in RR interval, QT interval (QT), corrected QT interval (QTc), QT dispersion (QTD), and corrected QT dispersion (QTcD) before and after administration of reversal agents were recorded using computerized measurements. Statistical analysis was performed using two-way analysis of variance.
The RR interval significantly decreased after reversal of the neuromuscular blockade in group N, compared with group S (p < 0.05). Compared with group S, the QT decreased, whereas QTc and QTcD increased, in group N (p < 0.05). Sugammadex was not found to alter QT, QTc, QTD, or QTcD throughout the study.
In the present study, a mixture of neostigmine and atropine, but not sugammadex, increased QTc and QTcD under propofol anesthesia. Thus, neostigmine may cause electrocardiogram abnormalities that could precede the development of fatal arrhythmias.
在全身麻醉下,非去极化神经肌肉阻滞剂新斯的明的逆转与QT间期延长有关。为了阐明新斯的明和舒更葡糖对血流动力学状态、神经肌肉阻滞逆转后的QT间期和QT离散度的影响,采用12导联心电图进行评估。为了排除七氟醚引起的QT间期延长,本研究在丙泊酚麻醉下进行。
获得独协医科大学医院伦理委员会批准后,将40例美国麻醉医师协会身体状况为I或II级的患者随机分为N组(n = 20)或S组(n = 20)。N组给予新斯的明(40μg/kg)和阿托品(20μg/kg),而S组给予舒更葡糖(4mg/kg)用于术后神经肌肉阻滞的逆转。使用计算机测量记录给予逆转剂前后RR间期、QT间期(QT)、校正QT间期(QTc)、QT离散度(QTD)和校正QT离散度(QTcD)的变化。采用双向方差分析进行统计分析。
与S组相比,N组神经肌肉阻滞逆转后RR间期显著缩短(p < 0.05)。与S组相比,N组QT缩短,而QTc和QTcD增加(p < 0.05)。在整个研究过程中,未发现舒更葡糖改变QT、QTc、QTD或QTcD。
在本研究中,在丙泊酚麻醉下,新斯的明和阿托品的混合物而非舒更葡糖增加了QTc和QTcD。因此,新斯的明可能会导致心电图异常,这可能是致命性心律失常发生的先兆。