Okajima Masaki, Takamura Masayuki, Taniguchi Takumi
Masaki Okajima, Takumi Taniguchi, Intensive Care Unit, Kanazawa University Hospital, Kanazawa 920-8641, Japan.
World J Crit Care Med. 2015 Aug 4;4(3):251-7. doi: 10.5492/wjccm.v4.i3.251.
To investigate whether landiolol, an ultra-short-acting β1-antagonist, can safely and effectively control heart rate in septic patients with supraventricular tachyarrhythmias.
We reviewed all patients with sepsis who admitted to our intensive care unit between January 2006 and December 2011. Sixty one septic patients suffered from supraventricular tachyarrhythmias (heart rate ≥ 120 bpm for > 1 h). Among 61 patients, 39 patients were treated with landiolol (landiolol group) and 22 patients were not treated with landiolol (control group). Arterial pressure, heart rate, cardiac rhythm, pulmonary arterial pressure and cardiac output (if a pulmonary arterial catheter was inserted) were compared between the 2 groups at 1, 8 and 24 h after the initiation of tachyarrhythmias.
Mean age and Acute Physiology and Chronic Health Evaluation II and Sequential Organ Failure Assessment scores were similar between the 2 groups. Paroxysmal atrial fibrillation/flutter (87%), paroxysmal atrial tachycardia (10%), and paroxysmal supraventricular tachycardia (3%) were observed. The initial landiolol dose administered was 6.3 ± 5.8 g/kg per minute. Rapid and substantial reduction of heart rate was observed in the landiolol group without any deterioration of hemodynamics. Landiolol significantly reduced heart rate (from 145 ± 14 bpm to 90 ± 20 bpm) compared to the control group (from 136 ± 21 bpm to 109 ± 18 bpm, P < 0.05). The conversion to sinus rhythm was observed more frequently in the landiolol group than in the control group at every point (P < 0.01 at 8 h; P < 0.05 at 1 and 24 h).
Landiolol safely reduced heart rate and, in part, converted to sinus rhythm in septic patients with supraventricular tachyarrhythmias.
研究超短效β1受体拮抗剂兰地洛尔能否安全有效地控制脓毒症合并室上性快速心律失常患者的心率。
我们回顾了2006年1月至2011年12月期间入住我院重症监护病房的所有脓毒症患者。61例脓毒症患者合并室上性快速心律失常(心率≥120次/分钟,持续时间>1小时)。61例患者中,39例接受兰地洛尔治疗(兰地洛尔组),22例未接受兰地洛尔治疗(对照组)。比较两组在快速心律失常发作后1小时、8小时和24小时的动脉压、心率、心律、肺动脉压和心输出量(如果插入肺动脉导管)。
两组患者的平均年龄、急性生理与慢性健康状况评分II和序贯器官衰竭评估评分相似。观察到阵发性心房颤动/扑动(87%)、阵发性房性心动过速(10%)和阵发性室上性心动过速(3%)。初始给予兰地洛尔的剂量为6.3±5.8微克/千克每分钟。兰地洛尔组心率迅速大幅下降,且血流动力学无任何恶化。与对照组相比,兰地洛尔显著降低了心率(从145±14次/分钟降至90±20次/分钟)(对照组从136±21次/分钟降至109±18次/分钟,P<0.05)。在各个时间点,兰地洛尔组比对照组更频繁地观察到转为窦性心律(8小时时P<0.01;1小时和24小时时P<0.05)。
兰地洛尔可安全降低脓毒症合并室上性快速心律失常患者的心率,并部分转为窦性心律。