Matek Jan, Cernohorsky Stanislav, Trca Stanislav, Krska Zdenek, Hoskovec David, Bruthans Jan, Sima Martin, Michalek Pavel
1st Department of Surgery-Department of Abdominal, Thoracic Surgery and Traumatology, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, 128 00 Prague, Czech Republic.
Medical Faculty, Masaryk University, 625 00 Brno, Czech Republic.
J Clin Med. 2020 May 9;9(5):1395. doi: 10.3390/jcm9051395.
The aim of this study was to compare plasma levobupivacaine concentrations in thoracic epidural and subpleural paravertebral analgesia.
Forty-four patients indicated for open lung resection had an epidural catheter inserted preoperatively or a subpleural catheter surgically. A bolus of 0.25% levobupivacaine at a dosage of 0.5 mg × kg was given after the thoracotomy closure. Plasma levobupivacaine level at 30 min was the primary outcome. Pharmacokinetic modeling was performed subsequently. Secondary outcomes included the quality of analgesia, complications, and patients'mobility.
Plasma concentrations were similar 30 min after application-0.389 mg × L in the epidural and 0.318 mg × L in the subpleural group ( = 0.33) and lower in the subpleural group at 120 min ( = 0.03). The areas under the curve but not maximum concentrations were lower in the subpleural group. The time to reach maximum plasma level was similar in both groups-27.6 vs. 24.2 min. No clinical symptoms of local anesthetic toxicity were recorded.
Levobupivacaine systemic concentrations were low in both groups without the symptoms of toxicity. This dosage should be safe for postoperative analgesia after thoracotomy.
本研究旨在比较胸段硬膜外镇痛和胸膜下椎旁镇痛时血浆左旋布比卡因的浓度。
44例拟行开胸肺切除术的患者在术前插入硬膜外导管或在手术中插入胸膜下导管。开胸手术关闭后给予0.25%左旋布比卡因,剂量为0.5mg/kg。主要观察指标为给药30分钟时的血浆左旋布比卡因水平。随后进行药代动力学建模。次要观察指标包括镇痛质量、并发症和患者活动度。
给药30分钟后,血浆浓度相似,硬膜外组为0.389mg/L,胸膜下组为0.318mg/L(P=0.33);120分钟时胸膜下组较低(P=0.03)。胸膜下组曲线下面积较低,但最大浓度无差异。两组达到血浆最高水平的时间相似,分别为27.6分钟和24.2分钟。未记录到局部麻醉药中毒的临床症状。
两组左旋布比卡因的全身浓度均较低,且无毒性症状。该剂量用于开胸术后镇痛应是安全的。