Shafei H, Chamberlain M, Natrajan K N, Khan M A, Gandhi R G
Department of Cardiothoracic Surgery, Victoria Hospital, Blackpool, England.
Thorac Cardiovasc Surg. 1990 Feb;38(1):38-41. doi: 10.1055/s-2007-1013989.
54 patients who had posterolateral thoracotomy were prospectively studied to compare the efficacy of intrapleural bupivacaine with that of bupivacaine intercostal block and cryofreezing. Patients were randomized into three groups. The intrapleural catheter group included 16 patients who had intermittent intrapleural instillation of 20 ml of 0.25% bupivacaine for forty-eight hours postoperatively. The second group included sixteen patients who were given perioperative bupivacaine intercostal block. The third group included fifteen patients treated by cryofreezing of the intercostal nerves. Visual analogue four-hourly pain score was compared between the three groups during the first forty-eight hours postoperatively. The analgesic requirements during the first postoperative week were also assessed. There was no significant difference between the three groups in the average pain score (3.61 +/- 1.37, 3.54 +/- 1.15, and 3.33 +/- 1.47 respectively). During the first forty-eight hours postoperatively, the percentage of patients who required papaveretum in the intrapleural catheter group (56.3%) was significantly less than that in the other two groups (both 100%). The average papaveretum requirement (mg per patient) in the intrapleural catheter group (27.33 +/- 25.27) was significantly less than that in the second group (52.66 +/- 26.85) but the difference was not statistically significant from that in the third group (37.66 +/- 20.95). No complications related to the use of the intrapleural catheter or to bupivacaine toxicity were encountered. In conclusion, the technique of intermittent intrapleural bupivacaine is safe and comparable in efficacy to bupivacaine intercostal block and cryofreezing. Narcotic requirements may be reduced when this technique is used.
对54例行后外侧开胸手术的患者进行前瞻性研究,以比较胸膜内布比卡因、布比卡因肋间阻滞和冷冻治疗的疗效。患者被随机分为三组。胸膜内导管组包括16例患者,术后48小时内间歇性胸膜内注入20 ml 0.25%布比卡因。第二组包括16例接受围手术期布比卡因肋间阻滞的患者。第三组包括15例接受肋间神经冷冻治疗的患者。术后48小时内,每4小时比较三组的视觉模拟疼痛评分。还评估了术后第一周的镇痛需求。三组的平均疼痛评分无显著差异(分别为3.61±1.37、3.54±1.15和3.33±1.47)。术后48小时内,胸膜内导管组需要哌替啶的患者百分比(56.3%)显著低于其他两组(均为100%)。胸膜内导管组的平均哌替啶需求量(mg/患者)(27.33±25.27)显著低于第二组(52.66±26.85),但与第三组(37.66±20.95)的差异无统计学意义。未遇到与胸膜内导管使用或布比卡因毒性相关的并发症。总之,间歇性胸膜内布比卡因技术安全,疗效与布比卡因肋间阻滞和冷冻治疗相当。使用该技术时可减少麻醉剂需求。