Abid A, Benhamou D, Labaille T
Service d'Anesthésie-Réanimation, Université Paris-Sud, Hôpital Antoine Béclère, Clamart.
Ann Fr Anesth Reanim. 1990;9(3):275-9. doi: 10.1016/s0750-7658(05)80186-8.
This study aimed to compare the efficacy and side-effects of sublingual buprenorphine, a synthetic opioid agonist antagonist, with those of subcutaneous morphine. Fifty ASA class 1 patients were included in the study after having given their informed consent. Caesarean section was carried out under epidural block with 0.5% bupivacaine; no opioids were used during the procedure. The first dose of opioid was given 2 h after the first dose of bupivacaine. Patients were randomly given either 10 mg morphine (n = 25) or 0.4 mg buprenorphine (n = 25), followed by the same dose every 6 h for 36 h. When analgesia was insufficient, tablets containing dextropropoxyphene and paracetamol were given. No attempt was made to blind the study to the patient, but the investigator assessing pain was unaware of the drug given to the patient. Pain intensity was assessed before, and 2 h after each dose of opioid with a 100 mm visual scale, as well as systolic, diastolic and mean arterial blood pressures, heart and breathing rates, and SpO2. Side-effects (pruritus, nausea, vomiting, drowsiness) were also noted. In 2 patients in each group, the protocol was stopped before the 36th h, but after the fourth dose, either because of side-effects, or at the patient's request. Results were similar in both groups of patients, whether for degree of pain relief, or physiological effects. There was no clinically detectable respiratory depression. Duration and intensity of episodes of arterial oxygen desaturation, and the incidence of nausea, were similar in the 2 groups; pruritus was more common in the morphine group.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究旨在比较合成阿片类激动剂拮抗剂舌下含服丁丙诺啡与皮下注射吗啡的疗效及副作用。50例美国麻醉医师协会(ASA)1级患者在签署知情同意书后纳入研究。剖宫产在0.5%布比卡因硬膜外阻滞下进行;手术过程中未使用阿片类药物。在第一剂布比卡因给药2小时后给予第一剂阿片类药物。患者被随机给予10毫克吗啡(n = 25)或0.4毫克丁丙诺啡(n = 25),随后每6小时给予相同剂量,持续36小时。当镇痛效果不足时,给予含右丙氧芬和对乙酰氨基酚的片剂。未对患者设盲,但评估疼痛的研究者不知道给予患者的药物。在每次给予阿片类药物前及给药后2小时,使用100毫米视觉模拟评分法评估疼痛强度,同时测量收缩压、舒张压和平均动脉压、心率、呼吸频率及血氧饱和度(SpO2)。还记录副作用(瘙痒、恶心、呕吐、嗜睡)。每组各有2例患者在第36小时前但在第四剂后因副作用或患者要求而停止试验。两组患者在疼痛缓解程度或生理效应方面结果相似。未发现临床上可检测到的呼吸抑制。两组患者动脉血氧饱和度降低发作的持续时间和强度以及恶心发生率相似;瘙痒在吗啡组更常见。(摘要截短至250字)