Hernández-Palazón J, Tortosa J A, Martínez-Lage J F, Pérez-Flores D
Department of Anesthesiology, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain.
Anesth Analg. 2001 Jun;92(6):1473-6. doi: 10.1097/00000539-200106000-00024.
We sought to determine the analgesic efficacy, opioid-sparing effects, and tolerability of propacetamol, an injectable prodrug of acetaminophen, in combination with morphine administered by patient-controlled analgesia (PCA) after spinal fusion surgery. Forty-two patients undergoing spinal stabilization surgery were randomized into two groups, which were given either an IV placebo or an IV injection of 2 g propacetamol every 6 h for 3 days after surgery. The postoperative opioid analgesic requirement was assessed with a PCA device used to self-administer morphine. Pain relief was evaluated by a visual analog pain scale and by verbal rating scores of pain relief at 8-h intervals for up to 72 h after surgery. The cumulative dose of morphine at 72 h was smaller in the Propacetamol group than in the Placebo group (60.3 +/- 20.5 vs 112.2 +/- 39.1 mg; P < 0.001). The pain scores were significantly lower in the Propacetamol group measured at two intervals of the study, although visual analog scale pain intensity scores were smaller than 3 in both groups. Most patients in the Placebo group obtained a greater degree of sedation on postoperative Day 3 (P < 0.05). This study demonstrates the usefulness of propacetamol as an adjunct to PCA morphine in the treatment of postoperative pain after spinal fusion.
我们试图确定对乙酰氨基酚的注射用前体药物丙帕他莫与吗啡联合用于患者自控镇痛(PCA)在脊柱融合手术后的镇痛效果、节省阿片类药物的作用及耐受性。42例行脊柱稳定手术的患者被随机分为两组,术后3天内一组静脉注射安慰剂,另一组每6小时静脉注射2 g丙帕他莫。使用PCA装置自行注射吗啡来评估术后阿片类镇痛药的需求量。通过视觉模拟疼痛量表以及术后长达72小时每隔8小时的疼痛缓解言语评分来评估疼痛缓解情况。丙帕他莫组72小时吗啡累积剂量低于安慰剂组(60.3±20.5 vs 112.2±39.1 mg;P<0.001)。在研究的两个时间点测量时,丙帕他莫组的疼痛评分显著更低,尽管两组的视觉模拟量表疼痛强度评分均小于3。安慰剂组的大多数患者在术后第3天镇静程度更高(P<0.05)。本研究证明丙帕他莫作为PCA吗啡的辅助药物在治疗脊柱融合术后疼痛方面的有效性。