Tucker P W, Smith J R, Adams D F
Department of Periodontology. Oregon Health Sciences University, Portland, USA.
J Periodontol. 1996 Feb;67(2):125-9. doi: 10.1902/jop.1996.67.2.125.
A single blind study of 24 patients compared the postoperative periodontal pain relief and adverse effects associated with a pretreatment regimen with etodolac, a nonsteroidal anti-inflammatory drug (NSAID), to a typical pro re nada (prn) regimen with a combination of acetaminophen with hydrocodone. Patients selected required one or more periodontal osseous surgeries that were judged to involve relatively similar degrees of surgical manipulation. Patients in the etodolac group received two 300 mg capsules 30 minutes prior to surgery and then redosed themselves prn. Patients who received the combination drug were not premedicated and followed a prn regimen. The subjects used a verbal analogue scale to report levels of pain hourly for the first 8 hours (starting 30 minutes prior to surgery) and also indicated any side effects experienced during the first week after surgery. Specific parameters monitored were the mean sum of hourly pain scores, mean hourly pain scores, time to first medication, number of postoperative doses, and adverse effects. Of the parameters studied, the only one that showed a statistically significant difference was the time to first medication. The time span from 30 minutes prior to the beginning of surgery to the first postsurgical dose was greater for etodolac than for the combination drug. However, the total number of medications taken under both regimens was similar. The side effects were minimal for both of the drugs studied. It was concluded that the analgesic regimens tested under clinical practice conditions were comparable in providing analgesia with minimum side effects in uncomplicated periodontal osseous surgery. Studies with larger numbers of patients are needed to definitively address whether these regimens are truly equivalent.
一项针对24名患者的单盲研究,比较了术前使用非甾体抗炎药依托度酸预处理方案与对乙酰氨基酚联合氢可酮的典型按需(prn)方案在术后牙周疼痛缓解及不良反应方面的情况。入选患者需接受一项或多项牙周骨手术,且这些手术被判定涉及相对相似程度的手术操作。依托度酸组患者在手术前30分钟服用两粒300毫克胶囊,然后按需自行再次给药。接受联合用药的患者未进行术前用药,而是遵循按需方案。受试者使用视觉模拟量表,在最初8小时(从手术前30分钟开始)每小时报告疼痛程度,并指出术后第一周内经历的任何副作用。监测的具体参数包括每小时疼痛评分的均值总和、每小时平均疼痛评分、首次用药时间、术后用药次数及不良反应。在所研究的参数中,唯一显示出统计学显著差异的是首次用药时间。从手术开始前30分钟到术后首次用药的时间跨度,依托度酸组比联合用药组更长。然而,两种方案下服用药物的总数相似。所研究的两种药物的副作用均最小。得出的结论是,在临床实践条件下测试的镇痛方案在为简单的牙周骨手术提供镇痛且副作用最小方面具有可比性。需要进行更多患者的研究来明确这些方案是否真的等效。