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机构地区:[1]青岛大学医学院附属医院海阳分院眼科,山东海阳265100
出 处:《中国实用眼科杂志》2013年第9期1135-1138,共4页Chinese Journal of Practical Ophthalmology
摘 要:目的评估分析尼美舒利在全视网膜光凝术(Panretinal photoeoagulation,PRP)中的镇痛效果。方法应用双盲法进行研究。收集接受PRP治疗的糖尿病视网膜病变患者48例58只眼,随机分为服药组和对照组。在激光治疗前24h开始服用药物2天。激光治疗应用标准化治疗,在治疗结束后应用简式的McGill疼痛问卷表(short form of the McGill pain questionnaire,SF—MPQ)进行评估,内容包括疼痛分级指数(pain rating index,PRI)、视觉模拟评分(visual analogous scale,VAS)和现有疼痛强度评分(present pain intensity,PPI)3部分,三者的累积分值作为疼痛系数。结果服药组的PRI为3.8333±2.3057,对照组为4.3333±3.1132,(P〉0.05)。服药组的VAS为(2.6167±1.1347)分,对照组为(3.2333±0.5942)分,(P〈0.05)。服药组的PPI为(1.3667±0.6149)分,对照组为(1.1111±0.7511)分,(P〉0.05)。服药组的疼痛系数为7.8167±3.4046,对照组为8.6778±3.5499,(P〉0.05)。二者差异无统计学意义。结论应用尼美舒利超前镇痛法对于缩减PRP疼痛的方法是不明显的。Objective To evaluate the effectiveness of nimesulide for the reduction of pain in panretinal photocoagulation (PRP). Methods A double-masked randomized controlled study was per-formed. Fifty-eight eyes in 48 patients undergoing PRP were enrolled and randomised to group nime-sulide or placebo, taken for 2 days starting 24 hours before the laser treatment. The laser treatment was performed following a standardized protocol. Pain after treatment was assessed using Short form of the McGill pain questionnaire (SF-MPQ), it included pain rating index (PRI), visual analogous scale (VAS) and present pain intensity (PPI). The score of them was the pain level. Results The PRI for group nimesulide was 3.8333±2.3057 and group placebo was 4.3333±3.1132, (P 〉0.05). The VAS for group nimesulide was 2.6167±1.1347 and group placebo was 3.2333±0.5942, (P 〈0.05). The PPI for group nimesulide was 1.3667±0.6149 and group placebo was 1.1111±0.7511, (P 〉0.05). The mean pain level for group nimesulide was 7.8167±3.4046 and group placebo was 8.6778±3.5499, (P 〉0.05). There was no significant difference for pain levels between nimesulide instilled and place-bo eyes (P 〉0.05). Conclusions Pre-emptive analgesia with nimesulide dose not significantly reduc-es pain associated with PRP.
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