首页> 外文期刊>International wound journal. >Analgesic efficacy of equimolar 50% nitrous oxide/oxygen gas premix (Kalinox?) as compared with a 5% eutectic mixture of lidocaine/prilocaine (EMLA?) in chronic leg ulcer debridement
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Analgesic efficacy of equimolar 50% nitrous oxide/oxygen gas premix (Kalinox?) as compared with a 5% eutectic mixture of lidocaine/prilocaine (EMLA?) in chronic leg ulcer debridement

机译:与慢性腿部溃疡清除血管干扰血管干扰率/普利卡因(EMLA?)的5%共晶混合物相比,等摩尔50%二氮氧化物/氧气预混物(Kalinoxα)的镇痛效果

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摘要

Abstract Chronic foot and leg ulcers are a common health problem worldwide. A mainstay of chronic ulcer therapy is sharp mechanical wound debridement requiring potent analgesia. In this prospective, controlled, single‐centre, crossover design study, patients were assigned to either the administration of topical analgesia with 5% lidocaine/prilocaine cream or the inhalation of an analgesic 50% N 2 O/O 2 gas premix. Primary outcome parameter was level of pain at maximum wound depth during debridement as measured by a visual analogue scale. Secondary outcomes included level of pain after debridement, overall duration of treatment session, duration and completeness of debridement, and the patient's subjective perception of analgesic quality during debridement. Pain level increased from 0·60/0·94 (first/second debridement; baseline) to 1·76/2·50 (debridement) with 5% lidocaine/prilocaine and from 1·00/1·35 (baseline) to 3·95/3·29 (debridement) with 50% N 2 O/O 2 gas premix. Patient satisfaction was 90·48%/94·44% (first/second debridement) with topical 5% lidocaine/prilocaine analgesia and 90·48%/76·47% with the inhalation of 50% N 2 O/O 2 gas premix. Debridement was completed in a significantly higher percentage of 85·71%/88·89% (first/second debridement) with 5% lidocaine/prilocaine than with 50% N 2 O/O 2 gas premix (42·86%/58·82%) (odds ratio 6·7; P = 0·001). This study provides sound evidence that analgesia with topically administered 5% lidocaine/prilocaine cream is superior to the use of inhaled 50% N 2 O/O 2 gas premix in chronic leg ulcer debridement.
机译:摘要慢性脚和腿部溃疡是全世界常见的健康问题。慢性溃疡疗法的主要机械伤口清创患者需要有效镇痛。在这项前瞻性,控制,单中心,交叉设计研究中,患者分配给局部镇痛的给药,用5%利多卡因/胰蛋白酶霜或吸入镇痛50%N 2 O / O 2气预混料。通过视觉模拟量表测量的清新过程中的最大伤口深度是疼痛的疼痛水平。二次结果包括清创后疼痛水平,治疗会议的总体持续时间,清卓人的持续时间和完整性,以及患者在清创中对镇痛质量的主观感知。疼痛程度从0·60/0·94(第一/第二种创新;基线)增加到1·76/2·50(清创),其中5%Lidocaine / prilocaine和1·00/1·35(基线)到3 ·95/3·29(清创),50%N 2 O / O 2气预混料。患者满意度为90·48%/ 94·44%(第一/第二种清创),具有局部5%利多卡因/胰岛素镇痛和90·48%/ 76·47%,吸入50%N 2 O / O 2气预混料。作品以85·71%/ 88·89%(第一/第二清创)的百分比明显高于5%Lidocaine / prilocaine,而不是50%N 2 O / O 2气预混物(42·86%/ 58· 82%)(差距6·7; P = 0·001)。本研究提供了合理的证据,即局部施用的5%利多卡因/胰蛋白酶霜的镇痛优于使用吸入的50%N 2 O / O 2气预混物在慢性腿部溃疡清除中。

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