首页> 外文期刊>Journal of clinical anesthesia >Effect of parecoxib pretreatment and venous occlusion on propofol injection pain: a prospective, randomized, double-blinded, placebo-controlled study.
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Effect of parecoxib pretreatment and venous occlusion on propofol injection pain: a prospective, randomized, double-blinded, placebo-controlled study.

机译:帕瑞昔布预处理和静脉阻塞对丙泊酚注射痛的影响:一项前瞻性,随机,双盲,安慰剂对照研究。

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STUDY OBJECTIVE: To investigate the effect of parecoxib pretreatment with venous occlusion on propofol injection pain. DESIGN: Prospective, randomized, double-blinded, placebo-controlled study. SETTING: Operating room of a tertiary-care medical center. PATIENTS: 150 ASA physical status I patients scheduled for elective surgery. INTERVENTIONS: Patients were randomized to three groups of 50 patients each to receive pretreatment with normal saline (Group NS), parecoxib 20 mg (Group P20), or parecoxib 40 mg (Group P40). All groups underwent venous occlusion for two minutes before propofol was injected. All pretreatment drugs were prepared in 5 mL doses. MEASUREMENTS: Pain scores were obtained by a study-blinded observer during propofol injection following the different pretreatment solutions. MAIN RESULTS: Pain scores among the three groups were significantly different (P < or = 0.001). In Group NS, 29 (58%) patients had pain during propofol injection compared with 22 (40%) Group P20 and 13 (26%) Group P40 patients (P < or = 0.005). Pain was significantly reduced in Group P40 (P < or = 0.001) compared with the control group. Moderate to severe pain was experienced by 18 (36%) Group NS and 4 (8%) Group P20 patients, whereas no Group P40 patient experienced moderate or severe pain (P < 0.001). Reduction in pain severity was statistically significant after pretreatment with either parecoxib 20 mg (P = 0.002) or parecoxib 40 mg (P < 0.001). CONCLUSION: Parecoxib 40 mg with venous occlusion is effective in reducing the frequency and severity of pain with propofol injection. Pretreatment with 20 mg of parecoxib reduces the severity of propofol injection pain significantly but does not reduce frequency compared with the control group.
机译:目的:探讨帕瑞昔布静脉闭塞预处理对异丙酚注射痛的影响。设计:前瞻性,随机,双盲,安慰剂对照研究。地点:三级医疗中心的手术室。患者:150名ASA身体状况I的患者计划进行择期手术。干预措施:将患者随机分为三组,每组50例,分别接受生理盐水(NS组),帕瑞昔布20 mg(P20组)或帕瑞昔布40 mg(P40组)预处理。在注射异丙酚之前,所有组均进行静脉闭塞2分钟。所有预处理药物均以5 mL剂量制备。测量:由盲研究者在不同的预处理溶液中注射异丙酚期间获得疼痛评分。主要结果:三组之间的疼痛评分显着不同(P <或= 0.001)。在NS组中,有29名(58%)患者在注射异丙酚时感到疼痛,而P20组有22名(40%),P40组有13名(26%)(P <或= 0.005)。与对照组相比,P40组的疼痛明显减轻(P <或= 0.001)。 NS组18名(36%)和P20组4名(8%)经历了中度至重度疼痛,而P40组没有中度或重度疼痛(P <0.001)。用帕瑞昔布20 mg(P = 0.002)或帕瑞昔布40 mg(P <0.001)进行预处理后,疼痛严重程度的降低具有统计学意义。结论:帕瑞昔布40 mg静脉阻塞可有效减少丙泊酚注射液的疼痛发生频率和严重程度。与对照组相比,用20 mg派瑞昔布进行预处理可显着降低丙泊酚注射痛的严重程度,但不会降低频率。

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