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曲马多或对乙酰氨基酚不会影响显著缓解疼痛的急性腹痛的诊断准确性-一项前瞻性、随机、安慰剂对照、双盲研究。

Tramadol or paracetamol do not effect the diagnostic accuracy of acute abdominal pain with significant pain relief - a prospective, randomized, placebo controlled double blind study.

机构信息

Department of Emergency Medicine, School of Medicine, Inonu University, Malatya, Turkey.

出版信息

Eur Rev Med Pharmacol Sci. 2012 Dec;16(14):1983-8.

Abstract

OBJECTIVES

To examine the effects of early administration of analgesics in patients with acute abdominal pain on pain severity, abdominal findings and diagnostic accuracy.

METHODS

210 patients with non-traumatic acute abdominal pain lasting less than 72 hours were enrolled to this trial. Patients were administrated by placebo, tramadol (1 mg/kg), or paracetamol (15 mg/kg) randomly after the first evaluation of pain severity scores (standard 100 mm visual analog scale) and abdominal findings (rebound, rigidity, tenderness). After 20 and 40 minutes of administrations, pain severity scores and abdominal findings were re-examined. Complete blood count, electrocardiography, plain abdominal x-ray, urine analysis and abdominal ultrasound were used for the initial diagnosis. The final diagnoses were decided after re-examinations, biochemical blood analysis, abdominal computed tomography in all patients and consultations or other diagnostic methods when necessary.

RESULTS

There were 70 patients in each group. Baseline pain severity scores and abdominal findings were similar at all groups. After 20 minutes, pain severity scores were decreased in tramadol and paracetamol groups compared with the placebo group as 55% and 45% vs 1% respectively (p < 0.001). After 40 minutes, decreases on pain severity scores were more significant at treatment groups, 67% and 60% vs 0 (p < 0.001). When compared to placebo tramadol and paracetamol increased the new onset or worsening nausea or vomiting. There was no difference on abdominal findings among the groups after 20 and 40 minutes examinations. Diagnostic accuracy of tramadol, paracetamol and placebo groups were 96%, 94% and 94% respectively.

CONCLUSIONS

Early administration of tramadol and paracetamol provided effective pain relief in patients with non-traumatic acute abdominal pain and those administrations did not interfere with diagnosis.

摘要

目的

探讨在急性腹痛患者中早期使用镇痛药对疼痛严重程度、腹部体征和诊断准确性的影响。

方法

本试验纳入了 210 例疼痛持续时间小于 72 小时的非创伤性急性腹痛患者。患者在首次评估疼痛严重程度评分(标准 100mm 视觉模拟评分)和腹部体征(反弹、僵硬、压痛)后,随机给予安慰剂、曲马多(1mg/kg)或扑热息痛(15mg/kg)。给药后 20 和 40 分钟,再次检查疼痛严重程度评分和腹部体征。所有患者均进行血常规、心电图、腹部平片、尿液分析和腹部超声检查以进行初步诊断。在所有患者中,根据复查、生化血液分析、腹部 CT 以及必要时咨询或其他诊断方法来确定最终诊断。

结果

每组各有 70 例患者。各组的基线疼痛严重程度评分和腹部体征相似。给药 20 分钟后,与安慰剂组相比,曲马多组和扑热息痛组的疼痛严重程度评分分别下降了 55%和 45%(p<0.001)。给药 40 分钟后,治疗组的疼痛严重程度评分下降更为显著,分别为 67%和 60%(p<0.001)。与安慰剂相比,曲马多和扑热息痛增加了新发或恶化的恶心或呕吐。给药 20 和 40 分钟后,各组的腹部体征无差异。曲马多、扑热息痛和安慰剂组的诊断准确率分别为 96%、94%和 94%。

结论

在非创伤性急性腹痛患者中早期使用曲马多和扑热息痛可有效缓解疼痛,且这些药物的使用不会干扰诊断。

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