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Do opiates affect the clinical evaluation of patients with acute abdominal pain?

机译:阿片类药物是否会影响急性腹痛患者的临床评估?

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CONTEXT: Clinicians have traditionally withheld opiate analgesia from patients with acute abdominal pain until after evaluation by a surgeon, out of concern that analgesia may alter the physical findings and interfere with diagnosis. OBJECTIVE: To determine the impact of opiate analgesics on the rational clinical examination and operative decision for patients with acute abdominal pain. DATA SOURCES AND STUDY SELECTION: MEDLINE (through May 2006), EMBASE, and hand searches of article bibliographies to identify placebo-controlled randomized trials of opiate analgesia reporting changes in the history, physical examination findings, or diagnostic errors (those resulting in "management errors," defined as the performance of unnecessary surgery or failure to perform necessary surgery in a timely fashion). DATA EXTRACTION: Two authors independently reviewed each study, abstracted data, and classified study quality. A third reviewer independently resolved discrepancies. DATA SYNTHESIS: Studies both in adults (9 trials) and in children (3 trials) showed trends toward increased risks of altered findings on the abdominal examination due to opiate administration, with risk ratios for changes in the examination of 1.51 (95% confidence interval [CI], 0.85 to 2.69) and 2.11 (95% CI, 0.60 to 7.35), respectively. When the analysis was restricted to the 8 adult and pediatric trials that reported significantly greater analgesia for patients who received opiates compared with those who received placebo, the risk of physical examination changes became significant (risk ratio, 2.13; 95% CI, 1.14 to 3.98). These trials exhibited significant heterogeneity (I2 = 68.6%; P = .002), and only 2 trials distinguished clinically significant changes such as loss of peritoneal signs from all other changes; consequently, we analyzed risk of management errors as a marker for important changes in the physical examination. Opiate administration had no significant association with management errors (+0.3% absolute increase; 95% CI, -4.1% to +4.7%). The 3 pediatric trials showed a nonsignificant absolute decrease in management errors (-0.8%; 95% CI, -8.6% to +6.9%). Across adult and pediatric trials with adequate analgesia, opiate administration was associated with a nonsignificant absolute decrease in the risk of management errors (-0.2%; 95% CI, -4.0% to +3.6%). CONCLUSIONS: Opiate administration may alter the physical examination findings, but these changes result in no significant increase in management errors. The existing literature does not rule out a small increase in errors, but this error rate reflects a conservative definition in which surgeries labeled as either delayed or unnecessary may have met appropriate standards of care. In published research reports, no patient experienced major morbidity or mortality attributable to opiate administration.
机译:语境:传统上,临床医生出于急腹痛可能会改变体格检查结果并干扰诊断的考虑,而对急性腹痛患者不进行鸦片类镇痛,直到医生对其进行评估之后。目的:确定阿片类镇痛药对急性腹痛患者合理临床检查和手术决策的影响。数据来源和研究选择:MEDLINE(至2006年5月),EMBASE和对文献书目的手工检索,以识别安慰剂对照的阿片类镇痛随机试验,这些试验报告了历史,体格检查结果或诊断错误的变化(这些导致“管理错误”,是指进行不必要的手术或未能及时进行必要的手术)。数据提取:两位作者独立审查了每项研究,提取了数据,并对研究质量进行了分类。第三位审稿人独立解决了差异。数据综合:成人(9个试验)和儿童(3个试验)的研究均显示,由于服用鸦片制剂而导致腹部检查改变的风险增加趋势,检查变化的风险比为1.51(95%置信区间) [CI],分别为0.85至2.69)和2.11(95%CI,0.60至7.35)。当分析仅限于8项成人和儿科试验,报告中接受鸦片制剂的患者比接受安慰剂的患者镇痛效果显着增强时,体格检查改变的风险变得显着(风险比,2.13; 95%CI,1.14至3.98 )。这些试验显示出显着的异质性(I2 = 68.6%; P = 0.002),只有2个试验将临床上显着的变化(例如腹膜征象的丧失)与所有其他变化区分开来;因此,我们分析了管理错误的风险,作为体格检查重要变化的标志。阿片类药物的施用与管理错误没有显着相关性(绝对增加+ 0.3%; CI从95%CI -4.1%增至+ 4.7%)。 3项儿科试验显示,管理错误的绝对减少无统计学意义(-0.8%; 95%CI,-8.6%至+ 6.9%)。在具有足够镇痛作用的成人和儿科试验中,鸦片类药物的使用与管理错误风险的绝对降低无明显关联(-0.2%; 95%CI,-4.0%至+ 3.6%)。结论:阿片类药物可能会改变体格检查的结果,但这些改变不会导致管理错误的明显增加。现有文献并没有排除错误的小幅增加,但是这种错误率反映了一个保守的定义,其中标记为延迟或不必要的手术可能已经达到适当的护理标准。在已发表的研究报告中,没有患者因服用鸦片制剂而出现严重的发病率或死亡率。

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