首页> 外文期刊>Journal of opioid management >Analgesic treatment for moderate-to-severe acute pain in the United States: patients' perspectives in the Physicians Partnering Against Pain (P3) survey.
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Analgesic treatment for moderate-to-severe acute pain in the United States: patients' perspectives in the Physicians Partnering Against Pain (P3) survey.

机译:在美国,中度至重度急性疼痛的止痛药治疗:《医师对疼痛的伙伴关系》(P3)调查中患者的观点。

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OBJECTIVES: To evaluate patients' perceptions of the adequacy of analgesia for moderate-to-severe acute pain and the influence of opioid-related side effects in outpatient pain management. SETTING: The Physicians Partnering Against Pain (P3) survey of analgesic treatment for moderate-to-severe acute pain in the United States. PATIENTS: Adults with moderate-to-severe acute pain at their first analgesic followup visit. MAIN OUTCOME MEASURES: Analgesic level was determined from the World Health Organization'spain ladder (0 = none; 1 = nonopioid; 2 = weak opioid; 3 = strong opioid). Pain intensity was derived from numeric rating scale (NRS) scores (0 = none [NRS = 0]; 1 = mild [NRS = 1-3]; 2 = moderate [NRS = 4-7]; 3 = severe [NRS = 8-10). Pain management index scores were calculated as the analgesic level minus the pain intensity. Opioid recipients responded to questions on the P3 survey regarding side effects and their management. RESULTS: Of the 50,869 patients with complete data for analysis, 22,267 (44 percent) had received potentially inadequate analgesia, including 43, 46, and 52 percent of patients aged < 65, 65-74, and > or = 75 years, respectively. Of the 39,6 75 patients treated with an opioid, 10,925 (28 percent) experienced at least one gastrointestinal side effect (nausea, vomiting or constipation). Many of these patients stopped taking the medication (13 percent) or reduced their dose (16 percent) to manage gastrointestinal side effects. CONCLUSIONS: In the P3 study, one of the largest outpatient surveys conducted in pain management, moderate-to-severe acute pain continued to be widely undertreated in outpatient settings in the United States, particularly among older patients. Opioids with improved tolerability profiles might help to alleviate this undertreatment of moderate-to-severe acute pain.
机译:目的:评估患者对中度至重度急性疼痛镇痛的适当性的认识,以及阿片类药物相关副作用在门诊疼痛管理中的影响。地点:美国医师合作抗痛(P3)镇痛药治疗中度至重度急性疼痛的调查。患者:首次镇痛随访时患有中度至重度急性疼痛的成年人。主要观察指标:根据世界卫生组织西班牙阶梯确定镇痛水平(0 =无; 1 =非阿片类药物; 2 =弱阿片类药物; 3 =强阿片类药物)。疼痛强度来自数字评分量表(NRS)评分(0 =无[NRS = 0]; 1 =轻度[NRS = 1-3]; 2 =轻度[NRS = 4-7]; 3 =严重[NRS = 8-10)。疼痛管理指数得分计算为镇痛水平减去疼痛强度。阿片类药物接受者回答了P3调查中有关副作用及其管理的问题。结果:在50869名具有完整分析数据的患者中,有22267名(44%)接受了可能不充分的镇痛,其中分别有43%,46%和52%的患者年龄<65岁,65-74岁和>或= 75岁。在39.6名阿片类药物治疗的75名患者中,有10,925名(28%)经历了至少一种胃肠道副作用(恶心,呕吐或便秘)。这些患者中有许多人停止服用药物(占13%)或减少剂量(占16%)来控制胃肠道副作用。结论:在P3研究中,这是在疼痛管理方面进行的最大的门诊调查之一,在美国,特别是在老年患者中,中度至重度急性疼痛继续被广泛地治疗不足。具有改善的耐受性的阿片类药物可能有助于减轻对中度至重度急性疼痛的这种治疗不足。

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