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静脉输注酚妥拉明后,疼痛缓解峰值延迟,缓解持续时间延长。初步报告。

Peak pain relief is delayed and duration of relief is extended following intravenous phentolamine infusion. Preliminary report.

作者信息

Galer B S

机构信息

Department of Anesthesiology, University of Washington School of Medicine, Seattle 98105, USA.

出版信息

Reg Anesth. 1995 Sep-Oct;20(5):444-7.

PMID:8519723
Abstract

BACKGROUND AND OBJECTIVES

Intravenous phentolamine infusion (i.v.P) has been shown to produce pain relief in some patients with sympathetically maintained pain. Animal models of neuropathic pain have reported decreases in pain behavior lasting 5 days following phentolamine injection. However, no clinical study has prospectively assessed pain relief for longer than 24 hours. The aim of this preliminary report was to assess prospectively daily pain relief scores for 1 week following i.v.P METHODS: Thirty-seven consecutive patients with neuropathic pain were asked to complete a pain relief scale for 7 days following i.v.P All patients were first administered 35 mg i.v.P At least 1 week later, 16 patients were administered i.v.P at a higher dose, 50 mg or 75 mg. Data from a total of 45 infusions were collected.

RESULTS

Sixteen patients experienced pain relief from i.v.P Twenty-seven infusions resulted in pain relief. Peak pain relief was delayed in 25 of 27 (93%) positive i.v.P: 7 patients experienced the onset of peak response the night immediately following an infusion, 13 the next day, 3 2 days later, and 1 each 4 and 5 days after infusion. All 16 patients who reported pain relief following i.v.P experienced at least 2 days of relief with each infusion. Eight patients experienced at least 1 week of pain relief. No differences in pain relief scores were seen with higher-dosage i.v.P.

CONCLUSIONS

A delay in peak pain relief was reported following 25/27 i.v.Ps. Peak pain relief occurred most often at least 24 hours after infusion completion. In these patients, duration of pain relief was at least 2 days. Placebo controlled studies are needed to verify these observations.

摘要

背景与目的

静脉注射酚妥拉明(i.v.P)已被证明能使一些患有交感神经维持性疼痛的患者缓解疼痛。神经性疼痛的动物模型报告称,注射酚妥拉明后疼痛行为的减轻可持续5天。然而,尚无临床研究对超过24小时的疼痛缓解情况进行前瞻性评估。本初步报告的目的是前瞻性评估静脉注射酚妥拉明后1周内的每日疼痛缓解评分。方法:37例连续性神经性疼痛患者被要求在静脉注射酚妥拉明后7天内完成疼痛缓解量表。所有患者首先接受35mg静脉注射酚妥拉明。至少1周后,16例患者接受更高剂量(50mg或75mg)的静脉注射酚妥拉明。共收集了45次注射的数据。

结果

16例患者通过静脉注射酚妥拉明获得疼痛缓解。27次注射导致疼痛缓解。27次阳性静脉注射酚妥拉明中有25次(93%)疼痛缓解峰值出现延迟:7例患者在注射后当晚出现峰值反应,13例在第二天出现,3例在2天后出现,1例在注射后4天和5天出现。所有16例报告静脉注射酚妥拉明后疼痛缓解的患者每次注射至少有2天的缓解期。8例患者经历了至少1周的疼痛缓解。更高剂量的静脉注射酚妥拉明在疼痛缓解评分上未见差异。

结论

27次静脉注射酚妥拉明中有25次报告疼痛缓解峰值出现延迟。疼痛缓解峰值最常出现在注射完成后至少24小时。在这些患者中,疼痛缓解持续时间至少为2天。需要进行安慰剂对照研究来验证这些观察结果。

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