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镰状细胞病住院青少年难治性疼痛的管理:从静脉注射阿片类药物改为持续输注硬膜外镇痛

Management of refractory pain in hospitalized adolescents with sickle cell disease: changing from intravenous opioids to continuous infusion epidural analgesia.

作者信息

New Tamara, Venable Claudia, Fraser Laura, Rosenberg Erin, Schmidt Jennifer, James-Herry Anne, Osunkwo Ifeyinwa, Dampier Carlton

机构信息

*Emory University School of Medicine †Children's Healthcare of Atlanta, Atlanta, GA.

出版信息

J Pediatr Hematol Oncol. 2014 Aug;36(6):e398-402. doi: 10.1097/MPH.0000000000000026.

DOI:10.1097/MPH.0000000000000026
PMID:24136017
Abstract

BACKGROUND

Prolonged hospitalizations for sickle cell disease painful episodes are not uncommon, as analgesic options are often suboptimal.

OBSERVATIONS

Seven patients (15.4 ± 3.7 y, 6 females) were treated with epidural analgesia for refractory pain. The median duration of epidural catheter placement was 4 days (interquartile range, 3 to 6 d). Mean pain scores changed from 6.8 ± 2.7 to 4.8 ± 2.2, whereas mean daily parenteral opioid requirements changed from 79.7 ± 100.4 to 13.0 ± 13.1 mg of morphine equivalents.

CONCLUSION

Continuous epidural analgesia is an alternative to continuing intravenous opioids in sickle cell disease patients with refractory pain, and may reduce opioid-related side effects and facilitate transition to oral analgesics.

摘要

背景

镰状细胞病疼痛发作导致的长期住院并不罕见,因为镇痛选择往往不尽人意。

观察结果

7例患者(年龄15.4±3.7岁,6名女性)接受硬膜外镇痛以治疗顽固性疼痛。硬膜外导管置入的中位持续时间为4天(四分位间距为3至6天)。平均疼痛评分从6.8±2.7降至4.8±2.2,而每日胃肠外阿片类药物平均需求量从79.7±100.4毫克吗啡当量降至13.0±13.1毫克。

结论

对于患有顽固性疼痛的镰状细胞病患者,持续硬膜外镇痛是持续静脉注射阿片类药物的一种替代方法,并且可能减少阿片类药物相关副作用并有助于向口服镇痛药过渡。

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