急性疼痛管理中影响脊髓阿片类药物生物利用度的关键因素

Borja Mugabure Bujedo
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引用次数: 2

摘要

虽然没有理想的镇痛药或神经轴给药途径,但临床医生都在继续寻找具有接近这一想法的品质的化合物。然而,事实证明,脊髓给药阿片类药物并不总是保证脊髓的节段性和选择性镇痛。这一点是有效的,因为药物在体循环中部分再摄取到达特定的脑阿片受体,而不是用脑脊液清除率的变化来解释差异。来自人类或动物实验研究的已发表证据表明,脊髓生物期的生物利用度与脂溶性呈负相关。因此,阿片类药物脊髓的生物利用度,亲水阿片类药物如吗啡,高于亲脂阿片类药物如芬太尼、舒芬太尼或阿芬太尼。
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Factores clave que afectan a la biodisponibilidad de los opioides sobre la médula espinal en el manejo del dolor agudo
Although there is no either ideal analgesic or route of neuraxial administration, clinicians alike continue to search for compounds with qualities which may approach this idea. However, it ́s a demonstrated fact that spinal administration of an opioid drug does not always guarantee segmental and selective analgesia into the spinal cord. This point is valid due to partial reuptake of the drug to systemic blood circulation reaching specifi c brain opioid receptors, rather than the differences are explained by variations in the clearance rate from the cerebrospinal fl uid. Published evidence from either human or animal experimental studies indicates that bioavailability in the spinal cord biophase is negatively correlated with liposolubility. Therefore, opioid spinal cord bioavailability is higher for hydrophilic opioids like morphine, than for lipophilic ones such as fentanyl, sufentanil or alfentanil.
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来源期刊
Revista de la Sociedad Espanola del Dolor
Revista de la Sociedad Espanola del Dolor Medicine-Anesthesiology and Pain Medicine
CiteScore
0.50
自引率
0.00%
发文量
22
期刊介绍: BOLETÍN INFORMATIVO de la Sociedad Española del Dolor. Sociedad Española del Dolor, Suscriptores, Hospitales, Bibliotecas y Facultades de Medicina.
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