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鞘内炎性肿块:每年阿片类药物剂量增加是否是早期指标?

Intrathecal inflammatory masses: is the yearly opioid dose increase an early indicator?

机构信息

Faculty of Health, Birmingham City University, Birmingham, UK; Department of Pain Management, Russells Hall Hospital, Dudley, UK; and Pain Management Unit, University Hospital Birmingham, Birmingham, UK.

出版信息

Neuromodulation. 2010 Apr;13(2):109-13. doi: 10.1111/j.1525-1403.2009.00259.x. Epub 2009 Nov 20.

Abstract

OBJECTIVES

The objective of this study is to investigate the association between intrathecal drug, flow rate, drug concentration, and drug dose with the formation of intrathecal inflammatory masses.

METHODS

A retrospective longitudinal study of 56 consecutive patients receiving long-term intrathecal analgesic administration was undertaken through screening of medical records. Data regarding drug flow rate, dose per day, and concentration of drugs administered were recorded for morphine, diamorphine, bupivicaine, clonidine and baclofen and averages computed.

RESULTS

The average follow-up time post-implant was 91 ± 55 months (range: 9-209). Four of the 56 patients were diagnosed with intrathecal granuloma indicating a rate of 7%, the equivalent to 0.009 events per patient year. Twenty-one of the patients had received morphine either alone or combined; 22 had received diamorphine either alone or mixed; and 13 crossed over from morphine to diamorphine or the inverse. None of the patients with granuloma crossed over before diagnosis. A significant correlation was found between opioid dose (r= 0.275, p < 0.05), yearly increase of the opioid dose (r= 0.433, p < 0.05), and granuloma formation. Clonidine appeared to have a protective effect for the non-granuloma patients. No association was found with flow rate (r= 0.056) or opioid concentration (r= 0.214).

CONCLUSION

This is the first detailed study showing an association of diamorphine with granulomas. This study supports the previous finding of intrathecal opioid dose being a risk factor for intrathecal granulomas and clonidine being protective. In addition we have found that the yearly increase in opioid dose is a risk factor for granulomas and could serve as an indicator for closer surveillance.

摘要

目的

本研究旨在探讨鞘内药物、流速、药物浓度和药物剂量与鞘内炎症肿块形成之间的关系。

方法

通过病历筛查,对 56 例连续接受长期鞘内镇痛治疗的患者进行了回顾性纵向研究。记录了吗啡、二氢吗啡酮、布比卡因、可乐定和巴氯芬的药物流速、每日剂量和给药浓度,并计算平均值。

结果

植入后平均随访时间为 91 ± 55 个月(范围:9-209)。56 例患者中有 4 例被诊断为鞘内肉芽肿,发生率为 7%,相当于 0.009 例/患者年。21 例患者单独或联合使用吗啡;22 例患者单独或混合使用二氢吗啡酮;13 例患者从吗啡转为二氢吗啡酮或反之。在诊断前,没有肉芽肿患者发生交叉。发现阿片类药物剂量(r=0.275,p<0.05)、阿片类药物剂量每年增加(r=0.433,p<0.05)与肉芽肿形成之间存在显著相关性。可乐定对非肉芽肿患者似乎有保护作用。未发现流速(r=0.056)或阿片类药物浓度(r=0.214)与肉芽肿之间存在关联。

结论

这是第一项详细研究,表明二氢吗啡酮与肉芽肿有关。本研究支持以前的发现,即鞘内阿片类药物剂量是鞘内肉芽肿的一个危险因素,可乐定具有保护作用。此外,我们发现阿片类药物剂量每年增加是肉芽肿的一个危险因素,并可作为密切监测的指标。

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