Oxaliplatin causes increased offset analgesia during chemotherapy - a feasibility study.

IF 1.5 Q4 CLINICAL NEUROLOGY Scandinavian Journal of Pain Pub Date : 2023-08-21 Print Date: 2023-10-26 DOI:10.1515/sjpain-2023-0037
Carsten Dahl Mørch, Joanna E Szpejewska, Laurids Ø Poulsen, Mette Nyholm Yilmaz, Ursula G Falkmer, Lars Arendt-Nielsen
{"title":"Oxaliplatin causes increased offset analgesia during chemotherapy - a feasibility study.","authors":"Carsten Dahl Mørch, Joanna E Szpejewska, Laurids Ø Poulsen, Mette Nyholm Yilmaz, Ursula G Falkmer, Lars Arendt-Nielsen","doi":"10.1515/sjpain-2023-0037","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Offset analgesia (OA) is the phenomenon where the perceived pain intensity to heat stimulation disproportionally decreases after a slight decrease in stimulation temperature. The neural mechanisms of OA are not fully understood, but it appears that both peripheral and central temporal filtering properties are involved. Chemotherapy with oxaliplatin often causes acute peripheral sensory neuropathy, and manifests primarily as a cold induced allodynia. The aim of this exploratory patient study was to investigate if OA was affected by the neurotoxic effects of adjuvant oxaliplatin treatment.</p><p><strong>Methods: </strong>OA was assessed in 17 colon cancer patients during 12 cycles of adjuvant oxaliplatin treatment. The OA response was estimated as the decrease in pain intensity caused by a temperature decrease from 46 °C to 45 °C. Changes in the OA during the treatment period was estimated using a mixed linear model and corrected for multiple comparisons by Sidak's test.</p><p><strong>Results: </strong>OA was increased significantly when assessed before the 2nd, 3rd, 5th, 6th, 9th, and 10th treatment cycle compared to the first (baseline) treatment (p<0.05).</p><p><strong>Conclusions: </strong>OA is generally decreased in persons suffering from chronic pain or peripheral neuropathy as compared to healthy controls. But in the present study, OA increased during chemotherapy with oxaliplatin. The underlying mechanism of this unexpected increase should be further explored.</p>","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":null,"pages":null},"PeriodicalIF":1.5000,"publicationDate":"2023-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Scandinavian Journal of Pain","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/sjpain-2023-0037","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/10/26 0:00:00","PubModel":"Print","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: Offset analgesia (OA) is the phenomenon where the perceived pain intensity to heat stimulation disproportionally decreases after a slight decrease in stimulation temperature. The neural mechanisms of OA are not fully understood, but it appears that both peripheral and central temporal filtering properties are involved. Chemotherapy with oxaliplatin often causes acute peripheral sensory neuropathy, and manifests primarily as a cold induced allodynia. The aim of this exploratory patient study was to investigate if OA was affected by the neurotoxic effects of adjuvant oxaliplatin treatment.

Methods: OA was assessed in 17 colon cancer patients during 12 cycles of adjuvant oxaliplatin treatment. The OA response was estimated as the decrease in pain intensity caused by a temperature decrease from 46 °C to 45 °C. Changes in the OA during the treatment period was estimated using a mixed linear model and corrected for multiple comparisons by Sidak's test.

Results: OA was increased significantly when assessed before the 2nd, 3rd, 5th, 6th, 9th, and 10th treatment cycle compared to the first (baseline) treatment (p<0.05).

Conclusions: OA is generally decreased in persons suffering from chronic pain or peripheral neuropathy as compared to healthy controls. But in the present study, OA increased during chemotherapy with oxaliplatin. The underlying mechanism of this unexpected increase should be further explored.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
奥沙利铂在化疗期间引起抵消性镇痛增加——一项可行性研究。
目的:偏移镇痛(OA)是指在刺激温度略有降低后,对热刺激的感知疼痛强度不成比例地降低的现象。OA的神经机制尚不完全清楚,但似乎涉及外围和中心时间滤波特性。奥沙利铂化疗经常引起急性周围感觉神经病变,主要表现为感冒引起的异常性疼痛。这项探索性患者研究的目的是调查OA是否受到奥沙利铂辅助治疗的神经毒性影响。方法:对17例癌症患者在奥沙利铂辅助治疗的12个周期内进行OA评估。OA反应被估计为温度从46下降引起的疼痛强度下降 °C至45 °C。使用混合线性模型估计治疗期间OA的变化,并通过Sidak检验进行多重比较校正。结果:OA在术后第2、3、5、6、9、10、10、11、12、12、13、13、14、14、15、15、16、16、17、18、18、19、18、21、21、22、21、23、21、24、21、25、,与第一次(基线)治疗相比,第10个治疗周期(P结论:与健康对照组相比,患有慢性疼痛或周围神经病变的人的OA通常会降低。但在本研究中,奥沙利铂化疗期间OA增加。这种意外增加的潜在机制应进一步探讨。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Scandinavian Journal of Pain
Scandinavian Journal of Pain CLINICAL NEUROLOGY-
CiteScore
3.30
自引率
6.20%
发文量
73
期刊最新文献
Neck and shoulder pain and inflammatory biomarkers in plasma among forklift truck operators - A case-control study. A positive scratch collapse test in anterior cutaneous nerve entrapment syndrome indicates its neuropathic character. Real-world evidence evaluation on consumer experience and prescription journey of diclofenac gel in Sweden. Differences in risk factors for flare-ups in patients with lumbar radicular pain may depend on the definition of flare. The "future" pain clinician: Competencies needed to provide psychologically informed care.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1