Concurrent validity of dynamic bedside quantitative sensory testing paradigms in breast cancer survivors with persistent pain.

IF 1.5 Q4 CLINICAL NEUROLOGY
Scandinavian Journal of Pain Pub Date : 2024-03-18 eCollection Date: 2024-01-01 DOI:10.1515/sjpain-2023-0093
Vincent Haenen, Mira Meeus, Nele Devoogdt, Bart Morlion, Lore Dams, Amber De Groote, Anthe Foubert, An De Groef
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Abstract

Background: Studies on the concurrent validity of clinically applicable testing protocols for conditioned pain modulation (CPM) and temporal summation of pain (TSP) in breast cancer survivors (BCS) with persistent pain are lacking.

Objectives: This study investigated the concurrent validity of two bedside protocols for CPM and TSP in comparison to a respective reference protocol. The participants' preferences for bedside CPM and TSP protocols were assessed.

Methods: Thirty BCS experiencing persistent pain were included in this study. Each participant underwent a reference test along with two bedside alternatives for assessing both TSP and CPM. For CPM, a cold pressor test (CPT) and blood pressure cuff (BPC) were used as conditioning stimulus. The test stimulus was elicited in parallel by pressure pain threshold after 45 and 90 s of conditioning at the lower limb. The CPM reference test consisted of parallel heat stimuli at the forearms using a two-thermode system. TSP was elicited using a von Frey monofilament (256 mN) and an algometer (98 kPa) at the affected site and opposite lower limb. The TSP reference test consisted of heat stimuli at the affected site and opposite lower limb. Participants' testing preference was examined using a purpose-designed questionnaire. Spearman's rank test examined the correlation between protocols.

Results: The two bedside CPM protocols were strongly correlated (r = 0.787-0.939, p < 0.005). A strong correlation was found between the BPC protocol and reference test using the relative effect magnitude (r = 0.541-0.555, p < 0.005). The bedside TSP protocols were moderately correlated with each other only at the lower limb using absolute change scores (r = 0.455, p = 0.012). No significant correlation was found between the bedside and reference TSP protocols.

Conclusion: The significantly moderate to very strong correlations between the bedside protocols validate their interchangeability. Researchers and clinicians should be able to choose which bedside protocol they utilize; however, participants favored the use of a BPC and algometer for the evaluation of CPM and TSP, respectively.

乳腺癌幸存者持续疼痛的动态床旁定量感官测试范例的并发有效性。
背景:目前还缺乏对乳腺癌幸存者(BCS)持续疼痛的条件性疼痛调节(CPM)和疼痛时间总和(TSP)的临床适用测试方案同时有效性的研究:本研究调查了两种床旁疼痛调节(CPM)和疼痛时间总和(TSP)测试方案与各自参考方案的并发有效性。评估了参与者对床边 CPM 和 TSP 方案的偏好:本研究纳入了 30 名持续疼痛的 BCS 患者。每位参与者都接受了一项参考测试以及两种床旁替代方案,以评估 TSP 和 CPM。对于 CPM,使用冷加压试验(CPT)和血压袖带(BPC)作为条件刺激。在下肢进行 45 秒和 90 秒的调节后,通过压痛阈值平行激发测试刺激。CPM 参考测试包括使用双温模式系统对前臂进行平行热刺激。在受累部位和对侧下肢使用 von Frey 单丝(256 毫牛顿)和压力计(98 千帕)诱发 TSP。TSP 参考测试包括在受影响部位和对侧下肢进行热刺激。使用专门设计的调查问卷对参与者的测试偏好进行了调查。斯皮尔曼秩检验检验了方案之间的相关性:结果:两种床旁 CPM 方案具有很强的相关性(r = 0.787-0.939,p < 0.005)。BPC方案与使用相对效应大小的参考测试之间存在很强的相关性(r = 0.541-0.555,p < 0.005)。床旁 TSP 方案仅在下肢使用绝对变化评分(r = 0.455,p = 0.012)时具有中度相关性。床旁 TSP 方案与参考 TSP 方案之间没有发现明显的相关性:结论:床旁方案之间存在明显的中度至高度相关性,这验证了它们之间的可互换性。研究人员和临床医生应该可以选择使用哪种床旁方案;不过,参与者更倾向于分别使用 BPC 和海藻糖度计来评估 CPM 和 TSP。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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
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