Predictors of neuropathic dysesthetic pain occurrence and chronification in multiple sclerosis (2-year prospective study).

Mykhaylo Delva, Kateryna Skoryk, Iryna Delva
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Abstract

Background: Patients with multiple sclerosis (MS) are a high-risk group for neuropathic pain.

Objective: to investigate predictors of neuropathic dysesthetic pain (NDP) occurrence and chronification in patients with MS during a 2-year observation period.

Methods: After the exclusion criteria application and signing of informed consent, we recruited in the study 241 patients among which 23 patients prematurely stopped participating in the study. During the 2-year observation period, new NDP was diagnosed on the PainDETECT questionnaire (>18). Patients with newly diagnosed NDP were examined at baseline, in 1, 3, and 6 months depending on pain duration. The socio-demographic, neuropsychological, cognitive, sleep quality, and clinical characteristics of patients were evaluated at the beginning of the study and updated at baseline examination in cases of newly diagnosed NDP.

Results: Over a 2-year observation period, NDP occurred in 34 patients (15.6%). Out of 34 cases of newly diagnosed NDP, in 20 cases (58.9%) pain became chronic (lasting longer than 3 months). In the Cox proportional hazards multifactorial model, progressive types of MS were an independent predictor of NDP occurrence (hazard ratio 2.60; 95% confidence interval, 1.30-5.18; p=0.01). In the multifactorial logistic regression analysis, subclinical depressive disorders (according to Hospital Anxiety and Depression Scale) were identified as an independent predictor of NDP chronification (odds ratio 7.14; 95% confidence interval, 1.12-45.59; p=0.04).

Conclusions: In MS predictors of NDP occurrence are progressive types of MS, whereas predictors of NDP chronification are subclinical depressive disorders.

多发性硬化症患者神经性疼痛发生和慢性化的预测因素(为期两年的前瞻性研究)。
背景:多发性硬化症(MS)患者是神经性疼痛的高危人群:多发性硬化症(MS)患者是神经病理性疼痛的高危人群。目的:研究MS患者在2年观察期内神经病理性疼痛(NDP)发生和慢性化的预测因素:在申请排除标准并签署知情同意书后,我们招募了 241 名患者参与研究,其中 23 名患者提前停止了参与研究。在 2 年的观察期内,根据疼痛检测问卷(PainDETECT)诊断出新的 NDP(大于 18)。新确诊的 NDP 患者根据疼痛持续时间在基线、1 个月、3 个月和 6 个月时接受检查。研究开始时对患者的社会人口学、神经心理学、认知能力、睡眠质量和临床特征进行了评估,并在基线检查时对新诊断的 NDP 病例进行了更新:在两年的观察期内,有 34 名患者(15.6%)发生了 NDP。在 34 例新确诊的 NDP 患者中,有 20 例(58.9%)的疼痛变成了慢性疼痛(持续时间超过 3 个月)。在 Cox 比例危险度多因素模型中,进行性多发性硬化症类型是 NDP 发生的独立预测因素(危险度比 2.60;95% 置信区间 1.30-5.18;P=0.01)。在多因素逻辑回归分析中,亚临床抑郁障碍(根据医院焦虑和抑郁量表)被认为是NDP慢性化的独立预测因素(几率比7.14;95%置信区间,1.12-45.59;P=0.04):在多发性硬化症中,NDP发生的预测因素是多发性硬化症的进行性类型,而NDP慢性化的预测因素是亚临床抑郁障碍。
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