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Detecting the neuropathic pain component in the clinical setting: a study protocol for validation of screening instruments for the presence of a neuropathic pain component

机译:检测临床环境中的神经疗法疼痛组分:用于验证筛查仪器的筛查仪器存在神经性疼痛组分的研究方案

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Background The presence of nerve damage plays a key role in the development and prognosis of chronic pain states. Assessment of the presence and severity of a neuropathic pain component (NePC) is key in diagnosing chronic pain patients. Low back pain (LBP) and neck and shoulder pain (NSP) are highly prevalent and clinically important medical and societal problems in which a NePC is frequently present. The more severe the NePC, the worse the course of the pain, its prognosis and the results of treatment. Reliable and standardised diagnosis of the NePC remains difficult to achieve. Standardized and validated screening tools may help to reliably identify the NePC in individual chronic pain patients. The aim of this study is to validate the Dutch language versions of the Pain DETECT Questionnaire (PDQ-Dlv) and the ‘Douleur Neuropathique 4 Questions’ (DN4-Dlv) for use in primary and specialist medical care settings to screen for a NePC in patients with chronic pain due to (1) LBP, (2) NSP or (3) known peripheral nerve damage (PND). Methods/design The study design is cross-sectional to assess the validity of the PDQ-Dlv and the DN4-Dlv with 2?weeks follow-up for test-retest reliability and 3?months follow-up for monitoring and prognosis. 438 patients with chronic pain due to (1) LBP, (2) NSP or (3) PND. will be included in this study. Based on the IASP definition of neuropathic pain, two physicians will independently assess whether the patient has a NEPC or not. This result will be compared with the outcome of the PDQ-Dlv & DN4-Dlv, the grading system for neuropathic pain, bed side examination and quantitative sensory testing. This study will further collect data regarding prevalence of NePC, general health status, mental health status, functioning, pain attribution and quality of life. Discussion The rationale for this study is to provide detailed information on the clinimetric quality of the PDQ-Dlv and DN4-Dlv in Dutch speaking countries. Our innovative multi-factorial approach should help achieve more reliable diagnosis and quantification of a NePC in patients with chronic pain. Trial registration The Netherlands National Trial Register ( NTR3030 ).
机译:背景神经损伤的存在在慢性疼痛状态的发展和预后起着关键作用。评估神经性疼痛组分(NEPC)的存在和严重程度是诊断慢性疼痛患者的关键。腰痛(LBP)和颈部和肩部疼痛(NSP)是高度普遍的,临床上重要的医学和核心问题,其中常态存在。 Nepc越严重,疼痛过程越差,其预后和治疗结果。可靠且标准化的NEPC诊断仍然难以实现。标准化和验证的筛选工具可能有助于可靠地识别单个慢性疼痛患者的NEPC。本研究的目的是验证止痛调查问卷(PDQ -DLV )和'Douleur Neuropathique 4问题'(DN4 -dlv )的荷兰语版本由于(1)LBP,(2)NSP或(3)已知的周围神经损伤(PND),在慢性疼痛患者中用于筛选慢性疼痛患者的核心和专业医疗环境。方法/设计研究设计是评估PDQ -DLV 和DN4 -dlv 的有效性,其中2个时间进行后续可靠性3?几个月的监测和预后随访。 438例慢性疼痛患者(1)LBP,(2)NSP或(3)PND。将包括在本研究中。基于IASP定义神经病疼痛,两名医生将独立评估患者是否有NEPC。该结果将与PDQ -DLV &dn4 -dlv ,用于神经性疼痛,床侧检查和定量感官测试的分级系统的结果进行比较。本研究将进一步收集有关Nepc患病率的数据,一般健康状况,心理健康状况,运作,疼痛归属和生活质量的数据。讨论本研究的基本原理是提供有关荷兰语国家的PDQ -dlv 和dn4 -dlv 的Clinetric质量的详细信息。我们创新的多因素方法应有助于实现慢性疼痛患者的更可靠的诊断和定量NEPC。审判登记荷兰国家试用寄存器(NTR3030)。

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