Department of Radiation Oncology, University Medical Center Utrecht, The Netherlands.
Department of Anesthesiology, University Medical Center Utrecht, The Netherlands.
Pain Physician. 2019 Jan;22(1):1-13.
Assessment of pain is important in daily clinical practice and as an endpoint in clinical studies. Because pain perception is highly subjective, pain measurement is complex. Self-rating pain scales are currently of great importance but have limitations. They depend on many more factors than pain, which could lead to an incorrect assessment of therapies or clinical studies. Therefore, there is need for valid, reliable, safe, and low-cost methods to determine and quantify patients' pain more objectively.
To provide an overview of devices and techniques that can be used to administer a pain stimulus with similar intensity as the endogenous pain experienced by the patient, in order to quantify and subsequently follow patients' pain more objectively.
In this systematic review, articles from PubMed, EMBASE, Cochrane library and Scopus were reviewed for eligibility.
Studies that described a device or technique that could be used to induce a variable, controlled, and measurable pain stimulus were included. Studies that made correlations with established pain scales or those who compared outcomes in multiple tests were selected to assessvalidity and reliability.
A total of 1,308 manuscripts were initially retrieved. After independent screening by a team of 4 reviewers, 19 studies were eventually included describing 15 different devices or techniques. These devices could be divided into groups based on stimulus administration: electrical, external pressure (probe) and miscellaneous pain stimulators. Electrical stimulators were found to be tested extensively and proven to be both valid and reliable.
To correlate new techniques with older methods such as the Numeric Rating Scale (NRS) and Visual Analogue Scale (VAS) for which an improvement is desired, is debatable. To (partially) address this problem, the reliability is added as an additional primary outcome to assess which device works best. Further limitations include the heterogeneity of studies found in both the types of pain measured as in outcome measures presented. In addition, it is important to note that part of the devices described cannot directly be used for clinical practice due to products that have cease to exist or the description of solely techniques rather than testing ready-to-use devices.
Several devices and techniques compared pain intensity experienced by patients with an external pain stimulus that potentially could be used as a new objective pain measurement tool. Given the results of our review, electrical stimulators that have been tested extensively with high validity, reliability, and feasibility would be recommended for use for clinical and research purposes. Moreover, normalization of pain intensity scores for current perception is important. Pain intensity normalization leads to higher correlations with established pain scales and possibly to increased inter-patient reliability.Registration number: Registered in the PROSPERO database (PROSPERO 2016:CRD42016041974)KEY WORDS: Systematic review, objective pain measurement, pain scales; devices, techniques, validity, reliability, safety, feasibility.
疼痛评估在日常临床实践和临床研究中作为终点都很重要。由于疼痛感知具有很强的主观性,因此疼痛测量非常复杂。自评疼痛量表目前非常重要,但也有其局限性。它们取决于比疼痛更多的因素,这可能导致对治疗或临床研究的评估不正确。因此,需要有有效、可靠、安全和低成本的方法来更客观地确定和量化患者的疼痛。
提供一种概述,可以使用该方法给予与患者内源性疼痛强度相似的疼痛刺激,以更客观地量化和随后跟踪患者的疼痛。
在本次系统评价中,对 PubMed、EMBASE、Cochrane 图书馆和 Scopus 的文章进行了筛选,以确定其是否符合入选标准。
纳入了可以用于诱导可变化、可控和可测量的疼痛刺激的设备或技术的研究。选择了与已建立的疼痛量表进行相关性研究或对多项测试结果进行比较的研究,以评估其有效性和可靠性。
最初检索到 1308 篇手稿。经过 4 名评审员组成的团队进行独立筛选后,最终纳入了 19 项研究,这些研究共描述了 15 种不同的设备或技术。这些设备可以根据刺激方式进行分组:电刺激、外部压力(探针)和其他疼痛刺激器。电刺激器已得到广泛测试,并被证明具有有效性和可靠性。
将新技术与希望改进的旧方法(如数字评分量表(NRS)和视觉模拟量表(VAS))进行相关联具有争议性。为了解决这个问题,将可靠性作为附加的主要结果之一进行评估,以确定哪种设备效果最好。进一步的局限性包括在测量的疼痛类型和呈现的结果测量中发现的研究的异质性。此外,需要注意的是,部分描述的设备由于已停产的产品或仅描述技术而非测试即用型设备而无法直接用于临床实践。
几种设备和技术将患者经历的疼痛强度与外部疼痛刺激进行了比较,这些刺激可能可以用作新的客观疼痛测量工具。根据我们的综述结果,具有广泛验证、可靠性、可行性的电刺激器将被推荐用于临床和研究目的。此外,对当前感知进行疼痛强度归一化很重要。疼痛强度归一化会导致与已建立的疼痛量表更高的相关性,并可能提高患者之间的可靠性。注册号:在 PROSPERO 数据库中注册(PROSPERO 2016:CRD42016041974)
系统评价、客观疼痛测量、疼痛量表、设备、技术、有效性、可靠性、安全性、可行性。