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dc.contributor.authorCuesta-Vargas, Antonio 
dc.contributor.authorNeblett, Randy
dc.contributor.authorNijs, Jo
dc.contributor.authorChiarotto, Alessandro
dc.contributor.authorKregel, Jeroen
dc.contributor.authorVan Wilgen, C Paul
dc.contributor.authorPitance, Laurent
dc.contributor.authorKnezevic, Aleksandar
dc.contributor.authorGatchel, Robert J
dc.contributor.authorMayer, Tom G
dc.contributor.authorViti, Carlotta
dc.contributor.authorRoldan-Jiménez, Cristina
dc.contributor.authorTesta, Marco
dc.contributor.authorCaumo, Wolnei
dc.contributor.authorJeremic-Knezevic, Milica
dc.contributor.authorNishigami, Tomohiko
dc.contributor.authorFeliu-Soler, Albert
dc.contributor.authorPérez-Aranda, Adrián
dc.contributor.authorLuciano, Juan V
dc.date.accessioned2025-01-13T09:49:12Z
dc.date.available2025-01-13T09:49:12Z
dc.date.issued2020-10-01
dc.identifier.citationCuesta-Vargas AI, Neblett R, Nijs J, Chiarotto A, Kregel J, van Wilgen CP, Pitance L, Knezevic A, Gatchel RJ, Mayer TG, Viti C, Roldan-Jiménez C, Testa M, Caumo W, Jeremic-Knezevic M, Nishigami T, Feliu-Soler A, Pérez-Aranda A, Luciano JV. Establishing Central Sensitization-Related Symptom Severity Subgroups: A Multicountry Study Using the Central Sensitization Inventory. Pain Med. 2020 Oct 1;21(10):2430-2440. doi: 10.1093/pm/pnaa210. PMID: 33118603.es_ES
dc.identifier.urihttps://hdl.handle.net/10630/36167
dc.description.abstractObjectives: The goal of this study was to identify central sensitization-related symptom severity subgroups in a large multicountry sample composed of patients with chronic pain and pain-free individuals using the Central Sensitization Inventory (CSI). Methods: A large, pooled international (N = 8 countries) sample of chronic pain patients plus healthy subjects (total N = 2,620) was randomly divided into two subsamples for cross-validation purposes. First, a hierarchical cluster analysis (HCA) was performed using CSI item-level data as clustering variables (test sample; N = 1,312). Second, a latent profile analysis (LPA) was conducted to confirm the optimal number of CSI clusters (validation sample; N = 1,308). Finally, to promote implementation in real-world clinical practice, we built a free online Central Sensitization Inventory Symptom Severity Calculator. Results: In both HCA (N = 1,219 valid cases) and LPA (N = 1,245 valid cases) analyses, a three-cluster and three-profile solution, respectively, emerged as the most statistically optimal and clinically meaningful. Clusters were labeled as follows: (i) Low Level of CS-Related Symptom Severity, (ii) Medium Level of CS-Related Symptom Severity, and (iii) High Level of CS-Related Symptom Severity. Conclusions: Our results indicated that a three-cluster solution clearly captured the heterogeneity of the CSI data. The calculator might provide an efficient way of classifying subjects into the cluster groups. Future studies should analyze the extent to which the CSI cluster classification correlates with other patient-reported and objective signs and symptoms of CS in patients with chronic pain, their associations with clinical outcomes, health-related costs, biomarkers, (etc.), and responsiveness to treatment.es_ES
dc.language.isoenges_ES
dc.publisherOxford University Presses_ES
dc.subjectDolores_ES
dc.subject.otherCentral Sensitivity Syndromees_ES
dc.subject.otherCentral Sensitizationes_ES
dc.subject.otherCentral Sensitization Inventoryes_ES
dc.subject.otherChronic Paines_ES
dc.subject.otherHierarchical Cluster Analysises_ES
dc.subject.otherLatent Profile Analysises_ES
dc.titleEstablishing Central Sensitization-Related Symptom Severity Subgroups: A Multicountry Study Using the Central Sensitization Inventoryes_ES
dc.typejournal articlees_ES
dc.identifier.doihttps://doi.org/10.1093/pm/pnaa210
dc.type.hasVersionAMes_ES
dc.departamentoFisioterapia
dc.rights.accessRightsopen accesses_ES


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