HELENA HIDEKO SEGUCHI KAZIYAMA

(Fonte: Lattes)
Índice h a partir de 2011
9
Lattes
Projetos de Pesquisa
Unidades Organizacionais
Instituto de Ortopedia e Traumatologia, Hospital das Clínicas, Faculdade de Medicina
LIM/62 - Laboratório de Fisiopatologia Cirúrgica, Hospital das Clínicas, Faculdade de Medicina

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Autor e Coautores FMUSP-HC Normalizados: JOACI OLIVEIRA DE ARAUJO ×

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  • bookPart
    Dor nos Membros Inferiores
    (2019) STUMP, Patrick; HERNANDEZ, Arnaldo José; ARAUJO, Joaci Oliveira de; KAZIYAMA, Helena Hideko Seguchi
  • bookPart
    Lombalgia
    (2019) YENG, Lin Tchia; TEIXEIRA, William Gemio Jacobsen; ARAUJO, Joaci Oliveira de; JR, Jefferson Rosi; KAZIYAMA, Helena Hideko Seguchi; TEIXEIRA, Manoel Jacobsen
  • article 43 Citação(ões) na Scopus
    Psychometric validation of the Portuguese version of the Neuropathic Pain Symptoms Inventory
    (2011) ANDRADE, Daniel Ciampi de; FERREIRA, Karine A. S. L.; NISHIMURA, Carine M.; YENG, Lyn T.; BATISTA, Abrahao F.; SA, Katia de; ARAUJO, Joaci; STUMP, Patrick R. N. A. G.; KAZIYAMA, Helena H.; GALHARDONI, Ricardo; FONOFF, Erich T.; BALLESTER, Gerson; ZAKKA, Telma; BOUHASSIRA, Didier; TEIXEIRA, Manoel J.
    Backgroud: It has been shown that different symptoms or symptom combinations of neuropathic pain (NeP) may correspond to different mechanistic backgrounds and respond differently to treatment. The Neuropathic Pain Symptom Inventory (NPSI) is able to detect distinct clusters of symptoms (i.e. dimensions) with a putative common mechanistic background. The present study described the psychometric validation of the Portuguese version (PV) of the NPSI. Methods: Patients were seen in two consecutive visits, three to four weeks apart. They were asked to: (i) rate their mean pain intensity in the last 24 hours on an 11-point (0-10) numerical scale; (ii) complete the PV-NPSI; (iii) provide the list of pain medications and doses currently in use. VAS and Global Impression of Change (GIC) were filled out in the second visit. Results: PV-NPSI underwent test-retest reliability, factor analysis, analysis of sensitivity to changes between both visits. The PV-NPSI was reliable in this setting, with a good intra-class correlation for all items. The factorial analysis showed that the PV-NPSI inventory assessed different components of neuropathic pain. Five different factors were found. The PV-NPSI was adequate to evaluate patients with neuropathic pain and to detect clusters of NeP symptoms. Conclusions: The psychometric properties of the PV-NPSI rendered it adequate to evaluate patients with both central and peripheral neuropathic pain syndromes and to detect clusters of NeP symptoms.