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Pain Catastrophizing Does Not Predict Spinal Cord Stimulation Outcomes: A Cohort Study of 259 Patients With Long-Term Follow-Up.
Poulsen, Dennis Møgeltoft; Sørensen, Jens Christian Hedemann; Blichfeldt-Eckhardt, Morten Rune; Gulisano, Helga Angela; Knudsen, Anne Lene Høst; Nikolajsen, Lone; Meier, Kaare.
Afiliação
  • Poulsen DM; Department of Neurosurgery, Aarhus University Hospital, Aarhus, Denmark.
  • Sørensen JCH; Center for Experimental Neuroscience (CENSE), Institute of Clinical Medicine, Aarhus University, Aarhus, Denmark.
  • Blichfeldt-Eckhardt MR; Department of Neurosurgery, Aarhus University Hospital, Aarhus, Denmark.
  • Gulisano HA; Center for Experimental Neuroscience (CENSE), Institute of Clinical Medicine, Aarhus University, Aarhus, Denmark.
  • Knudsen ALH; ESES Unit, Department of Neurosurgery, Odense University Hospital, Odense, Denmark.
  • Nikolajsen L; Department of Anesthesiology and Critical Care, Odense University Hospital, Odense, Denmark.
  • Meier K; Department of Neurosurgery, Aalborg University Hospital, Aalborg, Denmark.
Neuromodulation ; 24(1): 76-85, 2021 Jan.
Article em En | MEDLINE | ID: mdl-32929834
ABSTRACT

OBJECTIVE:

Spinal cord stimulation (SCS) is an important treatment modality used to treat chronic neuropathic pain. However, reported success rates of 26%-70% entail an increased focus on patient selection. An area of core interest is psychological evaluation, often using scales such as the Pain Catastrophizing Scale (PCS). The aim of this study was to assess the relation between baseline PCS scores obtained before implantation and SCS outcomes defined as (1) Rating on Patients' Global Impression of Change scale (PGIC), (2) Pain relief on the Numeric Rating Scale (NRS), (3) Cessation of pain medication, and (4) Risk of permanent explantation. MATERIALS AND

METHODS:

Using records from the Neurizon Neuromodulation Database, we performed a multicenter open cohort study of 259 permanently implanted SCS patients. Follow-up ranged from six months to nine years (median = three years). For each of the defined SCS outcomes, patients were grouped according to their latest follow-up registration. Subsequently, we used a one-way ANOVA and exact t-tests to compare mean baseline PCS scores between groups.

RESULTS:

No difference in mean baseline PCS scores was found between PGIC groups. Baseline PCS scores was not associated with the probability of obtaining 30% or 50% pain relief on latest registration. Baseline PCS scores of patients able to cease all usage of tricyclic antidepressants, antiepileptics, or opioids during SCS treatment did not differ from baseline scores of continuous users. We found no association between baseline PCS scores and risk of permanent explantation.

CONCLUSION:

This study did not demonstrate any associations between baseline PCS scores and SCS outcomes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dor Crônica / Estimulação da Medula Espinal Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Neuromodulation Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dor Crônica / Estimulação da Medula Espinal Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Neuromodulation Ano de publicação: 2021 Tipo de documento: Article