Your browser doesn't support javascript.
loading
OnabotulinumtoxinA injections in chronic migraine, targeted to sites of pericranial myofascial pain: an observational, open label, real-life cohort study.
Ranoux, Danièle; Martiné, Gaelle; Espagne-Dubreuilh, Gaëlle; Amilhaud-Bordier, Marlène; Caire, François; Magy, Laurent.
Afiliação
  • Ranoux D; Department of Neurosurgery, Centre Hospitalier Universitaire de Limoges, Limoges, France. daniele.ranoux@gmail.com.
  • Martiné G; Pain Center, Centre Hospitalier Universitaire de Limoges, Limoges, France.
  • Espagne-Dubreuilh G; Pain Center, Centre Hospitalier Universitaire de Limoges, Limoges, France.
  • Amilhaud-Bordier M; Pain Center, Centre Hospitalier de Guéret, Guéret, France.
  • Caire F; Department of Neurosurgery, Centre Hospitalier Universitaire de Limoges, Limoges, France.
  • Magy L; Department of Neurology, Centre Hospitalier Universitaire de Limoges, Limoges, France.
J Headache Pain ; 18(1): 75, 2017 Dec.
Article em En | MEDLINE | ID: mdl-28733943
BACKGROUND: OnabotulinumtoxinA has proven its efficacy in reducing the number of headache days in chronic migraine (CM) patients. The usual paradigm includes 31 pericranial injection sites with low dose (5 U) per site. The aim of this study is to present the results obtained using a simpler injection protocol of onabotulinumtoxinA, with injection sites targeted to pericranial myofascial sites of pain. METHODS: Observational, open label, real-life, cohort study. We enrolled 63 consecutive patients fulfilling the diagnostic criteria of CM, and refractory to conventional treatments. The patients were injected using a "follow-the-pain" pattern into the corrugator and/or temporalis and/or trapezius muscles. The doses per muscle were fixed. According to the number of muscles injected, the total dose could vary from 70 to 150 U per session. Patients were considered responders if they had a ≥ 50% decrease in number of headache days in at least two consecutive injection cycles. RESULTS: Forty one patients (65.1% in intention to treat analysis) responded to treatment. In 70.7% of responders, the effect size was even higher, with a reduction ≥70% in the number of headache days. The associated cervical pain and muscle tenderness, present in 33 patients, was reduced by ≥50% in 31 patients (94%). Triptan consumption dramatically decreased (81%) in responders. The trapezius was the most frequently injected muscle. We observed no serious adverse event. The mean patient satisfaction rate was 8.5/10. CONCLUSIONS: This study provides additional robust evidence supporting the efficacy of onabotulinumtoxinA injections in CM. Furthermore, the paradigm we used, with reduced number of injection sites targeted to pericranial myofascial sites of pain, may provide evidence in favor of the implication of myofascial trigger points in migraine chronicization. TRIAL REGISTRATION: ClinicalTrials.gov Protocol Record I17022 ClinicalTrials.gov Identifier: NCT03175263 . Date of registration: June 7, 2017. Retrospectively registered.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Toxinas Botulínicas Tipo A / Transtornos de Enxaqueca / Síndromes da Dor Miofascial Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Headache Pain Ano de publicação: 2017 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Toxinas Botulínicas Tipo A / Transtornos de Enxaqueca / Síndromes da Dor Miofascial Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Headache Pain Ano de publicação: 2017 Tipo de documento: Article País de afiliação: França