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ULTIMO FASCICOLOMINERVA ANESTESIOLOGICA

Rivista di Anestesia, Rianimazione, Terapia Antalgica e Terapia Intensiva

Official Journal of the Italian Society of Anesthesiology, Analgesia, Resuscitation and Intensive Care
Indexed/Abstracted in: Current Contents/Clinical Medicine, EMBASE, PubMed/MEDLINE, Science Citation Index Expanded (SciSearch), Scopus
Impact Factor 2,036

Periodicità: Mensile

ISSN 0375-9393

Online ISSN 1827-1596

 

Minerva Anestesiologica 2013 Giugno;79(6):634-42

 ORIGINAL ARTICLES

Acupuncture versus valproic acid in the prophylaxis of migraine without aura: a prospective controlled study

Facco E. 1, Liguori A. 2, Petti F. 2, Fauci A. J. 3, Cavallin F. 4, Zanette G. 1

1 Cattedra di Anestesiologia Generale e Speciale Odontostomatologica, Dipartimento Di Neuroscienze, Scienze Neurologiche, Psichiatriche, Sensoriali, Ricostruttive E Riabilitative, Università di Padova, Padova, Italy;
2 Dipartimento di Scienze Anatomiche, istologiche, Medico-Legali e dell’Apparato Locomotore, Istituto Paracelso, Master Agopuntura e Medicina Tradizionale Cinese, Università La Sapienza, Roma, Italy;
3 Istituto Superiore di Sanità, Joint Sino-Italian Laboratory for Traditional Chinese Medicine, Roma, Italy;
4 Independent Statistician, Free Practiotioner

Background: The pharmacologic treatment of migraine still remains below the expectations. The aim of this study is to compare the effectiveness of traditional acupuncture and valproic acid in migraine prophylaxis.
Methods: A prospective, controlled study was performed in 100 patients affected by migraine without aura lasting for over one year. The patients were stratified for sex and randomly divided into two groups of 50 patients each. Patients belonging to Group A (acupuncture) were submitted to 20 sessions of acupuncture, while patients belonging to Group V valproate) were administered Valproic acid (Depakin Chrono®) at a dose of 600 mg/day; 10 mg Rizatriptan wafers were allowed as needed to treat the attacks. The Midas Index (MI) and pain intensity (PI, by VAS) were recorded before treatment (T0), at three (T1) and six (T2) months; a six-point scale Pain Relief score (PRS), the Rizatriptan intake and adverse events were recorded at T1 and T2.
Results: Eighty-two out of 100 patients completed the study (9 dropouts in each group). In both groups the MI improved at T1 and T2 (P<0.0001). Pain intensity was better at T1 in group V (P<0.0001), but PI and PRS (P=0.02) as well as rizatriptan intake (P=0.001) were better in group A at T2. The rate of adverse events was 47.8% in group V and 0% in group A.
Conclusion: Our data show a lower pain intensity and lower Rizatriptan intake at six-months follow-up with no adverse events in acupuncture patients compared to those treated with valproic acid.

lingua: Inglese


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