A Retrospective Study on tDCS Treatment in Patients with Drug-Resistant Chronic Pain

Author:

Pérez-Borrego Yolanda A.1ORCID,Soto-León Vanesa1ORCID,Brocalero-Camacho Ángela12,Oliviero Antonio123,Carrasco-López Carmen45ORCID

Affiliation:

1. FENNSI Group, Hospital Nacional de Parapléjicos, SESCAM, 45071 Toledo, Spain

2. Unidad de Neurología, Hospital de Parapléjicos, SESCAM, 45071 Toledo, Spain

3. Hospital Los Madroños, 28690 Brunete, Spain

4. Internet of Things and People, University of Malmö, 211 19 Malmö, Sweden

5. Department of Anatomy, University of Seville, 41009 Seville, Spain

Abstract

Background. Transcranial direct current stimulation (tDCS) of the primary motor cortex (M1) has an analgesic effect superior to a placebo in chronic pain. Some years ago, tDCS was implemented at the Hospital Nacional of Paraplegics (Toledo, Spain) to treat patients with pharmacological resistance to chronic pain. Objective. The main objectives of this study with tDCS were (1) to confirm the safety of one-year treatment; (2) to estimate the number of patients after one year in treatment; (3) to describe the effects of tDCS on the pain intensity during one-year treatment; and (4) to identify factors related to treatment success. Methods. This was a retrospective study conducted at the National Hospital for Paraplegics with 155 patients with pharmacologically resistant chronic pain. Anodal tDCS was applied over the M1 for 20 min at 1.5 mA for 10 treatment sessions from Monday to Friday (Induction phase), followed by 2–3 sessions per month (Maintenance phase). Pain intensity was assessed using a Visual Analogue Scale (VAS). Results. Anodal tDCS on M1 confirmed the reduction in the pain intensity. Moreover, 58% of outpatients completed one year of treatment. Only the VAS values obtained during the baseline influenced the response to treatment. Patients with a very high VAS at the baseline were more likely to not respond adequately to tDCS treatment. Conclusions. Anodal tDCS over M1 is an adequate therapy (safe and efficient) to treat drug-resistant chronic pain. Moreover, pain intensity at the start of treatment could be a predictor of patients’ continuity with tDCS for at least one year.

Funder

European Union’s Horizon 2020 Marie Skłodowska-Curie Actions

Instituto de Salud Carlos III

Publisher

MDPI AG

Reference35 articles.

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