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Abstracts from the Annual Meeting of the German Society of Neuromodulation (DGNM) Joint Meeting with the Neuromodulation Society of the United Kingdom and Ireland (NSUKI). 23‐24 November 2012, Berlin, Germany

Identifieur interne : 000C62 ( Istex/Corpus ); précédent : 000C61; suivant : 000C63

Abstracts from the Annual Meeting of the German Society of Neuromodulation (DGNM) Joint Meeting with the Neuromodulation Society of the United Kingdom and Ireland (NSUKI). 23‐24 November 2012, Berlin, Germany

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RBID : ISTEX:993F0732D73B40A68E851DE672DD8F053DC81586
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DOI: 10.1111/ner.12040

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<title>Objectives: We performed more than 350 peripheral nerve stimulation procedures since 1991 We mostly treated patients with Causalgia (CRPS II) Incomplete or complete lesion of the stimulated peripheral nerves was determined in all patients. Surgical treatment failed or would not be indicated in all cases. All patients have extensively been treated with conservative pain therapy Material and method: The aim was to defi ne a standardised method, which would be as objective as possible, to verify the success of treatment, by measuring the pain-related disability assessment, the subjective intensity of pain and the subjective perception of pain. A long-term follow-up was arranged in addition to determine social and occupational re-integration. The implantation of the stimulating device, proximal to the lesion, was performed after microsurgical neurolysis of the peripheral nerves. Post surgically patients were to test stimulate with a stimulation unit externally connected to the lead. After concluding and discussing the results of the trial stimulation period, a stimulation unit was permanently implanted in most (more than 85%) cases, with a remarkable reduction of pain. Only in very few cases, the evaluation of the trial stimulation period was unsatisfactory to the patient and did not indicate the implantation of permanent devices. Results: After implanting the stimulator unit an average pain-related disability of 10% was achieved by all the patients fi tted with a permanent implant. More than 85% of the patients have used the permanent stimulation device implants with lasting</title>
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