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. 2022 Sep 22:2022:1217717.
doi: 10.1155/2022/1217717. eCollection 2022.

Analgesic Medication in Fibromyalgia Patients: A Cross-Sectional Study

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Analgesic Medication in Fibromyalgia Patients: A Cross-Sectional Study

H-C Aster et al. Pain Res Manag. .

Abstract

There is no approved drug for fibromyalgia syndrome (FMS) in Europe. In the German S3 guideline, amitriptyline, duloxetine, and pregabalin are recommended for temporary use. The aim of this study was to cross-sectionally investigate the current practice of medication in FMS patients in Germany. We systematically interviewed 156 patients with FMS, while they were participating in a larger study. The patients had been stratified into subgroups with and without a decrease in intraepidermal nerve fiber density. The drugs most commonly used to treat FMS pain were nonsteroidal anti-inflammatory drugs (NSAIDs) (41.0% of all patients), metamizole (22.4%), and amitriptyline (12.8%). The most frequent analgesic treatment regimen was "on demand" (53.9%), during pain attacks, while 35.1% of the drugs were administered daily and the remaining in other regimens. Median pain relief as self-rated by the patients on a numerical rating scale (0-10) was 2 points for NSAIDS, 2 for metamizole, and 1 for amitriptyline. Drugs that were discontinued due to lack of efficacy rather than side effects were acetaminophen, flupirtine, and selective serotonin reuptake inhibitors. Reduction in pain severity was best achieved by NSAIDs and metamizole. Our hypothesis that a decrease in intraepidermal nerve fiber density might represent a neuropathic subtype of FMS, which would be associated with better effectiveness of drugs targeting neuropathic pain, could not be confirmed in this cohort. Many FMS patients take "on-demand" medication that is not in line with current guidelines. More randomized clinical trials are needed to assess drug effects in FMS subgroups.

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Conflict of interest statement

HA, DE, and AB declare no conflicts of interest. NÜ has received honoraria for presentations from Sanofi Genzyme, Takeda, and Astellas; NÜ has received travel grants from Pfizer, Sanofi Genzyme, Takeda, Astellas; NÜ has received research support from Sanofi Genzyme, Takeda, and Idorsia. CS has received fees for consulting related to the treatment of neuropathic pain from the companies Algiax, Air Liquide, and Bayer.

Figures

Figure 1
Figure 1
Flowchart of the inclusion process of patients.

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