Somnolence and Dizziness During Mirogabalin Treatment in Patients With Neuropathic Pain Related to Lumbar Disease Who Switched From Pregabalin: A Retrospective Study

Author:

Akazawa Tsutomu12ORCID,Inoue Gen23ORCID,Tanaka Masahiro4,Umehara Tasuku5,Nagai Toshihiro26,Oshita Yusuke27ORCID,Imura Takayuki23,Miyagi Masayuki23,Saito Wataru23,Sako Kosuke4,Nomura Satoshi4,Hiyama Akihiko24ORCID,Katoh Hiroyuki24ORCID,Sakai Daisuke24,Sato Masato24,Yoshida Atsuhiro1,Iinuma Masahiro12,Niki Hisateru1,Takaso Masashi23,Watanabe Masahiko24

Affiliation:

1. Department of Orthopaedic Surgery, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan

2. Kanagawa Spine Research Society, Isehara, Kanagawa, Japan

3. Department of Orthopaedic Surgery, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan

4. Department of Orthopaedic Surgery, Tokai University School of Medicine, Isehara, Kanagawa, Japan

5. Department of Orthopaedic Surgery, St. Marianna University Yokohama Seibu Hospital, Yokohama, Kanagawa, Japan

6. Department of Orthopaedic Surgery, Tokai University Oiso Hospital, Oiso, Kanagawa, Japan

7. Department of Orthopaedic Surgery, Showa University Northern Yokohama Hospital, Yokohama, Kanagawa, Japan

Abstract

Study Design: Multicenter retrospective study. Objectives: To investigate adverse events (AEs) in patients with neuropathic pain related to lumbar disease who switched to mirogabalin from pregabalin. Methods: This study surveyed the records of 82 patients with peripheral neuropathic leg pain related to lumbar disease who switched to mirogabalin from pregabalin. We evaluated AEs associated with pregabalin and mirogabalin, the continuation rate of mirogabalin, and the pain-relieving effect at 4 weeks after switching from pregabalin to mirogabalin. We compared patients who switched due to lack of efficacy (LoE group) and patients who switched due to AEs (AE group). Results: The incidence rates of somnolence and dizziness with pregabalin were 12.2% and 14.6%, respectively, while the incidence rates with mirogabalin were reduced to 7.3% for somnolence and 4.9% for dizziness. The incidence of AEs with pregabalin was significantly higher in the AE group (LoE group: 11.1%, AE group 100%), especially for somnolence (LoE group: 3.2%, AE group: 47.1%) and dizziness (LoE group: 4.8%, AE: 52.9%). After switching, the incidences of AEs with mirogabalin were not significantly different between the 2 groups (LoE group: 15.9%, AE group: 23.5%), including for somnolence (LoE group: 7.9%, AE group: 5.9%) and dizziness (LoE group: 4.8%, AE group: 5.9%). There were no significant differences in continuation rate of mirogabalin or the pain-relieving effect between groups. Conclusions: The patients who experience somnolence and dizziness with pregabalin might be able to continue safely receiving treatment for their pain by switching to mirogabalin.

Publisher

SAGE Publications

Subject

Clinical Neurology,Orthopedics and Sports Medicine,Surgery

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