Safety, effectiveness, and duration of effect of BOTOX after switching from Dysport for blepharospasm, cervical dystonia, and hemifacial spasm

被引:60
|
作者
Bihari, K [1 ]
机构
[1] Natl Inst Neurosurg, H-1145 Budapest, Hungary
关键词
blepharospasm; botulinum toxin type A; cervical dystonia; hemifacial spasm;
D O I
10.1185/030079905X36396
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Local injection of botulinum toxin type A is first-line treatment of blepharospasm, cervical dystonia, and hemifacial spasm; however, there is uncertainty about the optimal dose of toxin for each indication as well as dose-conversion ratios that should be used when switching products in clinical practice. Objective: The goal of this study was to compare the safety, effectiveness, and duration of clinical effect of BOTOX* and Dysport dagger after drug switching (Dysport to BOTOX) among patents with movement disorders. Methods.-A total of 48 patients diagnosed with blepharospasm (n = 27), cervical dystonia (n = 12), or hemifacial spasm (n = 9) were evaluated during a single-arm, crossover-design study in which each patient was his/her own historical control using a 5:1 or 4:1 conversion ratio of Dysport to BOTOX units. Patients were assessed (using Jankovic, Visual Analog Scale, general pain scale, Toronto Western Spasmodic Tiorticollis Rating Scale [TWSTRS] scores) after the last injection of Dysport and the first injection of BOTOX. Moreover, each patient kept a diary during treatment to track onset and duration of therapeutic effect. Results: Although BOTOX and Dysport were both clinically effective, this effect was more significant with BOTOX compared to Dysport based on TWSTRS for cervical dystonia (P = 0.012), and Jankovic scores for blepharospasm (p = 0.006). Longer duration of effect also was noted with BOTOX than with Dysport (blepharospasm, 62.2 days vs 47.4 days (p = 0.001); cervical dystonia, 64.3 days vs 44.6 days (p = 0.014); hemifacial spasm, 65.1 days vs 41.8 days (p < 0.014), respectively). Of the 48 patients, 19 experienced at least one adverse drug reaction (ADR) during Dysport treatment, with the most commonly reported ADRs being ptosis for blepharospasm and hemifacial spasm and neck weakness for cervical dystonia. No patient reported an ADR during BOTOX treatment. Conclusions: Results suggest therapeutic effectiveness is enhanced with BOTOX compared to Dysport at a dosing ratio between 5:1 and 4:1 (Dysport:BOTOX). Safety and duration of therapeutic effect also are enhanced with BOTOX. Further research is needed.
引用
收藏
页码:433 / 438
页数:6
相关论文
共 38 条
  • [31] Adult cervical dystonia patients first treated with onabotulinumtoxinA exhibit comparable onset and duration of effect, time between visits, dose usage and safety profiles when switched to incobotulinumtoxinA
    Boileau, J.
    TOXICON, 2013, 68 : 107 - 107
  • [32] Effectiveness and Safety Data in Rheumatoid Arthritis Patients after Switching from Originator Rituximab to Biosimilar Rituximab (CT-P10)
    Ekin, Ali
    Misirci, Salim
    Lermi, Nihal
    Kutlu, Nagehan Dik
    Coskun, Belkis Nihan
    Yagiz, Burcu
    Dalkilic, Ediz
    Pehlivan, Yavuz
    AKTUELLE RHEUMATOLOGIE, 2025, 50 (01) : 71 - 82
  • [33] Effectiveness and Safety of Mirikizumab after switching from Ustekinumab in patients with moderate to severe Crohn's disease: results from a long-term extension study
    D'Haens, G.
    Laharie, D.
    Dulai, P. S.
    Seibold, F.
    Siegmund, B.
    Abraham, B.
    Malter, L.
    Protic, M.
    Morris, N.
    Hozak, R. R.
    Moses, R. E.
    Lopes, M. Ugolini
    Durand, F.
    Yu, G.
    Vermeire, S.
    JOURNAL OF CROHNS & COLITIS, 2025, 19 : i168 - i170
  • [34] Safety and Effectiveness of Glargine 300 U/ml After Switching from Basal Insulins in Patients with Type 1 Diabetes: COMET-T Study
    Goelz, Stefan
    Mader, Julia K.
    Bilz, Stefan
    Kenzler, Julia
    Danne, Thomas
    DIABETES THERAPY, 2025, 16 (01) : 121 - 134
  • [35] Long-term effectiveness, safety and immunogenicity of the biosimilar SB2 in inflammatory bowel disease patients after switching from originator infliximab
    Fischer, Sarah
    Cohnen, Sarah
    Klenske, Entcho
    Schmitt, Heike
    Vitali, Francesco
    Hirschmann, Simon
    Ramming, Andreas
    Zundler, Sebastian
    Rath, Timo
    Krebs, Sabine
    Dorje, Frank
    Uter, Wolfgang
    Nagore, Daniel
    Meyer, Sebastian
    Neurath, Markus F.
    Atreya, Raja
    THERAPEUTIC ADVANCES IN GASTROENTEROLOGY, 2021, 14
  • [36] Treatment satisfaction, safety, and effectiveness of biosimilar insulin glargine is comparable in patients with type 2 diabetes mellitus after switching from insulin glargine or insulin degludec: a post-marketing safety study
    Taki, Kentaro
    Koyanagi, Momoha
    Nagaoka, Soshi
    Shingaki, Tomotaka
    CURRENT MEDICAL RESEARCH AND OPINION, 2020, 36 (12) : 1975 - 1983
  • [37] Immunogenicity Analysis from a Randomized, Double-Blind Study To Compare the Efficacy and Safety of NeuroBloc® (Myobloc/RimabotulinumtoxinB;BoNT-B) with OnabotulinumtoxinA (Botox®; BoNT-A) in Patients with Cervical Dystonia (CD) Who Have Never Previously Received a Botulinum Toxin Product (402CD-EU)
    Birmingham, William
    Chinnapongse, Robert
    Lew, Mark
    Pagan, Fernando
    Reinhard, Sharon
    Ferreira, Joaquim
    NEUROLOGY, 2010, 74 (09) : A87 - A88
  • [38] The Effect of Preoperative Symptom Duration on Patient-Reported Outcomes After Anterior Cervical Discectomy and Fusion in Nonmyelopathic Patients: Analyses From the Michigan Spine Surgery Improvement Collaborative (MSSIC)
    Lawless, Michael H.
    Tong, Doris
    Claus, Chad F.
    Hanson, Connor
    Li, Chenxi
    Park, Paul
    Chang, Victor W.
    Abdulhak, Muwaffak M.
    Houseman, Clifford M.
    Bono, Peter L.
    Carr, Daniel A.
    Richards, Boyd F.
    Kelkar, Prashant S.
    Soo, Teck M.
    NEUROSURGERY, 2023, 92 (05) : 955 - 962