American Journal of Internal Medicine

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Aminaftone in the Treatment of Raynaud’s Phenomenon in Systemic Sclerosis: New Perspectives

Received: 03 August 2015    Accepted: 10 August 2015    Published: 19 August 2015
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Abstract

Objective: The aim of this study was to assess the efficacy (in terms of improved VAS Pain, Raynaud's Phenomenon attacks frequency and Raynaud’s Condition Score) of the Aminaftone in patients with Raynaud’s Phenomenon (RP) secondary to Systemic Sclerosis (SSc). Methods: Open label controlled study. We evaluated the efficacy of Aminaftone in the treatment of secondary RP in 108 patients with SSc consecutively recruited and divided in two groups. Group A: 51 Patients in treatment with Calcium Channel Blockers, prostanoids (iloprost 2ng [min/kg every 4 weeks), Endothelin Receptor Antagonist and Phosphodiesterase-5 inhibitors (Standard of Care). Group B: 57 Patients in treatment with Calcium Channel Blockers, Prostanoids, Endothelin Receptor Antagonist and Phosphodiesterase-5 inhibitors and Aminaftone (Standard of care + Aminaftone). Results: The number of RP attacks in group treated with Aminaftone (Group B) was lower than the group treated with standard therapy (Group A) from baseline to Week 48, obtaining statistically significance (Δ A -1.50 Δ B -2.10 p=0.02 95%CI). The RCS was statistically significantly different (Δ A -1.60 Δ B -2.50 p=0,04 95% CI), as was the pain VAS(Δ A -20.80 Δ B -30.60 p=0.04 95%CI) at week 48. Conclusion: The use of Aminaftone was well tolerated and improved RP as measured by RCS and pain when added to standard of care. A well-designed randomized controlled trial is needed to determine if these preliminary findings are supported

DOI 10.11648/j.ajim.20150305.12
Published in American Journal of Internal Medicine (Volume 3, Issue 5, September 2015)
Page(s) 204-209
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This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Raynaud’s Phenomenon, Systemic Sclerosis, Aminaftone, Endotheline

References
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Author Information
  • Department of General and Specialist Medicine, Division of Rheumatology, University Hospital Città della Salute e della Scienza di Torino, Turin, Italy

  • Department of General and Specialist Medicine, Division of Rheumatology, University Hospital Città della Salute e della Scienza di Torino, Turin, Italy

  • Department of General and Specialist Medicine, Division of Rheumatology, University Hospital Città della Salute e della Scienza di Torino, Turin, Italy

  • Department of General and Specialist Medicine, Division of Rheumatology, University Hospital Città della Salute e della Scienza di Torino, Turin, Italy

  • Department of General and Specialist Medicine, Division of Rheumatology, University Hospital Città della Salute e della Scienza di Torino, Turin, Italy

  • Department of General and Specialist Medicine, Division of Rheumatology, University Hospital Città della Salute e della Scienza di Torino, Turin, Italy

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  • APA Style

    Simone Parisi, Marco Scarati, Marta Priora, Clara Lisa Peroni, Angela Laganà, et al. (2015). Aminaftone in the Treatment of Raynaud’s Phenomenon in Systemic Sclerosis: New Perspectives. American Journal of Internal Medicine, 3(5), 204-209. https://doi.org/10.11648/j.ajim.20150305.12

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    ACS Style

    Simone Parisi; Marco Scarati; Marta Priora; Clara Lisa Peroni; Angela Laganà, et al. Aminaftone in the Treatment of Raynaud’s Phenomenon in Systemic Sclerosis: New Perspectives. Am. J. Intern. Med. 2015, 3(5), 204-209. doi: 10.11648/j.ajim.20150305.12

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    AMA Style

    Simone Parisi, Marco Scarati, Marta Priora, Clara Lisa Peroni, Angela Laganà, et al. Aminaftone in the Treatment of Raynaud’s Phenomenon in Systemic Sclerosis: New Perspectives. Am J Intern Med. 2015;3(5):204-209. doi: 10.11648/j.ajim.20150305.12

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  • @article{10.11648/j.ajim.20150305.12,
      author = {Simone Parisi and Marco Scarati and Marta Priora and Clara Lisa Peroni and Angela Laganà and Enrico Fusaro},
      title = {Aminaftone in the Treatment of Raynaud’s Phenomenon in Systemic Sclerosis: New Perspectives},
      journal = {American Journal of Internal Medicine},
      volume = {3},
      number = {5},
      pages = {204-209},
      doi = {10.11648/j.ajim.20150305.12},
      url = {https://doi.org/10.11648/j.ajim.20150305.12},
      eprint = {https://download.sciencepg.com/pdf/10.11648.j.ajim.20150305.12},
      abstract = {Objective: The aim of this study was to assess the efficacy (in terms of improved VAS Pain, Raynaud's Phenomenon attacks frequency and Raynaud’s Condition Score) of the Aminaftone in patients with Raynaud’s Phenomenon (RP) secondary to Systemic Sclerosis (SSc). Methods: Open label controlled study. We evaluated the efficacy of Aminaftone in the treatment of secondary RP in 108 patients with SSc consecutively recruited and divided in two groups. Group A: 51 Patients in treatment with Calcium Channel Blockers, prostanoids (iloprost 2ng [min/kg every 4 weeks), Endothelin Receptor Antagonist and Phosphodiesterase-5 inhibitors (Standard of Care). Group B: 57 Patients in treatment with Calcium Channel Blockers, Prostanoids, Endothelin Receptor Antagonist and Phosphodiesterase-5 inhibitors and Aminaftone (Standard of care + Aminaftone). Results: The number of RP attacks in group treated with Aminaftone (Group B) was lower than the group treated with standard therapy (Group A) from baseline to Week 48, obtaining statistically significance (Δ A -1.50 Δ B -2.10 p=0.02 95%CI). The RCS was statistically significantly different (Δ A -1.60 Δ B -2.50 p=0,04 95% CI), as was the pain VAS(Δ A -20.80 Δ B -30.60 p=0.04 95%CI) at week 48. Conclusion: The use of Aminaftone was well tolerated and improved RP as measured by RCS and pain when added to standard of care. A well-designed randomized controlled trial is needed to determine if these preliminary findings are supported},
     year = {2015}
    }
    

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  • TY  - JOUR
    T1  - Aminaftone in the Treatment of Raynaud’s Phenomenon in Systemic Sclerosis: New Perspectives
    AU  - Simone Parisi
    AU  - Marco Scarati
    AU  - Marta Priora
    AU  - Clara Lisa Peroni
    AU  - Angela Laganà
    AU  - Enrico Fusaro
    Y1  - 2015/08/19
    PY  - 2015
    N1  - https://doi.org/10.11648/j.ajim.20150305.12
    DO  - 10.11648/j.ajim.20150305.12
    T2  - American Journal of Internal Medicine
    JF  - American Journal of Internal Medicine
    JO  - American Journal of Internal Medicine
    SP  - 204
    EP  - 209
    PB  - Science Publishing Group
    SN  - 2330-4324
    UR  - https://doi.org/10.11648/j.ajim.20150305.12
    AB  - Objective: The aim of this study was to assess the efficacy (in terms of improved VAS Pain, Raynaud's Phenomenon attacks frequency and Raynaud’s Condition Score) of the Aminaftone in patients with Raynaud’s Phenomenon (RP) secondary to Systemic Sclerosis (SSc). Methods: Open label controlled study. We evaluated the efficacy of Aminaftone in the treatment of secondary RP in 108 patients with SSc consecutively recruited and divided in two groups. Group A: 51 Patients in treatment with Calcium Channel Blockers, prostanoids (iloprost 2ng [min/kg every 4 weeks), Endothelin Receptor Antagonist and Phosphodiesterase-5 inhibitors (Standard of Care). Group B: 57 Patients in treatment with Calcium Channel Blockers, Prostanoids, Endothelin Receptor Antagonist and Phosphodiesterase-5 inhibitors and Aminaftone (Standard of care + Aminaftone). Results: The number of RP attacks in group treated with Aminaftone (Group B) was lower than the group treated with standard therapy (Group A) from baseline to Week 48, obtaining statistically significance (Δ A -1.50 Δ B -2.10 p=0.02 95%CI). The RCS was statistically significantly different (Δ A -1.60 Δ B -2.50 p=0,04 95% CI), as was the pain VAS(Δ A -20.80 Δ B -30.60 p=0.04 95%CI) at week 48. Conclusion: The use of Aminaftone was well tolerated and improved RP as measured by RCS and pain when added to standard of care. A well-designed randomized controlled trial is needed to determine if these preliminary findings are supported
    VL  - 3
    IS  - 5
    ER  - 

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