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Publication Detail
Successful treatment of Raynaud's syndrome with Iloprost, a chemically stable prostacyclin analogue.
  • Publication Type:
    Journal article
  • Publication Sub Type:
    Clinical Trial
  • Authors:
    Yardumian DA, Isenberg DA, Rustin M, Belcher G, Snaith ML, Dowd PM, Machin SJ
  • Publication date:
    06/1988
  • Pagination:
    220, 226
  • Journal:
    Br J Rheumatol
  • Volume:
    27
  • Issue:
    3
  • Status:
    Published
  • Country:
    England
  • Print ISSN:
    0263-7103
  • Language:
    eng
  • Keywords:
    Aged, Body Temperature, Chronic Disease, Clinical Trials as Topic, Dose-Response Relationship, Drug, Epoprostenol, Female, Fingers, Humans, Iloprost, Infusions, Intravenous, Middle Aged, Platelet Aggregation, Random Allocation, Raynaud Disease, Regional Blood Flow, Time Factors
Abstract
Twelve female patients with severe secondary Raynaud's phenomenon were treated in a randomized order with both placebo and Iloprost infusions. Infusions were for 5 hours on 3 consecutive days and Iloprost was administered at variable dosage from 1.0 to 3.0 ng/kg/min. A 6-week follow-up period was used between the two sets of infusions. A significant number of patients reported Iloprost had improved Raynaud's symptomatology compared with placebo and this effect lasted for up to 6 weeks. The number of attacks of Raynaud's as recorded by patients in diary books was similarly reduced after Iloprost. Digital and nail-bed blood flows measured by laser-Doppler methods were increased for up to 6 weeks after Iloprost, but not after placebo infusions. Iloprost may be a useful therapeutic agent in the treatment of severe secondary Raynaud's syndrome.
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