INTRAVENOUS ILOPROST INFUSION IN PATIENTS WITH RAYNAUD PHENOMENON SECONDARY TO SYSTEMIC-SCLEROSIS - A MULTICENTER, PLACEBO-CONTROLLED, DOUBLE-BLIND-STUDY

被引:304
作者
WIGLEY, FM
WISE, RA
SEIBOLD, JR
MCCLOSKEY, DA
KUJALA, G
MEDSGER, TA
STEEN, VD
VARGA, J
JIMENEZ, S
MAYES, M
CLEMENTS, PJ
WEINER, SR
PORTER, J
ELLMAN, M
WISE, C
KAUFMAN, LD
WILLIAMS, J
DOLE, W
机构
[1] UNIV CALIF LOS ANGELES, SAN FERNANDO VALLEY PROGRAM, GRANADA HILLS, CA USA
[2] UMDNJ, ROBERT WOOD JOHNSON MED SCH, NEW BRUNSWICK, NJ 08903 USA
[3] W VIRGINIA UNIV, MORGANTOWN, WV 26506 USA
[4] UNIV PITTSBURGH, DEPT MED, PITTSBURGH, PA 15260 USA
[5] THOMAS JEFFERSON UNIV, PHILADELPHIA, PA 19107 USA
[6] WAYNE STATE UNIV, DETROIT, MI 48202 USA
[7] UNIV CALIF LOS ANGELES, SCH MED, DEPT MED, LOS ANGELES, CA 90024 USA
[8] UNIV OREGON, EUGENE, OR 97403 USA
[9] UNIV CHICAGO, CHICAGO, IL 60637 USA
[10] WAKE FOREST UNIV, BOWMAN GRAY SCH MED, WINSTON SALEM, NC 27103 USA
[11] SUNY STONY BROOK, DIV ALLERGY & RHEUMATOL, STONY BROOK, NY 11794 USA
[12] BERLEX LABS INC, WAYNE, NJ 07470 USA
关键词
D O I
10.7326/0003-4819-120-3-199402010-00004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To evaluate the efficacy and safety of iloprost, a prostacyclin analog, administered intravenously in patients with Raynaud phenomenon secondary to systemic sclerosis. Design: Multicenter, randomized, parallel placebo-controlled, double-blind study. Setting: University medical centers. Patients: 131 patients with systemic sclerosis (101 women, 30 men) ages 20 to 79 years. Intervention: Patients were randomly assigned to receive one of two parallel treatments of five daily sequential, 6-hour intravenous infusions of iloprost (0.5 to 2.0 ng/kg per min) or to receive a similar volume of placebo. Measurements: Frequency of Raynaud attacks, Raynaud severity score, physician's overall rating of treatment effect, and digital cutaneous lesion healing. Results: Of the 131 patients enrolled, 126 completed the 5-day infusion and 114 (87%) completed at least 6 weeks of follow-up. Sixty-four patients were randomly assigned to receive iloprost and 67 patients, to receive placebo. The mean weekly number of Raynaud attacks decreased 39.1% with iloprost and 22.2% with placebo (P = 0.005). In addition, the moan percentage of improvement in a global Raynaud severity score during the entire 9-week follow-up was greater in patients given iloprost (34.8%) than in those receiving placebo (19.7%) (P = 0.011). The physician's overall rating of, treatment effect showed greater improvement with iloprost than with placebo at week 6 (52.4% compared with 27.4%; P = 0.008) and week 9 (60.9% compared with 26.9%; P < 0.001). At week 3, 14.6% more patients receiving iloprost had 50% or more lesions heal compared with those given placebo (95% CI, 0.9% to 30%). During the infusion, 59 (92%) of the patients receiving iloprost had one or more side effects compared with 38 (57%) of the patients receiving placebo. Conclusion: iloprost is effective for the short-term palliation of severe Raynaud phenomenon in patients with systemic sclerosis.
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页码:199 / 206
页数:8
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