Combined oral contraceptives in women with systemic lupus erythematosus

被引:836
作者
Petri, M
Kim, MY
Kalunian, KC
Grossman, J
Hahn, BH
Sammaritano, LR
Lockshin, M
Merrill, JT
Belmont, HM
Askanase, AD
McCune, WJ
Hearth-Holmes, M
Dooley, MA
Von Feldt, J
Friedman, A
Tan, M
Davis, J
Cronin, M
Diamond, B
Mackay, M
Sigler, L
Fillius, M
Rupel, A
Licciardi, F
Buyon, JP
机构
[1] NYU, Hosp Joint Dis, Sch Med, Dept Rheumatol, New York, NY 10003 USA
[2] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[3] Montefiore Med Ctr, Albert Einstein Coll Med, Bronx, NY 10467 USA
[4] Univ Calif Los Angeles, Los Angeles, CA USA
[5] Hosp Special Surg, New York, NY 10021 USA
[6] Oklahoma Med Res Fdn, Oklahoma City, OK 73104 USA
[7] NYU, Sch Med, Bellevue Hosp, New York, NY USA
[8] Univ Michigan, Ann Arbor, MI 48109 USA
[9] Louisiana State Univ, Hlth Sci Ctr, Shreveport, LA 71105 USA
[10] Univ N Carolina, Chapel Hill, NC USA
[11] Univ Penn, Philadelphia, PA 19104 USA
[12] Univ Texas, Houston, TX USA
[13] Rheumatol Associates Long Isl, Port Jefferson Stn, NY USA
[14] Univ Calif San Francisco, San Francisco, CA 94143 USA
[15] Med Coll Wisconsin, Milwaukee, WI 53226 USA
关键词
D O I
10.1056/NEJMoa051135
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Oral contraceptives are rarely prescribed for women with systemic lupus erythematosus, because of concern about potential negative side effects. In this double-blind, randomized, noninferiority trial, we prospectively evaluated the effect of oral contraceptives on lupus activity in premenopausal women with systemic lupus erythematosus. METHODS: A total of 183 women with inactive (76 percent) or stable active (24 percent) systemic lupus erythematosus at 15 U.S. sites were randomly assigned to receive either oral contraceptives (triphasic ethinyl estradiol at a dose of 35 microg plus norethindrone at a dose of 0.5 to 1 mg for 12 cycles of 28 days each; 91 women) or placebo (92 women) and were evaluated at months 1, 2, 3, 6, 9, and 12. Subjects were excluded if they had moderate or high levels of anticardiolipin antibodies, lupus anticoagulant, or a history of thrombosis. RESULTS: The primary end point, a severe lupus flare, occurred in 7 of 91 subjects receiving oral contraceptives (7.7 percent) as compared with 7 of 92 subjects receiving placebo (7.6 percent). The 12-month rates of severe flare were similar: 0.084 for the group receiving oral contraceptives and 0.087 for the placebo group (P=0.95; upper limit of the one-sided 95 percent confidence interval for this difference, 0.069, which is within the prespecified 9 percent margin for noninferiority). Rates of mild or moderate flares were 1.40 flares per person-year for subjects receiving oral contraceptives and 1.44 flares per person-year for subjects receiving placebo (relative risk, 0.98; P=0.86). In the group that was randomized to receive oral contraceptives, there was one deep venous thrombosis and one clotted graft; in the placebo group, there was one deep venous thrombosis, one ocular thrombosis, one superficial thrombophlebitis, and one death (after cessation of the trial). CONCLUSIONS: Our study indicates that oral contraceptives do not increase the risk of flare among women with systemic lupus erythematosus whose disease is stable.
引用
收藏
页码:2550 / 2558
页数:9
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