| Literature DB >> 1771400 |
Abstract
The risk of a disease flare-up and the side-effects experienced during the use of oral contraceptives (OCs) were studied in 85 female SLE patients, 18-44 years old, regularly attending two specialist rheumatological clinics. Thirty-one patients had used combined oral contraceptives (cOCs) during or after the onset of SLE. Initial manifestations or exacerbations of SLE were noted in 4 (13%) of these patients during the first six months after starting cOCs and three of these four patients had major renal involvement. The incidence of disease flare-ups was the same as in patients not using cOCs. Two patients developed deep venous thrombosis during cOCs, and they both had antiphospholipid antibodies. Thirty-two patients had used progestagen-only contraceptives (PCs) and they were discontinued in 25 (78%) of the patients because of minor side-effects, mainly reflecting poor gynaecological tolerance. Albeit there is no definitive proof that cOCs actually precipitate or exacerbate SLE some patients may be more likely to have adverse effects while taking cOCs. It appears best to avoid cOCs in SLE patients with high levels of antiphospholipid antibodies and in patients with active nephritis. PCs cause many side-effects in SLE patients, but do not seem to activate the disease.Entities:
Keywords: Biology; Bleeding; Blood Coagulation Effects; Carbohydrate Metabolic Effects; Contraception; Contraceptive Agents; Contraceptive Agents, Estrogen; Contraceptive Agents, Female; Contraceptive Agents, Progestin; Contraceptive Methods; Developed Countries; Diseases; Economic Factors; Embolism; Ethinyl Estradiol; Europe; Family Planning; Gestodene; Hematological Effects; Hemic System; Levonorgestrel; Lipid Metabolic Effects; Lipids; Literature Review; Marketing; Metabolic Effects; Metrorrhagia; Northern Europe; Oral Contraceptives; Oral Contraceptives, Combined; Physiology; Pricing; Pulmonary Embolism; Signs And Symptoms; Systemic Lupus Erythematosus; United Kingdom; Vascular Diseases
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Year: 1991 PMID: 1771400 DOI: 10.3109/03009749109096822
Source DB: PubMed Journal: Scand J Rheumatol ISSN: 0300-9742 Impact factor: 3.641