Disease activity and thromboembolic events in women with systemic lupus erythematosus with and without anti-phospholipid syndrome: users of the 52-mg levonorgestrel-releasing intrauterine system.


Journal

Archives of gynecology and obstetrics
ISSN: 1432-0711
Titre abrégé: Arch Gynecol Obstet
Pays: Germany
ID NLM: 8710213

Informations de publication

Date de publication:
06 2019
Historique:
received: 26 10 2018
accepted: 25 03 2019
pubmed: 4 4 2019
medline: 31 3 2020
entrez: 4 4 2019
Statut: ppublish

Résumé

The disease status and thromboembolic events in women with systemic lupus erythematosus (SLE), with and without anti-phospholipid syndrome (APS), were evaluated before and after placement of the 52-mg levonorgestrel-releasing intrauterine system (LNG-IUS). A retrospective cohort study, with review of medical records of SLE women, who received an LNG-IUS placement between January 2007 and December 2016, carried out at the University of Campinas Medical School, Brazil. The outcomes included the disease activity (SLEDAI-2K) and damage index scores (SLICC/ACR-DI) presented for each year of device use, as well as venous/arterial thrombotic events, insertion up to a median of 5 years. The author's used χ The study evaluated 46 women with SLE, 18 with and 28 without APS; the mean age (± standard deviation [SD]) was 31.8 (SD ± 8.3) years old. The length of follow-up after LNG-IUS placement was 5.6 (SD ± 2.7) and 4.1 (SD ± 2.3) years for the groups with and without APS, respectively. Comparison of the groups found that the SLEDAI and SLICC mean scores were low for both at baseline, without variations through the follow-up. After LNG-IUS placement, two women presented three thrombotic arterial events, and one of them died from causes unrelated to LNG-IUS use. Our results, although restricted, provide information to policymakers and health professionals that the use of a 52 mg LNG-IUS over a 5-year median did not increase disease activity or damage index scores among women with SLE, with and without APS.

Identifiants

pubmed: 30941559
doi: 10.1007/s00404-019-05131-x
pii: 10.1007/s00404-019-05131-x
doi:

Substances chimiques

Levonorgestrel 5W7SIA7YZW

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1597-1605

Auteurs

Rafaella C Rebelo (RC)

Family Planning Clinic, Department of Obstetrics and Gynaecology, School of Medical Sciences, University of Campinas (UNICAMP), Caixa Postal 6181, Campinas, SP, 13083-970, Brazil.

Estephania Pignaton (E)

Rheumatology Division, Department of Clinical Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Rua Alexander Fleming, 101, Cidade Universitária, Campinas, SP, 13083-881, Brazil.

M Valeria Bahamondes (M)

Family Planning Clinic, Department of Obstetrics and Gynaecology, School of Medical Sciences, University of Campinas (UNICAMP), Caixa Postal 6181, Campinas, SP, 13083-970, Brazil.

Lilian T L Costallat (LTL)

Rheumatology Division, Department of Clinical Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Rua Alexander Fleming, 101, Cidade Universitária, Campinas, SP, 13083-881, Brazil.

Simone Appenzeller (S)

Rheumatology Division, Department of Clinical Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Rua Alexander Fleming, 101, Cidade Universitária, Campinas, SP, 13083-881, Brazil.

Luis Bahamondes (L)

Family Planning Clinic, Department of Obstetrics and Gynaecology, School of Medical Sciences, University of Campinas (UNICAMP), Caixa Postal 6181, Campinas, SP, 13083-970, Brazil.

Arlete Fernandes (A)

Family Planning Clinic, Department of Obstetrics and Gynaecology, School of Medical Sciences, University of Campinas (UNICAMP), Caixa Postal 6181, Campinas, SP, 13083-970, Brazil. arlete@fcm.unicamp.br.

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