Elevated Risk of Bacterial Vaginosis Among Users of the Copper Intrauterine Device: A Prospective Longitudinal Cohort Study.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
02 08 2021
Historique:
received: 17 12 2019
accepted: 01 06 2020
pubmed: 7 6 2020
medline: 7 8 2021
entrez: 7 6 2020
Statut: ppublish

Résumé

Limited evidence suggests that the nonhormonal contraceptive copper intrauterine device (Cu-IUD) may increase bacterial vaginosis (BV) risk, possibly due to increased volume and duration of menses, a common side effect of Cu-IUD use. Although increases in bleeding typically resolve within 6-12 months following initiation, evaluations of the association between Cu-IUD and BV have not included more than 6 months of follow-up. This secondary analysis of a human immunodeficiency virus type 1 prevention trial included 2585 African women ages 18-45 followed for up to 33 months. Women reported contraceptive use each month. BV was evaluated by Nugent score in 6-monthly intervals and, if clinically indicated, by Amsel criteria. Andersen-Gill proportional hazards models were used to (1) evaluate BV risk among Cu-IUD users relative to women using no/another nonhormonal contraceptive and (2) test changes in BV frequency before, while using, and following Cu-IUD discontinuation. BV frequency was highest among Cu-IUD users at 153.6 episodes per 100 person-years (95% confidence interval [CI]: 145.2, 162.4). In adjusted models, Cu-IUD users experienced 1.28-fold (95% CI: 1.12, 1.46) higher BV risk relative to women using no/another nonhormonal contraception. Compared to the 6 months prior to initiation, BV risk was 1.52-fold (95% CI: 1.16, 2.00) higher in the first 6 months of Cu-IUD use and remained elevated over 18 months of use (P < .05). Among women who discontinued Cu-IUD, BV frequency was similar to pre-initiation rates within 1 year. Cu-IUD users experienced elevated BV risk that persisted throughout use. Women and their providers may wish to consider BV risk when discussing contraceptive options.

Sections du résumé

BACKGROUND
Limited evidence suggests that the nonhormonal contraceptive copper intrauterine device (Cu-IUD) may increase bacterial vaginosis (BV) risk, possibly due to increased volume and duration of menses, a common side effect of Cu-IUD use. Although increases in bleeding typically resolve within 6-12 months following initiation, evaluations of the association between Cu-IUD and BV have not included more than 6 months of follow-up.
METHODS
This secondary analysis of a human immunodeficiency virus type 1 prevention trial included 2585 African women ages 18-45 followed for up to 33 months. Women reported contraceptive use each month. BV was evaluated by Nugent score in 6-monthly intervals and, if clinically indicated, by Amsel criteria. Andersen-Gill proportional hazards models were used to (1) evaluate BV risk among Cu-IUD users relative to women using no/another nonhormonal contraceptive and (2) test changes in BV frequency before, while using, and following Cu-IUD discontinuation.
RESULTS
BV frequency was highest among Cu-IUD users at 153.6 episodes per 100 person-years (95% confidence interval [CI]: 145.2, 162.4). In adjusted models, Cu-IUD users experienced 1.28-fold (95% CI: 1.12, 1.46) higher BV risk relative to women using no/another nonhormonal contraception. Compared to the 6 months prior to initiation, BV risk was 1.52-fold (95% CI: 1.16, 2.00) higher in the first 6 months of Cu-IUD use and remained elevated over 18 months of use (P < .05). Among women who discontinued Cu-IUD, BV frequency was similar to pre-initiation rates within 1 year.
CONCLUSIONS
Cu-IUD users experienced elevated BV risk that persisted throughout use. Women and their providers may wish to consider BV risk when discussing contraceptive options.

Identifiants

pubmed: 32505132
pii: 5854318
doi: 10.1093/cid/ciaa703
pmc: PMC8326546
doi:

Substances chimiques

Levonorgestrel 5W7SIA7YZW

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

513-520

Subventions

Organisme : NIAID NIH HHS
ID : UM1 AI068633
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068615
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI106707
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069518
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069463
Pays : United States

Investigateurs

Jared Baeten (J)
Thesla Palanee-Phillips (T)
Elizabeth Brown (E)
Lydia Soto-Torres (L)
Katie Schwartz (K)
Bonus Makanani (B)
Francis Martinson (F)
Linda-Gail Bekker (LG)
Vaneshree Govender (V)
Samantha Siva (S)
Zakir Gaffoor (Z)
Logashvari Naidoo (L)
Arendevi Pather (A)
Nitesha Jeenarain (N)
Gonasagrie Nair (G)
Thesla Palanee-Phillips (T)
Flavia Matovu (F)
Nyaradzo Mgodi (N)
Felix Mhlanga (F)

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Références

Contraception. 2009 May;79(5):356-62
pubmed: 19341847
Contraception. 2008 May;77(5):355-9
pubmed: 18402852
N Engl J Med. 2016 Dec;375(22):2121-2132
pubmed: 26900902
AIDS. 2015 Jun 1;29(9):1077-85
pubmed: 26125141
J Med Microbiol. 2018 Mar;67(3):308-313
pubmed: 29458551
PLoS Med. 2012;9(6):e1001251
pubmed: 22745608
Contraception. 2019 Sep;100(3):214-218
pubmed: 31226323
J Acquir Immune Defic Syndr. 2017 Oct 1;76(2):e47-e51
pubmed: 28542081
AIDS Care. 2018 Nov;30(11):1351-1355
pubmed: 29548268
Am J Med. 1983 Jan;74(1):14-22
pubmed: 6600371
PLoS One. 2010 Apr 15;5(4):e10197
pubmed: 20419168
BMC Infect Dis. 2015 Jul 29;15:292
pubmed: 26219949
J Med Microbiol. 2005 Dec;54(Pt 12):1199-1203
pubmed: 16278434
PLoS Med. 2011 Feb 15;8(2):e1000416
pubmed: 21358808
Open Access J Contracept. 2016 May 11;7:89-96
pubmed: 29386940
Eur J Clin Microbiol Infect Dis. 2017 Jan;36(1):43-48
pubmed: 27638008
Sex Transm Dis. 2013 Feb;40(2):117-22
pubmed: 23324974
J Clin Microbiol. 1991 Feb;29(2):297-301
pubmed: 1706728
Contraception. 2014 Aug;90(2):130-5
pubmed: 24835828
Sex Transm Dis. 2007 Dec;34(12):954-9
pubmed: 18077845
PLoS One. 2018 Nov 7;13(11):e0199724
pubmed: 30403671
Mil Med Res. 2016 Feb 13;3:4
pubmed: 26877884
Am J Obstet Gynecol. 2018 Jun;218(6):622.e1-622.e10
pubmed: 29505773
Glob Health Sci Pract. 2018 Mar 30;6(1):17-39
pubmed: 29559495
PLoS One. 2013 Sep 04;8(9):e73055
pubmed: 24023807
Contraception. 2017 Apr;95(4):405-413
pubmed: 27913230
N Engl J Med. 1995 Dec 28;333(26):1737-42
pubmed: 7491137
Sex Transm Dis. 2012 Mar;39(3):217-22
pubmed: 22337109

Auteurs

Kathryn Peebles (K)

Department of Epidemiology, University of Washington, Seattle, Washington, USA.

Flavia M Kiweewa (FM)

Makerere University - Johns Hopkins University Research Collaboration, Kampala, Uganda.
Makerere University School of Public Health, Kampala, Uganda.

Thesla Palanee-Phillips (T)

Wits Reproductive Health and HIV Institute, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Catherine Chappell (C)

Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Devika Singh (D)

Magee-Womens Research Institute, Pittsburgh, Pennsylvania, USA.

Katherine E Bunge (KE)

Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Logashvari Naidoo (L)

South African Medical Research Council, Durban, South Africa.

Bonus Makanani (B)

Malawi College of Medicine - Johns Hopkins University Research Project, Blantyre, Malawi.

Nitesha Jeenarain (N)

South African Medical Research Council, Durban, South Africa.

Doerieyah Reynolds (D)

University of Cape Town Medical School, Cape Town, South Africa.

Sharon L Hillier (SL)

Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Elizabeth R Brown (ER)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Department of Biostatistics, University of Washington, Seattle, Washington, USA.

Jared M Baeten (JM)

Department of Epidemiology, University of Washington, Seattle, Washington, USA.
Department of Global Health, University of Washington, Seattle, Washington, USA.
Department of Medicine, University of Washington, Seattle, Washington, USA.

Jennifer E Balkus (JE)

Department of Epidemiology, University of Washington, Seattle, Washington, USA.
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Department of Global Health, University of Washington, Seattle, Washington, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH