Logo: to the web site of Uppsala University

uu.sePublications from Uppsala University
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Placement of an intrauterine device within 48 hours after second-trimester medical abortion: a randomized controlled trial
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Disciplinary Domain of Medicine and Pharmacy, research centers etc., Center for Clinical Research Dalarna. Karolinska Inst, Danderyd Hosp, Dept Clin Sci, Stockholm, Sweden.;Falun Cent Hosp, Dept Obstet & Gynecol, Falun, Sweden..ORCID iD: 0000-0001-6061-3982
Univ Gothenburg, Dept Obstet & Gynecol, Gothenburg, Sweden..
Karolinska Inst, Danderyd Hosp, Dept Clin Sci, Stockholm, Sweden.;Dalarna Univ, Sch Hlth & Welf, Falun, Sweden.;Karolinska Inst, Dept Womens & Childrens Hlth, Stockholm, Sweden..
Lund Univ, Dept Clin Sci, Lund, Sweden.;Skane Univ Hosp, Dept Gynaecol & Obstet, Lund, Sweden..
Show others and affiliations
2024 (English)In: American Journal of Obstetrics and Gynecology, ISSN 0002-9378, E-ISSN 1097-6868, Vol. 231, no 5, p. 530e1-530e8Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: International guidelines recommend placement of intrauterine devices immediately after second-trimester medical abortion, but evidence concerning the optimal time for intrauterine device placement is lacking from clinical trials. OBJECTIVE: This study aimed to investigate effectiveness, safety, and acceptability of intrauterine device placement within 48 hours, compared with placement at 2 to 4 weeks after second-trimester medical abortion. We hypothesized that intrauterine device placement within 48 hours would be superior compared with placement at 2 to 4 weeks after the abortion, in terms of the proportion of intrauterine device use after 6 months, with maintained safety and acceptability. STUDY DESIGN: In this open-label, randomized, controlled, superiority trial, we recruited participants at 8 abortion clinics in Sweden. Eligible participants were aged >= 18 years, requesting medical abortion with gestation >= 85 days, and opting for use of a postabortion intrauterine device. Participants were randomized (1:1) to intrauterine device placement either within 48 hours of complete abortion (intervention) or after 2 to 4 weeks (control). Our primary outcome was self-reported use of an intrauterine device after 6 months. Secondary outcomes included expulsion rates, pain at placement, adverse events and complications, acceptability, and subsequent pregnancies and abortions. Differences in nonnormal continuous variables were analyzed with the Mann-Whitney U test, and differences in dichotomous variables with the chi-square or Fisher exact tests. A P value <.05 was considered statistically significant. Group differences are presented by modified intention-to-treat and per-protocol analyses. RESULTS: Between January 2019 and June 2022, we enrolled 179 participants, of whom 90 were assigned to the intervention and 89 to the control arm. Enrollment was prematurely stopped after an interim analysis exceeded a predefined intrauterine device expulsion rate of 20%. According to modified intention-to-treat analysis, use of intrauterine device after 6 months was 50.7% (34/67) in the intervention group vs 71.6% (48/ 67) in the control group (proportion difference, 20.9%; 95% confidence interval, 4.4%-35.9%; P=.02). The intrauterine device expulsion rate was 30.1% (22/73) in the intervention group vs 2.9% (2/70; P<.001) in the control group. Other adverse events were rare and patient acceptability was high in both groups. CONCLUSION: Intrauterine device placement within 48 hours after second-trimester medical abortion was nonsuperior in terms of the proportion of intrauterine device use after 6 months when compared with placement after 2 to 4 weeks. Placement within 48 hours after second- trimester abortion can be used in selected individuals after counseling on expulsion risk.

Place, publisher, year, edition, pages
Elsevier, 2024. Vol. 231, no 5, p. 530e1-530e8
Keywords [en]
health services accessibility, induced abortion, intrauterine device expulsion, long-acting reversible contraception, medicated intra-uterine devices, postabortion contraception, repeated abortion seekers, contraception, copper intrauterine devices, family planning services
National Category
Gynaecology, Obstetrics and Reproductive Medicine
Identifiers
URN: urn:nbn:se:uu:diva-543285DOI: 10.1016/j.ajog.2024.05.041ISI: 001347132200001PubMedID: 38796039Scopus ID: 2-s2.0-85195668981OAI: oai:DiVA.org:uu-543285DiVA, id: diva2:1918810
Available from: 2024-12-06 Created: 2024-12-06 Last updated: 2025-02-11Bibliographically approved

Open Access in DiVA

dataset(410 kB)65 downloads
File information
File name DATASET01.pdfFile size 410 kBChecksum SHA-512
b96e62efaf87463eb41265d752c4536d645f7ec277f1942c055f94a0b48754c85ad8ea60959ea978c4270fd68ccc565165a3a39143af6e6ed5f1c62194a1abf0
Type datasetMimetype application/pdf

Other links

Publisher's full textPubMedScopus

Authority records

Hogmark, Sara

Search in DiVA

By author/editor
Hogmark, Sara
By organisation
Center for Clinical Research Dalarna
In the same journal
American Journal of Obstetrics and Gynecology
Gynaecology, Obstetrics and Reproductive Medicine

Search outside of DiVA

GoogleGoogle Scholar
Total: 0 downloads
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 220 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf