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Effectiveness, safety and overall satisfaction of early postpartum placement of hormonal IUD compared with standard procedure: An open-label, randomized, multicenter study.
Lichtenstein Liljeblad, Karin; Kopp Kallner, Helena; Brynhildsen, Jan.
Afiliação
  • Lichtenstein Liljeblad K; Department of Clinical Sciences at Danderyd Hospital, Karolinska Institutet, Stockholm, Sweden.
  • Kopp Kallner H; Department of Obstetrics and Gynecology, Danderyd Hospital, Stockholm, Sweden.
  • Brynhildsen J; Department of Clinical Sciences at Danderyd Hospital, Karolinska Institutet, Stockholm, Sweden.
Acta Obstet Gynecol Scand ; 101(4): 424-430, 2022 Apr.
Article em En | MEDLINE | ID: mdl-35141886
INTRODUCTION: In this open-label, randomized controlled, non-inferiority, multicenter study we aimed to study the risk of termination of pregnancy within 1 year postpartum, the safety profile and patient acceptability after early postpartum insertion of a hormonal intrauterine device (LNG-IUS, Mirena®) compared with standard placement 6-8 weeks postpartum. MATERIAL AND METHODS: April 2018 to January 2020 women with uncomplicated vaginal delivery at four urban birth centers in Sweden, were randomized to either early placement within 48 h after delivery (early group) or standard placement 6-8 weeks postpartum (standard group) of a hormonal intrauterine device. The main outcome measure was the proportion of terminations of pregnancies in each group during the first year after placement of the intrauterine device. Registration EudraCT database no. 2017-001945-29. RESULTS: The study was prematurely stopped according to the protocol due to an expulsion rate >20% in the early group. No pregnancies occurred. Fifty-two women were randomized to early and 49 women to standard insertion. In the early group, 23/52 (44.2%) of the intrauterine devices were expelled. After expulsion, 10 women chose to have another hormonal intrauterine device placed but still significantly fewer women (39/52, 75%, p = 0.22) in the early group used the hormonal intrauterine device method at study completion. No expulsions occurred in the standard group, but 5/49 (10.2%) requested removal and 41/49 (83.7%, p = 0.22) had used the hormonal intrauterine device method continuously for 1 year. CONCLUSIONS: Early hormonal intrauterine device insertion after vaginal delivery is associated with high expulsion rates. Despite this, a high continuation rate of the hormonal intrauterine device method is seen among women once choosing the method. In the light of high continuation rates, the advantages of early insertion could balance the risk of expulsion for well-informed women.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anticoncepcionais Femininos / Dispositivos Intrauterinos / Dispositivos Intrauterinos Medicados / Dispositivos Intrauterinos de Cobre Tipo de estudo: Clinical_trials Limite: Female / Humans / Pregnancy Idioma: En Revista: Acta Obstet Gynecol Scand Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Suécia País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anticoncepcionais Femininos / Dispositivos Intrauterinos / Dispositivos Intrauterinos Medicados / Dispositivos Intrauterinos de Cobre Tipo de estudo: Clinical_trials Limite: Female / Humans / Pregnancy Idioma: En Revista: Acta Obstet Gynecol Scand Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Suécia País de publicação: Estados Unidos