Intrauterine contraceptive device rupture. Follow-up of a retrospective cohort and clinical protocol. RUDIUS study

Objective: Intrauterine device fracture, as we know it today, is an infrequent event, usually described as isolated cases. The purpose of this study was to look for factors influencing intrauterine fragment retention after device rupture. Study design: Retrospective cohort study. A total of 135 pati...

Full description

Bibliographic Details
Main Authors: Esther Cánovas, Duska Beric, Rebeca Jara, Eduardo Cazorla
Format: Article
Language:English
Published: Elsevier 2022-01-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844022000391
_version_ 1798018338220146688
author Esther Cánovas
Duska Beric
Rebeca Jara
Eduardo Cazorla
author_facet Esther Cánovas
Duska Beric
Rebeca Jara
Eduardo Cazorla
author_sort Esther Cánovas
collection DOAJ
description Objective: Intrauterine device fracture, as we know it today, is an infrequent event, usually described as isolated cases. The purpose of this study was to look for factors influencing intrauterine fragment retention after device rupture. Study design: Retrospective cohort study. A total of 135 patients were recruited, and the cohort follow-up ran for three full years from 2018 to 2020. Results: Thirty-three percent of patients had a retained intrauterine fragment compared to 82 of 123 (66.7%) who had expelled it spontaneously. In the group of patients who had at least one intercurrent period between device fracture and confirmatory fragment persistent test, we found persistence of intrauterine fragment in 18 of 71 (25.4%) patients compared to 53 of 71 (74.6%) who did not (p = 0.047). A total of 6 of 39 (15.4%) of the patients with spontaneous rupture of the device presented with persistence of the intrauterine fragment compared to 32 of 81 (39.2%) of the group with fracture after manipulation (p = 0.006). The mean time elapsed from the fracture to the confirmatory test in the patients who had persistence of the fragment was 26.97 days (range from 0 to 116), while in those who expelled it spontaneously, a mean of 45.59 days (range 7–267) had elapsed (p = 0.003). Conclusions: The main factors positively influencing complete expulsion of the fragmented IUD were elapsed time of 45 days or more, intercurrent menstruation or spontaneous fracture. Therefore, the proposed protocol calls for expectant management for at least 1.5 months after fracture, allowing at least one intercurrent period to elapse prior to any therapeutic manoeuvre.
first_indexed 2024-04-11T16:22:24Z
format Article
id doaj.art-a023c73b05c34f39a0ea97923d82e1e5
institution Directory Open Access Journal
issn 2405-8440
language English
last_indexed 2024-04-11T16:22:24Z
publishDate 2022-01-01
publisher Elsevier
record_format Article
series Heliyon
spelling doaj.art-a023c73b05c34f39a0ea97923d82e1e52022-12-22T04:14:19ZengElsevierHeliyon2405-84402022-01-0181e08751Intrauterine contraceptive device rupture. Follow-up of a retrospective cohort and clinical protocol. RUDIUS studyEsther Cánovas0Duska Beric1Rebeca Jara2Eduardo Cazorla3Department of Obstetrics and Gynaecology, University Hospital of Torrevieja, Alicante, Carretera CV 95, s/n, 03186, Torrevieja, Alicante, SpainDepartment of Obstetrics and Gynaecology, University Hospital of Torrevieja, Alicante, Carretera CV 95, s/n, 03186, Torrevieja, Alicante, SpainDepartment of Obstetrics and Gynaecology, University Hospital of Vinalopó, Alicante, Carrer Tonico Sansano Mora, 14, 03293, Elche, Alicante, SpainDepartment of Obstetrics and Gynaecology, University Hospital of Torrevieja, Alicante, Carretera CV 95, s/n, 03186, Torrevieja, Alicante, Spain; Corresponding author.Objective: Intrauterine device fracture, as we know it today, is an infrequent event, usually described as isolated cases. The purpose of this study was to look for factors influencing intrauterine fragment retention after device rupture. Study design: Retrospective cohort study. A total of 135 patients were recruited, and the cohort follow-up ran for three full years from 2018 to 2020. Results: Thirty-three percent of patients had a retained intrauterine fragment compared to 82 of 123 (66.7%) who had expelled it spontaneously. In the group of patients who had at least one intercurrent period between device fracture and confirmatory fragment persistent test, we found persistence of intrauterine fragment in 18 of 71 (25.4%) patients compared to 53 of 71 (74.6%) who did not (p = 0.047). A total of 6 of 39 (15.4%) of the patients with spontaneous rupture of the device presented with persistence of the intrauterine fragment compared to 32 of 81 (39.2%) of the group with fracture after manipulation (p = 0.006). The mean time elapsed from the fracture to the confirmatory test in the patients who had persistence of the fragment was 26.97 days (range from 0 to 116), while in those who expelled it spontaneously, a mean of 45.59 days (range 7–267) had elapsed (p = 0.003). Conclusions: The main factors positively influencing complete expulsion of the fragmented IUD were elapsed time of 45 days or more, intercurrent menstruation or spontaneous fracture. Therefore, the proposed protocol calls for expectant management for at least 1.5 months after fracture, allowing at least one intercurrent period to elapse prior to any therapeutic manoeuvre.http://www.sciencedirect.com/science/article/pii/S2405844022000391Intrauterine dispositiveFractured IUDIUD breakageCohort studyClinical protocol
spellingShingle Esther Cánovas
Duska Beric
Rebeca Jara
Eduardo Cazorla
Intrauterine contraceptive device rupture. Follow-up of a retrospective cohort and clinical protocol. RUDIUS study
Heliyon
Intrauterine dispositive
Fractured IUD
IUD breakage
Cohort study
Clinical protocol
title Intrauterine contraceptive device rupture. Follow-up of a retrospective cohort and clinical protocol. RUDIUS study
title_full Intrauterine contraceptive device rupture. Follow-up of a retrospective cohort and clinical protocol. RUDIUS study
title_fullStr Intrauterine contraceptive device rupture. Follow-up of a retrospective cohort and clinical protocol. RUDIUS study
title_full_unstemmed Intrauterine contraceptive device rupture. Follow-up of a retrospective cohort and clinical protocol. RUDIUS study
title_short Intrauterine contraceptive device rupture. Follow-up of a retrospective cohort and clinical protocol. RUDIUS study
title_sort intrauterine contraceptive device rupture follow up of a retrospective cohort and clinical protocol rudius study
topic Intrauterine dispositive
Fractured IUD
IUD breakage
Cohort study
Clinical protocol
url http://www.sciencedirect.com/science/article/pii/S2405844022000391
work_keys_str_mv AT esthercanovas intrauterinecontraceptivedevicerupturefollowupofaretrospectivecohortandclinicalprotocolrudiusstudy
AT duskaberic intrauterinecontraceptivedevicerupturefollowupofaretrospectivecohortandclinicalprotocolrudiusstudy
AT rebecajara intrauterinecontraceptivedevicerupturefollowupofaretrospectivecohortandclinicalprotocolrudiusstudy
AT eduardocazorla intrauterinecontraceptivedevicerupturefollowupofaretrospectivecohortandclinicalprotocolrudiusstudy