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Two Years Follow-Up of Patients With Abnormal Uterine Bleeding After Insertion of the Levonorgestrel-Releasing Intrauterine System

dc.authorid Tolunay, Harun Egemen/0000-0002-8922-4400
dc.authorid Cim, Numan/0000-0003-0983-3204
dc.authorscopusid 35955724600
dc.authorscopusid 57197539213
dc.authorscopusid 57199508019
dc.authorscopusid 13404207800
dc.authorscopusid 42262158200
dc.authorscopusid 55818321300
dc.authorscopusid 55354165200
dc.authorwosid Tolunay, Harun/Aag-4620-2020
dc.authorwosid Yildizhan, Recep/Aaa-8400-2021
dc.authorwosid Karaman, Erbil/Afu-7129-2022
dc.authorwosid Cim, Numan/A-4305-2016
dc.contributor.author Cim, Numan
dc.contributor.author Soysal, Sunullah
dc.contributor.author Sayan, Sena
dc.contributor.author Yildizhan, Begum
dc.contributor.author Karaman, Erbil
dc.contributor.author Cetin, Orkun
dc.contributor.author Yildizhan, Recep
dc.date.accessioned 2025-05-10T17:11:09Z
dc.date.available 2025-05-10T17:11:09Z
dc.date.issued 2018
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp [Cim, Numan; Karaman, Erbil; Cetin, Orkun; Tolunay, Harun Egemen; Yildizhan, Recep] Yuzuncu Yil Univ, Med Fac, Dept Obstet & Gynecol, TR-65080 Van, Turkey; [Soysal, Sunullah; Sayan, Sena; Yildizhan, Begum] Marmara Univ, Med Fac, Dept Obstet & Gynecol, Istanbul, Turkey en_US
dc.description Tolunay, Harun Egemen/0000-0002-8922-4400; Cim, Numan/0000-0003-0983-3204 en_US
dc.description.abstract Aim: To evaluate the efficacy and safety of levonorgestrel-releasing intrauterine system (LNG-IUS) in the long-term treatment of heavy menstrual blood loss in women unrelated to intrauterine pathology. Methods: One hundred and six parous women aged 33-48 years with recurrent heavy menstrual bleeding (HMB) participated in this study. The women were followed up for 24 months and were assessed for intensity of bleeding both for pre- and post-insertion periods. An LNG-IUS was inserted in each patient within 7 days of the start of menstrual flow. The women were followed up at 1, 3, 6, 12, 18, and 24 months following the insertion of the intrauterine device. Results: One hundred and two women completed the follow-up period and had a significant reduction in the amount of menstrual blood loss. The LNG-IUS was well tolerated by all women. Pre-treatment of the use of the LNG-IUS, endometrial biopsy patterns for irregular proliferative endometrium and for atypical simple hyperplasia were 34/106 (32.08%) and 61/106 (57.55%) respectively and after treatment no abnormal pathologic findings were determined (p < 0.001). Conclusion: Our findings indicate that the LNG-IUS is effective for significantly reducing the amount of menstrual blood loss in women with HMB. (c) 2017 S. Karger AG, Basel en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.1159/000480012
dc.identifier.endpage 575 en_US
dc.identifier.issn 0378-7346
dc.identifier.issn 1423-002X
dc.identifier.issue 6 en_US
dc.identifier.pmid 29223999
dc.identifier.scopus 2-s2.0-85038117177
dc.identifier.scopusquality Q2
dc.identifier.startpage 569 en_US
dc.identifier.uri https://doi.org/10.1159/000480012
dc.identifier.uri https://hdl.handle.net/20.500.14720/7653
dc.identifier.volume 83 en_US
dc.identifier.wos WOS:000454454600008
dc.identifier.wosquality Q3
dc.language.iso en en_US
dc.publisher Karger en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Levonorgestrel en_US
dc.subject Lng-Ius en_US
dc.subject Heavy Menstrual Bleeding en_US
dc.subject Uterine Volume en_US
dc.subject Pulsatile Index en_US
dc.subject Endometrial Biopsy en_US
dc.title Two Years Follow-Up of Patients With Abnormal Uterine Bleeding After Insertion of the Levonorgestrel-Releasing Intrauterine System en_US
dc.type Article en_US

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