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- Publisher Website: 10.1111/j.1479-828X.2010.01152.x
- Scopus: eid_2-s2.0-77953833819
- PMID: 20618247
- WOS: WOS:000278915200014
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Article: Levonorgestrel-releasing intrauterine system (Mirena®) and Depot medroxyprogesterone acetate (Depoprovera) as long-term maintenance therapy for patients with moderate and severe endometriosis: A randomised controlled trial
Title | Levonorgestrel-releasing intrauterine system (Mirena®) and Depot medroxyprogesterone acetate (Depoprovera) as long-term maintenance therapy for patients with moderate and severe endometriosis: A randomised controlled trial |
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Authors | |
Keywords | Bone mineral density Depot medroxyprogesterone acetate Endometriosis Levonorgestrel-releasing intrauterine system Recurrence |
Issue Date | 2010 |
Publisher | Blackwell Publishing Asia. The Journal's web site is located at http://www.blackwellpublishing.com/journals/ANZJOG |
Citation | Australian And New Zealand Journal Of Obstetrics And Gynaecology, 2010, v. 50 n. 3, p. 273-279 How to Cite? |
Abstract | Background: Progestogen therapy has been found to be useful in controlling endometriosis. For patients after conservative surgery, long-term medical maintenance therapy should be sought to prevent recurrence and control symptoms. Levonorgestrel-releasing intrauterine system (LNG-IUS) may be a useful form of prolonged progestogen therapy for endometriosis. Aims: To evaluate and compare the efficacy and safety of LNG-IUS to depot medroxyprogesterone acetate (MPA) for patients with moderate or severe endometriosis following conservative surgery, in terms of symptoms control, recurrence prevention and patients' acceptance. Methods: A total of 30 patients after conservative surgery for endometriosis underwent randomisation. Of these patients, 15 received LNG-IUS and 15 had three-monthly depot MPA for three years. Their symptom control, recurrence, compliance and change in bone mineral density (BMD) were compared. The data were analysed using student's t-test and chi-square test. Results: Symptoms and recurrence were controlled by both therapies. The compliance was better in LNG-IUS Group with 13 patients staying on their therapy versus seven patients in Depot MPA Group. LNG-IUS users had a significantly better change in BMD (+0.023, +0.071 g/cm2) than Depot MPA users (-0.030, -0.017 g/cm2) in both hip and lumbar regions. Conclusions: Levonorgestrel-releasing intrauterine system was effective in symptom control and prevention of recurrence. LNG-IUS users showed a better compliance. After three years, bone gain was noted with LNG-IUS, but bone loss with depot MPA. © 2010 The Royal Australian and New Zealand College of Obstetricians and Gynaecologists. |
Persistent Identifier | http://hdl.handle.net/10722/184212 |
ISSN | 2023 Impact Factor: 1.4 2023 SCImago Journal Rankings: 0.630 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Wong, AYK | en_US |
dc.contributor.author | Tang, LCH | en_US |
dc.contributor.author | Chin, RKH | en_US |
dc.date.accessioned | 2013-06-25T03:01:25Z | - |
dc.date.available | 2013-06-25T03:01:25Z | - |
dc.date.issued | 2010 | en_US |
dc.identifier.citation | Australian And New Zealand Journal Of Obstetrics And Gynaecology, 2010, v. 50 n. 3, p. 273-279 | en_US |
dc.identifier.issn | 0004-8666 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/184212 | - |
dc.description.abstract | Background: Progestogen therapy has been found to be useful in controlling endometriosis. For patients after conservative surgery, long-term medical maintenance therapy should be sought to prevent recurrence and control symptoms. Levonorgestrel-releasing intrauterine system (LNG-IUS) may be a useful form of prolonged progestogen therapy for endometriosis. Aims: To evaluate and compare the efficacy and safety of LNG-IUS to depot medroxyprogesterone acetate (MPA) for patients with moderate or severe endometriosis following conservative surgery, in terms of symptoms control, recurrence prevention and patients' acceptance. Methods: A total of 30 patients after conservative surgery for endometriosis underwent randomisation. Of these patients, 15 received LNG-IUS and 15 had three-monthly depot MPA for three years. Their symptom control, recurrence, compliance and change in bone mineral density (BMD) were compared. The data were analysed using student's t-test and chi-square test. Results: Symptoms and recurrence were controlled by both therapies. The compliance was better in LNG-IUS Group with 13 patients staying on their therapy versus seven patients in Depot MPA Group. LNG-IUS users had a significantly better change in BMD (+0.023, +0.071 g/cm2) than Depot MPA users (-0.030, -0.017 g/cm2) in both hip and lumbar regions. Conclusions: Levonorgestrel-releasing intrauterine system was effective in symptom control and prevention of recurrence. LNG-IUS users showed a better compliance. After three years, bone gain was noted with LNG-IUS, but bone loss with depot MPA. © 2010 The Royal Australian and New Zealand College of Obstetricians and Gynaecologists. | en_US |
dc.language | eng | en_US |
dc.publisher | Blackwell Publishing Asia. The Journal's web site is located at http://www.blackwellpublishing.com/journals/ANZJOG | en_US |
dc.relation.ispartof | Australian and New Zealand Journal of Obstetrics and Gynaecology | en_US |
dc.subject | Bone mineral density | - |
dc.subject | Depot medroxyprogesterone acetate | - |
dc.subject | Endometriosis | - |
dc.subject | Levonorgestrel-releasing intrauterine system | - |
dc.subject | Recurrence | - |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Contraceptive Agents, Female - Therapeutic Use | en_US |
dc.subject.mesh | Endometriosis - Drug Therapy - Surgery | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Levonorgestrel - Therapeutic Use | en_US |
dc.subject.mesh | Medroxyprogesterone Acetate - Therapeutic Use | en_US |
dc.title | Levonorgestrel-releasing intrauterine system (Mirena®) and Depot medroxyprogesterone acetate (Depoprovera) as long-term maintenance therapy for patients with moderate and severe endometriosis: A randomised controlled trial | en_US |
dc.type | Article | en_US |
dc.identifier.email | Tang, LCH: lchtang@hku.hk | en_US |
dc.identifier.authority | Tang, LCH=rp01756 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1111/j.1479-828X.2010.01152.x | en_US |
dc.identifier.pmid | 20618247 | - |
dc.identifier.scopus | eid_2-s2.0-77953833819 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77953833819&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 50 | en_US |
dc.identifier.issue | 3 | en_US |
dc.identifier.spage | 273 | en_US |
dc.identifier.epage | 279 | en_US |
dc.identifier.isi | WOS:000278915200014 | - |
dc.publisher.place | Australia | en_US |
dc.identifier.f1000 | 6106956 | - |
dc.identifier.scopusauthorid | Wong, AYK=7403147449 | en_US |
dc.identifier.scopusauthorid | Tang, LCH=7402081111 | en_US |
dc.identifier.scopusauthorid | Chin, RKH=24358899900 | en_US |
dc.identifier.issnl | 0004-8666 | - |