A Canadian, Multicentre Study Comparing the Efficacy of a Levonorgestrel-releasing Intrauterine System to an Oral Contraceptive in Women With Idiopathic Menorrhagia
Abstract Objectives To evaluate the efficacy of a levonorgestrel-releasing intrauterine system (LNG-IUS) compared with a combined oral contraceptive containing 1 mg norethindrone acetate and 20 μg ethinyl estradiol (OC1/20) in reducing menstrual blood loss (MBL) in women with idiopathic menorrhagia....
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Veröffentlicht in: | Journal of obstetrics and gynaecology Canada 2009-04, Vol.31 (4), p.340-347 |
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creator | Endrikat, Jan, MD, PhD Shapiro, Heather, MD, FRCRC Lukkari-Lax, Eeva, MD Kunz, Michael, PhD Schmidt, Werner, MD, PhD Fortier, Michel, MD |
description | Abstract Objectives To evaluate the efficacy of a levonorgestrel-releasing intrauterine system (LNG-IUS) compared with a combined oral contraceptive containing 1 mg norethindrone acetate and 20 μg ethinyl estradiol (OC1/20) in reducing menstrual blood loss (MBL) in women with idiopathic menorrhagia. Methods A prospective, randomized, open-label study was conducted in nine centres in Canada. Healthy women over 30 years of age suffering from idiopathic menorrhagia were treated either with LNG-IUS (n = 20) or with OC1/20 (n = 19) over 12 months. The primary endpoint was the change in MBL from baseline to 12 months. Secondary endpoints included treatment success (defined as a MBL score < 100 after 12 months), hemoglobin levels, and the menorrhagia severity score. Results In both treatment groups, MBL decreased significantly from baseline to 12 months ( P < 0.001). For the primary endpoint, the MBL score decreased significantly more in the LNG-IUS group (median from 228 to 13, mean percent change–83%) compared to the OC1/20 group (median from 290 to 72; mean percent change–68%) ( P = 0.002) after 12 months. In the LNG-IUS group, 80% of subjects had treatment success compared with 36.8 % in the OC1/20 group ( P < 0.009). Both treatments increased hemoglobin concentrations significantly between baseline and 12 months. The menorrhagia severity score was consistently lower in the LNG-IUS group at all study time points and was significantly lower ( P = 0.045) at six months. Both treatments were well tolerated. Conclusion Both the LNG-IUS and the combined oral contraceptive effectively decreased menstrual blood loss in women with idiopathic menorrhagia. The overall clinical benefit was more pronounced with LNG-IUS than with OC1/20. |
doi_str_mv | 10.1016/S1701-2163(16)34151-2 |
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Methods A prospective, randomized, open-label study was conducted in nine centres in Canada. Healthy women over 30 years of age suffering from idiopathic menorrhagia were treated either with LNG-IUS (n = 20) or with OC1/20 (n = 19) over 12 months. The primary endpoint was the change in MBL from baseline to 12 months. Secondary endpoints included treatment success (defined as a MBL score < 100 after 12 months), hemoglobin levels, and the menorrhagia severity score. Results In both treatment groups, MBL decreased significantly from baseline to 12 months ( P < 0.001). For the primary endpoint, the MBL score decreased significantly more in the LNG-IUS group (median from 228 to 13, mean percent change–83%) compared to the OC1/20 group (median from 290 to 72; mean percent change–68%) ( P = 0.002) after 12 months. In the LNG-IUS group, 80% of subjects had treatment success compared with 36.8 % in the OC1/20 group ( P < 0.009). Both treatments increased hemoglobin concentrations significantly between baseline and 12 months. The menorrhagia severity score was consistently lower in the LNG-IUS group at all study time points and was significantly lower ( P = 0.045) at six months. Both treatments were well tolerated. Conclusion Both the LNG-IUS and the combined oral contraceptive effectively decreased menstrual blood loss in women with idiopathic menorrhagia. The overall clinical benefit was more pronounced with LNG-IUS than with OC1/20.</description><identifier>ISSN: 1701-2163</identifier><identifier>DOI: 10.1016/S1701-2163(16)34151-2</identifier><identifier>PMID: 19497153</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Adult ; Canada ; Contraceptive Agents, Female - administration & dosage ; Contraceptives, Oral, Synthetic - therapeutic use ; Estrogens - therapeutic use ; Ethinyl Estradiol - therapeutic use ; Female ; Hemoglobins - analysis ; Humans ; idiopathic menorrhagia ; Intrauterine Devices, Medicated ; Levonorgestrel - administration & dosage ; Levonorgestrel-releasing intrauterine system ; Menorrhagia - drug therapy ; Norethindrone - analogs & derivatives ; Norethindrone - therapeutic use ; Obstetrics and Gynecology ; oral contraceptive ; Prospective Studies ; Severity of Illness Index</subject><ispartof>Journal of obstetrics and gynaecology Canada, 2009-04, Vol.31 (4), p.340-347</ispartof><rights>Society of Obstetricians and Gynaecologists of Canada</rights><rights>2009 Society of Obstetricians and Gynaecologists of Canada</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-ac285141b45dc4ed03290b6a960a39dab724266c6c755439dcd87cbdb6b8547b3</citedby><cites>FETCH-LOGICAL-c418t-ac285141b45dc4ed03290b6a960a39dab724266c6c755439dcd87cbdb6b8547b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19497153$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Endrikat, Jan, MD, PhD</creatorcontrib><creatorcontrib>Shapiro, Heather, MD, FRCRC</creatorcontrib><creatorcontrib>Lukkari-Lax, Eeva, MD</creatorcontrib><creatorcontrib>Kunz, Michael, PhD</creatorcontrib><creatorcontrib>Schmidt, Werner, MD, PhD</creatorcontrib><creatorcontrib>Fortier, Michel, MD</creatorcontrib><title>A Canadian, Multicentre Study Comparing the Efficacy of a Levonorgestrel-releasing Intrauterine System to an Oral Contraceptive in Women With Idiopathic Menorrhagia</title><title>Journal of obstetrics and gynaecology Canada</title><addtitle>J Obstet Gynaecol Can</addtitle><description>Abstract Objectives To evaluate the efficacy of a levonorgestrel-releasing intrauterine system (LNG-IUS) compared with a combined oral contraceptive containing 1 mg norethindrone acetate and 20 μg ethinyl estradiol (OC1/20) in reducing menstrual blood loss (MBL) in women with idiopathic menorrhagia. Methods A prospective, randomized, open-label study was conducted in nine centres in Canada. Healthy women over 30 years of age suffering from idiopathic menorrhagia were treated either with LNG-IUS (n = 20) or with OC1/20 (n = 19) over 12 months. The primary endpoint was the change in MBL from baseline to 12 months. Secondary endpoints included treatment success (defined as a MBL score < 100 after 12 months), hemoglobin levels, and the menorrhagia severity score. Results In both treatment groups, MBL decreased significantly from baseline to 12 months ( P < 0.001). For the primary endpoint, the MBL score decreased significantly more in the LNG-IUS group (median from 228 to 13, mean percent change–83%) compared to the OC1/20 group (median from 290 to 72; mean percent change–68%) ( P = 0.002) after 12 months. In the LNG-IUS group, 80% of subjects had treatment success compared with 36.8 % in the OC1/20 group ( P < 0.009). Both treatments increased hemoglobin concentrations significantly between baseline and 12 months. The menorrhagia severity score was consistently lower in the LNG-IUS group at all study time points and was significantly lower ( P = 0.045) at six months. Both treatments were well tolerated. Conclusion Both the LNG-IUS and the combined oral contraceptive effectively decreased menstrual blood loss in women with idiopathic menorrhagia. The overall clinical benefit was more pronounced with LNG-IUS than with OC1/20.</description><subject>Adult</subject><subject>Canada</subject><subject>Contraceptive Agents, Female - administration & dosage</subject><subject>Contraceptives, Oral, Synthetic - therapeutic use</subject><subject>Estrogens - therapeutic use</subject><subject>Ethinyl Estradiol - therapeutic use</subject><subject>Female</subject><subject>Hemoglobins - analysis</subject><subject>Humans</subject><subject>idiopathic menorrhagia</subject><subject>Intrauterine Devices, Medicated</subject><subject>Levonorgestrel - administration & dosage</subject><subject>Levonorgestrel-releasing intrauterine system</subject><subject>Menorrhagia - drug therapy</subject><subject>Norethindrone - analogs & derivatives</subject><subject>Norethindrone - therapeutic use</subject><subject>Obstetrics and Gynecology</subject><subject>oral contraceptive</subject><subject>Prospective Studies</subject><subject>Severity of Illness Index</subject><issn>1701-2163</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhnMA0VL4CSCfEEgE4nw4mwuoWpV2pa16KIijNbEnuy6JHWxnpfwffiiT7gokLkj-0IzfeUaeN0le8ewDz7j4eM_rjKc5F8VbLt4VJa8oepKc_0mfJc9DeMiyqi7q5llyxpuyqXlVnCe_LtkaLGgD9j27nfpoFNrokd3HSc9s7YYRvLE7FvfIrrrOKFAzcx0DtsWDs87vMJC-T2kjhEW6IQBMEamOOHOIOLDoGFh256En5vKucIzmgMxY9t0NSKeJe7bRxo0Q90axWyS438POwIvkaQd9wJen-yL59uXq6_om3d5db9aX21SVfBVTUPmq4iVvy0qrEnVW5E3WCmhEBkWjoa3zMhdCCVVXVUkZpVe1anUr2lVV1m1xkbw5ckfvfk70LzmYoLDvwaKbghQ1ERshSFgdhcq7EDx2cvRmAD9LnsnFEvloiVxmLyl6tETmVPf61GBqB9R_q05-kODzUYD0zYNBL4MyaBVq41FFqZ35b4tP_xBUbyzZ1v_AGcODm7ylGUouQy6zI2Rh0FoIefEb11W0_Q</recordid><startdate>20090401</startdate><enddate>20090401</enddate><creator>Endrikat, Jan, MD, PhD</creator><creator>Shapiro, Heather, MD, FRCRC</creator><creator>Lukkari-Lax, Eeva, MD</creator><creator>Kunz, Michael, PhD</creator><creator>Schmidt, Werner, MD, PhD</creator><creator>Fortier, Michel, MD</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20090401</creationdate><title>A Canadian, Multicentre Study Comparing the Efficacy of a Levonorgestrel-releasing Intrauterine System to an Oral Contraceptive in Women With Idiopathic Menorrhagia</title><author>Endrikat, Jan, MD, PhD ; Shapiro, Heather, MD, FRCRC ; Lukkari-Lax, Eeva, MD ; Kunz, Michael, PhD ; Schmidt, Werner, MD, PhD ; Fortier, Michel, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-ac285141b45dc4ed03290b6a960a39dab724266c6c755439dcd87cbdb6b8547b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Canada</topic><topic>Contraceptive Agents, Female - administration & dosage</topic><topic>Contraceptives, Oral, Synthetic - therapeutic use</topic><topic>Estrogens - therapeutic use</topic><topic>Ethinyl Estradiol - therapeutic use</topic><topic>Female</topic><topic>Hemoglobins - analysis</topic><topic>Humans</topic><topic>idiopathic menorrhagia</topic><topic>Intrauterine Devices, Medicated</topic><topic>Levonorgestrel - administration & dosage</topic><topic>Levonorgestrel-releasing intrauterine system</topic><topic>Menorrhagia - drug therapy</topic><topic>Norethindrone - analogs & derivatives</topic><topic>Norethindrone - therapeutic use</topic><topic>Obstetrics and Gynecology</topic><topic>oral contraceptive</topic><topic>Prospective Studies</topic><topic>Severity of Illness Index</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Endrikat, Jan, MD, PhD</creatorcontrib><creatorcontrib>Shapiro, Heather, MD, FRCRC</creatorcontrib><creatorcontrib>Lukkari-Lax, Eeva, MD</creatorcontrib><creatorcontrib>Kunz, Michael, PhD</creatorcontrib><creatorcontrib>Schmidt, Werner, MD, PhD</creatorcontrib><creatorcontrib>Fortier, Michel, MD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of obstetrics and gynaecology Canada</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Endrikat, Jan, MD, PhD</au><au>Shapiro, Heather, MD, FRCRC</au><au>Lukkari-Lax, Eeva, MD</au><au>Kunz, Michael, PhD</au><au>Schmidt, Werner, MD, PhD</au><au>Fortier, Michel, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Canadian, Multicentre Study Comparing the Efficacy of a Levonorgestrel-releasing Intrauterine System to an Oral Contraceptive in Women With Idiopathic Menorrhagia</atitle><jtitle>Journal of obstetrics and gynaecology Canada</jtitle><addtitle>J Obstet Gynaecol Can</addtitle><date>2009-04-01</date><risdate>2009</risdate><volume>31</volume><issue>4</issue><spage>340</spage><epage>347</epage><pages>340-347</pages><issn>1701-2163</issn><abstract>Abstract Objectives To evaluate the efficacy of a levonorgestrel-releasing intrauterine system (LNG-IUS) compared with a combined oral contraceptive containing 1 mg norethindrone acetate and 20 μg ethinyl estradiol (OC1/20) in reducing menstrual blood loss (MBL) in women with idiopathic menorrhagia. Methods A prospective, randomized, open-label study was conducted in nine centres in Canada. Healthy women over 30 years of age suffering from idiopathic menorrhagia were treated either with LNG-IUS (n = 20) or with OC1/20 (n = 19) over 12 months. The primary endpoint was the change in MBL from baseline to 12 months. Secondary endpoints included treatment success (defined as a MBL score < 100 after 12 months), hemoglobin levels, and the menorrhagia severity score. Results In both treatment groups, MBL decreased significantly from baseline to 12 months ( P < 0.001). For the primary endpoint, the MBL score decreased significantly more in the LNG-IUS group (median from 228 to 13, mean percent change–83%) compared to the OC1/20 group (median from 290 to 72; mean percent change–68%) ( P = 0.002) after 12 months. In the LNG-IUS group, 80% of subjects had treatment success compared with 36.8 % in the OC1/20 group ( P < 0.009). Both treatments increased hemoglobin concentrations significantly between baseline and 12 months. The menorrhagia severity score was consistently lower in the LNG-IUS group at all study time points and was significantly lower ( P = 0.045) at six months. Both treatments were well tolerated. Conclusion Both the LNG-IUS and the combined oral contraceptive effectively decreased menstrual blood loss in women with idiopathic menorrhagia. The overall clinical benefit was more pronounced with LNG-IUS than with OC1/20.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>19497153</pmid><doi>10.1016/S1701-2163(16)34151-2</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Canada Contraceptive Agents, Female - administration & dosage Contraceptives, Oral, Synthetic - therapeutic use Estrogens - therapeutic use Ethinyl Estradiol - therapeutic use Female Hemoglobins - analysis Humans idiopathic menorrhagia Intrauterine Devices, Medicated Levonorgestrel - administration & dosage Levonorgestrel-releasing intrauterine system Menorrhagia - drug therapy Norethindrone - analogs & derivatives Norethindrone - therapeutic use Obstetrics and Gynecology oral contraceptive Prospective Studies Severity of Illness Index |
title | A Canadian, Multicentre Study Comparing the Efficacy of a Levonorgestrel-releasing Intrauterine System to an Oral Contraceptive in Women With Idiopathic Menorrhagia |
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