{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,25]],"date-time":"2026-04-25T02:33:06Z","timestamp":1777084386460,"version":"3.51.4"},"reference-count":26,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2013,10,1]],"date-time":"2013-10-01T00:00:00Z","timestamp":1380585600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["obgyn.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["BJOG"],"published-print":{"date-parts":[[2014,1]]},"abstract":"<jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To investigate the anatomical cure rate and complications related to collagen\u2010coated mesh for cystocele, compared with a conventional anterior colporrhaphy.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Design<\/jats:title>\n                    <jats:p>A randomised controlled study.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Setting<\/jats:title>\n                    <jats:p>Six departments of obstetrics and gynaecology in Norway, Sweden, Finland, and Denmark.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Population<\/jats:title>\n                    <jats:p>Women aged 55\u00a0years or older, referred for surgery with a prolapse of the anterior vaginal wall of stage\u00a02 or higher.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Women scheduled for primary cystocoele surgery were randomised to either anterior colporrhaphy or a collagen\u2010coated Prolene mesh. Power analysis indicated that 130 patients had to be randomised. All patients were evaluated using the Pelvic Organ Prolapse\u2010Quantification (\n                      <jats:styled-content style=\"fixed-case\">POP<\/jats:styled-content>\n                      \u2010Q) measurement. Quality of life, symptoms, and sexual function were evaluated using the Pelvic Floor Impact Questionnaire, the Pelvic Floor Distress Inventory, and the Pelvic Organ Prolapse\/Urinary Incontinence Sexual Questionnaire.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Main outcome measures<\/jats:title>\n                    <jats:p>\n                      The primary outcome was objective cure, defined as prolapse below\n                      <jats:styled-content style=\"fixed-case\">POP<\/jats:styled-content>\n                      \u2010Q stage\u00a02 at the 12\u2010months follow\u2010up. Secondary outcomes were quality of life, symptoms, and presence (or not) of complications.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      In total, 161 women were randomised to either anterior colporrhaphy or mesh (participant ages 64.9\u00a0\u00b1\u00a06.4\u00a0years versus 64.7\u00a0\u00b1\u00a06.6\u00a0years, respectively; mean\u00a0\u00b1\u00a0\n                      <jats:styled-content style=\"fixed-case\">SD<\/jats:styled-content>\n                      ). The objective cure rate was 39.8% (95%\u00a0\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      28.6\u201350.9%) in the anterior colporrhaphy group, compared with 88.1% (95%\u00a0\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      80.7\u201395.6%) in the mesh group (\n                      <jats:italic>P<\/jats:italic>\n                      \u00a0&lt;\u00a00.001). Vaginal mesh exposure occurred in ten women (13.3%) and dyspareunia occurred in two women (2.7%, not significant) in the mesh group at the 12\u2010months follow\u2010up. Questionnaires revealed no difference between the groups.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Our study demonstrates a significantly improved objective cure rate associated with a high exposure rate among women with mesh surgery as opposed to conventional surgery.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/1471-0528.12454","type":"journal-article","created":{"date-parts":[[2013,10,11]],"date-time":"2013-10-11T21:26:49Z","timestamp":1381526809000},"page":"102-111","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":46,"title":["Anterior colporrhaphy compared with collagen\u2010coated transvaginal mesh for anterior vaginal wall prolapse: a randomised controlled trial"],"prefix":"10.1111","volume":"121","author":[{"given":"M","family":"Rudnicki","sequence":"first","affiliation":[{"name":"Department of Obstetrics and Gynaecology Roskilde University Hospital Roskilde Denmark"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E","family":"Laurikainen","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynaecology Turku University Hospital Turku Finland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R","family":"Pogosean","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynaecology Lidk\u00f6ping Hospital Lidk\u00f6ping Sweden"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I","family":"Kinne","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynaecology Ahus University Hospital Ahus Norway"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"U","family":"Jakobsson","sequence":"additional","affiliation":[{"name":"Center for Primary Healthcare Research Faculty of Medicine Lund University Lund Sweden"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P","family":"Teleman","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynaecology Skane University Hospital Lund Lund University Lund Sweden"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2013,10]]},"reference":[{"key":"e_1_2_7_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0029-7844(97)00058-6"},{"key":"e_1_2_7_3_1","doi-asserted-by":"publisher","DOI":"10.1067\/mob.2001.119081"},{"key":"e_1_2_7_4_1","doi-asserted-by":"publisher","DOI":"10.1097\/AOG.0b013e31816a2489"},{"key":"e_1_2_7_5_1","doi-asserted-by":"publisher","DOI":"10.1007\/s00192-009-1018-3"},{"key":"e_1_2_7_6_1","doi-asserted-by":"publisher","DOI":"10.1007\/s00192-010-1153-x"},{"key":"e_1_2_7_7_1","doi-asserted-by":"publisher","DOI":"10.1097\/AOG.0b013e318237edc4"},{"key":"e_1_2_7_8_1","doi-asserted-by":"publisher","DOI":"10.1056\/NEJMoa1009521"},{"issue":"360","key":"e_1_2_7_9_1","first-page":"e1","article-title":"Laparoscopic sacral colpopey versus total vaginal mesh for vaginal vault prolapse: a randomized trial","volume":"204","author":"Maher CF","year":"2011","journal-title":"Am J Obstet Gynecol"},{"issue":"83","key":"e_1_2_7_10_1","first-page":"e1","article-title":"Surgical intervention after transvaginal Prolift mesh repair: retrospective single\u2010center study including 524 patients with 3\u00a0years' median follow\u2010up","volume":"206","author":"Landsheere L","year":"2012","journal-title":"Am J Obstet Gynecol"},{"key":"e_1_2_7_11_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1471-0528.2009.02254.x"},{"key":"e_1_2_7_12_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1471-0528.2011.03082.x"},{"key":"e_1_2_7_13_1","doi-asserted-by":"publisher","DOI":"10.1002\/nau.21064"},{"key":"e_1_2_7_14_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jmig.2007.02.003"},{"key":"e_1_2_7_15_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajog.2007.12.029"},{"key":"e_1_2_7_16_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ejogrb.2011.01.027"},{"key":"e_1_2_7_17_1","unstructured":"[http:\/\/www.fda.gov\/downloads\/advisorycommittees\/committeesmeetingmaterials\/medicaldevices\/medicaldevicesadvisorycommittee\/obstetricsandgynecologydevices\/ucm270402.pdf]. 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