{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,2]],"date-time":"2026-09-02T10:13:23Z","timestamp":1788344003650,"version":"build-2803163510"},"reference-count":27,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2015,12,21]],"date-time":"2015-12-21T00:00:00Z","timestamp":1450656000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["bjui-journals.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["BJU International"],"published-print":{"date-parts":[[2016,5]]},"abstract":"<jats:sec>\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>\n                      To report the results from a prospective multicentric study of patients with Peyronie's disease (\n                      <jats:styled-content style=\"fixed-case\">PD<\/jats:styled-content>\n                      ) treated with the \u2018sliding\u2019 technique (\n                      <jats:styled-content style=\"fixed-case\">ST<\/jats:styled-content>\n                      ).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Patients and Methods<\/jats:title>\n                    <jats:p>\n                      From June 2010 to January 2014, 28 consecutive patients affected by stable\n                      <jats:styled-content style=\"fixed-case\">PD<\/jats:styled-content>\n                      with severe penile shortening and end\u2010stage erectile dysfunction (\n                      <jats:styled-content style=\"fixed-case\">ED<\/jats:styled-content>\n                      ) were enrolled in three European\n                      <jats:styled-content style=\"fixed-case\">PD<\/jats:styled-content>\n                      tertiary referral centres. The validated International Index of Erectile Function (\n                      <jats:styled-content style=\"fixed-case\">IIEF<\/jats:styled-content>\n                      ) questionnaire, the Sexual Encounter Profile (\n                      <jats:styled-content style=\"fixed-case\">SEP<\/jats:styled-content>\n                      ) Questions 2 and 3, and the Peyronie's disease questionnaire (\n                      <jats:styled-content style=\"fixed-case\">PDQ<\/jats:styled-content>\n                      ) were completed preoperatively by all patients. At the follow\u2010up visits (at 3, 6 and 12 months), the\n                      <jats:styled-content style=\"fixed-case\">IIEF<\/jats:styled-content>\n                      , the\n                      <jats:styled-content style=\"fixed-case\">SEP<\/jats:styled-content>\n                      Questions 2 and 3, the\n                      <jats:styled-content style=\"fixed-case\">PDQ<\/jats:styled-content>\n                      , and the Erectile Dysfunction Inventory of Treatment Satisfaction (\n                      <jats:styled-content style=\"fixed-case\">EDITS<\/jats:styled-content>\n                      ) were completed. The outcome analysis was focused on penile length restoration, and intra\u2010 and postoperative complications classified according the Clavien\u2013Dindo Classification.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The mean (range) follow\u2010up was 37 (9\u201360) months. A malleable penile prosthesis (\n                      <jats:styled-content style=\"fixed-case\">PP<\/jats:styled-content>\n                      ) was implanted in seven patients, while an inflatable three\u2010pieces\n                      <jats:styled-content style=\"fixed-case\">PP<\/jats:styled-content>\n                      was placed in the remainder. In the case of inflatable\n                      <jats:styled-content style=\"fixed-case\">PP<\/jats:styled-content>\n                      implantation, porcine small intestinal submucosa and acellular porcine dermal matrix were used to cover the tunical defects. While in patients undergoing malleable\n                      <jats:styled-content style=\"fixed-case\">PP<\/jats:styled-content>\n                      implantation, collagen\u2010fibrin sponge was used. The mean operative time was 145 min in the inflatable\n                      <jats:styled-content style=\"fixed-case\">PP<\/jats:styled-content>\n                      group and 115 min in the malleable\n                      <jats:styled-content style=\"fixed-case\">PP<\/jats:styled-content>\n                      group. There were no intraoperative complications. Postoperative complications included profuse bleeding requiring a blood transfusion in one patient (3.5%) on anticoagulation therapy for a mechanical heart valve (Grade\n                      <jats:styled-content style=\"fixed-case\">II<\/jats:styled-content>\n                      ) and\n                      <jats:styled-content style=\"fixed-case\">PP<\/jats:styled-content>\n                      infection requiring the removal of the device (7%) (Grade\n                      <jats:styled-content style=\"fixed-case\">III<\/jats:styled-content>\n                      ). There were no late recurrences of the shaft deformation. The postoperative functional data showed a progressive improvement in the score of all questionnaires, peaking at 12 months postoperatively. The mean (range) penile lengthening was 3.2 (2.5\u20134) cm and no patient reported recurrence of the curvature.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      The present series suggests that, in the hands of experienced high\u2010volume surgeons, penile length restoration with the use of the\n                      <jats:styled-content style=\"fixed-case\">ST<\/jats:styled-content>\n                      represents an effective option for end\u2010stage\n                      <jats:styled-content style=\"fixed-case\">PD<\/jats:styled-content>\n                      associated with\n                      <jats:styled-content style=\"fixed-case\">ED<\/jats:styled-content>\n                      and severe shortening of the shaft. Larger series and longer follow\u2010up will be required to fully establish the efficacy of this procedure.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/bju.13371","type":"journal-article","created":{"date-parts":[[2015,12,21]],"date-time":"2015-12-21T00:53:54Z","timestamp":1450659234000},"page":"814-820","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":64,"title":["A prospective multicentric international study on the surgical outcomes and patients\u2019 satisfaction rates of the \u2018sliding\u2019 technique for end\u2010stage Peyronie's disease with severe shortening of the penis and erectile dysfunction"],"prefix":"10.1111","volume":"117","author":[{"given":"Luigi","family":"Rolle","sequence":"first","affiliation":[{"name":"Department of Urology Citt\u00e0 della Salute e della Scienza University of Turin  Turin 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