{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,19]],"date-time":"2026-06-19T11:43:54Z","timestamp":1781869434348,"version":"3.54.5"},"reference-count":37,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2014,3,17]],"date-time":"2014-03-17T00:00:00Z","timestamp":1395014400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100000938","name":"Australian Government Department of Veterans' Affairs","doi-asserted-by":"crossref","id":[{"id":"10.13039\/501100000938","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J American Geriatrics Society"],"published-print":{"date-parts":[[2014,4]]},"abstract":"<jats:sec>\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>\n                      To determine whether there is greater risk of initiation of oxybutynin to treat urinary incontinence (\n                      <jats:styled-content style=\"fixed-case\">UI<\/jats:styled-content>\n                      ) after initiation of medicines reported to be associated with\n                      <jats:styled-content style=\"fixed-case\">UI<\/jats:styled-content>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Design<\/jats:title>\n                    <jats:p>\n                      Prescription sequence symmetry analysis (\n                      <jats:styled-content style=\"fixed-case\">PSSA<\/jats:styled-content>\n                      ).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Setting<\/jats:title>\n                    <jats:p>\n                      Administrative claims data from the\n                      <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>\n                      ustralian\n                      <jats:styled-content style=\"fixed-case\">G<\/jats:styled-content>\n                      overnment\n                      <jats:styled-content style=\"fixed-case\">D<\/jats:styled-content>\n                      epartment of\n                      <jats:styled-content style=\"fixed-case\">V<\/jats:styled-content>\n                      eterans'\n                      <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>\n                      ffairs.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Participants<\/jats:title>\n                    <jats:p>\n                      Individuals who initiated oxybutynin and a medicine reported to be associated with\n                      <jats:styled-content style=\"fixed-case\">UI<\/jats:styled-content>\n                      in a 12\u2010month period.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Measurements<\/jats:title>\n                    <jats:p>\n                      Between\n                      <jats:styled-content style=\"fixed-case\">J<\/jats:styled-content>\n                      anuary 1, 2001, and\n                      <jats:styled-content style=\"fixed-case\">D<\/jats:styled-content>\n                      ecember 31, 2011, the distribution of incident dispensing of medicines reported to be associated with\n                      <jats:styled-content style=\"fixed-case\">UI<\/jats:styled-content>\n                      (prazosin, diuretics, calcium channel blockers (\n                      <jats:styled-content style=\"fixed-case\">CCB<\/jats:styled-content>\n                      s), angiotensin\u2010converting enzyme inhibitors (\n                      <jats:styled-content style=\"fixed-case\">ACE<\/jats:styled-content>\n                      Is), angiotensin receptor blockers (\n                      <jats:styled-content style=\"fixed-case\">ARB<\/jats:styled-content>\n                      s), hormone replacement therapy (\n                      <jats:styled-content style=\"fixed-case\">HRT<\/jats:styled-content>\n                      ), opioid analgesics, anticonvulsants, levodopa, antipsychotics, sedatives, selective serotonin reuptake inhibitors (\n                      <jats:styled-content style=\"fixed-case\">SSRI<\/jats:styled-content>\n                      s), venlafaxine, anticholinesterases) was assessed before and after incident dispensing of oxybutynin (to treat\n                      <jats:styled-content style=\"fixed-case\">UI<\/jats:styled-content>\n                      ). Crude and adjusted sequence ratios (\n                      <jats:styled-content style=\"fixed-case\">ASR<\/jats:styled-content>\n                      s) with 95% confidence intervals (\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      s) were calculated.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Significant associations between initiation of\n                      <jats:styled-content style=\"fixed-case\">CCB<\/jats:styled-content>\n                      s,\n                      <jats:styled-content style=\"fixed-case\">ACEI<\/jats:styled-content>\n                      s,\n                      <jats:styled-content style=\"fixed-case\">ARB<\/jats:styled-content>\n                      s, and hypnotic\u2010sedatives and subsequent initiation of oxybutynin were found.\n                      <jats:styled-content style=\"fixed-case\">ASR<\/jats:styled-content>\n                      s ranged from 1.28 (95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      \u00a0=\u00a01.19\u20131.39) for\n                      <jats:styled-content style=\"fixed-case\">ACEI<\/jats:styled-content>\n                      s to 1.59 (95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      \u00a0=\u00a01.29\u20131.96) for verapamil. In women, there was greater risk of initiation of oxybutynin after prazosin (\n                      <jats:styled-content style=\"fixed-case\">ASR<\/jats:styled-content>\n                      \u00a0=\u00a01.84, 95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      \u00a0=\u00a01.29\u20132.63) and\n                      <jats:styled-content style=\"fixed-case\">HRT<\/jats:styled-content>\n                      (\n                      <jats:styled-content style=\"fixed-case\">ASR<\/jats:styled-content>\n                      \u00a0= 1.54, 95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      \u00a0=\u00a01.42\u20131.67) initiation.\n                      <jats:styled-content style=\"fixed-case\">PSSA<\/jats:styled-content>\n                      showed no significant association with initiation of opioids, anticonvulsants, levodopa,\n                      <jats:styled-content style=\"fixed-case\">SSRI<\/jats:styled-content>\n                      s, venlafaxine, or anticholinesterases and subsequent initiation of oxybutynin.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      This study highlights the potential for initiation of commonly used medicines to be associated with subsequent initiation of oxybutynin to treat\n                      <jats:styled-content style=\"fixed-case\">UI<\/jats:styled-content>\n                      . Greater awareness of the potential for medicines to contribute to\n                      <jats:styled-content style=\"fixed-case\">UI<\/jats:styled-content>\n                      is required.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/jgs.12741","type":"journal-article","created":{"date-parts":[[2014,3,17]],"date-time":"2014-03-17T15:43:14Z","timestamp":1395070994000},"page":"690-695","source":"Crossref","is-referenced-by-count":20,"title":["Risk of Medication\u2010Associated Initiation of Oxybutynin in Elderly Men and Women"],"prefix":"10.1111","volume":"62","author":[{"given":"Lisa M.","family":"Kalisch Ellett","sequence":"first","affiliation":[{"name":"Quality Use of Medicines and Pharmacy Research Centre School of Pharmacy and Medical Sciences University of South Australia Adelaide South Australia Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nicole L.","family":"Pratt","sequence":"additional","affiliation":[{"name":"Quality Use of Medicines and Pharmacy Research Centre School of Pharmacy and Medical Sciences University of South Australia Adelaide South Australia Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"John D.","family":"Barratt","sequence":"additional","affiliation":[{"name":"Quality Use of Medicines and Pharmacy Research Centre School of Pharmacy and Medical Sciences University of South Australia Adelaide South Australia Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Debra","family":"Rowett","sequence":"additional","affiliation":[{"name":"Quality Use of Medicines and Pharmacy Research Centre School of Pharmacy and Medical Sciences University of South Australia Adelaide South Australia Australia"},{"name":"Drug and Therapeutics Information Service Repatriation General Hospital Adelaide South Australia Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Elizabeth E.","family":"Roughead","sequence":"additional","affiliation":[{"name":"Quality Use of Medicines and Pharmacy Research Centre School of Pharmacy and Medical Sciences University of South Australia Adelaide South Australia Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2014,3,17]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.1002\/(SICI)1520-6777(1999)18:6<567::AID-NAU7>3.0.CO;2-F"},{"key":"e_1_2_6_3_1","doi-asserted-by":"publisher","DOI":"10.1093\/ageing\/afq025"},{"key":"e_1_2_6_4_1","unstructured":"Health Canada.Canada vigilance adverse reaction online database [on\u2010line]. 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