{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,5]],"date-time":"2026-06-05T10:11:13Z","timestamp":1780654273486,"version":"3.54.1"},"reference-count":35,"publisher":"Cambridge University Press (CUP)","issue":"4","license":[{"start":{"date-parts":[[2015,10,21]],"date-time":"2015-10-21T00:00:00Z","timestamp":1445385600000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/www.cambridge.org\/core\/terms"}],"content-domain":{"domain":["journals.cambridge.org"],"crossmark-restriction":true},"short-container-title":["Prim Health Care Res Dev"],"published-print":{"date-parts":[[2016,7]]},"abstract":"<jats:sec id=\"S1463423615000456_abs1\" sec-type=\"general\">\n                    <jats:title>Background and aim<\/jats:title>\n                    <jats:p>Current health-care delivery requires increasingly proactive and\n                     inter-professional work. Therefore, collecting patient information and\n                     knowledge management is of paramount importance. General practitioners (GPs)\n                     are well placed to lead these evolving models of care delivery. However, it is\n                     unclear how they are handling these changes. To gain an insight into this\n                     matter, the HIV epidemic was chosen as a test case.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S1463423615000456_abs2\" sec-type=\"methods\">\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>Data were collected and analysed from 13 semi-structured interviews with\n                     GPs, working in urban communities in Flanders.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S1463423615000456_abs3\" sec-type=\"general\">\n                    <jats:title>Findings<\/jats:title>\n                    <jats:p>\n                      GPs use various types of patient information to estimate patients\u2019 risk of\n                     HIV. The way in which sexual health information is collected and registered,\n                     depends on the type of information under discussion.\n                      <jats:italic>General\n                        patient information<\/jats:italic>\n                      and\n                      <jats:italic>medical history\n                        data<\/jats:italic>\n                      are often automatically collected and registered.\n                     Proactively collecting\n                      <jats:italic>sexual health information<\/jats:italic>\n                      is\n                     uncommon. Moreover, the registration of the latter is not obvious, mostly owing\n                     to insufficient space in the electronic medical record (EMR).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"S1463423615000456_abs4\" sec-type=\"conclusions\">\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      GPs seem willing to systematically collect and register\n                      <jats:italic>sexual health information<\/jats:italic>\n                      , in particular about\n                     HIV-risk factors. They expressed a need for guidance together with practical\n                     adjustments of the EMR to adequately capture and share this\n                     information.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1017\/s1463423615000456","type":"journal-article","created":{"date-parts":[[2015,10,21]],"date-time":"2015-10-21T00:03:07Z","timestamp":1445385787000},"page":"333-350","update-policy":"https:\/\/doi.org\/10.1017\/policypage","source":"Crossref","is-referenced-by-count":8,"title":["Collecting and registering sexual health information in the context of HIV\n                  risk in the electronic medical record of general practitioners: a qualitative\n                  exploration of the preference of general practitioners in urban communities in\n                  Flanders (Belgium)"],"prefix":"10.1017","volume":"17","author":[{"given":"Jolien","family":"Vos","sequence":"first","affiliation":[{"name":"University of Lincoln"},{"name":"Ghent University"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Peter","family":"Pype","sequence":"additional","affiliation":[{"name":"Ghent University"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jessika","family":"Deblonde","sequence":"additional","affiliation":[{"name":"Belgian Scientific Institute of Public Health"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sandra","family":"Van den Eynde","sequence":"additional","affiliation":[{"name":"Sensoa"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Karolien","family":"Aelbrecht","sequence":"additional","affiliation":[{"name":"Ghent University"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Myriam","family":"Deveugele","sequence":"additional","affiliation":[{"name":"Ghent University"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dirk","family":"Avonts","sequence":"additional","affiliation":[{"name":"Ghent 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