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The main objective of this study was to examine pain medication regimens according to pain intensity following PFF. Furthermore, we explored the utilization of medication plans.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>The \u201cProFem\u201d\u2010study on healthcare provision, functional ability, and quality of life after PFF is a German population\u2010based prospective cohort study based on statutory health insurance data and individually linked survey data from different time points including information on the currently used medication. This present analysis refers to the participants' baseline interviews (about 3\u2009months following PFF) conducted from 2018 to 2019 in the participants' private surroundings.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>The study population comprised 444 participants (mean age: 81.2\u2009years, 71.0% female). Half of them reported high intensity pain, and the mean value for the EuroQol visual analogue scale was 50.8. Most commonly used analgesics were metamizole and tilidine\/naloxone. Among participants with high intensity pain, 21.9% received only PRN pain medication and 17.2% no pain medication at all. Overall, 61.5% of participants presented any (printed) medication plan and only 25.2% a \u201cfederal standardized medication plan\u201d (BMP).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>As a substantial number of patients reports high intensity pain about 3\u2009months following a PFF, the large proportion of those receiving no or only PRN pain medication raises questions regarding the appropriateness of the therapy. The overall low utilization of the BMP indicates potential for improvement.<\/jats:p><\/jats:sec>","DOI":"10.1002\/pds.5865","type":"journal-article","created":{"date-parts":[[2024,8,13]],"date-time":"2024-08-13T07:14:54Z","timestamp":1723533294000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Pain Medication and Pain Intensity Following Hip Fractures\u2014Analyses Based on the <scp>ProFem<\/scp> Cohort Study"],"prefix":"10.1002","volume":"33","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3957-9721","authenticated-orcid":false,"given":"Kathrin","family":"Jobski","sequence":"first","affiliation":[{"name":"Department of Health Services Research Carl von Ossietzky Universit\u00e4t Oldenburg  Oldenburg Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michaela","family":"Ritschel","sequence":"additional","affiliation":[{"name":"Institute for Health Services Research and Health Economics, 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