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    <Identifier>26gaa21</Identifier>
    <IdentifierDoi>10.3205/26gaa21</IdentifierDoi>
    <IdentifierUrn>urn:nbn:de:0183-26gaa216</IdentifierUrn>
    <ArticleType>Meeting Abstract</ArticleType>
    <TitleGroup>
      <Title language="en">Pharmacological Stratification of Fall-Risk-Increasing Drugs for Prevention of Fall-related Injuries in Older Adults:  A Population-Based Cohort Study</Title>
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        <PersonNames>
          <Lastname>Schechner</Lastname>
          <LastnameHeading>Schechner</LastnameHeading>
          <Firstname>Miriam</Firstname>
          <Initials>M</Initials>
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        <Address>
          <Affiliation>Institute of General Practice and Family Medicine, LMU University Hospital, LMU Munich, Munich, Germany</Affiliation>
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        <Email>Miriam.Schechner&#64;med.uni-muenchen.de</Email>
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          <Lastname>Rottenkolber</Lastname>
          <LastnameHeading>Rottenkolber</LastnameHeading>
          <Firstname>Marietta</Firstname>
          <Initials>M</Initials>
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        <Address>
          <Affiliation>Institute of General Practice and Family Medicine, LMU University Hospital, LMU Munich, Munich, Germany</Affiliation>
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          <Lastname>Oehler</Lastname>
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          <Firstname>Patrick</Firstname>
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          <Affiliation>Institute of General Practice and Family Medicine, LMU University Hospital, LMU Munich, Munich, Germany</Affiliation>
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        <PersonNames>
          <Lastname>Guthrie</Lastname>
          <LastnameHeading>Guthrie</LastnameHeading>
          <Firstname>Bruce</Firstname>
          <Initials>B</Initials>
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        <Address>
          <Affiliation>Advanced Care Research Centre, Usher Institute, University of Edinburgh, Edinburgh, United Kingdom</Affiliation>
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      <Creator>
        <PersonNames>
          <Lastname>Grill</Lastname>
          <LastnameHeading>Grill</LastnameHeading>
          <Firstname>Eva</Firstname>
          <Initials>E</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Institute for Medical Information Processing, Biometry, and Epidemiology (IBE), Faculty of Medicine, LMU Munich, Munich, Germany</Affiliation>
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        <PersonNames>
          <Lastname>Hoffmann</Lastname>
          <LastnameHeading>Hoffmann</LastnameHeading>
          <Firstname>Sabine</Firstname>
          <Initials>S</Initials>
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        <Address>
          <Affiliation>Department of Statistics, LMU Munich, Munich, Germany</Affiliation>
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      <Creator>
        <PersonNames>
          <Lastname>Piller</Lastname>
          <LastnameHeading>Piller</LastnameHeading>
          <Firstname>Johannes</Firstname>
          <Initials>J</Initials>
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        <Address>
          <Affiliation>Statistical Consulting Unit (StaBLab), LMU Munich, Munich, Germany</Affiliation>
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      <Creator>
        <PersonNames>
          <Lastname>Bender</Lastname>
          <LastnameHeading>Bender</LastnameHeading>
          <Firstname>Andreas</Firstname>
          <Initials>A</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Munich Center for Machine Learning, LMU Munich, Munich, Germany</Affiliation>
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      <Creator>
        <PersonNames>
          <Lastname>Dreischulte</Lastname>
          <LastnameHeading>Dreischulte</LastnameHeading>
          <Firstname>Tobias</Firstname>
          <Initials>T</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Institute of General Practice and Family Medicine, LMU University Hospital, LMU Munich, Munich, Germany</Affiliation>
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        <Email>Tobias.Dreischulte&#64;med.uni-muenchen.de</Email>
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    <PublisherList>
      <Publisher>
        <Corporation>
          <Corporatename>German Medical Science GMS Publishing House</Corporatename>
        </Corporation>
        <Address>D&#252;sseldorf</Address>
      </Publisher>
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    <SubjectGroup>
      <SubjectheadingDDB>610</SubjectheadingDDB>
    </SubjectGroup>
    <DatePublishedList>
      <DatePublished>20261021</DatePublished>
    </DatePublishedList>
    <Language>engl</Language>
    <License license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
      <AltText language="en">This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License.</AltText>
      <AltText language="de">Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung).</AltText>
    </License>
    <SourceGroup>
      <Meeting>
        <MeetingId>M0661</MeetingId>
        <MeetingSequence>21</MeetingSequence>
        <MeetingCorporation>Gesellschaft f&#252;r Arzneimittelanwendungsforschung und Arzneimittelepidemiologie e.V. (GAA)</MeetingCorporation>
        <MeetingName>33. Jahrestagung der Gesellschaft f&#252;r Arzneimittelanwendungsforschung und Arzneimittelepidemiologie</MeetingName>
        <MeetingTitle></MeetingTitle>
        <MeetingSession>Abstracts</MeetingSession>
        <MeetingCity>M&#252;nchen</MeetingCity>
        <MeetingDate>
          <DateFrom>20261129</DateFrom>
          <DateTo>20261130</DateTo>
        </MeetingDate>
      </Meeting>
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    <ArticleNo>26gaa21</ArticleNo>
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      <MainHeadline>Text</MainHeadline><Pgraph><Mark1>Background&#47;Aim: </Mark1>Falls are a major cause of morbidity among older adults. While deprescribing fall-risk-increasing drugs (FRIDs) is recommended for secondary prevention, their high prevalence limits efficient targeting in primary prevention. Stratification by pharmacological FRID subclasses or drugs with fall-risk-increasing adverse reactions (FRIAR-drugs) may improve identification of high-risk patients, yet their added value in routine care is uncertain.</Pgraph><Pgraph>Therefore, the aim of this study is to compare pharmacological FRID classifications with a FRIAR-based framework for predicting fall-related hospitalisations and to identify drug subgroups that differentiate fall-risk among exposed older adults in a primary prevention context.</Pgraph><Pgraph><Mark1>Methods: </Mark1>We conducted a retrospective cohort study including 120,867 adults aged &#8805;65 years prescribed at least one FRID or FRIAR-drug at baseline. Fall-related hospitalisations in 2019 were identified using ICD-10 codes. Multivariate logistic regression evaluated pharmacological FRID (sub)groups and FRIAR-drug classifications, adjusted for established general predictors. Model performance was assessed using internal validation and sensitivity analyses.</Pgraph><Pgraph><Mark1>Results: </Mark1>During follow-up, 2,788 individuals (2.3&#37;) experienced a fall-related hospitalisation. Pharmacological subgroups associated with higher risk included serotonin re-uptake inhibitors, older antiepileptics, and drugs with moderate anticholinergic properties. In contrast, the FRIAR-drug framework added little prognostic information beyond established FRID classifications. The final model demonstrated moderate discrimination (AUC 0.73) with stable predictive performance on internal validation.</Pgraph><Pgraph><Mark1>Discussion&#47;Conclusion: </Mark1>Pharmacological stratification of FRIDs allows clinically useful differentiation of fall-risk among exposed older adults, whereas FRIAR-based classification adds limited prognostic value. These findings support more selective prioritisation of medication review in primary-preventive fall strategies, although external validation and evaluation of decision-relevant risk stratification are required.</Pgraph></TextBlock>
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