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    <subfield code="2">doi</subfield>
    <subfield code="a">10.3399/bjgp12X659295</subfield>
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    <subfield code="2">sideral</subfield>
    <subfield code="a">80055</subfield>
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    <subfield code="a">ART-2012-80055</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Calderón-Larrañaga, A.</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Multimorbidity, polypharmacy, referrals, and adverse drug events: Are we doing things well?</subfield>
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  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2012</subfield>
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  <datafield tag="520" ind1="3" ind2=" ">
    <subfield code="a">Background The consequences of multimorbidity include polypharmacy and repeated referrals for specialised care, which may increase the risk of adverse drug events (ADEs).

Aim The objective of this study was to analyse the influence of multimorbidity, polypharmacy, and multiple referrals on the frequency of ADEs, as an indicator of therapeutic safety, in the context of a national healthcare system.

Design and setting This was a multicentre, retrospective, observational study of 79 089 adult patients treated during 2008 in primary care centres.

Method The explanatory patient variables sex, age, level of multimorbidity, polypharmacy, number of primary care physician visits, and number of different specialties attended were analysed. The response variable was the occurrence of ADEs. Logistic regression models were used to identify associations among the analysed variables.

Results The prevalence of individuals with at least one ADE was 0.88%. Multivariate analysis identified the following variables as risk factors for the occurrence of ADE in descending order of effect size: multimorbidity level (odds ratio [OR]Veryhigh/Low = 45.26; ORHigh/Low = 17.58; ORModerate/Low = 4.25), polypharmacy (OR = 1.34), female sex (OR = 1.31), number of different specialties (OR = 1.20), and number of primary care physician visits (OR = 1.01). Age, however, did not show statistical significance (OR = 1.00; 95% confidence interval = 0.996 to 1.005).

Conclusion The results of this study demonstrate that multimorbidity is strongly related to the occurrence of ADEs, insofar as it requires the intervention of multiple specialties and the prescription of multiple medications. Further research should shed light on the causal pathway between multimorbidity and increased risk of adverse events.</subfield>
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    <subfield code="a">All rights reserved</subfield>
    <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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    <subfield code="a">2.034</subfield>
    <subfield code="b">2012</subfield>
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    <subfield code="a">PRIMARY HEALTH CARE</subfield>
    <subfield code="b">3 / 18 = 0.167</subfield>
    <subfield code="c">2012</subfield>
    <subfield code="d">Q1</subfield>
    <subfield code="e">T1</subfield>
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    <subfield code="a">MEDICINE, GENERAL &amp; INTERNAL</subfield>
    <subfield code="b">41 / 153 = 0.268</subfield>
    <subfield code="c">2012</subfield>
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    <subfield code="a">Poblador-Plou, B.</subfield>
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    <subfield code="a">González-Rubio, F.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-2580-2002</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Gimeno-Feliu, L.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-2928-6623</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Abad-Díez, J. M.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-9466-3902</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Prados-Torres, A.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-5704-6056</subfield>
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  <datafield tag="710" ind1="2" ind2=" ">
    <subfield code="1">1007</subfield>
    <subfield code="2">610</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Medicina, Psiqu. y Derm.</subfield>
    <subfield code="c">Area Medicina</subfield>
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  <datafield tag="710" ind1="2" ind2=" ">
    <subfield code="1">1008</subfield>
    <subfield code="2">615</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Microb.Med.Pr.,Sal.Públ.</subfield>
    <subfield code="c">Área Medic.Prevent.Salud Públ.</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">62, 605 (2012), e821-e826</subfield>
    <subfield code="p">Br. j. gen. pract.</subfield>
    <subfield code="t">BRITISH JOURNAL OF GENERAL PRACTICE</subfield>
    <subfield code="x">0960-1643</subfield>
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