La maladie de Parkinson au Canada (serveur d'exploration)

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Associations between Anticholinergic Burden and Adverse Health Outcomes in Parkinson Disease

Identifieur interne : 000435 ( Main/Exploration ); précédent : 000434; suivant : 000436

Associations between Anticholinergic Burden and Adverse Health Outcomes in Parkinson Disease

Auteurs : James A. G. Crispo [Canada, États-Unis] ; Allison W. Willis [États-Unis] ; Dylan P. Thibault [États-Unis] ; Yannick Fortin [Canada] ; Harlen D. Hays [États-Unis] ; Douglas S. Mcnair [États-Unis] ; Lise M. Bjerre [Canada] ; Dafna E. Kohen [Canada] ; Santiago Perez-Lloret [Argentine] ; Donald R. Mattison [Canada] ; Daniel Krewski [Canada]

Source :

RBID : PMC:4777375

English descriptors

Abstract

Background

Elderly adults should avoid medications with anticholinergic effects since they may increase the risk of adverse events, including falls, delirium, and cognitive impairment. However, data on anticholinergic burden are limited in subpopulations, such as individuals with Parkinson disease (PD). The objective of this study was to determine whether anticholinergic burden was associated with adverse outcomes in a PD inpatient population.

Methods

Using the Cerner Health Facts® database, we retrospectively examined anticholinergic medication use, diagnoses, and hospital revisits within a cohort of 16,302 PD inpatients admitted to a Cerner hospital between 2000 and 2011. Anticholinergic burden was computed using the Anticholinergic Risk Scale (ARS). Primary outcomes were associations between ARS score and diagnosis of fracture and delirium. Secondary outcomes included associations between ARS score and 30-day hospital revisits.

Results

Many individuals (57.8%) were prescribed non-PD medications with moderate to very strong anticholinergic potential. Individuals with the greatest ARS score (≥4) were more likely to be diagnosed with fractures (adjusted odds ratio (AOR): 1.56, 95% CI: 1.29–1.88) and delirium (AOR: 1.61, 95% CI: 1.08–2.40) relative to those with no anticholinergic burden. Similarly, inpatients with the greatest ARS score were more likely to visit the emergency department (adjusted hazard ratio (AHR): 1.32, 95% CI: 1.10–1.58) and be readmitted (AHR: 1.16, 95% CI: 1.01–1.33) within 30-days of discharge.

Conclusions

We found a positive association between increased anticholinergic burden and adverse outcomes among individuals with PD. Additional pharmacovigilance studies are needed to better understand risks associated with anticholinergic medication use in PD.


Url:
DOI: 10.1371/journal.pone.0150621
PubMed: 26939130
PubMed Central: 4777375


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="aff011">
<addr-line>Risk Sciences International, Ottawa, Ontario, Canada</addr-line>
</nlm:aff>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Risk Sciences International, Ottawa, Ontario</wicri:regionArea>
<wicri:noRegion>Ontario</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Krewski, Daniel" sort="Krewski, Daniel" uniqKey="Krewski D" first="Daniel" last="Krewski">Daniel Krewski</name>
<affiliation wicri:level="1">
<nlm:aff id="aff001">
<addr-line>McLaughlin Centre for Population Health Risk Assessment, University of Ottawa, Ottawa, Ontario, Canada</addr-line>
</nlm:aff>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>McLaughlin Centre for Population Health Risk Assessment, University of Ottawa, Ottawa, Ontario</wicri:regionArea>
<wicri:noRegion>Ontario</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="aff011">
<addr-line>Risk Sciences International, Ottawa, Ontario, Canada</addr-line>
</nlm:aff>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Risk Sciences International, Ottawa, Ontario</wicri:regionArea>
<wicri:noRegion>Ontario</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series>
<title level="j">PLoS ONE</title>
<idno type="eISSN">1932-6203</idno>
<imprint>
<date when="2016">2016</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Accidental Falls (prevention & control)</term>
<term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Cholinergic Antagonists (adverse effects)</term>
<term>Cognition Disorders (chemically induced)</term>
<term>Cognition Disorders (complications)</term>
<term>Cohort Studies</term>
<term>Databases, Factual</term>
<term>Delirium (chemically induced)</term>
<term>Delirium (complications)</term>
<term>Emergency Service, Hospital</term>
<term>Female</term>
<term>Fractures, Bone (complications)</term>
<term>Fractures, Bone (prevention & control)</term>
<term>Hospitalization</term>
<term>Humans</term>
<term>Inpatients</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Parkinson Disease (complications)</term>
<term>Parkinson Disease (therapy)</term>
<term>Proportional Hazards Models</term>
<term>Retrospective Studies</term>
<term>Risk Factors</term>
<term>Treatment Outcome</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="adverse effects" xml:lang="en">
<term>Cholinergic Antagonists</term>
</keywords>
<keywords scheme="MESH" qualifier="chemically induced" xml:lang="en">
<term>Cognition Disorders</term>
<term>Delirium</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en">
<term>Cognition Disorders</term>
<term>Delirium</term>
<term>Fractures, Bone</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="prevention & control" xml:lang="en">
<term>Accidental Falls</term>
<term>Fractures, Bone</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en">
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Cohort Studies</term>
<term>Databases, Factual</term>
<term>Emergency Service, Hospital</term>
<term>Female</term>
<term>Hospitalization</term>
<term>Humans</term>
<term>Inpatients</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Proportional Hazards Models</term>
<term>Retrospective Studies</term>
<term>Risk Factors</term>
<term>Treatment Outcome</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<sec id="sec001">
<title>Background</title>
<p>Elderly adults should avoid medications with anticholinergic effects since they may increase the risk of adverse events, including falls, delirium, and cognitive impairment. However, data on anticholinergic burden are limited in subpopulations, such as individuals with Parkinson disease (PD). The objective of this study was to determine whether anticholinergic burden was associated with adverse outcomes in a PD inpatient population.</p>
</sec>
<sec id="sec002">
<title>Methods</title>
<p>Using the Cerner Health Facts® database, we retrospectively examined anticholinergic medication use, diagnoses, and hospital revisits within a cohort of 16,302 PD inpatients admitted to a Cerner hospital between 2000 and 2011. Anticholinergic burden was computed using the Anticholinergic Risk Scale (ARS). Primary outcomes were associations between ARS score and diagnosis of fracture and delirium. Secondary outcomes included associations between ARS score and 30-day hospital revisits.</p>
</sec>
<sec id="sec003">
<title>Results</title>
<p>Many individuals (57.8%) were prescribed non-PD medications with moderate to very strong anticholinergic potential. Individuals with the greatest ARS score (≥4) were more likely to be diagnosed with fractures (adjusted odds ratio (AOR): 1.56, 95% CI: 1.29–1.88) and delirium (AOR: 1.61, 95% CI: 1.08–2.40) relative to those with no anticholinergic burden. Similarly, inpatients with the greatest ARS score were more likely to visit the emergency department (adjusted hazard ratio (AHR): 1.32, 95% CI: 1.10–1.58) and be readmitted (AHR: 1.16, 95% CI: 1.01–1.33) within 30-days of discharge.</p>
</sec>
<sec id="sec004">
<title>Conclusions</title>
<p>We found a positive association between increased anticholinergic burden and adverse outcomes among individuals with PD. Additional pharmacovigilance studies are needed to better understand risks associated with anticholinergic medication use in PD.</p>
</sec>
</div>
</front>
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<name sortKey="Fortin, Yannick" sort="Fortin, Yannick" uniqKey="Fortin Y" first="Yannick" last="Fortin">Yannick Fortin</name>
<name sortKey="Kohen, Dafna E" sort="Kohen, Dafna E" uniqKey="Kohen D" first="Dafna E." last="Kohen">Dafna E. Kohen</name>
<name sortKey="Krewski, Daniel" sort="Krewski, Daniel" uniqKey="Krewski D" first="Daniel" last="Krewski">Daniel Krewski</name>
<name sortKey="Krewski, Daniel" sort="Krewski, Daniel" uniqKey="Krewski D" first="Daniel" last="Krewski">Daniel Krewski</name>
<name sortKey="Mattison, Donald R" sort="Mattison, Donald R" uniqKey="Mattison D" first="Donald R." last="Mattison">Donald R. Mattison</name>
<name sortKey="Mattison, Donald R" sort="Mattison, Donald R" uniqKey="Mattison D" first="Donald R." last="Mattison">Donald R. Mattison</name>
</country>
<country name="États-Unis">
<region name="Pennsylvanie">
<name sortKey="Crispo, James A G" sort="Crispo, James A G" uniqKey="Crispo J" first="James A. G." last="Crispo">James A. G. Crispo</name>
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<name sortKey="Hays, Harlen D" sort="Hays, Harlen D" uniqKey="Hays H" first="Harlen D." last="Hays">Harlen D. Hays</name>
<name sortKey="Mcnair, Douglas S" sort="Mcnair, Douglas S" uniqKey="Mcnair D" first="Douglas S." last="Mcnair">Douglas S. Mcnair</name>
<name sortKey="Thibault, Dylan P" sort="Thibault, Dylan P" uniqKey="Thibault D" first="Dylan P." last="Thibault">Dylan P. Thibault</name>
<name sortKey="Thibault, Dylan P" sort="Thibault, Dylan P" uniqKey="Thibault D" first="Dylan P." last="Thibault">Dylan P. Thibault</name>
<name sortKey="Thibault, Dylan P" sort="Thibault, Dylan P" uniqKey="Thibault D" first="Dylan P." last="Thibault">Dylan P. Thibault</name>
<name sortKey="Willis, Allison W" sort="Willis, Allison W" uniqKey="Willis A" first="Allison W." last="Willis">Allison W. Willis</name>
<name sortKey="Willis, Allison W" sort="Willis, Allison W" uniqKey="Willis A" first="Allison W." last="Willis">Allison W. Willis</name>
<name sortKey="Willis, Allison W" sort="Willis, Allison W" uniqKey="Willis A" first="Allison W." last="Willis">Allison W. Willis</name>
</country>
<country name="Argentine">
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<name sortKey="Perez Lloret, Santiago" sort="Perez Lloret, Santiago" uniqKey="Perez Lloret S" first="Santiago" last="Perez-Lloret">Santiago Perez-Lloret</name>
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</record>

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EXPLOR_STEP=$WICRI_ROOT/Wicri/Canada/explor/ParkinsonCanadaV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000435 | SxmlIndent | more

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Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Canada
   |area=    ParkinsonCanadaV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     PMC:4777375
   |texte=   Associations between Anticholinergic Burden and Adverse Health Outcomes in Parkinson Disease
}}

Pour générer des pages wiki

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