Anticholinergic Activity of 107 Medications Commonly Used by Older Adults
The objective of this study was to measure the anticholinergic activity (AA) of medications commonly used by older adults. A radioreceptor assay was used to investigate the AA of 107 medications. Six clinically relevant concentrations were assessed for each medication. Rodent forebrain and striatum...
Gespeichert in:
Veröffentlicht in: | Journal of the American Geriatrics Society (JAGS) 2008-07, Vol.56 (7), p.1333-1341 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1341 |
---|---|
container_issue | 7 |
container_start_page | 1333 |
container_title | Journal of the American Geriatrics Society (JAGS) |
container_volume | 56 |
creator | Chew, Marci L. Mulsant, Benoit H. Pollock, Bruce G. Lehman, Mark E. Greenspan, Andrew Mahmoud, Ramy A. Kirshner, Margaret A. Sorisio, Denise A. Bies, Robert R. Gharabawi, Georges |
description | The objective of this study was to measure the anticholinergic activity (AA) of medications commonly used by older adults. A radioreceptor assay was used to investigate the AA of 107 medications. Six clinically relevant concentrations were assessed for each medication. Rodent forebrain and striatum homogenate was used with tritiated quinuclidinyl benzilate. Drug‐free serum was added to medication and atropine standard‐curve samples. For medications that showed detectable AA, average steady‐state peak plasma and serum concentrations (Cmax) in older adults were used to estimate relationships between in vitro dose and AA. All results are reported in pmol/mL of atropine equivalents. At typical doses administered to older adults, amitriptyline, atropine, clozapine, dicyclomine, doxepin, L‐hyoscyamine, thioridazine, and tolterodine demonstrated AA exceeding 15 pmol/mL. Chlorpromazine, diphenhydramine, nortriptyline, olanzapine, oxybutynin, and paroxetine had AA values of 5 to 15 pmol/mL. Citalopram, escitalopram, fluoxetine, lithium, mirtazapine, quetiapine, ranitidine, and temazepam had values less than 5 pmol/mL. Amoxicillin, celecoxib, cephalexin, diazepam, digoxin, diphenoxylate, donepezil, duloxetine, fentanyl, furosemide, hydrocodone, lansoprazole, levofloxacin, metformin, phenytoin, propoxyphene, and topiramate demonstrated AA only at the highest concentrations tested (patients with above‐average Cmax values, who receive higher doses, or are frail may show AA). The remainder of the medications investigated did not demonstrate any AA at the concentrations examined. Psychotropic medications were particularly likely to demonstrate AA. Each of the drug classifications investigated (e.g., antipsychotic, cardiovascular) had at least one medication that demonstrated AA at therapeutic doses. Clinicians can use this information when choosing between equally efficacious medications, as well as in assessing overall anticholinergic burden. |
doi_str_mv | 10.1111/j.1532-5415.2008.01737.x |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_210383716</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1523114871</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5287-7f70b2069e21b6b3d2eb347374c739f898c9667f5b785754cf5ac016f097d7133</originalsourceid><addsrcrecordid>eNqNkE1P3DAQhq2KqizQv4CsSj0mHdvxRw49rFZlS6HlAKhHK3Fs8JJNwM62m3-P011tr_gyluZ5Z0YPQphATtL7ssoJZzTjBeE5BVA5EMlkvn2HZofGEZoBAM2UIMUxOolxBUAoKPUBHRPFCXDFZuhy3g3ePPat72x48AbPzeD_-GHEvUvrJP5pG2-qwfddxIt-ve67dsT30Ta4HvFN29iA582mHeIZeu-qNtqP-3qK7i--3S2-Z9c3y8vF_DoznCqZSSehpiBKS0ktatZQW7MiXV8YyUqnSmVKIaTjtVRc8sI4XhkgwkEpG0kYO0WfdnOfQ_-ysXHQq34TurRSUwJMMUlEgtQOMqGPMVinn4NfV2HUBPSkUK_0ZEpPpvSkUP9TqLcper6fv6nXtvkf3DtLwOc9UEVTtS5UnfHxwCXFpFBFmbivO-6vb-345gP0j-Xt9Ev5bJf3cbDbQ74KT1qkPte_fy31kklxx6-u9AV7BdIPmJ0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>210383716</pqid></control><display><type>article</type><title>Anticholinergic Activity of 107 Medications Commonly Used by Older Adults</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Chew, Marci L. ; Mulsant, Benoit H. ; Pollock, Bruce G. ; Lehman, Mark E. ; Greenspan, Andrew ; Mahmoud, Ramy A. ; Kirshner, Margaret A. ; Sorisio, Denise A. ; Bies, Robert R. ; Gharabawi, Georges</creator><creatorcontrib>Chew, Marci L. ; Mulsant, Benoit H. ; Pollock, Bruce G. ; Lehman, Mark E. ; Greenspan, Andrew ; Mahmoud, Ramy A. ; Kirshner, Margaret A. ; Sorisio, Denise A. ; Bies, Robert R. ; Gharabawi, Georges</creatorcontrib><description>The objective of this study was to measure the anticholinergic activity (AA) of medications commonly used by older adults. A radioreceptor assay was used to investigate the AA of 107 medications. Six clinically relevant concentrations were assessed for each medication. Rodent forebrain and striatum homogenate was used with tritiated quinuclidinyl benzilate. Drug‐free serum was added to medication and atropine standard‐curve samples. For medications that showed detectable AA, average steady‐state peak plasma and serum concentrations (Cmax) in older adults were used to estimate relationships between in vitro dose and AA. All results are reported in pmol/mL of atropine equivalents. At typical doses administered to older adults, amitriptyline, atropine, clozapine, dicyclomine, doxepin, L‐hyoscyamine, thioridazine, and tolterodine demonstrated AA exceeding 15 pmol/mL. Chlorpromazine, diphenhydramine, nortriptyline, olanzapine, oxybutynin, and paroxetine had AA values of 5 to 15 pmol/mL. Citalopram, escitalopram, fluoxetine, lithium, mirtazapine, quetiapine, ranitidine, and temazepam had values less than 5 pmol/mL. Amoxicillin, celecoxib, cephalexin, diazepam, digoxin, diphenoxylate, donepezil, duloxetine, fentanyl, furosemide, hydrocodone, lansoprazole, levofloxacin, metformin, phenytoin, propoxyphene, and topiramate demonstrated AA only at the highest concentrations tested (patients with above‐average Cmax values, who receive higher doses, or are frail may show AA). The remainder of the medications investigated did not demonstrate any AA at the concentrations examined. Psychotropic medications were particularly likely to demonstrate AA. Each of the drug classifications investigated (e.g., antipsychotic, cardiovascular) had at least one medication that demonstrated AA at therapeutic doses. Clinicians can use this information when choosing between equally efficacious medications, as well as in assessing overall anticholinergic burden.</description><identifier>ISSN: 0002-8614</identifier><identifier>EISSN: 1532-5415</identifier><identifier>DOI: 10.1111/j.1532-5415.2008.01737.x</identifier><identifier>PMID: 18510583</identifier><identifier>CODEN: JAGSAF</identifier><language>eng</language><publisher>Malden, USA: Blackwell Publishing Inc</publisher><subject>Aged ; anticholinergic activity ; Biological and medical sciences ; Cholinesterase Inhibitors - adverse effects ; Cholinesterase Inhibitors - classification ; Cholinesterase Inhibitors - pharmacokinetics ; Cognition Disorders - chemically induced ; elderly ; Female ; General aspects ; Geriatrics ; Humans ; Male ; Medical sciences ; medications ; Miscellaneous ; Models, Biological ; Older people ; Pharmaceuticals ; Public health. Hygiene ; Public health. Hygiene-occupational medicine ; Side effects ; Tissue Distribution</subject><ispartof>Journal of the American Geriatrics Society (JAGS), 2008-07, Vol.56 (7), p.1333-1341</ispartof><rights>2008, Copyright the Authors. Journal compilation © 2008, The American Geriatrics Society</rights><rights>2008 INIST-CNRS</rights><rights>Journal compilation 2008 The American Geriatrics Society/Blackwell Publishing</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5287-7f70b2069e21b6b3d2eb347374c739f898c9667f5b785754cf5ac016f097d7133</citedby><cites>FETCH-LOGICAL-c5287-7f70b2069e21b6b3d2eb347374c739f898c9667f5b785754cf5ac016f097d7133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1532-5415.2008.01737.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1532-5415.2008.01737.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20814849$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18510583$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chew, Marci L.</creatorcontrib><creatorcontrib>Mulsant, Benoit H.</creatorcontrib><creatorcontrib>Pollock, Bruce G.</creatorcontrib><creatorcontrib>Lehman, Mark E.</creatorcontrib><creatorcontrib>Greenspan, Andrew</creatorcontrib><creatorcontrib>Mahmoud, Ramy A.</creatorcontrib><creatorcontrib>Kirshner, Margaret A.</creatorcontrib><creatorcontrib>Sorisio, Denise A.</creatorcontrib><creatorcontrib>Bies, Robert R.</creatorcontrib><creatorcontrib>Gharabawi, Georges</creatorcontrib><title>Anticholinergic Activity of 107 Medications Commonly Used by Older Adults</title><title>Journal of the American Geriatrics Society (JAGS)</title><addtitle>J Am Geriatr Soc</addtitle><description>The objective of this study was to measure the anticholinergic activity (AA) of medications commonly used by older adults. A radioreceptor assay was used to investigate the AA of 107 medications. Six clinically relevant concentrations were assessed for each medication. Rodent forebrain and striatum homogenate was used with tritiated quinuclidinyl benzilate. Drug‐free serum was added to medication and atropine standard‐curve samples. For medications that showed detectable AA, average steady‐state peak plasma and serum concentrations (Cmax) in older adults were used to estimate relationships between in vitro dose and AA. All results are reported in pmol/mL of atropine equivalents. At typical doses administered to older adults, amitriptyline, atropine, clozapine, dicyclomine, doxepin, L‐hyoscyamine, thioridazine, and tolterodine demonstrated AA exceeding 15 pmol/mL. Chlorpromazine, diphenhydramine, nortriptyline, olanzapine, oxybutynin, and paroxetine had AA values of 5 to 15 pmol/mL. Citalopram, escitalopram, fluoxetine, lithium, mirtazapine, quetiapine, ranitidine, and temazepam had values less than 5 pmol/mL. Amoxicillin, celecoxib, cephalexin, diazepam, digoxin, diphenoxylate, donepezil, duloxetine, fentanyl, furosemide, hydrocodone, lansoprazole, levofloxacin, metformin, phenytoin, propoxyphene, and topiramate demonstrated AA only at the highest concentrations tested (patients with above‐average Cmax values, who receive higher doses, or are frail may show AA). The remainder of the medications investigated did not demonstrate any AA at the concentrations examined. Psychotropic medications were particularly likely to demonstrate AA. Each of the drug classifications investigated (e.g., antipsychotic, cardiovascular) had at least one medication that demonstrated AA at therapeutic doses. Clinicians can use this information when choosing between equally efficacious medications, as well as in assessing overall anticholinergic burden.</description><subject>Aged</subject><subject>anticholinergic activity</subject><subject>Biological and medical sciences</subject><subject>Cholinesterase Inhibitors - adverse effects</subject><subject>Cholinesterase Inhibitors - classification</subject><subject>Cholinesterase Inhibitors - pharmacokinetics</subject><subject>Cognition Disorders - chemically induced</subject><subject>elderly</subject><subject>Female</subject><subject>General aspects</subject><subject>Geriatrics</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>medications</subject><subject>Miscellaneous</subject><subject>Models, Biological</subject><subject>Older people</subject><subject>Pharmaceuticals</subject><subject>Public health. Hygiene</subject><subject>Public health. Hygiene-occupational medicine</subject><subject>Side effects</subject><subject>Tissue Distribution</subject><issn>0002-8614</issn><issn>1532-5415</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1P3DAQhq2KqizQv4CsSj0mHdvxRw49rFZlS6HlAKhHK3Fs8JJNwM62m3-P011tr_gyluZ5Z0YPQphATtL7ssoJZzTjBeE5BVA5EMlkvn2HZofGEZoBAM2UIMUxOolxBUAoKPUBHRPFCXDFZuhy3g3ePPat72x48AbPzeD_-GHEvUvrJP5pG2-qwfddxIt-ve67dsT30Ta4HvFN29iA582mHeIZeu-qNtqP-3qK7i--3S2-Z9c3y8vF_DoznCqZSSehpiBKS0ktatZQW7MiXV8YyUqnSmVKIaTjtVRc8sI4XhkgwkEpG0kYO0WfdnOfQ_-ysXHQq34TurRSUwJMMUlEgtQOMqGPMVinn4NfV2HUBPSkUK_0ZEpPpvSkUP9TqLcper6fv6nXtvkf3DtLwOc9UEVTtS5UnfHxwCXFpFBFmbivO-6vb-345gP0j-Xt9Ev5bJf3cbDbQ74KT1qkPte_fy31kklxx6-u9AV7BdIPmJ0</recordid><startdate>200807</startdate><enddate>200807</enddate><creator>Chew, Marci L.</creator><creator>Mulsant, Benoit H.</creator><creator>Pollock, Bruce G.</creator><creator>Lehman, Mark E.</creator><creator>Greenspan, Andrew</creator><creator>Mahmoud, Ramy A.</creator><creator>Kirshner, Margaret A.</creator><creator>Sorisio, Denise A.</creator><creator>Bies, Robert R.</creator><creator>Gharabawi, Georges</creator><general>Blackwell Publishing Inc</general><general>Blackwell</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>K9.</scope><scope>NAPCQ</scope></search><sort><creationdate>200807</creationdate><title>Anticholinergic Activity of 107 Medications Commonly Used by Older Adults</title><author>Chew, Marci L. ; Mulsant, Benoit H. ; Pollock, Bruce G. ; Lehman, Mark E. ; Greenspan, Andrew ; Mahmoud, Ramy A. ; Kirshner, Margaret A. ; Sorisio, Denise A. ; Bies, Robert R. ; Gharabawi, Georges</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5287-7f70b2069e21b6b3d2eb347374c739f898c9667f5b785754cf5ac016f097d7133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Aged</topic><topic>anticholinergic activity</topic><topic>Biological and medical sciences</topic><topic>Cholinesterase Inhibitors - adverse effects</topic><topic>Cholinesterase Inhibitors - classification</topic><topic>Cholinesterase Inhibitors - pharmacokinetics</topic><topic>Cognition Disorders - chemically induced</topic><topic>elderly</topic><topic>Female</topic><topic>General aspects</topic><topic>Geriatrics</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>medications</topic><topic>Miscellaneous</topic><topic>Models, Biological</topic><topic>Older people</topic><topic>Pharmaceuticals</topic><topic>Public health. Hygiene</topic><topic>Public health. Hygiene-occupational medicine</topic><topic>Side effects</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chew, Marci L.</creatorcontrib><creatorcontrib>Mulsant, Benoit H.</creatorcontrib><creatorcontrib>Pollock, Bruce G.</creatorcontrib><creatorcontrib>Lehman, Mark E.</creatorcontrib><creatorcontrib>Greenspan, Andrew</creatorcontrib><creatorcontrib>Mahmoud, Ramy A.</creatorcontrib><creatorcontrib>Kirshner, Margaret A.</creatorcontrib><creatorcontrib>Sorisio, Denise A.</creatorcontrib><creatorcontrib>Bies, Robert R.</creatorcontrib><creatorcontrib>Gharabawi, Georges</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><jtitle>Journal of the American Geriatrics Society (JAGS)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chew, Marci L.</au><au>Mulsant, Benoit H.</au><au>Pollock, Bruce G.</au><au>Lehman, Mark E.</au><au>Greenspan, Andrew</au><au>Mahmoud, Ramy A.</au><au>Kirshner, Margaret A.</au><au>Sorisio, Denise A.</au><au>Bies, Robert R.</au><au>Gharabawi, Georges</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anticholinergic Activity of 107 Medications Commonly Used by Older Adults</atitle><jtitle>Journal of the American Geriatrics Society (JAGS)</jtitle><addtitle>J Am Geriatr Soc</addtitle><date>2008-07</date><risdate>2008</risdate><volume>56</volume><issue>7</issue><spage>1333</spage><epage>1341</epage><pages>1333-1341</pages><issn>0002-8614</issn><eissn>1532-5415</eissn><coden>JAGSAF</coden><abstract>The objective of this study was to measure the anticholinergic activity (AA) of medications commonly used by older adults. A radioreceptor assay was used to investigate the AA of 107 medications. Six clinically relevant concentrations were assessed for each medication. Rodent forebrain and striatum homogenate was used with tritiated quinuclidinyl benzilate. Drug‐free serum was added to medication and atropine standard‐curve samples. For medications that showed detectable AA, average steady‐state peak plasma and serum concentrations (Cmax) in older adults were used to estimate relationships between in vitro dose and AA. All results are reported in pmol/mL of atropine equivalents. At typical doses administered to older adults, amitriptyline, atropine, clozapine, dicyclomine, doxepin, L‐hyoscyamine, thioridazine, and tolterodine demonstrated AA exceeding 15 pmol/mL. Chlorpromazine, diphenhydramine, nortriptyline, olanzapine, oxybutynin, and paroxetine had AA values of 5 to 15 pmol/mL. Citalopram, escitalopram, fluoxetine, lithium, mirtazapine, quetiapine, ranitidine, and temazepam had values less than 5 pmol/mL. Amoxicillin, celecoxib, cephalexin, diazepam, digoxin, diphenoxylate, donepezil, duloxetine, fentanyl, furosemide, hydrocodone, lansoprazole, levofloxacin, metformin, phenytoin, propoxyphene, and topiramate demonstrated AA only at the highest concentrations tested (patients with above‐average Cmax values, who receive higher doses, or are frail may show AA). The remainder of the medications investigated did not demonstrate any AA at the concentrations examined. Psychotropic medications were particularly likely to demonstrate AA. Each of the drug classifications investigated (e.g., antipsychotic, cardiovascular) had at least one medication that demonstrated AA at therapeutic doses. Clinicians can use this information when choosing between equally efficacious medications, as well as in assessing overall anticholinergic burden.</abstract><cop>Malden, USA</cop><pub>Blackwell Publishing Inc</pub><pmid>18510583</pmid><doi>10.1111/j.1532-5415.2008.01737.x</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0002-8614 |
ispartof | Journal of the American Geriatrics Society (JAGS), 2008-07, Vol.56 (7), p.1333-1341 |
issn | 0002-8614 1532-5415 |
language | eng |
recordid | cdi_proquest_journals_210383716 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Aged anticholinergic activity Biological and medical sciences Cholinesterase Inhibitors - adverse effects Cholinesterase Inhibitors - classification Cholinesterase Inhibitors - pharmacokinetics Cognition Disorders - chemically induced elderly Female General aspects Geriatrics Humans Male Medical sciences medications Miscellaneous Models, Biological Older people Pharmaceuticals Public health. Hygiene Public health. Hygiene-occupational medicine Side effects Tissue Distribution |
title | Anticholinergic Activity of 107 Medications Commonly Used by Older Adults |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T07%3A02%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Anticholinergic%20Activity%20of%20107%20Medications%20Commonly%20Used%20by%20Older%20Adults&rft.jtitle=Journal%20of%20the%20American%20Geriatrics%20Society%20(JAGS)&rft.au=Chew,%20Marci%20L.&rft.date=2008-07&rft.volume=56&rft.issue=7&rft.spage=1333&rft.epage=1341&rft.pages=1333-1341&rft.issn=0002-8614&rft.eissn=1532-5415&rft.coden=JAGSAF&rft_id=info:doi/10.1111/j.1532-5415.2008.01737.x&rft_dat=%3Cproquest_cross%3E1523114871%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=210383716&rft_id=info:pmid/18510583&rfr_iscdi=true |