4CPS-083 Aging with HIV: optimising pharmacotherapy beyond interactions

BackgroundPharmacotherapeutic complexity and potentially inappropriate medication (PIM) negatively affect therapeutic goals in HIV +adult patients and increase frailty and risk of falls. The POINT study carried out in Spain in 2017 alerted polypharmacy and pharmacotherapeutic complexity, and low adh...

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Veröffentlicht in:European journal of hospital pharmacy. Science and practice 2019-03, Vol.26 (Suppl 1), p.A107-A107
Hauptverfasser: Gallardo-Anciano, J, Gonzalez-Perez, Y, Calvo-Aragüete, ME, Blanco-Ramos, JR
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container_issue Suppl 1
container_start_page A107
container_title European journal of hospital pharmacy. Science and practice
container_volume 26
creator Gallardo-Anciano, J
Gonzalez-Perez, Y
Calvo-Aragüete, ME
Blanco-Ramos, JR
description BackgroundPharmacotherapeutic complexity and potentially inappropriate medication (PIM) negatively affect therapeutic goals in HIV +adult patients and increase frailty and risk of falls. The POINT study carried out in Spain in 2017 alerted polypharmacy and pharmacotherapeutic complexity, and low adherence in HIV +adults.PurposeTo describe treatment complexity, fall-risk-increasing drugs (FRIDs) burden, and the presence of PIM in middle-aged and elderly HIV +patients in our clinical setting.Material and methodsObservational, cross-sectional study was conducted in the referral hospital for HIV infection of our region in April 2018. We selected patients aged ≥45 y. Exclusion criteria: no medication information available in electronic clinical history. Age, gender and active chronic medication were collected. We calculated: overall treatment complexity and complexity due to concomitant one (MRCI-E tool); FRIDs with the most consistent association with a higher risk (antipsychotics, antidepressants, benzodiazepines, loop diuretics, opioids, antiepileptics and polypharmacy, according to the Systematic Review and Meta-Analysis of the EUGMS Task and Finish Group on FRIDs); anticholinergic drug burden (DBI score); and STOPP criteria. Polypharmacy was defined as ≥5 medications. Fix-dose combinations were counted as one drug.ResultsA total of 143 HIV +patients were included, all of them on antirretroviral treatment (ART), 92.3% received concomitant non-HIV drugs (non-ART). Median age: 54y (SD 7.6; range 45 to 84y) and 94 (65.7%) male. Eighty-two patients (57.3%) received ≥1 FRID (35.7%≥1 benzodiazepine), 71 (49.7%) had ≥1 anticholinergic drug and at least one STOPP criteria was detected in 55 patients (38.4%).Abstract 4CPS-083 Table 1 Pharmacological profile N (%) Median (SD) Range Total chronic drugs (ART+non ART)1434 (3.1)1–17 ART 143 (100%) 2 (0.9) 1– 5 Non-ART 132 (92.3%) 3 (2.8) 1– 14 ≥5 non-ART 40 (28%) 7 (2.3) 5– 14Overall complexity (ART+non ART) (points)1438 (7.1)2–38.5 ART complexity 143 3 (1.6) 2– 12.5 Non-ART complexity 132 5 (6.6) 0.5– 32 % non-ART complexity/overall 132 63.6% (19.9) 11.1%– 94 %Number of FRIDs/patient82 (57.3%)2 (1.1)1–5 Benzodiazepine 51 (35.7%) 1 (0.4) 1– 2Anticholinergic drug burden (DBI points)71 (49.7%)0.75 (0.7)0.2–3.46 High-risk DBI score (≥1 ) 33 (23.1%) 1.58 (0.5) 1.05– 3.46Number of STOPP criteria55 (38.5%)1 (0.6)1–3ConclusionThe impact of non-HIV drugs on overall pharmacotherapeutic complexity, and the frequent use of PIM in p
doi_str_mv 10.1136/ejhpharm-2019-eahpconf.232
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The POINT study carried out in Spain in 2017 alerted polypharmacy and pharmacotherapeutic complexity, and low adherence in HIV +adults.PurposeTo describe treatment complexity, fall-risk-increasing drugs (FRIDs) burden, and the presence of PIM in middle-aged and elderly HIV +patients in our clinical setting.Material and methodsObservational, cross-sectional study was conducted in the referral hospital for HIV infection of our region in April 2018. We selected patients aged ≥45 y. Exclusion criteria: no medication information available in electronic clinical history. Age, gender and active chronic medication were collected. We calculated: overall treatment complexity and complexity due to concomitant one (MRCI-E tool); FRIDs with the most consistent association with a higher risk (antipsychotics, antidepressants, benzodiazepines, loop diuretics, opioids, antiepileptics and polypharmacy, according to the Systematic Review and Meta-Analysis of the EUGMS Task and Finish Group on FRIDs); anticholinergic drug burden (DBI score); and STOPP criteria. Polypharmacy was defined as ≥5 medications. Fix-dose combinations were counted as one drug.ResultsA total of 143 HIV +patients were included, all of them on antirretroviral treatment (ART), 92.3% received concomitant non-HIV drugs (non-ART). Median age: 54y (SD 7.6; range 45 to 84y) and 94 (65.7%) male. Eighty-two patients (57.3%) received ≥1 FRID (35.7%≥1 benzodiazepine), 71 (49.7%) had ≥1 anticholinergic drug and at least one STOPP criteria was detected in 55 patients (38.4%).Abstract 4CPS-083 Table 1 Pharmacological profile N (%) Median (SD) Range Total chronic drugs (ART+non ART)1434 (3.1)1–17 ART 143 (100%) 2 (0.9) 1– 5 Non-ART 132 (92.3%) 3 (2.8) 1– 14 ≥5 non-ART 40 (28%) 7 (2.3) 5– 14Overall complexity (ART+non ART) (points)1438 (7.1)2–38.5 ART complexity 143 3 (1.6) 2– 12.5 Non-ART complexity 132 5 (6.6) 0.5– 32 % non-ART complexity/overall 132 63.6% (19.9) 11.1%– 94 %Number of FRIDs/patient82 (57.3%)2 (1.1)1–5 Benzodiazepine 51 (35.7%) 1 (0.4) 1– 2Anticholinergic drug burden (DBI points)71 (49.7%)0.75 (0.7)0.2–3.46 High-risk DBI score (≥1 ) 33 (23.1%) 1.58 (0.5) 1.05– 3.46Number of STOPP criteria55 (38.5%)1 (0.6)1–3ConclusionThe impact of non-HIV drugs on overall pharmacotherapeutic complexity, and the frequent use of PIM in patients≥45 y justifies the need for periodical reassessment of the treatment in order to optimise adequacy and benefit/risk balance.References and/or acknowledgementsPOINT study.https://ejhp.bmj.com/content/25/Suppl_1/A249.2No conflict of interest.</description><identifier>ISSN: 2047-9956</identifier><identifier>EISSN: 2047-9964</identifier><identifier>DOI: 10.1136/ejhpharm-2019-eahpconf.232</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><subject>Drug therapy ; HIV ; Human immunodeficiency virus ; Polypharmacy ; Systematic review</subject><ispartof>European journal of hospital pharmacy. Science and practice, 2019-03, Vol.26 (Suppl 1), p.A107-A107</ispartof><rights>2019, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>2019 2019, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids></links><search><creatorcontrib>Gallardo-Anciano, J</creatorcontrib><creatorcontrib>Gonzalez-Perez, Y</creatorcontrib><creatorcontrib>Calvo-Aragüete, ME</creatorcontrib><creatorcontrib>Blanco-Ramos, JR</creatorcontrib><title>4CPS-083 Aging with HIV: optimising pharmacotherapy beyond interactions</title><title>European journal of hospital pharmacy. Science and practice</title><description>BackgroundPharmacotherapeutic complexity and potentially inappropriate medication (PIM) negatively affect therapeutic goals in HIV +adult patients and increase frailty and risk of falls. The POINT study carried out in Spain in 2017 alerted polypharmacy and pharmacotherapeutic complexity, and low adherence in HIV +adults.PurposeTo describe treatment complexity, fall-risk-increasing drugs (FRIDs) burden, and the presence of PIM in middle-aged and elderly HIV +patients in our clinical setting.Material and methodsObservational, cross-sectional study was conducted in the referral hospital for HIV infection of our region in April 2018. We selected patients aged ≥45 y. Exclusion criteria: no medication information available in electronic clinical history. Age, gender and active chronic medication were collected. We calculated: overall treatment complexity and complexity due to concomitant one (MRCI-E tool); FRIDs with the most consistent association with a higher risk (antipsychotics, antidepressants, benzodiazepines, loop diuretics, opioids, antiepileptics and polypharmacy, according to the Systematic Review and Meta-Analysis of the EUGMS Task and Finish Group on FRIDs); anticholinergic drug burden (DBI score); and STOPP criteria. Polypharmacy was defined as ≥5 medications. Fix-dose combinations were counted as one drug.ResultsA total of 143 HIV +patients were included, all of them on antirretroviral treatment (ART), 92.3% received concomitant non-HIV drugs (non-ART). Median age: 54y (SD 7.6; range 45 to 84y) and 94 (65.7%) male. Eighty-two patients (57.3%) received ≥1 FRID (35.7%≥1 benzodiazepine), 71 (49.7%) had ≥1 anticholinergic drug and at least one STOPP criteria was detected in 55 patients (38.4%).Abstract 4CPS-083 Table 1 Pharmacological profile N (%) Median (SD) Range Total chronic drugs (ART+non ART)1434 (3.1)1–17 ART 143 (100%) 2 (0.9) 1– 5 Non-ART 132 (92.3%) 3 (2.8) 1– 14 ≥5 non-ART 40 (28%) 7 (2.3) 5– 14Overall complexity (ART+non ART) (points)1438 (7.1)2–38.5 ART complexity 143 3 (1.6) 2– 12.5 Non-ART complexity 132 5 (6.6) 0.5– 32 % non-ART complexity/overall 132 63.6% (19.9) 11.1%– 94 %Number of FRIDs/patient82 (57.3%)2 (1.1)1–5 Benzodiazepine 51 (35.7%) 1 (0.4) 1– 2Anticholinergic drug burden (DBI points)71 (49.7%)0.75 (0.7)0.2–3.46 High-risk DBI score (≥1 ) 33 (23.1%) 1.58 (0.5) 1.05– 3.46Number of STOPP criteria55 (38.5%)1 (0.6)1–3ConclusionThe impact of non-HIV drugs on overall pharmacotherapeutic complexity, and the frequent use of PIM in patients≥45 y justifies the need for periodical reassessment of the treatment in order to optimise adequacy and benefit/risk balance.References and/or acknowledgementsPOINT study.https://ejhp.bmj.com/content/25/Suppl_1/A249.2No conflict of interest.</description><subject>Drug therapy</subject><subject>HIV</subject><subject>Human immunodeficiency virus</subject><subject>Polypharmacy</subject><subject>Systematic review</subject><issn>2047-9956</issn><issn>2047-9964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNo9kM9KxDAQxoMouKz7DkXPWZNJ2jTelkXdwoKCf64hadNtim1q20V68-KL-iS2rutc5pvhY77hh9AlJUtKWXRty6IpdFthIFRiq4sm9XW-BAYnaAaECyxlxE__dRido0XXOUNCxmLJmZyhhK8fnzCJ2ffn12rn6l3w4foi2CSvN4Fvele5blr-5ujU94VtdTMExg6-zgJX9-Oc9s7X3QU6y_VbZxd_fY5e7m6f1xu8fbhP1qstNhQiwNJmhIcagJKM5VybGFIaZhBbJkZJxu8ZCCZTwanMKCehia3goCVYLk3E5ujqcLdp_fvedr0q_b6tx0gFVJKxYkFGV3hwmapUTesq3Q6KEjWBU0dwagKnjuDUFP0DVqtlMA</recordid><startdate>201903</startdate><enddate>201903</enddate><creator>Gallardo-Anciano, J</creator><creator>Gonzalez-Perez, Y</creator><creator>Calvo-Aragüete, ME</creator><creator>Blanco-Ramos, JR</creator><general>BMJ Publishing Group LTD</general><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>201903</creationdate><title>4CPS-083 Aging with HIV: optimising pharmacotherapy beyond interactions</title><author>Gallardo-Anciano, J ; Gonzalez-Perez, Y ; Calvo-Aragüete, ME ; Blanco-Ramos, JR</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1262-9ed045a2210d3f4ab82c15d28e3782c023232739c7419d1405b8e742a92e49b63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Drug therapy</topic><topic>HIV</topic><topic>Human immunodeficiency virus</topic><topic>Polypharmacy</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gallardo-Anciano, J</creatorcontrib><creatorcontrib>Gonzalez-Perez, Y</creatorcontrib><creatorcontrib>Calvo-Aragüete, ME</creatorcontrib><creatorcontrib>Blanco-Ramos, JR</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>European journal of hospital pharmacy. Science and practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gallardo-Anciano, J</au><au>Gonzalez-Perez, Y</au><au>Calvo-Aragüete, ME</au><au>Blanco-Ramos, JR</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>4CPS-083 Aging with HIV: optimising pharmacotherapy beyond interactions</atitle><jtitle>European journal of hospital pharmacy. Science and practice</jtitle><date>2019-03</date><risdate>2019</risdate><volume>26</volume><issue>Suppl 1</issue><spage>A107</spage><epage>A107</epage><pages>A107-A107</pages><issn>2047-9956</issn><eissn>2047-9964</eissn><abstract>BackgroundPharmacotherapeutic complexity and potentially inappropriate medication (PIM) negatively affect therapeutic goals in HIV +adult patients and increase frailty and risk of falls. The POINT study carried out in Spain in 2017 alerted polypharmacy and pharmacotherapeutic complexity, and low adherence in HIV +adults.PurposeTo describe treatment complexity, fall-risk-increasing drugs (FRIDs) burden, and the presence of PIM in middle-aged and elderly HIV +patients in our clinical setting.Material and methodsObservational, cross-sectional study was conducted in the referral hospital for HIV infection of our region in April 2018. We selected patients aged ≥45 y. Exclusion criteria: no medication information available in electronic clinical history. Age, gender and active chronic medication were collected. We calculated: overall treatment complexity and complexity due to concomitant one (MRCI-E tool); FRIDs with the most consistent association with a higher risk (antipsychotics, antidepressants, benzodiazepines, loop diuretics, opioids, antiepileptics and polypharmacy, according to the Systematic Review and Meta-Analysis of the EUGMS Task and Finish Group on FRIDs); anticholinergic drug burden (DBI score); and STOPP criteria. Polypharmacy was defined as ≥5 medications. Fix-dose combinations were counted as one drug.ResultsA total of 143 HIV +patients were included, all of them on antirretroviral treatment (ART), 92.3% received concomitant non-HIV drugs (non-ART). Median age: 54y (SD 7.6; range 45 to 84y) and 94 (65.7%) male. Eighty-two patients (57.3%) received ≥1 FRID (35.7%≥1 benzodiazepine), 71 (49.7%) had ≥1 anticholinergic drug and at least one STOPP criteria was detected in 55 patients (38.4%).Abstract 4CPS-083 Table 1 Pharmacological profile N (%) Median (SD) Range Total chronic drugs (ART+non ART)1434 (3.1)1–17 ART 143 (100%) 2 (0.9) 1– 5 Non-ART 132 (92.3%) 3 (2.8) 1– 14 ≥5 non-ART 40 (28%) 7 (2.3) 5– 14Overall complexity (ART+non ART) (points)1438 (7.1)2–38.5 ART complexity 143 3 (1.6) 2– 12.5 Non-ART complexity 132 5 (6.6) 0.5– 32 % non-ART complexity/overall 132 63.6% (19.9) 11.1%– 94 %Number of FRIDs/patient82 (57.3%)2 (1.1)1–5 Benzodiazepine 51 (35.7%) 1 (0.4) 1– 2Anticholinergic drug burden (DBI points)71 (49.7%)0.75 (0.7)0.2–3.46 High-risk DBI score (≥1 ) 33 (23.1%) 1.58 (0.5) 1.05– 3.46Number of STOPP criteria55 (38.5%)1 (0.6)1–3ConclusionThe impact of non-HIV drugs on overall pharmacotherapeutic complexity, and the frequent use of PIM in patients≥45 y justifies the need for periodical reassessment of the treatment in order to optimise adequacy and benefit/risk balance.References and/or acknowledgementsPOINT study.https://ejhp.bmj.com/content/25/Suppl_1/A249.2No conflict of interest.</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/ejhpharm-2019-eahpconf.232</doi><oa>free_for_read</oa></addata></record>
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subjects Drug therapy
HIV
Human immunodeficiency virus
Polypharmacy
Systematic review
title 4CPS-083 Aging with HIV: optimising pharmacotherapy beyond interactions
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