CP-204 Observational study on the use of different therapeutic alternatives for multiple sclerosis treatment
BackgroundMultiple sclerosis (MS) is a chronic demyelinating CNS disease. The recent commercialisation of new drugs for its treatment can change prescriber and patient treatment preferences.PurposeTo determinate the most prescribed drugs at the beginning of the disease and to observe if the emergenc...
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Veröffentlicht in: | European journal of hospital pharmacy. Science and practice 2017-03, Vol.24 (Suppl 1), p.A91-A91 |
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description | BackgroundMultiple sclerosis (MS) is a chronic demyelinating CNS disease. The recent commercialisation of new drugs for its treatment can change prescriber and patient treatment preferences.PurposeTo determinate the most prescribed drugs at the beginning of the disease and to observe if the emergence of new drugs for MS (dimethyl fumarate, alemtuzumab, pegylated interferon and teriflunomide) has changed the prescription tendency, or if they are preserved as a secondline treatment. Also, to quantify the outbreaks/year, reasons for discontinuation and adverse events of treatment.Material and methodsThis was a retrospective observational study including all treated MS patients (January 2004–March 2016). The data were obtained from their medical records and dispensation register.Results55 patients were included in the study, 69% women. Average age was 36±9 years. The most prescribed drugs after diagnosis were: interferon-β1b (25%), interferon-β1a 30 µg (20%), interferon-β1a 44 µg (18%), glatiramer acetate (GA) (18%), natalizumab (7%), fingolimod (7%) and dimethyl fumarate (5%). Among these, there were 8 prescriptions after the commercialisation of the new MS drugs: 3 dimethyl fumarate, 2 interferon-β1a 44 µg, 1 GA, 1 fingolimod and 1 natalizumab. With those initial treatments, 27 (49%) patients did not have outbreaks, 17 (31%) had 1 outbreak/year, 8 (15%) had 2 outbreaks/year and 3 (6%) had 3 outbreaks/year. 69% of patients were treated with 1 drug, 20% with 2 different drugs and 11% were treated with ≥3 drugs. The reasons for the change were: disease progression (52%), adverse events (47%) and patient’s decision (1%).27 patients did not present adverse events, 15 had flu-like syndrome, 5 redness, 5 discomfort at the injection site, 2 lymphopenia, 2 paresthesias, 2 mood disturbance, 1 transaminase elevation and 1 palpitations.ConclusionMS affects young adults, especially women. Interferon and GA are the most common initial treatments but with the appearance of new MS drugs, the use of dimethyl fumarate has increased. New MS drugs are mostly used as a secondline treatments but natalizumab is still the most used when there is no response to initial treatment. 85% of patients tolerated the treatment and no medication change was necessary. This drug has been demonstrated to be effectives because 69% of patients needed one treatment line to control their illness.No conflict of interest |
doi_str_mv | 10.1136/ejhpharm-2017-000640.202 |
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fullrecord | <record><control><sourceid>proquest_bmj_p</sourceid><recordid>TN_cdi_proquest_journals_2552764002</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2552764002</sourcerecordid><originalsourceid>FETCH-LOGICAL-b1002-171fc7f1a89d24d52dce121d80b98b0f19df3d0b4e62863e60ddab29761f64ed3</originalsourceid><addsrcrecordid>eNp9kUtLAzEUhYMoWGr_Q8D11JvHZCZLKb6goAtdD0lzQ6fMyyRT6M6Nf9Rf4pSqS1f3cDnncjkfIZTBkjGhbnC3HbYmtBkHVmQAoCQsOfAzMuMgi0xrJc__dK4uySLG2kIuRKml0DPSrV6msPz6-Hy2EcPepLrvTENjGt2B9h1NW6RjRNp76mrvMWCXjstgBhxTvaGmSRi6KbfHSH0faDs2qR4apHHTYOhjHWkKaFI7Ja_IhTdNxMXPnJO3-7vX1WO2fn54Wt2uM8sAeMYK5jeFZ6bUjkuXc7dBxpkrwerSgmfaeeHASlS8VAIVOGcs14ViXkl0Yk6uT3eH0L-PGFO168fpyyZWPM95MfUE_D8XKwsxlZQzmFzi5LLtrhpC3ZpwqBhURwLVL4HqSKA6EZg0F990fH00</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1873338510</pqid></control><display><type>article</type><title>CP-204 Observational study on the use of different therapeutic alternatives for multiple sclerosis treatment</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>de Dios López, A ; Montaña, S Jornet ; Parada, L Sánchez ; Broseta, PA López ; Marqués, M Martín ; Subirada, M Canela</creator><creatorcontrib>de Dios López, A ; Montaña, S Jornet ; Parada, L Sánchez ; Broseta, PA López ; Marqués, M Martín ; Subirada, M Canela</creatorcontrib><description>BackgroundMultiple sclerosis (MS) is a chronic demyelinating CNS disease. The recent commercialisation of new drugs for its treatment can change prescriber and patient treatment preferences.PurposeTo determinate the most prescribed drugs at the beginning of the disease and to observe if the emergence of new drugs for MS (dimethyl fumarate, alemtuzumab, pegylated interferon and teriflunomide) has changed the prescription tendency, or if they are preserved as a secondline treatment. Also, to quantify the outbreaks/year, reasons for discontinuation and adverse events of treatment.Material and methodsThis was a retrospective observational study including all treated MS patients (January 2004–March 2016). The data were obtained from their medical records and dispensation register.Results55 patients were included in the study, 69% women. Average age was 36±9 years. The most prescribed drugs after diagnosis were: interferon-β1b (25%), interferon-β1a 30 µg (20%), interferon-β1a 44 µg (18%), glatiramer acetate (GA) (18%), natalizumab (7%), fingolimod (7%) and dimethyl fumarate (5%). Among these, there were 8 prescriptions after the commercialisation of the new MS drugs: 3 dimethyl fumarate, 2 interferon-β1a 44 µg, 1 GA, 1 fingolimod and 1 natalizumab. With those initial treatments, 27 (49%) patients did not have outbreaks, 17 (31%) had 1 outbreak/year, 8 (15%) had 2 outbreaks/year and 3 (6%) had 3 outbreaks/year. 69% of patients were treated with 1 drug, 20% with 2 different drugs and 11% were treated with ≥3 drugs. The reasons for the change were: disease progression (52%), adverse events (47%) and patient’s decision (1%).27 patients did not present adverse events, 15 had flu-like syndrome, 5 redness, 5 discomfort at the injection site, 2 lymphopenia, 2 paresthesias, 2 mood disturbance, 1 transaminase elevation and 1 palpitations.ConclusionMS affects young adults, especially women. Interferon and GA are the most common initial treatments but with the appearance of new MS drugs, the use of dimethyl fumarate has increased. New MS drugs are mostly used as a secondline treatments but natalizumab is still the most used when there is no response to initial treatment. 85% of patients tolerated the treatment and no medication change was necessary. This drug has been demonstrated to be effectives because 69% of patients needed one treatment line to control their illness.No conflict of interest</description><identifier>ISSN: 2047-9956</identifier><identifier>EISSN: 2047-9964</identifier><identifier>DOI: 10.1136/ejhpharm-2017-000640.202</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><subject>Drugs ; Epidemics ; Interferon ; Multiple sclerosis ; Observational studies ; Patients</subject><ispartof>European journal of hospital pharmacy. Science and practice, 2017-03, Vol.24 (Suppl 1), p.A91-A91</ispartof><rights>2017, 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>Copyright: 2017 (c) 2017, 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>2017 2017, 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><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>de Dios López, A</creatorcontrib><creatorcontrib>Montaña, S Jornet</creatorcontrib><creatorcontrib>Parada, L Sánchez</creatorcontrib><creatorcontrib>Broseta, PA López</creatorcontrib><creatorcontrib>Marqués, M Martín</creatorcontrib><creatorcontrib>Subirada, M Canela</creatorcontrib><title>CP-204 Observational study on the use of different therapeutic alternatives for multiple sclerosis treatment</title><title>European journal of hospital pharmacy. Science and practice</title><description>BackgroundMultiple sclerosis (MS) is a chronic demyelinating CNS disease. The recent commercialisation of new drugs for its treatment can change prescriber and patient treatment preferences.PurposeTo determinate the most prescribed drugs at the beginning of the disease and to observe if the emergence of new drugs for MS (dimethyl fumarate, alemtuzumab, pegylated interferon and teriflunomide) has changed the prescription tendency, or if they are preserved as a secondline treatment. Also, to quantify the outbreaks/year, reasons for discontinuation and adverse events of treatment.Material and methodsThis was a retrospective observational study including all treated MS patients (January 2004–March 2016). The data were obtained from their medical records and dispensation register.Results55 patients were included in the study, 69% women. Average age was 36±9 years. The most prescribed drugs after diagnosis were: interferon-β1b (25%), interferon-β1a 30 µg (20%), interferon-β1a 44 µg (18%), glatiramer acetate (GA) (18%), natalizumab (7%), fingolimod (7%) and dimethyl fumarate (5%). Among these, there were 8 prescriptions after the commercialisation of the new MS drugs: 3 dimethyl fumarate, 2 interferon-β1a 44 µg, 1 GA, 1 fingolimod and 1 natalizumab. With those initial treatments, 27 (49%) patients did not have outbreaks, 17 (31%) had 1 outbreak/year, 8 (15%) had 2 outbreaks/year and 3 (6%) had 3 outbreaks/year. 69% of patients were treated with 1 drug, 20% with 2 different drugs and 11% were treated with ≥3 drugs. The reasons for the change were: disease progression (52%), adverse events (47%) and patient’s decision (1%).27 patients did not present adverse events, 15 had flu-like syndrome, 5 redness, 5 discomfort at the injection site, 2 lymphopenia, 2 paresthesias, 2 mood disturbance, 1 transaminase elevation and 1 palpitations.ConclusionMS affects young adults, especially women. Interferon and GA are the most common initial treatments but with the appearance of new MS drugs, the use of dimethyl fumarate has increased. New MS drugs are mostly used as a secondline treatments but natalizumab is still the most used when there is no response to initial treatment. 85% of patients tolerated the treatment and no medication change was necessary. This drug has been demonstrated to be effectives because 69% of patients needed one treatment line to control their illness.No conflict of interest</description><subject>Drugs</subject><subject>Epidemics</subject><subject>Interferon</subject><subject>Multiple sclerosis</subject><subject>Observational studies</subject><subject>Patients</subject><issn>2047-9956</issn><issn>2047-9964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kUtLAzEUhYMoWGr_Q8D11JvHZCZLKb6goAtdD0lzQ6fMyyRT6M6Nf9Rf4pSqS1f3cDnncjkfIZTBkjGhbnC3HbYmtBkHVmQAoCQsOfAzMuMgi0xrJc__dK4uySLG2kIuRKml0DPSrV6msPz6-Hy2EcPepLrvTENjGt2B9h1NW6RjRNp76mrvMWCXjstgBhxTvaGmSRi6KbfHSH0faDs2qR4apHHTYOhjHWkKaFI7Ja_IhTdNxMXPnJO3-7vX1WO2fn54Wt2uM8sAeMYK5jeFZ6bUjkuXc7dBxpkrwerSgmfaeeHASlS8VAIVOGcs14ViXkl0Yk6uT3eH0L-PGFO168fpyyZWPM95MfUE_D8XKwsxlZQzmFzi5LLtrhpC3ZpwqBhURwLVL4HqSKA6EZg0F990fH00</recordid><startdate>201703</startdate><enddate>201703</enddate><creator>de Dios López, A</creator><creator>Montaña, S Jornet</creator><creator>Parada, L Sánchez</creator><creator>Broseta, PA López</creator><creator>Marqués, M Martín</creator><creator>Subirada, M Canela</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>201703</creationdate><title>CP-204 Observational study on the use of different therapeutic alternatives for multiple sclerosis treatment</title><author>de Dios López, A ; Montaña, S Jornet ; Parada, L Sánchez ; Broseta, PA López ; Marqués, M Martín ; Subirada, M Canela</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1002-171fc7f1a89d24d52dce121d80b98b0f19df3d0b4e62863e60ddab29761f64ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Drugs</topic><topic>Epidemics</topic><topic>Interferon</topic><topic>Multiple sclerosis</topic><topic>Observational studies</topic><topic>Patients</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Dios López, A</creatorcontrib><creatorcontrib>Montaña, S Jornet</creatorcontrib><creatorcontrib>Parada, L Sánchez</creatorcontrib><creatorcontrib>Broseta, PA López</creatorcontrib><creatorcontrib>Marqués, M Martín</creatorcontrib><creatorcontrib>Subirada, M Canela</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Health & 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 & 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>de Dios López, A</au><au>Montaña, S Jornet</au><au>Parada, L Sánchez</au><au>Broseta, PA López</au><au>Marqués, M Martín</au><au>Subirada, M Canela</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CP-204 Observational study on the use of different therapeutic alternatives for multiple sclerosis treatment</atitle><jtitle>European journal of hospital pharmacy. Science and practice</jtitle><date>2017-03</date><risdate>2017</risdate><volume>24</volume><issue>Suppl 1</issue><spage>A91</spage><epage>A91</epage><pages>A91-A91</pages><issn>2047-9956</issn><eissn>2047-9964</eissn><abstract>BackgroundMultiple sclerosis (MS) is a chronic demyelinating CNS disease. The recent commercialisation of new drugs for its treatment can change prescriber and patient treatment preferences.PurposeTo determinate the most prescribed drugs at the beginning of the disease and to observe if the emergence of new drugs for MS (dimethyl fumarate, alemtuzumab, pegylated interferon and teriflunomide) has changed the prescription tendency, or if they are preserved as a secondline treatment. Also, to quantify the outbreaks/year, reasons for discontinuation and adverse events of treatment.Material and methodsThis was a retrospective observational study including all treated MS patients (January 2004–March 2016). The data were obtained from their medical records and dispensation register.Results55 patients were included in the study, 69% women. Average age was 36±9 years. The most prescribed drugs after diagnosis were: interferon-β1b (25%), interferon-β1a 30 µg (20%), interferon-β1a 44 µg (18%), glatiramer acetate (GA) (18%), natalizumab (7%), fingolimod (7%) and dimethyl fumarate (5%). Among these, there were 8 prescriptions after the commercialisation of the new MS drugs: 3 dimethyl fumarate, 2 interferon-β1a 44 µg, 1 GA, 1 fingolimod and 1 natalizumab. With those initial treatments, 27 (49%) patients did not have outbreaks, 17 (31%) had 1 outbreak/year, 8 (15%) had 2 outbreaks/year and 3 (6%) had 3 outbreaks/year. 69% of patients were treated with 1 drug, 20% with 2 different drugs and 11% were treated with ≥3 drugs. The reasons for the change were: disease progression (52%), adverse events (47%) and patient’s decision (1%).27 patients did not present adverse events, 15 had flu-like syndrome, 5 redness, 5 discomfort at the injection site, 2 lymphopenia, 2 paresthesias, 2 mood disturbance, 1 transaminase elevation and 1 palpitations.ConclusionMS affects young adults, especially women. Interferon and GA are the most common initial treatments but with the appearance of new MS drugs, the use of dimethyl fumarate has increased. New MS drugs are mostly used as a secondline treatments but natalizumab is still the most used when there is no response to initial treatment. 85% of patients tolerated the treatment and no medication change was necessary. This drug has been demonstrated to be effectives because 69% of patients needed one treatment line to control their illness.No conflict of interest</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/ejhpharm-2017-000640.202</doi></addata></record> |
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subjects | Drugs Epidemics Interferon Multiple sclerosis Observational studies Patients |
title | CP-204 Observational study on the use of different therapeutic alternatives for multiple sclerosis treatment |
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