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Adherence with levodopa/carbidopa/entacapone versus levodopa/carbidopa and entacapone as separate tablets in patients with Parkinson's disease

Observational studies suggest that single-tablet formulations are associated with improved adherence versus the same components taken as separate tablets. The objective of this study was to compare adherence in patients with Parkinson's disease (PD) receiving levodopa therapy as levodopa/carbid...

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Published in:Current medical research and opinion 2010-07, Vol.26 (7), p.1543-1552
Main Authors: Delea, Thomas E., Thomas, Simu K., Hagiwara, May, Mancione, L.
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description Observational studies suggest that single-tablet formulations are associated with improved adherence versus the same components taken as separate tablets. The objective of this study was to compare adherence in patients with Parkinson's disease (PD) receiving levodopa therapy as levodopa/carbidopa/entacapone tablets (LCE) versus levodopa/carbidopa (LC) tablets and entacapone (E) as separate tablets (LC and E). This was a retrospective, observational cohort study using a large health insurance claims database. Subjects included persons with a PD diagnosis who were receiving LC without E and then received either an add-on therapy with E as a separate tablet (LC and E) or LCE as one tablet (LCE). The primary study outcome was treatment adherence, estimated from pharmacy refills based on the 'percent of days covered' (PDC) with LCE or LC and E during follow-up and compared for patients receiving LCE and LC and E using multivariate regression analyses. In multivariate analyses controlling for differences between groups in baseline characteristics, including pre-index dosage of and adherence with LC, receipt of LCE (n = 388) was associated with 79% lower mean non-adherence during follow-up (95% CI: 73-83%; p 
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The objective of this study was to compare adherence in patients with Parkinson's disease (PD) receiving levodopa therapy as levodopa/carbidopa/entacapone tablets (LCE) versus levodopa/carbidopa (LC) tablets and entacapone (E) as separate tablets (LC and E). This was a retrospective, observational cohort study using a large health insurance claims database. Subjects included persons with a PD diagnosis who were receiving LC without E and then received either an add-on therapy with E as a separate tablet (LC and E) or LCE as one tablet (LCE). The primary study outcome was treatment adherence, estimated from pharmacy refills based on the 'percent of days covered' (PDC) with LCE or LC and E during follow-up and compared for patients receiving LCE and LC and E using multivariate regression analyses. In multivariate analyses controlling for differences between groups in baseline characteristics, including pre-index dosage of and adherence with LC, receipt of LCE (n = 388) was associated with 79% lower mean non-adherence during follow-up (95% CI: 73-83%; p &lt; 0.001) versus LC and E (n = 823), 86% lower odds of unsatisfactory adherence (95% CI: 80-91%; p &lt; 0.001), and a 26% lower risk of discontinuation (95% CI: 6-42%; p &lt; 0.013). This was an observational study with the inherent potential for selection bias. Pharmacy claims may not provide an accurate estimate of adherence. Requiring subjects to have a certain number of prescriptions before and after the index date may yield a sample that is not representative of all patients initiating levodopa therapy in typical clinical practice. Better adherence with LCE may have important implications for maintaining function in patients receiving chronic oral levodopa therapy. 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The objective of this study was to compare adherence in patients with Parkinson's disease (PD) receiving levodopa therapy as levodopa/carbidopa/entacapone tablets (LCE) versus levodopa/carbidopa (LC) tablets and entacapone (E) as separate tablets (LC and E). This was a retrospective, observational cohort study using a large health insurance claims database. Subjects included persons with a PD diagnosis who were receiving LC without E and then received either an add-on therapy with E as a separate tablet (LC and E) or LCE as one tablet (LCE). The primary study outcome was treatment adherence, estimated from pharmacy refills based on the 'percent of days covered' (PDC) with LCE or LC and E during follow-up and compared for patients receiving LCE and LC and E using multivariate regression analyses. In multivariate analyses controlling for differences between groups in baseline characteristics, including pre-index dosage of and adherence with LC, receipt of LCE (n = 388) was associated with 79% lower mean non-adherence during follow-up (95% CI: 73-83%; p &lt; 0.001) versus LC and E (n = 823), 86% lower odds of unsatisfactory adherence (95% CI: 80-91%; p &lt; 0.001), and a 26% lower risk of discontinuation (95% CI: 6-42%; p &lt; 0.013). This was an observational study with the inherent potential for selection bias. Pharmacy claims may not provide an accurate estimate of adherence. Requiring subjects to have a certain number of prescriptions before and after the index date may yield a sample that is not representative of all patients initiating levodopa therapy in typical clinical practice. Better adherence with LCE may have important implications for maintaining function in patients receiving chronic oral levodopa therapy. Further research is needed to confirm these results and examine the association between improved adherence and clinical and economic outcomes.</description><subject>Adherence</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Algorithms</subject><subject>Antiparkinson Agents - administration &amp; dosage</subject><subject>Antiparkinson Agents - adverse effects</subject><subject>Carbidopa - administration &amp; dosage</subject><subject>Carbidopa - adverse effects</subject><subject>Catechols - administration &amp; dosage</subject><subject>Catechols - adverse effects</subject><subject>Cohort Studies</subject><subject>Dosage Forms</subject><subject>Drug Combinations</subject><subject>Female</subject><subject>Humans</subject><subject>Levodopa - administration &amp; dosage</subject><subject>Levodopa - adverse effects</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Motor complications</subject><subject>Nitriles - administration &amp; dosage</subject><subject>Nitriles - adverse effects</subject><subject>Parkinson Disease - drug therapy</subject><subject>Parkinson Disease - epidemiology</subject><subject>Parkinson's disease</subject><subject>Patient Compliance - statistics &amp; 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Thomas, Simu K. ; Hagiwara, May ; Mancione, L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-3af51aacbe4ed93036ceb80939f34b3ffd99878cef5d191d349d9fbfb324c8813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adherence</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Algorithms</topic><topic>Antiparkinson Agents - administration &amp; dosage</topic><topic>Antiparkinson Agents - adverse effects</topic><topic>Carbidopa - administration &amp; dosage</topic><topic>Carbidopa - adverse effects</topic><topic>Catechols - administration &amp; dosage</topic><topic>Catechols - adverse effects</topic><topic>Cohort Studies</topic><topic>Dosage Forms</topic><topic>Drug Combinations</topic><topic>Female</topic><topic>Humans</topic><topic>Levodopa - administration &amp; dosage</topic><topic>Levodopa - adverse effects</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Motor complications</topic><topic>Nitriles - administration &amp; dosage</topic><topic>Nitriles - adverse effects</topic><topic>Parkinson Disease - drug therapy</topic><topic>Parkinson Disease - epidemiology</topic><topic>Parkinson's disease</topic><topic>Patient Compliance - statistics &amp; numerical data</topic><topic>Retrospective Studies</topic><topic>Tablets</topic><topic>Wearing-off</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Delea, Thomas E.</creatorcontrib><creatorcontrib>Thomas, Simu K.</creatorcontrib><creatorcontrib>Hagiwara, May</creatorcontrib><creatorcontrib>Mancione, L.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Current medical research and opinion</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Delea, Thomas E.</au><au>Thomas, Simu K.</au><au>Hagiwara, May</au><au>Mancione, L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adherence with levodopa/carbidopa/entacapone versus levodopa/carbidopa and entacapone as separate tablets in patients with Parkinson's disease</atitle><jtitle>Current medical research and opinion</jtitle><addtitle>Curr Med Res Opin</addtitle><date>2010-07-01</date><risdate>2010</risdate><volume>26</volume><issue>7</issue><spage>1543</spage><epage>1552</epage><pages>1543-1552</pages><issn>0300-7995</issn><eissn>1473-4877</eissn><abstract>Observational studies suggest that single-tablet formulations are associated with improved adherence versus the same components taken as separate tablets. The objective of this study was to compare adherence in patients with Parkinson's disease (PD) receiving levodopa therapy as levodopa/carbidopa/entacapone tablets (LCE) versus levodopa/carbidopa (LC) tablets and entacapone (E) as separate tablets (LC and E). This was a retrospective, observational cohort study using a large health insurance claims database. Subjects included persons with a PD diagnosis who were receiving LC without E and then received either an add-on therapy with E as a separate tablet (LC and E) or LCE as one tablet (LCE). The primary study outcome was treatment adherence, estimated from pharmacy refills based on the 'percent of days covered' (PDC) with LCE or LC and E during follow-up and compared for patients receiving LCE and LC and E using multivariate regression analyses. In multivariate analyses controlling for differences between groups in baseline characteristics, including pre-index dosage of and adherence with LC, receipt of LCE (n = 388) was associated with 79% lower mean non-adherence during follow-up (95% CI: 73-83%; p &lt; 0.001) versus LC and E (n = 823), 86% lower odds of unsatisfactory adherence (95% CI: 80-91%; p &lt; 0.001), and a 26% lower risk of discontinuation (95% CI: 6-42%; p &lt; 0.013). This was an observational study with the inherent potential for selection bias. Pharmacy claims may not provide an accurate estimate of adherence. Requiring subjects to have a certain number of prescriptions before and after the index date may yield a sample that is not representative of all patients initiating levodopa therapy in typical clinical practice. Better adherence with LCE may have important implications for maintaining function in patients receiving chronic oral levodopa therapy. Further research is needed to confirm these results and examine the association between improved adherence and clinical and economic outcomes.</abstract><cop>England</cop><pub>Taylor &amp; Francis</pub><pmid>20429819</pmid><doi>10.1185/03007991003780628</doi><tpages>10</tpages></addata></record>
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subjects Adherence
Aged
Aged, 80 and over
Algorithms
Antiparkinson Agents - administration & dosage
Antiparkinson Agents - adverse effects
Carbidopa - administration & dosage
Carbidopa - adverse effects
Catechols - administration & dosage
Catechols - adverse effects
Cohort Studies
Dosage Forms
Drug Combinations
Female
Humans
Levodopa - administration & dosage
Levodopa - adverse effects
Male
Middle Aged
Motor complications
Nitriles - administration & dosage
Nitriles - adverse effects
Parkinson Disease - drug therapy
Parkinson Disease - epidemiology
Parkinson's disease
Patient Compliance - statistics & numerical data
Retrospective Studies
Tablets
Wearing-off
title Adherence with levodopa/carbidopa/entacapone versus levodopa/carbidopa and entacapone as separate tablets in patients with Parkinson's disease
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