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Differences in compliance patterns across the selective serotonin reuptake inhibitors (SSRIs)
ABSTRACT Objective: To evaluate differential compliance rates between immediate-release (IR) selective serotonin reuptake inhibitors (SSRI) and a controlled-release (CR) SSRI in patients initiating SSRI therapy. Methods: A retrospective analysis of patients initiating treatment with SSRIs identified...
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Published in: | Current medical research and opinion 2005-10, Vol.21 (10), p.1651-1658 |
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creator | Keene, Matthew S. Eaddy, Michael T. Mauch, Robert P. Regan, Timothy S. Shah, Manan Chiao, Evelyn |
description | ABSTRACT
Objective: To evaluate differential compliance rates between immediate-release (IR) selective serotonin reuptake inhibitors (SSRI) and a controlled-release (CR) SSRI in patients initiating SSRI therapy.
Methods: A retrospective analysis of patients initiating treatment with SSRIs identified in the IHCIS National Managed Care Database between July 2001 and December 2002 was conducted. Logistic regression models were used to assess differences in 6‐month compliance rates, controlling for age, gender, utilization of mental health specialty care services, titration rates, diagnoses, and comorbidities. Compliance was defined as having a minimum medication possession ratio of 80% over a 180-day period without evidence of a 15‐day gap prior to 90 days of therapy.
Results: There were 116 090 patients included in the study, with approximately 4% receiving a CR SSRI and 96% receiving IR SSRIs. Approximately 25% of patients had a diagnosis for depression, 16% had a diagnosis for anxiety, and 13% had a diagnosis for both anxiety and depression. Overall, 54.2% were noncompliant with therapy, while 30.2% of patients were compliant with therapy, and 15.7% had evidence of a therapy change. After controlling for baseline covariates, patients initiating IR SSRIs were 14% less likely to be compliant compared to those initiating paroxetine CR ( p < 0.0001). Patients initiating on paroxetine IR were least likely to be compliant (odds ratio [OR] 0.788; p < 0.0001), followed by escitalopram (OR 0.850; p = 0.0179), sertraline (OR 0.877; p = 0.0005), citalopram (0.909; p = 0.0114), and fluoxetine (OR 0.916; p = 0.0250).
Conclusions: Approximately 54% of patients initiating SSRI therapy were noncompliant with SSRI therapy over a 6‐month period, with the lowest level of compliance found in patients receiving IR SSRI agents. Future studies should assess the effect of compliance on economic measures and determine if reductions in resource utilization are found across specific SSRI agents. |
doi_str_mv | 10.1185/030079905X65420 |
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Objective: To evaluate differential compliance rates between immediate-release (IR) selective serotonin reuptake inhibitors (SSRI) and a controlled-release (CR) SSRI in patients initiating SSRI therapy.
Methods: A retrospective analysis of patients initiating treatment with SSRIs identified in the IHCIS National Managed Care Database between July 2001 and December 2002 was conducted. Logistic regression models were used to assess differences in 6‐month compliance rates, controlling for age, gender, utilization of mental health specialty care services, titration rates, diagnoses, and comorbidities. Compliance was defined as having a minimum medication possession ratio of 80% over a 180-day period without evidence of a 15‐day gap prior to 90 days of therapy.
Results: There were 116 090 patients included in the study, with approximately 4% receiving a CR SSRI and 96% receiving IR SSRIs. Approximately 25% of patients had a diagnosis for depression, 16% had a diagnosis for anxiety, and 13% had a diagnosis for both anxiety and depression. Overall, 54.2% were noncompliant with therapy, while 30.2% of patients were compliant with therapy, and 15.7% had evidence of a therapy change. After controlling for baseline covariates, patients initiating IR SSRIs were 14% less likely to be compliant compared to those initiating paroxetine CR ( p < 0.0001). Patients initiating on paroxetine IR were least likely to be compliant (odds ratio [OR] 0.788; p < 0.0001), followed by escitalopram (OR 0.850; p = 0.0179), sertraline (OR 0.877; p = 0.0005), citalopram (0.909; p = 0.0114), and fluoxetine (OR 0.916; p = 0.0250).
Conclusions: Approximately 54% of patients initiating SSRI therapy were noncompliant with SSRI therapy over a 6‐month period, with the lowest level of compliance found in patients receiving IR SSRI agents. Future studies should assess the effect of compliance on economic measures and determine if reductions in resource utilization are found across specific SSRI agents.</description><identifier>ISSN: 0300-7995</identifier><identifier>EISSN: 1473-4877</identifier><identifier>DOI: 10.1185/030079905X65420</identifier><identifier>PMID: 16238905</identifier><identifier>CODEN: CMROCX</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Adult ; Antidepressant ; Anxiety ; Anxiety - drug therapy ; Comorbidity ; Compliance ; Delayed-Action Preparations ; Depression ; Depression - drug therapy ; Female ; Humans ; Male ; Patient Compliance ; Retrospective Studies ; Selective serotonin reuptake inhibitor ; Serotonin Uptake Inhibitors - administration & dosage</subject><ispartof>Current medical research and opinion, 2005-10, Vol.21 (10), p.1651-1658</ispartof><rights>2005 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2005</rights><rights>Copyright Librapharm Oct 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-a77f93d60f51550f30e326838b43f777855a552451e2e57728b04a90e0d643d3</citedby><cites>FETCH-LOGICAL-c423t-a77f93d60f51550f30e326838b43f777855a552451e2e57728b04a90e0d643d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16238905$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Keene, Matthew S.</creatorcontrib><creatorcontrib>Eaddy, Michael T.</creatorcontrib><creatorcontrib>Mauch, Robert P.</creatorcontrib><creatorcontrib>Regan, Timothy S.</creatorcontrib><creatorcontrib>Shah, Manan</creatorcontrib><creatorcontrib>Chiao, Evelyn</creatorcontrib><title>Differences in compliance patterns across the selective serotonin reuptake inhibitors (SSRIs)</title><title>Current medical research and opinion</title><addtitle>Curr Med Res Opin</addtitle><description>ABSTRACT
Objective: To evaluate differential compliance rates between immediate-release (IR) selective serotonin reuptake inhibitors (SSRI) and a controlled-release (CR) SSRI in patients initiating SSRI therapy.
Methods: A retrospective analysis of patients initiating treatment with SSRIs identified in the IHCIS National Managed Care Database between July 2001 and December 2002 was conducted. Logistic regression models were used to assess differences in 6‐month compliance rates, controlling for age, gender, utilization of mental health specialty care services, titration rates, diagnoses, and comorbidities. Compliance was defined as having a minimum medication possession ratio of 80% over a 180-day period without evidence of a 15‐day gap prior to 90 days of therapy.
Results: There were 116 090 patients included in the study, with approximately 4% receiving a CR SSRI and 96% receiving IR SSRIs. Approximately 25% of patients had a diagnosis for depression, 16% had a diagnosis for anxiety, and 13% had a diagnosis for both anxiety and depression. Overall, 54.2% were noncompliant with therapy, while 30.2% of patients were compliant with therapy, and 15.7% had evidence of a therapy change. After controlling for baseline covariates, patients initiating IR SSRIs were 14% less likely to be compliant compared to those initiating paroxetine CR ( p < 0.0001). Patients initiating on paroxetine IR were least likely to be compliant (odds ratio [OR] 0.788; p < 0.0001), followed by escitalopram (OR 0.850; p = 0.0179), sertraline (OR 0.877; p = 0.0005), citalopram (0.909; p = 0.0114), and fluoxetine (OR 0.916; p = 0.0250).
Conclusions: Approximately 54% of patients initiating SSRI therapy were noncompliant with SSRI therapy over a 6‐month period, with the lowest level of compliance found in patients receiving IR SSRI agents. Future studies should assess the effect of compliance on economic measures and determine if reductions in resource utilization are found across specific SSRI agents.</description><subject>Adult</subject><subject>Antidepressant</subject><subject>Anxiety</subject><subject>Anxiety - drug therapy</subject><subject>Comorbidity</subject><subject>Compliance</subject><subject>Delayed-Action Preparations</subject><subject>Depression</subject><subject>Depression - drug therapy</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Patient Compliance</subject><subject>Retrospective Studies</subject><subject>Selective serotonin reuptake inhibitor</subject><subject>Serotonin Uptake Inhibitors - administration & dosage</subject><issn>0300-7995</issn><issn>1473-4877</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp1kE1rFTEUhoNY7LW6dieDC6mLaU--Jhl30vpRKBRsF24k5M6ccFNnJmOSUfrvze29UCx0lYTzPC8nLyFvKJxQquUpcADVtiB_NFIweEZWVCheC63Uc7LaTusylofkZUq3AJTptn1BDmnDuC7Wivw8985hxKnDVPmp6sI4D96WZzXbnDFOqbJdDClVeYNVwgG77P9sbzHkMBUl4jJn-wuLvvFrn0NM1fH19feL9OEVOXB2SPh6fx6Rmy-fb86-1ZdXXy_OPl3WnWA811Yp1_K-ASeplOA4IGeN5notuFNKaSmtlExIigylUkyvQdgWEPpG8J4fkfe72DmG3wumbEafOhwGO2FYkmm0At2AKOC7R-BtWOJUVjMMNABr2RY63UH3347ozBz9aOOdoWC2rZtHrRfj7T52WY_YP_D7mgvwcQf4yYU42r8hDr3J9m4I0cXStk-GP53e_idv0A5509mID9s_5f4DeOigZQ</recordid><startdate>20051001</startdate><enddate>20051001</enddate><creator>Keene, Matthew S.</creator><creator>Eaddy, Michael T.</creator><creator>Mauch, Robert P.</creator><creator>Regan, Timothy S.</creator><creator>Shah, Manan</creator><creator>Chiao, Evelyn</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><general>Informa Healthcare</general><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>20051001</creationdate><title>Differences in compliance patterns across the selective serotonin reuptake inhibitors (SSRIs)</title><author>Keene, Matthew S. ; Eaddy, Michael T. ; Mauch, Robert P. ; Regan, Timothy S. ; Shah, Manan ; Chiao, Evelyn</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-a77f93d60f51550f30e326838b43f777855a552451e2e57728b04a90e0d643d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>Antidepressant</topic><topic>Anxiety</topic><topic>Anxiety - drug therapy</topic><topic>Comorbidity</topic><topic>Compliance</topic><topic>Delayed-Action Preparations</topic><topic>Depression</topic><topic>Depression - drug therapy</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Patient Compliance</topic><topic>Retrospective Studies</topic><topic>Selective serotonin reuptake inhibitor</topic><topic>Serotonin Uptake Inhibitors - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Keene, Matthew S.</creatorcontrib><creatorcontrib>Eaddy, Michael T.</creatorcontrib><creatorcontrib>Mauch, Robert P.</creatorcontrib><creatorcontrib>Regan, Timothy S.</creatorcontrib><creatorcontrib>Shah, Manan</creatorcontrib><creatorcontrib>Chiao, Evelyn</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</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><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</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>Keene, Matthew S.</au><au>Eaddy, Michael T.</au><au>Mauch, Robert P.</au><au>Regan, Timothy S.</au><au>Shah, Manan</au><au>Chiao, Evelyn</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differences in compliance patterns across the selective serotonin reuptake inhibitors (SSRIs)</atitle><jtitle>Current medical research and opinion</jtitle><addtitle>Curr Med Res Opin</addtitle><date>2005-10-01</date><risdate>2005</risdate><volume>21</volume><issue>10</issue><spage>1651</spage><epage>1658</epage><pages>1651-1658</pages><issn>0300-7995</issn><eissn>1473-4877</eissn><coden>CMROCX</coden><abstract>ABSTRACT
Objective: To evaluate differential compliance rates between immediate-release (IR) selective serotonin reuptake inhibitors (SSRI) and a controlled-release (CR) SSRI in patients initiating SSRI therapy.
Methods: A retrospective analysis of patients initiating treatment with SSRIs identified in the IHCIS National Managed Care Database between July 2001 and December 2002 was conducted. Logistic regression models were used to assess differences in 6‐month compliance rates, controlling for age, gender, utilization of mental health specialty care services, titration rates, diagnoses, and comorbidities. Compliance was defined as having a minimum medication possession ratio of 80% over a 180-day period without evidence of a 15‐day gap prior to 90 days of therapy.
Results: There were 116 090 patients included in the study, with approximately 4% receiving a CR SSRI and 96% receiving IR SSRIs. Approximately 25% of patients had a diagnosis for depression, 16% had a diagnosis for anxiety, and 13% had a diagnosis for both anxiety and depression. Overall, 54.2% were noncompliant with therapy, while 30.2% of patients were compliant with therapy, and 15.7% had evidence of a therapy change. After controlling for baseline covariates, patients initiating IR SSRIs were 14% less likely to be compliant compared to those initiating paroxetine CR ( p < 0.0001). Patients initiating on paroxetine IR were least likely to be compliant (odds ratio [OR] 0.788; p < 0.0001), followed by escitalopram (OR 0.850; p = 0.0179), sertraline (OR 0.877; p = 0.0005), citalopram (0.909; p = 0.0114), and fluoxetine (OR 0.916; p = 0.0250).
Conclusions: Approximately 54% of patients initiating SSRI therapy were noncompliant with SSRI therapy over a 6‐month period, with the lowest level of compliance found in patients receiving IR SSRI agents. Future studies should assess the effect of compliance on economic measures and determine if reductions in resource utilization are found across specific SSRI agents.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>16238905</pmid><doi>10.1185/030079905X65420</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Antidepressant Anxiety Anxiety - drug therapy Comorbidity Compliance Delayed-Action Preparations Depression Depression - drug therapy Female Humans Male Patient Compliance Retrospective Studies Selective serotonin reuptake inhibitor Serotonin Uptake Inhibitors - administration & dosage |
title | Differences in compliance patterns across the selective serotonin reuptake inhibitors (SSRIs) |
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