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Treatment Nonadherence Leads to Dose Escalation in Many Depressed Patients

BOSTON – Nearly one-third of patients on antidepressant pharmacotherapy in a large-scale analysis did not take their original antidepressant dose as prescribed within the 6 months prior to dose escalation, a study has shown.

The findings suggest that the lack of adequate treatment response that drives dosage increases in many patients may be linked to suboptimal medication adherence rather than to dose insufficiency, Dr. David J. Muzina reported at the American Psychiatric Association’s Institute on Psychiatric Services.

To evaluate patient nonadherence to chronic antidepressant therapy and a resulting upward dosage titration of the same medication, Dr. Muzina of Medco Health Solutions Inc. and his colleagues identified 53,530 patients from Medco’s administrative patient claims database who were on antidepressant medications at the same dosage level for at least 6 months, followed by a subsequent submission of claims for a higher dose.

Patients with only one claim for antidepressant medication in a 6-month period were excluded from the analysis, as were those taking multiple antidepressants, Dr. Muzina explained.

To measure adherence status – which was determined by the proportion of days the patient possessed a supply of the medication, or the medication possession ratio (MPR) – a minimum of two claims for the same antidepressant drug was required. According to the National Committee for Quality Assurance’s antidepressant performance measures, adherence was defined as an MPR of at least 80%, Dr. Muzina said.

With respect to patient demographics and prescription characteristics, the study cohort was predominantly female (72%), with a mean age of 51 years. More than two-thirds of the sample (68%) filled their antidepressant prescriptions at retail pharmacies, and 62% received generic medications, Dr. Muzina said. Most of the prescriptions were ordered by nonpsychiatrists, with only 15% ordered by psychiatrists; nearly half of the 49,524 patients for whom Chronic Disease Scores (CDS) were available had scores indicating a high degree of comorbidity, he said.

Of the full study cohort, “only 70.3% were adherent to their antidepressant medication in the 6 months prior to their dosage increase. Nearly 30% were nonadherent,” Dr. Muzina reported. Among the nonadherent patients, “one in four was in possession of their prescribed medication during less than 3 months of the 6-month period,” he said.

An analysis of medication adherence by study subgroup – including age, sex, comorbidity, pharmacy channel (mail vs. retail), formulation (brand vs. generic), and prescriber (psychiatrist vs. nonpsychiatrist) – showed significant differences for all but the type of clinician prescriber, Dr. Muzina said, noting that similarly high rates of nonadherence were observed among the psychiatrist (30.4%) and nonpsychiatrist (29.5%) groups.

Regarding pharmacy channel and formulation, 19.2% of patients who filled their prescriptions by mail were nonadherent, which was significantly lower than the 34.6% of those who used a retail pharmacy. Those receiving generic-only drugs had a small but significantly higher nonadherence rate (30.2%) than the 28.9% rate that was observed among patients receiving brand-name drugs.

Older age, male sex, and a higher CDS – perhaps because of the increased interaction with clinicians required by sicker patients –were also associated with significantly improved adherence relative to their respective corollaries, he said.

Although the study did not investigate the reasons for patient nonadherence, some possibilities include undesired or intolerable side effects, negative stigma, and forgetfulness, Dr. Muzina hypothesized.

Although the findings are limited by the study’s retrospective design and the use of an administrative claims database, which doesn’t provide certain relevant clinical information, according to Dr. Muzina, the results indicate that clinicians should investigate and address adherence issues in all patients on antidepressant medications prior to prescribing a dose increase “to enable patients with depression to fully benefit from their medications.” Additionally, factors associated with adherence to antidepressant treatment should be investigated in future studies, he said.

Medco Health provided funding for the extraction of data from the patient claims database and statistical analysis. Dr. Muzina became national practice leader of Medco Neuroscience Resource Center after the study began and received no compensation for his participation.

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BOSTON – Nearly one-third of patients on antidepressant pharmacotherapy in a large-scale analysis did not take their original antidepressant dose as prescribed within the 6 months prior to dose escalation, a study has shown.

The findings suggest that the lack of adequate treatment response that drives dosage increases in many patients may be linked to suboptimal medication adherence rather than to dose insufficiency, Dr. David J. Muzina reported at the American Psychiatric Association’s Institute on Psychiatric Services.

To evaluate patient nonadherence to chronic antidepressant therapy and a resulting upward dosage titration of the same medication, Dr. Muzina of Medco Health Solutions Inc. and his colleagues identified 53,530 patients from Medco’s administrative patient claims database who were on antidepressant medications at the same dosage level for at least 6 months, followed by a subsequent submission of claims for a higher dose.

Patients with only one claim for antidepressant medication in a 6-month period were excluded from the analysis, as were those taking multiple antidepressants, Dr. Muzina explained.

To measure adherence status – which was determined by the proportion of days the patient possessed a supply of the medication, or the medication possession ratio (MPR) – a minimum of two claims for the same antidepressant drug was required. According to the National Committee for Quality Assurance’s antidepressant performance measures, adherence was defined as an MPR of at least 80%, Dr. Muzina said.

With respect to patient demographics and prescription characteristics, the study cohort was predominantly female (72%), with a mean age of 51 years. More than two-thirds of the sample (68%) filled their antidepressant prescriptions at retail pharmacies, and 62% received generic medications, Dr. Muzina said. Most of the prescriptions were ordered by nonpsychiatrists, with only 15% ordered by psychiatrists; nearly half of the 49,524 patients for whom Chronic Disease Scores (CDS) were available had scores indicating a high degree of comorbidity, he said.

Of the full study cohort, “only 70.3% were adherent to their antidepressant medication in the 6 months prior to their dosage increase. Nearly 30% were nonadherent,” Dr. Muzina reported. Among the nonadherent patients, “one in four was in possession of their prescribed medication during less than 3 months of the 6-month period,” he said.

An analysis of medication adherence by study subgroup – including age, sex, comorbidity, pharmacy channel (mail vs. retail), formulation (brand vs. generic), and prescriber (psychiatrist vs. nonpsychiatrist) – showed significant differences for all but the type of clinician prescriber, Dr. Muzina said, noting that similarly high rates of nonadherence were observed among the psychiatrist (30.4%) and nonpsychiatrist (29.5%) groups.

Regarding pharmacy channel and formulation, 19.2% of patients who filled their prescriptions by mail were nonadherent, which was significantly lower than the 34.6% of those who used a retail pharmacy. Those receiving generic-only drugs had a small but significantly higher nonadherence rate (30.2%) than the 28.9% rate that was observed among patients receiving brand-name drugs.

Older age, male sex, and a higher CDS – perhaps because of the increased interaction with clinicians required by sicker patients –were also associated with significantly improved adherence relative to their respective corollaries, he said.

Although the study did not investigate the reasons for patient nonadherence, some possibilities include undesired or intolerable side effects, negative stigma, and forgetfulness, Dr. Muzina hypothesized.

Although the findings are limited by the study’s retrospective design and the use of an administrative claims database, which doesn’t provide certain relevant clinical information, according to Dr. Muzina, the results indicate that clinicians should investigate and address adherence issues in all patients on antidepressant medications prior to prescribing a dose increase “to enable patients with depression to fully benefit from their medications.” Additionally, factors associated with adherence to antidepressant treatment should be investigated in future studies, he said.

Medco Health provided funding for the extraction of data from the patient claims database and statistical analysis. Dr. Muzina became national practice leader of Medco Neuroscience Resource Center after the study began and received no compensation for his participation.

BOSTON – Nearly one-third of patients on antidepressant pharmacotherapy in a large-scale analysis did not take their original antidepressant dose as prescribed within the 6 months prior to dose escalation, a study has shown.

The findings suggest that the lack of adequate treatment response that drives dosage increases in many patients may be linked to suboptimal medication adherence rather than to dose insufficiency, Dr. David J. Muzina reported at the American Psychiatric Association’s Institute on Psychiatric Services.

To evaluate patient nonadherence to chronic antidepressant therapy and a resulting upward dosage titration of the same medication, Dr. Muzina of Medco Health Solutions Inc. and his colleagues identified 53,530 patients from Medco’s administrative patient claims database who were on antidepressant medications at the same dosage level for at least 6 months, followed by a subsequent submission of claims for a higher dose.

Patients with only one claim for antidepressant medication in a 6-month period were excluded from the analysis, as were those taking multiple antidepressants, Dr. Muzina explained.

To measure adherence status – which was determined by the proportion of days the patient possessed a supply of the medication, or the medication possession ratio (MPR) – a minimum of two claims for the same antidepressant drug was required. According to the National Committee for Quality Assurance’s antidepressant performance measures, adherence was defined as an MPR of at least 80%, Dr. Muzina said.

With respect to patient demographics and prescription characteristics, the study cohort was predominantly female (72%), with a mean age of 51 years. More than two-thirds of the sample (68%) filled their antidepressant prescriptions at retail pharmacies, and 62% received generic medications, Dr. Muzina said. Most of the prescriptions were ordered by nonpsychiatrists, with only 15% ordered by psychiatrists; nearly half of the 49,524 patients for whom Chronic Disease Scores (CDS) were available had scores indicating a high degree of comorbidity, he said.

Of the full study cohort, “only 70.3% were adherent to their antidepressant medication in the 6 months prior to their dosage increase. Nearly 30% were nonadherent,” Dr. Muzina reported. Among the nonadherent patients, “one in four was in possession of their prescribed medication during less than 3 months of the 6-month period,” he said.

An analysis of medication adherence by study subgroup – including age, sex, comorbidity, pharmacy channel (mail vs. retail), formulation (brand vs. generic), and prescriber (psychiatrist vs. nonpsychiatrist) – showed significant differences for all but the type of clinician prescriber, Dr. Muzina said, noting that similarly high rates of nonadherence were observed among the psychiatrist (30.4%) and nonpsychiatrist (29.5%) groups.

Regarding pharmacy channel and formulation, 19.2% of patients who filled their prescriptions by mail were nonadherent, which was significantly lower than the 34.6% of those who used a retail pharmacy. Those receiving generic-only drugs had a small but significantly higher nonadherence rate (30.2%) than the 28.9% rate that was observed among patients receiving brand-name drugs.

Older age, male sex, and a higher CDS – perhaps because of the increased interaction with clinicians required by sicker patients –were also associated with significantly improved adherence relative to their respective corollaries, he said.

Although the study did not investigate the reasons for patient nonadherence, some possibilities include undesired or intolerable side effects, negative stigma, and forgetfulness, Dr. Muzina hypothesized.

Although the findings are limited by the study’s retrospective design and the use of an administrative claims database, which doesn’t provide certain relevant clinical information, according to Dr. Muzina, the results indicate that clinicians should investigate and address adherence issues in all patients on antidepressant medications prior to prescribing a dose increase “to enable patients with depression to fully benefit from their medications.” Additionally, factors associated with adherence to antidepressant treatment should be investigated in future studies, he said.

Medco Health provided funding for the extraction of data from the patient claims database and statistical analysis. Dr. Muzina became national practice leader of Medco Neuroscience Resource Center after the study began and received no compensation for his participation.

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Treatment Nonadherence Leads to Dose Escalation in Many Depressed Patients
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antidepressant pharmacotherapy, antidepressant dose, dose escalation, adequate treatment response, dosage increase, Dr. David J. Muzina, American Psychiatric Association
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antidepressant pharmacotherapy, antidepressant dose, dose escalation, adequate treatment response, dosage increase, Dr. David J. Muzina, American Psychiatric Association
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Major Finding: Treatment nonadherence is behind dose escalation in one-third of patients who receive antidepressant therapy.

Data Source: A large-scale analysis of patient nonadherence to chronic antidepressant therapy and subsequent prescribed dose escalation of the same medication using a national patient claims administrative database.

Disclosures: Medco Health Solutions Inc. provided funding for the study. Dr. Muzina became an employee of Medco Neuroscience Resource Center after the study began and received no compensation for his participation.