Joseph B. Straton, MD

ABSTRACT

BACKGROUND: Although selective serotonin reuptake inhibitors (SSRIs) are the most commonly prescribed antidepressants, data comparing the effectiveness of the members of this class of antidepressants are limited. This study compared the effectiveness of 3 SSRIs in a naturalistic study designed to mimic typical primary care prescribing.

POPULATION STUDIED: Adult outpatients from 2 primary care research networks were eligible for the study if their primary care doctor had diagnosed a depressive disorder requiring medication. Patients were excluded if they were cognitively impaired, terminally ill, or suicidal; lived in a nursing home; were currently taking a non-SSRI antidepressant; or had recently taken an SSRI antidepressant. Data were analyzed from 546 patients (79% of those invited to participate), who were randomized and completed at least 1 follow-up interview.

STUDY DESIGN AND VALIDITY: This was a randomized, controlled, unblinded trial designed to reflect actual primary care practice. After being diagnosed by their primary care physician (PCP) with clinical depression, with the PCP using his or her usual methods to make the diagnosis, patients were randomized through a concealed allocation procedure to receive daily doses of 20 mg paroxetine (Paxil), 20 mg fluoxetine (Prozac), or 50 mg sertraline (Zoloft). Both the patients and doctors were aware of the medication assignment. The PCP could adjust the dose to clinical response or change patients to a different medication. By the end of the study, less than half of the patients were taking the medication they had originally started.

OUTCOMES MEASURED: The primary outcome was change in the Mental Component Score (MCS) of the Medical Outcomes Study 36-Item Short Form Health Survey (SF-36). The scoring of the MCS incorporates elements of the 8 subscales of the SF-36 and ranges from 0 to 100, with higher scores representing better mental health. Several other measures of depression and social functioning provided secondary outcomes.

RESULTS: Forty-one percent to 50% of participants stopped their initially assigned medication during the 9-month follow-up period. About 20% of participants switched to another antidepressant. Roughly 25% stopped taking antidepressants altogether before completion of the follow-up period.

ABSTRACT

BACKGROUND: Although selective serotonin reuptake inhibitors (SSRIs) are the most commonly prescribed antidepressants, data comparing the effectiveness of the members of this class of antidepressants are limited. This study compared the effectiveness of 3 SSRIs in a naturalistic study designed to mimic typical primary care prescribing.

POPULATION STUDIED: Adult outpatients from 2 primary care research networks were eligible for the study if their primary care doctor had diagnosed a depressive disorder requiring medication. Patients were excluded if they were cognitively impaired, terminally ill, or suicidal; lived in a nursing home; were currently taking a non-SSRI antidepressant; or had recently taken an SSRI antidepressant. Data were analyzed from 546 patients (79% of those invited to participate), who were randomized and completed at least 1 follow-up interview.

STUDY DESIGN AND VALIDITY: This was a randomized, controlled, unblinded trial designed to reflect actual primary care practice. After being diagnosed by their primary care physician (PCP) with clinical depression, with the PCP using his or her usual methods to make the diagnosis, patients were randomized through a concealed allocation procedure to receive daily doses of 20 mg paroxetine (Paxil), 20 mg fluoxetine (Prozac), or 50 mg sertraline (Zoloft). Both the patients and doctors were aware of the medication assignment. The PCP could adjust the dose to clinical response or change patients to a different medication. By the end of the study, less than half of the patients were taking the medication they had originally started.

OUTCOMES MEASURED: The primary outcome was change in the Mental Component Score (MCS) of the Medical Outcomes Study 36-Item Short Form Health Survey (SF-36). The scoring of the MCS incorporates elements of the 8 subscales of the SF-36 and ranges from 0 to 100, with higher scores representing better mental health. Several other measures of depression and social functioning provided secondary outcomes.

RESULTS: Forty-one percent to 50% of participants stopped their initially assigned medication during the 9-month follow-up period. About 20% of participants switched to another antidepressant. Roughly 25% stopped taking antidepressants altogether before completion of the follow-up period.

ABSTRACT

BACKGROUND: Although selective serotonin reuptake inhibitors (SSRIs) are the most commonly prescribed antidepressants, data comparing the effectiveness of the members of this class of antidepressants are limited. This study compared the effectiveness of 3 SSRIs in a naturalistic study designed to mimic typical primary care prescribing.

POPULATION STUDIED: Adult outpatients from 2 primary care research networks were eligible for the study if their primary care doctor had diagnosed a depressive disorder requiring medication. Patients were excluded if they were cognitively impaired, terminally ill, or suicidal; lived in a nursing home; were currently taking a non-SSRI antidepressant; or had recently taken an SSRI antidepressant. Data were analyzed from 546 patients (79% of those invited to participate), who were randomized and completed at least 1 follow-up interview.

STUDY DESIGN AND VALIDITY: This was a randomized, controlled, unblinded trial designed to reflect actual primary care practice. After being diagnosed by their primary care physician (PCP) with clinical depression, with the PCP using his or her usual methods to make the diagnosis, patients were randomized through a concealed allocation procedure to receive daily doses of 20 mg paroxetine (Paxil), 20 mg fluoxetine (Prozac), or 50 mg sertraline (Zoloft). Both the patients and doctors were aware of the medication assignment. The PCP could adjust the dose to clinical response or change patients to a different medication. By the end of the study, less than half of the patients were taking the medication they had originally started.

OUTCOMES MEASURED: The primary outcome was change in the Mental Component Score (MCS) of the Medical Outcomes Study 36-Item Short Form Health Survey (SF-36). The scoring of the MCS incorporates elements of the 8 subscales of the SF-36 and ranges from 0 to 100, with higher scores representing better mental health. Several other measures of depression and social functioning provided secondary outcomes.

RESULTS: Forty-one percent to 50% of participants stopped their initially assigned medication during the 9-month follow-up period. About 20% of participants switched to another antidepressant. Roughly 25% stopped taking antidepressants altogether before completion of the follow-up period.