Depressive Disorder, Treatment-Resistant
Conditions
Brief summary
The purpose of this study is to describe the epidemiology of Treatment Resistant Depression (TRD) in the US, including the population incidence of TRD, and TRD as a proportion of Pharmacologically Treated Depression (PTD), and stratify the estimates by sex and age group, with separate estimates for the Medicaid population, the Medicare population, and the privately insured population. Anonymized participants data will be used for the analysis.
Interventions
None listed
Sponsors
Janssen Research & Development, LLC
Study design
Observational model
COHORT
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
14 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Have been in the database for the past year (ignoring breaks of \< 30 days) * Have not had, an excluded diagnosis or dispensing of an AD medication during the past year * Are aged 14 to 60 years (if in the CCAE or MCDC databases), or are aged greater than or equal to (\>=) 65 years (if in the MCDR database). Age is defined as age on Jan 1, 2011. The boundary at age 60 for the first two databases is intended to avoid loss to follow-up due to transfer to Medicare at age 65. The boundary at age 65 for the MCDR database reflects the fact that very few people described by that database are aged less than 65
Exclusion criteria
\- Participants will be excluded when they receive diagnoses Schizophrenia, Bipolar disorder including mania or Dementia
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Incidence Rate of Treatment Resistant Depression | Up to 4 years | TRD will be defined as the failure of two medications, as marked by their replacement or supplementation with other medications using three alternative definitions. In one the time for a medication regimen to fail is limited to less than or equal to (\<=) 3 months and in the second the time for a medication regimen to fail is limited to \<= 6 months, both corresponding to the medication never providing adequate relief. In the third, the time for a medication regimen to fail will be limited to \<= 2 years, corresponding to the medication not providing permanent or very long lasting relief. |
| Treatment Resistant Depression as a Proportion of Pharmacologically Treated Depression | Up to 4 years | An episode of PTD begins when a member of the study cohort receives a dispensing of an antidepressant (AD) medication and receives a diagnosis of depression between 180 days before that dispensing and 30 days after that dispensing. |
| Incidence Rate of Treatment Resistant Depression by Age Group and Sex | Up to 4 years | TRD incidence will be stratified by age group and sex under each of the three definitions of failure of a medication regimen. |
| Incidence Rate of TRD as Separate Estimates for the Medicaid Population, the Medicare Population, and the Privately Insured Population | Up to 4 years | TRD incidence will be stratified by data population (database): Medicaid, Medicare, Privately insured. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Incidence on TRD Based on Sensitivity Analysis | Up to 4 years | Sensitivity analyses are intended to clarify how the results of the present study will compare to the results of other studies that may define as The maximum time for failure of a regimen is changed to: 60, 120, 150, or 365 days, or is not limited; the requirement that a regimen include greater than or equal to (\>=) 28 days' supply of the antidepressant medication and antipsychotic medication (if present) is changed to \>= 42 days and 14 days supply; participants who get an excluded diagnosis are retroactively excluded from the study cohort; or the definition of an incident case adds a requirement for no depression diagnosis in the prior year. |
| Number of Participants With Selected Markers for Severity of Depression | Up to 4 years | The following markers of severity will be tabulated during the PTD episodes and stratified according to whether the participant develops or does not develop TRD during the study period: Electro-convulsive therapy, hospitalization with a diagnosis of depression, receiving a diagnosis of suicidal thoughts, receiving a diagnosis of self-harm, emergency department visit with a diagnosis of injury, emergency department visit with a diagnosis of poisoning. |
Outcome results
None listed