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Epidemiology and current treatment patterns of treatment-resistant depression in Scotland: a CPRD study

AIMS: To assess the incidence and treatments currently used in clinical practice for the treatment of treatment-resistant depression (TRD) in Scotland. BACKGROUND: Patients with major depressive disorder (MDD) who have not responded to at least two successive antidepressant (AD) treatments in a sing...

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Autores principales: Ming, Timothy, Denee, Tom, Scott, Gemma, Morrens, Joachim, Weatherburn, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8771495/
http://dx.doi.org/10.1192/bjo.2021.876
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author Ming, Timothy
Denee, Tom
Scott, Gemma
Morrens, Joachim
Weatherburn, Christopher
author_facet Ming, Timothy
Denee, Tom
Scott, Gemma
Morrens, Joachim
Weatherburn, Christopher
author_sort Ming, Timothy
collection PubMed
description AIMS: To assess the incidence and treatments currently used in clinical practice for the treatment of treatment-resistant depression (TRD) in Scotland. BACKGROUND: Patients with major depressive disorder (MDD) who have not responded to at least two successive antidepressant (AD) treatments in a single episode are described as having Treatment-Resistant Depression (TRD). Epidemiological data on TRD in Scotland is lacking. Furthermore, there is no data to our knowledge on therapies prescribed in Scottish clinical practice to treat TRD. METHOD: A retrospective, longitudinal cohort study was conducted using Clinical Practice Research Datalink (CPRD) medical records. Adult patients were indexed on AD prescription, requiring MDD diagnosis within 90 days, from Jan 2011-May 2018 with 360-day baseline and 180-day minimum follow-up periods. Failure of ≥2 adequate oral AD regimens following indexing constituted TRD classification. Incidence rates of MDD and TRD (within the MDD cohort) and treatment lines following TRD classification were derived. RESULT: The analysis included 20,059 patients with MDD (mean age 44 years, 63% female, median follow-up 59 months); 1,374 (6.8%) were classified as TRD. Median time-to-TRD classification was 25 months. The incidence rate of MDD was 15.9 per 1,000 patient-years and for TRD was 14.7 per 1,000 MDD-patient-years. For all first four post-TRD treatment lines, SSRI monotherapy was the most commonly prescribed therapy, followed by combination (dual/triple) therapy and augmentation therapy (at least one oral AD supplemented with lithium, an antipsychotic or an anticonvulsant therapy). At first-line of TRD treatment, 1,050 (76.4%) patients received monotherapy AD, 212 (15.4%) received combination AD therapy and 112 (8.2%) received augmentation therapy. The most common monotherapy treatments at first-line TRD were sertraline (15.6%), mirtazapine (13.8%), fluoxetine (12.2%) and venlafaxine (11.6%). Among combination therapies, mirtazapine, venlafaxine, sertraline and amitriptyline were frequently used. Among the TRD and MDD cohort, no somatic treatments were coded in CPRD, although the use of these treatments was likely underestimated. CONCLUSION: Monotherapy AD treatment was the most common therapy type for all four post-TRD treatment lines. These data support the need for new treatments that can achieve and maintain therapeutic response, and avoid continuous cycling through similar AD therapies. This study was sponsored by Janssen Cilag Ltd.
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spelling pubmed-87714952022-01-31 Epidemiology and current treatment patterns of treatment-resistant depression in Scotland: a CPRD study Ming, Timothy Denee, Tom Scott, Gemma Morrens, Joachim Weatherburn, Christopher BJPsych Open Service Evaluation AIMS: To assess the incidence and treatments currently used in clinical practice for the treatment of treatment-resistant depression (TRD) in Scotland. BACKGROUND: Patients with major depressive disorder (MDD) who have not responded to at least two successive antidepressant (AD) treatments in a single episode are described as having Treatment-Resistant Depression (TRD). Epidemiological data on TRD in Scotland is lacking. Furthermore, there is no data to our knowledge on therapies prescribed in Scottish clinical practice to treat TRD. METHOD: A retrospective, longitudinal cohort study was conducted using Clinical Practice Research Datalink (CPRD) medical records. Adult patients were indexed on AD prescription, requiring MDD diagnosis within 90 days, from Jan 2011-May 2018 with 360-day baseline and 180-day minimum follow-up periods. Failure of ≥2 adequate oral AD regimens following indexing constituted TRD classification. Incidence rates of MDD and TRD (within the MDD cohort) and treatment lines following TRD classification were derived. RESULT: The analysis included 20,059 patients with MDD (mean age 44 years, 63% female, median follow-up 59 months); 1,374 (6.8%) were classified as TRD. Median time-to-TRD classification was 25 months. The incidence rate of MDD was 15.9 per 1,000 patient-years and for TRD was 14.7 per 1,000 MDD-patient-years. For all first four post-TRD treatment lines, SSRI monotherapy was the most commonly prescribed therapy, followed by combination (dual/triple) therapy and augmentation therapy (at least one oral AD supplemented with lithium, an antipsychotic or an anticonvulsant therapy). At first-line of TRD treatment, 1,050 (76.4%) patients received monotherapy AD, 212 (15.4%) received combination AD therapy and 112 (8.2%) received augmentation therapy. The most common monotherapy treatments at first-line TRD were sertraline (15.6%), mirtazapine (13.8%), fluoxetine (12.2%) and venlafaxine (11.6%). Among combination therapies, mirtazapine, venlafaxine, sertraline and amitriptyline were frequently used. Among the TRD and MDD cohort, no somatic treatments were coded in CPRD, although the use of these treatments was likely underestimated. CONCLUSION: Monotherapy AD treatment was the most common therapy type for all four post-TRD treatment lines. These data support the need for new treatments that can achieve and maintain therapeutic response, and avoid continuous cycling through similar AD therapies. This study was sponsored by Janssen Cilag Ltd. Cambridge University Press 2021-06-18 /pmc/articles/PMC8771495/ http://dx.doi.org/10.1192/bjo.2021.876 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Service Evaluation
Ming, Timothy
Denee, Tom
Scott, Gemma
Morrens, Joachim
Weatherburn, Christopher
Epidemiology and current treatment patterns of treatment-resistant depression in Scotland: a CPRD study
title Epidemiology and current treatment patterns of treatment-resistant depression in Scotland: a CPRD study
title_full Epidemiology and current treatment patterns of treatment-resistant depression in Scotland: a CPRD study
title_fullStr Epidemiology and current treatment patterns of treatment-resistant depression in Scotland: a CPRD study
title_full_unstemmed Epidemiology and current treatment patterns of treatment-resistant depression in Scotland: a CPRD study
title_short Epidemiology and current treatment patterns of treatment-resistant depression in Scotland: a CPRD study
title_sort epidemiology and current treatment patterns of treatment-resistant depression in scotland: a cprd study
topic Service Evaluation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8771495/
http://dx.doi.org/10.1192/bjo.2021.876
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