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Targeted provider education and pre-visit planning increase rates of formal depression screening in childhood-onset SLE
BACKGROUND: Despite being at high risk for depression, patients with childhood-onset systemic lupus erythematosus (c-SLE) are infrequently and inconsistently screened for depression by their pediatric rheumatologists. We aimed to systematically increase rates of formal depression screening for c-SLE...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330037/ https://www.ncbi.nlm.nih.gov/pubmed/34344396 http://dx.doi.org/10.1186/s12969-021-00576-4 |
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author | Mulvihill, Evan Furru, Rebecca Goldstein-Leever, Alana Driest, Kyla Lemle, Stephanie MacDonald, Darby Frost, Emily Sivaraman, Vidya |
author_facet | Mulvihill, Evan Furru, Rebecca Goldstein-Leever, Alana Driest, Kyla Lemle, Stephanie MacDonald, Darby Frost, Emily Sivaraman, Vidya |
author_sort | Mulvihill, Evan |
collection | PubMed |
description | BACKGROUND: Despite being at high risk for depression, patients with childhood-onset systemic lupus erythematosus (c-SLE) are infrequently and inconsistently screened for depression by their pediatric rheumatologists. We aimed to systematically increase rates of formal depression screening for c-SLE patients in an academic Pediatric Rheumatology clinic. METHODS: Our multi-disciplinary quality improvement (QI) team used electronic health record (EHR) documentation to retroactively calculate baseline rates of documented depression screening using the Patient Health Questionnaire-9 (PHQ-9). We then engaged key stakeholders to develop a clinical workflow for formal depression screening in the clinic. We also provided education to providers regarding mental health disorders in c-SLE, with an emphasis on prevalence, screening methods, and management of positive screens. We then used the Plan-Do-Study Act (PDSA) method of QI to systematically evaluate and adjust our process in real time. The primary outcome was the percentage of patients with c-SLE seen per month who had a documented PHQ-9 screening within the past year. RESULTS: The percentage of children with documented PHQ-9 results ranged from 0 to 4.5 % at baseline to 91.0 % within 12 months of project initiation. By the end of the project, monthly screening rates greater than 80 % has been sustained for 10 months. As a result of these efforts, twenty-seven (48.2 %) patients with at least mild depressive symptoms were identified while seven (12.5 %) with thoughts of self-harm were referred to appropriate mental health resources. CONCLUSIONS: Routine formal depression screening is feasible in a busy subspecialty clinic. Using QI methods, rates of formal depression screening among children with c-SLE were increased from an average of 3.3 % per month to a sustained monthly rate of greater than 80 %. Individuals with depressive symptoms and/or thoughts of self-harm were identified and referred to appropriate mental health resources. |
format | Online Article Text |
id | pubmed-8330037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-83300372021-08-03 Targeted provider education and pre-visit planning increase rates of formal depression screening in childhood-onset SLE Mulvihill, Evan Furru, Rebecca Goldstein-Leever, Alana Driest, Kyla Lemle, Stephanie MacDonald, Darby Frost, Emily Sivaraman, Vidya Pediatr Rheumatol Online J Research Article BACKGROUND: Despite being at high risk for depression, patients with childhood-onset systemic lupus erythematosus (c-SLE) are infrequently and inconsistently screened for depression by their pediatric rheumatologists. We aimed to systematically increase rates of formal depression screening for c-SLE patients in an academic Pediatric Rheumatology clinic. METHODS: Our multi-disciplinary quality improvement (QI) team used electronic health record (EHR) documentation to retroactively calculate baseline rates of documented depression screening using the Patient Health Questionnaire-9 (PHQ-9). We then engaged key stakeholders to develop a clinical workflow for formal depression screening in the clinic. We also provided education to providers regarding mental health disorders in c-SLE, with an emphasis on prevalence, screening methods, and management of positive screens. We then used the Plan-Do-Study Act (PDSA) method of QI to systematically evaluate and adjust our process in real time. The primary outcome was the percentage of patients with c-SLE seen per month who had a documented PHQ-9 screening within the past year. RESULTS: The percentage of children with documented PHQ-9 results ranged from 0 to 4.5 % at baseline to 91.0 % within 12 months of project initiation. By the end of the project, monthly screening rates greater than 80 % has been sustained for 10 months. As a result of these efforts, twenty-seven (48.2 %) patients with at least mild depressive symptoms were identified while seven (12.5 %) with thoughts of self-harm were referred to appropriate mental health resources. CONCLUSIONS: Routine formal depression screening is feasible in a busy subspecialty clinic. Using QI methods, rates of formal depression screening among children with c-SLE were increased from an average of 3.3 % per month to a sustained monthly rate of greater than 80 %. Individuals with depressive symptoms and/or thoughts of self-harm were identified and referred to appropriate mental health resources. BioMed Central 2021-08-03 /pmc/articles/PMC8330037/ /pubmed/34344396 http://dx.doi.org/10.1186/s12969-021-00576-4 Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Mulvihill, Evan Furru, Rebecca Goldstein-Leever, Alana Driest, Kyla Lemle, Stephanie MacDonald, Darby Frost, Emily Sivaraman, Vidya Targeted provider education and pre-visit planning increase rates of formal depression screening in childhood-onset SLE |
title | Targeted provider education and pre-visit planning increase rates of formal depression screening in childhood-onset SLE |
title_full | Targeted provider education and pre-visit planning increase rates of formal depression screening in childhood-onset SLE |
title_fullStr | Targeted provider education and pre-visit planning increase rates of formal depression screening in childhood-onset SLE |
title_full_unstemmed | Targeted provider education and pre-visit planning increase rates of formal depression screening in childhood-onset SLE |
title_short | Targeted provider education and pre-visit planning increase rates of formal depression screening in childhood-onset SLE |
title_sort | targeted provider education and pre-visit planning increase rates of formal depression screening in childhood-onset sle |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330037/ https://www.ncbi.nlm.nih.gov/pubmed/34344396 http://dx.doi.org/10.1186/s12969-021-00576-4 |
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