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  1. Article ; Online: A Descriptive Study of the Caregiver's Experience of Managing Care for Children and Adolescents With Attention-Deficit/Hyperactivity Disorder During the COVID-19 Pandemic: The UNCOVER Study.

    Raveendran, Subhara / Burke, Mary C / Klahn, Karen / McCue, Maggie / Roy, Anit / Martin, Michael / Sarkey, Sara

    The primary care companion for CNS disorders

    2024  Volume 26, Issue 1

    MeSH term(s) Adult ; Child ; Humans ; Adolescent ; COVID-19 ; Attention Deficit Disorder with Hyperactivity/therapy ; Caregivers ; Pandemics ; Quality of Life
    Language English
    Publishing date 2024-01-02
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2675414-9
    ISSN 2155-7780 ; 2155-7780
    ISSN (online) 2155-7780
    ISSN 2155-7780
    DOI 10.4088/PCC.23m03587
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Correction to: Using the Goal Attainment Scale adapted for depression to better understand treatment outcomes in patients with major depressive disorder switching to vortioxetine: a phase 4, single-arm, open-label, multicenter study.

    McCue, Maggie / Sarkey, Sara / Eramo, Anna / François, Clement / Parikh, Sagar V

    BMC psychiatry

    2022  Volume 22, Issue 1, Page(s) 170

    Language English
    Publishing date 2022-03-07
    Publishing country England
    Document type Published Erratum
    ZDB-ID 2050438-X
    ISSN 1471-244X ; 1471-244X
    ISSN (online) 1471-244X
    ISSN 1471-244X
    DOI 10.1186/s12888-022-03798-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Correction: Using the Goal Attainment Scale adapted for depression to better understand treatment outcomes in patients with major depressive disorder switching to vortioxetine: a phase 4, single-arm, open-label, multicenter study.

    McCue, Maggie / Sarkey, Sara / Eramo, Anna / François, Clement / Parikh, Sagar V

    BMC psychiatry

    2022  Volume 22, Issue 1, Page(s) 388

    Language English
    Publishing date 2022-06-08
    Publishing country England
    Document type Published Erratum
    ZDB-ID 2050438-X
    ISSN 1471-244X ; 1471-244X
    ISSN (online) 1471-244X
    ISSN 1471-244X
    DOI 10.1186/s12888-022-03975-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: The Experience of Adults With Attention-Deficit/Hyperactivity Disorder in 2021 During the COVID-19 Pandemic: The UNCOVER Study.

    Raveendran, Subhara / Burke, Mary C / Klahn, Karen / McCue, Maggie / Roy, Anit / Martin, Michael / Sarkey, Sara

    The primary care companion for CNS disorders

    2023  Volume 25, Issue 4

    MeSH term(s) Humans ; Adult ; Attention Deficit Disorder with Hyperactivity/drug therapy ; Attention Deficit Disorder with Hyperactivity/epidemiology ; Pandemics ; Quality of Life ; Cross-Sectional Studies ; COVID-19/epidemiology ; Central Nervous System Stimulants/therapeutic use
    Chemical Substances Central Nervous System Stimulants
    Language English
    Publishing date 2023-07-13
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2675414-9
    ISSN 2155-7780 ; 2155-7780
    ISSN (online) 2155-7780
    ISSN 2155-7780
    DOI 10.4088/PCC.22m03474
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Using the Goal Attainment Scale adapted for depression to better understand treatment outcomes in patients with major depressive disorder switching to vortioxetine: a phase 4, single-arm, open-label, multicenter study.

    McCue, Maggie / Sarkey, Sara / Eramo, Anna / François, Clement / Parikh, Sagar V

    BMC psychiatry

    2021  Volume 21, Issue 1, Page(s) 622

    Abstract: Background: Major depressive disorder (MDD) is the leading cause of disability worldwide. Response to pharmacologic treatment is generally evaluated by traditional clinician- and patient-reported rating scales. Assessing therapeutic efficacy using the ... ...

    Abstract Background: Major depressive disorder (MDD) is the leading cause of disability worldwide. Response to pharmacologic treatment is generally evaluated by traditional clinician- and patient-reported rating scales. Assessing therapeutic efficacy using the Goal Attainment Scale offers a complementary measure that focuses on recovery-oriented outcomes that patients consider valuable and vital to their well-being. This study aimed to examine outcomes using the Goal Attainment Scale adapted for depression (GAS-D).
    Methods: A phase 4, single-arm, open-label, multicenter study enrolled patients with MDD who were switching antidepressant medication. Patients received vortioxetine 10-20 mg over 12 weeks. Three specific, measurable, attainable, relevant, and time-bound goals were collaboratively set by patients with their clinicians. One goal was determined by the patient's self-defined objectives; 2 were related to predefined domain categories. Prespecified domains included psychological, motivational, emotional, physical/functional, and cognitive categories. The primary endpoint was the proportion of patients who achieved a GAS-D score ≥ 50 at week 12. Secondary and exploratory endpoints included changes from baseline in several clinical and patient-reported measures of depression and cognitive function. Safety and tolerability were also assessed.
    Results: At week 12, of the 122 adults participating in the study, 57.8% achieved a GAS-D score ≥ 50. Depression severity, cognitive function, cognitive performance, well-being, employment, and quality of life also significantly improved. Treatment response and remission rates were 65 and 40%, respectively. Vortioxetine was well tolerated, with adverse events consistent with product labeling.
    Conclusions: A majority of patients with MDD switching to vortioxetine achieved their treatment goals, including improvement in specific functional outcomes relating to physical and emotional goals, as assessed by the GAS-D and standard patient- and clinician-reported measures. When assayed for convergent validity in a separate analysis, changes in goal scores on the GAS-D were statistically significantly correlated with multiple commonly used clinical measures of depression assessed in this study. The GAS-D approach provides a new patient-centric paradigm for the collaborative development and assessment of progress toward meaningful treatment goals, contributing to a comprehensive evaluation of treatment outcomes in patients with MDD. Longer studies against a control intervention are justified.
    Trial registration: ClinicalTrials.gov identifier: NCT02972632 . Registered 21 November 2016.
    MeSH term(s) Adult ; Depression ; Depressive Disorder, Major/drug therapy ; Double-Blind Method ; Goals ; Humans ; Quality of Life ; Treatment Outcome ; Vortioxetine
    Chemical Substances Vortioxetine (3O2K1S3WQV)
    Language English
    Publishing date 2021-12-11
    Publishing country England
    Document type Clinical Trial, Phase IV ; Journal Article ; Multicenter Study ; Research Support, Non-U.S. Gov't
    ZDB-ID 2050438-X
    ISSN 1471-244X ; 1471-244X
    ISSN (online) 1471-244X
    ISSN 1471-244X
    DOI 10.1186/s12888-021-03608-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Design and Implementation of a Digitally Enabled Care Pathway to Improve Management of Depression in a Large Health Care System: Protocol for the Implementation of a Patient Care Platform.

    Khatib, Rasha / McCue, Maggie / Blair, Chris / Roy, Anit / Franco, John / Fehnert, Ben / King, James / Sarkey, Sara / Chrones, Lambros / Martin, Michael / Kabir, Christopher / Kemp, David E

    JMIR research protocols

    2023  Volume 12, Page(s) e43788

    Abstract: Background: Major depressive disorder (MDD) is a serious public health concern worldwide. A treatment approach that incorporates measurement-based care (MBC) and shared decision-making between patients with MDD and their providers may foster patient ... ...

    Abstract Background: Major depressive disorder (MDD) is a serious public health concern worldwide. A treatment approach that incorporates measurement-based care (MBC) and shared decision-making between patients with MDD and their providers may foster patient engagement and improve clinical outcomes. While digital tools such as mobile apps show promise for expanding health interventions, these apps are rarely integrated into clinical practice.
    Objective: The primary objective of this ongoing study is to determine whether implementation of a digital tool-the Pathway Platform-in primary care improves adherence to MBC practices; here, we present the study methods.
    Methods: This large-scale, real-world implementation study is based on a pilot study of an earlier iteration of a mobile app (the Pathway app) that confirmed the feasibility of using the app in patients with MDD and showed a positive trend in patient engagement in the app arm. In addition, a user-centered design approach that included qualitative assessments from patients and providers was used to improve understanding of the patient journey and care team workflows. User feedback highlighted the need for enhanced features, education modules, and real-time data sharing via integration with the electronic health record. The current iteration of the Platform includes the newest version of the Pathway app, education modules for both patients and providers, and real-time patient-level data sharing with the electronic health record. The study takes place in primary care sites within the Advocate Aurora Health system in Illinois and includes adult patients with MDD who were recently prescribed monotherapy antidepressant medication (defined as a new start, medication switch, or dose change in the past 3 months). Clinical performance and selected patient outcomes will be compared before and after the implementation of the Platform.
    Results: Patient recruitment was completed in July 2022, with initial results expected in mid-2023.
    Conclusions: This study will provide useful insights into real-world integration of a digital platform within a large health system. The methods presented here highlight the unique user-centric development of the Pathway Platform, which has resulted in an enhanced digital tool with the potential to foster MBC and shared decision-making, improve patient-provider communication, and ultimately lead to optimized treatment outcomes for patients with MDD.
    Trial registration: ClinicalTrials.gov NCT04891224; https://clinicaltrials.gov/ct2/show/NCT04891224.
    International registered report identifier (irrid): DERR1-10.2196/43788.
    Language English
    Publishing date 2023-06-23
    Publishing country Canada
    Document type Journal Article
    ZDB-ID 2719222-2
    ISSN 1929-0748
    ISSN 1929-0748
    DOI 10.2196/43788
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Real-world clinical outcomes and treatment patterns in patients with MDD treated with vortioxetine: a retrospective study.

    McDaniel, Brandon T / Cornet, Victor / Carroll, Jeanne / Chrones, Lambros / Chudzik, Joseph / Cochran, Jeanette / Guha, Shion / Lawrence, Debra F / McCue, Maggie / Sarkey, Sara / Lorenz, Betty / Fawver, Jay

    BMC psychiatry

    2023  Volume 23, Issue 1, Page(s) 938

    Abstract: Background: This study included evaluation of the effectiveness of vortioxetine, a treatment for adults with major depressive disorder (MDD), using patient-reported outcome measures (PROMs) in a real-world setting.: Methods: This retrospective chart ... ...

    Abstract Background: This study included evaluation of the effectiveness of vortioxetine, a treatment for adults with major depressive disorder (MDD), using patient-reported outcome measures (PROMs) in a real-world setting.
    Methods: This retrospective chart review analyzed the care experiences of adult patients with a diagnosis of MDD from Parkview Physicians Group - Mind-Body Medicine, Midwestern United States. Patients with a prescription for vortioxetine, an initial baseline visit, and ≥ 2 follow-up visits within 16 weeks from September 2014 to December 2018 were included. The primary outcome measure was effectiveness of vortioxetine on depression severity as assessed by change in Patient Health Questionnaire-9 (PHQ-9) scores ~ 12 weeks after initiation of vortioxetine. Secondary outcomes included changes in depression-related symptoms (i.e., sexual dysfunction, sleep disturbance, cognitive function, work/social function), clinical characteristics, response, remission, and medication persistence. Clinical narrative notes were also analyzed to examine sleep disturbance, sexual dysfunction, appetite, absenteeism, and presenteeism. All outcomes were examined at index (start of vortioxetine) and at ~ 12 weeks, and mean differences were analyzed using pairwise t tests.
    Results: A total of 1242 patients with MDD met inclusion criteria, and 63.9% of these patients had ≥ 3 psychiatric diagnoses and 65.9% were taking ≥ 3 medications. PHQ-9 mean scores decreased significantly from baseline to week 12 (14.15 ± 5.8 to 9.62 ± 6.03, respectively; p < 0.001). At week 12, the response and remission rates in all patients were 31.0% and 23.1%, respectively, and 67% continued vortioxetine treatment. Overall, results also showed significant improvements by week 12 in anxiety (p < 0.001), sexual dysfunction (p < 0.01), sleep disturbance (p < 0.01), cognitive function (p < 0.001), work/social functioning (p = 0.021), and appetite (p < 0.001). A significant decrease in presenteeism was observed at week 12 (p < 0.001); however, no significant change was observed in absenteeism (p = 0.466).
    Conclusions: Using PROMs, our study results suggest that adults with MDD prescribed vortioxetine showed improvement in depressive symptoms in the context of a real-world clinical practice setting. These patients had multiple comorbid psychiatric and physical diagnoses and multiple previous antidepressant treatments had failed.
    MeSH term(s) Adult ; Humans ; Vortioxetine/therapeutic use ; Depressive Disorder, Major/psychology ; Retrospective Studies ; Antidepressive Agents/therapeutic use ; Sexual Dysfunction, Physiological ; Treatment Outcome ; Double-Blind Method
    Chemical Substances Vortioxetine (3O2K1S3WQV) ; Antidepressive Agents
    Language English
    Publishing date 2023-12-13
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2050438-X
    ISSN 1471-244X ; 1471-244X
    ISSN (online) 1471-244X
    ISSN 1471-244X
    DOI 10.1186/s12888-023-05439-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Patient Perspective of Cognitive Symptoms in Major Depressive Disorder: Retrospective Database and Prospective Survey Analyses.

    Chiauzzi, Emil / Drahos, Jennifer / Sarkey, Sara / Curran, Christopher / Wang, Victor / Tomori, Dapo

    Journal of participatory medicine

    2019  Volume 11, Issue 2, Page(s) e11167

    Abstract: Background: Major depressive disorder (MDD) is a common and burdensome condition. The clinical understanding of MDD is shaped by current research, which lacks insight into the patient perspective.: Objective: This two-part study aimed to generate ... ...

    Abstract Background: Major depressive disorder (MDD) is a common and burdensome condition. The clinical understanding of MDD is shaped by current research, which lacks insight into the patient perspective.
    Objective: This two-part study aimed to generate data from PatientsLikeMe, an online patient network, on the perception of cognitive symptoms and their prioritization in MDD.
    Methods: A retrospective data analysis (study 1) was used to analyze data from the PatientsLikeMe community with self-reported MDD. Information on patient demographics, comorbidities, self-rated severity of MDD, treatment effectiveness, and specific symptoms of MDD was analyzed. A prospective electronic survey (study 2) was emailed to longstanding and recently active members of the PatientsLikeMe MDD community. Study 1 analysis informed the objectives of the study 2 survey, which were to determine symptom perception and prioritization, cognitive symptoms of MDD, residual symptoms, and medication effectiveness.
    Results: In study 1 (N=17,166), cognitive symptoms were frequently reported, including "severe" difficulty in concentrating (28%). Difficulty in concentrating was reported even among patients with no/mild depression (80%) and those who considered their treatment successful (17%). In study 2 (N=2525), 23% (118/508) of patients cited cognitive symptoms as a treatment priority. Cognitive symptoms correlated with depression severity, including difficulty in making decisions, concentrating, and thinking clearly (r
    Conclusions: Patients acknowledge that cognitive dysfunction in MDD limits their ability to recover fully and return to a normal level of social and occupational functioning. Further clinical understanding and characterization of MDD for symptom prioritization and relapse risk due to residual cognitive impairment are required to help patients return to normal cognitive function and aid their overall recovery.
    Language English
    Publishing date 2019-05-16
    Publishing country Canada
    Document type Journal Article
    ZDB-ID 2573853-7
    ISSN 2152-7202 ; 2152-7202
    ISSN (online) 2152-7202
    ISSN 2152-7202
    DOI 10.2196/11167
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Mobile App to Enhance Patient Activation and Patient-Provider Communication in Major Depressive Disorder Management: Collaborative, Randomized Controlled Pilot Study.

    McCue, Maggie / Blair, Christopher / Fehnert, Ben / King, James / Cormack, Francesca / Sarkey, Sara / Eramo, Anna / Kabir, Christopher / Khatib, Rasha / Kemp, David

    JMIR formative research

    2022  Volume 6, Issue 10, Page(s) e34923

    Abstract: Background: Enhanced patient-provider engagement can improve patient health outcomes in chronic conditions, including major depressive disorder (MDD).: Objective: We evaluated the impact of a digitally enabled care mobile app, Pathway, designed to ... ...

    Abstract Background: Enhanced patient-provider engagement can improve patient health outcomes in chronic conditions, including major depressive disorder (MDD).
    Objective: We evaluated the impact of a digitally enabled care mobile app, Pathway, designed to improve MDD patient-provider engagement. Patients used a mobile interface to assess treatment progress and share this information with primary care providers (PCPs).
    Methods: In this 52-week, real-world effectiveness and feasibility study conducted in primary care clinics, 40 patients with MDD who were recently prescribed antidepressant monotherapy were randomized to use a mobile app with usual care (20/40, 50%) or usual care alone (20/40, 50%). Patients in the app arm engaged with the app daily for 18 weeks; a report was generated at 6-week intervals and shared with the PCPs to facilitate shared treatment decision-making discussions. The patients discontinued the app at week 18 and were followed through year 1. Coprimary outcome measures, assessed via research visits, included change from baseline in the 13-item Patient Activation Measure (PAM-13) and 7-item Patient-Provider Engagement Scale scores at week 18. Additional outcome measures included depression severity (9-item Patient Health Questionnaire [PHQ-9]) and cognitive symptoms (5-item Perceived Deficits Questionnaire-Depression).
    Results: All 37 patients (app arm: n=18, 49%; usual care arm: n=19, 51%) who completed the 18-week follow-up period (n=31, 84% female, mean age 36, SD 11.3 years) had moderate to moderately severe depression. Improvements in PAM-13 and PHQ-9 scores were observed in both arms. Increases in PAM-13 scores from baseline to 18 weeks were numerically greater in the app arm than in the usual care arm (mean 10.5, SD 13.2 vs mean 8.8, SD 9.4; P=.65). At 52 weeks, differences in PAM-13 scores from baseline demonstrated significantly greater improvements in the app arm than in the usual care arm (mean 20.2, SD 17.7 vs mean 1.6, SD 14.2; P=.04). Compared with baseline, PHQ-9 scores decreased in both the app arm and the usual care arm at 18 weeks (mean 7.8, SD 7.2 vs mean 7.0, SD 6.5; P=.73) and 52 weeks (mean 9.5, SD 4.0 vs mean 4.7, SD 6.0; P=.07). Improvements in 7-item Patient-Provider Engagement Scale and WHO-5 scores were observed in both arms at 18 weeks and were sustained through 52 weeks in the app arm. Improvements in WHO-5 scores at 52 weeks were significantly greater in the app arm than in the usual care arm (41.5 vs 20.0; P=.02).
    Conclusions: Patients with MDD will engage with a mobile app designed to track treatment and disease progression. PCPs will use the data generated as part of their assessment to inform clinical care. The study results suggest that an app-enabled clinical care pathway may enhance patient activation and benefit MDD management.
    Trial registration: ClinicalTrials.gov NCT03242213; https://clinicaltrials.gov/ct2/show/NCT03242213.
    Language English
    Publishing date 2022-10-27
    Publishing country Canada
    Document type Journal Article
    ISSN 2561-326X
    ISSN (online) 2561-326X
    DOI 10.2196/34923
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Patient attitudes toward and goals for MDD treatment: a survey study.

    McNaughton, Emily C / Curran, Christopher / Granskie, Jamie / Opler, Mark / Sarkey, Sara / Mucha, Lisa / Eramo, Anna / François, Clement / Webber-Lind, Briana / McCue, Maggie

    Patient preference and adherence

    2019  Volume 13, Page(s) 959–967

    Abstract: Background/Objectives: ...

    Abstract Background/Objectives:
    Language English
    Publishing date 2019-06-14
    Publishing country New Zealand
    Document type Journal Article
    ZDB-ID 2455848-5
    ISSN 1177-889X
    ISSN 1177-889X
    DOI 10.2147/PPA.S204198
    Database MEDical Literature Analysis and Retrieval System OnLINE

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