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. 2023 Dec 13;23(1):938.
doi: 10.1186/s12888-023-05439-8.

Real-world clinical outcomes and treatment patterns in patients with MDD treated with vortioxetine: a retrospective study

Affiliations

Real-world clinical outcomes and treatment patterns in patients with MDD treated with vortioxetine: a retrospective study

Brandon T McDaniel et al. BMC Psychiatry. .

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.

Keywords: Cognitive functioning; Comorbid psychiatric diagnoses; Depression severity; Major depressive disorder; Patient-reported outcome measures; Previous antidepressant treatments; Real-world clinical practice setting; Sexual dysfunction; Social functioning; Vortioxetine.

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Conflict of interest statement

Brandon T. McDaniel, Victor Cornet, and Jeanne Carroll are employees of Parkview Mirro Center for Research and Innovation, which received funding from Takeda for the study. Victor Cornet also holds stock in Axcella Health. Joseph Chudzik is an intern/contractor with Parkview Mirro Center. Lambros Chrones, Maggie McCue, Sara Sarkey, and Betty Lorenz are employees of Takeda Pharmaceuticals U.S.A., Inc. Lambros Chrones, Maggie McCue, and Sara Sarkey have stock or stock options with Takeda. Betty Lorenz received funding for attending meetings and/or travel from Takeda and holds stock options with Takeda. Debra F. Lawrence was an employee of Takeda Pharmaceuticals U.S.A., Inc., at the time of the study and holds stock or stock options with Takeda. Shion Guha is an external contractor for Parkview Mirro Center, which received funds from Takeda for the study, and is an employee of the University of Toronto. Jay Fawver was a consultant with Takeda Pharmaceuticals U.S.A., Inc., at the time of the study and is an employee of Parkview Physicians Group – Mind-Body Medicine. He also is on the speakers’ bureau for Takeda. Jeanette Cochran is an employee of Parkview Physicians Group – Mind-Body Medicine.

Figures

Fig. 1
Fig. 1
Response and remission rates at 12 weeks based on PHQ-9 scores. Note: We also examined patients who began at index with PHQ-9 scores of 5 or greater, as the definition of remission was that patients’ PHQ-9 scores decreased to below 5. Thus, this sensitivity analysis excludes patients who were already meeting the definition of remission at index. PHQ-9, Patient Health Questionnaire-9

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