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Lisa Harding

Depression MD, Mood Disorder Institute, Milton, CT, United States.

4 papers in the library · 13 citations · publishing 2024-2025

Papers

Treatment Patterns, Acute Healthcare Resource Use, and Costs of Patients with Treatment-Resistant Depression Completing Induction Phase of Esketamine in the United States.

Drugs - real world outcomes June 1, 2024 Lisa Harding, Kruti Joshi, Maryia Zhdanava et al. 5 citations

Adults with treatment-resistant depression who completed induction treatment with esketamine nasal spray showed reductions in acute healthcare costs, particularly among those who had prior mental health-related hospitalizations or emergency visits. In a cohort of 322 patients, mean all-cause acute healthcare costs per patient per month fell from $837 before treatment to $770 after, while mental health-related costs dropped from $648 to $577. Among 111 patients with prior acute care use, all-cause costs decreased from $2,323 to $1,423, driven by mental health-related cost reductions from $1,880 to $1,139. Patients generally took longer than the label-recommended 28 days to complete the eight induction sessions, averaging 73 days. Most patients continued with maintenance sessions.

Health Care Resource Use and Medical Costs Among Patients With Major Depressive Disorder and Acute Suicidal Ideation or Behavior Initiated on Esketamine Nasal Spray or Traditional Treatments in the United States.

Clinical therapeutics March 1, 2025 Lisa Harding, Maryia Zhdanava, Amanda Teeple et al. 3 citations

Patients with major depressive disorder accompanied by acute suicidal ideation or behavior who were started on esketamine nasal spray had fewer acute care hospital days and lower medical costs per month than those receiving electroconvulsive therapy or an antidepressant augmented with a second-generation antipsychotic. Among 122 esketamine users, mean acute care use was 0.59 days per month, a 58% decrease from before treatment, compared with 3.17 days (44% increase) for 336 ECT patients and 0.92 days (21% decrease) for 9,958 patients on augmentation therapy. Medical costs per patient per month were $1,869 for esketamine, $4,624 for ECT, and $2,163 for augmentation. The findings suggest esketamine may be associated with lower resource use and cost reductions relative to other treatments.

Music mindfulness acutely modulates autonomic activity and improves psychological state in anxiety and depression.

Frontiers in neuroscience January 1, 2025 Christine Ramirez, Gertrude Asumpaame Alayine, Cyril Selase Kwaku Akafia et al. 3 citations

Music mindfulness—combining music listening with mindfulness activities—acutely increases heart rate variability and alters brain activity in frontotemporal regions, as measured by wearable electrocardiography and electroencephalography in people with moderate anxiety and depression. Both live and virtual sessions reduce stress and shift state of consciousness, but only live sessions enhance social connection. Effects on physiology and psychology differ by self-reported sex. The findings suggest music mindfulness engages autonomic and neural mechanisms that may help treat anxiety and depression symptoms.

Understanding profiles of patients with treatment-resistant depression by stringency of health plan prior authorization criteria for approval of esketamine nasal spray.

Current medical research and opinion September 1, 2024 Lisa Harding, Maryia Zhdanava, Aditi Shah et al. 2 citations

Among US adults with treatment-resistant depression who initiated esketamine nasal spray, those whose health plans had prior authorization criteria stricter than the drug label (stringent cohort, 168 patients) and those with less or equally strict criteria (non-stringent cohort, 400 patients) had similar treatment histories. Both groups completed about four antidepressant treatment courses on average before starting esketamine, and roughly 95% used augmentation therapy, with about 59% using an antipsychotic. These averages exceeded the number of antidepressant trials mandated by the esketamine label, suggesting that requiring additional prior authorization steps beyond the label may not be necessary.