# Deutetrabenazine and Modified Electroconvulsive Therapy for Tardive Dyskinesia With Recurrent Depression: A Case Report

**Authors:** Zhiying Wan, Xiaofen Li, Yu Fang, Chao Zeng, Meiyu Shen

PMC · DOI: 10.7759/cureus.102749 · Cureus · 2026-01-31

## TL;DR

A patient with tardive dyskinesia and depression showed significant improvement after stopping anticholinergic drugs and starting deutetrabenazine with electroconvulsive therapy.

## Contribution

This case report demonstrates a novel combination of deutetrabenazine and MECT for treating TD and depression.

## Key findings

- TD symptoms completely resolved after 15 days of combined treatment.
- Depressive symptoms improved by 60% as measured by HAMD-17 scores.
- No recurrence was observed during a 10-day follow-up.

## Abstract

This study reports a case of tardive dyskinesia (TD) and depression in a patient with long-term use of antipsychotic and anticholinergic drugs, through the tapering and discontinuation of anticholinergic drugs and the concurrent use of deutetrabenazine combined with modified electroconvulsive therapy (MECT). Her TD symptoms have completely improved. The score on the Hamilton Depression Rating Scale (HAMD-17) has dropped from 20 points to eight points, and the depressive symptoms have improved by 60%. A 31-year-old woman with a mood disorder, treated with risperidone (dose range: 4 mL/day, duration: 11 months), olanzapine (dose range: 10 mg/day, duration: 11 months), and benztropine (dose range: 6 mg/day, duration: four months) for recurrent depression, developed lip twitching, bradykinesia, and worsened depression. Upon admission on February 4, benztropine was tapered and discontinued by February 22. A new regimen of deutetrabenazine combined with MECT was initiated on February 7. Following 15 days of this combined treatment, the patient’s TD symptoms completely resolved. The HAMD-17 score dropped from 20 to eight, and the Brief Psychiatric Rating Scale (BPRS) score initially fluctuated but then stabilized and improved. No recurrence was observed during a 10-day follow-up post-discharge. This case study indicates that stopping anticholinergic drugs and using vesicular monoamine transporter 2 (VMAT2) inhibitors with MECT can quickly alleviate symptoms in patients with TD and mood disorders. Clinicians should be aware of the long-term motor disorder risks of antipsychotics, perform regular screenings, and focus on multi-target interventions. Future research should increase sample sizes to confirm the treatment's general applicability and long-term safety.

## Linked entities

- **Chemicals:** deutetrabenazine (PubChem CID 73442840), risperidone (PubChem CID 5073), olanzapine (PubChem CID 135398745), benztropine (PubChem CID 1201549)
- **Diseases:** tardive dyskinesia (MONDO:0010096), depression (MONDO:0002050), mood disorder (MONDO:0005371)

## Full-text entities

- **Genes:** DRD2 (dopamine receptor D2) [NCBI Gene 1813] {aka D2DR, D2R}, SLC18A2 (solute carrier family 18 member A2) [NCBI Gene 6571] {aka PKDYS2, SVAT, SVMT, VAT2, VMAT2}
- **Diseases:** Emotional disorders (MESH:D009358), seizure (MESH:D012640), fatigue (MESH:D005221), lip (MESH:D008047), involuntary mouth opening/closing movements (MESH:D009059), suicidal ideation (MESH:D001072), mood (MESH:D019964), anxiety (MESH:D001007), emotional and behavioral disorders (MESH:D001523), substance abuse (MESH:D019966), jaw pain (MESH:D010146), anhedonia (MESH:D059445), inattention (MESH:D001308), tension (MESH:D018781), trauma (MESH:D014947), headaches (MESH:D006261), memory impairment (MESH:D008569), motor disorder (MESH:D000068079), cognitive decline (MESH:D003072), extrapyramidal reactions (MESH:D001480), movement disorder (MESH:D009069), parkinsonism (MESH:D010302), involuntary, repetitive movements (MESH:D020820), hypersensitivity (MESH:D004342), bipolar disorder (MESH:D001714), Abnormal Involuntary Movement (MESH:D004409), Depression (MESH:D003866), temporomandibular joint pain (MESH:D013706), psychosis (MESH:D011618), attention was impaired (MESH:D001289), MECT (MESH:D016609), cardiovascular disease (MESH:D002318), bradykinesia (MESH:D018476), tremors (MESH:D014202), delusions (MESH:D063726), death (MESH:D003643), auditory hallucinations (MESH:D006212), neurotransmitter abnormalities (MESH:D000014)
- **Chemicals:** risperidone (MESH:D018967), testosterone (MESH:D013739), oxygen (MESH:D010100), lithium carbonate (MESH:D016651), clozapine (MESH:D003024), Benztropine (MESH:D001590), dopamine (MESH:D004298), DC (MESH:D003841), valbenazine (MESH:C000603978), Deutetrabenazine (MESH:C000609690), depakine (MESH:D014635), lorazepam (MESH:D008140), olanzapine (MESH:D000077152), MECT (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12955273/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12955273/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12955273/full.md

---
Source: https://tomesphere.com/paper/PMC12955273