Evidence map›Paper›PMID 38131059›Full record

ArticleThe mental health clinician2023

Exploring real-world symptom impact and improvement in well-being domains for tardive dyskinesia in VMAT2 inhibitor-treated patients via clinician survey and chart review.

Jonathan M Meyer, Craig Chepke, Rimal B Bera, M Mercedes Pérez-Rodríguez, Leslie Lundt, Ericha G Franey, Rahul Dhanda, Betsy Benning, Morgan Bron, Chuck Yonan

Open access · goldAbstract read
In one paragraph

Article in The mental health clinician, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 43% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 4 countries.

Jonathan M MeyerVoluntary Clinical Professor, University of California, San Diego School of Medicine, Department of Psychiatry, La Jolla, California.
Craig ChepkeMedical Director, Excel Psychiatric Associates, Huntersville, North Carolina.
Rimal B BeraClinical Professor of Psychiatry, Psychiatry and Human Behavior, University of California, Irvine School of Medicine, Department of Psychiatry, Orange, California.
M Mercedes Pérez-RodríguezAssociate Professor, Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, New York.
Leslie LundtExecutive Medical Director, Neurocrine Biosciences, Inc., San Diego, California.
Ericha G FraneySenior Manager, Health Economics and Outcomes Research, Clinical Development, Neurocrine Biosciences, Inc, San Diego, California.
Rahul DhandaDirector, Neurocrine Biosciences, Inc, San Diego, California.
Betsy BenningPrincipal, Consulting Services, IQVIA, San Mateo, California.
Morgan BronDirector, Health Economics and Outcomes Research, Neurocrine Biosciences, Inc, San Diego, California.
Chuck YonanVoluntary Clinical Professor, University of California, San Diego School of Medicine, Department of Psychiatry, La Jolla, California.
Neurocrine Biosciences (United States) · USAlkermes (Ireland) · IEIcahn School of Medicine at Mount Sinai · USIQVIA (United States) · USUniversity of California, Irvine · USUniversity of California San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Two vesicular monoamine transporter 2 (VMAT2) inhibitors are approved in the United States (US) for the treatment of tardive dyskinesia (TD). There is a paucity of information on the impact of VMAT2 inhibitor treatment on patient social and physical well-being. The study objective was to elucidate clinician-reported improvement in symptoms and any noticeable changes in social or physical well-being in patients receiving VMAT2 inhibitors. Methods: A web-based survey was offered to physicians, nurse practitioners, and physician assistants based in the US who prescribed valbenazine for TD within the past 24 months. Clinicians reported data from the charts of patients who met the inclusion criteria and were allowed to recall missing information. Results: Respondents included 163 clinicians who reviewed charts of 601 VMAT2-treated patients with TD: 47% had TD symptoms in ≥2 body regions, with the most common being in the head or face and upper extremities. Prior to treatment, 93% of patients showed impairment in ≥1 social domain, and 88% were impaired in ≥1 physical domain. Following treatment, among those with improvement in TD symptoms (n = 540), 80% to 95% showed improvement in social domains, 90% to 95% showed improvement in physical domains, and 73% showed improvement in their primary psychiatric condition. Discussion: In VMAT2-treated patients with TD symptom improvement, clinicians reported concomitant improvement in psychiatric disorder symptoms and in social and physical well-being. Regular assessment of TD impact on these types of domains should occur simultaneously with movement disorder ratings when evaluating the value of VMAT2 inhibitor therapy.

Indexed as

antipsychoticsdeutetrabenazinedisease burdenpatient awarenesspatient-centric outcomespsychiatric diseasestardive dyskinesiatetrabenazinevalbenazinevesicular monoamine transport inhibitors

Identifiers

PMID38131059
PMCPMC10732123
OpenAlexW4387234605

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.