Evidence map›Paper›PMID 36865636›Full record

ReviewNeurology. Clinical practice2023

Health Services in Huntington Disease: A Systematic Literature Review.

Adys Mendizabal, Jennifer M Diaz, Arturo V Bustamante, Yvette Bordelon

Open access · greenAbstract readReview
In one paragraph

Review in Neurology. Clinical practice, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Systemic Symptoms in Huntington's Disease: A Comprehensive Review.Movement disorders clinical practice · 2024
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
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

4 authors at 1 institution in 1 country.

Adys MendizabalDepartment of Neurology (AM, JMD, YB), David Geffen School of Medicine, University of California Los Angeles (UCLA); Institute of Society and Genetics (AM), College of Life Sciences, University of California Los Angeles (UCLA); and Department of Health Policy and Management (AVB), Fielding School of Public Health, University of California Los Angeles (UCLA).
Jennifer M DiazDepartment of Neurology (AM, JMD, YB), David Geffen School of Medicine, University of California Los Angeles (UCLA); Institute of Society and Genetics (AM), College of Life Sciences, University of California Los Angeles (UCLA); and Department of Health Policy and Management (AVB), Fielding School of Public Health, University of California Los Angeles (UCLA).
Arturo V BustamanteDepartment of Neurology (AM, JMD, YB), David Geffen School of Medicine, University of California Los Angeles (UCLA); Institute of Society and Genetics (AM), College of Life Sciences, University of California Los Angeles (UCLA); and Department of Health Policy and Management (AVB), Fielding School of Public Health, University of California Los Angeles (UCLA).
Yvette BordelonDepartment of Neurology (AM, JMD, YB), David Geffen School of Medicine, University of California Los Angeles (UCLA); Institute of Society and Genetics (AM), College of Life Sciences, University of California Los Angeles (UCLA); and Department of Health Policy and Management (AVB), Fielding School of Public Health, University of California Los Angeles (UCLA).
University of California, Los Angeles · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose of Review: Clinical trials for Huntington disease (HD) have primarily focused on managing chorea and, more recently, the development of disease-modifying therapies (DMTs). Nonetheless, understanding health services among patients with HD is essential for assessing new therapeutics, development of quality metrics, and overall quality of life of patients and families with HD. Health services assess health care utilization patterns, outcomes, and health care-associated costs, which can help shape the development of therapeutics and aid in policies that affect patients with a specific condition. In this systematic literature review, we analyze data of published studies looking at causes of hospitalization, outcomes, and health care costs in HD. Recent Findings: The search yielded 8 articles published in the English language and comprising data from the United States, Australia, New Zealand, and Israel. The most common cause of hospitalization among patients with HD was dysphagia or dysphagia-related complications (e.g., aspiration pneumonia or malnutrition), followed by psychiatric or behavioral symptoms. Patients with HD had more prolonged hospitalizations than non-HD patients, and it was most prominent among those with advanced disease. Patients with HD were more likely to be discharged to a facility. A small percentage received inpatient palliative care consultation, and behavioral symptoms were a primary cause of discharge to another facility. Interventions such as gastrostomy tube placement had associated morbidity, and it was common among patients with HD with a diagnosis of dementia. Palliative care consultation and specialized nursing care were associated with more routine discharges and fewer hospitalizations. In terms of cost, patients with HD with private and public insurances had the highest expenditure with more advanced disease, and expenses were associated with hospitalization and medication costs. Summary: In addition to DMTs, HD clinical trial development should also consider the leading causes of hospitalization, morbidity, and mortality in patients with HD, including dysphagia and psychiatric disease. No research study, to our knowledge, has systematically reviewed health services research studies in HD. Evidence from health services research is needed to evaluate the efficacy of pharmacologic and supportive therapies. This type of research is also critical in understanding health care costs associated with the disease and to better advocate and shape policies that can benefit this patient population.

Identifiers

PMID36865636
PMCPMC9973320
OpenAlexW4315606076

What OpenQuestion holds

Textmetadata
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.