Evidence map›Paper›PMID 30363491›Full record

ArticleMovement disorders clinical practice

Hospitalizations of Children with Huntington's Disease in the United States.

Adys Mendizabal, Anh-Thu Ngo Vu, Dylan Thibault, Pedro Gonzalez-Alegre, Allison Willis

Open access · bronzeAbstract read
In one paragraph

Article in Movement disorders clinical practice. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.1field-weighted citation impact, top 58% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Clinical Review of Juvenile Huntington's Disease.Journal of Huntington's disease · 2024
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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

5 authors at 2 institutions in 1 country.

Adys MendizabalDepartment of Neurology University of Pennsylvania School of Medicine Philadelphia Pennsylvania.
Anh-Thu Ngo VuDepartment of Neurology Emory University School of Medicine Atlanta Georgia.
Dylan ThibaultDepartment of Neurology University of Pennsylvania School of Medicine Philadelphia Pennsylvania.
Pedro Gonzalez-AlegreDepartment of Neurology University of Pennsylvania School of Medicine Philadelphia Pennsylvania.
Allison WillisDepartment of Neurology University of Pennsylvania School of Medicine Philadelphia Pennsylvania.
University of Pennsylvania · USEmory University · US

Funding

Parkinson Disease Disparities and OutcomesK23NS081087 · NINDS · WASHINGTON UNIVERSITY · PI WILLIS, ALLISON · 2012 to 2015
$669k
NINDS NIH HHS K23 NS081087
6 · The paper itself

Abstract

backgroundJuvenile Huntington's disease (JHD) is a childhood-onset neurodegenerative disorder. Although it is caused by the same pathologic expansion of CGA repeats as adult-onset Huntington's disease, JHD has distinct clinical features. Most clinical research in HD focuses in the adult-onset disease; therefore, little is known about acute care outcomes for patients with JHD.

methodsThe Kids' Inpatient Database (KID) was used to examine hospitalizations of children with JHD and to determine the diagnoses and procedures associated with inpatient care for JHD. Regression models were built to examine acute care outcomes, including death, length of stay, and disposition at discharge in patients with JHD compared with patients in the general KID data.

resultsThe proportion of JHD cases among hospitalized children was 1.23 per 100,000 KID inpatient stays. Seizures/convulsions (58.5%) and psychiatric conditions (26.1%) were the most common primary or secondary diagnoses among JHD patient hospitalizations. The most common procedure was percutaneous endoscopic gastrostomy tube placement (8.6%). Compared with hospitalizations of the general population, hospitalizations of patients with JHD had a lower odds of discharge to home (adjusted odds ratio [AOR], 0.23; 95% confidence interval [CI], 0.14-0.37) and an increased likelihood of death (AOR, 8.03; 95% CI, 2.98-21.60) or discharge to a short-term care facility (AOR, 4.44; 95% CI, 2.59-7.61). A diagnosis of JHD was associated with increased length of stay (7.04 vs. 3.75 days;

conclusionsChildren with JHD have unique acute care patterns. Future studies are needed to determine the extent to which coordinated care may impact inpatient and disposition needs.

Indexed as

EpidemiologyHuntington's diseasejuvenile Huntington's diseasepediatric neurology

Identifiers

PMID30363491
PMCPMC6174499
OpenAlexW2611737256

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.