Evidence map›Paper›PMID 38160372›Full record

ArticleJournal of pediatric rehabilitation medicine2023

Addressing social determinants of health through customization: Quality improvement, telemedicine, and care coordination to serve immigrant families.

Heidi Castillo, Mary M Locastro, Ellen Fremion, Anjali Malhotra, Rosanna Morales, Kelly Timmons, Susan Jarosz, Nienke P Dosa, Jonathan Castillo

Abstract read
In one paragraph

Article in Journal of pediatric rehabilitation medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

9 authors.

Heidi CastilloDevelopmental Medicine, Department of Pediatrics, Children's Nebraska Hospital, Omaha, NE, USA.
Mary M LocastroSpina Bifida Center of Central New York, Department of Pediatrics, SUNY Upstate Medical University, Syracuse, NY, USA.
Ellen FremionTransition Medicine, Department of Internal Medicine, Baylor College of Medicine, Houston, TX, USA.
Anjali MalhotraSpina Bifida Center of Central New York, Department of Pediatrics, SUNY Upstate Medical University, Syracuse, NY, USA.
Rosanna MoralesTexas Children's Hospital, Houston, TX, USA.
Kelly TimmonsTexas Children's Hospital, Houston, TX, USA.
Susan JaroszDivision of Pediatric Urology, Department of Surgery, Texas Children's Hospital and Scott Department of Urology, Baylor College of Medicine, Houston, TX, USA.
Nienke P DosaSpina Bifida Center of Central New York, Department of Pediatrics, SUNY Upstate Medical University, Syracuse, NY, USA.
Jonathan CastilloDevelopmental Medicine, Department of Pediatrics, Children's Nebraska Hospital, Omaha, NE, USA.

Funding

ACL HHS U01DD001265NCBDD CDC HHS U01 DD001265
6 · The paper itself

Abstract

purposeThe purpose of this project was to establish a pathway for electronic medical record (EMR) customization, utilizing quality improvement methodology, to both identify and address adverse social determinants of health (SDOH) among a diverse spina bifida (SB) population.

methodsStarting in September 2020, the four fundamental steps were to (1) facilitate an advisory committee to safeguard the standard clinical protocols, (2) characterize barriers to implementation, (3) evaluate workflow to sustain data entry capture, and (4) manage the technology platform for seamless integration. The SB clinic was the first clinic within the enterprise to rollout the use of an adverse SDOH mitigation activity. A Spanish-speaking interpreter was scheduled for all clinics, as many families were limited in English proficiency.

resultsThe customization of the EMR to support an efficient workflow to address SDOH was feasible in a large and diverse urban medical center. Of the 758 patients served in the clinic, a myelomeningocele diagnosis was present in 86% of individuals. While 52% of participants were female, ethnically 52% of individuals served were Latino. Many of these individuals disclosed being recent immigrants to the United States. Often immigration and asylum related issues were at the forefront of the SDOH issues addressed.

conclusionGiven the occurrence of adverse SDOH among individuals with SB, many of whom are new Latin-American immigrants, meaningful clinical efforts are needed to both identify and address the causes of the observed disparities. EMR customization is feasible and can identify and, through social prescriptions, address SDOH to support the provision of safe, high quality, and equitable care for vulnerable and medically complex populations at home and potentially abroad.

Indexed as

Emigrants and ImmigrantsSpinal DysraphismTelemedicineEmigration and ImmigrationFemaleHumansMaleQuality ImprovementSocial Determinants of HealthUnited Statesglobal healthHealth disparitiesminority healthmyelomeningocelesocialprescribingspina bifidathree-hit model

Identifiers

PMID38160372
PMCPMC10789335

What OpenQuestion holds

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LicenceCC BY-NC
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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.