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1.
J Autism Dev Disord ; 52(2): 871-876, 2022 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-33761061

RESUMEN

This study examined if listening to music will improve the accuracy of blood pressure (BP) readings in children with Williams syndrome (WS). Fifty-two participants (7-12 years) were randomly assigned to a music or non-music group. BPs were obtained at two time points. There was a significant decrease in both systolic and diastolic BP from Time 1 to Time 2 for everyone. Participants from the music group had lower systolic BP readings at Time 2 than participants in the non-music group (Cohen's d = 0.33). Systolic BP readings were approximately 3.8 mmHg lower in the music group. Music may be beneficial in obtaining more accurate systolic BP readings in children with WS.


Asunto(s)
Trastorno del Espectro Autista , Hipotensión , Música , Síndrome de Williams , Presión Sanguínea , Niño , Humanos
2.
Pediatrics ; 149(1)2022 01 01.
Artículo en Inglés | MEDLINE | ID: mdl-34972222

RESUMEN

A physician workforce that reflects the patient population is associated with improved patient outcomes and promotes health equity. Notwithstanding, racial and ethnic disparities persist within US medical schools, making some individuals underrepresented in medicine (URM). We sought to increase the percentage of URM residents who matched into our pediatric residency programs from a baseline of 5% to 35% to achieve demographic parity with our patients. We developed a multifaceted approach using multiple iterative tests of change, with the primary strategy being increased visibility of URM trainees and faculty to residency applicants. Strategies included applicant interviews with URM faculty, interview dinners with URM residents, visibility at academic conferences for URM trainees, development of targeted marketing materials, and a visiting student program supported by networking with URM residents. The primary outcome measure was the percentage of matched residents in the categorical pediatrics, child neurology, and medical genetics training programs who identified as URM. The percentage of URM residents increased to 16% (6 of 37) in 2018, 26% (11 of 43) in 2019, 19% (8 of 43) in 2020, and 21% (9 of 43) in 2021 (a four-year average of 22% URM residents; P = .0002). This progress toward a more representative residency program was met by challenges, such as pipeline concerns, the minority tax, and recruitment during a pandemic. We were able to implement small, low-resource strategies that had a large cumulative impact and could be implemented in other residency programs. Specific tactics and challenges encountered are discussed in this special article.


Asunto(s)
Internado y Residencia/organización & administración , Grupos Minoritarios/estadística & datos numéricos , Pediatría/educación , Desarrollo de Programa , COVID-19/epidemiología , Equidad en Salud , Humanos , Internado y Residencia/estadística & datos numéricos , Pandemias , Pediatras/provisión & distribución , Estados Unidos/epidemiología
3.
Pediatrics ; 148(6)2021 12 01.
Artículo en Inglés | MEDLINE | ID: mdl-34814178

Asunto(s)
Médicos , Humanos
4.
Pediatr Clin North Am ; 68(5): 1133-1145, 2021 10.
Artículo en Inglés | MEDLINE | ID: mdl-34538304

RESUMEN

The coronavirus disease 2019 (COVID-19) pandemic has uncovered long-standing health disparities in marginalized communities, including racial and ethnic minorities and children with underlying medical and social problems. African Americans, Hispanics, and Native Americans have higher rates of COVID-19 infections and deaths than their population percentages in the United States. Unique populations of children, including children with developmental disabilities, children in the foster care system, children with chronic medical problems, and children who are homeless are particularly vulnerable to COVID-19 infection. This article explores how the COVID-19 pandemic superimposed on health disparities directly and indirectly affects children, adolescents, and their caregivers.


Asunto(s)
COVID-19/epidemiología , Etnicidad/estadística & datos numéricos , Disparidades en el Estado de Salud , Disparidades en Atención de Salud/estadística & datos numéricos , Adolescente , Niño , Humanos , Estados Unidos
5.
Am J Med Genet A ; 173(5): 1159-1171, 2017 May.
Artículo en Inglés | MEDLINE | ID: mdl-28371210

RESUMEN

Williams Syndrome (WS) is a contiguous gene deletion disorder, caused by the deletion of approximately 26-28 genes from chromosome 7 (7q11.23). Individuals with WS have complex medical, developmental, and behavioral features, requiring multidisciplinary and interdisciplinary collaboration. Guidelines detailing the identification, evaluation, and monitoring of individuals with WS need clarification, especially for primary care providers who are first-line in their management. This report summarizes the proceedings of the 2016 Professional Conference on WS in Columbus, OH. Presentations were directed towards primary care providers and subspecialists, emphasizing evidence-based practices for treating the prevalent medical and behavioral features of WS. Included in this report are findings from a panel of cardiovascular experts discussing three case studies on treatment of hypertension and the use of sedation or anesthesia for non-cardiac procedures. Abstracts from individual expert presenters are included, covering various medical and behavioral topics, and providing updates in management of WS individuals. The following topics were discussed: differences in phenotypes of 7q11.23 deletion versus duplication, growth parameters, endocrine concerns, sleep difficulties, behaviors to monitor, and pharmacological options, the neurodevelopmental profile of WS individuals, and the importance of monitoring medical and behavioral concerns as WS individuals transition to adulthood.


Asunto(s)
Eliminación de Gen , Guías como Asunto , Síndrome de Williams/genética , Cromosomas Humanos Par 7/genética , Humanos , Síndrome de Williams/diagnóstico , Síndrome de Williams/terapia
6.
J Behav Health Serv Res ; 41(4): 539-47, 2014 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-24435226
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