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1.
Am J Med Genet A ; 173(6): 1539-1545, 2017 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-28332275

RESUMEN

The goals of this undertaking were to assess the outcomes of thyroid screening tests and adherence to thyroid screening guidelines across five Down syndrome (DS) specialty clinics in various states. Data related to thyroid screening were collected for 663 individuals across five clinics specializing in the comprehensive care of individuals with DS for a period of 1 year. Of the 663 participants, 47.7% of participants had a TSH and free T4 ordered at their DS specialty clinic visit. Approximately 19.0% (60/316) had a new thyroid disorder diagnosis made. We conclude that a sizable proportion of the patients with DS are not up-to-date on current guidelines when they present to a DS specialty clinic, while adherence to thyroid screening guidelines helps facilitate early diagnoses. Hypothyroidism is prevalent in the population, consistent with reported literature. DS specialty clinics can help patients stay current on screening guidelines.


Asunto(s)
Síndrome de Down/fisiopatología , Hipotiroidismo/fisiopatología , Enfermedades de la Tiroides/fisiopatología , Adolescente , Adulto , Anciano , Niño , Preescolar , Síndrome de Down/sangre , Síndrome de Down/complicaciones , Femenino , Humanos , Hipotiroidismo/sangre , Hipotiroidismo/complicaciones , Lactante , Masculino , Persona de Mediana Edad , Sistema de Registros , Enfermedades de la Tiroides/sangre , Enfermedades de la Tiroides/complicaciones , Pruebas de Función de la Tiroides , Glándula Tiroides/fisiopatología , Tirotropina/sangre , Tiroxina/sangre
2.
Am J Med Genet A ; 170(12): 3098-3105, 2016 12.
Artículo en Inglés | MEDLINE | ID: mdl-27605215

RESUMEN

The main purposes of this undertaking were to determine how often patients with Down syndrome (DS) are screened for celiac disease (CD) across five DS specialty clinics, which symptoms of CD are most often reported to DS specialty providers at these clinics, and, how many individuals were diagnosed with CD by these clinics. This was accomplished by following 663 individuals with DS for 1 year, across five clinics in different states specializing in the comprehensive care of people with DS. Of the 663 participants, 114 individuals were screened for CD at their visit to a DS specialty clinic. Protracted constipation (43.2%) and refractory behavioral problems (23.7%) were symptoms most often reported to DS specialty providers. During the 1 year study period, 13 patients screened positive for CD by serology. Of those, eight underwent duodenal biopsy, and three were diagnosed with CD. We conclude that CD is an important consideration in the comprehensive care of individuals with DS. However, while symptoms are common, diagnoses are infrequent in DS specialty clinics. © 2016 Wiley Periodicals, Inc.


Asunto(s)
Enfermedad Celíaca/diagnóstico , Síndrome de Down/diagnóstico , Asesoramiento Genético , Adolescente , Adulto , Biopsia , Enfermedad Celíaca/complicaciones , Enfermedad Celíaca/fisiopatología , Niño , Preescolar , Síndrome de Down/complicaciones , Síndrome de Down/fisiopatología , Femenino , Humanos , Lactante , Recién Nacido , Masculino , Adulto Joven
3.
Am J Med Genet A ; 167A(11): 2520-6, 2015 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-26249752

RESUMEN

The Down Syndrome Study Group (DSSG) was founded in 2012 as a voluntary, collaborative effort with the goal of supporting evidenced-based health care guidelines for individuals with Down syndrome (DS). Since then, 5 DS specialty clinics have collected prospective, longitudinal data on medical conditions that co-occur with DS. Data were entered by clinical staff or trained designees into the National Down Syndrome Patient Database, which we created using REDCap software. In our pilot year, we enrolled 663 participants across the U.S., ages 36 days to 70 years, from multiple racial and ethnic backgrounds. Here we report: (i) the demographic distribution of participants enrolled, (ii) a detailed account of our database infrastructure, and (iii) lessons learned during our pilot year to assist future researchers with similar goals for other patient populations.


Asunto(s)
Bases de Datos Factuales , Síndrome de Down/epidemiología , Estudios Multicéntricos como Asunto , Sistema de Registros , Adolescente , Adulto , Niño , Preescolar , Conducta Cooperativa , Demografía , Femenino , Humanos , Lactante , Recién Nacido , Estudios Interdisciplinarios , Masculino , Estados Unidos/epidemiología , Adulto Joven
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