Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
J Grad Med Educ ; 12(6): 745-752, 2020 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-33391599

RESUMO

BACKGROUND: Despite increasing use of telehealth, there are limited published curricula training primary care providers in utilizing telehealth to deliver complex interdisciplinary care. OBJECTIVE: To describe and evaluate a telehealth curriculum with a longitudinal objective structured clinical examination (OSCE) to improve internal medicine residents' confidence and skills in coordinating complex interdisciplinary primary care via televisits, electronic consultation, and teleconferencing. METHODS: In 2019, 56 first- and third-year residents participated in a 3-part, 5-week OSCE training them to use telehealth to manage complex primary care. Learners conducted a standardized patient (SP) televisit in session 1, coordinated care via inter-visit e-messaging, and led a simulated interdisciplinary teleconference in session 2. Surveys measured confidence before session 1 (pre), post-session 1 (post-1), and post-session 2 (post-2). SP televisit checklists and investigators' assessment of e-messages evaluated residents' telehealth skills. RESULTS: Response rates were pre 100%, post-1 95% (53 of 56), and post-2 100%. Post-intervention, more residents were "confident/very confident" in adjusting their camera (33%, 95% CI 20-45 vs 85%, 95% CI 75-95, P < .0001), e-messaging (pre 36%, 95% CI 24-49 vs post-2 80%, 95% CI 70-91, P < .0001), and coordinating interdisciplinary care (pre 35%, 95% CI 22-47 vs post-2 84%, 95% CI 74-94, P < .0001). More residents were "likely/very likely" to use telemedicine in the future (pre 56%, 95% CI 43-69, vs post-2 79%, 95% CI 68-89, P = .001). CONCLUSIONS: A longitudinal, interdisciplinary telehealth simulation is feasible and can improve residents' confidence in using telemedicine to provide complex patient care.


Assuntos
Internato e Residência , Telemedicina , Competência Clínica , Currículo , Humanos , Assistência ao Paciente , Simulação de Paciente , Atenção Primária à Saúde
2.
Hemoglobin ; 32(6): 588-91, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-19065337

RESUMO

Neonatal screening for hemoglobinopathies occasionally results in the detection of novel hemoglobin (Hb) variants. Two heterozygous infants were found with different beta chain mutations, neither of which produced obvious clinical or laboratory abnormalities on routine examinations. The variants were characterized by cation exchange high performance liquid chromatography (HPLC), reversed phase HPLC, and sequencing of amplified beta-globin genes. Functional studies could not be performed at this time.


Assuntos
Mutação , Globinas beta/genética , Alanina/química , Alanina/genética , Substituição de Aminoácidos , Ácido Aspártico/química , Ácido Aspártico/genética , Sequência de Bases , Pré-Escolar , Cromatografia Líquida de Alta Pressão , Humanos , Lactente , Isoleucina/química , Isoleucina/genética , Masculino , Dados de Sequência Molecular , Valina/química , Valina/genética , Globinas beta/química
3.
Hemoglobin ; 32(6): 596-600, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-19065339

RESUMO

Neonatal cyanosis can result from a multitude of acquired and inherited causes. Cyanosis resulting from fetal M hemoglobin (Hb) variants is very rare. Only two (G)gamma variants causing methemoglobinemia and cyanosis in the newborn have been reported to date. Here we describe a novel fetal Hb variant, Hb F-Circleville [Ggamma63(E7)His-->Leu], associated with methemoglobinemia and cyanosis in the newborn. The patient's sister also had neonatal cyanosis at birth.


Assuntos
Cianose/genética , Hemoglobina Fetal/genética , Globinas/genética , Substituição de Aminoácidos , Sequência de Bases , Cianose/etiologia , Feminino , Hemoglobinas Anormais , Histidina/química , Histidina/genética , Humanos , Recém-Nascido , Leucina/química , Leucina/genética , Masculino , Dados de Sequência Molecular , Mutação/genética
4.
Blood ; 105(2): 545-7, 2005 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-15454485

RESUMO

The efficacy of hydroxyurea (HU) and its role in the reduction in mortality in sickle cell patients has been established. Nevertheless, many patients still die of complications of this disease while on HU. Of the 226 patients treated with HU at our center, 38 died (34 of sickle cell-related causes). Acute chest syndrome (ACS) was the most common (35%) cause of death. Deceased and surviving patients did not differ significantly in average HU dose, baseline fetal hemoglobin (Hb F), or maximum Hb F response. However, the deceased patients were significantly older when HU was instituted, were more anemic, and more likely to have BAN or CAM haplotypes. They also had significantly higher serum blood-urea-nitrogen (BUN) and creatinine levels. Sickle cell patients who die while on HU therapy may represent a subgroup of older patients, possibly with more severe disease and more severe organ damage. Such patients need early identification and prompt HU institution.


Assuntos
Anemia Falciforme/tratamento farmacológico , Anemia Falciforme/mortalidade , Antidrepanocíticos/administração & dosagem , Hidroxiureia/administração & dosagem , Doença Aguda , Adolescente , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Resultado do Tratamento
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...