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1.
J Racial Ethn Health Disparities ; 7(6): 1150-1159, 2020 12.
Artigo em Inglês | MEDLINE | ID: mdl-32297304

RESUMO

INTRODUCTION: An abundance of research investigates the health of often referred to as "at risk" or "high risk" youth from underserved communities and usually racial/ethnic minorities. These ubiquitous terms relate to poverty, violence, and unsafe behaviors (e.g., sex without condoms, alcohol, and drug use). METHODS: This analysis distinguished the heterogeneity of risks among African American female adolescents recruited for an intervention study from underserved communities in North Carolina. Eligibility included: ages 16-19, considered or dropped out of school, never completed high school, and during the past 3 months had sex with a male partner and used drugs or alcohol. A variable was created to represent the continuum of risk comprised of history of homelessness, or trading sex, or current heavy alcohol and marijuana use. Participants fell into 0, 1, or 2-3 categories. Ordinal logistic regression estimated the odds of adverse poor outcomes by category. Linear regression estimated reduction in material and emotional support by category. RESULTS: Of the 237 participants, 59.5%, 27.8%, and 12.7% were in 0, 1, or 2-3 categories, respectively. Relative to adolescents in 0 categories, participants in other categories were more likely to report food insecurity (OR = 3.27, 95%CI [1.8, 5.94]); past arrest (OR = 3.56 [2.08, 6.09]); run away (OR = 3.30 [1.79, 6.10]); multiple sex partners (2.97 [1.61, 5.48]); and vaginal/anal sexual abuse (OR = 3.21[1.73, 5.96]). Material and emotional support was significantly lower for participants in 2-3 risk categories. CONCLUSIONS: Vague use of "at risk" fails to recognize the heterogeneity of experiences and needs of underserved African American youth.


Assuntos
Negro ou Afro-Americano , Assunção de Riscos , Adolescente , Feminino , Humanos , Modelos Logísticos , North Carolina , Pobreza , Comportamento Sexual , Transtornos Relacionados ao Uso de Substâncias , Inquéritos e Questionários , Adulto Jovem
2.
Br J Dermatol ; 179(6): 1297-1306, 2018 12.
Artigo em Inglês | MEDLINE | ID: mdl-29727479

RESUMO

BACKGROUND: Oral systemic immunomodulatory medication is regularly used off-licence in children with severe atopic eczema. However, there is no firm evidence regarding the effectiveness, safety, cost-effectiveness and impact on quality of life from an adequately powered randomized controlled trial (RCT) using systemic medication in children. OBJECTIVES: To assess whether there is a difference in the speed of onset, effectiveness, side-effect profile and reduction in flares post-treatment between ciclosporin (CyA) and methotrexate (MTX), and also the cost-effectiveness of the drugs. Treatment impact on quality of life will also be examined in addition to whether FLG genotype influences treatment response. In addition, the trial studies the immune-metabolic effects of CyA and MTX. METHODS: Multicentre, parallel group, assessor-blind, pragmatic RCT of 36 weeks' duration with a 24-week follow-up period. In total, 102 children aged 2-16 years with moderate-to-severe atopic eczema, unresponsive to topical treatment will be randomized (1 : 1) to receive MTX (0·4 mg kg-1 per week) or CyA (4 mg kg-1 per day). RESULTS: The trial has two primary outcomes: change from baseline to 12 weeks in Objective Severity Scoring of Atopic Dermatitis (o-SCORAD) and time to first significant flare following treatment cessation. CONCLUSIONS: This trial addresses important therapeutic questions, highlighted in systematic reviews and treatment guidelines for atopic eczema. The trial design is pragmatic to reflect current clinical practice.


Assuntos
Análise Custo-Benefício , Ciclosporina/administração & dosagem , Dermatite Atópica/tratamento farmacológico , Fármacos Dermatológicos/administração & dosagem , Metotrexato/administração & dosagem , Administração Oral , Adolescente , Criança , Pré-Escolar , Ciclosporina/efeitos adversos , Ciclosporina/economia , Dermatite Atópica/diagnóstico , Dermatite Atópica/economia , Dermatite Atópica/genética , Fármacos Dermatológicos/efeitos adversos , Fármacos Dermatológicos/economia , Feminino , Proteínas Filagrinas , Humanos , Proteínas de Filamentos Intermediários/genética , Masculino , Metotrexato/efeitos adversos , Metotrexato/economia , Estudos Multicêntricos como Assunto , Ensaios Clínicos Pragmáticos como Assunto , Ensaios Clínicos Controlados Aleatórios como Assunto , Índice de Gravidade de Doença , Resultado do Tratamento
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