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1.
J Am Acad Child Adolesc Psychiatry ; 59(4): 468-496, 2020 04.
Artigo em Inglês | MEDLINE | ID: mdl-33928910

RESUMO

Intellectual disability (intellectual developmental disorder) (ID/IDD) is both a psychiatric disorder and a risk factor for co-occurring psychiatric disorders in children and adolescents. DSM-5 introduced important changes in the conceptualization and diagnosis of ID/IDD, and current research studies clarify assessment and treatment of co-occurring psychiatric disorders in this population. Optimal assessment and treatment of psychiatric illness in children and adolescents with ID/IDD includes modifications in diagnostic and treatment techniques, appreciation of variations in the clinical presentation of psychiatric disorders, an understanding of the spectrum of etiologies of behavioral disturbance, and knowledge of psychosocial and medical interventions.


Assuntos
Deficiência Intelectual , Transtornos Mentais , Adolescente , Criança , Comorbidade , Deficiências do Desenvolvimento , Manual Diagnóstico e Estatístico de Transtornos Mentais , Humanos , Deficiência Intelectual/diagnóstico , Deficiência Intelectual/epidemiologia , Deficiência Intelectual/terapia , Transtornos Mentais/diagnóstico , Transtornos Mentais/epidemiologia , Transtornos Mentais/terapia , Fatores de Risco
2.
Adm Policy Ment Health ; 41(4): 552-67, 2014 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-23709285

RESUMO

When compared with the general United States child population, children entering foster care have elevated rates of mental health problems. This study examines: (1) state approaches to mental health evaluations for children entering foster care for the first time, (2) the consistency of these approaches with professional guidelines, and (3) whether the specific instruments endorsed are supported by available evidence. Semi-structured qualitative interviews and a document review of available protocols/policies were conducted for 47 states and the District of Columbia. All states endorsed mental health evaluations; variation existed between states in approach, timeframe, administrator, and specific instruments endorsed.


Assuntos
Cuidados no Lar de Adoção/organização & administração , Política de Saúde , Transtornos Mentais/diagnóstico , Serviços de Saúde Mental/organização & administração , Saúde Mental , Guias de Prática Clínica como Assunto , Adolescente , Criança , Pré-Escolar , Feminino , Fidelidade a Diretrizes , Necessidades e Demandas de Serviços de Saúde , Humanos , Lactente , Masculino , Programas de Rastreamento , Avaliação das Necessidades , Pesquisa Qualitativa , Estados Unidos
3.
Pediatr Blood Cancer ; 54(3): 398-402, 2010 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19827138

RESUMO

BACKGROUND: Pulmonary hypertension (PHTN) is increasingly recognized as a serious complication of sickle cell disease (SCD). Our objective was to determine the prevalence of PHTN and identify factors associated with PHTN among children and young adults with SCD in Lebanon. PROCEDURE: From June 2004 to June 2008, 90 patients were studied. Correlation of TRV with LDH, mean corpuscular volume (MCV), fetal hemoglobin (HbF), hydroxyurea use, and G6PD deficiency was performed. Transthoracic Doppler echocardiography was performed during steady-state at each patient's initial visit and yearly thereafter. PHT was defined as a tricuspid regurgitant jet velocity (TRV) > or =2.5 m/sec. RESULTS: Twenty-seven patients (31.8%) were found to have PHTN. They had significantly higher LDH levels (P = 0.008) and MCV (P = 0.024). There was a higher percentage of patients on hydroxyurea in the group with PHTN (78% vs. 50%, P = 0.015). Furthermore, five children, mean age 9.8 years (range, 6-13 years), with initially normal TRV developed PHTN while on hydroxyurea for at least 3 years, at a mean dose of 19.2 mg/kg/day (range, 14-24). PHTN clustered in families and was found in all members with SCD in 7 of the 21 families studied; they contributed 16 of the 27 patients with PHTN. None of the 21 patients with PHTN were G6PD deficient compared to 4 of 36 without PHTN. CONCLUSIONS: PHTN was common, associated with increased hemolysis but not G6PD deficiency, and clustered in families. Moreover, PHTN developed despite hydroxyurea therapy in five patients.


Assuntos
Anemia Falciforme/complicações , Anemia Falciforme/genética , Hipertensão Pulmonar/etiologia , Hipertensão Pulmonar/genética , Adolescente , Adulto , Anemia Falciforme/tratamento farmacológico , Antidrepanocíticos/uso terapêutico , Criança , Pré-Escolar , Ecocardiografia , Feminino , Humanos , Hidroxiureia/uso terapêutico , Hipertensão Pulmonar/prevenção & controle , Líbano , Masculino , Linhagem , Adulto Jovem
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