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1.
J Infect Dis ; 215(2): 171-174, 2017 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-28073857

RESUMO

A neonate born to an Ebola virus-positive woman was diagnosed with Ebola virus infection on her first day of life. The patient was treated with monoclonal antibodies (ZMapp), a buffy coat transfusion from an Ebola survivor, and the broad-spectrum antiviral GS-5734. On day 20, a venous blood specimen tested negative for Ebola virus by quantitative reverse-transcription polymerase chain reaction. The patient was discharged in good health on day 33 of life. Further follow-up consultations showed age-appropriate weight gain and neurodevelopment at the age of 12 months. This patient is the first neonate documented to have survived congenital infection with Ebola virus.


Assuntos
Alanina/análogos & derivados , Anticorpos Monoclonais/administração & dosagem , Antivirais/administração & dosagem , Doença pelo Vírus Ebola/congênito , Doença pelo Vírus Ebola/terapia , Fatores Imunológicos/administração & dosagem , Ribonucleotídeos/administração & dosagem , Terapias em Estudo/métodos , Monofosfato de Adenosina/análogos & derivados , Alanina/administração & dosagem , Sangue/virologia , Feminino , Humanos , Recém-Nascido , Gravidez , Resultado do Tratamento , Adulto Jovem
2.
Matern Child Nutr ; 9(1): 74-89, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22784020

RESUMO

In Haiti, initiation of breastfeeding is high, but early mixed feeding is the norm. In a situation of crisis, mothers' worries about insufficiency of breast milk, disruption of social networks and free unmonitored distribution of breast milk substitutes impact feeding practices. This study was conducted to explore the attitudes, practices and understandings of breastfeeding in the post-earthquake situation in Haiti. A mixed-method study was conducted in Léogâne, Haiti, a town close to the epicentre of the 2010 earthquake. In a household survey, 1131 mothers of children under 24 months were interviewed about feeding practices. In the quantitative component, we conducted 25 in-depth interviews and seven focus group discussions with mothers, grandmothers, traditional birth attendants, fathers and health care professionals. Mothers described breastfeeding as a challenging responsibility to ensure the infants' health. They understood breast milk as a dynamic substance, the quality of which would deteriorate if the mother's diet was poor or if the mother was afflicted with a psychosocial condition called move san or colere, 'bad blood'. To protect the child in these situations, early supplementary feeding is introduced. Only 20% of informants exclusively breastfed infants under 6 months. Because of a lack of confidence in the quality of breast milk, Haitian mothers tend to wean children earlier. The abiding concerns of Haitian mothers over the quality of their breast milk suggest a number of ways - such as dietary advice - that post-earthquake aid agencies could enhance breastfeeding support.


Assuntos
Atitude Frente a Saúde , Aleitamento Materno/psicologia , Fenômenos Fisiológicos da Nutrição do Lactente/fisiologia , Fenômenos Fisiológicos da Nutrição Materna/fisiologia , Mães/psicologia , Estado Nutricional , Adulto , Fatores Etários , Características Culturais , Terremotos , Feminino , Haiti , Humanos , Lactente , Recém-Nascido , Masculino , Fatores de Tempo , Desmame
3.
Malar J ; 6: 29, 2007 Mar 12.
Artigo em Inglês | MEDLINE | ID: mdl-17352806

RESUMO

BACKGROUND: Artesunate-amodiaquine combination for the treatment of childhood malaria is one of the artemisinin combination therapies (ACTs) recommended by National authorities in many African countries today. Effectiveness data on this combination in young children is scarce. METHODS: The effectiveness of three daily doses of artesunate plus amodiaquine combination given unsupervised (n = 32), compared with the efficacy when given under full supervision (n = 29) to children with falciparum malaria were assessed in an unrandomized study. RESULTS: 61 patients analysed revealed a PCR-corrected day-28 cure rate of 86 % (25 of 29 patients; CI 69-95 %) in the supervised group and 63 % (20 of 32 patients; CI 45-77 %) in the unsupervised group. The difference in outcome between both groups was statistically significant (p = 0.04). No severe adverse events were reported. CONCLUSION: The effectiveness of this short course regimen in young children with falciparum malaria could be augmented by increased adherence and improved formulation.


Assuntos
Amodiaquina/uso terapêutico , Antimaláricos/uso terapêutico , Artemisininas/uso terapêutico , Malária Falciparum/tratamento farmacológico , Plasmodium falciparum/efeitos dos fármacos , Sesquiterpenos/uso terapêutico , Amodiaquina/administração & dosagem , Amodiaquina/efeitos adversos , Animais , Antimaláricos/administração & dosagem , Antimaláricos/efeitos adversos , Artemisininas/administração & dosagem , Artemisininas/efeitos adversos , Artesunato , Pré-Escolar , Quimioterapia Combinada , Gabão , Humanos , Lactente , Malária Falciparum/parasitologia , Sesquiterpenos/administração & dosagem , Sesquiterpenos/efeitos adversos , Resultado do Tratamento
4.
J Infect Dis ; 196(11): 1595-602, 2007 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-18008242

RESUMO

BACKGROUND: Intermittent preventive treatment aims to maximize the protective effects of malaria chemoprophylaxis while minimizing the deleterious effects. METHODS: In Gabon, 1189 infants received either sulfadoxine-pyrimethamine (SP; 250 and 12.5 mg, respectively) or placebo at 3, 9, and 15 months of age. Children were actively followed-up until 18 months of age. RESULTS: In the intention-to-treat population at 18 months of follow-up, 84 children (17%) in the SP group had > or =1 episode of anemia, versus 108 (21%) in the placebo group (protective efficacy, 22% [95% confidence interval {CI}, -1% to 40%]; P=.06). In the intervention group, there were 66 episodes during 485 person-years at risk, compared with 79 episodes during 497 years in the placebo group (protective efficacy, 17% [95% CI, -24% to 45%; P=.36). The effects were similar at 12 months of follow-up. The study drug was safe and well tolerated. CONCLUSIONS: The intervention was efficacious, producing a reduction in risk for anemia but a smaller effect against malaria. It is a valuable additional tool to control malaria in a highly vulnerable age group. Remaining important questions are currently being addressed in further studies. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT00167843.


Assuntos
Antimaláricos/administração & dosagem , Malária Falciparum/prevenção & controle , Parasitemia/prevenção & controle , Pirimetamina/administração & dosagem , Sulfadoxina/administração & dosagem , Anemia/induzido quimicamente , Anemia/epidemiologia , Antimaláricos/efeitos adversos , Método Duplo-Cego , Esquema de Medicação , Combinação de Medicamentos , Feminino , Gabão/epidemiologia , Hematócrito , Hemoglobinas/metabolismo , Humanos , Incidência , Lactente , Estimativa de Kaplan-Meier , Malária Falciparum/sangue , Malária Falciparum/epidemiologia , Masculino , Parasitemia/sangue , Parasitemia/epidemiologia , Parasitemia/parasitologia , Seleção de Pacientes , Pirimetamina/efeitos adversos , Projetos de Pesquisa , Sulfadoxina/efeitos adversos , Resultado do Tratamento
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