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1.
J Infect Dis ; 215(2): 171-174, 2017 Jan 15.
Artículo en Inglés | MEDLINE | ID: mdl-28073857

RESUMEN

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.


Asunto(s)
Alanina/análogos & derivados , Anticuerpos Monoclonales/administración & dosificación , Antivirales/administración & dosificación , Fiebre Hemorrágica Ebola/congénito , Fiebre Hemorrágica Ebola/terapia , Factores Inmunológicos/administración & dosificación , Ribonucleótidos/administración & dosificación , Terapias en Investigación/métodos , Adenosina Monofosfato/análogos & derivados , Alanina/administración & dosificación , Sangre/virología , Femenino , Humanos , Recién Nacido , Embarazo , Resultado del Tratamiento , Adulto Joven
2.
Matern Child Nutr ; 9(1): 74-89, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-22784020

RESUMEN

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.


Asunto(s)
Actitud Frente a la Salud , Lactancia Materna/psicología , Fenómenos Fisiológicos Nutricionales del Lactante/fisiología , Fenómenos Fisiologicos Nutricionales Maternos/fisiología , Madres/psicología , Estado Nutricional , Adulto , Factores de Edad , Características Culturales , Terremotos , Femenino , Haití , Humanos , Lactante , Recién Nacido , Masculino , Factores de Tiempo , Destete
3.
Malar J ; 6: 29, 2007 Mar 12.
Artículo en Inglés | MEDLINE | ID: mdl-17352806

RESUMEN

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.


Asunto(s)
Amodiaquina/uso terapéutico , Antimaláricos/uso terapéutico , Artemisininas/uso terapéutico , Malaria Falciparum/tratamiento farmacológico , Plasmodium falciparum/efectos de los fármacos , Sesquiterpenos/uso terapéutico , Amodiaquina/administración & dosificación , Amodiaquina/efectos adversos , Animales , Antimaláricos/administración & dosificación , Antimaláricos/efectos adversos , Artemisininas/administración & dosificación , Artemisininas/efectos adversos , Artesunato , Preescolar , Quimioterapia Combinada , Gabón , Humanos , Lactante , Malaria Falciparum/parasitología , Sesquiterpenos/administración & dosificación , Sesquiterpenos/efectos adversos , Resultado del Tratamiento
4.
J Infect Dis ; 196(11): 1595-602, 2007 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-18008242

RESUMEN

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.


Asunto(s)
Antimaláricos/administración & dosificación , Malaria Falciparum/prevención & control , Parasitemia/prevención & control , Pirimetamina/administración & dosificación , Sulfadoxina/administración & dosificación , Anemia/inducido químicamente , Anemia/epidemiología , Antimaláricos/efectos adversos , Método Doble Ciego , Esquema de Medicación , Combinación de Medicamentos , Femenino , Gabón/epidemiología , Hematócrito , Hemoglobinas/metabolismo , Humanos , Incidencia , Lactante , Estimación de Kaplan-Meier , Malaria Falciparum/sangre , Malaria Falciparum/epidemiología , Masculino , Parasitemia/sangre , Parasitemia/epidemiología , Parasitemia/parasitología , Selección de Paciente , Pirimetamina/efectos adversos , Proyectos de Investigación , Sulfadoxina/efectos adversos , Resultado del Tratamiento
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