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1.
HIV Med ; 19(1): e1-e42, 2018 01.
Artigo em Inglês | MEDLINE | ID: mdl-25649230

RESUMO

The 2015 Paediatric European Network for Treatment of AIDS (PENTA) guidelines provide practical recommendations on the management of HIV-1 infection in children in Europe and are an update to those published in 2009. Aims of treatment have progressed significantly over the last decade, moving far beyond limitation of short-term morbidity and mortality to optimizing health status for adult life and minimizing the impact of chronic HIV infection on immune system development and health in general. Additionally, there is a greater need for increased awareness and minimization of long-term drug toxicity. The main updates to the previous guidelines include: an increase in the number of indications for antiretroviral therapy (ART) at all ages (higher CD4 thresholds for consideration of ART initiation and additional clinical indications), revised guidance on first- and second-line ART recommendations, including more recently available drug classes, expanded guidance on management of coinfections (including tuberculosis, hepatitis B and hepatitis C) and additional emphasis on the needs of adolescents as they approach transition to adult services. There is a new section on the current ART 'pipeline' of drug development, a comprehensive summary table of currently recommended ART with dosing recommendations. Differences between PENTA and current US and World Health Organization guidelines are highlighted and explained.


Assuntos
Síndrome de Imunodeficiência Adquirida/diagnóstico , Síndrome de Imunodeficiência Adquirida/tratamento farmacológico , Antirretrovirais/uso terapêutico , Infecções Oportunistas Relacionadas com a AIDS/tratamento farmacológico , Síndrome de Imunodeficiência Adquirida/complicações , Adolescente , Criança , Pré-Escolar , Coinfecção/tratamento farmacológico , Europa (Continente) , Feminino , Humanos , Lactente , Recém-Nascido , Masculino
3.
HIV Med ; 18(3): 171-180, 2017 03.
Artigo em Inglês | MEDLINE | ID: mdl-27625109

RESUMO

OBJECTIVES: The aim of the study was to determine the time to, and risk factors for, triple-class virological failure (TCVF) across age groups for children and adolescents with perinatally acquired HIV infection and older adolescents and adults with heterosexually acquired HIV infection. METHODS: We analysed individual patient data from cohorts in the Collaboration of Observational HIV Epidemiological Research Europe (COHERE). A total of 5972 participants starting antiretroviral therapy (ART) from 1998, aged < 20 years at the start of ART for those with perinatal infection and 15-29 years for those with heterosexual infection, with ART containing at least two nucleoside reverse transcriptase inhibitors (NRTIs) and a nonnucleoside reverse transcriptase inhibitor (NNRTI) or a boosted protease inhibitor (bPI), were followed from ART initiation until the most recent viral load (VL) measurement. Virological failure of a drug was defined as VL > 500 HIV-1 RNA copies/mL despite ≥ 4 months of use. TCVF was defined as cumulative failure of two NRTIs, an NNRTI and a bPI. RESULTS: The median number of weeks between diagnosis and the start of ART was higher in participants with perinatal HIV infection compared with participants with heterosexually acquired HIV infection overall [17 (interquartile range (IQR) 4-111) vs. 8 (IQR 2-38) weeks, respectively], and highest in perinatally infected participants aged 10-14 years [49 (IQR 9-267) weeks]. The cumulative proportion with TCVF 5 years after starting ART was 9.6% [95% confidence interval (CI) 7.0-12.3%] in participants with perinatally acquired infection and 4.7% (95% CI 3.9-5.5%) in participants with heterosexually acquired infection, and highest in perinatally infected participants aged 10-14 years when starting ART (27.7%; 95% CI 13.2-42.1%). Across all participants, significant predictors of TCVF were those with perinatal HIV aged 10-14 years, African origin, pre-ART AIDS, NNRTI-based initial regimens, higher pre-ART viral load and lower pre-ART CD4. CONCLUSIONS: The results suggest a beneficial effect of starting ART before adolescence, and starting young people on boosted PIs, to maximize treatment response during this transitional stage of development.


Assuntos
Antirretrovirais/uso terapêutico , Farmacorresistência Viral , Infecções por HIV/tratamento farmacológico , Grupos Populacionais , Adolescente , Adulto , Criança , Pré-Escolar , Estudos de Coortes , Europa (Continente) , Feminino , Humanos , Lactente , Masculino , Fatores de Tempo , Falha de Tratamento , Adulto Jovem
4.
Int J Tuberc Lung Dis ; 20(10): 1293-1299, 2016 10.
Artigo em Inglês | MEDLINE | ID: mdl-27725037

RESUMO

SETTING: In June 2014, we became aware that shortages of purified protein derivative (PPD), the test substance used for the tuberculin skin test (TST), had occurred in several European health care institutions providing care for children with tuberculosis (TB). OBJECTIVE: To establish the extent of the shortage, a survey was performed. DESIGN: Survey conducted over a 1-month period (June-July 2014) among members of the Paediatric Tuberculosis Network European Trials Group (ptbnet). RESULTS: Thirty-five physicians from 23 European countries contributed data. The most commonly used PPD product was RT23 (Statens Serum Institut; n = 22, 63%). Twenty-one (60%) participants reported that their institution was experiencing a PPD shortage. The majority (n = 17, 81%) of those reporting a shortage were using RT23. Thirteen (37%) participants reported changes in screening practices resulting from the shortage, including sourcing PPD from alternative manufacturers, restricting remaining supplies to patients at greatest risk or replacing TST by an interferon-gamma release assay. CONCLUSIONS: The data show that a PPD shortage occurred in 2014, affecting multiple European countries. The shortage resulted in changes in TB screening capabilities and practices, potentially compromising both patient care as well as public health efforts. Appropriate actions to prevent future PPD shortages should be explored urgently by public health agencies and key stakeholders.


Assuntos
Necessidades e Demandas de Serviços de Saúde , Programas de Rastreamento , Teste Tuberculínico , Tuberculina , Tuberculose/diagnóstico , Europa (Continente) , Humanos , Testes de Liberação de Interferon-gama , Prevalência
5.
Clin Microbiol Infect ; 22(7): 643.e1-6, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27107685

RESUMO

Staphylococcus aureus is the main pathogen responsible for bone and joint infections worldwide and is also capable of causing pneumonia and other invasive severe diseases. Panton-Valentine leukocidin (PVL) and methicillin-resistant S. aureus (MRSA) have been studied as factors related with severity in these infections. The aims of this study were to describe invasive community-acquired S. aureus (CA-SA) infections and to analyse factors related to severity of disease. Paediatric patients (aged 0-16 years) who had a CA-SA invasive infection were prospectively recruited from 13 centres in 7 European countries. Demographic, clinical and microbiological data were collected. Severe infection was defined as invasive infection leading to death or admission to intensive care due to haemodynamic instability or respiratory failure. A total of 152 children (88 boys) were included. The median age was 7.2 years (interquartile range, 1.3-11.9). Twenty-six (17%) of the 152 patients had a severe infection, including 3 deaths (2%). Prevalence of PVL-positive CA-SA infections was 18.6%, and 7.8% of the isolates were MRSA. The multivariate analysis identified pneumonia (adjusted odds ratio (aOR) 13.39 (95% confidence interval (CI) 4.11-43.56); p 0.008), leukopenia at admission (<3000/mm(3)) (aOR 18.3 (95% CI 1.3-259.9); p 0.03) and PVL-positive infections (aOR 4.69 (95% CI 1.39-15.81); p 0.01) as the only factors independently associated with severe outcome. There were no differences in MRSA prevalence between severe and nonsevere cases (aOR 4.30 (95% CI 0.68- 28.95); p 0.13). Our results show that in European children, PVL is associated with more severe infections, regardless of methicillin resistance.


Assuntos
Infecções Comunitárias Adquiridas/patologia , Índice de Gravidade de Doença , Infecções Estafilocócicas/patologia , Staphylococcus aureus/isolamento & purificação , Toxinas Bacterianas/análise , Criança , Pré-Escolar , Infecções Comunitárias Adquiridas/epidemiologia , Infecções Comunitárias Adquiridas/mortalidade , Cuidados Críticos , Europa (Continente)/epidemiologia , Exotoxinas/análise , Feminino , Humanos , Lactente , Leucocidinas/análise , Masculino , Estudos Prospectivos , Fatores de Risco , Infecções Estafilocócicas/epidemiologia , Infecções Estafilocócicas/mortalidade , Staphylococcus aureus/genética , Staphylococcus aureus/patogenicidade , Análise de Sobrevida , Fatores de Virulência/análise
6.
An. pediatr. (2003. Ed. impr.) ; 83(4): 285.e1-285.e8, oct. 2015. tab, ilus
Artigo em Espanhol | IBECS | ID: ibc-143981

RESUMO

El cribado de tuberculosis (TB) gestacional mediante la realización de la prueba de tuberculina (PT) se recomienda a las embarazadas con síntomas compatibles, contacto íntimo con TB bacilífera o riesgo de progresión a formas activas. Las nuevas técnicas de diagnóstico interferon gamma release assay (IGRA) están indicadas en gestantes sin factores de riesgo, con PT positiva y antecedente de vacunación BCG, y en inmunodeprimidas con sospecha clínica y PT negativa. El diagnóstico de enfermedad es difícil, ya que los síntomas pueden ser inespecíficos y hay más formas extrapulmonares, por el retraso en las exploraciones radiológicas y por la mayor tasa de anergia a la tuberculina. La TB neonatal puede adquirirse de forma intrauterina (TB congénita) o por vía respiratoria tras el parto (TB posnatal). La TB congénita es excepcional, no produce malformaciones fetales y, aunque puede estar presente en el nacimiento, suele iniciarse a partir de la segunda semana de vida. En ausencia de antecedentes familiares, la TB neonatal debe sospecharse en caso de neumonía con patrón miliar, hepatoesplenomegalia con lesiones focales o meningitis linfocitaria con hipoglucorraquia, especialmente si la madre procede de áreas de alta endemia de TB. La PT es habitualmente negativa y la sensibilidad de los IGRA es inferior a la de niños de más edad. Sin embargo, la baciloscopia y el cultivo de jugo gástrico tienen una rentabilidad superior, especialmente en la TB congénita. Las técnicas de diagnóstico molecular permiten un diagnóstico precoz y la detección de mutaciones de resistencia farmacológica. El riesgo de formas diseminadas y la mortalidad son elevados


Tuberculosis (TB) screening in pregnancy using tuberculin skin test (TST) is recommended in case of symptoms of TB disease, close contact with a patient with infectious TB, or high risk of developing active disease. The new interferon gamma release assay (IGRA) tests are recommended in BCG-vaccinated pregnant women with positive TST and no known risk factors for TB, and in those immunocompromised, with clinical suspicion of TB but negative TST. TB diagnosis is difficult due to the non-specific symptoms, the increased frequency of extrapulmonary disease, the delay in radiological examinations, and the high rate of tuberculin anergy. Neonatal TB can be acquired in utero (congenital TB), or through airborne transmission after delivery (postnatal TB). Congenital TB is extremely rare and does not cause fetal malformations. It may be evident at birth, although it usually presents after the second week of life. In newborns with no family history of TB, the disease should be considered in cases of miliary pneumonia, hepatosplenomegaly with focal lesions, or lymphocytic meningitis with hypoglycorrhachia, especially in those born to immigrants from high TB-burden countries. TST is usually negative, and IGRAs have lower sensitivity than in older children. However, the yield of acid-fast smear and culture is higher, mostly in congenital TB. Molecular diagnosis techniques enable early diagnosis and detection of drug resistance mutations. There is a substantial risk of disseminated disease and death


Assuntos
Adulto , Criança , Feminino , Humanos , Recém-Nascido , Masculino , Gravidez , Tuberculose/congênito , Tuberculose/diagnóstico , Tuberculose/epidemiologia , Teste Tuberculínico/instrumentação , Teste Tuberculínico/métodos , Teste Tuberculínico , Testes de Liberação de Interferon-gama/instrumentação , Testes de Liberação de Interferon-gama/métodos , Testes de Liberação de Interferon-gama , Tuberculose/prevenção & controle , Sociedades Médicas/normas , Sociedades Médicas , Programas de Rastreamento/métodos , Algoritmos , Diagnóstico Diferencial , Radiografia Torácica , Escarro/microbiologia
7.
An. pediatr. (2003. Ed. impr.) ; 83(4): 286.e1-286.e7, oct. 2015. tab, ilus
Artigo em Espanhol | IBECS | ID: ibc-143982

RESUMO

En la embarazada expuesta a tuberculosis (TB) no se recomienda profilaxis primaria con isoniazida salvo en gestantes inmunodeprimidas, con enfermedades crónicas o factores de riesgo obstétrico y antecedente de contacto íntimo mantenido con un enfermo bacilífero. En la infección tuberculosa latente (ITBL) se iniciará profilaxis con isoniazida si existe contacto reciente con TB o factores de riesgo de progresión a TB activa. En caso contrario, se retrasará hasta al menos 3 semanas después del parto. El tratamiento de la enfermedad tuberculosa es el mismo que fuera de la gestación. Los recién nacidos de madres con historia gestacional de TB diseminada o extrapulmonar, con TB activa en el parto o con contacto TB posnatal conocido, asintomáticos y con pruebas diagnósticas negativas, deben recibir profilaxis primaria con isoniazida durante al menos 12 semanas. Transcurrido ese tiempo se repiten los test diagnósticos, y si son negativos, se interrumpe la profilaxis. En la ITBL, se administrará isoniazida durante 9 meses. En la enfermedad tuberculosa, el tratamiento es el mismo que en el niño mayor pero mantenido al menos 9 meses. Se recomienda aislamiento respiratorio en la TB congénita y en la TB posnatal con baciloscopia positiva en jugo gástrico o aspirado bronquial. La separación madre-hijo solo está indicada en madres que han recibido tratamiento durante menos de 2 semanas, presentan baciloscopia positiva o tienen TB resistente. La lactancia materna no está contraindicada y en las situaciones de separación la madre puede extraerse la leche para que sea administrada en biberón al recién nacido


In pregnant women who have been exposed to tuberculosis (TB), primary isoniazid prophylaxis is only recommended in cases of immunosuppression, chronic medical conditions or obstetric risk factors, and close and sustained contact with a patient with infectious TB. Isoniazid prophylaxis for latent tuberculosis infection (LTBI) is recommended in women who have close contact with an infectious TB patient or have risk factors for progression to active disease. Otherwise, it should be delayed until at least three weeks after delivery. Treatment of TB disease during pregnancy is the same as for the general adult population. Infants born to mothers with disseminated or extrapulmonary TB in pregnancy, with active TB at delivery, or with postnatal exposure to TB, should undergo a complete diagnostic evaluation. Primary isoniazid prophylaxis for at least 12 weeks is recommended for those with negative diagnostic tests and no evidence of disease. Repeated negative diagnostic tests are mandatory before interrupting prophylaxis. Isoniazid for 9 months is recommended in LTBI. Treatment of neonatal TB disease is similar to that of older children, but should be maintained for at least 9 months. Respiratory isolation is recommended in congenital TB, and in postnatal TB with positive gastric or bronchial aspirate acid-fast smears. Separation of mother and infant is only necessary when the mother has received treatment for less than 2 weeks, is sputum smear-positive, or has drug-resistant TB. Breastfeeding is not contraindicated, and in case of mother-infant separation expressed breast milk feeding is recommended


Assuntos
Adulto , Feminino , Humanos , Recém-Nascido , Masculino , Tuberculose/terapia , Isoniazida/uso terapêutico , Aleitamento Materno/tendências , Resistência a Medicamentos , Coinfecção/complicações , Coinfecção/terapia , Antirretrovirais/uso terapêutico , Antibióticos Antituberculose/metabolismo , Antibióticos Antituberculose/uso terapêutico , Fatores de Risco , Monitorização Imunológica/métodos , Vacina BCG/imunologia
12.
An Pediatr (Barc) ; 83(4): 285.e1-8, 2015 Oct.
Artigo em Espanhol | MEDLINE | ID: mdl-25754313

RESUMO

Tuberculosis (TB) screening in pregnancy using tuberculin skin test (TST) is recommended in case of symptoms of TB disease, close contact with a patient with infectious TB, or high risk of developing active disease. The new interferon gamma release assay (IGRA) tests are recommended in BCG-vaccinated pregnant women with positive TST and no known risk factors for TB, and in those immunocompromised, with clinical suspicion of TB but negative TST. TB diagnosis is difficult due to the non-specific symptoms, the increased frequency of extrapulmonary disease, the delay in radiological examinations, and the high rate of tuberculin anergy. Neonatal TB can be acquired in utero (congenital TB), or through airborne transmission after delivery (postnatal TB). Congenital TB is extremely rare and does not cause fetal malformations. It may be evident at birth, although it usually presents after the second week of life. In newborns with no family history of TB, the disease should be considered in cases of miliary pneumonia, hepatosplenomegaly with focal lesions, or lymphocytic meningitis with hypoglycorrhachia, especially in those born to immigrants from high TB-burden countries. TST is usually negative, and IGRAs have lower sensitivity than in older children. However, the yield of acid-fast smear and culture is higher, mostly in congenital TB. Molecular diagnosis techniques enable early diagnosis and detection of drug resistance mutations. There is a substantial risk of disseminated disease and death.


Assuntos
Complicações Infecciosas na Gravidez/diagnóstico , Tuberculose/congênito , Tuberculose/diagnóstico , Algoritmos , Feminino , Humanos , Recém-Nascido , Gravidez , Complicações Infecciosas na Gravidez/epidemiologia , Tuberculose/epidemiologia
13.
An Pediatr (Barc) ; 83(4): 286.e1-7, 2015 Oct.
Artigo em Espanhol | MEDLINE | ID: mdl-25754314

RESUMO

In pregnant women who have been exposed to tuberculosis (TB), primary isoniazid prophylaxis is only recommended in cases of immunosuppression, chronic medical conditions or obstetric risk factors, and close and sustained contact with a patient with infectious TB. Isoniazid prophylaxis for latent tuberculosis infection (LTBI) is recommended in women who have close contact with an infectious TB patient or have risk factors for progression to active disease. Otherwise, it should be delayed until at least three weeks after delivery. Treatment of TB disease during pregnancy is the same as for the general adult population. Infants born to mothers with disseminated or extrapulmonary TB in pregnancy, with active TB at delivery, or with postnatal exposure to TB, should undergo a complete diagnostic evaluation. Primary isoniazid prophylaxis for at least 12 weeks is recommended for those with negative diagnostic tests and no evidence of disease. Repeated negative diagnostic tests are mandatory before interrupting prophylaxis. Isoniazid for 9 months is recommended in LTBI. Treatment of neonatal TB disease is similar to that of older children, but should be maintained for at least 9 months. Respiratory isolation is recommended in congenital TB, and in postnatal TB with positive gastric or bronchial aspirate acid-fast smears. Separation of mother and infant is only necessary when the mother has received treatment for less than 2 weeks, is sputum smear-positive, or has drug-resistant TB. Breastfeeding is not contraindicated, and in case of mother-infant separation expressed breast milk feeding is recommended.


Assuntos
Antituberculosos/uso terapêutico , Isoniazida/uso terapêutico , Complicações Infecciosas na Gravidez/tratamento farmacológico , Tuberculose/congênito , Tuberculose/tratamento farmacológico , Feminino , Humanos , Recém-Nascido , Gravidez , Complicações Infecciosas na Gravidez/prevenção & controle , Tuberculose/prevenção & controle
18.
Emergencias (St. Vicenç dels Horts) ; 25(1): 55-57, feb. 2013. ilus
Artigo em Espanhol | IBECS | ID: ibc-110608

RESUMO

Se describen las características de las consultas en urgencias entre 2000 y 2010 por pinchazo accidental y se analiza la probabilidad de seroconversión para los virus de la hepatitis B (VHB), C (VHC) y el virus de la inmunodeficiencia humana (VIH). Se revisan160 pacientes; 108 (67,5%) son varones; la edad mediana es de 6,3 (p25-p75: 4,8-9,1) años. La incidencia es de 1,2 (p25-75: 0,8-2,0) consultas por pinchazo accidental/10.000 consultas y año, con tendencia a decrecer. Los accidentes se produjeron con mayor frecuencia en los parques y los dedos de las manos fueron el sitio anatómico más afectado. En la muestra estudiada es nulo el riesgo de transmisión para los virus estudiados (AU)


To describe the characteristics of visits to a pediatric emergency department after accidental needlestick injuries and between 2000 and 2010 to estimate the likelihood of hepatitis B and C virus or human immunodeficiency virus seroconversion. A total of 160 cases were studied; 108 patients (67.5%) were boys. The median age (25th-75thpercentile) was 6.3 (4.8-9.1) years. The department attended a median of 1.2 (0.8-2.0) patients with accidental needle puncture per 10 000 visits annually. The incidence tended to decrease over time. Accidents occurred most often in parks, and fingers were the most common place of puncture. No seroconversions occurred (AU)


Assuntos
Humanos , Masculino , Feminino , Lactente , Pré-Escolar , Criança , Ferimentos Penetrantes Produzidos por Agulha/epidemiologia , Transmissão de Doença Infecciosa/estatística & dados numéricos , Fatores de Risco , Serviços de Saúde da Criança/estatística & dados numéricos , Serviços Médicos de Emergência/estatística & dados numéricos , Soropositividade para HIV/epidemiologia , Anticorpos Anti-Hepatite/isolamento & purificação
19.
An. pediatr. (2003, Ed. impr.) ; 76(6): 360-360[e1-e9], jun. 2012. tab, ilus
Artigo em Espanhol | IBECS | ID: ibc-101491

RESUMO

La transmisión vertical del virus de inmunodeficiencia humana en los países desarrollados se ha reducido drásticamente a menos del 2% en los últimos 15 años, tras la aplicación de distintas medidas profilácticas: el uso de antirretrovirales, la cesárea electiva y la lactancia artificial exclusiva. El seguimiento de estos niños sanos es la situación más común relacionada con la infección por el VIH que los pediatras no especialistas deben afrontar en la actualidad en la práctica clínica habitual en España. Estas recomendaciones, emitidas por la Sociedad Española de Infectología Pediátrica, pretenden resumir los principales aspectos de este seguimiento, incluyendo el manejo en sala de partos, el tipo de lactancia, la profilaxis antirretroviral neonatal, el diagnóstico de la infección por el VIH, las comorbilidades en la época neonatal, la toxicidad a corto y a medio plazo, las inmunizaciones y otras medidas profilácticas y el seguimiento a largo plazo(AU)


Human immunodeficiency virus vertical transmission in developed countries has dramatically decreased to less than 2% over the last 15 years due to the consecutive implementation of different prophylactic measures, including the use of antiretrovirals, elective cesarean section and refraining from breastfeeding. The follow-up of these otherwise healthy children is, by far, the most common situation related to HIV infection that general pediatricians currently face in routine clinical care in Spain. These Recommendations issued by the Spanish Society of Pediatric Infectious Diseases attempt to summarize the main aspects of this follow-up, including birth management, type of feeding, neonatal antiretroviral prophylaxis, HIV infection diagnosis, common early comorbidities, short- and mid-term toxicities, vaccination and other prophylactic measures and long-term follow-up(AU)


Assuntos
Humanos , Masculino , Feminino , Criança , Sociedades Médicas/normas , Sociedades Médicas , Infecções/epidemiologia , Controle de Infecções/organização & administração , Síndrome de Imunodeficiência Adquirida/epidemiologia , Síndrome de Imunodeficiência Adquirida/prevenção & controle , Antirretrovirais/uso terapêutico , Assistência Perinatal/métodos , Assistência Perinatal/organização & administração , Assistência Perinatal/normas , Controle de Infecções/tendências , Antirretrovirais/imunologia , HIV/imunologia , Sociedades Médicas/organização & administração , Controle de Infecções/normas , Antirretrovirais/metabolismo , Assistência Perinatal/tendências , Assistência Perinatal
20.
An Pediatr (Barc) ; 76(6): 360.e1-9, 2012 Jun.
Artigo em Espanhol | MEDLINE | ID: mdl-22406157

RESUMO

Human immunodeficiency virus vertical transmission in developed countries has dramatically decreased to less than 2% over the last 15 years due to the consecutive implementation of different prophylactic measures, including the use of antiretrovirals, elective cesarean section and refraining from breastfeeding. The follow-up of these otherwise healthy children is, by far, the most common situation related to HIV infection that general pediatricians currently face in routine clinical care in Spain. These recommendations issued by the Spanish Society of Pediatric Infectious Diseases attempt to summarize the main aspects of this follow-up, including birth management, type of feeding, neonatal antiretroviral prophylaxis, HIV infection diagnosis, common early comorbidities, short- and mid-term toxicities, vaccination and other prophylactic measures and long-term follow-up.


Assuntos
Antirretrovirais/uso terapêutico , Infecções por HIV/prevenção & controle , Infecções por HIV/transmissão , Transmissão Vertical de Doenças Infecciosas/prevenção & controle , Complicações Infecciosas na Gravidez/tratamento farmacológico , Algoritmos , Antirretrovirais/efeitos adversos , Feminino , Seguimentos , Infecções por HIV/diagnóstico , Infecções por HIV/tratamento farmacológico , Humanos , Recém-Nascido , Gravidez , Efeitos Tardios da Exposição Pré-Natal/induzido quimicamente
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