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1.
Pediatr Infect Dis J ; 20(10): 1009-10, 2001 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11642621

RESUMO

Patients with advanced HIV disease have a poor response to some immunizations. A case is presented of a Class C1 HIV-infected child who suffered three episodes of Streptococcus pneumoniae serotype 6B bacteremia despite having received the heptavalent conjugate and 23-valent polysaccharide pneumococcal vaccines. Clinicians should expect some vaccine failures with the heptavalent conjugate vaccine in children with advanced HIV disease.


Assuntos
Infecções Oportunistas Relacionadas com a AIDS/imunologia , Infecções Oportunistas Relacionadas com a AIDS/prevenção & controle , Bacteriemia/prevenção & controle , Vacinas Pneumocócicas/uso terapêutico , Infecções Estreptocócicas/prevenção & controle , Feminino , Humanos , Hospedeiro Imunocomprometido , Lactente , Fatores de Risco , Prevenção Secundária , Falha de Tratamento , Vacinas Conjugadas/uso terapêutico
2.
Pediatr Infect Dis J ; 20(10): 946-50, 2001 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11642628

RESUMO

BACKGROUND: Bacterial infections cause significant morbidity and mortality in cardiac transplant patients. Because Streptococcus pneumoniae is the most prominent bacterial pathogen of childhood, the objective of this study was to define the role of S. pneumoniae as a pathogen in the cardiac transplant population. METHODS: Medical records of cardiac transplant patients from March, 1990, through November, 2000, were reviewed to identify invasive pneumococcal infections after transplantation. Demographic, clinical and microbiologic data were reviewed. RESULTS: Nine (11%) of 80 patients had 12 episodes of pneumococcal bacteremia for an incidence rate of 39 cases/1,000 patient years. Patients who were African-American, transplanted before 2 years of age and transplanted because of idiopathic dilated cardiomyopathy were at increased risk of invasive pneumococcal disease (P < 0.05). Six patients were eligible for the 23-valent pneumococcal polysaccharide vaccine before their first invasive infection, but only 1 had received it at the recommended age. Most isolates (82%) were penicillin-susceptible, and no single serotype predominated. There were 2 deaths in the study group, but each was unrelated to infection. Three patients (33%) had recurrent invasive disease with a second serotype an average of 12 months after the first infection. CONCLUSIONS: The incidence of pneumococcal bacteremia in cardiac transplant patients is higher than in the general pediatric population. Risks for infection were being African-American, being younger than 2 years at the time of transplant and being transplanted because of idiopathic cardiomyopathy. It is plausible that pneumococcal vaccine would decrease this risk.


Assuntos
Transplante de Coração/efeitos adversos , Infecções Pneumocócicas/epidemiologia , Infecções Pneumocócicas/etiologia , Arkansas/epidemiologia , Distribuição de Qui-Quadrado , Pré-Escolar , Humanos , Hospedeiro Imunocomprometido , Incidência , Lactente , Recém-Nascido , Prontuários Médicos , Recidiva , Estudos Retrospectivos , Fatores de Risco , Índice de Gravidade de Doença
3.
J Ark Med Soc ; 95(6): 239-41, 1998 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-9821745

RESUMO

In 1994, the Centers for Disease Control and Prevention (CDC) recommended zidovudine (ZDV) prophylaxis to reduce perinatal transmission of HIV. Caregivers at the University of Arkansas for Medical Sciences (UAMS) instituted a program of universal voluntary HIV testing of pregnant females combined with maternal education regarding ZDV prophylaxis in October 1994. Since that time, 7 of 39 (18%) infants referred to Arkansas Children's Hospital (ACH) for evaluation of perinatal HIV exposure have been infected compared to 21 of 53 (40%) referred prior to October 1994, (p = 0.042). Unfortunately, of the 39 infants referred to ACH after October 1994, 21 were born to HIV-infected mothers who did not comply with prophylaxis. Fifteen of these mothers were not offered intravenous ZDV during delivery; five have children infected with HIV. These data indicate the need for increased efforts by health officials in Arkansas to institute nationally recommended methods of prevention of perinatal HIV.


Assuntos
Infecções por HIV/prevenção & controle , Infecções por HIV/transmissão , Transmissão Vertical de Doenças Infecciosas/prevenção & controle , Complicações Infecciosas na Gravidez , Fármacos Anti-HIV/uso terapêutico , Arkansas , Feminino , Infecções por HIV/tratamento farmacológico , Humanos , Gravidez , Complicações Infecciosas na Gravidez/tratamento farmacológico , Zidovudina/uso terapêutico
4.
J Ark Med Soc ; 92(4): 165-8, 1995 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-7592235

RESUMO

Pediatric human immunodeficiency virus (HIV) infection is a disease of mother-to-infant transmission. The World Health Organization estimates there will be ten million HIV-infected children by the end of this century. It is now thought that both intrauterine and intrapartum transmission of HIV occurs. Infants infected in utero develop clinical signs and symptoms at an earlier age than those who are infected at the time of delivery. We describe two cases that demonstrate early-onset and late-onset pediatric HIV disease, respectively. Recently, it was determined that perinatal transmission of HIV can be significantly reduced by the administration of the antiretroviral drug, zidovudine (ZDV), to HIV-positive pregnant women and their newborns, making HIV screening of pregnant women more desirable than ever. A program of universal voluntary HIV testing for pregnant women has been successfully implemented at the University of Arkansas for Medical Sciences. Details of this program are described herein.


Assuntos
Infecções por HIV , Complicações Infecciosas na Gravidez , Evolução Fatal , Feminino , Infecções por HIV/congênito , Infecções por HIV/prevenção & controle , Infecções por HIV/transmissão , Humanos , Lactente , Recém-Nascido , Transmissão Vertical de Doenças Infecciosas , Gravidez , Complicações Infecciosas na Gravidez/prevenção & controle , Zidovudina/uso terapêutico
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