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Pediatrics
June 1996
Department of Pediatrics, National Taiwan University Hospital, Taipei.
Objective: To investigate the effects of 3-week versus 4-week administration of benzathine penicillin G (BPG) on the incidence of Group A streptococcal infections and the recurrences of rheumatic fever (RF).
Study Design: We started, in 1979, randomly allocating all patients with RF to a 3-week or 4-week BPG prophylaxis program. They were examined at the RF clinic, every 3 to 6 months, and at any time they did not feel well.
Am J Med Sci
April 1995
Department of Pediatrics, Louisiana State University Medical Center, New Orleans 70112-2822.
This article reports the case of a boy aged 2 years 6 months, who had fever, arthritis, and necrotizing cutaneous vasculitis. Evaluation revealed no evidence of direct infectious causes. However, high anti-streptolysin and streptozyme titers during the acute phase support the possibility that streptococcal infection played an important role in the pathogenesis of this disease.
View Article and Find Full Text PDFArch Inst Cardiol Mex
September 1995
Departamento de Inmunologia, Instituto Nacional de Cardiología Ignacio Chávez, México, D.F.
Streptococcal throat infection is a sine qua non for the development of rheumatic fever (RF) in genetically susceptible people. Demonstration of such infection is not easy. In overt RF less than 10% of patients still carry streptococci in their throat and immunologic methods are required to identify antibodies against streptococcal products (SP).
View Article and Find Full Text PDFPediatr Infect Dis J
October 1991
Department of Pediatrics, University of Florida, Gainesville 32610.
Pediatr Infect Dis J
February 1991
Department of Microbiology and Pathology, Faculty of Medicine, Jordan University of Science and Technology, Irbid.
Three hundred six children with probable Group A beta-hemolytic streptococcal pharyngitis were enrolled in a randomized double blind trial to compare the effects of immediate vs. delayed treatment with oral penicillin V. Among the 229 culture-positive patients, 111 were randomly assigned to receive penicillin V immediately and 118 to receive a placebo for 48 to 52 hours followed by penicillin V.
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