Citation
Gerber, Angela, et al. "Clinical Course and the Role of Shiga Toxin-producing Escherichia Coli Infection in the Hemolytic-uremic Syndrome in Pediatric Patients, 1997-2000, in Germany and Austria: a Prospective Study." The Journal of Infectious Diseases, vol. 186, no. 4, 2002, pp. 493-500.
Gerber A, Karch H, Allerberger F, et al. Clinical course and the role of shiga toxin-producing Escherichia coli infection in the hemolytic-uremic syndrome in pediatric patients, 1997-2000, in Germany and Austria: a prospective study. J Infect Dis. 2002;186(4):493-500.
Gerber, A., Karch, H., Allerberger, F., Verweyen, H. M., & Zimmerhackl, L. B. (2002). Clinical course and the role of shiga toxin-producing Escherichia coli infection in the hemolytic-uremic syndrome in pediatric patients, 1997-2000, in Germany and Austria: a prospective study. The Journal of Infectious Diseases, 186(4), 493-500.
Gerber A, et al. Clinical Course and the Role of Shiga Toxin-producing Escherichia Coli Infection in the Hemolytic-uremic Syndrome in Pediatric Patients, 1997-2000, in Germany and Austria: a Prospective Study. J Infect Dis. 2002 Aug 15;186(4):493-500. PubMed PMID: 12195376.
TY - JOUR
T1 - Clinical course and the role of shiga toxin-producing Escherichia coli infection in the hemolytic-uremic syndrome in pediatric patients, 1997-2000, in Germany and Austria: a prospective study.
AU - Gerber,Angela,
AU - Karch,Helge,
AU - Allerberger,Franz,
AU - Verweyen,Hege M,
AU - Zimmerhackl,Lothar B,
Y1 - 2002/08/02/
PY - 2002/02/04/received
PY - 2002/04/12/revised
PY - 2002/8/27/pubmed
PY - 2002/9/18/medline
PY - 2002/8/27/entrez
SP - 493
EP - 500
JF - The Journal of infectious diseases
JO - J Infect Dis
VL - 186
IS - 4
N2 - Hemolytic-uremic syndrome (HUS) is mainly associated with foodborne infections by Shiga toxin-producing Escherichia coli (STEC). From January 1997 through December 2000, 394 children with HUS were evaluated in a prospective multicenter surveillance study in Germany and Austria (incidences, 0.7/100,000 and 0.4/100,000 children <15 years old, respectively). Blood leukocytosis was associated with increased detection of STEC in stool cultures (P<.01) and a more severe disease course. Risk of death was associated with cerebral involvement (P<.01). Most strikingly, non-O157:H7 STEC were detected in 43% of stool cultures of patients with HUS: O26 was detected in 15%, sorbitol-fermenting O157:H(-) in 10%, O145 in 9%, O103 in 3%, and O111 in 43%. Patients with O157:H7 serotypes required dialysis for a longer time and had bloody diarrhea detected more frequently, compared with patients with non-O157:H7 serotypes (P<.05). This large study in children with HUS underlines the rising importance of non-O157:H7 serotypes, and, despite increased public awareness, the number of patients remained unchanged.
SN - 0022-1899
UR - https://www.unboundmedicine.com/medline/citation/12195376/Clinical_course_and_the_role_of_shiga_toxin_producing_Escherichia_coli_infection_in_the_hemolytic_uremic_syndrome_in_pediatric_patients_1997_2000_in_Germany_and_Austria:_a_prospective_study_
DB - PRIME
DP - Unbound Medicine
ER -