SciELO - Scientific Electronic Library Online

 
vol.114 issue6Humoral immunity to tetanus, measles and rubella in children with acute lymphoblastic leukemia after chemotherapyA new challenge for the world: the eradication of polio author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

  • Have no cited articlesCited by SciELO

Related links

  • Have no similar articlesSimilars in SciELO

Share


Archivos argentinos de pediatría

Print version ISSN 0325-0075On-line version ISSN 1668-3501

Abstract

EYMANN, Alfredo et al. Prevalence and clinical course of typical hemolytic uremic syndrome among siblings. Arch. argent. pediatr. [online]. 2016, vol.114, n.6, pp.553-556. ISSN 0325-0075.  http://dx.doi.org/10.5546/aap.2016.553.

Introduction. Hemolytic uremic syndrome (HUS) isaninfectious disease caused by Shiga toxin-producing Escherichia coli. The objective of this study was to assess the risk of transmission and clinical course between siblings with typical HUS. Population and methods. Medical records of children with typical HUS between 1997 and 2012 were reviewed. Sibling pairs were established as inclusion criteria. A severity score was defined. Results. A total of 133 patients with HUS were recorded; 40 had siblings and 4 progressed to HUS (10%). The mean age of the 4 sibling pairs was 29.3 months old (SD ± 11.5); 5 (62.5%) were girls. The mean time between each case was 5.7 days (SD ± 3). HUS was more severe in the siblings who became infected in the second place. Conclusion. The risk of HUS transmission between siblings was 10%, and the clinical course of the second sibling was less favorable.

Keywords : Hemolytic uremic syndrome; Siblings; Escherichia coli; Risk; Argentina.

        · abstract in Spanish     · text in English | Spanish     · English ( pdf ) | Spanish ( pdf )

 

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License