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Childhood Hemolytic Uremic Syndrome, United Kingdom and Ireland
We conducted prospective surveillance of childhood hemolytic uremic syndrome (HUS) from 1997 to 2001 to describe disease incidence and clinical, epidemiologic and microbiologic characteristics. We compared our findings, where possible, with those of a previous study conducted from 1985 to 1988. The...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Centers for Disease Control and Prevention
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3320351/ https://www.ncbi.nlm.nih.gov/pubmed/15829199 http://dx.doi.org/10.3201/eid1104.040833 |
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author | Lynn, Richard M. O'Brien, Sarah J. Taylor, C. Mark Adak, Goutam K. Chart, Henrik Cheasty, Tom Coia, John E. Gillespie, Iain A. Locking, Mary E. Reilly, William J. Smith, Henry R. Waters, Aoife Willshaw, Geraldine A. |
author_facet | Lynn, Richard M. O'Brien, Sarah J. Taylor, C. Mark Adak, Goutam K. Chart, Henrik Cheasty, Tom Coia, John E. Gillespie, Iain A. Locking, Mary E. Reilly, William J. Smith, Henry R. Waters, Aoife Willshaw, Geraldine A. |
author_sort | Lynn, Richard M. |
collection | PubMed |
description | We conducted prospective surveillance of childhood hemolytic uremic syndrome (HUS) from 1997 to 2001 to describe disease incidence and clinical, epidemiologic and microbiologic characteristics. We compared our findings, where possible, with those of a previous study conducted from 1985 to 1988. The average annual incidence of HUS for the United Kingdom and Ireland (0.71/100,000) was unchanged from 1985 to 1988. The overall early mortality had halved, but the reduction in mortality was almost entirely accounted for by improved outcome in patients with diarrhea-associated HUS. The principal infective cause of diarrhea-associated HUS was Shiga toxin–producing Escherichia coli O157 (STEC O157), although in the 1997–2001 survey STEC O157 phage type (PT) 21/28 had replaced STEC O157 PT2 as the predominant PT. The risk of developing diarrhea-associated HUS was significantly higher in children infected with STEC O157 PT 2 and PT 21/28 compared with other PTs. Hypertension as a complication of HUS was greatly reduced in patients with diarrhea-associated HUS. |
format | Online Article Text |
id | pubmed-3320351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Centers for Disease Control and Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-33203512012-04-20 Childhood Hemolytic Uremic Syndrome, United Kingdom and Ireland Lynn, Richard M. O'Brien, Sarah J. Taylor, C. Mark Adak, Goutam K. Chart, Henrik Cheasty, Tom Coia, John E. Gillespie, Iain A. Locking, Mary E. Reilly, William J. Smith, Henry R. Waters, Aoife Willshaw, Geraldine A. Emerg Infect Dis Research We conducted prospective surveillance of childhood hemolytic uremic syndrome (HUS) from 1997 to 2001 to describe disease incidence and clinical, epidemiologic and microbiologic characteristics. We compared our findings, where possible, with those of a previous study conducted from 1985 to 1988. The average annual incidence of HUS for the United Kingdom and Ireland (0.71/100,000) was unchanged from 1985 to 1988. The overall early mortality had halved, but the reduction in mortality was almost entirely accounted for by improved outcome in patients with diarrhea-associated HUS. The principal infective cause of diarrhea-associated HUS was Shiga toxin–producing Escherichia coli O157 (STEC O157), although in the 1997–2001 survey STEC O157 phage type (PT) 21/28 had replaced STEC O157 PT2 as the predominant PT. The risk of developing diarrhea-associated HUS was significantly higher in children infected with STEC O157 PT 2 and PT 21/28 compared with other PTs. Hypertension as a complication of HUS was greatly reduced in patients with diarrhea-associated HUS. Centers for Disease Control and Prevention 2005-04 /pmc/articles/PMC3320351/ /pubmed/15829199 http://dx.doi.org/10.3201/eid1104.040833 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited. |
spellingShingle | Research Lynn, Richard M. O'Brien, Sarah J. Taylor, C. Mark Adak, Goutam K. Chart, Henrik Cheasty, Tom Coia, John E. Gillespie, Iain A. Locking, Mary E. Reilly, William J. Smith, Henry R. Waters, Aoife Willshaw, Geraldine A. Childhood Hemolytic Uremic Syndrome, United Kingdom and Ireland |
title | Childhood Hemolytic Uremic Syndrome, United Kingdom and Ireland |
title_full | Childhood Hemolytic Uremic Syndrome, United Kingdom and Ireland |
title_fullStr | Childhood Hemolytic Uremic Syndrome, United Kingdom and Ireland |
title_full_unstemmed | Childhood Hemolytic Uremic Syndrome, United Kingdom and Ireland |
title_short | Childhood Hemolytic Uremic Syndrome, United Kingdom and Ireland |
title_sort | childhood hemolytic uremic syndrome, united kingdom and ireland |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3320351/ https://www.ncbi.nlm.nih.gov/pubmed/15829199 http://dx.doi.org/10.3201/eid1104.040833 |
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