Cargando…
Thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome
BACKGROUND: Hemolytic and uremic syndrome (HUS) diagnosis involves association of non immune hemolytic anemia, thrombocytopenia, and renal failure. HUS without thrombocytopenia has been observed, we call it partial HUS. Its real frequency and outcome are unknown. The aim of this study was to determi...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554580/ https://www.ncbi.nlm.nih.gov/pubmed/23298275 http://dx.doi.org/10.1186/1471-2369-14-3 |
_version_ | 1782256924141551616 |
---|---|
author | Sallée, Marion Ismail, Khalil Fakhouri, Fadi Vacher-Coponat, Henri Moussi-Francés, Julie Frémaux-Bacchi, Véronique Burtey, Stéphane |
author_facet | Sallée, Marion Ismail, Khalil Fakhouri, Fadi Vacher-Coponat, Henri Moussi-Francés, Julie Frémaux-Bacchi, Véronique Burtey, Stéphane |
author_sort | Sallée, Marion |
collection | PubMed |
description | BACKGROUND: Hemolytic and uremic syndrome (HUS) diagnosis involves association of non immune hemolytic anemia, thrombocytopenia, and renal failure. HUS without thrombocytopenia has been observed, we call it partial HUS. Its real frequency and outcome are unknown. The aim of this study was to determine the prevalence of patients with normal platelets count in two HUS cohorts and to compare their outcome to patients with thrombocytopenia. METHODS: We retrospectively identified HUS diagnosis in two different cohorts. The first cohort was from a single center and consisted of all cases of HUS whatever the aetiology, the second was multicentric and consisted of atypical HUS patients. These cohorts were divided into two groups depending on the presence or absence of thrombocytopenia. Clinical and biological data were compared between thrombopenic and non thrombopenic group. RESULTS: We identified 13% (20/150) of patients with normal platelets count: 10 episodes (18%) of HUS in six patients (14%) in the monocentric cohort and 14 patients (13%) with 17 episodes (12%) in the multicentric cohort of atypical HUS. Groups differed in platelets count and LDH level. In both cohorts, renal outcome was similar to patient presenting with thrombocytopenia. CONCLUSION: HUS with normal platelets count is not infrequent. Relative to classical clinical presentation of HUS, partial HUS has similar characteristics and identical poor renal outcome and so must be treated in the same way. |
format | Online Article Text |
id | pubmed-3554580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35545802013-01-29 Thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome Sallée, Marion Ismail, Khalil Fakhouri, Fadi Vacher-Coponat, Henri Moussi-Francés, Julie Frémaux-Bacchi, Véronique Burtey, Stéphane BMC Nephrol Research Article BACKGROUND: Hemolytic and uremic syndrome (HUS) diagnosis involves association of non immune hemolytic anemia, thrombocytopenia, and renal failure. HUS without thrombocytopenia has been observed, we call it partial HUS. Its real frequency and outcome are unknown. The aim of this study was to determine the prevalence of patients with normal platelets count in two HUS cohorts and to compare their outcome to patients with thrombocytopenia. METHODS: We retrospectively identified HUS diagnosis in two different cohorts. The first cohort was from a single center and consisted of all cases of HUS whatever the aetiology, the second was multicentric and consisted of atypical HUS patients. These cohorts were divided into two groups depending on the presence or absence of thrombocytopenia. Clinical and biological data were compared between thrombopenic and non thrombopenic group. RESULTS: We identified 13% (20/150) of patients with normal platelets count: 10 episodes (18%) of HUS in six patients (14%) in the monocentric cohort and 14 patients (13%) with 17 episodes (12%) in the multicentric cohort of atypical HUS. Groups differed in platelets count and LDH level. In both cohorts, renal outcome was similar to patient presenting with thrombocytopenia. CONCLUSION: HUS with normal platelets count is not infrequent. Relative to classical clinical presentation of HUS, partial HUS has similar characteristics and identical poor renal outcome and so must be treated in the same way. BioMed Central 2013-01-08 /pmc/articles/PMC3554580/ /pubmed/23298275 http://dx.doi.org/10.1186/1471-2369-14-3 Text en Copyright ©2013 Sallée et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sallée, Marion Ismail, Khalil Fakhouri, Fadi Vacher-Coponat, Henri Moussi-Francés, Julie Frémaux-Bacchi, Véronique Burtey, Stéphane Thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome |
title | Thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome |
title_full | Thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome |
title_fullStr | Thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome |
title_full_unstemmed | Thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome |
title_short | Thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome |
title_sort | thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554580/ https://www.ncbi.nlm.nih.gov/pubmed/23298275 http://dx.doi.org/10.1186/1471-2369-14-3 |
work_keys_str_mv | AT salleemarion thrombocytopeniaisnotmandatorytodiagnosehaemolyticanduremicsyndrome AT ismailkhalil thrombocytopeniaisnotmandatorytodiagnosehaemolyticanduremicsyndrome AT fakhourifadi thrombocytopeniaisnotmandatorytodiagnosehaemolyticanduremicsyndrome AT vachercoponathenri thrombocytopeniaisnotmandatorytodiagnosehaemolyticanduremicsyndrome AT moussifrancesjulie thrombocytopeniaisnotmandatorytodiagnosehaemolyticanduremicsyndrome AT fremauxbacchiveronique thrombocytopeniaisnotmandatorytodiagnosehaemolyticanduremicsyndrome AT burteystephane thrombocytopeniaisnotmandatorytodiagnosehaemolyticanduremicsyndrome |