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Asthma is a risk factor for acute chest syndrome and cerebral vascular accidents in children with sickle cell disease

BACKGROUND: Asthma and sickle cell disease are common conditions that both may result in pulmonary complications. We hypothesized that children with sickle cell disease with concomitant asthma have an increased incidence of vaso-occlusive crises that are complicated by episodes of acute chest syndro...

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Autores principales: Nordness, Mark E, Lynn, John, Zacharisen, Michael C, Scott, Paul J, Kelly, Kevin J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC548142/
https://www.ncbi.nlm.nih.gov/pubmed/15663785
http://dx.doi.org/10.1186/1476-7961-3-2
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author Nordness, Mark E
Lynn, John
Zacharisen, Michael C
Scott, Paul J
Kelly, Kevin J
author_facet Nordness, Mark E
Lynn, John
Zacharisen, Michael C
Scott, Paul J
Kelly, Kevin J
author_sort Nordness, Mark E
collection PubMed
description BACKGROUND: Asthma and sickle cell disease are common conditions that both may result in pulmonary complications. We hypothesized that children with sickle cell disease with concomitant asthma have an increased incidence of vaso-occlusive crises that are complicated by episodes of acute chest syndrome. METHODS: A 5-year retrospective chart analysis was performed investigating 48 children ages 3–18 years with asthma and sickle cell disease and 48 children with sickle cell disease alone. Children were matched for age, gender, and type of sickle cell defect. Hospital admissions were recorded for acute chest syndrome, cerebral vascular accident, vaso-occlusive pain crises, and blood transfusions (total, exchange and chronic). Mann-Whitney test and Chi square analysis were used to assess differences between the groups. RESULTS: Children with sickle cell disease and asthma had significantly more episodes of acute chest syndrome (p = 0.03) and cerebral vascular accidents (p = 0.05) compared to children with sickle cell disease without asthma. As expected, these children received more total blood transfusions (p = 0.01) and chronic transfusions (p = 0.04). Admissions for vasoocclusive pain crises and exchange transfusions were not statistically different between cases and controls. SS disease is more severe than SC disease. CONCLUSIONS: Children with concomitant asthma and sickle cell disease have increased episodes of acute chest syndrome, cerebral vascular accidents and the need for blood transfusions. Whether aggressive asthma therapy can reduce these complications in this subset of children is unknown and requires further studies.
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spelling pubmed-5481422005-02-05 Asthma is a risk factor for acute chest syndrome and cerebral vascular accidents in children with sickle cell disease Nordness, Mark E Lynn, John Zacharisen, Michael C Scott, Paul J Kelly, Kevin J Clin Mol Allergy Research BACKGROUND: Asthma and sickle cell disease are common conditions that both may result in pulmonary complications. We hypothesized that children with sickle cell disease with concomitant asthma have an increased incidence of vaso-occlusive crises that are complicated by episodes of acute chest syndrome. METHODS: A 5-year retrospective chart analysis was performed investigating 48 children ages 3–18 years with asthma and sickle cell disease and 48 children with sickle cell disease alone. Children were matched for age, gender, and type of sickle cell defect. Hospital admissions were recorded for acute chest syndrome, cerebral vascular accident, vaso-occlusive pain crises, and blood transfusions (total, exchange and chronic). Mann-Whitney test and Chi square analysis were used to assess differences between the groups. RESULTS: Children with sickle cell disease and asthma had significantly more episodes of acute chest syndrome (p = 0.03) and cerebral vascular accidents (p = 0.05) compared to children with sickle cell disease without asthma. As expected, these children received more total blood transfusions (p = 0.01) and chronic transfusions (p = 0.04). Admissions for vasoocclusive pain crises and exchange transfusions were not statistically different between cases and controls. SS disease is more severe than SC disease. CONCLUSIONS: Children with concomitant asthma and sickle cell disease have increased episodes of acute chest syndrome, cerebral vascular accidents and the need for blood transfusions. Whether aggressive asthma therapy can reduce these complications in this subset of children is unknown and requires further studies. BioMed Central 2005-01-21 /pmc/articles/PMC548142/ /pubmed/15663785 http://dx.doi.org/10.1186/1476-7961-3-2 Text en Copyright © 2005 Nordness 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
Nordness, Mark E
Lynn, John
Zacharisen, Michael C
Scott, Paul J
Kelly, Kevin J
Asthma is a risk factor for acute chest syndrome and cerebral vascular accidents in children with sickle cell disease
title Asthma is a risk factor for acute chest syndrome and cerebral vascular accidents in children with sickle cell disease
title_full Asthma is a risk factor for acute chest syndrome and cerebral vascular accidents in children with sickle cell disease
title_fullStr Asthma is a risk factor for acute chest syndrome and cerebral vascular accidents in children with sickle cell disease
title_full_unstemmed Asthma is a risk factor for acute chest syndrome and cerebral vascular accidents in children with sickle cell disease
title_short Asthma is a risk factor for acute chest syndrome and cerebral vascular accidents in children with sickle cell disease
title_sort asthma is a risk factor for acute chest syndrome and cerebral vascular accidents in children with sickle cell disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC548142/
https://www.ncbi.nlm.nih.gov/pubmed/15663785
http://dx.doi.org/10.1186/1476-7961-3-2
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