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The prevalence of hypertension and abnormal kidney function in children with sickle cell disease –a cross sectional review
BACKGROUND: Renal disease is a known contributor to mortality in adults with sickle cell disease (SCD) and renal abnormalities are evident in childhood. Hyperfiltration (evidenced by elevated glomerular filtration rate, GFR) occurs in children with SCD early in disease. However, the incidence of low...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231610/ https://www.ncbi.nlm.nih.gov/pubmed/24168027 http://dx.doi.org/10.1186/1471-2369-14-237 |
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author | Bodas, Prasad Huang, Alex O’Riordan, Mary Ann Sedor, John R Dell, Katherine MacRae |
author_facet | Bodas, Prasad Huang, Alex O’Riordan, Mary Ann Sedor, John R Dell, Katherine MacRae |
author_sort | Bodas, Prasad |
collection | PubMed |
description | BACKGROUND: Renal disease is a known contributor to mortality in adults with sickle cell disease (SCD) and renal abnormalities are evident in childhood. Hyperfiltration (evidenced by elevated glomerular filtration rate, GFR) occurs in children with SCD early in disease. However, the incidence of low GFR (<90 ml/min/1.73 m2) suggestive of chronic kidney disease (CKD), is not well established. The prevalence of hypertension is also not well known. The goal of this study was to determine the prevalence of hypertension and CKD in a cohort of children with SCD. METHODS: We performed a retrospective chart review of patients followed at the Rainbow Babies and Children’s Sickle Cell Disease Clinic who were seen during routine follow up visits. Inclusion criteria were all patients ages 3–18. Exclusion criteria included recent (within 2 weeks) hospitalization and/or episode of acute chest, pain crises, febrile illness or red blood cell transfusion. Data collected included serum creatinine, blood pressure and history of sickle cell complications (acute chest syndrome, stroke or stroke risk). Estimated GFR (eGFR) was calculated using the updated Schwartz creatinine-based estimating formula. Analysis examined the associations among eGFR, blood pressure and sickle cell complications. The Institutional Review Board at University Hospitals Case Medical Center approved this study. RESULTS: A total of 48 children had complete data available. Mean eGFR was 140 mL/min/1.73 m(2) +/- 34.9 (range 71.9-404.2 mL/min/1.73 m(2)). Four patients (8.3%) had eGFRs < 90 mL/min/1.73 m(2), 35 patients (72.9%) had eGFRs > 120 mL/min/1.73 m(2) and 9 patients (18.8%) had eGFRs in the normal range. Eight patients (16.7%) had evidence of elevated blood pressures (pre-hypertension or hypertension). There was no correlation between eGFR and age, and no association of eGFR with acute chest or stroke risk. CONCLUSION: In this SCD cohort, we identified abnormally low eGFR (suggestive of early CKD) in 8.3% of patients and elevated blood pressure in 16.7%. These findings are in contrast to other published studies that show primarily normal or elevated GFR and the absence of or minimal hypertension. These findings indicate that elevated blood pressure and decreased eGFR are not uncommon in children with SCD, and should be more rigorously studied. |
format | Online Article Text |
id | pubmed-4231610 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42316102014-11-18 The prevalence of hypertension and abnormal kidney function in children with sickle cell disease –a cross sectional review Bodas, Prasad Huang, Alex O’Riordan, Mary Ann Sedor, John R Dell, Katherine MacRae BMC Nephrol Research Article BACKGROUND: Renal disease is a known contributor to mortality in adults with sickle cell disease (SCD) and renal abnormalities are evident in childhood. Hyperfiltration (evidenced by elevated glomerular filtration rate, GFR) occurs in children with SCD early in disease. However, the incidence of low GFR (<90 ml/min/1.73 m2) suggestive of chronic kidney disease (CKD), is not well established. The prevalence of hypertension is also not well known. The goal of this study was to determine the prevalence of hypertension and CKD in a cohort of children with SCD. METHODS: We performed a retrospective chart review of patients followed at the Rainbow Babies and Children’s Sickle Cell Disease Clinic who were seen during routine follow up visits. Inclusion criteria were all patients ages 3–18. Exclusion criteria included recent (within 2 weeks) hospitalization and/or episode of acute chest, pain crises, febrile illness or red blood cell transfusion. Data collected included serum creatinine, blood pressure and history of sickle cell complications (acute chest syndrome, stroke or stroke risk). Estimated GFR (eGFR) was calculated using the updated Schwartz creatinine-based estimating formula. Analysis examined the associations among eGFR, blood pressure and sickle cell complications. The Institutional Review Board at University Hospitals Case Medical Center approved this study. RESULTS: A total of 48 children had complete data available. Mean eGFR was 140 mL/min/1.73 m(2) +/- 34.9 (range 71.9-404.2 mL/min/1.73 m(2)). Four patients (8.3%) had eGFRs < 90 mL/min/1.73 m(2), 35 patients (72.9%) had eGFRs > 120 mL/min/1.73 m(2) and 9 patients (18.8%) had eGFRs in the normal range. Eight patients (16.7%) had evidence of elevated blood pressures (pre-hypertension or hypertension). There was no correlation between eGFR and age, and no association of eGFR with acute chest or stroke risk. CONCLUSION: In this SCD cohort, we identified abnormally low eGFR (suggestive of early CKD) in 8.3% of patients and elevated blood pressure in 16.7%. These findings are in contrast to other published studies that show primarily normal or elevated GFR and the absence of or minimal hypertension. These findings indicate that elevated blood pressure and decreased eGFR are not uncommon in children with SCD, and should be more rigorously studied. BioMed Central 2013-10-30 /pmc/articles/PMC4231610/ /pubmed/24168027 http://dx.doi.org/10.1186/1471-2369-14-237 Text en Copyright © 2013 Bodas 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 Bodas, Prasad Huang, Alex O’Riordan, Mary Ann Sedor, John R Dell, Katherine MacRae The prevalence of hypertension and abnormal kidney function in children with sickle cell disease –a cross sectional review |
title | The prevalence of hypertension and abnormal kidney function in children with sickle cell disease –a cross sectional review |
title_full | The prevalence of hypertension and abnormal kidney function in children with sickle cell disease –a cross sectional review |
title_fullStr | The prevalence of hypertension and abnormal kidney function in children with sickle cell disease –a cross sectional review |
title_full_unstemmed | The prevalence of hypertension and abnormal kidney function in children with sickle cell disease –a cross sectional review |
title_short | The prevalence of hypertension and abnormal kidney function in children with sickle cell disease –a cross sectional review |
title_sort | prevalence of hypertension and abnormal kidney function in children with sickle cell disease –a cross sectional review |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231610/ https://www.ncbi.nlm.nih.gov/pubmed/24168027 http://dx.doi.org/10.1186/1471-2369-14-237 |
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