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Evaluating the prevalence of lipid assessments in children in Alberta, Canada

BACKGROUND: Familial hypercholesterolemia is a common, inherited, life-threatening and treatable condition that is characterized by marked elevations of low-density lipoprotein cholesterol (LDL-C), resulting in a high risk of cardiovascular disease, but treatment starting in childhood dramatically r...

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Autores principales: Christian, Susan, Ridsdale, Ross, Lin, Mu, Khoury, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: CMA Impact Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516684/
https://www.ncbi.nlm.nih.gov/pubmed/37726114
http://dx.doi.org/10.9778/cmajo.20220163
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author Christian, Susan
Ridsdale, Ross
Lin, Mu
Khoury, Michael
author_facet Christian, Susan
Ridsdale, Ross
Lin, Mu
Khoury, Michael
author_sort Christian, Susan
collection PubMed
description BACKGROUND: Familial hypercholesterolemia is a common, inherited, life-threatening and treatable condition that is characterized by marked elevations of low-density lipoprotein cholesterol (LDL-C), resulting in a high risk of cardiovascular disease, but treatment starting in childhood dramatically reduces this risk. We sought to evaluate the prevalence of pediatric lipid assessments among children in Alberta. METHODS: We reviewed laboratory and administrative data from Alberta Health between Apr. 1, 2012, and Dec. 31, 2021. We evaluated 2 pediatric cohorts (children aged 2–10 yr and children aged 9–17 yr) to allow for longitudinal assessments throughout the pediatric period. We also reviewed annual frequencies of lipid assessment for all children between 2013 and 2021. RESULTS: Pediatric lipid assessments were performed for 1972 (4.3%) of 46 170 children aged 2–10 years and for 8158 (19.9%) of 40 926 children aged 9–17 years. Female children (aged 2–10 yr) and those living in rural communities were significantly less likely to have a lipid assessment, compared with male children and those in nonrural communities. Among those with lipid assessments, 23 (1.2%) and 86 (1.1%) children aged 2–10 years and 9–17 years, respectively, had an LDL-C level suggestive of probable familial hypercholesterolemia (≥ 4.0 mmol/L). Statin therapy was prescribed in 16 children during the study period. The frequency of lipid assessments was relatively stable, with the exception of a decrease in 2020. INTERPRETATION: Rates of pediatric lipid assessment in Alberta are suboptimal. These findings highlight the need to increase awareness of the benefits of early diagnosis and treatment of familial hypercholesterolemia with regard to long-term health and identify and overcome barriers to diagnosis and treatment.
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spelling pubmed-105166842023-09-23 Evaluating the prevalence of lipid assessments in children in Alberta, Canada Christian, Susan Ridsdale, Ross Lin, Mu Khoury, Michael CMAJ Open Research BACKGROUND: Familial hypercholesterolemia is a common, inherited, life-threatening and treatable condition that is characterized by marked elevations of low-density lipoprotein cholesterol (LDL-C), resulting in a high risk of cardiovascular disease, but treatment starting in childhood dramatically reduces this risk. We sought to evaluate the prevalence of pediatric lipid assessments among children in Alberta. METHODS: We reviewed laboratory and administrative data from Alberta Health between Apr. 1, 2012, and Dec. 31, 2021. We evaluated 2 pediatric cohorts (children aged 2–10 yr and children aged 9–17 yr) to allow for longitudinal assessments throughout the pediatric period. We also reviewed annual frequencies of lipid assessment for all children between 2013 and 2021. RESULTS: Pediatric lipid assessments were performed for 1972 (4.3%) of 46 170 children aged 2–10 years and for 8158 (19.9%) of 40 926 children aged 9–17 years. Female children (aged 2–10 yr) and those living in rural communities were significantly less likely to have a lipid assessment, compared with male children and those in nonrural communities. Among those with lipid assessments, 23 (1.2%) and 86 (1.1%) children aged 2–10 years and 9–17 years, respectively, had an LDL-C level suggestive of probable familial hypercholesterolemia (≥ 4.0 mmol/L). Statin therapy was prescribed in 16 children during the study period. The frequency of lipid assessments was relatively stable, with the exception of a decrease in 2020. INTERPRETATION: Rates of pediatric lipid assessment in Alberta are suboptimal. These findings highlight the need to increase awareness of the benefits of early diagnosis and treatment of familial hypercholesterolemia with regard to long-term health and identify and overcome barriers to diagnosis and treatment. CMA Impact Inc. 2023-09-19 /pmc/articles/PMC10516684/ /pubmed/37726114 http://dx.doi.org/10.9778/cmajo.20220163 Text en © 2023 CMA Impact Inc. or its licensors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY-NC-ND 4.0) licence, which permits use, distribution and reproduction in any medium, provided that the original publication is properly cited, the use is noncommercial (i.e., research or educational use), and no modifications or adaptations are made. See: https://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Research
Christian, Susan
Ridsdale, Ross
Lin, Mu
Khoury, Michael
Evaluating the prevalence of lipid assessments in children in Alberta, Canada
title Evaluating the prevalence of lipid assessments in children in Alberta, Canada
title_full Evaluating the prevalence of lipid assessments in children in Alberta, Canada
title_fullStr Evaluating the prevalence of lipid assessments in children in Alberta, Canada
title_full_unstemmed Evaluating the prevalence of lipid assessments in children in Alberta, Canada
title_short Evaluating the prevalence of lipid assessments in children in Alberta, Canada
title_sort evaluating the prevalence of lipid assessments in children in alberta, canada
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516684/
https://www.ncbi.nlm.nih.gov/pubmed/37726114
http://dx.doi.org/10.9778/cmajo.20220163
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