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Primary Aldosteronism Screening Rates Differ with Sex, Race, and Comorbidities
BACKGROUND: Primary aldosteronism (PA) is a common but under‐recognized cause of secondary hypertension. Data directly comparing screening rates across single and overlapping indications are lacking. METHODS AND RESULTS: We conducted a retrospective review of adults with hypertension seen in outpati...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9707846/ https://www.ncbi.nlm.nih.gov/pubmed/35861830 http://dx.doi.org/10.1161/JAHA.122.025952 |
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author | Turcu, Adina F. Nhan, Winnie Grigoryan, Seda Zhang, Lei Urban, Caitlin Liu, Haiping Holevinski, Lynn Zhao, Lili |
author_facet | Turcu, Adina F. Nhan, Winnie Grigoryan, Seda Zhang, Lei Urban, Caitlin Liu, Haiping Holevinski, Lynn Zhao, Lili |
author_sort | Turcu, Adina F. |
collection | PubMed |
description | BACKGROUND: Primary aldosteronism (PA) is a common but under‐recognized cause of secondary hypertension. Data directly comparing screening rates across single and overlapping indications are lacking. METHODS AND RESULTS: We conducted a retrospective review of adults with hypertension seen in outpatient clinics at a tertiary referral academic center between January 1, 2017, and June 30, 2020. We included patients with hypertension plus at least one of the following: resistant hypertension; age<35 years; obstructive sleep apnea; hypokalemia; or an adrenal mass. We excluded patients with adrenal insufficiency, severe renal disease, or heart failure, and renovascular hypertension. Of 203 535 patients with hypertension, 86044 (42.3%) met at least 1 PA screening criterion, and of these, 2898 (3.4%) were screened for PA. Screening occurred in 2.7% of patients with resistant hypertension; 4.2% of those with obstructive sleep apnea; 5.1% of those <35 years; 10.0% of those with hypokalemia; and 47.3% of patients with an adrenal mass. Screening rates were higher in patients with multiple risk factors: 16.8% for ≥3, 5.7% for 2, and 2.5% for 1 criterion. Multiple logistic regression showed that the odds of PA screening were higher in patients with hypokalemia: odds ratio (95% CI): 3.0 (2.7–3.3); women: 1.3 (1.2–1.4); Black versus White: 1.5 (1.4–1.7); those with obstructive sleep apnea, chronic renal disease, stroke, and dyslipidemia. CONCLUSIONS: Consideration for PA is given in a small subset of at‐risk patients, and typically after comorbidities have developed. |
format | Online Article Text |
id | pubmed-9707846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97078462022-11-30 Primary Aldosteronism Screening Rates Differ with Sex, Race, and Comorbidities Turcu, Adina F. Nhan, Winnie Grigoryan, Seda Zhang, Lei Urban, Caitlin Liu, Haiping Holevinski, Lynn Zhao, Lili J Am Heart Assoc Original Research BACKGROUND: Primary aldosteronism (PA) is a common but under‐recognized cause of secondary hypertension. Data directly comparing screening rates across single and overlapping indications are lacking. METHODS AND RESULTS: We conducted a retrospective review of adults with hypertension seen in outpatient clinics at a tertiary referral academic center between January 1, 2017, and June 30, 2020. We included patients with hypertension plus at least one of the following: resistant hypertension; age<35 years; obstructive sleep apnea; hypokalemia; or an adrenal mass. We excluded patients with adrenal insufficiency, severe renal disease, or heart failure, and renovascular hypertension. Of 203 535 patients with hypertension, 86044 (42.3%) met at least 1 PA screening criterion, and of these, 2898 (3.4%) were screened for PA. Screening occurred in 2.7% of patients with resistant hypertension; 4.2% of those with obstructive sleep apnea; 5.1% of those <35 years; 10.0% of those with hypokalemia; and 47.3% of patients with an adrenal mass. Screening rates were higher in patients with multiple risk factors: 16.8% for ≥3, 5.7% for 2, and 2.5% for 1 criterion. Multiple logistic regression showed that the odds of PA screening were higher in patients with hypokalemia: odds ratio (95% CI): 3.0 (2.7–3.3); women: 1.3 (1.2–1.4); Black versus White: 1.5 (1.4–1.7); those with obstructive sleep apnea, chronic renal disease, stroke, and dyslipidemia. CONCLUSIONS: Consideration for PA is given in a small subset of at‐risk patients, and typically after comorbidities have developed. John Wiley and Sons Inc. 2022-07-08 /pmc/articles/PMC9707846/ /pubmed/35861830 http://dx.doi.org/10.1161/JAHA.122.025952 Text en © 2022 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Research Turcu, Adina F. Nhan, Winnie Grigoryan, Seda Zhang, Lei Urban, Caitlin Liu, Haiping Holevinski, Lynn Zhao, Lili Primary Aldosteronism Screening Rates Differ with Sex, Race, and Comorbidities |
title | Primary Aldosteronism Screening Rates Differ with Sex, Race, and Comorbidities |
title_full | Primary Aldosteronism Screening Rates Differ with Sex, Race, and Comorbidities |
title_fullStr | Primary Aldosteronism Screening Rates Differ with Sex, Race, and Comorbidities |
title_full_unstemmed | Primary Aldosteronism Screening Rates Differ with Sex, Race, and Comorbidities |
title_short | Primary Aldosteronism Screening Rates Differ with Sex, Race, and Comorbidities |
title_sort | primary aldosteronism screening rates differ with sex, race, and comorbidities |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9707846/ https://www.ncbi.nlm.nih.gov/pubmed/35861830 http://dx.doi.org/10.1161/JAHA.122.025952 |
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