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The association between drospirenone and hyperkalemia: a comparative-safety study

BACKGROUND: Drospirenone/ethinyl-estradiol is an oral contraceptive (OC) that possesses unique antimineralocorticoid activity. It is conjectured that drospirenone, taken alone or concomitantly with spironolactone, may be associated with an increased risk of hyperkalemia. METHODS: A retrospective coh...

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Autores principales: Bird, Steven T, Pepe, Salvatore R, Etminan, Mahyar, Liu, Xinyue, Brophy, James M, Delaney, Joseph AC
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265420/
https://www.ncbi.nlm.nih.gov/pubmed/22208934
http://dx.doi.org/10.1186/1472-6904-11-23
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author Bird, Steven T
Pepe, Salvatore R
Etminan, Mahyar
Liu, Xinyue
Brophy, James M
Delaney, Joseph AC
author_facet Bird, Steven T
Pepe, Salvatore R
Etminan, Mahyar
Liu, Xinyue
Brophy, James M
Delaney, Joseph AC
author_sort Bird, Steven T
collection PubMed
description BACKGROUND: Drospirenone/ethinyl-estradiol is an oral contraceptive (OC) that possesses unique antimineralocorticoid activity. It is conjectured that drospirenone, taken alone or concomitantly with spironolactone, may be associated with an increased risk of hyperkalemia. METHODS: A retrospective cohort study was conducted evaluating women between 18-46 years of age in the Lifelink™ Health Plan Claims Database. The study was restricted to new users of OCs between 1997-2009. Cox proportional hazards models were used to estimate the time to first occurrence of hyperkalemia diagnosis. The main analysis compared OCs containing drospirenone with OCs containing levonorgestrel, a second generation OC not known to impact potassium homeostasis. Logistic regression evaluated concomitant prescribing of drospirenone and spironolactone RESULTS: The cohort included 1,148,183 women, averaging 28.8 years of age and 280 days of OC therapy. 2325 cases of hyperkalemia were identified. The adjusted hazard ratio (HR) for hyperkalemia with drospirenone compared to levonorgestrel was 1.10 (95%CI 0.95-1.26). There was an increased risk of hyperkalemia with norethindrone HR 1.15 (95%CI: 1.00-1.33) and norgestimate HR 1.27 (95%CI: 1.11-1.46). Other OCs were unassociated with hyperkalemia. The odds of receiving spironolactone while taking drospirenone were 2.66 (95%CI 2.53-2.80) times higher than the odds of receiving spironolactone and levonorgestrel. Only 6.5% of patients taking drospirenone and spironolactone had a serum potassium assay within 180 days of starting concomitant therapy. CONCLUSIONS: A clinically significant signal for hyperkalemia with drospirenone was not demonstrated in the current study. Despite the bolded warning for hyperkalemia with joint drospirenone and spironolactone administration, physicians are actually using them together preferentially, and are not following the recommended potassium monitoring requirements in the package insert.
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spelling pubmed-32654202012-01-25 The association between drospirenone and hyperkalemia: a comparative-safety study Bird, Steven T Pepe, Salvatore R Etminan, Mahyar Liu, Xinyue Brophy, James M Delaney, Joseph AC BMC Clin Pharmacol Research Article BACKGROUND: Drospirenone/ethinyl-estradiol is an oral contraceptive (OC) that possesses unique antimineralocorticoid activity. It is conjectured that drospirenone, taken alone or concomitantly with spironolactone, may be associated with an increased risk of hyperkalemia. METHODS: A retrospective cohort study was conducted evaluating women between 18-46 years of age in the Lifelink™ Health Plan Claims Database. The study was restricted to new users of OCs between 1997-2009. Cox proportional hazards models were used to estimate the time to first occurrence of hyperkalemia diagnosis. The main analysis compared OCs containing drospirenone with OCs containing levonorgestrel, a second generation OC not known to impact potassium homeostasis. Logistic regression evaluated concomitant prescribing of drospirenone and spironolactone RESULTS: The cohort included 1,148,183 women, averaging 28.8 years of age and 280 days of OC therapy. 2325 cases of hyperkalemia were identified. The adjusted hazard ratio (HR) for hyperkalemia with drospirenone compared to levonorgestrel was 1.10 (95%CI 0.95-1.26). There was an increased risk of hyperkalemia with norethindrone HR 1.15 (95%CI: 1.00-1.33) and norgestimate HR 1.27 (95%CI: 1.11-1.46). Other OCs were unassociated with hyperkalemia. The odds of receiving spironolactone while taking drospirenone were 2.66 (95%CI 2.53-2.80) times higher than the odds of receiving spironolactone and levonorgestrel. Only 6.5% of patients taking drospirenone and spironolactone had a serum potassium assay within 180 days of starting concomitant therapy. CONCLUSIONS: A clinically significant signal for hyperkalemia with drospirenone was not demonstrated in the current study. Despite the bolded warning for hyperkalemia with joint drospirenone and spironolactone administration, physicians are actually using them together preferentially, and are not following the recommended potassium monitoring requirements in the package insert. BioMed Central 2011-12-30 /pmc/articles/PMC3265420/ /pubmed/22208934 http://dx.doi.org/10.1186/1472-6904-11-23 Text en Copyright ©2011 Bird 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
Bird, Steven T
Pepe, Salvatore R
Etminan, Mahyar
Liu, Xinyue
Brophy, James M
Delaney, Joseph AC
The association between drospirenone and hyperkalemia: a comparative-safety study
title The association between drospirenone and hyperkalemia: a comparative-safety study
title_full The association between drospirenone and hyperkalemia: a comparative-safety study
title_fullStr The association between drospirenone and hyperkalemia: a comparative-safety study
title_full_unstemmed The association between drospirenone and hyperkalemia: a comparative-safety study
title_short The association between drospirenone and hyperkalemia: a comparative-safety study
title_sort association between drospirenone and hyperkalemia: a comparative-safety study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265420/
https://www.ncbi.nlm.nih.gov/pubmed/22208934
http://dx.doi.org/10.1186/1472-6904-11-23
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