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Transfer of rosuvastatin into breast milk: liquid chromatography–mass spectrometry methodology and clinical recommendations

INTRODUCTION: Rosuvastatin reduces concentrations of total cholesterol (TC) and is used for the management of hypercholesterolemia and prevention of acute coronary syndromes. There are no published reports estimating infant exposure to rosuvastatin through breast milk. PURPOSE: The aims of this stud...

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Autores principales: Lwin, Ei Mon Phyo, Leggett, Catherine, Ritchie, Usha, Gerber, Cobus, Song, Yunmei, Hague, William, Turner, Sean, Upton, Richard, Garg, Sanjay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6211583/
https://www.ncbi.nlm.nih.gov/pubmed/30464396
http://dx.doi.org/10.2147/DDDT.S184053
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author Lwin, Ei Mon Phyo
Leggett, Catherine
Ritchie, Usha
Gerber, Cobus
Song, Yunmei
Hague, William
Turner, Sean
Upton, Richard
Garg, Sanjay
author_facet Lwin, Ei Mon Phyo
Leggett, Catherine
Ritchie, Usha
Gerber, Cobus
Song, Yunmei
Hague, William
Turner, Sean
Upton, Richard
Garg, Sanjay
author_sort Lwin, Ei Mon Phyo
collection PubMed
description INTRODUCTION: Rosuvastatin reduces concentrations of total cholesterol (TC) and is used for the management of hypercholesterolemia and prevention of acute coronary syndromes. There are no published reports estimating infant exposure to rosuvastatin through breast milk. PURPOSE: The aims of this study were to quantify concentrations of rosuvastatin in human milk and plasma from a lactating woman taking rosuvastatin and to investigate potential infant exposure. MATERIALS AND METHODS: A 38-year-old breastfeeding mother was commenced on rosuvastatin 20 mg daily for secondary prevention of an acute coronary syndrome. Eight maternal breast milk samples and a single plasma sample were collected over a 24-hour period. The samples were quantified using a sensitive liquid chromatography–mass spectrometry (LC-MS/MS) method. RESULTS: The average concentration of rosuvastatin in breast milk was 30.84 ng/mL, and a peak concentration of 58.59 ng/mL occurred at 17 hours after oral administration. Although the milk-to-plasma (M/P) ratio was 16.49 at 14 hours, the theoretical infant dosage (TID) and relative infant dose (RID) were 0.005 mg/kg/day and 1.50%, respectively. CONCLUSION: The findings suggest that only small amounts of rosuvastatin pass into breast milk. Should the maternal condition necessitate treatment, consideration could be given to the use of rosuvastatin during breastfeeding provided the infant is monitored.
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spelling pubmed-62115832018-11-21 Transfer of rosuvastatin into breast milk: liquid chromatography–mass spectrometry methodology and clinical recommendations Lwin, Ei Mon Phyo Leggett, Catherine Ritchie, Usha Gerber, Cobus Song, Yunmei Hague, William Turner, Sean Upton, Richard Garg, Sanjay Drug Des Devel Ther Original Research INTRODUCTION: Rosuvastatin reduces concentrations of total cholesterol (TC) and is used for the management of hypercholesterolemia and prevention of acute coronary syndromes. There are no published reports estimating infant exposure to rosuvastatin through breast milk. PURPOSE: The aims of this study were to quantify concentrations of rosuvastatin in human milk and plasma from a lactating woman taking rosuvastatin and to investigate potential infant exposure. MATERIALS AND METHODS: A 38-year-old breastfeeding mother was commenced on rosuvastatin 20 mg daily for secondary prevention of an acute coronary syndrome. Eight maternal breast milk samples and a single plasma sample were collected over a 24-hour period. The samples were quantified using a sensitive liquid chromatography–mass spectrometry (LC-MS/MS) method. RESULTS: The average concentration of rosuvastatin in breast milk was 30.84 ng/mL, and a peak concentration of 58.59 ng/mL occurred at 17 hours after oral administration. Although the milk-to-plasma (M/P) ratio was 16.49 at 14 hours, the theoretical infant dosage (TID) and relative infant dose (RID) were 0.005 mg/kg/day and 1.50%, respectively. CONCLUSION: The findings suggest that only small amounts of rosuvastatin pass into breast milk. Should the maternal condition necessitate treatment, consideration could be given to the use of rosuvastatin during breastfeeding provided the infant is monitored. Dove Medical Press 2018-10-29 /pmc/articles/PMC6211583/ /pubmed/30464396 http://dx.doi.org/10.2147/DDDT.S184053 Text en © 2018 Lwin et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Lwin, Ei Mon Phyo
Leggett, Catherine
Ritchie, Usha
Gerber, Cobus
Song, Yunmei
Hague, William
Turner, Sean
Upton, Richard
Garg, Sanjay
Transfer of rosuvastatin into breast milk: liquid chromatography–mass spectrometry methodology and clinical recommendations
title Transfer of rosuvastatin into breast milk: liquid chromatography–mass spectrometry methodology and clinical recommendations
title_full Transfer of rosuvastatin into breast milk: liquid chromatography–mass spectrometry methodology and clinical recommendations
title_fullStr Transfer of rosuvastatin into breast milk: liquid chromatography–mass spectrometry methodology and clinical recommendations
title_full_unstemmed Transfer of rosuvastatin into breast milk: liquid chromatography–mass spectrometry methodology and clinical recommendations
title_short Transfer of rosuvastatin into breast milk: liquid chromatography–mass spectrometry methodology and clinical recommendations
title_sort transfer of rosuvastatin into breast milk: liquid chromatography–mass spectrometry methodology and clinical recommendations
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6211583/
https://www.ncbi.nlm.nih.gov/pubmed/30464396
http://dx.doi.org/10.2147/DDDT.S184053
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