The Direct Factor Xa Inhibitor Rivaroxaban Passes Into Human Breast Milk

Standard

The Direct Factor Xa Inhibitor Rivaroxaban Passes Into Human Breast Milk. / Wiesen, Martin H J; Blaich, Cornelia; Müller, Carsten; Streichert, Thomas; Pfister, Roman; Michels, Guido.

in: CHEST, Jahrgang 150, Nr. 1, 07.2016, S. e1-4.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Wiesen, MHJ, Blaich, C, Müller, C, Streichert, T, Pfister, R & Michels, G 2016, 'The Direct Factor Xa Inhibitor Rivaroxaban Passes Into Human Breast Milk', CHEST, Jg. 150, Nr. 1, S. e1-4. https://doi.org/10.1016/j.chest.2016.01.021

APA

Wiesen, M. H. J., Blaich, C., Müller, C., Streichert, T., Pfister, R., & Michels, G. (2016). The Direct Factor Xa Inhibitor Rivaroxaban Passes Into Human Breast Milk. CHEST, 150(1), e1-4. https://doi.org/10.1016/j.chest.2016.01.021

Vancouver

Wiesen MHJ, Blaich C, Müller C, Streichert T, Pfister R, Michels G. The Direct Factor Xa Inhibitor Rivaroxaban Passes Into Human Breast Milk. CHEST. 2016 Jul;150(1):e1-4. https://doi.org/10.1016/j.chest.2016.01.021

Bibtex

@article{34b8a9fd582641b4ab2d8eb11b13b363,
title = "The Direct Factor Xa Inhibitor Rivaroxaban Passes Into Human Breast Milk",
abstract = "Thromboembolic disorders frequently require antithrombotic treatment during pregnancy and lactation. Vitamin K antagonists and heparins are the treatment options of choice in breastfeeding women. Factors including the route of administration, discomfort during treatment, and fetal and neonatal safety affect women's choices about anticoagulant therapy. Direct-acting oral anticoagulants (DOACs) have emerged as alternatives to these agents and may offer advantages compared with vitamin K antagonists. As breastfeeding women were excluded from clinical trials evaluating DOACs, no safety and efficacy data are available for these special patients and, crucially, estimates for infant exposure are lacking. Therefore, the manufacturer recommends against using DOACs during the lactation period. We present the case of a patient who stopped breastfeeding owing to a diagnosis of postpartum cardiomyopathy. Anticoagulation with enoxaparin that commenced after the diagnosis of postpartum pulmonary embolism was switched to rivaroxaban. At that time, breast milk samples were collected and rivaroxaban concentrations were determined by liquid chromatography tandem-mass spectrometry. Rivaroxaban appears in human breast milk in comparatively small amounts; its safety has not been determined.",
keywords = "Journal Article",
author = "Wiesen, {Martin H J} and Cornelia Blaich and Carsten M{\"u}ller and Thomas Streichert and Roman Pfister and Guido Michels",
note = "Copyright {\textcopyright} 2016 American College of Chest Physicians. Published by Elsevier Inc. All rights reserved.",
year = "2016",
month = jul,
doi = "10.1016/j.chest.2016.01.021",
language = "English",
volume = "150",
pages = "e1--4",
journal = "CHEST",
issn = "0012-3692",
publisher = "American College of Chest Physicians",
number = "1",

}

RIS

TY - JOUR

T1 - The Direct Factor Xa Inhibitor Rivaroxaban Passes Into Human Breast Milk

AU - Wiesen, Martin H J

AU - Blaich, Cornelia

AU - Müller, Carsten

AU - Streichert, Thomas

AU - Pfister, Roman

AU - Michels, Guido

N1 - Copyright © 2016 American College of Chest Physicians. Published by Elsevier Inc. All rights reserved.

PY - 2016/7

Y1 - 2016/7

N2 - Thromboembolic disorders frequently require antithrombotic treatment during pregnancy and lactation. Vitamin K antagonists and heparins are the treatment options of choice in breastfeeding women. Factors including the route of administration, discomfort during treatment, and fetal and neonatal safety affect women's choices about anticoagulant therapy. Direct-acting oral anticoagulants (DOACs) have emerged as alternatives to these agents and may offer advantages compared with vitamin K antagonists. As breastfeeding women were excluded from clinical trials evaluating DOACs, no safety and efficacy data are available for these special patients and, crucially, estimates for infant exposure are lacking. Therefore, the manufacturer recommends against using DOACs during the lactation period. We present the case of a patient who stopped breastfeeding owing to a diagnosis of postpartum cardiomyopathy. Anticoagulation with enoxaparin that commenced after the diagnosis of postpartum pulmonary embolism was switched to rivaroxaban. At that time, breast milk samples were collected and rivaroxaban concentrations were determined by liquid chromatography tandem-mass spectrometry. Rivaroxaban appears in human breast milk in comparatively small amounts; its safety has not been determined.

AB - Thromboembolic disorders frequently require antithrombotic treatment during pregnancy and lactation. Vitamin K antagonists and heparins are the treatment options of choice in breastfeeding women. Factors including the route of administration, discomfort during treatment, and fetal and neonatal safety affect women's choices about anticoagulant therapy. Direct-acting oral anticoagulants (DOACs) have emerged as alternatives to these agents and may offer advantages compared with vitamin K antagonists. As breastfeeding women were excluded from clinical trials evaluating DOACs, no safety and efficacy data are available for these special patients and, crucially, estimates for infant exposure are lacking. Therefore, the manufacturer recommends against using DOACs during the lactation period. We present the case of a patient who stopped breastfeeding owing to a diagnosis of postpartum cardiomyopathy. Anticoagulation with enoxaparin that commenced after the diagnosis of postpartum pulmonary embolism was switched to rivaroxaban. At that time, breast milk samples were collected and rivaroxaban concentrations were determined by liquid chromatography tandem-mass spectrometry. Rivaroxaban appears in human breast milk in comparatively small amounts; its safety has not been determined.

KW - Journal Article

U2 - 10.1016/j.chest.2016.01.021

DO - 10.1016/j.chest.2016.01.021

M3 - SCORING: Journal article

C2 - 27396794

VL - 150

SP - e1-4

JO - CHEST

JF - CHEST

SN - 0012-3692

IS - 1

ER -