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Clinical Lactation Studies of Lithium: A Systematic Review

Background: There is substantial evidence that postpartum prophylaxis with lithium lowers the rate of relapse in bipolar disorder. However, it is contraindicated during breastfeeding due to the high variability of the transfer into breast milk. Aims: We conducted a systematic review of the current e...

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Autores principales: Imaz, Maria Luisa, Torra, Mercè, Soy, Dolors, García-Esteve, Lluïsa, Martin-Santos, Rocio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6746934/
https://www.ncbi.nlm.nih.gov/pubmed/31551795
http://dx.doi.org/10.3389/fphar.2019.01005
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author Imaz, Maria Luisa
Torra, Mercè
Soy, Dolors
García-Esteve, Lluïsa
Martin-Santos, Rocio
author_facet Imaz, Maria Luisa
Torra, Mercè
Soy, Dolors
García-Esteve, Lluïsa
Martin-Santos, Rocio
author_sort Imaz, Maria Luisa
collection PubMed
description Background: There is substantial evidence that postpartum prophylaxis with lithium lowers the rate of relapse in bipolar disorder. However, it is contraindicated during breastfeeding due to the high variability of the transfer into breast milk. Aims: We conducted a systematic review of the current evidence of studies assessing the transfer of lithium to lactating infants and short-term infant outcomes. Methods: An a priori protocol was designed based on PRISMA guidelines. Searches in PubMed and LactMed were conducted until September 2018. Studies assessing lithium pharmacokinetic parameters and short-term infant outcomes were included. Quality was assessed using a checklist based on international guidelines (i.e., FDA). Results: From 344 initial studies, 13 case reports/series with 39 mother–child dyads were included. Only 15% of studies complied with ≥50% of the items on the quality assessment checklist. Infants breastfeed a mean (SD) of 58.9 (83.3) days. Mean maternal lithium dose was 904 (293) mg/day, corresponding lithium plasma/serum concentration was 0.73(0.26) mEq/L, and breast milk concentration was 0.84(0.14) mEq/L. Mean infant lithium plasma/serum concentration was 0.23(0.26) mEq/L. Twenty-six (80%) infants had concentrations ≤0.30 mEq/L without adverse effects. Eight (20%) showed a transient adverse event (i.e., acute toxicity or thyroid alterations). All of them were also prenatally exposed to lithium monotherapy or polytherapy. Conclusion: The current evidence comes from studies with a degree of heterogeneity and of low-moderate quality. However, it identifies areas of improvement for future clinical lactation studies of lithium and provides support for some clinical recommendations.
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spelling pubmed-67469342019-09-24 Clinical Lactation Studies of Lithium: A Systematic Review Imaz, Maria Luisa Torra, Mercè Soy, Dolors García-Esteve, Lluïsa Martin-Santos, Rocio Front Pharmacol Pharmacology Background: There is substantial evidence that postpartum prophylaxis with lithium lowers the rate of relapse in bipolar disorder. However, it is contraindicated during breastfeeding due to the high variability of the transfer into breast milk. Aims: We conducted a systematic review of the current evidence of studies assessing the transfer of lithium to lactating infants and short-term infant outcomes. Methods: An a priori protocol was designed based on PRISMA guidelines. Searches in PubMed and LactMed were conducted until September 2018. Studies assessing lithium pharmacokinetic parameters and short-term infant outcomes were included. Quality was assessed using a checklist based on international guidelines (i.e., FDA). Results: From 344 initial studies, 13 case reports/series with 39 mother–child dyads were included. Only 15% of studies complied with ≥50% of the items on the quality assessment checklist. Infants breastfeed a mean (SD) of 58.9 (83.3) days. Mean maternal lithium dose was 904 (293) mg/day, corresponding lithium plasma/serum concentration was 0.73(0.26) mEq/L, and breast milk concentration was 0.84(0.14) mEq/L. Mean infant lithium plasma/serum concentration was 0.23(0.26) mEq/L. Twenty-six (80%) infants had concentrations ≤0.30 mEq/L without adverse effects. Eight (20%) showed a transient adverse event (i.e., acute toxicity or thyroid alterations). All of them were also prenatally exposed to lithium monotherapy or polytherapy. Conclusion: The current evidence comes from studies with a degree of heterogeneity and of low-moderate quality. However, it identifies areas of improvement for future clinical lactation studies of lithium and provides support for some clinical recommendations. Frontiers Media S.A. 2019-09-10 /pmc/articles/PMC6746934/ /pubmed/31551795 http://dx.doi.org/10.3389/fphar.2019.01005 Text en Copyright © 2019 Imaz, Torra, Soy, García-Esteve and Martin-Santos http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Imaz, Maria Luisa
Torra, Mercè
Soy, Dolors
García-Esteve, Lluïsa
Martin-Santos, Rocio
Clinical Lactation Studies of Lithium: A Systematic Review
title Clinical Lactation Studies of Lithium: A Systematic Review
title_full Clinical Lactation Studies of Lithium: A Systematic Review
title_fullStr Clinical Lactation Studies of Lithium: A Systematic Review
title_full_unstemmed Clinical Lactation Studies of Lithium: A Systematic Review
title_short Clinical Lactation Studies of Lithium: A Systematic Review
title_sort clinical lactation studies of lithium: a systematic review
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6746934/
https://www.ncbi.nlm.nih.gov/pubmed/31551795
http://dx.doi.org/10.3389/fphar.2019.01005
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