Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Excretion of hydroxyurea into milk.

R K Sylvester1, M Lobell, M E Teresi

  • 1Department of Pharmacy, United Hospital, Inc. St. Paul, MN 55102.

Cancer
|November 1, 1987
PubMed
Summary

This study examines whether hydroxyurea, a drug used in cancer treatment, is excreted into breast milk. The authors review existing literature and find evidence that hydroxyurea is present in breast milk samples. This suggests that nursing infants may be exposed to the drug. The study also considers findings for other antineoplastic agents. The authors propose that these findings should inform clinical decisions about drug use during lactation. The review does not resolve whether the drug is entirely safe for lactation but highlights the need for further research.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Cardiovascular effects of a novel potent and highly selective azaindole-based inhibitor of Rho-kinase.

British journal of pharmacology·2007
Same author

A conserved arginine plays a role in the catalytic cycle of the protein disulphide isomerases.

Journal of molecular biology·2003
Same author

Asthma stability after oral prednisone: a clinical model for comparing inhaled steroid potency.

American journal of respiratory and critical care medicine·2001
Same author

Multicenter survey of pharmacy faculty and student metered-dose inhaler knowledge.

Journal of the American Pharmaceutical Association (Washington, D.C. : 1996)·2001
Same author

In vitro characteristics of tobramycin aerosol from ultrasonic and jet nebulizers.

Pharmacotherapy·2001
Same author

Antibiotic activity and characterization of BB-3497, a novel peptide deformylase inhibitor.

Antimicrobial agents and chemotherapy·2001

Area of Science:

  • Pharmacology of antineoplastic drugs
  • Lactation and drug excretion
  • Clinical oncology drug safety

Background:

Prior research has shown that certain medications are excreted into breast milk, but gaps remain regarding specific antineoplastic agents. No prior work had resolved whether hydroxyurea, a drug used in cancer treatment, is excreted in breast milk. This uncertainty drove the need for a focused review of available evidence. The literature on other antineoplastic drugs suggests variable milk excretion patterns. However, the specific case of hydroxyurea had not been clearly established. This gap motivated a systematic review of existing studies. The absence of data on hydroxyurea excretion in breast milk highlights a critical need for maternal and infant safety assessments. Understanding drug transfer into milk is essential for guiding clinical decisions in lactating patients. This review aims to clarify the current state of evidence for hydroxyurea and similar agents.

Purpose Of The Study:

The aim of this study is to determine whether hydroxyurea is excreted into human breast milk. The specific problem involves assessing the safety of lactation in patients receiving hydroxyurea therapy. The motivation stems from the lack of clear evidence on this topic. The authors propose to synthesize existing literature to address this gap. The study focuses on evaluating the transfer of hydroxyurea from mother to infant via breast milk. This information is crucial for informing clinical guidelines on drug use during lactation. The review also considers other antineoplastic agents to provide a broader context. The ultimate goal is to support safer decision-making for lactating patients undergoing cancer treatment.

Keywords:
hydroxyurea breast milk excretionantineoplastic drug safetylactation drug transferoncology pharmacology

Frequently Asked Questions

Hydroxyurea is detected in breast milk samples, suggesting passive diffusion or active transport mechanisms.

Excretion into breast milk may pose risks to nursing infants, requiring careful clinical evaluation.

Hydroxyurea excretion into milk may lead to infant exposure, potentially affecting their health.

Pharmacokinetic studies help quantify drug transfer into milk and assess potential infant exposure.

Case reports and pharmacokinetic data confirm hydroxyurea presence in breast milk samples.

Related Experiment Videos

Main Methods:

The authors conducted a literature review focusing on hydroxyurea excretion into breast milk. They analyzed existing studies that measured drug concentrations in maternal milk samples. The review approach included examining case reports and pharmacokinetic data. The authors compared findings with those of other antineoplastic agents. No new experiments were performed; all conclusions are based on prior research. The synthesis of evidence involved evaluating the consistency of results across studies. The literature review approach prioritized human studies over animal models. The findings were contextualized within broader discussions of drug safety in lactation.

Main Results:

Hydroxyurea was detected in breast milk samples from treated patients. The concentration levels suggest potential exposure to the nursing infant. The study found no prior evidence of hydroxyurea being completely absent in breast milk. Other antineoplastic agents showed variable excretion patterns in milk. The data suggest that hydroxyurea transfer into milk is not negligible. The authors propose that this finding should inform clinical recommendations. The review highlights the need for caution in recommending lactation during hydroxyurea therapy. These results suggest a need for further pharmacokinetic studies in this population.

Conclusions:

The authors conclude that hydroxyurea is excreted into human breast milk. This finding suggests a potential risk for infant exposure through lactation. The review does not propose definitive safety thresholds for this drug in breastfeeding. The authors suggest that these findings should guide clinical decision-making. The synthesis of evidence does not resolve whether the drug is entirely safe for lactation. The study does not assign essentiality to any specific drug monitoring strategy. The authors suggest that further research is needed to quantify infant exposure risks. These conclusions are based solely on the available literature and do not propose new therapeutic directions.

The authors suggest caution in recommending lactation during hydroxyurea therapy due to potential infant exposure.