PEDIATRICS Vol. 108 No. 3
September 2001,
pp. 776-789
AMERICAN ACADEMY OF PEDIATRICS:
The Transfer of Drugs and Other Chemicals Into Human Milk
Committee on Drugs
 |
ABSTRACT |
The American Academy of Pediatrics places emphasis
on increasing breastfeeding in the United States. A common reason for
the cessation of breastfeeding is the use of medication by the nursing mother and advice by her physician to stop nursing. Such advice may not
be warranted. This statement is intended to supply the pediatrician,
obstetrician, and family physician with data, if known, concerning the
excretion of drugs into human milk. Most drugs likely to be prescribed
to the nursing mother should have no effect on milk supply or on infant
well-being. This information is important not only to protect nursing
infants from untoward effects of maternal medication but also to allow
effective pharmacologic treatment of breastfeeding mothers. Nicotine,
psychotropic drugs, and silicone implants are 3 important topics
reviewed in this statement.
 |
INTRODUCTION |
A statement on the transfer of drugs and chemicals into
human milk was first published in 1983,1 with revisions in 19892 and 1994.3 Information continues to
become available. The current statement is intended to revise the lists of agents transferred into human milk and describe their possible effects on the infant or on lactation, if known (Tables 1-7). If a
pharmacologic or chemical agent does not appear in the tables, it does
not mean that it is not transferred into human milk or that it does not
have an effect on the infant; it only indicates that there were no
reports found in the literature. These tables should assist the
physician in counseling a nursing mother regarding breastfeeding when
the mother has a condition for which a drug is medically indicated.
 |
BREASTFEEDING AND SMOKING |
In the previous edition of this statement, the Committee on Drugs
placed nicotine (smoking) in Table 2, "Drugs of Abuse-Contraindicated
During Breastfeeding." The reasons for placing nicotine and, thus,
smoking in Table 2 were documented decrease in milk production and
weight gain in the infant of the smoking mother and exposure of the
infant to environmental tobacco smoke as demonstrated by the presence
of nicotine and its primary metabolite, cotinine, in human
milk.4-12 There is controversy regarding the effects of
nicotine on infant size at 1 year of age.13,14 There are
hundreds of compounds in tobacco smoke; however, nicotine and its
metabolite acotinine are most often used as markers of tobacco
exposure. Nicotine is not necessarily the only component that might
cause an increase in respiratory illnesses (including otitis media) in
the nursing infant attributable to both transmammary secretion of
compounds and environmental exposure. Nicotine is present in milk in
concentrations between 1.5 and 3.0 times the simultaneous maternal
plasma concentration,15 and elimination half-life is
similar
60 to 90 minutes in milk and plasma.7 There is no
evidence to document whether this amount of nicotine presents a health
risk to the nursing infant.
The Committee on Drugs wishes to support the emphasis of the American
Academy of Pediatrics on increasing breastfeeding in the United States.
Pregnancy and lactation are ideal occasions for physicians to urge
cessation of smoking. It is recognized that there are women who are
unable to stop smoking cigarettes. One study reported that, among women
who continue to smoke throughout breastfeeding, the incidence of acute
respiratory illness is decreased among their infants, compared with
infants of smoking mothers who are bottle fed.16 It may be
that breastfeeding and smoking is less detrimental to the child than
bottle feeding and smoking. The Committee on Drugs awaits more data on
this issue. The Committee on Drugs therefore has not placed nicotine
(and thus smoking) in any of the Tables but hopes that the interest in
breastfeeding by a smoking woman will serve as a point of discussion about smoking cessation between the pediatrician and the prospective lactating woman or nursing mother. Alternate (oral, transcutaneous) sources of nicotine to assist with smoking cessation, however, have not
been studied sufficiently for the Committee on Drugs to make a
recommendation for or against them in breastfeeding women.
 |
PSYCHOTROPIC DRUGS |
Anti-anxiety drugs, antidepressants, and neuroleptic drugs have
been placed in Table 4, "Drugs for Which the Effect on Nursing
Infants is Unknown but May Be of Concern." These drugs appear in low
concentrations (usually with a milk-to-plasma ratio of 0.5-1.0) in
milk after maternal ingestion. Because of the long half-life of these
compounds and some of their metabolites, nursing infants may have
measurable amounts in their plasma and tissues, such as the brain. This
is particularly important in infants during the first few months of
life, with immature hepatic and renal function. Nursing mothers should
be informed that if they take one of these drugs, the infant will be
exposed to it. Because these drugs affect neurotransmitter function in
the developing central nervous system, it may not be possible to
predict long-term neurodevelopmental effects.
 |
SILICONE BREAST IMPLANTS AND BREASTFEEDING |
Approximately 800 000 to 1 million women in the United States
have received breast implants containing silicone (elemental silicon
with chemical bonds to oxygen) in the implant envelope or in the
envelope and the interior gel. Concern has been raised about the
possible effects to the nursing infant if mothers with implants
breastfeed. This concern was initially raised in reports that described
esophageal dysfunction in 11 children whose mothers had
implants.17,18 This finding has not been confirmed by
other reports. Silicone chemistry is extremely complex; the polymer
involved in the covering and the interior of the breast implant
consists of a polymer of alternating silicon and oxygen atoms with
methyl groups attached to the oxygen groups (methyl polydimethylsiloxane).19 The length of the polymer
determines whether it is a solid, gel, or liquid. There are only a few
instances of the polymer being assayed in the milk of women with
implants; the concentrations are not elevated over control
samples.20 There is no evidence at the present time that
this polymer is directly toxic to human tissues; however, concern also
exists that toxicity may be mediated through an immunologic mechanism. This has yet to be confirmed in humans. Except for the study cited above, there have been no other reports of clinical problems in infants
of mothers with silicone breast implants.21 It is unlikely
that elemental silicon causes difficulty, because silicon is present in
higher concentrations in cow milk and formula than in milk of humans
with implants.22 The anticolic compound simethicone is a
silicone and has a structure very similar to the methyl
polydimethylsiloxane in breast implants. Simethicone has been used for
decades in this country and Europe without any evidence of toxicity to
infants. The Committee on Drugs does not feel that the evidence
currently justifies classifying silicone implants as a contraindication
to breastfeeding.
 |
DRUG THERAPY OF THE LACTATING WOMAN |
The following should be considered before prescribing drugs to
lactating women:
- Is drug therapy really necessary? If drugs are required,
consultation between the pediatrician and the mother's physician can
be most useful in determining what options to choose.
- The safest drug should be chosen, for example,
acetaminophen rather than aspirin for analgesia.
- If there is a possibility that a drug may present a risk to the
infant, consideration should be given to measurement of blood concentrations in the nursing infant.
- Drug exposure to the nursing infant may be minimized by having
the mother take the medication just after she has breastfed the infant
or just before the infant is due to have a lengthy sleep period.
Data have been obtained from a search of the medical literature.
Because methodologies used to quantitate drugs in milk continue to
improve, this information will require frequent updating. Drugs cited
in Tables 1 through 7 are listed in alphabetical order by generic name;
brand names are available from the current Physicians' Desk
Reference,23 USP DI 2001: Drug
Information for the Health Care Professional, Volume
I,24 and USP Dictionary of USAN and
International Drug Names.25 The reference list is not
inclusive of all articles published on the topic.
Physicians who encounter adverse effects in infants who have been
receiving drug-contaminated human milk are urged to document these
effects in a communication to the Food and Drug Administration (http://www.fda.gov/medwatch/index.html) and to the Committee on Drugs.
This communication should include the generic and brand names of the
drug, the maternal dose and mode of administration, the concentration
of the drug in milk and maternal and infant blood in relation to the
time of ingestion, the method used for laboratory identification, the
age of the infant, and the adverse effects. Such reports may
substantially increase the pediatric community's fund of knowledge
regarding drug transfer into human milk and the potential or actual
risk to the infant.
View this table:
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|
TABLE 5
Drugs That Have Been Associated With Significant Effects on Some
Nursing Infants and Should Be Given to Nursing Mothers With
Caution*
|
|
Committee on Drugs, 2000-2001
Robert M. Ward, MD, Chairperson
Brian A. Bates, MD
William E. Benitz, MD
David J. Burchfield, MD
John C. Ring, MD
Richard P. Walls, MD, PhD
Philip D. Walson, MD
Liaisons
John Alexander, MD
Food and Drug Administration Alternate
Donald R. Bennett, MD, PhD
American Medical Association/United States Pharmacopeia
Therese Cvetkovich, MD
Food and Drug Administration
Owen R. Hagino, MD
American Academy of Child and Adolescent Psychiatry
Stuart M. MacLeod, MD, PhD
Canadian Paediatric Society
Siddika Mithani, MD
Bureau of Pharmaceutical Assessment Health Protection Branch, Canada
Joseph Mulinare, MD, MSPH
Centers for Disease Control and Prevention
Laura E. Riley, MD
American College of Obstetricians and Gynecologists
Sumner J. Yaffe, MD
National Institutes of Health
Section Liaisons
Charles J. Coté, MD
Section on Anesthesiology
Eli O. Meltzer, MD
Section on Allergy and Immunology
Consultant
Cheston M. Berlin, Jr, MD
Staff
Raymond J. Koteras, MHA
 |
ACKNOWLEDGMENT |
The Committee on Drugs would like to thank Linda Watson for her
work in reference identification, document retrieval, and manuscript
preparation.
 |
FOOTNOTES |
The recommendations in this statement do not indicate an exclusive course of treatment or serve as a standard of medical care. Variations, taking into account individual circumstances, may be appropriate.
 |
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