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Use of a sparse sampling study design to assess transfer of tramadol and its O ‐desmethyl metabolite into transitional breast milk
Author(s) -
Ilett Kenneth F.,
Paech Michael J.,
PageSharp Madhu,
Sy Sherwin K.,
Kristensen Judith H.,
Goy Raymond,
Chua Sebastian,
Christmas Tracey,
Scott Karen L.
Publication year - 2008
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1111/j.1365-2125.2008.03117.x
Subject(s) - tramadol , metabolite , breastfeeding , breast milk , medicine , pharmacokinetics , desmethyl , infant formula , breast feeding , anesthesia , pharmacology , chemistry , analgesic , pediatrics , biochemistry
WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT • There are presently no published data on tramadol transfer into breast milk or on its effects in the breastfed infant. WHAT THIS STUDY ADDS • We have provided quantitative data on the absolute and relative infant doses of rac‐ tramadol and it rac‐O ‐desmethyl metabolite for the breastfed infant. • We have also demonstrated a novel sparse sampling data collection method for investigating infant exposure via milk. AIMS To investigate the transfer of rac‐ tramadol and its rac‐O‐ desmethyl metabolite into transitional milk, and assess unwanted effects in the breastfed infant. METHODS Tramadol HCl (100 mg six hourly) was administered to 75 breastfeeding mothers for postoperative analgesia on days 2–4 after Caesarian section. Milk and plasma samples were collected after administration of four or more doses. Rac‐ tramadol and rac‐O ‐desmethyltramadol were measured by high performance liquid chromatography. Milk : plasma ratio (M : P) and infant doses were calculated by standard methods. The behavioural characteristics of the exposed breastfed infants and a matched control group of infants not exposed to tramadol were also studied. RESULTS At steady‐state, mean (95% CI) M : P was 2.2 (2.0, 2.4) for rac‐ tramadol and 2.8 (2.5, 3.1) for rac‐O‐ desmethyltramadol. The estimated absolute and relative infant doses were 112 (102, 122) μg kg −1 day −1 and 30 (28, 32) μg kg −1 day −1 , and 2.24% (2.04, 2.44)% and 0.64% (0.59, 0.69)% for rac‐ tramadol and rac‐O‐ desmethyltramadol, respectively. The exposed infants and control breastfed infants had similar characteristics, including Apgar scores at birth and Neurologic and Adaptive Capacity Scores. CONCLUSIONS The combined relative infant dose of 2.88% at steady‐state was low. The similarity of NACS in exposed infants and controls suggests that there were no significant behavioural adverse effects. We conclude that short‐term maternal use of tramadol during establishment of lactation is compatible with breastfeeding.