Advertisement
Journal Home
Search for

Volume 155, Issue 4, Pages 495-499.e2 (October 2009)


View previous. 23 of 54 View next.

Mercury Levels in Premature and Low Birth Weight Newborn Infants after Receipt of Thimerosal-Containing Vaccines

Michael E. Pichichero, MDaCorresponding Author Informationemail address, Angela Gentile, MDb, Norberto Giglio, MDb, Margarita Martin Alonso, MDc, Maria Veronica Fernandez Mentaberri, MDc, Grazyna Zareba, PhDa, Thomas Clarkson, PhDa, Carlos Gotelli, PhDd, Mariano Gotelli, PhDd, Lihan Yan, PhDe, John Treanor, MDa

Received 13 August 2008; received in revised form 9 February 2009; accepted 8 April 2009. published online 29 June 2009.

Objective

We conducted a population-based pharmacokinetic study to assess blood levels and elimination of mercury after vaccination of premature infants born at ≥32 and <37 weeks of gestation and with birth weight ≥2000 but <3000 g.

Study design

Blood, stool, and urine samples were obtained before vaccination and 12 hours to 30 days after vaccination from 72 premature newborn infants. Total mercury levels were measured by atomic absorption.

Results

The mean ± standard deviation (SD) birth weight was 2.4 ± 0.3 kg for the study population. Maximal mean ± SD blood mercury level was 3.6 ± 2.1 ng/mL, occurring at 1 day after vaccination; maximal mean ± SD stool mercury level was 35.4 ± 38.0 ng/g, occurring on day 5 after vaccination; and urine mercury levels were mostly nondetectable. The blood mercury half-life was calculated to be 6.3 (95% CI, 3.85 to 8.77) days, and mercury levels returned to prevaccination levels by day 30.

Conclusions

The blood half-life of intramuscular ethyl mercury from thimerosal in vaccines given to premature infants is substantially shorter than that of oral methyl mercury in adults. Because of the differing pharmacokinetics, exposure guidelines based on oral methyl mercury in adults may not be accurate for children who receive thimerosal-containing vaccines.

a University of Rochester, Rochester, NY

b R. Gutierrez Children's Hospital, Buenos Aires, Argentina

c Hospital Durand, Buenos Aires, Argentina

d Center of Toxicology Research, Buenos Aires, Argentina

e EMMES Corp, Rockville, MD

Corresponding Author InformationReprint requests: Dr Michael E. Pichichero, Rochester General Hospital, Research Institute, 1425 Portland Avenue, Rochester, NY 14621.

 Supported by NIH NIAID contract AI 25460. The authors declare no conflicts of interest.

PII: S0022-3476(09)00370-9

doi:10.1016/j.jpeds.2009.04.011


View previous. 23 of 54 View next.

Advertisement