Anthropometric indices of Gambian children after one or three annual rounds of mass drug administration with azithromycin for trachoma control

Sarah E. Burr*, John Hart, Tansy Edwards, Emma Harding-Esch, Martin J. Holland, David C.W. Mabey, Ansumana Sillah, Robin L. Bailey

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Citations (Scopus)


Background: Mass drug administration (MDA) with azithromycin, carried out for the control of blinding trachoma, has been linked to reduced mortality in children. While the mechanism behind this reduction is unclear, it may be due, in part, to improved nutritional status via a potential reduction in the community burden of infectious disease. To determine whether MDA with azithromycin improves anthropometric indices at the community level, we measured the heights and weights of children aged 1 to 4 years in communities where one (single MDA arm) or three annual rounds (annual MDA arm) of azithromycin had been distributed. Methods: Data collection took place three years after treatment in the single MDA arm and one year after the final round of treatment in the annual MDA arm. Mean height-for-age, weight-for-age and weight-for-height z scores were compared between treatment arms. Results: No significant differences in mean height-for-age, weight-for-age or weight-for-height z scores were found between the annual MDA and single MDA arms, nor was there a significant reduction in prevalence of stunting, wasting or underweight between arms. Conclusions: Our data do not provide evidence that community MDA with azithromycin improved anthropometric outcomes of children in The Gambia. This may suggest reductions in mortality associated with azithromycin MDA are due to a mechanism other than improved nutritional status.

Original languageEnglish
Article number1176
JournalBMC Public Health
Issue number1
Publication statusPublished - 2014

Bibliographical note

Funding Information:
We are grateful to the community leaders and villagers for their participation in the study. We also thank Pateh Makalo, Mass Laye, Sarjo Dibba, Muhamed Jallow, Robyn Damary-Homan, Jane Whitton, Anita Wadagni, Hassan Joof, Ousman Jallow, Omar Manneh and Omar Camara for their work in the field and David Jeffries for helpful discussion of the data. The PRET trial ( NCT00792922) was funded by the Bill and Melinda Gates Foundation (grant number 48027). SEB receives salary funding from the Bill and Melinda Gates Foundation (grant number OPP1066930). MJH receives salary funding from the Wellcome Trust (grant number 079246/Z/06/Z). TE receives salary support from MRC and DFID (grant number G0700837).

Publisher Copyright:
© 2014 Burr et al.


  • Anthropometry
  • Azithromycin
  • Mass drug administration
  • Trachoma control


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