Mass Oral Azithromycin for Childhood Mortality: Timing of Death After Distribution in the MORDOR Trial

Travis C Porco, John Hart, Ahmed M Arzika, Jerusha Weaver, Khumbo Kalua, Zakayo Mrango, Sun Y Cotter, Nicole E Stoller, Kieran S O'Brien, Dionna M Fry, Benjamin Vanderschelden, Catherine E Oldenburg, Sheila K West, Robin L Bailey, Jeremy D Keenan, Thomas M Lietman, Macrolides Oraux pour Réduire les Décès avec un Oeil sur la Résistance (MORDOR) Study Group, Travis C Porco, John Hart, Ahmed M Arzika, Jerusha Weaver, Khumbo Kalua, Zakayo Mrango, Sun Y Cotter, Nicole E Stoller, Kieran S O'Brien, Dionna M Fry, Benjamin Vanderschelden, Catherine E Oldenburg, Sheila K West, Robin L Bailey, Jeremy D Keenan, Thomas M Lietman, Macrolides Oraux pour Réduire les Décès avec un Oeil sur la Résistance (MORDOR) Study Group

Abstract

In a large community-randomized trial, biannual azithromycin distributions significantly reduced postneonatal childhood mortality in sub-Saharan African sites. Here, we present a prespecified secondary analysis showing that much of the protective effect was in the first 3 months postdistribution. Distributing more frequently than biannually could be considered if logistically feasible. Clinical Trials Registration. NCT02047981.

Keywords: azithromycin; childhood mortality; sub-Saharan Africa.

© The Author(s) 2018. Published by Oxford University Press for the Infectious Diseases Society of America.

Figures

Figure 1.
Figure 1.
Excess mortality in the first 2 months in the control group, compared to the treatment group, is seen in the difference between estimated mortality time density estimates. The horizontal axis depicts time in days from the beginning of each phase. The vertical axis shows the difference between the density of mortality times in the control and treatment groups (smoothed with a Gaussian kernel of bandwidth 0.1 month). Results from Malawi are presented in red, Niger in purple, Tanzania in green, and total in black. Note that this displays the difference between 2 probability distributions, and thus an excess at one time would necessarily be balanced by a deficit at another.

References

    1. Emerson PM, Hooper PJ, Sarah V. Progress and projections in the program to eliminate trachoma. PLoS Negl Trop Dis 2017; 11:e0005402.
    1. Whitty CJ, Glasgow KW, Sadiq ST, Mabey DC, Bailey R. Impact of community-based mass treatment for trachoma with oral azithromycin on general morbidity in Gambian children. Pediatr Infect Dis J 1999; 18:955–8.
    1. Fry AM, Jha HC, Lietman TM, et al. . Adverse and beneficial secondary effects of mass treatment with azithromycin to eliminate blindness due to trachoma in Nepal. Clin Infect Dis 2002; 35:395–402.
    1. Coles CL, Levens J, Seidman JC, Mkocha H, Munoz B, West S. Mass distribution of azithromycin for trachoma control is associated with short-term reduction in risk of acute lower respiratory infection in young children. Pediatr Infect Dis J 2012; 31:341–6.
    1. Coles CL, Seidman JC, Levens J, Mkocha H, Munoz B, West S. Association of mass treatment with azithromycin in trachoma-endemic communities with short-term reduced risk of diarrhea in young children. Am J Trop Med Hyg 2011; 85:691–6.
    1. Gaynor BD, Amza A, Kadri B, et al. . Impact of mass azithromycin distribution on malaria parasitemia during the low-transmission season in Niger: a cluster-randomized trial. Am J Trop Med Hyg 2014; 90:846–51.
    1. Schachterle SE, Mtove G, Levens JP, et al. . Short-term malaria reduction by single-dose azithromycin during mass drug administration for trachoma, Tanzania. Emerg Infect Dis 2014; 20:941–9.
    1. Keenan JD, Ayele B, Gebre T, et al. . Childhood mortality in a cohort treated with mass azithromycin for trachoma. Clin Infect Dis 2011; 52:883–8.
    1. Porco TC, Gebre T, Ayele B, et al. . Effect of mass distribution of azithromycin for trachoma control on overall mortality in Ethiopian children: a randomized trial. JAMA 2009; 302:962–8.
    1. Keenan JD, Bailey RL, West SK, et al. MORDOR Study Group. Azithromycin to reduce childhood mortality in sub-Saharan Africa. N Engl J Med 2018; 378:1583–92.
    1. Schachter J, West SK, Mabey D, et al. . Azithromycin in control of trachoma. Lancet 1999; 354:630–5.
    1. See CW, O’Brien KS, Keenan JD, et al. . The effect of mass azithromycin distribution on childhood mortality: beliefs and estimates of efficacy. Am J Trop Med Hyg 2015; 93:1106–9.
    1. Gao D, Amza A, Nassirou B, et al. . Optimal seasonal timing of oral azithromycin for malaria. Am J Trop Med Hyg 2014; 91:936–42.
    1. Sié A, Tapsoba C, Dah C, et al. . Dietary diversity and nutritional status among children in rural Burkina Faso. Int Health 2018; 10:157–62.
    1. Becher H, Kynast-Wolf G, Sié A, et al. . Patterns of malaria: cause-specific and all-cause mortality in a malaria-endemic area of west Africa. Am J Trop Med Hyg 2008; 78:106–13.
    1. Yusuf S, Collins R, Peto R. Why do we need some large, simple randomized trials?Stat Med 1984; 3:409–22.

Source: PubMed

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