Biannual azithromycin distribution and child mortality among malnourished children: A subgroup analysis of the MORDOR cluster-randomized trial in Niger

Abstract

Background: Biannual azithromycin distribution has been shown to reduce child mortality as well as increase antimicrobial resistance. Targeting distributions to vulnerable subgroups such as malnourished children is one approach to reaching those at the highest risk of mortality while limiting selection for resistance. The objective of this analysis was to assess whether the effect of azithromycin on mortality differs by nutritional status.

Methods and findings: A large simple trial randomized communities in Niger to receive biannual distributions of azithromycin or placebo to children 1-59 months old over a 2-year timeframe. In exploratory subgroup analyses, the effect of azithromycin distribution on child mortality was assessed for underweight subgroups using weight-for-age Z-score (WAZ) thresholds of -2 and -3. Modification of the effect of azithromycin on mortality by underweight status was examined on the additive and multiplicative scale. Between December 2014 and August 2017, 27,222 children 1-11 months of age from 593 communities had weight measured at their first study visit. Overall, the average age among included children was 4.7 months (interquartile range [IQR] 3-6), 49.5% were female, 23% had a WAZ < -2, and 10% had a WAZ < -3. This analysis included 523 deaths in communities assigned to azithromycin and 661 deaths in communities assigned to placebo. The mortality rate was lower in communities assigned to azithromycin than placebo overall, with larger reductions among children with lower WAZ: -12.6 deaths per 1,000 person-years (95% CI -18.5 to -6.9, P < 0.001) overall, -17.0 (95% CI -28.0 to -7.0, P = 0.001) among children with WAZ < -2, and -25.6 (95% CI -42.6 to -9.6, P = 0.003) among children with WAZ < -3. No statistically significant evidence of effect modification was demonstrated by WAZ subgroup on either the additive or multiplicative scale (WAZ < -2, additive: 95% CI -6.4 to 16.8, P = 0.34; WAZ < -2, multiplicative: 95% CI 0.8 to 1.4, P = 0.50, WAZ < -3, additive: 95% CI -2.2 to 31.1, P = 0.14; WAZ < -3, multiplicative: 95% CI 0.9 to 1.7, P = 0.26). The estimated number of deaths averted with azithromycin was 388 (95% CI 214 to 574) overall, 116 (95% CI 48 to 192) among children with WAZ < -2, and 76 (95% CI 27 to 127) among children with WAZ < -3. Limitations include the availability of a single weight measurement on only the youngest children and the lack of power to detect small effect sizes with this rare outcome. Despite the trial's large size, formal tests for effect modification did not reach statistical significance at the 95% confidence level.

Conclusions: Although mortality rates were higher in the underweight subgroups, this study was unable to demonstrate that nutritional status modified the effect of biannual azithromycin distribution on mortality. Even if the effect were greater among underweight children, a nontargeted intervention would result in the greatest absolute number of deaths averted.

Trial registration: The MORDOR trial is registered at clinicaltrials.gov NCT02047981.

Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1. CONSORT participant flow diagram.

CONSORT, Consolidated Standards of Reporting Trials.

Fig 2. Comparison of mortality rates by treatment arm and WAZ subgroup with interaction contrasts.

(A, B) Comparisons of mortality rate (deaths per 1,000 person-years) by treatment arm overall and by WAZ subgroup on the additive (A) and multiplicative (B) scales. (A) Mortality rate differences (mortality rate in communities assigned to azithromycin minus mortality rate in communities assigned to placebo). (B) Mortality rate ratios (mortality rate in communities assigned to azithromycin divided by mortality rate in communities assigned to placebo). (C, D) Interaction contrasts on the additive (C) and multiplicative (D) scales. Interaction contrasts defined subgroups such that the groups with the lowest mortality rates were the reference categories (i.e., R00 = mortality rate among higher-weight children in communities assigned to azithromycin, R01 = mortality rate among underweight in communities assigned to azithromycin, R10 = mortality rate among higher-weight children in communities assigned to placebo, and R11 = mortality rate among underweight children in communities assigned to placebo). (C) Interaction contrasts on the additive scale. (D) Interaction contrasts on the multiplicative scale. WAZ, weight-for-age Z-score.

Fig 3. Kaplan-Meier estimates of survival probability by treatment arm and the moderate to severe underweight subgroup.

Each curve depicts a different subgroup, with placebo represented by dotted lines in shades of blue and azithromycin represented by solid lines in shades of red. The darker shades indicate the higher-weight subgroup (WAZ ≥ −2), and the lighter shades indicate the underweight subgroup (WAZ

Fig 4. Kaplan-Meier estimates of survival probability by treatment arm and the severe underweight subgroup.

Each curve depicts a different subgroup, with placebo represented by dotted lines in shades of blue and azithromycin represented by solid lines in shades of red. The darker shades indicate the higher-weight subgroup (WAZ ≥ −3), and the lighter shades indicate the underweight subgroup (WAZ