# Supplementation with ready-to-use therapeutic food has no effect on adverse outcomes among undernourished children aged 6–59 months with severe pneumonia

**Authors:** Damalie Nalwanga, Elisa Giallongo, Victor Musiime, Sarah Kiguli, Peter Olupot Olupot, Florence Alaroker, Robert Opoka, Abner Tagoola, Mainga Hamaluba, Christabel Mogaka, Eva Nabawanuka, Charles Karamagi, André Briend, Kathryn Maitland

PMC · DOI: 10.3389/fnut.2025.1507360 · 2025-06-06

## TL;DR

Adding ready-to-use therapeutic food to the diet of undernourished children with severe pneumonia did not improve their outcomes.

## Contribution

This study shows that RUTF supplementation does not reduce adverse outcomes in undernourished children with severe pneumonia.

## Key findings

- RUTF supplementation had no significant effect on adverse outcomes like mortality or re-admission.
- Adverse outcomes decreased with increasing age, regardless of RUTF use.
- High rates of adverse events persisted despite RUTF supplementation.

## Abstract

To investigate the effect of supplementation with ready-to-use therapeutic food (RUTF) on adverse outcomes among undernourished children aged 6–59 months with severe pneumonia.

This secondary analysis of the COAST-Nutrition (ISRCTN10829073) included children hospitalized for severe pneumonia in Uganda and Kenya. Undernutrition was defined as having either a weight-for-age z score, height-for-age z score, or weight-for-height/length z score below the median of the WHO reference population (< 0) or mid-upper arm circumference (MUAC) below 13.5 cm. Participants were randomized to receive 1 sachet of RUTF daily for 8 weeks in addition to the usual diet (intervention) or usual diet alone (control). The primary composite outcome for adverse events was any one of mortality, re-admission, or deterioration of nutritional status by day 90 of follow-up.

Of 846 main trial participants, 741 (88%) met the inclusion criteria (intervention: 374 versus control: 367). Of 687 (93%) participants in whom the primary outcome was assessed, 370 (54%) experienced an adverse event, [intervention: 184/348 (53%) versus control: 186/339(54%)]. There was no difference in the primary outcome between groups, aOR 0.92 (95% CI 0.68, 1.24), p = 0.572. Adverse outcome risk reduced with increasing age, aOR 0.53, (95% CI 0.45, 0.62), p < 0.001.

RUTF supplementation did not reduce the high frequency of adverse outcomes in children aged 6–59 months following hospital admission with severe pneumonia. Nutritional support directly targeting metabolic needs post-pneumonia should be considered in the future.

ISRCTN10829073, PACTR202106635355751.

## Full-text entities

- **Diseases:** pneumonia (MESH:D011014), Undernutrition (MESH:D044342)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12178878/full.md

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Source: https://tomesphere.com/paper/PMC12178878