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Caregiver Screening for Relapse Among Children Recently Recovered From Severe Acute Malnutrition: A Randomized
Mamadou Bountogo1, Clarisse Dah1, Moussa Ouédraogo1
1Centre de Recherche en Santé de Nouna, Nouna, Burkina Faso.
Insights
Training caregivers to screen for relapse using mid-upper arm circumference (MUAC) tapes is feasible for children recovering from severe acute malnutrition (SAM). This approach may reduce relapse detection time and hospitalizations, warranting further investigation in larger trials.
Area of Science:
- Public Health and Nutrition
- Pediatric Malnutrition Research
- Global Health Interventions
Background:
- Relapse to acute malnutrition is a significant challenge for children recovering from severe acute malnutrition (SAM).
- Existing interventions primarily focus on the acute phase, with limited resources for post-discharge follow-up.
- Early detection of relapse is crucial for timely intervention and improved outcomes in children recovering from SAM.
Purpose of the Study:
- To evaluate the feasibility of training caregivers to screen for malnutrition relapse using mid-upper arm circumference (MUAC) tapes.
- To assess the impact of caregiver-led MUAC screening on the time to detection of relapse in children recently recovered from SAM.
- To compare hospitalization and mortality rates between caregiver screening and standard care follow-up.
Main Methods:
- A randomized controlled trial involving 200 caregiver-child dyads in Burkina Faso.
- Intervention group: Caregivers trained for weekly MUAC screening for 6 months.
- Control group: Standard of care (SOC) with monthly clinic visits for 3 months post-discharge.
Main Results:
- The caregiver MUAC screening group showed a trend towards a lower hazard of relapse detection (HR 0.65).
- Significantly fewer hospitalizations and/or deaths occurred in the MUAC screening group (3%) compared to the SOC group (14%).
- Caregiver training for MUAC screening was feasible and well-accepted.
Conclusions:
- Training caregivers in MUAC screening is a feasible strategy to monitor children after recovery from SAM.
- This approach may reduce the time to detect relapse and decrease adverse health events like hospitalization.
- A larger-scale trial is recommended to confirm these findings and establish the effectiveness of caregiver-led MUAC screening.
Abstract:
Relapse to acute malnutrition after recovery from severe acute malnutrition (SAM) is common. However, most programmatic resources are devoted to the acute phase of recovery, and fewer interventions are available for children recently discharged from outpatient nutritional programs. We evaluated the feasibility of training caregivers to screen for relapse using mid-upper arm circumference (MUAC) tapes for reducing time to detection of relapse among children recently recovered from SAM in Burkina Faso. Caregiver-child dyads were enrolled and randomized in a 1:1 fashion to either caregiver MUAC screening or local standard of care (SOC), which consists of monthly clinic-based follow-up visits for 3 months following discharge. In the MUAC screening group, caregivers were trained on how to use a standard MUAC tape and asked to screen their child weekly with a provided MUAC tape for the 6-month duration of the study. The primary outcome was time to relapse detection, defined as MUAC < 12.5 cm and/or weight-for-height Z-score < -2. Secondary outcomes included hospitalization and/or death over the 6-month study period. Of 200 caregiver-child dyads enrolled in the trial, 99 were randomized to the MUAC screening group and 101 to the SOC group. By 6 months after enrollment, the hazard of relapse detection was lower in the MUAC screening group compared to the SOC group (hazard ratio, HR, 0.65, 95% confidence interval, CI, 0.38-1.12). Fewer hospitalizations and/or deaths occurred in the MUAC screening group compared to the SOC group (MUAC: 3%; SOC: 14%, risk ratio 0.23, 95% CI, 0.07-0.79). Training caregivers to screen for relapse after recovery from SAM was feasible and may lead to modestly reduced time to detection of relapse, suggesting a full-scale trial is warranted. Trial Registration: This study was prospectively registered on clinicaltrials.gov (NCT05932992, registered June 27, 2023).
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