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Oxygen therapy for children with an oxygen saturation of 90-93% in Malawi: the NoGoLO2 pilot randomised controlled
Kristen S Joseph1,2, Tisungane Mvalo3,4, Nicole Shilkofski5
1Department of Anesthesia and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA kjosep24@jh.edu.
Insights
A randomized trial comparing standard care, low-flow nasal cannula (LFNC), and high-flow nasal cannula (HFNC) oxygen for children with pneumonia and low oxygen saturation (SpO2) is feasible. The study demonstrated high enrollment and successful follow-up, indicating potential for future research in low-income settings.
Area of Science:
- Pediatric critical care
- Respiratory medicine
- Global health
Background:
- Oxygen therapy is crucial for childhood pneumonia with hypoxemia.
- World Health Organization guidelines recommend oxygen for SpO2 <90%.
- Children with SpO2 90-93% in low- and middle-income countries face increased mortality risk.
Purpose of the Study:
- To determine the feasibility of a randomized controlled trial.
- To compare standard care (no oxygen), low-flow nasal cannula (LFNC), and high-flow nasal cannula (HFNC).
- To evaluate oxygen therapy for children with pneumonia and SpO2 of 90-93%.
Main Methods:
- Pilot, open-label, three-armed randomized controlled trial (NCT06176664).
- Conducted at Salima District Hospital, Malawi.
- Included children aged 1-59 months with WHO-defined pneumonia and SpO2 90-93%.
Main Results:
- 21 out of 29 eligible children (72%) were enrolled.
- An average of 0.8 protocol deviations per participant occurred.
- No participants withdrew, and all were followed for 14-day outcomes; 14.3% experienced treatment failure.
Conclusions:
- A three-armed randomized controlled trial comparing standard care, LFNC, and HFNC oxygen is feasible.
- This approach is suitable for children with pneumonia and SpO2 90-93% in Malawi.
- The study design supports future trials in similar settings.
Objective:
Oxygen is a cornerstone treatment for pneumonia with hypoxaemia. WHO guidelines recommend oxygen therapy for children with a peripheral arterial haemoglobin oxygen saturation (SpO2) <90%. Children in low- and middle-income countries with an SpO2 of 90-93% are at increased risk of mortality and may benefit from oxygen therapy. We aimed to determine the feasibility of a randomised controlled trial comparing standard of care (no oxygen), low-flow nasal cannula (LFNC) and high-flow nasal cannula (HFNC) among children with pneumonia and an SpO2 of 90-93%.
Design:
Pilot, open-label, three-armed randomised control trial (NCT06176664).
Setting:
Salima District Hospital, Malawi.
Patients:
Children 1-59 months old with WHO-defined pneumonia and an SpO2 of 90-93%.
Interventions:
Standard care (no oxygen), LFNC or HFNC.
Main Outcome Measures:
The primary outcome was feasibility defined as an average of ≤2 protocol deviations per participant. Secondary outcomes included consent refusal, participant attrition and treatment failure within 14 days. Treatment failure was defined as an SpO2 <90% for standard care participants or <94% in the LFNC and HFNC arms despite maximum therapy as described, any new severe respiratory distress (grunting, very severe chest indrawing) or any new WHO-defined emergency sign.
Results:
Of the 29 eligible patients, 21 (72%) were enrolled and randomised. There was an average of 0.8 (16/21) deviations per participant. Seven (43.8%) protocol violations were related to study intervention protocols and nine (56.3%) to medication availability and routine care. No participants withdrew from the study. Three of 21 participants (14.3%) had treatment failure. All participants were successfully followed to obtain the 14-day outcome.
Conclusions:
A three-armed, open-label randomised control trial is feasible to compare standard of care, LFNC and HFNC oxygen for children with pneumonia and an SpO2 of 90-93% in Malawi.
Trial Registration Number:
NCT06176664.
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