Cost‐effectiveness of nasal high‐flow in children with acute hypoxaemic respiratory failure

Author:

Gannon Brenda12,Franklin Donna34567ORCID,Vo Vinh1,Babl Franz E78910,Schibler Andreas7111213

Affiliation:

1. School of Economics University of Queensland Brisbane Queensland Australia

2. University of Queensland Centre for the Business and Economics of Health Brisbane Queensland Australia

3. Children's Emergency and Critical Care Research Gold Coast University Hospital Gold Coast Queensland Australia

4. Emergency Department Gold Coast University Hospital Gold Coast Queensland Australia

5. Faculty of Medicine The University of Queensland Brisbane Queensland Australia

6. Menzies Health Institute Queensland Griffith University Gold Coast Queensland Australia

7. Paediatric Research in Emergency Departments International Collaborative (PREDICT) Melbourne Victoria Australia

8. Emergency Department Royal Children's Hospital Melbourne Victoria Australia

9. Murdoch Children's Research Institute Melbourne Victoria Australia

10. Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences University of Melbourne Melbourne Victoria Australia

11. St Andrew's War Memorial Hospital Brisbane Queensland Australia

12. Critical Care Research Group, St Andrew's War Memorial Hospital Brisbane Queensland Australia

13. Wesley Medical Research Brisbane Queensland Australia

Abstract

AimA pilot randomised controlled trial assessed the early application of nasal high‐flow (NHF) therapy compared with standard oxygen therapy (SOT), in children aged 0 to 16 years presenting to paediatric emergency departments with acute hypoxaemic respiratory failure (AHRF). The study estimated the need to escalate therapy and hospital length of stay in the NHF group compared with SOT. This sub‐study then assessed the subsequent cost‐effectiveness.MethodsA decision tree‐based model was developed, alongside the clinical study, to estimate cost‐effectiveness, from the healthcare sector perspective. The primary health economics outcome is measured as incremental cost per length of hospital stay avoided. Incremental cost effectiveness ratios (ICER) measuring change in cost per change in length of stay, were obtained for four samples, depending on responder status and obstructive airways disease. These were (1) obstructive and responder, (2) non‐obstructive and responder, (3) obstructive and non‐responder and (4) non obstructive and non‐responder. Bootstrapping of parameters accounted for uncertainty in estimates of cost and outcome.ResultsThe ICER for patients randomised to NHF, indicated an additional A$367.20 for a lower hospital length of stay (in days) in the non‐obstructive/non‐responder sample. In the bootstrap sample, this was found to be cost effective above a willingness to pay threshold of A$10 000. The ICER was A$440.86 in the obstructive/responder sample and A$469.56 in the non‐obstructive/responder sample – but both resulted in a longer length of stay. The ICER in the obstructive/non‐responder sample was A$52 167.76, also with a longer length of stay, mainly impacted by a small sample of severe cases.ConclusionAs first‐line treatment, NHF is unlikely to be cost‐effective compared with SOT, but for non‐obstructive patients who required escalation in care (non‐obstructive non‐responder), NHF is likely to be cost‐effective if willingness‐to‐pay per reduced hospital length of stay is more than A$10 000 per patient.

Funder

National Health and Medical Research Council

Publisher

Wiley

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