Resuscitation With Vitamin C, Hydrocortisone, and Thiamin in Children With Septic Shock: A Multicenter Randomized Pilot Study

Author:

Schlapbach Luregn J.,Raman Sainath12,Buckley David3,George Shane145,King Megan4,Ridolfi Roberta12,Harley Amanda146,Cree Michele12,Long Debbie17,Erickson Simon8,Singh Puneet9,Festa Marino1011,Gibbons Kristen1,Bellomo Rinaldo,

Affiliation:

1. Child Health Research Centre, The University of Queensland, Brisbane, QLD, Australia.

2. Paediatric Intensive Care Unit, Queensland Children’s Hospital, Children’s Health Queensland, Brisbane, QLD, Australia.

3. Paediatric Intensive Care Unit, Starship Children’s Hospital, Auckland, New Zealand.

4. Departments of Emergency Medicine and Children’s Critical Care, Gold Coast University Hospital, Southport, QLD, Australia.

5. School of Medicine and Menzies Health Institute Queensland, Griffith University, Southport, QLD, Australia.

6. School of Nursing, Midwifery and Social Work, University of Queensland, QLD, Australia.

7. School of Nursing, Centre for Healthcare Transformation, Queensland University of Technology, Brisbane, QLD, Australia.

8. Paediatric Critical Care Unit, Perth Children`s Hospital, Perth, WA, Australia.

9. Paediatric Intensive Care Unit, Sydney Children’s Hospital, Sydney, NSW, Australia.

10. Paediatric Intensive Care Unit, Children’s Hospital Westmead, Sydney, NSW, Australia.

11. Kids Critical Care Research Group, Kids Research, Sydney Children’s Hospitals Network, Sydney, NSW, Australia.

Abstract

OBJECTIVES: Adjunctive therapy with vitamin C, hydrocortisone, and thiamin has been evaluated in adults, but randomized controlled trial (RCT) data in children are lacking. We aimed to test the feasibility of vitamin C, hydrocortisone, and thiamin in PICU patients with septic shock; and to explore whether the intervention is associated with increased survival free of organ dysfunction. DESIGN: Open-label parallel, pilot RCT multicenter study. The primary endpoint was feasibility. Clinical endpoints included survival free of organ dysfunction censored at 28 days and nine secondary outcomes, shock reversal, and two proxy measures of intervention efficacy. SETTING: Six PICUs in Australia and New Zealand. PATIENTS: Children of age between 28 days and 18 years requiring vasoactive drugs for septic shock between August 2019 and March 2021. INTERVENTIONS: Patients were assigned 1:1 to receive 1 mg/kg hydrocortisone every 6 hours (q6h), 30 mg/kg ascorbic acid q6h, and 4 mg/kg thiamin every 12 hours (n = 27), or standard septic shock management (n = 33). MEASUREMENTS AND MAIN RESULTS: Sixty of 77 (78%) eligible patients consented with 91% of approached parents providing consent. The median time from randomization to intervention was 44 (interquartile range [IQR] 29–120) min. Seventy of seventy-seven (28%) patients had received IV steroids before randomization. Median survival alive and free of organ dysfunction was 20.0 (0.0–26.0) days in the intervention and 21.0 (0.0–25.0) days in the standard care group. Median PICU length of stay was 5.3 (2.5–11.3) days in the intervention group versus 6.9 (3.0–11.5) days in the control group. Shock reversal occurred at a median of 35.2 (14.6–101.2) hours in the intervention group versus 47.3 (22.4–106.8) hours in the standard care group (median difference –12 hr; 95% CI, –56.8 to 32.7 hr). CONCLUSIONS: In children requiring vasopressors for septic shock, a protocol comparing adjunctive treatment with high-dose vitamin C, hydrocortisone, and thiamin versus standard care was feasible. These findings assist in making modifications to the trial protocol to enable a better-designed larger RCT.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Critical Care and Intensive Care Medicine,Pediatrics, Perinatology and Child Health

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