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DOI 10.1097/pcc.0000000000003516

Медицинская библиотека · Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies · 2024

Protocol for a Randomized Controlled Trial to Evaluate a Permissive Blood Pressure Target Versus Usual Care in Critically Ill Children with Hypotension (PRESSURE).

Darnell Robert, Brown Alanna, Laing Emma, Edwards Julia, Harrison David A, Manning Joseph C, Peters Mark J, Ramnarayan Padmanabhan, Ray Samiran, Sadique Zia, Scholefield Barnaby R, Shortt Dermot, Lampro Lamprini, Au Carly, Rowan Kathy M, Mouncey Paul, Inwald David P, Protocolised Evaluation of Permissive Blood Pressure Targets Versus Usual Care (PRESSURE) Trial Investigators on behalf of the U.K. Paediatric Critical Care Society Study Group (PCCS-SG)

СтатьяПротокол клинического исследованияПеревод в очереди

Аннотация

OBJECTIVES

Management of hypotension is a fundamental part of pediatric critical care, with cardiovascular support in the form of fluids or vasoactive drugs offered to every hypotensive child. However, optimal blood pressure (BP) targets are unknown. The PRotocolised Evaluation of PermiSSive BP Targets Versus Usual CaRE (PRESSURE) trial aims to evaluate the clinical and cost-effectiveness of a permissive mean arterial pressure (MAP) target of greater than a fifth centile for age compared with usual care.

DESIGN

Pragmatic, open, multicenter, parallel-group randomized control trial (RCT) with integrated economic evaluation.

SETTING

Eighteen PICUs across the United Kingdom.

PATIENTS: Infants and children older than 37 weeks corrected gestational age to 16 years accepted to a participating PICU, on mechanical ventilation and receiving vasoactive drugs for hypotension.

INTERVENTIONS: Adjustment of hemodynamic support to achieve a permissive MAP target greater than fifth centile for age during invasive mechanical ventilation.

MEASUREMENTS AND MAIN

RESULTS

Randomization is 1:1 to a permissive MAP target or usual care, stratified by site and age group. Due to the emergency nature of the treatment, approaching patients for written informed consent will be deferred until after randomization. The primary clinical outcome is a composite of death and days of ventilatory support at 30 days. Baseline demographics and clinical status will be recorded as well as daily measures of BP and organ support, and discharge outcomes. This RCT received Health Research Authority approval (reference 289545), and a favorable ethical opinion from the East of England-Cambridge South Research Ethics Committee on May 10, 2021 (reference number 21/EE/0084). The trial is registered and has an International Standard RCT Number (reference 20609635).

CONCLUSIONS

Trial findings will be disseminated in U.K. national and international conferences and in peer-reviewed journals.

Для цитирования: Darnell Robert, Brown Alanna, Laing Emma, Edwards Julia, Harrison David A, Manning Joseph C, Peters Mark J, Ramnarayan Padmanabhan, Ray Samiran, Sadique Zia, Scholefield Barnaby R, Shortt Dermot, Lampro Lamprini, Au Carly, Rowan Kathy M, Mouncey Paul, Inwald David P, Protocolised Evaluation of Permissive Blood Pressure Targets Versus Usual Care (PRESSURE) Trial Investigators on behalf of the U.K. Paediatric Critical Care Society Study Group (PCCS-SG). Protocol for a Randomized Controlled Trial to Evaluate a Permissive Blood Pressure Target Versus Usual Care in Critically Ill Children with Hypotension (PRESSURE).. Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies. 2024. DOI: 10.1097/pcc.0000000000003516.

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