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Transnasal Humidified Rapid Insufflation Ventilatory Exchange in children requiring emergent intubation (Kids THRIVE): a protocol for a randomised controlled trial.
George, Shane; Humphreys, Susan; Williams, Tara; Gelbart, Ben; Chavan, Arjun; Rasmussen, Katie; Ganeshalingham, Anusha; Erickson, Simon; Ganu, Subodh Suhas; Singhal, Nitesh; Foster, Kelly; Gannon, Brenda; Gibbons, Kristen; Schlapbach, Luregn J; Festa, Marino; Dalziel, Stuart; Schibler, Andreas.
Afiliação
  • George S; Children's Critical Care Service, Gold Coast University Hospital, Southport, Queensland, Australia.
  • Humphreys S; School of Medicine, Griffith University, Southport, Queensland, Australia.
  • Williams T; Paediatric Critical Care Research Group (PCCRG), Queensland Children's Hospital and The University of Queensland, Brisbane, Queensland, Australia.
  • Gelbart B; Paediatric Research in Emergency Departments International Collaborative (PREDICT), Parkville, Victoria, Australia.
  • Chavan A; Paediatric Study Group, Australia and New Zealand Intensive Care Society (ANZICS PSG), Melbourne, Victoria, Australia.
  • Rasmussen K; Paediatric Critical Care Research Group (PCCRG), Queensland Children's Hospital and The University of Queensland, Brisbane, Queensland, Australia.
  • Ganeshalingham A; Paediatric Critical Care Research Group (PCCRG), Queensland Children's Hospital and The University of Queensland, Brisbane, Queensland, Australia.
  • Erickson S; Paediatric Intensive Care Unit, Royal Children's Hospital Melbourne, Parkville, Victoria, Australia.
  • Ganu SS; Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Singhal N; Paediatric Intensive Care Unit, The Townsville Hospital, Townsville, Queensland, Australia.
  • Foster K; Critical Care Division, Queensland Children's Hospital, Brisbane, Queensland, Australia.
  • Gannon B; Paediatric Emergency Research Unit, Centre for Children's Health Research, Children's Health Queensland, Brisbane, Queensland, Australia.
  • Gibbons K; Starship Children's Hospital, Auckland, Auckland, New Zealand.
  • Schlapbach LJ; Paediatric Critical Care, Perth Children's Hospital, Perth, Western Australia, Australia.
  • Festa M; Department of Paediatric Critical Care Medicine, Women's and Children's Hospital, North Adelaide, South Australia, Australia.
  • Dalziel S; Paediatric Intensive Care Unit, Royal Alexandra Hospital for Children, Westmead, New South Wales, Australia.
  • Schibler A; Paediatric Research in Emergency Departments International Collaborative (PREDICT), Parkville, Victoria, Australia.
BMJ Open ; 9(2): e025997, 2019 02 20.
Article em En | MEDLINE | ID: mdl-30787094
INTRODUCTION: Emergency intubation of children with abnormal respiratory or cardiac physiology is a high-risk procedure and associated with a high incidence of adverse events including hypoxemia. Successful emergency intubation is dependent on inter-related patient and operator factors. Preoxygenation has been used to maximise oxygen reserves in the patient and to prolong the safe apnoeic time during the intubation phase. Transnasal Humidified Rapid Insufflation Ventilatory Exchange (THRIVE) prolongs the safe apnoeic window for a safe intubation during elective intubation. We designed a clinical trial to test the hypothesis that THRIVE reduces the frequency of adverse and hypoxemic events during emergency intubation in children and to test the hypothesis that this treatment is cost-effective compared with standard care. METHODS AND ANALYSIS: The Kids THRIVE trial is a multicentre randomised controlled trial performed in participating emergency departments and paediatric intensive care units. 960 infants and children aged 0-16 years requiring emergency intubation for all reasons will be enrolled and allocated to THRIVE or control in a 1:1 allocation with stratification by site, age (<1, 1-7 and >7 years) and operator (junior and senior). Children allocated to THRIVE will receive weight appropriate transnasal flow rates with 100% oxygen, whereas children in the control arm will not receive any transnasal oxygen insufflation. The primary outcomes are defined as follows: (1) hypoxemic event during the intubation phase defined as SpO2 <90% (patient-dependent variable) and (2) first intubation attempt success without hypoxemia (operator-dependent variable). Analyses will be conducted on an intention-to-treat basis. ETHICS AND DISSEMINATION: Ethics approval for the protocol and consent process has been obtained (HREC/16/QRCH/81). The trial has been actively recruiting since May 2017. The study findings will be submitted for publication in a peer-reviewed journal. TRIAL REGISTRATION NUMBER: ACTRN12617000147381.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxigenoterapia / Apneia / Insuflação / Manuseio das Vias Aéreas Tipo de estudo: Clinical_trials / Guideline Aspecto: Ethics Limite: Child / Humans Idioma: En Revista: BMJ Open Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Austrália País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxigenoterapia / Apneia / Insuflação / Manuseio das Vias Aéreas Tipo de estudo: Clinical_trials / Guideline Aspecto: Ethics Limite: Child / Humans Idioma: En Revista: BMJ Open Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Austrália País de publicação: Reino Unido