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Transnasal humidified rapid insufflation ventilatory exchange for oxygenation of children during apnoea: a prospective randomised controlled trial.
Riva, T; Pedersen, T H; Seiler, S; Kasper, N; Theiler, L; Greif, R; Kleine-Brueggeney, M.
Afiliación
  • Riva T; Department of Anaesthesiology & Pain Therapy, Bern University Hospital, Inselspital, Freiburgstrasse 8, 3010 Bern, Switzerland.
  • Pedersen TH; Department of Anaesthesiology & Pain Therapy, Bern University Hospital, Inselspital, Freiburgstrasse 8, 3010 Bern, Switzerland. Electronic address: tinaheidipedersen@yahoo.dk.
  • Seiler S; Department of Anaesthesiology & Pain Therapy, Bern University Hospital, Inselspital, Freiburgstrasse 8, 3010 Bern, Switzerland.
  • Kasper N; Department of Anaesthesiology & Pain Therapy, Bern University Hospital, Inselspital, Freiburgstrasse 8, 3010 Bern, Switzerland.
  • Theiler L; Department of Anaesthesiology & Pain Therapy, Bern University Hospital, Inselspital, Freiburgstrasse 8, 3010 Bern, Switzerland.
  • Greif R; Department of Anaesthesiology & Pain Therapy, Bern University Hospital, Inselspital, Freiburgstrasse 8, 3010 Bern, Switzerland.
  • Kleine-Brueggeney M; Department of Anaesthesiology & Pain Therapy, Bern University Hospital, Inselspital, Freiburgstrasse 8, 3010 Bern, Switzerland; Department of Anaesthesia, Evelina London Children's Hospital, Guy's and St. Thomas' NHS Foundation Trust, London, UK.
Br J Anaesth ; 120(3): 592-599, 2018 Mar.
Article en En | MEDLINE | ID: mdl-29452816
ABSTRACT

BACKGROUND:

Transnasal humidified rapid insufflation ventilatory exchange (THRIVE) comprises the administration of heated, humidified, and blended air/oxygen mixtures via nasal cannula at rates of ≥2 litres kg-1 min-1. The aim of this randomized controlled study was to evaluate the length of the safe apnoea time using THRIVE with two different oxygen concentrations (100% vs 30% oxygen) compared with standard low-flow 100% oxygen administration.

METHODS:

Sixty patients, aged 1-6 yr, weighing 10-20 kg, undergoing general anaesthesia for elective surgery, were randomly allocated to receive one of the following oxygen administration methods during apnoea 1) low-flow 100% oxygen at 0.2 litres kg-1 min-1; 2) THRIVE 100% oxygen at 2 litres kg-1 min-1; and 3) THRIVE 30% oxygen at 2 litres kg-1 min-1. Primary outcome was time to desaturation to 95%. Termination criteria included SpO2 decreased to 95%, transcutaneous CO2 increased to 65 mmHg, or apnoea time of 10 min.

RESULTS:

The median (interquartile range) [range] apnoea time was 6.9 (5.7-7.8) [2.8-10.0] min for low-flow 100% oxygen, 7.6 (6.2-9.1) [5.2-10.0] min for THRIVE 100% oxygen, and 3.0 (2.4-3.7) [0.2-5.3] min for THRIVE 30% oxygen. No significant difference was detected between apnoea times with low-flow and THRIVE 100% oxygen administration (P=0.15). THRIVE with 30% oxygen demonstrated significantly shorter apnoea times (P<0.001) than both 100% oxygen modalities. The overall rate of transcutaneous CO2 increase was 0.57 (0.49-0.63) [0.29-8.92] kPa min-1 without differences between the 3 groups (P=0.25).

CONCLUSIONS:

High-flow 100% oxygen (2 litres kg-1 min-1) administered via nasal cannulas did not extend the safe apnoea time for children weighing 10-20 kg compared with low-flow nasal cannula oxygen (0.2 litres kg-1 min-1). No ventilatory effect was observed with THRIVE at 2.0 litres kg-1 min-1. CLINICAL TRIAL REGISTRATION NCT02979067.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Terapia por Inhalación de Oxígeno / Apnea / Insuflación Tipo de estudio: Clinical_trials / Observational_studies Límite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Terapia por Inhalación de Oxígeno / Apnea / Insuflación Tipo de estudio: Clinical_trials / Observational_studies Límite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Año: 2018 Tipo del documento: Article