Publication: Transnasal humidified rapid insufflation ventilatory exchange for oxygenation of children during apnoea: a prospective randomised controlled trial.
cris.virtual.author-orcid | 0000-0003-0160-2073 | |
cris.virtualsource.author-orcid | fdb89231-ae93-44c3-883b-e935477637a2 | |
cris.virtualsource.author-orcid | 7bda0f28-8f88-4e8d-ac3a-2bf06e9e3d3c | |
cris.virtualsource.author-orcid | d46ddc6f-681c-44bc-bb9f-814c5539d2ed | |
cris.virtualsource.author-orcid | f58b9e1d-82f4-4d4f-ae01-23be2c56211e | |
cris.virtualsource.author-orcid | 58a5f25a-95b8-4367-9219-cb7fdf2fc922 | |
cris.virtualsource.author-orcid | 3e5f9518-08b5-4b2c-8b0f-3b03d7aad0bb | |
cris.virtualsource.author-orcid | 07bf9ea1-8ad5-485d-a1a1-bad09dfb5e7e | |
datacite.rights | restricted | |
dc.contributor.author | Riva, Thomas | |
dc.contributor.author | Pedersen, Tina Heidi | |
dc.contributor.author | Seiler, Stefan Jürg | |
dc.contributor.author | Kasper, Nina Elisabeth | |
dc.contributor.author | Theiler, Lorenz | |
dc.contributor.author | Greif, Robert | |
dc.contributor.author | Kleine-Brüggeney, Maren | |
dc.date.accessioned | 2024-10-25T14:08:05Z | |
dc.date.available | 2024-10-25T14:08:05Z | |
dc.date.issued | 2018-03 | |
dc.description.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 min. 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 min; 2) THRIVE 100% oxygen at 2 litres kg min; and 3) THRIVE 30% oxygen at 2 litres kg min. Primary outcome was time to desaturation to 95%. Termination criteria included SpOdecreased to 95%, transcutaneous COincreased 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 COincrease was 0.57 (0.49-0.63) [0.29-8.92] kPa minwithout differences between the 3 groups (P=0.25). CONCLUSIONS High-flow 100% oxygen (2 litres kg min) 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 min). No ventilatory effect was observed with THRIVE at 2.0 litres kg min. CLINICAL TRIAL REGISTRATION NCT02979067. | |
dc.description.numberOfPages | 8 | |
dc.description.sponsorship | Universitätsklinik für Anästhesiologie und Schmerztherapie | |
dc.identifier.doi | 10.7892/boris.112644 | |
dc.identifier.pmid | 29452816 | |
dc.identifier.publisherDOI | 10.1016/j.bja.2017.12.017 | |
dc.identifier.uri | https://boris-portal.unibe.ch/handle/20.500.12422/159227 | |
dc.language.iso | en | |
dc.publisher | Elsevier | |
dc.relation.ispartof | British journal of anaesthesia | |
dc.relation.issn | 0007-0912 | |
dc.relation.organization | DCD5A442BADCE17DE0405C82790C4DE2 | |
dc.subject | THRIVE apnoeic oxygenation high-flow nasal cannula oxygen paediatric anaesthesia safe apnoea time | |
dc.subject.ddc | 600 - Technology::610 - Medicine & health | |
dc.title | Transnasal humidified rapid insufflation ventilatory exchange for oxygenation of children during apnoea: a prospective randomised controlled trial. | |
dc.type | article | |
dspace.entity.type | Publication | |
dspace.file.type | text | |
oaire.citation.endPage | 599 | |
oaire.citation.issue | 3 | |
oaire.citation.startPage | 592 | |
oaire.citation.volume | 120 | |
oairecerif.author.affiliation | Universitätsklinik für Anästhesiologie und Schmerztherapie | |
oairecerif.author.affiliation | Universitätsklinik für Anästhesiologie und Schmerztherapie | |
oairecerif.author.affiliation | Universitätsklinik für Anästhesiologie und Schmerztherapie | |
oairecerif.author.affiliation | Universitätsklinik für Anästhesiologie und Schmerztherapie | |
oairecerif.author.affiliation | Universitätsklinik für Anästhesiologie und Schmerztherapie | |
oairecerif.author.affiliation | Universitätsklinik für Anästhesiologie und Schmerztherapie | |
oairecerif.author.affiliation | Universitätsklinik für Anästhesiologie und Schmerztherapie | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.date.licenseChanged | 2019-11-03 14:01:01 | |
unibe.description.ispublished | pub | |
unibe.eprints.legacyId | 112644 | |
unibe.journal.abbrevTitle | BRIT J ANAESTH | |
unibe.refereed | true | |
unibe.subtype.article | journal |
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