dc.contributor.author
Kirkegaard, Hans
dc.contributor.author
Rasmussen, Bodil S.
dc.contributor.author
de Haas, Inge
dc.contributor.author
Nielsen, Jorgen Feldbaek
dc.contributor.author
Ilkjaer, Susanne
dc.contributor.author
Kaltoft, Anne
dc.contributor.author
Jeppesen, Anni Norregaard
dc.contributor.author
Grejs, Anders
dc.contributor.author
Duez, Christophe Henri Valdemar
dc.contributor.author
Larsen, Alf Inge
dc.contributor.author
Pettila, Ville
dc.contributor.author
Toome, Valdo
dc.contributor.author
Arus, Urmet
dc.contributor.author
Taccone, Fabio Silvio
dc.contributor.author
Storm, Christian
dc.contributor.author
Skrifvars, Markus B.
dc.contributor.author
Soreide, Eldar
dc.date.accessioned
2018-06-08T04:13:33Z
dc.date.available
2016-05-30T08:31:50.908Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/16847
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-21028
dc.description.abstract
Background The application of therapeutic hypothermia (TH) for 12 to 24 hours
following out-of-hospital cardiac arrest (OHCA) has been associated with
decreased mortality and improved neurological function. However, the optimal
duration of cooling is not known. We aimed to investigate whether targeted
temperature management (TTM) at 33 ± 1 °C for 48 hours compared to 24 hours
results in a better long-term neurological outcome. Methods The TTH48 trial is
an investigator-initiated pragmatic international trial in which patients
resuscitated from OHCA are randomised to TTM at 33 ± 1 °C for either 24 or 48
hours. Inclusion criteria are: age older than 17 and below 80 years; presumed
cardiac origin of arrest; and Glasgow Coma Score (GCS) <8, on admission. The
primary outcome is neurological outcome at 6 months using the Cerebral
Performance Category score (CPC) by an assessor blinded to treatment
allocation and dichotomised to good (CPC 1–2) or poor (CPC 3–5) outcome.
Secondary outcomes are: 6-month mortality, incidence of infection, bleeding
and organ failure and CPC at hospital discharge, at day 28 and at day 90
following OHCA. Assuming that 50 % of the patients treated for 24 hours will
have a poor outcome at 6 months, a study including 350 patients (175/arm) will
have 80 % power (with a significance level of 5 %) to detect an absolute 15 %
difference in primary outcome between treatment groups. A safety interim
analysis was performed after the inclusion of 175 patients. Discussion This is
the first randomised trial to investigate the effect of the duration of TTM at
33 ± 1 °C in adult OHCA patients. We anticipate that the results of this trial
will add significant knowledge regarding the management of cooling procedures
in OHCA patients.
en
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
Out-of-hospital cardiac arrest
dc.subject
Target temperature management
dc.subject
Mild therapeutic hypothermia
dc.subject
Prolonged target temperature management
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit
dc.title
Time-differentiated target temperature management after out-of-hospital
cardiac arrest
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Trials. - 17 (2016), Artikel Nr. 228
dc.title.subtitle
a multicentre, randomised, parallel-group, assessor-blinded clinical trial
(the TTH48 trial): study protocol for a randomised controlled trial
dcterms.bibliographicCitation.doi
10.1186/s13063-016-1338-9
dcterms.bibliographicCitation.url
http://trialsjournal.biomedcentral.com/articles/10.1186/s13063-016-1338-9
refubium.affiliation
Charité - Universitätsmedizin Berlin
de
refubium.mycore.fudocsId
FUDOCS_document_000000024628
refubium.note.author
Der Artike wurde in einer Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000006474
dcterms.accessRights.openaire
open access