Time to start of cardiopulmonary resuscitation and the effect of target temperature management at 33°C and 36°C
Jazyk angličtina Země Irsko Médium print-electronic
Typ dokumentu časopisecké články, randomizované kontrolované studie, práce podpořená grantem
PubMed
26705972
DOI
10.1016/j.resuscitation.2015.10.013
PII: S0300-9572(15)00873-4
Knihovny.cz E-zdroje
- Klíčová slova
- Cardiac arrest, Neurological function, Targeted temperature management,
- MeSH
- časové faktory MeSH
- kardiopulmonální resuscitace metody MeSH
- lidé středního věku MeSH
- lidé MeSH
- senioři MeSH
- tělesná teplota * MeSH
- zástava srdce mimo nemocnici terapie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
INTRODUCTION: The optimal temperature during targeted temperature management (TTM) for comatose patients resuscitated from out-of-hospital cardiac arrest is unknown. It has been hypothesized that patients with long no-flow times, for example those without bystander CPR would have the most to gain from temperature management at lower temperatures. METHODS: We analysed data from an international clinical trial randomizing cardiac arrest patients to targeted temperature management at 33°C and 36°C for an interaction between no-flow time and intervention group, with neurological function at six months after cardiac arrest as the primary outcome. A cerebral performance category (CPC) score of 1 or 2 was considered a good outcome. RESULTS: No-flow time (min) was associated with poor neurological outcome (OR 1.13, 95% confidence interval 1.06-1.20, p<0.001). There was no statistically significant interaction between no flow-time and intervention group (p=0.11), which may imply that the non-superior effect of 33°C was consistent for all no-flow times. Bystander CPR was not independently associated with neurological function. CONCLUSIONS: TTM at 33°C compared to 36°C was not associated with an increased probability of a good neurological function for patients with longer no-flow times.
Adult Critical Care University Hospital of Wales Cardiff United Kingdom
Department of Anesthesiology Rikshospitalet Oslo University Hospital Oslo Norway
Department of Intensive Care Academic Medical Centre Amsterdam The Netherlands
Department of Intensive Care Geneva University Hospital Geneva Switzerland
Department of Intensive Care Leeuwarden Hospital Leeuwarden The Netherlands
Department of Intensive Care Liverpool Hospital Sydney NSW Australia
Department of Intensive Care Royal Berkshire Hospital Reading United Kingdom
Department of Intensive Care Santa Maria degli Ángeli Pordenone Italy
The Heart Centre Copenhagen University Hospital Rigshospitalet Copenhagen Denmark
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