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Scandinavian clinical practice guideline on mechanical ventilation in adults with the acute respiratory distress syndrome
Claesson, J; Freundlich, M; Gunnarsson, I; Laake, J. H; Vandvik, P. O; Varpula, T; Aasmundstad, T. A.
Affiliation
  • Claesson, J; Umeå University Hospital. Department of Intensive Care. Surgical Division. Umeå, Sweden. SE
  • Freundlich, M; Aalborg University Hospital. Clinic for Anaesthesiology. Aalborg. DK
  • Gunnarsson, I; Landspitali University Hospital. Department of Anaesthesiology and Intensive Care Medicine. Reykjaviki. IS
  • Laake, J. H; Oslo University Hospital. Department of Anaesthesiology. Division of Critical Care. Oslo. NO
  • Vandvik, P. O; Innlandet Hospital Trust. Department of Medicine. Division Gjøvik. NO
  • Varpula, T; Helsinki University Hospital. Department of Intensive Care Medicine. Helsinki. FI
  • Aasmundstad, T. A; Oslo University Hospital. Department of Anaesthesiology. Division of Critical Care. Oslo. NO
Acta anaesthesiol. scand ; 59(3)Mar. 2015. tab
Article in English | BIGG - GRADE guidelines | ID: biblio-965786
Responsible library: BR1.1
ABSTRACT

BACKGROUND:

The objective of the Scandinavian Society of Anaesthesiology and Intensive Care Medicine (SSAI) task force on mechanical ventilation in adults with the acute respiratory distress syndrome (ARDS) is to formulate treatment recommendations based on available evidence from systematic reviews and randomised trials.

METHODS:

This guideline was developed according to standards for trustworthy guidelines through a systematic review of the literature and the use of the Grading of Recommendations Assessment, Development and Evaluation system for assessment of the quality of evidence and for moving from evidence to recommendations in a systematic and transparent process.

RESULTS:

We found evidence of moderately high quality to support a strong recommendation for pressure limitation and small tidal volumes in patients with ARDS. Also, we suggest positive end-expiratory pressure (PEEP) > 5 cm H2O in moderate to severe ARDS and prone ventilation 16/24 h for the first week in moderate to severe ARDS (weak recommendation, low quality evidence). Volume controlled ventilation or pressure control may be equally beneficial or harmful and partial modes of ventilatory support may be used if clinically feasible (weak recommendation, very low quality evidence). We suggest utilising recruitment manoeuvres as a rescue measure in catastrophic hypoxaemia only (weak recommendation, low quality evidence). Based on high-quality evidence, we strongly recommend not to use high-frequency oscillatory ventilation. We could find no relevant data from randomised trials to guide decisions on choice of FiO2 or utilisation of non-invasive ventilation.

CONCLUSION:

We strongly recommend pressure- and volume limitation and suggest using higher PEEP and prone ventilation in patients with severe respiratory failure.(AU)
Subject(s)

Full text: Available Collection: Tematic databases Database: BIGG - GRADE guidelines Main subject: Respiration, Artificial / Respiratory Distress Syndrome, Newborn / High-Frequency Ventilation Type of study: Controlled clinical trial / Practice guideline / Prognostic study Language: English Journal: Acta anaesthesiol. scand Year: 2015 Document type: Article Institution/Affiliation country: Aalborg University Hospital/DK / Helsinki University Hospital/FI / Innlandet Hospital Trust/NO / Landspitali University Hospital/IS / Oslo University Hospital/NO / Umeå University Hospital/SE

Full text: Available Collection: Tematic databases Database: BIGG - GRADE guidelines Main subject: Respiration, Artificial / Respiratory Distress Syndrome, Newborn / High-Frequency Ventilation Type of study: Controlled clinical trial / Practice guideline / Prognostic study Language: English Journal: Acta anaesthesiol. scand Year: 2015 Document type: Article Institution/Affiliation country: Aalborg University Hospital/DK / Helsinki University Hospital/FI / Innlandet Hospital Trust/NO / Landspitali University Hospital/IS / Oslo University Hospital/NO / Umeå University Hospital/SE
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