The Cochrane database of systematic reviews

Automated versus manual breathing support weaning to shorten ventilation time in critically ill adults and children

Updated

Abstract

Automated closed loop systems reduced the geometric mean duration of weaning by 30%.

  • Automated systems may decrease the overall duration of ventilation by 10%.
  • Length of stay in the intensive care unit may be reduced by 8% with automated systems.
  • Mixed or medical ICU populations experienced a greater reduction in weaning duration of 42%.
  • Automated systems may lower the risk of prolonged mechanical ventilation (> 21 days) and the need for tracheostomy.
  • There was no strong evidence indicating an effect on mortality rates or hospital length of stay.

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Full Text

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Funding

Competing interests

Bronagh Blackwood, Chris R Cardwell, Danny F McAuley: none known. Louise Rose has completed an RCT comparing automated weaning using SmartCare/PS™ with usual care that was included in this systematic review. Dr Rose received no funding from Draeger Medical for this study. SmartCare/PS software, and associated technical upgrades for two ventilators, were provided free of charge to the Intensive Care Unit of The Royal Melbourne Hospital by Draeger Medical, Australia. Marcus J Schultz received a research fund of EUR 12,000 for a study on weaning with ASV by Hamilton Medical, Switzerland. Hamilton Medical provided Professor Schultz's hospital research group with EUR 12,000 for performing a study of weaning with ASV in cardiac surgical patients. The money was used to buy equipment, a computer, statistician time, and to cover costs involved with the presentation of the results at a scientific meeting and publication of an article. Philippe Jouvet has completed an RCT comparing automated weaning using SmartCare/PS™ with usual care, included in this systematic review. Dr Jouvet did not receive any funding from Draeger for this study though, for the purposes of the study, Draeger Medical provided one ventilator. Dr Jouvet received two grants as support from Hamilton Medical for two clinical studies, including a prospective trial on automation of weaning with ASV in children (NCT01095406) and a clinical study on criteria for mechanical ventilation adjustments in children. These two studies were not eligible for inclusion in the systematic review. Dr Jouvet also conducted a clinical trial on weaning with NAVA in infants (NCT00603174) that was not eligible for inclusion in the systematic review. Dr Jouvet did not receive any funding from Maquet for this study though, for the purposes of the study, Maquet provided one ventilator.
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