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Development and preclinical testing of an adaptive algorithm for automated control of inspired oxygen in the preterm infant.
Dargaville, Peter A; Sadeghi Fathabadi, Omid; Plottier, Gemma K; Lim, Kathleen; Wheeler, Kevin I; Jayakar, Rohan; Gale, Timothy J.
Afiliação
  • Dargaville PA; Neonatal Respiratory Group, Menzies Institute for Medical Research, University of Tasmania, Hobart, Tasmania, Australia.
  • Sadeghi Fathabadi O; Department of Paediatrics, Royal Hobart Hospital, Hobart, Tasmania, Australia.
  • Plottier GK; School of Engineering and ICT, University of Tasmania, Hobart, Tasmania, Australia.
  • Lim K; Department of Paediatrics, Royal Hobart Hospital, Hobart, Tasmania, Australia.
  • Wheeler KI; School of Medicine, University of Tasmania, Hobart, Tasmania, Australia.
  • Jayakar R; Department of Paediatrics, Royal Hobart Hospital, Hobart, Tasmania, Australia.
  • Gale TJ; Neonatal Unit, Royal Children's Hospital, Melbourne, Victoria, Australia.
Arch Dis Child Fetal Neonatal Ed ; 102(1): F31-F36, 2017 Jan.
Article em En | MEDLINE | ID: mdl-27634820
ABSTRACT

OBJECTIVE:

To assess the performance of a novel algorithm for automated oxygen control using a simulation of oxygenation founded on in vivo data from preterm infants.

METHODS:

A proportional-integral-derivative (PID) control algorithm was enhanced by (i) compensation for the non-linear SpO2-PaO2 relationship, (ii) adaptation to the severity of lung dysfunction and (iii) error attenuation within the target range. Algorithm function with and without enhancements was evaluated by iterative linking with a computerised simulation of oxygenation. Data for this simulation (FiO2 and SpO2 at 1 Hz) were sourced from extant recordings from preterm infants (n=16), and converted to a datastream of values for ventilationperfusion ratio and shunt. Combination of this datastream second by second with the FiO2 values from the algorithm under test produced a sequence of novel SpO2 values, allowing time in the SpO2 target range (91%-95%) and in various degrees of hypoxaemia and hyperoxaemia to be determined. A PID algorithm with 30 s lockout after each FiO2 adjustment, and a proportional-derivative (PD) algorithm were also evaluated.

RESULTS:

Separate addition of each enhancing feature to the PID algorithm showed a benefit, but not with uniformly positive effects. The fully enhanced algorithm was optimal for the combination of targeting the desired SpO2 range and avoiding time in, and episodes of, hypoxaemia and hyperoxaemia. This algorithm performed better than one with a 30 s lockout, and considerably better than PD control.

CONCLUSIONS:

An enhanced PID algorithm was very effective for automated oxygen control in a simulation of oxygenation, and deserves clinical evaluation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oxigênio / Oxigenoterapia / Respiração Artificial / Automação / Algoritmos / Recém-Nascido Prematuro / Doenças do Prematuro Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male / Newborn Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oxigênio / Oxigenoterapia / Respiração Artificial / Automação / Algoritmos / Recém-Nascido Prematuro / Doenças do Prematuro Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male / Newborn Idioma: En Ano de publicação: 2017 Tipo de documento: Article