Literature DB >> 21424827

Daily titration of neurally adjusted ventilatory assist using the diaphragm electrical activity.

Hadrien Rozé1, Abdelghani Lafrikh, Virginie Perrier, Arnaud Germain, Antoine Dewitte, Francis Gomez, Gérard Janvier, Alexandre Ouattara.   

Abstract

PURPOSE: To determine the feasibility of daily titration of the neurally adjusted ventilatory assist (NAVA) level in relation to the maximal diaphragmatic electrical activity (EAdi(maxSBT)) measured during a spontaneous breathing trial (SBT) during pressure support ventilation (PSV).
METHODS: The study included 15 consecutive patients in whom mechanical ventilation weaning was initiated with the NAVA mode. EAdi(maxSBT) was determined daily during an SBT using PSV with 7 cmH2O of inspiratory pressure and no positive end-expiratory pressure (PEEP). If the SBT was unsuccessful, NAVA was used and the level was then adjusted to obtain an EAdi of ~60% of the EAdi(maxSBT). Arterial blood gas analyses were performed 20 min after each change in NAVA level.
RESULTS: Three patients were dropped from the study at day 4 because of worsening of their sickness. The median duration of NAVA ventilation was 4.5 days (IQR 3-6.5). From day 1 to extubation, EAdi(maxSBT) and EAdi increased significantly from 16.6 (9.6) to 21.7 (10.3) μV (P = 0.013) and from 10.0 (5.5) to 15.1 (9.2) μV (P = 0.026), respectively. The pressure delivered significantly decreased from 20 (8) to 10 (5) cmH2O (P = 0.003). Conversely, tidal volume, carbon dioxide tension, and pH values remained unchanged during the same period.
CONCLUSION: These results suggest that daily titration of NAVA level with an electrical goal of ~60% EAdi(maxSBT) is feasible and well tolerated. The respiratory mechanics improvement and increase in respiratory drive allowed for a daily reduction of the NAVA level while preserving breathing, oxygenation, and alveolar ventilation until extubation.

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Year:  2011        PMID: 21424827     DOI: 10.1007/s00134-011-2209-1

Source DB:  PubMed          Journal:  Intensive Care Med        ISSN: 0342-4642            Impact factor:   17.440


  24 in total

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2.  Neurally adjusted ventilatory assist improves patient-ventilator interaction.

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4.  Neurally adjusted ventilatory assist increases respiratory variability and complexity in acute respiratory failure.

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Authors:  J-M Boles; J Bion; A Connors; M Herridge; B Marsh; C Melot; R Pearl; H Silverman; M Stanchina; A Vieillard-Baron; T Welte
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7.  Patient-ventilator interaction during pressure support ventilation and neurally adjusted ventilatory assist.

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8.  Titration and implementation of neurally adjusted ventilatory assist in critically ill patients.

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Authors:  Timothy D Girard; John P Kress; Barry D Fuchs; Jason W W Thomason; William D Schweickert; Brenda T Pun; Darren B Taichman; Jan G Dunn; Anne S Pohlman; Paul A Kinniry; James C Jackson; Angelo E Canonico; Richard W Light; Ayumi K Shintani; Jennifer L Thompson; Sharon M Gordon; Jesse B Hall; Robert S Dittus; Gordon R Bernard; E Wesley Ely
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  15 in total

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2.  Respiratory pattern during neurally adjusted ventilatory assist in acute respiratory failure patients.

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3.  Evolution of inspiratory diaphragm activity in children over the course of the PICU stay.

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6.  Impact of prolonged assisted ventilation on diaphragmatic efficiency: NAVA versus PSV.

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Review 7.  Respiratory drive in the acute respiratory distress syndrome: pathophysiology, monitoring, and therapeutic interventions.

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8.  Patient-ventilator synchrony in Neurally Adjusted Ventilatory Assist (NAVA) and Pressure Support Ventilation (PSV): a prospective observational study.

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9.  Effects of Neurally Adjusted Ventilatory Assist (NAVA) levels in non-invasive ventilated patients: titrating NAVA levels with electric diaphragmatic activity and tidal volume matching.

Authors:  Yeong Shiong Chiew; J Geoffrey Chase; Bernard Lambermont; Jean Roeseler; Christopher Pretty; Emilie Bialais; Thierry Sottiaux; Thomas Desaive
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10.  Neurally Adjusted Ventilatory Assist (NAVA) or Pressure Support Ventilation (PSV) during spontaneous breathing trials in critically ill patients: a crossover trial.

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