Journal Club American Journal of Respiratory and Critical Care Medicine. Zhang Junyi

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Transcription:

Journal Club 2018 American Journal of Respiratory and Critical Care Medicine Zhang Junyi 2018.11.23

Background Mechanical Ventilation A life-saving technique used worldwide 15 million patients annually 30% patients required prolonged mechanical weaning Prolonged mechanical ventilation is associated with an increased risk of death, poor long term functional outcomes and markedly higher healthcare costs Mortality starts to increase after the first unsuccessful separation attempt Am J Respir Crit Care Med, 2017; 195(6

Background Diaphragm weakness is a leading cause of difficult weaning from mechanical ventilation. Diaphragm dysfunction is independently associated with weaning failure Am J Respir Crit Care Med. 2017; 195(1):57-66.

Background Mechanical ventilation per se can cause acute diaphragm injury and weakness medications Mechanical Ventilation shock Diaphragm Injury neuromyopathy sepsi s Diaphragm weakness electrolyte imbalancd Am J Respir Crit Care Med. 2013; 188(2

Background diaphragm muscle thickness changes over time during ventilation Changes in diaphragm thickness (increases and decreases) occurred predominantly during the early course of ventilation and rapid early decreases in diaphragm thickness were observed during both controlled ventilation and partially assisted ventilation Am J Respir Crit Care Med. 2015; 192( 9): 1080 1

Background Ventilatory assistance suppressing inspiratory effort results in rapid diaphragm atrophy fully controlled mode short-term group: patients anesthetized and supported with MV for 2 3 hours during thoracic surgery for localized lung cancers; long-term group: patients with brain death destined for organ donation, who had received MV for at least 24 hours before organ harvest. Am J Respir Crit Care Med,2011;183

Background Insufficient ventilatory support: load-induced diaphragmatic inflammation and The origin of the augmented level of these cytokines(il-6, IL-10, eotaxin, and EGF) during AECOPD could partly be the strenuously contracting respiratory muscles and/or the mechanically stressed lung. Am J Respir Crit Care Med. 2016

Background Excessive or inadequate ventilatory support that may impair muscle function (VIDD). muscle-protective ventilation strategies High Inspiratory Effort Low Inspiratory Effort diaphragm thickening fraction(tfdi a surrogate measure of inspiratory ef Am J Respir Crit Care Med. 2015; 192( 9): 1080 1

Am J Respir Crit Care Med.2013;188(2):213 219 Background The specific effect of diaphragm atrophy and injury caused by ventilation on clinical outcomes remains unknown. two-thirds of ventilated patients exhibit diaphragm weakness at the time of ICU admission before any effect of mechanical ventilation Diaphragm dysfunction on intensive care unit admission is frequent and is related to sepsis and the severity of the ongoing disease. Diaphragm dysfunction is associated with a poorer prognosis but not with a longer duration of mechanical ventilation.

Objectives To establish the impact of diaphragm injury resulting from ventilation on clinical outcomes. Evaluate the effect of both decreases and increases in T di on the risk of prolonged ventilator dependence. Examine whether mean thickening fraction over the first 3 days of ventilation predicted the duration of ventilation, hypothesizing a priori that the duration of ventilation would be lowest at an intermediate level

Methods- Study Population and Setting

Methods- Inclusion and Exclusion Criteria for the Research Protocols

Methods- Measurement Techniques Technique for measuring diaphragm thickness and thickening fraction by ultra right hemidiaphragm : using a high frequency (13 MHz) linear array transducer placed in the 9 th or 10 th intercostal space between the anterior and midaxillary lines in the zone of apposition location was marked : enhance day-to-day measurement consistency TFdi = (Tdi, ei Tdi, ee) / Tdi, ee (TFdi = diaphragm thickening fraction during inspiration, Tdi,ei = end-inspiratory diaphragm thickness, Tdi,ee = end-expiratory diaphragm thickness ) : Measurements were repeated and averaged over several consecutive breaths. Observers: competence was demonstrated by achieving agreement within 0.1 mm on 15 consecutive ultrasound examinations.

Methods- Measurement Techniques Diaphragm electrical activity monitoring protocol Upon enrollment, a nasogastric catheter fitted multiple-array electrodes to acquire crural diaphragm electromyograms (EMG) was placed. Airway pressure (Paw), flow and EAdi were recorded in real time. ΔEAdi and ΔPaw were averaged across all mechanical or spontaneous breaths for each 5-minute recording.

Methods- Measurement Techniques Diaphragm function measurement protocol achieve maximal inspiratory effort transient reduction of ventilator setting, coached inspiratory effort, transient occlusion of the endotracheal tube if necessary TF di, max was measured after 1 week of mechanical ventilation: 1 once the patient was awake and breathing spontaneously 2 in CPAP mode 3 The highest value obtained for TFdi, max during repeated measurements was taken as the measurement of muscle function. TF di, max was measured on the day of extubation 1 If the patient was extubated before 1 week of ventilation was completed 2 either before or immediately after extubation

Methods-Patient Characteristics and Clinical Outcomes Demographic data, comorbidities, admission diagnosis, and severity of were collected at baseline. Ventilator settings, arterial blood gas tensions, criteria for sepsis, Riker Sedation-Agitation Scale (SAS), exposure to neuromuscular blockade, and Sequential Organ Failure Assessment (SOFA) scores were recorded daily.

Methods-Patient Characteristics and Clinical Outcomes Primary outcome Secondary outcome Time to final disconnection from mechanical ventilation (due to liberation or death) Survival status at time of final disconnection from mechanical ventilation (alive or dead) Survival status at time of hospital discharge Survival status at day 60 Ventilator-free days to day 60 Reintubation Tracheostomy Prolonged ventilator-dependence (time to liberation > 14 days) Complications of respiratory failure (composite of at least one of reintubation, tracheostomy, time to liberation > 14 days, death in hospital) Time to ICU discharge Time to hospital discharge

Statistical Analysis The primary analysis (time-varying exposure approach) - Primary outcome: relative hazard of liberation from mechanical ventilation Assess the relationship between T di (expressed as a percentage of baseline T di ) on any given day and the hazard of liberation from mechanical ventilation on that day. This time-varying covariate model was constructed by splitting the interval between each diaphragm thickness ultrasound measurement into separate intervals (n=928 intervals). The percentage change in T di from baseline was computed for each interval. We then restricted the intervals under analysis to those where patients were at risk of liberation (i.e. where ventilator settings were low enough such that patients where the decision to extubated was at least possible: PEEP 10 cm H 2 O and FiO2 0.5), yielding 646 intervals.

Statistical Analysis The secondary analysis ( classification based approach) - Secondary outcomes and change in diaphragm thickness Three groups of classification: >10% decrease <10% change >10% increase Differences in groups: bivariate Poisson regression logistic regression The day on which the patient was classified was recorded. This approach was employed in order to classify patients according to the earliest changes in diaphragm thickness following initiation of ventilation while permitting some flexibility in the timing of the development of these changes. To estimate the absolute risk of remaining ventilator-dependent at 21 days, we computed cumulative incidence functions for liberation from mechanical ventilation and the competing risk of death

Statistical Analysis Determinants of change in diaphragm thickness - Impact of Inspiratory Inspiratory effort diaphragm thickening fraction hourly mean diaphragm electrical activity mode of ventilation (control, assisted) applied driving pressure (i.e. peak pressure PEEP) in partially assisted mode The effect of inspiratory effort on the change in thickness over time was modelled using an interaction term for the covariate of interest and time. All statistical analyses were conducted using R version 3

Results Study cohort

Results Changes in Diaphragm Thickness and Clinical Outcomes

Results Changes in Diaphragm Thickness and Clinical Outcomes

Results Changes in Diaphragm Thickness and Clinical Outcomes

Results Reasons for missing measurements of maximal diaphragm thickening fraction.

Results Changes in Diaphragm Thickness and Diaphragm Function weakness frequently

Results Inspiratory Effort and Changes in Diaphragm Thickness

Results Inspiratory Effort and Changes in Diaphragm Thickness

Results Inspiratory Effort and Clinical Outcomes

Discussion The central finding of this study is that the progressive development of diaphragm atrophy during mechanical ventilation is associated with prolonged mechanical ventilation and ICU admission and an increased risk of complications of acute respiratory failure. We also found that rapid early increases in diaphragm thickness predicted prolonged ventilation. Rapid early increases in diaphragm thickness predicted prolonged ventilation, raising the possibility of clinically significant diaphragm injury caused by insufficient respiratory muscle unloading during ventilation The histologic basis of increases in T di during ventilation has not been characterized. T di tended to decrease at lower inspiratory effort levels and increase at higher inspiratory effort levels, suggesting that some intermediate level may be optimal. Because competing issues of respiratory muscle oxygen consumption and lung injury can modify the safest inspiratory effort level during ventilation, the optimal level of patient inspiratory effort during ventilation has been uncertain. These data raise the possibility that titrating ventilatory support to maintain this range of inspiratory effort might accelerate liberation from ventilation.

Limitations First, despite attempts to account for confounding, observed associations may derive from residual confounding related to unmeasured patient or illness characteristics, so that we cannot definitively conclude a causal effect. Second, we did not record the use of noninvasive ventilation after extubation and consequently the frequency of noninvasive ventilation for postextubation respiratory distress in our study is uncertain. Third, we have no histologic data correlating with the observed changes in diaphragm thickness.

Limitations Fourth, measurements were not collected on weekends, resulting in some missing values for T di measurements. To mitigate this problem, we did not enroll patients on Fridays. Consequently, any such missing values would be expected to bias the effect toward the null. Fifth, quantifying diaphragm function by maximal diaphragm thickening fraction relies on patient volitional effort, potentially limiting measurement reliability in a clinical context where it is sometimes challenging to obtain maximal volitional efforts. Sixth, we did not measure posthospital outcomes and their long-term functional status.

Conclusion In summary, the progressive development of diaphragm atrophy during the early course of mechanical ventilation predicts prolonged ventilation and an increased risk of complications of acute respiratory failure. Similar but weaker results were found for increased T di. Efforts to prevent and treat diaphragm atrophy or increased T di may significantly improve outcomes in patients with acute respiratory failure.