Influence of Respiratory Mechanics on Diaphragmatic Dysfunction in COPD Patients Who Have Failed NIV (RHYDIAN)
RHYDIAN
1 other identifier
observational
30
1 country
1
Brief Summary
Although non-invasive mechanical ventilation (NIV) is the gold standard treatment for patients with acute exacerbation of COPD (AECOPD) who develop respiratory acidosis, failure rate are still high ranging from 5% to 40%. Recent studies have shown that the onset of severe diaphragmatic dysfunction (DD) during AECOPD increases risk of NIV failure and mortality in this subset of patients. Although the imbalance between the load and the contractile capacity of inspiratory muscles seems the main cause of AECOPD-induced hypercapnic respiratory failure, data regarding the influence of mechanical derangement on diaphragmatic performance in this acute phase are lacking. With this study we aim at investigating the impact of respiratory mechanics on diaphragm function in AECOPD patients who experienced NIV failure. AECOPD with respiratory acidosis admitted to the ICU of the University Hospital of Modena from 2017-2018 undergoing mechanical ventilation (MV) due to NIV failure were enrolled. The study protocol consisted of two consecutive phases; in the first step measurements of static respiratory mechanics and end expiratory lung volume (EELV) were performed after 30 minutes of MV in volume control mode. In the second step transdiaphragmatic pressure (Pdi) was calculated by means of a sniff maneuver (Maximal Pdi) after 30 minutes of spontaneous breathing trial. Linear regression analysis and Pearson's correlation coefficient was used to asses the association between Maximal Pdi values and static and dynamic mechanical features and the association between Maximal Pdi and Pdi/Maximal Pdi.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Jan 2017
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2018
CompletedFirst Submitted
Initial submission to the registry
February 21, 2019
CompletedFirst Posted
Study publicly available on registry
February 25, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2022
CompletedApril 7, 2022
April 1, 2022
1.5 years
February 21, 2019
April 5, 2022
Conditions
Outcome Measures
Primary Outcomes (2)
Impact of static elastance on diaphragm function in AECOPD patient who failed NIV
Correlation between static elastance and Maximal Pdi in patients undergoing mechanical ventilation for AECOPD
30 days from Respiratory Intensive Care Unit admission
Impact of dynamic intrinsic Positive End Expiratory Pressure on diaphragm function in AECOPD patient who failed NIV
Correlation between dynamic intrinsic Positive End Expiratory Pressure and Maximal Pdi in patients undergoing mechanical ventilation for AECOPD
30 days from Respiratory Intensive Care Unit admission
Interventions
The study protocol consisted of two consecutive phases; in the first step measurements of static respiratory mechanics and end expiratory lung volume (EELV) were performed after 30 minutes of MV in volume control mode. In the second step transdiaphragmatic pressure (Pdi) was calculated by means of a sniff maneuver (Maximal Pdi) after 30 minutes of spontaneous breathing trial. Linear regression analysis and Pearson's correlation coefficient was used to asses the association between Maximal Pdi values and static and dynamic mechanical features and the association between Maximal Pdi and Pdi/Maximal Pdi.
Eligibility Criteria
Cohort study
You may qualify if:
- age over 18 years
- AECOPD with respiratory acidosis admitted to the Respiratory Intensive Care Unit of the University Hospital of Modena (Italy) undergoing endotracheal intubation due to NIV failure.
You may not qualify if:
- history of neuromuscular disease,
- presence of chest wall deformities,
- coexistence of interstitial lung disease,
- presence of pulmonary edema,
- severe hemodynamic instability,
- septic shock,
- evidence of lobar pneumonia or bilateral parenchymal consolidation at chest X-ray on admission,
- contraindication to NIV,
- previously assessed diaphragmatic palsy,
- intracranial hypertension,
- known pregnancy,
- need for immediate endotracheal intubation,
- neurologic impairment,
- lack of collaboration,
- unreliable maneuver to calculate maximal transdiaphragmatic pressure.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Hospital of Modena Policlinico di Modena
Modena, Italy
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
February 21, 2019
First Posted
February 25, 2019
Study Start
January 1, 2017
Primary Completion
July 1, 2018
Study Completion
March 1, 2022
Last Updated
April 7, 2022
Record last verified: 2022-04