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Ventilator-associated Injury (VAI) in Chronic Home Mechanical Ventilation

Ventilator-associated Injury (VAI) in Chronic Home Mechanical Ventilation: a Paradigm Switch in Order to Improve Ventilatory Support

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04521426
Enrollment
15
Registered
2020-08-20
Start date
2020-10-01
Completion date
2023-09-01
Last updated
2023-11-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Long-term Non-invasive Ventilation, Respiratory Failure

Keywords

COPD, Lung fibrosis, non-invasive ventilation, respiratory muscles, diaphragm, lung inflammation, ventilator-induced lung injury

Brief summary

Rationale: The pathophysiological changes in respiratory muscle morphology and functioning in patients with end-stage pulmonary disease are not very well known. Furthermore, in COPD, long-term high-intensity NIV is applied without knowing the exact consequences on the lungs and respiratory muscles. Objective: The aims of the study are to get insight in: A. changes respiratory muscles in end-stage respiratory disease, comparing COPD with restrictive lung disease (RLD) due to pulmonary fibrosis B. the effects of long-term HI-NIV in severe COPD patients on the respiratory muscles and the lungs; by comparing COPD patients that had been treated with long-term NIV to COPD patients that were not treated with long-term NIV. Study design: In order to investigate this, the investigators will include in a small pilot cohort study patients being lung transplanted. In these patients there is lung tissue available and respiratory muscle biopsies will be performed during lung-transplant surgery. Study population: Patients that are listed for lung transplantation for an underlying diagnosis of COPD or RLD will be asked to participate. Three groups will be included: patients with a RLD due to pulmonary fibrosis, COPD patients that had been treated with long-term NIV prior to being lung transplanted and COPD patients that were not treated with long-term NIV. Patients will be included definitely once being lung transplanted. Main study parameters/endpoints: The study is an exploratory pilot study. Both contractile strength and the structure of single diaphragm and intercostal muscle fibres as well as lung injury; i.e. alveolar structure and damage and inflammation in the alveoli, will be investigated.

Detailed description

Rationale: Chronic Obstructive Pulmonary Disease (COPD) is a progressive inflammatory disease characterised by airway and lung parenchyma damage. At end-stage disease patients may develop chronic hypercapnic respiratory failure, a disease characteristic that is however not uniformly seen in other end-stage lung diseases, such as in patients with pulmonary fibrosis. The underlying process for the development of chronic hypercapnic respiratory failure is incompletely understood and the role of respiratory muscle alterations is unclear. Home noninvasive ventilation with high-intensity ventilatory settings (HI-NIV) has been shown to be effective in these severe COPD patients. However, in patients being mechanically ventilated on the intensive care unit for diverse reasons, high-intensity ventilation, especially high tidal volumes, has been shown to result in ventilator associated lung and diaphragm injury. Whether this occurs in home high-intensity NIV, is however completely unknown. Objective: The aims of the study are to get insight in: A. changes respiratory muscles in end-stage respiratory disease, comparing COPD with restrictive lung disease (RLD) due to pulmonary fibrosis B. the effects of long-term HI-NIV in severe COPD patients on the respiratory muscles; i.e. the contractile strength and the structure of single diaphragm and intercostal muscle fibres and the lungs; i.e. alveolar structure and damage and inflammation, by comparing COPD patients that had been treated with long-term NIV to COPD patients that were not treated with long-term NIV. Study design: In order to investigate this, the investigators will include in a small pilot cohort study patients being lung transplanted. In these patients there is lung tissue available and respiratory muscle biopsies will be performed during lung-transplant surgery. Study population: Patients that are listed for lung transplantation for an underlying diagnosis of COPD or RLD will be asked to participate. Three groups will be included: patients with a RLD due to pulmonary fibrosis, COPD patients that had been treated with long-term NIV prior to being lung transplanted and COPD patients that were not treated with long-term NIV. Patients will be included definitely once being lung transplanted. Main study parameters/endpoints: The study is an exploratory pilot study. The study aims to get data on respiratory muscle and lung and airway pathology in order to, if important results are observed, set up a larger prospective trial investigating both clinical outcomes and pathology of the respiratory muscles/lungs. Both contractile strength and the structure of single diaphragm and intercostal muscle fibres as well as lung injury; i.e. alveolar structure and damage and inflammation in the alveoli, will be investigated.

Interventions

OTHERNo other than standard care

No other than standard care.

Sponsors

University Medical Center Groningen
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. RLD: probable or confirmed diagnosis of interstitial pulmonary fibrosis (IPF) or other fibrotic lung disease of unknown origin. 2. COPD: GOLD stage III or IV 3. Being listed for lung transplantation

Exclusion criteria

1. Concomitant neuromuscular or systemic/collagen-vascular disease 2. Prior lung surgery (except for lung biopsies) or lung volume reduction treatment 3. Being unable to understand the patient information and consent for the study

Design outcomes

Primary

MeasureTime frameDescription
Ventilator-associated lung injury gene-expressionduring surgeryGene-expression profiling of epithelial cells with regard to inflammatory factors
Ventilator-associated lung injury BAL IL-1betaduring surgeryBAL IL-1beta
Ventilator-associated lung injury BAL IL-8during surgeryBAL IL-8
Ventilator-associated lung injury BAL MIP-2during surgeryBAL MIP-2
Ventilator-associated lung injury BAL sRAGEduring surgeryBAL sRAGE
Ventilator-associated lung injury basal membraneduring surgeryhistopathological changes to the basal membrane
Ventilator-associated lung injury alveolar cellsduring surgeryhistopathological changes to type I alveolar cells
Ventilator-associated lung injury edemaduring surgeryedema in the alveoli and interstitium
Ventilator-associated lung injury fibrinduring surgeryinterstitial fibrin
Ventilator-associated lung injury inflammatory cellsduring surgeryInflammatory cells influx in the alveoli
Respiratory muscle morphology and functioningduring surgeryBiopsies of the diaphragm and intercostal muscles will be taken during surgery
Ventilator-associated lung injury serum TNF-alfaduring surgeryserum TNF-alfa
Ventilator-associated lung injury serum IL-6during surgeryserum IL-6
Ventilator-associated lung injury serum IL-1betaduring surgeryserum IL-1beta
Ventilator-associated lung injury serum IL-8during surgeryserum IL-8
Ventilator-associated lung injury serum MIP-2during surgeryserum MIP-2
Ventilator-associated lung injury serum sRAGEduring surgeryserum sRAGE
Ventilator-associated lung injury BAL TNF-alfaduring surgeryBAL TNF-alfa
Ventilator-associated lung injury BAL IL-6during surgeryBAL IL-6

Secondary

MeasureTime frameDescription
Demographics_BMIduring surgeryBMI
Lung Function_FEV1during surgeryFEV1
Lung Function_FVCduring surgeryFVC
Ventilatory useduring surgeryDuration of usage (longitudinally and use per day)
Ventilatory settingsduring surgerySettings of the NIV
Demographics_ageduring surgeryage
Blood gasses_PaCO2during surgeryPaCO2
Blood gasses_HCO3-during surgeryHCO3-
Demographics_genderduring surgerygender

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026