Austin Health

Title
Respiratory function and respiratory complications in spinal cord injury: protocol for a prospective, multicentre cohort study in high-income countries.
Publication Date
2020-11-05
Author(s)
Raab, Anja M
Brinkhof, Martin W G
Berlowitz, David J
Postma, Karin
Gobets, David
Hirschfeld, Sven
Hopman, Maria T E
Huber, Burkhart
Hund-Georgiadis, Margret
Jordan, Xavier
Schubert, Martin
Wildburger, Renate
Mueller, Gabi
Subject
epidemiology
rehabilitation medicine
respiratory infections
Type of document
Journal Article
OrcId
0000-0002-4139-2173
0000-0002-9319-665X
0000-0003-2543-8722
0000-0002-0729-6778
0000-0003-0270-5672
0000-0001-9504-5452
0000-0002-4415-2888
0000-0003-3389-0057
0000-0001-9820-3823
0000-0001-6391-3737
DOI
10.1136/bmjopen-2020-038204
Abstract
Pneumonia is one of the leading complications and causes of death after a spinal cord injury (SCI). After a cervical or thoracic lesion, impairment of the respiratory muscles decreases respiratory function, which increases the risk of respiratory complications. Pneumonia substantially reduces patient's quality of life, may prolong inpatient rehabilitation time, increase healthcare costs or at worse, lead to early death. Respiratory function and coughing can be improved through various interventions after SCI, but the available evidence as to which aspect of respiratory care should be optimised is inconclusive. Furthermore, ability of respiratory function parameters to predict pneumonia risk is insufficiently established. This paper details the protocol for a large-scale, multicentre research project that aims to evaluate the ability of parameters of respiratory function to predict and understand variation in inpatient risk of pneumonia in SCI. RESCOM, a prospective cohort study, began recruitment in October 2016 across 10 SCI rehabilitation centres from Australia, Austria, Germany, the Netherlands and Switzerland. Inpatients with acute SCI, with complete or incomplete cervical or thoracic lesions, 18 years or older and not/no more dependent on 24-hour mechanical ventilation within the first 3 months after injury are eligible for inclusion. The target sample size is 500 participants. The primary outcome is an occurrence of pneumonia; secondary outcomes include pneumonia-related mortality and quality of life. We will use the longitudinal data for prognostic models on inpatient pneumonia risk factors. The study has been reviewed and approved by all local ethics committees of all participating centres. Study results will be disseminated to the scientific community through peer-reviewed journals and conference presentations, to the SCI community, other stakeholders and via social media, newsletters and engagement activities. ClinicalTrials.gov NCT02891096.
Link
Citation
BMJ open 2020; 10(11): e038204
Jornal Title
BMJ open

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