To develop a screening test to predict ICU-AW at an early stage in patients admitted to the ICU. Also by prospectively following the patient group in time, this study aims to describe the natural history and functional limitations in patients…
ID
Source
Brief title
Condition
- Ancillary infectious topics
- Neuromuscular disorders
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Sensitivity and specificity of the different electrophysiological studies for
predicting ICU-AW.
Secondary outcome
Functional impairments after 3,6 and 12 months; risk factors for developing
ICU-AW; feasibility of the different electrophysiological studies.
Background summary
Intensive care unit - acquired weakness (ICU-AW) is a frequent and important
complication of critical illness. Patients suffer from severe weakness
affecting extremities but also respiratory muscles. ICU-AW causes increased
mortality, longer duration of mechanical ventilation and protracted recovery
after a critical illness. The most important risk factors for development of
ICU-AW are sepsis and the systemic inflammatory response syndrome (SIRS).
Diagnosing ICU-AW is difficult. Due to concomitant disorders of consciousness
conventional diagnostic methods for diagnosing weakness, i.e the neurological
examination, is not possible at an early stage. This leads to a delayed
diagnosis of ICU-AW which hampers clinical decision making on for example
tracheostomy and rehabilitation strategies.
Study objective
To develop a screening test to predict ICU-AW at an early stage in patients
admitted to the ICU. Also by prospectively following the patient group in time,
this study aims to describe the natural history and functional limitations in
patients suffering from ICU-AW.
Study design
Prospective cohort study.
Study burden and risks
Depending on when the patient awakens, he or she will be screened once or
multiple times. Every screening examination will take about 10 minutes. After
awakening, a clinical neurological examination will be preformed also taking
about 10 minutes. If the patients consents to partcipate in the follow up
study, he or she will be contacted via telephone three times. One interview at
3, 6 and 12 months after discharge. Every interview will take about 15 minutes
to complete.
Electrophysiological studies used in this project are used and accepted
worldwide. For this project extra stringent safety requirements have been
developed which will be evaluated before every examination. The risk for the
patient will be negligible.
Meibergdreef 9
Postbus 22700, 1100 DE Amsterdan
NL
Meibergdreef 9
Postbus 22700, 1100 DE Amsterdan
NL
Listed location countries
Age
Inclusion criteria
>2 days on mechanical ventilation
Exclusion criteria
Stroke as reason for admission, quadriplegia due to spinal cord disorder, out of hospital cardiac arrest, neuromuscular disorder as reason for admission
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL33385.018.10 |