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Chest Physiotherapy Effects on Intracranial Pressure

Not Applicable
Completed
Conditions
Acute Brain Injury
Interventions
Procedure: inferior limb passive mobilization
Procedure: rapid thoracic compression technique
Registration Number
NCT03609866
Lead Sponsor
University of Santiago de Compostela
Brief Summary

The investigators will study the effects of a chest physiotherapy technique (rapid thoracic compression) on the intracranial pressure of individuals with acute cerebral injury and with need of intubated mechanical ventilation

Detailed Description

Patients with acute brain injury often require invasive mechanical ventilation connection, increasing the risk of developing complications such as respiratory secretions retention. Thethoracic compression is a manual chest physiotherapy technique that can improve clearance of secretions in these patients. Although today the scientific evidence is contradictory, the manual abdomino-thoracic compression may be associated with increased intracranial pressure in patients with acute brain injury.

Objectives: The aim of this work to study the effects of manual thoracic compression technique in intracranial pressure in mechanically ventilated patients. Furthermore, the effects of the technique in different volumes and flows recorded by the ventilator and the relationship between the pressure applied in the intervention group and the different variables will also be studied.

Methodology: It will be a randomized clinical trial, single-blind in the application of the techniques. Patients with acute brain injury in invasive mechanical ventilation will be included, randomized into two groups. In the control group, a technique of passive inferior limbs mobilization will be applied and in the intervention group it will be performed the manual thoracic compression technique. The data of the primary variable, intracranial pressure will be collected with a monitoring system and continuous recording (Integra Camino).

A descriptive analysis of the values collected from the variables in the study will be performed, studying the measures of central tendency. In the presence of normal distribution will be presented mean and standard deviation, and median and interquartile range in case of non-observation of normal distribution. The normality of the samples will be verified with the Kolmogorov-Smirnov test. The verification of the hypothesis in study will be assessed using the Student T test for independent samples in case of sample normality and by the Wilcoxon test otherwise. A multiple linear regression analysis will be performed: considering as a dependent variable the differences in intracranial pressure, difference or volume / minute gain and expiratory flow and between the covariates, the type of technique, the pressure applied in the technique under study, the type of brain injury, age, sex, etc.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
Inclusion Criteria
  • intubated patients for 48 hours in vc, pc, vcrp
  • hemodynamically stable (MAP>60mmHg)
  • respiratory stability (PEEP<15cmH2O and FiO2<60%)
  • ICP stable (0<icp<20mmHg)
  • RASS of 5
  • informed consent signed
Exclusion Criteria
  • thoracic fractures
  • abdominal injuries that limits local pressure
  • systemic or local changes that undergoes with abdominal volume increase
  • inferior limbs fractures that contraindicates passive mobilization techniques

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
controlinferior limb passive mobilizationwill be performed inferior limbs passive mobilization
experimentalrapid thoracic compression techniquerapid thoracic compression technique will be applied
Primary Outcome Measures
NameTimeMethod
intracranial pressure changes5 minutes before start procedure, immediately after procedure, 5 minutes after the end of procedure and 10 minutes after the end of procedure

with Camino ICP monitoring

Secondary Outcome Measures
NameTimeMethod
heart rate changes5 minutes before start procedure, immediately after procedure, 5 minutes after the end of procedure and 10 minutes after the end of procedure

with philips monitoring device

cerebral perfusion pressure changes5 minutes before start procedure, immediately after procedure, 5 minutes after the end of procedure and 10 minutes after the end of procedure

with philips monitoring device

oxygen saturation changes5 minutes before start procedure, immediately after procedure, 5 minutes after the end of procedure and 10 minutes after the end of procedure

with philips monitoring device

peak expiratory flow changesall the respiratory cycles will be recorded 30 seconds before procedure and during the procedure

with maquet servo u and servo i ventilators, the purpose is to identify the best peak expiratory flow before and during the procedure, and to compare them.

Trial Locations

Locations (1)

Hospital Álvaro Cunqueiro

🇪🇸

Vigo, Galicia, Spain

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