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Correlation of Two Methods for Cough Peak Flow Measurement in Intubated Patients (COUGH-ICU)

C

Centre Hospitalier Régional d'Orléans

Status

Completed

Conditions

Ventilator Weaning
Respiratory Insufficiency

Study type

Observational

Funder types

Other

Identifiers

NCT03357198
CHRO-2017-02

Details and patient eligibility

About

Cough Peak Flow (CPF) seems to be an efficient tool to assess cough capacity for the intensive care unit (ICU) ventilated patient. CPF can be used in the ventilator weaning process, as reflecting the upper airways protection capacity.

CPF requires disconnection of the patient from the ICU ventilator, supplemental material (handheld spirometer, antibacterial filter) and an excellent synchronization between the specialized caregiver and the patient.

We aimed that CPF with the ventilator built-in flow-meter is correlated with CPF using a handheld flowmeter connected to the endotracheal tube.

Enrollment

62 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age > 18 years
  • Mechanically ventilated patient > 24 hours
  • Weaning ventilator phase (PEEP < 9 cmH2O and Support < 15 cm H2O)
  • Richmond Agitation Sedation Scale between -1 and +1
  • Patient's agreement to participate

Exclusion criteria

  • Pregnant women
  • Bronchospasm
  • FiO2 > 70%
  • Thoracic surgery < 7 days
  • Abdominal surgery < 7 days
  • Thoracic injury with rib fracture < 21 days
  • Pneumothorax < 24 hours

Trial design

62 participants in 1 patient group

cough peak flow measurement
Description:
All enrolled patients will undergo measurement of cough peak flow by two methods, i.e. using a handheld electronic spirometer, and using the ventilator flowmeter, in a randomized order.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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