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Neurophysiological Diagnosis for ICU Septic Shock Patients (EDX)

V

Vaud University Hospital Center

Status

Unknown

Conditions

ICU Acquired Weakness

Treatments

Diagnostic Test: Nerve conduction study

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Patients hospitalized in the Intensive Care Unit (ICU) are at risk for developing severe disabilities, physical or cognitive. In particular, ICU-acquired weakness is frequent. The causes of this weakness are multiple and the physiopathology is still not fully understood. Immobilization in bed and sepsis are known risk factors.

ICU-acquired weakness has been associated with prolonged mechanical ventilation duration, and increased in ICU and hospital length of stay. It has also been associated with significant decrease in functional capacity and with higher mortality. An early screening using a specific diagnostic protocol could help improving the management of patients suffering from ICU acquired weakness.

The aim of this study is to early detect ICU acquired weakness in patients suffering from septic shock and ventilated for more than 72 hours.

Enrollment

20 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

• Patients admitted to the ICU with a septic shock and ventilated for more than 72 hours.

Exclusion criteria

  • Hospitalization for more than 7 days before intubation.
  • Functional disability at admission of ≥4 (Requires constant nursing care and attention, bedridden, incontinent) in the Modified Rankin Scale.
  • Lower limb disorders precluding nerve conduction studies (NCV) and electromyography (EMG), such as clinical edema of the lower limbs, or fractures, amputation, and plaster casts of the lower limbs.
  • Evidence of altered neuromuscular transmission at repetitive stimulation test either caused by neuromuscular blocking agents or disease.
  • Burn patients admitted to ICU.
  • Patient requesting withdrawal of therapies.

Trial contacts and locations

1

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Central trial contact

CAROLINE ATTWELL

Data sourced from clinicaltrials.gov

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