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O2 Consumption And CO2 Production After Hemodynamic Optimization In Shock (OxyCarDio)

I

Institute of Hospitalization and Scientific Care (IRCCS)

Status

Enrolling

Conditions

Hemodynamic Instability
Oxygen Consumption (V̇O2)

Treatments

Other: Fluid bolus
Other: Noradrenalin

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this prospective observational study is to analyse change in VO2 and VCO2 measured via a dedicated ventilator after hemodynamic optimization maneuvers in adult patients admitted to the ICU with any sign of shock.

The main questions it aims to answer are:

  1. Do common maneuvers for hemodynamic optimization (fluid bolus and/or vasopressor administration) have any impact on tissue perfusion in terms of oxygen consumption (VO2) and carbon dioxide production (VCO2) measured by a dedicated ventilator?
  2. Are the values measured by exhaled gas comparable to those calculated by the measurement of dissolved veno-arterial gas?

Participants enrolled in the study will receive advanced hemodynamic monitoring with MostCare Up (Vygon ®) and their hemodynamic instability will be managed according to most recent guidelines and based on clinical decision of treating physicians.

Enrollment

36 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Hypotension (MAP< 65mmHg or sudden drop in MAP > 15 mmHg) and one of the following conditions:

  • Heart rate > 120 bpm
  • Urinary output < 0.5 ml/kg/h for at least two hours
  • Lactate > 2 mmol/L

Exclusion criteria

  • Urgent need for surgery
  • Urgent need for veno-arterial ECMO or severe hemodynamic instability
  • Consistent risk of imminent death
  • Severe ARDS or severe respiratory failure (p/F < 100 mmHg) and/or FiO2>0.8
  • Severe heart failure (NYHA 4 and/or EF<25%)
  • Need for intermittent or continuous renal replacement therapy (IRRT or CRRT)
  • Anemia defined as Hb<8 g/dL
  • VO2 variability < 5% throughout ten minutes of stabilization before procedure start
  • Intraabdominal hypertension, defined as intraabdominal pressure > 18 mmHg
  • Pregnancy
  • Withdrawal or refuse of informed consent
  • Terminal disease
  • Do-not-resuscitate order.

Trial contacts and locations

1

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Central trial contact

Antonio M Dell'Anna

Data sourced from clinicaltrials.gov

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