Insufficient Oxygenation in Septic Patients

Sanquin-LUMC J.J van Rood Center for Clinical Transfusion Research81 enrolled

Overview

This study will describe the change of mitochondrial oxygen tension (mitoPO2) compared to traditional parameters of oxygenation and oxygen balance in the first 24 hours of septic patients admitted to the intensive care unit of an academic hospital. The mitoPO2 will be measured on prespecified measurement moments in the ICU. With each measurement moment, arterial and central venous blood gasses will be taken too.

Evidence is increasing that there is no clear parameter for tissue oxygenation in critically ill septic patients to guide resuscitation. New studies have shown the potential of protoporphyrin IX-triple state lifetime technique to measure mitochondrial oxygenation tension (mitoPO2) in vivo, which possibly is an early indicator of oxygen disbalance in the cell and therefore a physiological trigger for fluid therapy. Objectives: 1. To describe mitoPO2 measurements in patients with sepsis who are about to receive fluid therapy 2. To describe the effects of fluid therapy and the associated change in mitoPO2 and change in other physiologic measures of tissue oxygenation and oxygen balance 3.To describe the association between mitoPO2 and vital organ (dis)functions and change of SOFA (Sequential organ failure assessment) score after 24hrs 5. To describe the microcirculatory, cellular and mitochondrial function during the first 24 hours of septic patients. Study population: critically ill patients with sepsis which are admitted to the intensive care unit through the emergency department or hospital ward and in whom fluid therapy (crystalloid, albumin and red cell transfusion) is planned. Main study endpoints Primary endpoint: Change in mitoPO2 after fluid therapy. This will be compared to traditional parameters used to measure oxygenation and oxygen balance Secondary endpoints: * Association of mitoPO2 trend with separate (ischemic) organ (dis)function. The SOFA score after 24 hours will also be assessed. * Safety of mitoPO2 measurements in critically ill septic patients. * Description of the association of sepsis with microcirculatory function, cellular function and mitochondrial function. * Description of the association between mitoPO2 change and clinical outcomes , like length of stay(both ICU and in-hospital) and mortality (both ICU and in-hospital).

Study Type

OBSERVATIONAL

Enrollment

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Age of patient is at least 18 years * Patients diagnosed with sepsis in the emergency department or hospital ward * Patients are admitted to the ICU via the hospital ward or emergency department * Informed consent is given either by the patient or if the patient is too ill to give informed consent, by his or her legal representative. * Patients have an arterial catheter in situ, since blood samples will be taken for the study. Most patients admitted to the ICU have an arterial catheter in place since it is part of standard care. Exclusion Criteria: * Patients younger than 18 years * Patients with sepsis discharged after emergency department visit * Patients admitted to a hospital ward other than the ICU after emergency department visit * Patients who cannot give informed consent themselves and without a legal representative will be excluded since no informed consent can be obtained * Patients known with porphyria and/or photodermatosis will be excluded, since the risk of phototoxicity * Patients with hypersensitivity to the active substance or to the plaster material of ALA (5-aminolevulinic acid) * Pregnant or breast feeding women since there is no adequate data form the use of ALA in pregnant or breast feeding women * Insufficient comprehensibility of the Dutch language

Outcomes

Primary Outcomes

Change of mitoPO2 during first 24 hours of a septic patient

The primary endpoint is the change of mitoPO2(mitochondrial oxygenation) before and after fluid therapy in patients with sepsis. This will be compared to traditional parameters used to measure tissue oxygenation and oxygen balance (central venous oxygen saturation, mean arterial pressure and lactate).

Time frame: 24 hours

Secondary Outcomes

SOFA (sequential organ failure assessment) score after 24 hours

The association of mitoPO2 change in 24 hours with the Sequential Organ Failure Assessment score after 24 hours will be assessed. With the help of this information, more insight can be given in how much information the cutaneous mitoPO2 measurement gives about the organs separately and together.

Time frame: 24 hours

Organ (dis)function

To describe the association between mitoPO2 change and separate organ functions.

Time frame: 24 hours

Validation of mitoPO2 measurement with blood based biomarkers of cellular function

Cellular function will be assessed with blood-based biomarkers mitochondrial membrane potential (MMP), presence of cellular reactive oxygen species (ROS) molecules and glutathione (GSH) activity. Mitochondrial function will be assessed with mitoPO2 measurements.

Time frame: 24 hours

Safety (incidence of adverse and serious adverse events)

The adverse and serious adverse events of the mitoPO2 measurements will be assessed.

Time frame: 24 hours

Length of ICU stay

Association of mitoPO2 change and length of intensive care unit-stay.

Time frame: 3 months

Length of hospital stay

Association of mitoPO2 change and length of hospital stay.

Time frame: 3 months

ICU mortality

Association of mitoPO2 change and intensive care unit mortality.

Time frame: 3 months

In-hospital mortality

Association of mitoPO2 change and in-hospital mortality.

Time frame: 3 months

Insufficient Oxygenation in Septic Patients

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes

Secondary Outcomes