Blood Volume Assessment in COVID-19 and Bacterial Sepsis

Covid19 Clinical Trial

— BVAC19  

Official title:

Blood Volume, Components and Capillary Leak in ICU Patients With SARS-CoV-2 and Bacterial Infections

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04517695
• Other study ID #: 20-00896
• Status: Completed
• Start date: August 1, 2020
• Est. completion date: April 9, 2023

Study information

• Verified date: September 2023
• Source: NYU Langone Health
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

In patients with SARS-CoV-2 or bacterial infection admitted to the intensive care unit (ICU), the state of the intravascular volume, the characteristics of the blood volume components, and the development of a vascular leak is currently unknown. The relationship of these parameters with parameters of cardiac performance, lung edema and sublingual microcirculatory perfusion parameters have never been studied.

Description:

Acute respiratory failure related to infection by the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), is the main reason for ICU admission in in the majority of patients admitted to the ICU in this viral syndrome, and it presents a significant clinical challenge. Severe hypoxemia in these patients is thought to be related in part to generation of alveolar edema. This would be related to the specific infection related injury of the alveoli-capillary membrane, however other factors could be related to edema formation. Although patients meet criteria for the Acute Respiratory Distress Syndrome (ARDS), there is significant controversy about whether the lungs of the COVID-19 patients have the characteristics of ARDS and thus whether the treatment should mimic treatment of ARDS due to other causes. A general principle in ARDS patients is to avoid positive fluid balances as this may contribute to alveolar edema. Also, the guidelines on the management of COVID-19 patients by the Society of Critical Care Medicine advocate a conservative fluid strategy. However, uncorrected hypovolemia may result in additional organ dysfunction (especially kidney injury). The clinical fluid status is usually estimated by the presence of peripheral edema and daily fluid balances and thus prone to errors as these are poorly related to the circulating blood volume. Management of patients with sepsis based on blood volume measurements and red blood cell volume, to disclose true anemia, has been shown to improve outcome. Finally, the transudation of albumin in the extravascular space has been shown to be associated with outcome of critically ill patients. It is highly plausible that these parameters could help guide the care of COVID-19 patients given the available data in the literature, thus promoting better treatment of these patients.

This is a prospective multicenter study where the treatment team is blinded to the results of the study. The primary objective of the study is to describe the blood volume, the volume of blood components, the capillary leak and parameters of cardiac performance, lung edema and sublingual microcirculatory perfusion and their trajectory during the early phase of hospitalization of patients with SARS-CoV-2 or bacterial infection.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 39
• Est. completion date: April 9, 2023
• Est. primary completion date: April 9, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 95 Years

Eligibility

Inclusion Criteria:

• Confirmed SARS-CoV-2 or bacterial infection

• Patient admitted to the ICU

• Patient age is between 18 and 95 years

• Patent peripheral or central venous line from which blood draws can be made and through which the 131I bolus can be administered

• Arterial catheter considered indicated by primary team caring for the patient

Exclusion Criteria:

• Refused informed consent to participate in the study

• Pregnant or possible pregnant women

• Patient unlikely to survive more than 72h

• Patient with life sustaining treatment limitations (use of renal replacement therapy)

• Patient already on or likely to be placed on extra-corporeal membrane oxygenation support within 48h after admission

• Known allergy to iodine or iodinated 131I albumin

• Patients with chronic renal failure requiring renal replacement therapy

Related Conditions & MeSH terms

• Acute Lung Injury
• Acute Respiratory Distress Syndrome
• Bacterial Infections
• Bacterial Sepsis
• COVID-19
• Covid19
• Infections
• Respiratory Distress Syndrome
• Respiratory Distress Syndrome, Newborn
• Sepsis

Intervention

Device:
• BVA-100
The BVA-100 is a software package designed to calculate human blood volume using the method of tracer dilution. It uses tagged serum albumin.
• Transpulmonary Thermodilution (TPTD)
TPTD consists of placing a thermistor-equipped catheter in a central artery (usually the femoral or axillary artery) and injecting cold saline solution into a central vein through a central venous catheter.
• Sublingual Microcirculation
With incident dark field imaging, the CytoCam device can record digital image sequences using a handheld camera. In the current study the camera will be used to non-invasively record images of the sublingual microcirculation.

Locations

Country	Name	City	State
United States	Uniformed Services University of the Health Sciences	Bethesda	Maryland
United States	NYU Langone Health	New York	New York
United States	Wake Forest Baptist Health	Winston-Salem	North Carolina

Sponsors (2)

Lead Sponsor	Collaborator
NYU Langone Health	Daxor Corporation

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Absolute Total Blood Volume	Absolute total blood volume calculated using BVA-100 software.	Day 1, Day of ICU Discharge (up to day 21)
Primary	Change in Total Blood Volume Relative to Ideal Body Weight	Total blood volume relative to ideal body weight calculated using the BVA-100 software.	Day 1, Day of ICU Discharge (up to day 21)
Primary	Change in Absolute Red Blood Cell Volume	Absolute red blood cell volume calculated using the BVA-100 software.	Day 1, Day of ICU Discharge (up to day 21)
Primary	Change in Red Blood Cell Volume Relative to Ideal Body Weight	Red blood cell volume relative to ideal body weight calculated using the BVA-100 software.	Day 1, Day of ICU Discharge (up to day 21)
Primary	Change in Absolute Plasma Volume	Absolute plasma volume calculated using the BVA-100 software.	Day 1, Day of ICU Discharge (up to day 21)
Primary	Change in Plasma Volume Relative to Ideal Body Weight	Plasma volume relative to ideal body weight calculated using the BVA-100 software.	Day 1, Day of ICU Discharge (up to day 21)
Primary	Change in Transudation Rate of Albumin	Transudation rate of albumin calculated using the BVA-100 software. An increase indicates the transudation rate increased during the observational period.	Day 1, Day of ICU Discharge (up to day 21)
Primary	Change in Heart Rate	Measured using PICCO. Heart rate expressed as beats per minute (BPM).	Day 1, Day of ICU Discharge (up to day 21)
Primary	Change in Cardiac Output	Measured using PICCO. Cardiac output expressed in liters per minute (L/min).	Day 1, Day of ICU Discharge (up to day 21)
Primary	Change in Stroke Volume	Measured using PICCO. Stroke volume expressed in milliliters per square meter (mL/m2).	Day 1, Day of ICU Discharge (up to day 21)
Primary	Change in Systemic Vascular Resistance (SVR)	Measured using PICCO. SVR expressed in dynes/second/cm^5.	Day 1, Day of ICU Discharge (up to day 21)
Primary	Change in Global End Diastolic Volume (GEDV) Index	Measured using PICCO. GEDV expressed in mL/m2.	Day 1, Day of ICU Discharge (up to day 21)
Primary	Change in Intra-Thoracic Blood Volume Index (ITBVI)	Measured using PICCO. ITBVI expressed in mL/m2.	Day 1, Day of ICU Discharge (up to day 21)
Primary	Change in Extravascular Lung Water (EVLW)	Measured using PICCO. EVLW expressed in mL/kg.	Day 1, Day of ICU Discharge (up to day 21)
Primary	Maximum Stroke Volume	Measured using PICCO. Stroke volume expressed in mL/m2.	Up to Day of ICU Discharge (up to day 21)
Primary	Minimum Stroke Volume	Measured using PICCO. Stroke volume expressed in mL/m2.	Up to Day of ICU Discharge (up to day 21)
Primary	Maximum Pulse Pressure	Measured using PICCO. Pulse pressure expressed in millimeters of mercury (mmHg).	Up to Day of ICU Discharge (up to day 21)
Primary	Minimum Pulse Pressure	Measured using PICCO. Pulse pressure expressed in millimeters of mercury (mmHg).	Up to Day of ICU Discharge (up to day 21)
Primary	Change in Systolic Blood Pressure	Measured using PICCO. Systolic blood pressure expressed in mmHg.	Day 1, Day of ICU Discharge (up to day 21)
Primary	Change in Diastolic Blood Pressure	Measured using PICCO. Diastolic blood pressure expressed in mmHg.	Day 1, Day of ICU Discharge (up to day 21)
Primary	Mean Blood Pressure	Measured using PICCO. Blood pressure expressed in mmHg.	Up to Day of ICU Discharge (up to day 21)
Primary	Change in Central Venous Pressure (CVP)	Measured using PICCO. CVP expressed in mmHg.	Day 1, Day of ICU Discharge (up to day 21)
Secondary	Number of Participants with New Onset Renal Injury		Up to Day of ICU Discharge (up to day 21)
Secondary	Number of Participants Requiring Renal Replacement Therapy		Up to Day of ICU Discharge (up to day 21)