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The goal of this observational study is to observe brachial-to-radial pressure gradient in critically-ill patients receiving vasoactive agents. The main questions it aims to answer are:
Pathological conditions, such as arterial stenosis, use of vasoconstrictive drugs, or massive vasodilatation, can cause significant differences in mean arterial pressure (MAP) in different parts of the arterial system. For example, in the case of stenosis between the brachial and radial arteries, the pressure behind the stenosis is lower than in front of it, which can lead to erroneous conclusions about the actual arterial pressure. The use of vasoconstrictive drugs in patients with circulatory insufficiency can result in reduced peripheral arterial pressure transmission, as evidenced by studies showing lower pressures in the radial artery compared to the femoral artery. Inadequate MAP assessments can lead to excessive use of vasoactive drugs and fluids, increasing the risk of complications such as cardiac ischemia, atrial fibrillation, and renal failure. One method to detect a significant gradient between central MAP (e.g., aorta or femoral artery) and peripheral MAP is non-invasive, oscillometric measurement of MAP on the brachial artery and comparing it to MAP obtained from invasive radial access (known as NIBR-APG). The brachial-radial MAP gradient is highly correlated with the femoral-radial gradient and may be indicative of significantly higher central pressure. The aim of this project is to evaluate the frequency of the brachial-radial gradient phenomenon in patients undergoing vasoconstrictive treatment in intensive care units.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Adult critically-ill patients receiving vasoactive agents | Adult critically-ill patients receiving vasoactive agents and undergoing invasive blood pressure monitoring in the radial artery |
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| Measure | Description | Time Frame |
|---|---|---|
| Frequency of significant brachial-to-radial gradient | Frequency of significant brachial-to-radial gradient > 11 mmHg MAP | At baseline (after initial resuscitation). The gradient will be assessed only once, in a cross-sectional manner. |
| Measure | Description | Time Frame |
|---|---|---|
| Determinants of the brachial-to-radial gradient | Odds ratio (OR) of norepinephrine equivalent dose and OR of other potential risk factors (diabetes, age and body surface area) for significant brachial-radial gradient (>11 mmHg MAP) | At baseline (after initial resuscitation). The variables will be collected only once in a cross-sectional manner. |
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Inclusion Criteria:
Exclusion Criteria:
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Adult patients admitted to the intensive care unit, requiring invasive blood pressure monitoring, and undergoing vasoactive therapy.
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| Name | Affiliation | Role |
|---|---|---|
| Zbigniew Putowski, MD PhD | Center for Intensive Care and Perioperative Medicine, Jagiellonian University Medical College, Cracow, Poland | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| 5 Szpital Wojskowy z PoliklinikÄ… w Krakowie | Krakow | Poland | ||||
| Uniwersytecki Szpital w Opolu |
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| ID | Term |
|---|---|
| D012769 | Shock |
| D016638 | Critical Illness |
| ID | Term |
|---|---|
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D020969 | Disease Attributes |
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| Brachial-to-radial gradient and capillary refill time | Correlation between brachial-to-radial gradient and capillary refill time | At baseline (after initial resuscitation). Variables will be collected only once in a cross-sectional manner. |
| Brachial-to-radial gradient and lactates | Correlation between brachial-to-radial gradient and lactate concentration | At baseline (after initial resuscitation). Variables will be collected only once in a cross-sectional manner. |
| Opole |
| Poland |
| Uniwersyteckie Centrum Kliniczne w Warszawie | Warsaw | Poland |