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Grant: Master's Award: Canada Graduate Scholarships

Queen's University (Kingston, Ontario)

$27,000.00

The Peripheral Use of Low-dose Vasopressors for Safety and Efficacy in the Intensive Care Unit: A Pilot Feasibility Study

EF 2024-25

Résumé
The use of medications to increase blood pressure called vasopressors are invaluable in the treatment of patients who have difficulty maintaining a stable blood pressure. Vasopressors are usually infused through a central venous catheter (CVC), which is a flexible tube placed in the large vein of the neck, arm or groin. CVCs require a skilled clinician and often with an ultrasound to prevent complications such as a collapsed lung or bleeding. These complications can cause significant harm and may occur in up to 15% of patients. Alternatively, the infusion of vasopressors through a peripheral venous catheter (PVC), a thin tube placed in the smaller veins of the arm or hand, have been avoided due to the risk of extravasation, which is the leakage of fluid to surrounding tissues. This can lead to potential tissue death requiring surgery. However, emerging research shows the safety of infusing vasopressors through a PVC, referred to as peripheral vasopressors. There is a growing interest in peripheral vasopressors for two main reasons: to expedite vasopressor initiation in patients with refractory shock and to potentially avoid CVC placement and its complications. However, a standardized protocol for administration is lacking and many clinicians still avoid peripheral vasopressors due to lack of high quality evidence. We will examine the effectiveness of implementing a peripheral vasopressor protocol by conducting a feasibility study and assess outcomes such as safety of peripheral vasopressors and acceptability rate by healthcare providers. By conducting this study, we hope to provide the framework to conduct larger, multi-center trials and to provide high quality data for the future use of a standardized peripheral vasopressor protocol.
Programme
Master's Award: Canada Graduate Scholarships
Emplacement
Ontario, Canada
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
530010
Name
Wiseman Jessica F
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Prcname2
Special Cases - Awards Programs
Projecttitle
The Peripheral Use of Low-dose Vasopressors for Safety and Efficacy in the Intensive Care Unit: A Pilot Feasibility Study
Programtype2
Studentship Programs
Orgnameinp2
Queen's University (Kingston, Ontario)
Cihramount2
$27,000
Cihrequipment2
$0
Programname2
Master's Award: Canada Graduate Scholarships
Keyworddelim
Clinical Study; Hospital-Based; Intensive Care Unit; Peripheral Vasopressor Use; Shock
Abstract
The use of medications to increase blood pressure called vasopressors are invaluable in the treatment of patients who have difficulty maintaining a stable blood pressure. Vasopressors are usually infused through a central venous catheter (CVC), which is a flexible tube placed in the large vein of the neck, arm or groin. CVCs require a skilled clinician and often with an ultrasound to prevent complications such as a collapsed lung or bleeding. These complications can cause significant harm and may occur in up to 15% of patients. Alternatively, the infusion of vasopressors through a peripheral venous catheter (PVC), a thin tube placed in the smaller veins of the arm or hand, have been avoided due to the risk of extravasation, which is the leakage of fluid to surrounding tissues. This can lead to potential tissue death requiring surgery. However, emerging research shows the safety of infusing vasopressors through a PVC, referred to as peripheral vasopressors. There is a growing interest in peripheral vasopressors for two main reasons: to expedite vasopressor initiation in patients with refractory shock and to potentially avoid CVC placement and its complications. However, a standardized protocol for administration is lacking and many clinicians still avoid peripheral vasopressors due to lack of high quality evidence. We will examine the effectiveness of implementing a peripheral vasopressor protocol by conducting a feasibility study and assess outcomes such as safety of peripheral vasopressors and acceptability rate by healthcare providers. By conducting this study, we hope to provide the framework to conduct larger, multi-center trials and to provide high quality data for the future use of a standardized peripheral vasopressor protocol.
Competitiondate
202412
Approvedterm2
1 yr 0 mth
Pinamesdelim
Wiseman, Jessica F
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $27,000~ $0~