Burns Clinical Trial
Official title:
A Single-centre Prospective Observational Study of MIcrocirculatory Perfusion Alterations in Severe Burn Injury
The main objective of our study is to focus on the efficiency of standard fluid resuscitation
in promoting tissue perfusion in severe burns patients (>15% TBSA). The incidence of
microcirculatory perfusion alterations, according to a predefined arbitrary cut off value, in
patients with severe burns injury (>15%TBSA) will be assessed during standard resuscitation
in the first 24 hours.
Secondary objectives are to assess differences in microcirculatory perfusion alterations
between early (<12 hours post burn injury) and late standard resuscitation (>12 hours post
burn injury) with addition of albumin to the regime.
And to measure several biomarkers of glycocalyx shedding, oxidative stress and inflammation.
Rationale: There are valid concerns that resuscitation in burns shock is inadequate. A
tendency to over resuscitate patients seem to exist. Current guidelines were developed 35
years ago and clinical burn resuscitation has not advanced significantly, despite ongoing
research. The main goal of resuscitation is achieving organ perfusion and tissue oxygenation.
Inadequate fluid resuscitation of severe acute burns may result in hypovolemic shock and
death. Excessive fluid resuscitation may result in fluid overload, lung edema,
intra-abdominal hypertension, abdominal compartment syndrome and burn depth conversion with
increased requirement for escharotomies, fasciotomies and skin grafting. Monitoring of
adequacy of resuscitation in burns patients has always been guided by systemic hemodynamic
variables (macro circulation) like blood pressure, heart rate, stroke volume and urinary
output, being urine output the major indicator of successful resuscitation. Whether these end
points are successful in achieving adequate perfusion and oxygen transport to the tissues is
unknown and relies on the assumption that there is a hemodynamic coherence between the macro
and microcirculation whereby improving the macro circulation causes a parallel improvement in
the microcirculation Objective: The main objective of our study is to focus on the efficacy
of standard fluid resuscitation in promoting tissue perfusion.
Study design: Single-center, prospective, observational clinical study in the Maasstad
Hospital.
Study population: All adult patients who are admitted to the Intensive Care Unit with severe
burns over 15%TBSA and resuscitated with the standard resuscitation protocol will be
included.
Main study parameters/endpoints: Measurement of sublingual microcirculation with vessel
density and flow parameters. Also skin perfusion maps (Laser Speckle Imaging) will be
recorded. Blood and urine samples will also be used for measuring glycocalyx shedding
products.
Nature and extent of the burden and risks associated with participation, benefit and group
relatedness:
Microcirculation assessment and laser speckle imaging are non-invasive procedures, and there
are negligible risks. Blood tests will be used for measuring glycocalyx shedding products,
this is an invasive procedure which may increase the risk of contamination, patient
discomfort and in some extreme cases blood sample collection may be a burden on patient
haemoglobin levels which is prone to decrease in critical patients. Assessment is essential
for determining whether action is required to change our existing resuscitation regime for
critically ill burned patients. If the results show that the current resuscitation regime is
suboptimal, then motivation for changing the existing practice can lead to improved clinical
care and a reduction in over- or under resuscitation in the ICU environment with its
potential harmful effects.
The risks associated with participation can be considered negligible and the burden can be
considered minimal in this observational study. The patients taking part in this study will
have no direct benefit.
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