Critical Illness Clinical Trial
Official title:
Microcirculatory Alterations in Critical Disease. New Ultrasound Technology for Assessment of Small-vessel Circulation Pathophysiology
Aim of this study is (1) to test and further develop a new non-invasive ultrasound method,
and (2) to gain new insight into microcirculatory alterations during critical disease,
particularly in critical septic shock patients.
Although early identification and treatment of sepsis have had top priority among the working
tasks of the international 'Surviving Sepsis Campaign' society (collaboration of the Society
of Critical Care Medicine and the European Society of Intensive Care Medicine) for several
years, which have led to improved survival over the last two decades, there is no objective
validated diagnostic test to identify or to support the clinical diagnosis at an early stage.
Analogous, there is no validated monitoring system available to guide and evaluate the
effects of stabilizing measurements in sepsis, or other critical disease, at the
microcirculatory level. And thus, there is an enormous knowledge gap regarding dynamic
changes at the microcirculatory level during sepsis and other critical disease.
Goal with this study is to investigate the robustness of this new US-technology, regarding
its ability to identify and monitor critical microcirculatory impairment during critical
disease. The investigators believe this technology may improve early diagnosis and thus early
initiation of adequate treatment in septic shock. Its mobile and non-invasive qualities, as
in most ultrasound methods, substantiate its availability to a wide range of clinical
settings.
Critical disease, e.g. life threatening septic shock triggered from infections with
multiorgan failure, demands aggressive medical treatment in specialized intensive care units
(ICU). Incidences and mortality of sepsis vary significant, depending on regional medical
culture, diagnostic criteria and the time span and method of data collection.
Common clinical appearance of critical disease is often life threatening low blood pressure,
impaired consciousness up to coma, abnormal breathing patterns, and then subsequently
secondary organ failures which further increases mortality. The influence of these
'macro-haemodynamic symptoms', i.e. physiologic aberrations that can be assessed using
standard patient monitoring systems, on the tissue micro-circulation where organ damage and
finally cell death occurs, is only indirectly available for assessment. Basically, the coarse
therapeutic approach to circulatory shock is to normalize macro-haemodynamic parameters,
without any robust method to evaluate and monitor micro-circulatory effects. Thus, following
current guidelines and clinical practice, it is sometimes not known for sure, on an
individual basis, whether treatment and stabilization measures increase survival chances.
Studies of the microcirculation have been performed using invasive micro-dialysis, direct
orthogonal polarization spectral imaging and direct side-stream dark-field microscopy. The
wide use of these methods is challenged by the fact that they are very expensive and demand
extended operator expertise.
The investigators think there is sufficient evidence to claim that further improvement in
early diagnostic and therapy guidance of sepsis, septic shock and other critical disease,
depends on increased knowledge of microcirculatory alterations, and widespread affordable
technical solutions to detect and monitor the course of sepsis and other critical disease at
the microcirculatory level.
At the Norwegian University of Technology and Science (NTNU), Department of Circulation and
Medical Imaging (ISB), new ultrasound technology has been developed by Professor Hans Torp,
which may offer an operator-independent, affordable and non-invasive method to evaluate
microcirculation in humans.
In general, ultrasound is unique in that sense that it facilitates non-invasive imaging of
anatomy and physiology. The unique with this new probe is the emittance of ultrasound waves
from the whole cross-section of the probe surface.
To describe the expected spectrum of microcirculatory impairment during different stages of
sepsis, septic shock and comparable critical disease, firstly US registrations are needed
from persons with known normal microcirculation. Then, registrations of normal
microcirculation are needed in persons exposed to increasing amounts of circulatory stress.
Finally, microcirculatory conditions will be observed in patients with critical septic shock.
Thus, firstly healthy volunteers are included, then stabile patients undergoing major planned
surgery, and finally patients in critical septic shock demanding advanced intensive care
treatment and monitoring.
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