Ventricular Function, Left Clinical Trial
Official title:
Evaluation of Radial Strain Versus Fractional Shortening and Fractional Area Change for Assessment of Left Ventricular Function in Transesophageal Echocardiography
Assessment of left ventricular function is an essential determinant of overall hemodynamics
and heart function and therefore of central interest in intra-operative transesophageal
echocardiography.
Currently, the most frequently used methods for quantification of left ventricular function
are fractional shortening (FS) and fractional area change (FAC).
Radial strain is a new parameter to asses left ventricular function. The investigators want
to assess left ventricular function with radial strain, fractional shortening (FS) and
fractional area change (FAC) in non-cardiac patients during non-cardiac operations. The aim
of this study is to show that radial strain is as reliable as FS and FAC in left ventricular
function assessment and more robust to changes in preload and afterload conditions.
Assessment of left ventricular function is an essential determinant of overall hemodynamics
and heart function and therefore of central interest in intra-operative transesophageal
echocardiography.
Currently, the most frequently used methods for quantification of left ventricular function
are fractional shortening (FS) and fractional area change (FAC). These parameters can be
assessed in the transgastric mid papillary short axis view (TG SAX) to quantify left
ventricular systolic function. Limitations of these methods are the experience of the
investigator - the more experienced the investigator the more reliable and reproducible the
data are, load dependency of these methods and the geometrical assumption of a
one-dimensional measurement for assessment of a three-dimensional contracting left
ventricle. Therefore, LV-function will either be over- or underestimated by influence of
segmental wall motion abnormalities or by missing them.
Radial strain allows reliable and reproducible evaluation of left ventricular function and
also allows assessment of myocardial deformation from representative segments of each wall
of the left ventricle. Myocardial strain is described as the relative deformation of a
myocardial fiber, normalized to its original length:L1-L0/L0(%). Strain is positive (radial
thickening) if L1>L0 and negative (longitudinal shortening and circumferential thinning) if
L1<L0. Radial strain is sensitive to changes in contractility and less influenced by loading
conditions which occur frequently during anaesthesia in a wide spectrum of non-cardiac
surgery as a result of blood loss or loss of hemodynamic autoregulation due to anesthetic
drugs.
Therefore we want to assess left ventricular function with radial strain, fractional
shortening (FS) and fractional area change (FAC) in non-cardiac patients during non-cardiac
operations. The aim of this study is to show that radial strain is as reliable as FS and FAC
in left ventricular function assessment and more robust to changes in preload and afterload
conditions.
Study hypothesis
The aim of the study is to compare fractional shortening (FS) and fractional area change
(FAC) with radial strain from TG mid SAX using TEE in the anaesthetized patient undergoing
non-cardiac surgery. Furthermore we want to investigate the influence of changes in loading
conditions on these parameters in the anaesthetized non-cardiac patient undergoing
non-cardiac surgery. Therefore patients are examined in zero position, trendelenburg- and
anti-trendelenburg-position.
Hypothesis:
- Radial strain correlates with FAC and FS in assessment of left ventricular function in
patients undergoing non-cardiac surgery. FAC is of primary interest because it has
several advantages: it is very easy to calculate, it´s considered a surrogate of
ejection fraction, and several studies have shown that it is an excellent measure of
left ventricular function even in patients with heterogeneity of regional function.
- The parameters radial strain, fractional shortening and fractional area change
correlate during are changes in loading conditions (zero-position, trendelenburg- and
anti-trendelenburg-maneuver).
Study design: prospective cohort study Inclusion criteria
- Planned non-cardiac surgery with a minimum duration of 60 minutes, where intubation is
indicated
- Age above 18 years
- Signed informed consent Exclusion criteria
- No patient's consent
- Subjects not able to understand study procedures
- Contraindications to transesophageal echocardiography (oesophageal-, gastric disorders,
hematologic disorders with increased bleeding incidence, ENT-surgery, surgery of the
oesophagus or stomach)
- Medical history of any kind of heart disease, dyspnea or angina pectoris
- Hypertension (medically treated)
- Diabetes
- Atrial fibrillation Study protocol One day prior to surgery the patients are screened
and invited to participate in the study by the principle investigator. If they consent
the principle investigator does a physical examination and takes their medical history.
On the day of surgery patients receive premedication as usual. Arriving at the operating
room the patients are monitored with ECG, pulse oximetry and blood pressure (either invasive
with insertion of an arterial catheter, when indicated, or non-invasive blood pressure). A
peripheral venous line is needed for induction of anaesthesia. Induction and maintenance of
anaesthesia is performed using standard protocols. After induction of anaesthesia and
insertion of all needed catheters (central venous catheter, bladder catheter, arterial
catheter, and eventually pulmonary artery catheter) the transoesophageal probe, covered with
a special condom, will be inserted.
The examination will be done by the principle investigator (Dr. Ulrike Weber) under
supervision of an expierenced investigator.
Intraoperative TEE-Examinations (T1, T2, T3)
At T1, T2, T3 TEE-study examinations are performed in zero position, Trendelenburg position,
and anti-Trendelenburg position. Positioning will follow a random order according to a
blinded randomization list.
Trendelenburg-position shall be defined for the study with 10cm head-down from horizontal
position, anti-trendelenburg position with 10cm head-up (from horizontal position). After
positioning examination will start after a 3 min delay for reaching a steady-state in
loading conditions.
T1 - after induction of anesthesia
After insertion of the probe a transesophageal echo examination (TEE) is performed -
including a complete routine clinical examination (T1):
T2 - Intraoperative TEE, 3min after positioning
Positioning (zero position, Trendelenburg, anti-trendelenburg) will be performed according
to randomization. 3min after positioning, under stable hemodynamics, recordings of HR, blood
pressure, FS, FAC, Radial strain
T3 - Intraoperative TEE, 3min after positioning
Positioning (zero position, Trendelenburg, anti-trendelenburg) will be performed according
to randomization. 3min after positioning, under stable hemodynamics, recordings of HR, blood
pressure, FS, FAC, Radial strain
The following measurements are taken for the study (3 times during sinus rhythm):
- FS in the transgastric short axis mid papillary view
- FAC in the transgastric short axis mid papillary view
- Radial strain in the transgastric short axis mid papillary view
Recordings of the 2D-mode images of the TG SAX shall be taken in triplicate with 3 heart
cycles per stored clip. The images will be stored digitally in the EchoPAC-raw data format.
Analysis of data will be performed offline in a dedicated work station (EchoPAC, GE Vingmed,
Horten, Norway). Three different investigators will analyse all data two times at two
different time points.
Expected study population: 33 patients
;
Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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