The Role of Left Ventricular Outflow Tract (LVOT) Velocity-time Integral (VTI) and Respiratory Variability at Peak Rate (Vpeak) in Predicting Hypotension After General Anesthesia Induction

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorAydin Adnan Menderes University

About this trial

Preoperatively, patients will undergo transthoracic echocardiography measurements approximately 15-30 minutes before induction. TTE will be performed on all patients by an experienced observer; the echocardiography device will be equipped with an S4-2 transducer (4-2 MHz frequency range) in the left lateral decubitus position.

VTI and Vpeak values of the LVOT were measured from manually drawn contours using pulsatile wave Doppler technique in the apical five-chamber view. The Doppler beam was aligned with the aortic blood flow, and the signal was captured at an appropriate angle (\<20°).

The maximum (VTImax) and minimum (VTImin) VTI, as well as the maximum (Vpeakmax) and minimum (Vpeakmin) Vpeak values, were determined over three respiratory cycles. ΔVTI was calculated with the following formula:

ΔVTI = \[2 × (VTImax - VTImin) / (VTImax + VTImin)\] × 100%.

ΔVpeak was calculated with the following formula:

ΔVpeak = \[2 × (Vpeakmax - Vpeakmin) / (Vpeakmax + Vpeakmin)\] × 100%. These parameters were analyzed to evaluate the hemodynamic status of patients and estimate fluid responsiveness.

Patients with a 30% decrease from baseline in SBP and a decrease in MAP below 60 mmHg in the first 10 minutes after anesthesia induction were considered to have hypotension. Patients were divided into two groups: "with" and "without" hypotension.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

18-75 years

ASA Physical Status 1-3;

Patients scheduled for general anesthesia

Disqualifiers

Patient is pregnant

Post-cardiac surgery

Severe pulmonary hypertension

Severe valvular disease

Trial population

This study will be conducted on hemodynamically stable patients aged between 18 and 75 years, with an American Society of Anesthesiologists (ASA) physical status classification of I-III, who are scheduled for elective surgery and will undergo general anesthesia.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Inotrope

    Drug

    Hypotensive attacks with MAP below 55 mmHg or prolonged duration (2 minutes or more) will be treated with ephedrine 0.1 mg/kg.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: with hypotension1 intervention
Group B: none hypotension0 interventions

Trial outcomes

Primary outcomes

1

lvot-vtı

The relationship between hypotension following induction of general anesthesia and respiratory variability in left ventricular outflow tract VTI peak velocity (Vpeak variability).

Time frame
1 hour

Secondary outcomes

1

lv echo

The relationship between hypotension following induction of general anesthesia and left ventricular function parameters measured by transthoracic echocardiography (TTE).

Time frame
1 hour

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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