Early Goal-directed Therapy and Myocardial Dysfunction

NCT ID: NCT01312688

Last Updated: 2011-03-11

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 300 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-07-31
• Study Completion Date: 2013-12-31

Brief Summary

The cardiovascular system plays a central role in the pathophysiology and prognosis of sepsis, yet the correct hemodynamic management of septic patients is still vigorously debated. Despite guidelines, the use of CVP and PAOP is seriously criticized for inaccurate prediction of fluid requirement. Recently studies showed that early goal-directed therapy (EGDT) aimed at achieving a ScvO2 of ≥70% significantly improved survival of septic shock patients, yet EGDT has not been adopted by all intensivists. The investigators have recently found using 2D echocardiography in 262 patients with severe sepsis or septic shock and treated by the conventional guidelines (without ScvO2) that diastolic dysfunction and reduced stroke volume index are strong independent predictors of mortality. In the present study the investigators intend to test the effect of EGDT on resuscitation, on long term myocardial function and left ventricular volumes and on survival in ICU patients with severe sepsis and septic shock. Patients will be randomized to EGDT (resuscitation directed by ScvO2) or standard of therapy for the first six hours after diagnosis of severe sepsis or septic shock and admission to the ICU. After six hours patients in septic shock will be further monitored with non invasive cardiac output (PiCCO, Pulsion Technologies). All patients will be followed daily by 2D & 3D transthoracic echocardiography with detailed measurements of systolic and diastolic left and right ventricular volumes and functions. Patients in the EGDT group will be compared to the control group for parameters of initial resuscitation (fluid volumes, ScvO2 achieved, inotrope use), initial values from non invasive cardiac output at six hours, interventions required from institution of non invasive cardiac output, early and long term effects on cardiac function and volumes from echo measurements, and mortality. The effectiveness of EGDT will thus be examined in the short and long terms.

Detailed Description

Design: Prospective randomized controlled trial, approved (now submitted for approval) by the Institutional Review Board. Over a period of 2 years, 300 patients with severe sepsis or septic shock will be randomized to either the currently accepted standard hemodynamic treatment in our ICU or to the standard plus goal-directed therapy according to the Rivers protocol and the SSC guidelines, i.e. including the addition of ScvO2 measurements and consequently derived treatments to achieve ScvO2 ≥70% for the first 6 hours after appearance of sepsis or septic shock in the ICU (Fig. 2).

After the first 6 hours all patients in septic shock (62% of the patients according to our preliminary data) will be monitored by continuous cardiac output monitoring. Additionally, all patients will be followed daily by transthoracic echocardiography for up 19 to 5 days (Fig 3). Since the patients themselves will not be able to sign an informed consent, the inclusion to the study will be approved by the attending physician in charge of the ICU who will also be able to decide on stopping the study protocol at any time according to his clinical judgment as to the best interest of the patient.

Conditions

Sepsis; Septic Shock; Myocardial Dysfunction

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Standard hemodynamic therapy

Standard hemodynamic therapy currently accepted in our ICU

Group Type: OTHER

Early Goal Directed Hemodynamic Therapy in Sepsis

Intervention Type: OTHER

Early Goal Directed Hemodynamic Therapy according to the SSC guidelines

Early Goal Directed Hemodynamic Therapy

Early Goal Directed Hemodynamic Therapy according to the Surviving Sepsis Campaign Guidelines

Group Type: EXPERIMENTAL

Early Goal Directed Hemodynamic Therapy in Sepsis

Intervention Type: OTHER

Early Goal Directed Hemodynamic Therapy according to the SSC guidelines

Interventions

Early Goal Directed Hemodynamic Therapy in Sepsis

Early Goal Directed Hemodynamic Therapy according to the SSC guidelines

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Intensive care unit patients with severe sepsis or septic shock, age 18 or above.

Exclusion Criteria

• Pregnant women
• Patients with known significant valvular or coronary heart disease
• Patients with poor quality echocardiography imaging

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Hadassah Medical Organization

OTHER

Sponsor Role: lead

Responsible Party

Hadassah Medical Center

Principal Investigators

Giora Landesberg, MD, DSc

Role: PRINCIPAL_INVESTIGATOR

Hadassah Medical Organization

Locations

Hadassah Medical Center

Jerusalem, , Israel

Countries

Israel

Central Contacts

Giora 'Landesberg, MD, DSc

Role: CONTACT

gio@cc.huji.ac.il

972-54-4512874

Facility Contacts

Giora Landesberg

Role: primary

972-54-4512874

Other Identifiers

0034-11-HMO-CTIL

Identifier Type: -

Identifier Source: org_study_id