Stroke-free Survival Comparison Between Early Surgery and Conventional Therapy in Left Infective Endocarditis

Maria Vittoria Hospital

Status: Terminated

Conditions: Endocarditis

Treatments: Procedure: Conventional therapy; Procedure: Early surgery

Study type: Interventional

Funder types: Other

Identifiers

NCT03411499

Protocol RF-2013-020358691

Details and patient eligibility

About

The purpose of the EARLY study is to evaluate the efficacy and effectiveness of early surgery in patients with Infective Endocarditis (IE).

Full description

Infective endocarditis (IE) is a relatively rare disease and has a high in-hospital mortality (15-30%) and morbidity due to complications like embolic events, especially in the central nervous system, and heart failure. International guidelines give indications on the optimal timing for surgery, and they strongly recommend early surgery for patients in the active phase of IE with acute cardiac complications (e.g., acute heart failure, uncontrolled infection, and persistent large vegetations after an embolic event). However, at present there is no clear evidence supporting the effectiveness of early surgery or indicating the best time to perform surgery, especially in patients without such conditions. Primary objective of the study is to evaluate whether, in patients with IE and no emergency surgery indication, an early surgical strategy (performed within 72 hours from IE diagnosis) is more effective than conventional therapy in terms of 1-year stroke-free survival. Secondary objectives are: overall survival, risk of embolic, risk of strokes, event-free survival, IE relapse, heart failure, length of hospital stay, hospital re-admission and hospitalization days, strategy compliance, quality of life and health care costs.

This study design consist of a two-arm, open-label, multicenter randomized controlled trial, but patients who decline to be randomized and prefer a certain therapy strategy will be treated according to best practice and included into a prospective observational study after given informed consent. This parallel constructed observational study will be performed with a maximum of consistency to treatment and observation compared to the Randomized clinical trial (RCT). Patients who agree to the randomized trial will be stratified according to centre and clinical features (prosthetic valve,vegetations, valve regurgitation) and randomized with a 1: 1 ratio to 2 different strategies.

According to O'Brien and Fleming group sequential design with a maximum of two stages and a drop-out rate of 10%, a total of 400 randomized patients (200 per group) are required to detect an increase in the stroke-free survival from 82% to 89.5% (corresponding to an Hazard Ratio=0.56) considering a significance level of 5% and a power of 80% and expecting a risk for mortality or stroke at one year with standard treatment equal to 0.18.

EARLY study may help to demonstrate early surgery impact on the contemporary management of the disease.

Enrollment: 6 patients

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Left-sided Infective Endocarditis (IE) according to modified Duke criteria, fulfilling at least one of the following features:

   • IE on native or prosthetic valve with severe mitral or aortic valve regurgitation, without heart failure;
   • IE on native or prosthetic valve, during the first week of antibiotic therapy, have very large (15-30 mm) or large (>10mm), mobile isolated vegetations due to Staphylococcus aureus, Streptococcus bovis, HACEK or Abiotrophia, without any other indication for surgery;
   • IE on native or prosthetic valve with severe valve regurgitation without heart failure and with large vegetations (> 10 mm) and Euroscore I 5-19;
   • IE on native or prosthetic valve with moderate o moderate-severe valve regurgitation with large vegetations (> 10 mm)
   • IE on prosthetic valve due to Staphylococcus aureus or gram negative non HACEK microorganisms.

2. Compliance to study treatments

3. Euroscore I <20

4. Informed consent signature

Exclusion criteria

1. Patients with right-side IE and IE on a cardiac device

2. Patients with IE and:

   • heart failure , refractory pulmonary oedema, cardiogenic shock or untreatable heart failure
   • fistula involving cardiac chambers or pericardium
   • persistent heart failure or unstable echocardiographic signs or poor haemodynamic tolerance
   • uncontrolled local infection (abscess, pseudoaneurism, fistula, increase in size vegetations)
   • fever and positive blood cultures lasting >7 days
   • fungal IE or other multi-resistant microorganisms
   • large vegetations (> 10 mm) after embolic event
   • large vegetations (> 10 mm) and other predictors of complicated course (heart failure, abscess)
   • vegetations >30 mm

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

6 participants in 2 patient groups

Early surgery

Experimental group

Description:

Surgery within 72 hours from endocarditis diagnosis

Treatment:

Procedure: Early surgery

Conventional therapy

Active Comparator group

Description:

Medical treatment and a possible delayed surgical intervention according to the current guidelines

Treatment:

Procedure: Conventional therapy