Sepsis in the ICU-II
Study Details
Study Description
Brief Summary
Sepsis-induced cardiac dysfunction (SIMD) is a well-known phenomenon yet its diagnosis remains elusive with no accepted definition, or defining pathophysiological mechanism associated with this disease. Systolic dysfunction occurs in 20-70% of patients, and may be severe, yet does not appear to have any prognostic value for mortality. Diastolic function has also been variably described and seems to be related to short-term mortality. However, the contribution of left ventricular systolic and diastolic dysfunction to mortality in sepsis are still far from clear, with uncertain contribution from previous cardiovascular disease, vasopressor and inotropic drugs and mechanical ventilation. Another poorly investigated area is right ventricular dysfunction. Cor pulmonale occurs in up to 25% of patients with septic shock, and is invariably related to pulmonary haemodynamics and mechanical ventilation, yet very little is known about how this affects prognosis. Finally, although the outcome of disease is a function of multiple parameters, septic cardiomyopathy is most frequently characterized based on individual echocardiographic parameters, without considering their interactions or placing them in the context of biomarkers and clinically available haemodynamic data. Available relevant studies are often monocentric, and many fail to consider the various confounders that influence the clinical outcome in sepsis. Therefore, the diagnostic and prognostic value of combinations of clinical, biochemical and haemodynamic variables remains to be established.
Accordingly, the purpose of this study is to identify biomarkers and echocardiographic and haemodynamic signatures characteristic of specific outcomes in SIMD to support the diagnosis and prognosis in SIMD. Specific aims are:
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To determine the association between left ventricular systolic and diastolic dysfunction, and adverse outcome in SIMD;
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To determine the association between right ventricular systolic and diastolic dysfunction, and adverse outcome in SIMD;
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To determine the association between novel biomarkers and adverse outcome in SIMD;
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To determine the combined value of biomarker, echocardiographic, and haemodynamic variables for predicting adverse outcomes in SIMD;
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To explore if there are different phenotypes of SIMD using unsupervised machine learning algorithms, and whether they are associated with adverse outcomes.
50 patients will be enrolled in a feasibility study to evaluate the logistical setup for acute echocardiography and biobanking facilities. A further 300 patients will be enrolled with inclusion from peripheral centers once feasibility is confirmed.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
UPDATE 26 Feb 2022:
A pilot project was completedafter recruitment of 50 patients confirming the feasibility of data collection, study logistics, biomarker assay set-up and frequency of outcomes. Cancellation of non-COVID related research in 2020&2021 has caused significant delays. Recruitment of patients will continue during 2022&2023. At the time of writing 70 patients have been recruited across 4 centres.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Adult patients with septic shock All adult (>=18 yo) patients admitted to participating ICUs with septic shock defined according to the Sepsis III criteria. Purely observation study with no intervention. Patients are exposed to septic shock and treatment according to standard departmental protocols at each centre. |
Other: Exposure is septic shock (defined according to Sepsis-III) and standard treatment according to departmental protocols.
Collection of data, biomarker and echocardiography analysis will be centralized and blinded. Assessment of endpoints will be blinded.
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Outcome Measures
Primary Outcome Measures
- Myocardial injury [any time during ICU stay within the study period, up to 10 days]
increased hsTnT
- Organ failure free days [30 days of study inclusion]
Organ failure
Secondary Outcome Measures
- 30 day mortality [30 days after study inclusion]
Short term mortality
- 365 day mortality [365 days after study inclusion]
Long term mortality
Other Outcome Measures
- Exploratory outcomes [during ICU stay, up to 10 days]
Vasopressor inotropic score
- Exploratory outcomes [30 days of study inclusion]
Days free of mechanical ventilation
Eligibility Criteria
Criteria
Inclusion Criteria:
- Adult patients admitted to ICU and fulfilling the Sepsis-III criteria for septic shock
Exclusion Criteria:
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No informed consent
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Acute coronary syndromes
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | CHU Dijon-Bourgogne | Dijon | France | 21000 | |
| 2 | CHU Georges Pompidou | Paris | France | 75015 | |
| 3 | Ryhov Sjukhus Jönköping | Jönköping | Sweden | 55305 | |
| 4 | Dept of Anaesthesia and Intensive Care | Linköping | Sweden | 58185 |
Sponsors and Collaborators
- Linkoeping University
- Hospitaux Universitaires Paris Sud
- Hôpital Dupuytren
- CHU Dijon Bourgogne
- CHU George Pompidou, Paris
- Ryhov Hospital, Jönköping
Investigators
- Study Chair: Michelle Chew, MBBS, PhD, Linkoeping University Hospital
- Principal Investigator: Bernard Cholley, MD, PhD, CHU George Pompidou
- Principal Investigator: Belaid Bouhemad, MD, PhD, CHU Dijon
- Principal Investigator: Fredrik Hammarsköjld, MD, PhD, Ryhov Hospital, Jönköping
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- SICU-II