Long-term Cognitive and Cerebral Changes in Sepsis Survivors and Their Predictors (BonSEP)

German Center for Neurodegenerative Diseases (DZNE)

Status: Unknown

Conditions: Severe Sepsis Without Septic Shock; Severe Sepsis With Septic Shock

Treatments: Procedure: Blood Sample; Other: Resting State EEG; Behavioral: Neurocognitive Assessment; Other: MRI; Procedure: Lumbar Puncture

Study type: Interventional

Funder types: Other

Identifiers

NCT02339649

BN005

2011-003014-16 (EudraCT Number)

Details and patient eligibility

About

The main goals of this study are to provide a cognitive, neurological, brain morphological, and serological profile of sepsis survivors in order to make long-term prognosis of recovery and estimate the need for rehabilitation measures in order to help patients reintegrate into normal daily life.

Full description

Comparison of cognitive function in severe septic/septic shock ICU patients with non-septic postoperative ICU patients and actively recruited healthy controls at several time points up to 12 months after leaving the ICU.

Secondary aims:

• Profiling specific cognitive deficits in sepsis survivors over time.
• Identifying possible subclasses of long-term cognitive impairment according to facets of disease, therapy and ICU experience.
• Investigating long-term brain morphological changes, with hippocampus as region of interest (ROI).
• Determining values of Serum- and CSF-Biomarkers
• Evaluation of diagnostic and prognostic value of non-routine biomarkers for systemic- and neuroinflammation in the acute phase and in the long-term
• Investigate associations between brain morphological changes, cognitive changes, neurological status, psychiatric burden, disability level, employment status and health-related quality of life (HRQOL).
• Investigating brain-activity changes in resting state electro-encephalogram (EEG)

Enrollment: 308 estimated patients

Sex: All

Ages: 25 to 80 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

sepsis/septic shock subjects will only be included in the study if they meet all of the following criteria:

• Written informed consent of the subject. or legal representative patient at the Anesthesiological-Operative Intensive Care Unit of the University Hospital Bonn, the Department of Anesthesiology, Intensive Care and Pain Therapy of the Malteser Hospital, or the Department of Anesthesiology, Intensive Care Medicine and Pain Medicine of the Gemeinschaftskrankenhaus Bonn St. Petrus Hospital. At the Anesthesiological-Operative Intensive Care Unit of the University Hospital Bonn, only, or 1) documentation of presumed will via a relative or legal representative . together with 2) Documentation of verification by a doctor independent of the study that the patient's study participation is unobjectionable. Written informed consent of patient will be obtained at the earliest time possible.
• Aged 25-80 years
• Male or female
• Admitted to the intensive care units of the Anesthesiological-Operative Intensive Care Unit of the University Hospital Bonn, from the Department of Anesthesiology, Intensive Care and Pain Therapy of the Malteser Hospital or from the Department of Anesthesiology, Intensive Care Medicine and Pain Medicine of the Gemeinschaftskrankenhaus Bonn St. Petrus Hospital.
• Duration of ICU stay must be a minimum of 24 hours. In case of transfer to intermediate care or the observation ward before the 24 hour ICU period is complete, study parameters must be allowed to be assessed.
• Fulfill the criteria of sepsis and/or septic shock patients according to theThird International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3, Singer et al, 2016).

Postoperative ICU Patients will only be included in the study if they meet all of the following criteria:

• Written informed consent of the subject.
• Aged 25-80 years
• Male or female
• Admitted to the intensive care units of the Anesthesiological-Operative Intensive Care Unit of the University Hospital Bonn, which includes a surgical ICU, an anesthesiological ICU, and a cardio-surgical ICU
• Duration of ICU stay must be a minimum of 24 hours. In case of transfer to intermediate care or the observation ward before the 24 hour ICU period is complete, study parameters must be allowed to be assessed.
• Mini-Mental Status Examination (MMSE) Score of 25 or above

Healthy Controls will only be included in the study if they meet all of the following criteria:

• Written informed consent of the subject
• Aged 25-80 years
• Male or female

Exclusion criteria

Subjects presenting with any of the following exclusion criteria may not be included in the study:

• Simultaneous participation in any clinical treatment study involving administration of an investigational medicinal product within 30 days prior to study beginning
• Physical or psychiatric condition which at the investigator's discretion may put the subject at risk, may confound the study results, or may interfere with the subject's participation in this study
• Prior to the start of this study existence of preexisting severe diseases and/or conduction of surgery necessarily imply life expectancy less than 12 months
• Known or suspected persistent abuse of medication, drugs or alcohol now or in the past
• Known cerebral lesions, cerebral infarction or malignomas
• Dementia or history of other central nervous system diseases
• Cranial-cerebral injury
• Known HIV-Infection
• Known liver cirrhosis with a documented Child-Pugh Score of C prior to this study
• Liver transplants
• Prior to start of this study nursing care level of 2 or 3
• Prior to start of this study residing in a nursing home

Additional Exclusion Criteria For Non-Septic Postoperative ICU Patients:

• Fulfill the criteria of sepsis and/or septic shock patients according to theThird International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3, Singer et al, 2016).
• In the case that a postoperative ICU patient fulfills the criteria for sepsis during ICU stay, he/she will be moved to the sepsis group.

Additional Exclusion Criteria For Healthy:

• Executing third-party cognitive and functional assessments of another patient-subject also included in this investigation
• History of ICU stay in the last 12 months

Trial design

Primary purpose: Other

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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308 participants in 3 patient groups

Sepsis/septic Shock

Other group

Description:

Men and women seen at the intensive care units of the Anesthesiology Department of the University Hospital Bonn aged 25-80; fulfill the criteria of sepsis and/or septic shock patients according to theThird International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3, Singer et al, 2016). Interventions: Neurocognitive Assessment, Clinical Scales, Questionnaires, Blood Sample, voluntary Lumbar Puncture, Resting State EEG, MRI

Treatment:

Other: MRI

Procedure: Lumbar Puncture

Behavioral: Neurocognitive Assessment

Other: Resting State EEG

Procedure: Blood Sample

Postoperative ICU Patients

Other group

Description:

Men and women seen at the intensive care units of the Anesthesiology Department of the University Hospital Bonn aged 25-80: * Admitted to the intensive care units of the Anesthesiological-Operative Intensive Care Unit of the University Hospital Bonn, which includes a surgical ICU, an anesthesiological ICU, and a cardio-surgical ICU * Duration of ICU stay must be a minimum of 24 hours. * Mini-Mental State Examination (MMSE) Score of 25 or above Interventions: Neurocognitive Assessment, Clinical Scales, Questionnaires, Blood Sample, voluntary Lumbar Puncture, Resting State EEG, MRI

Treatment:

Other: MRI

Procedure: Lumbar Puncture

Behavioral: Neurocognitive Assessment

Other: Resting State EEG

Procedure: Blood Sample

Healthy Controls

Other group

Description:

Healthy Controls will only be included in the study if they meet all of the following criteria: Written informed consent of the subject, Aged 25-80 years, Male or female. Interventions: Neurocognitive Assessment, Clinical Scales, Questionnaires, Blood Sample, voluntary Lumbar Puncture, Resting State EEG, MRI

Treatment:

Other: MRI

Procedure: Lumbar Puncture

Behavioral: Neurocognitive Assessment

Other: Resting State EEG

Procedure: Blood Sample