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Background: Recent studies have questioned the safety of current fluid resuscitation strategies in patients with septic shock as prospective and observational data suggesting that the resulting fluid overload is associated with mortality. Two strategies have evolved to prevent or minimize fluid overload: restrictive fluid administration or active removal of accumulated fluid. While several small trials show benefits with a restrictive fluid administration regimen, active protocolized de-resuscitation was scarcely evaluated. The combination of both strategies yet warrants systematic evaluation.
Aim: This study aims to assess the efficacy and feasibility of an early active de-resuscitation protocol in patients with septic shock. We hypothesize that the application of a structured early de-resuscitation protocol versus standard of care will lead to less fluid overload at day three after ICU admission.
Study Intervention: Patients admitted to the ICU with confirmed or suspected septic shock (Sepsis-3 definition) will be randomized (1:1) to either the intervention or standard of care. In the intervention arm, patients are managed according to the REDUCE fluid management protocol during resuscitation and de-resuscitation.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention: REDUCE Protocol | Experimental | Fluid resuscitation and de-resuscitation is based on the REDUCE fluid management protocol. |
|
| Standard of Care | Active Comparator | Fluid resuscitation and de-resuscitation according to the standard of care |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Fluid management according to the REDUCE Fluid Protocol | Other | Fluid management according to the protocol will be guided by pre-defined clinical signs for impaired perfusion and fluid overload. |
| Measure | Description | Time Frame |
|---|---|---|
| Proportion of patient with a negative fluid balance on day 3 | Proportion of patients with a negative cumulative fluid balance on day 3 | Up to day 3 after ICU admission |
| Measure | Description | Time Frame |
|---|---|---|
| Number of patients with fluid overload at day 3 and ICU discharge | Fluid overload as defined as ((input-output)/admission weight)*100 | From hospital admission to the end of ICU stay, on average after 7 days |
| Feasibility of the REDUCE fluid protocol |
| Measure | Description | Time Frame |
|---|---|---|
| Daily cumulative fluid balance up to day 7 | Cumulative fluid balance is total input - total output | Throughout the ICU stay, on average 7 days |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Anna S Messmer, MD | Department of Intensive Care, Inselspital, Bern University Hospital, Bern, Switzerland | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Hospital Basel | Basel | 4031 | Switzerland | |||
| University Hospital Bern, Inselspital |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 37734896 | Background | Messmer A, Pietsch U, Siegemund M, Buehler P, Waskowski J, Muller M, Uehlinger DE, Hollinger A, Filipovic M, Berger D, Schefold JC, Pfortmueller CA. Protocolised early de-resuscitation in septic shock (REDUCE): protocol for a randomised controlled multicentre feasibility trial. BMJ Open. 2023 Sep 21;13(9):e074847. doi: 10.1136/bmjopen-2023-074847. |
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| ID | Term |
|---|---|
| D012772 | Shock, Septic |
| ID | Term |
|---|---|
| D018805 | Sepsis |
| D007239 | Infections |
| D018746 | Systemic Inflammatory Response Syndrome |
| D007249 | Inflammation |
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| ID | Term |
|---|---|
| D059039 | Standard of Care |
| ID | Term |
|---|---|
| D019984 | Quality Indicators, Health Care |
| D011787 | Quality of Health Care |
| D006298 | Health Services Administration |
| D017530 | Health Care Quality, Access, and Evaluation |
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Patients will be randomized to receive either fluid resuscitation/de-resuscitation according to the REDUCE protocol or standard of care.
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Outcome assessors will be blinded to the treatment allocation.
|
| Standard of care | Other | Fluid resuscitation and de-resuscitation will be managed according to the standard of care |
|
Number of REDUCE fluid protocol violations
| From randomisation until the end of ICU stay, on average after 7 days |
| Incidence of ischemic events and severe AKI | Number of patients with:ischaemic events, severe AKI (AKIN stage 2 or more); respectively episodes of: severe hypernatremia (sodium >/= 155mmol/l), severe hypokalemia (< 3.0 mmol/l), severe metabolic alkalosis (pH >/= 7.55, bicarbonate >/= 35 mmol/l), anaphylactic reaction to diuretic drug | Ischemic events and AKI: From randomisation until the end of ICU stay (on average after 7 days), and at day 30; electrolyte and acid-base/medication associated safety endpoints: during ICU stay (on average 7 days) |
| Ventilator-free days at day 30 | Ventilator free days up to day 30 | Up to 30 days after randomisation |
| Vasopressor-free days at day 30 | Vasopressor free days up to day 30 | Up to 30 days after randomisation |
| Renal replacement therapy | Need for and time on renal replacement therapy | Up to 90 days after randomisation |
| Number of patients with need for renal replacement at 90days | Number of patients with on-going need for renal replacement at 90days | Up to 90 days after randomisation |
| All-cause mortality | At 30days and 90 days after randomization | Up to 90 days after randomisation |
| Bern |
| 3010 |
| Switzerland |
| Cantonal Hospital St. Gallen | Sankt Gallen | 9000 | Switzerland |
| Kantonsspital Winterthur | Winterthur | 8400 | Switzerland |
| D010335 |
| Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D012769 | Shock |