Crystalloid Liberal or Vasopressors Early Resuscitation in Sepsis
Status: | Recruiting |
---|---|
Conditions: | Hospital, Hospital |
Therapuetic Areas: | Other |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/8/2019 |
Start Date: | March 7, 2018 |
End Date: | June 2021 |
Contact: | Katie Oldmixon, RN |
Email: | coldmixon@mgh.harvard.edu |
Phone: | 617 726-4777 |
Multicenter, prospective, phase 3 randomized non-blinded interventional trial of fluid
treatment strategies in the first 24 hours for patients with sepsis-induced hypotension. The
aim of the study is to determine the impact of a restrictive fluids strategy (vasopressors
first followed by rescue fluids) as compared to a liberal fluid strategy (fluids first
followed by rescue vasopressors) on 90-day in-hospital mortality in patients with
sepsis-induced hypotension.
treatment strategies in the first 24 hours for patients with sepsis-induced hypotension. The
aim of the study is to determine the impact of a restrictive fluids strategy (vasopressors
first followed by rescue fluids) as compared to a liberal fluid strategy (fluids first
followed by rescue vasopressors) on 90-day in-hospital mortality in patients with
sepsis-induced hypotension.
Primary Hypothesis: Restrictive (vs liberal) fluid treatment strategy during the first 24
hours of resuscitation for sepsis-induced hypotension will reduce 90-day in-hospital
mortality.
1. We will emphasize early screening and protocol initiation, and enroll a maximum of 2320
patients with suspected sepsis-induced hypotension.
- All patients will receive at least 1 liter of fluids prior to meeting study
inclusion criteria (and no more than 3 liters prior to randomization).
- Patients will be enrolled within 4 hours of meeting study inclusion criteria
- Any type of isotonic crystalloid (normal saline, ringers lactate, or a balanced
solution such as plasmalyte) is permitted.
2. Restrictive Fluids (Early Vasopressors) Group
- Norepinephrine will be used as preferred vasopressor and titrated to achieve mean
arterial pressure (MAP) between 65 mmHg and 75 mmHg
- "Rescue fluids" may be administered as 500ml boluses if predefined rescue criteria
are met
3. Liberal Fluids (Fluids First) Group
- Additional 2 liter intravenous fluid bolus upon enrollment
- Administer 500ml fluid boluses for fluid triggers until 5 liters administered or
development of clinical signs of acute volume overload develop
- "Rescue vasopressors" may be administered after 5 liters of fluid, for development
of acute volume overload, or if other predefined rescue criteria are met
hours of resuscitation for sepsis-induced hypotension will reduce 90-day in-hospital
mortality.
1. We will emphasize early screening and protocol initiation, and enroll a maximum of 2320
patients with suspected sepsis-induced hypotension.
- All patients will receive at least 1 liter of fluids prior to meeting study
inclusion criteria (and no more than 3 liters prior to randomization).
- Patients will be enrolled within 4 hours of meeting study inclusion criteria
- Any type of isotonic crystalloid (normal saline, ringers lactate, or a balanced
solution such as plasmalyte) is permitted.
2. Restrictive Fluids (Early Vasopressors) Group
- Norepinephrine will be used as preferred vasopressor and titrated to achieve mean
arterial pressure (MAP) between 65 mmHg and 75 mmHg
- "Rescue fluids" may be administered as 500ml boluses if predefined rescue criteria
are met
3. Liberal Fluids (Fluids First) Group
- Additional 2 liter intravenous fluid bolus upon enrollment
- Administer 500ml fluid boluses for fluid triggers until 5 liters administered or
development of clinical signs of acute volume overload develop
- "Rescue vasopressors" may be administered after 5 liters of fluid, for development
of acute volume overload, or if other predefined rescue criteria are met
Inclusion Criteria:
- Age ≥ 18 years
- A suspected or confirmed infection (broadly defined by administration or planned
administration of antibiotics)
- Sepsis-induced hypotension defined as systolic blood pressure < 100 mmHg or MAP < 65
mmHg after a minimum of at least 1 liter of fluid (*Fluids inclusive of pre-hospital
fluids; blood pressure must be below any known or reported pre-morbid baseline).
Exclusion Criteria:
- More than 4 hours elapsed since meeting inclusion criteria or 24 hours elapsed since
admission to the hospital
- Patient already received 3 liters of intravenous fluid (includes prehospital volumes)
- Unable to obtain informed consent
- Known pregnancy
- Hypotension suspected to be due to non-sepsis cause (e.g. hemorrhagic shock)
- Blood pressure is at known or reported baseline level
- Severe Volume Depletion from an acute condition other than sepsis. In the judgment of
the treating physician, the patient has an acute condition other than sepsis causing
(or indicative) of *severe volume depletion; Examples include: Diabetic ketoacidosis,
high volume vomiting or diarrhea, hyperosmolar hyperglycemic state, and nonexertional
hyperthermia (heat stroke); severe is defined by the need for substantial intravenous
fluid administration as part of routine clinical care
- Pulmonary edema or clinical signs of new fluid overload (e.g. bilateral crackles, new
oxygen requirement, new peripheral edema, fluid overload on chest x-ray)
- Treating physician unwilling to give additional fluids as directed by the liberal
protocol
- Treating physician unwilling to use vasopressors as directed by the restrictive
protocol.
- Current or imminent decision to withhold most/all life-sustaining treatment; this does
not exclude those patients committed to full support except cardiopulmonary
resuscitation
- Immediate surgical intervention planned such that study procedures could not be
followed
- Prior enrollment in this study
We found this trial at
50
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1211 Medical Center Dr
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(615) 322-5000
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Charleston, South Carolina 29425
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