EBQ:Lactate clearance vs central venous oxygen saturation
(Redirected from Lactate clearance vs central venous oxygen saturation)
Complete Journal Club Article
Jones AE.. "Lactate clearance vs central venous oxygen saturation as goals of early sepsis therapy: a randomized clinical trial". JAMA. 2010. 303(8):739-746.
PubMed Full text PDF
PubMed Full text PDF
Clinical Question
Is lactate clearance as good as SVO2 as a measure of oxygen delivery to tissues in patients presenting with severe sepsis and septic shock?
Conclusion
For patients with septic shock who were treated by normalizing CVP and MAP; attempt to normalize lactate clearance as opposed to normalize SVO2 showed no significant difference in in-hospital mortality.
Major Points
- Lactate clearance-directed therapy was non-inferior to ScvO2-directed therapy for in-hospital mortality in severe sepsis and septic shock
- Lactate clearance of >=10% over 6 hours was used as the resuscitation target in the intervention group
- Both groups received early antibiotics, fluid resuscitation, and vasopressors per an EGDT-based protocol
- The lactate group had fewer central venous catheter hours, which may reduce catheter-related complications
- Results suggested that lactate clearance could serve as a simpler, more accessible alternative to continuous ScvO2 monitoring
Study Design
- Prospective, randomized, non-inferiority trial
- Single center: Beth Israel Deaconess Medical Center, Boston
- N = 300 patients with severe sepsis or septic shock
- Non-inferiority margin: 10% absolute difference in in-hospital mortality
- Study period: January 2007 - January 2009
Population
Inclusion Criteria
- Severe sepsis or septic shock meeting SIRS criteria with suspected or confirmed infection
- Lactate >=4 mmol/L or SBP <90 mmHg after fluid bolus
Exclusion Criteria
- Age <18 years
- Need for immediate surgery
- Anticipated survival <24 hours
- Contraindication to central venous catheter placement
Inclusion Criteria
- >17 years old AND
- confirmed or presumed infection meeting criteria for severe sepsis or septic shock:
- 2 or more SIRS criteria AND
- SBP <90 after 20 mL/kg bolus or blood lactate at least 36 mg/dL
Exclusion Criteria
- Pregnancy
- Primary diagnosis other than sepsis
- Likely surgery required within 6 hours of diagnosis
- Contraindication to chest or neck CVC
- Cardiopulmonary resuscitation
- Transfer from an institution with sepsis protocol already underway
- Advance directive restricting study protocol
Interventions
- Randomized into 1 of 2 resuscitation groups
- CVP was managed first in both groups to achieve a CVP of at least 8
- Isotonic boluses given
- SBP was managed second to maintain a MAP of at least 65
- Fluid resuscitation followed by vasopressors (dopamine and norepi)
- The groups differed in the third physiologic parameter that was targeted: SVO2 vs. lactate clearance
- SVO2 of 70%
- lactate clearance of 10%
- If hematocrit <30 and either target not achieved, PRBC transfusion to achieve hematocrit of at least 30
- If hematocrit was at least 30 and either target not achieved, then dopamine titrated to achieve effect
Outcome
*Intention to treat analysis
Primary Outcomes
- Absolute in-hospital mortality rate
- SVO2: 23%
- Lactate: 17%
- Did not reach -10% threshold
Secondary Outcomes
- ICU length of stay
- SVO2: 8.46%
- Lactate: 7.39%
- p-value = 0.75
- Hospital length of stay
- SVO2: 10.89%
- Lactate: 11.68%
- p-value = 0.60
- Ventilator-free days
- SVO2: 10.39%
- Lactate: 11.09%
- p-value = 0.67
- New onset of multiple organ failure
- SVO2: 25%
- Lactate: 22%
- p-value = 0.68
Subgroup analysis
Criticisms
- Single-center study limits generalizability
- Non-inferiority design with a wide 10% margin may not detect clinically meaningful differences
- Both groups still required central venous access, so the practical advantage of the lactate strategy was limited
- A single lactate measurement at 6 hours may miss important trends in the intervening period
- The study was underpowered to detect superiority of either approach
Funding
- National Institutes of Health (NIH)
