Diferencia entre revisiones de «EBQ:Lactate clearance vs central venous oxygen saturation»
(Created page with "PMID 20179283") |
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{{JC info | |||
| title= Lactate clearance vs central venous oxygen saturation as goals of early sepsis therapy: a randomized clinical trial | |||
| abbreviation= Lactate clearance vs central venous oxygen saturation as goals of early sepsis therapy: a randomized clinical trial | |||
| expansion= Lactate clearance vs central venous oxygen saturation as goals of early sepsis therapy: a randomized clinical trial | |||
| published= 2010 | |||
| author= Jones AE. | |||
| journal= JAMA | |||
| year= 2010 | |||
| volume= 303 | |||
| issue= 8 | |||
| pages= 739-746 | |||
| pmid= 20179283 | |||
| fulltexturl= http://jama.jamanetwork.com/article.aspx?articleid=185405 | |||
| pdfurl= http://jama.jamanetwork.com/data/Journals/JAMA/4501/jce05001_739_746.pdf | |||
| status = Complete | |||
}} | |||
==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) | |||
==Sources== | |||
<references/> | |||
[[Category:EBQ]] | |||
Revisión actual - 23:01 21 mar 2026
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)
