EBQ:ARDSnet Trial: Difference between revisions

(Added Study Design and Criticisms sections)
 
Line 34: Line 34:
*Enrollment: March 1996 to March 1999 (terminated early after the fourth interim analysis)
*Enrollment: March 1996 to March 1999 (terminated early after the fourth interim analysis)
*Follow-up: 180 days or until home breathing independently
*Follow-up: 180 days or until home breathing independently
==Study Design==
*Multicenter, randomized, controlled trial
*ARDS Network - 10 university medical centers
*N = 861 patients
*Primary Outcome: mortality before discharge with unassisted breathing
*Enrollment period: March 1996 - March 1999


==Population==
==Population==
Line 106: Line 113:


==Criticisms==
==Criticisms==
 
*Control group tidal volume (12 mL/kg) was higher than what many clinicians were already using at the time
*Plateau pressures were not controlled independently of tidal volume, so it is unclear whether the benefit was from lower volume or lower pressure
*PEEP levels were relatively low in both groups; higher PEEP strategies were not evaluated
*Predicted body weight was used for calculations, which requires accurate height measurement
*The trial was stopped early for efficacy, which may have overestimated treatment effect
==Funding==
==Funding==
The National Heart, Lung, and Blood Institute.
The National Heart, Lung, and Blood Institute.

Latest revision as of 22:36, 21 March 2026

Complete Journal Club Article
Brower RG, et al. "Ventilation With Lower Tidal Volumes As Compared With Traditional Tidal Volumes For Acute Lung Injury And The Acute Respiratory Distress Syndrome". The New England Journal of Medicine. 2000. 342(18):1301-1308.
PubMed Full text PDF

Clinical Question

Does a lung protective strategy of low tidal volumes in patients with Acute Lung Injury (ALI) and Acute Respiratory Distress Syndrome (ARDS) decrease mortality and ventilator-free days when compared to traditional ventilation strategies.

Conclusion

In patients with ALI/ARDS, lower tidal volumes of 6mL/kg predicted body weight reduces mortality and decreases length of time on mechanical ventilation.

Major Points

  • Acute Respiratory Distress Syndrome results from alveolar damage and barotrauma are associated with elevated plateau pressures and higher tidal volume ventilations
  • The trial was stopped early when patients in the low tidal volumes arm showed a significant decrease in mortality and more ventilator-free days compared to the traditional tidal volumes arm.

Guidelines

See Sepsis for guideline recommendations

Design

  • Multicenter, randomized trial of 861 patients in parallel-group in 10 university-affiliated ARDSNet centers
    • Low tidal volumes: Starting at 6ml/kg PBW and plateau pressure ≤30cmH2O (n=432)
    • Traditional tidal volumes: starting at 12ml/kg PBW and plateau pressure of ≤50cmH2O (n=429)
  • Enrollment: March 1996 to March 1999 (terminated early after the fourth interim analysis)
  • Follow-up: 180 days or until home breathing independently

Study Design

  • Multicenter, randomized, controlled trial
  • ARDS Network - 10 university medical centers
  • N = 861 patients
  • Primary Outcome: mortality before discharge with unassisted breathing
  • Enrollment period: March 1996 - March 1999

Population

Inclusion Criteria

  • Age ≥18 years
  • Receiving mechanical ventilation
  • Diagnosis of ALI/ARDS ≤36h prior to enrollment; defined as:
    • Acute decrease in PaO2/FiO2ratio to ≤300
    • CXR: Bilateral pulmonary infiltrates
    • PCWP of ≤18mmHg without evidence of left atrial hypertension

Exclusion Criteria

  • Pregnancy
  • Increased ICP, neuromuscular disease imparing spontaneous breathing, sickle cell disease, or severe chronic respiratory disease
  • Weight more than 1kg/cm of height
  • Burns >30% of BSA
  • Estimated 6-month mortality rate >50%
  • History of bone marrow or lung transplantation
  • Child-Pugh class C liver disease
  • Participation in other trials w/in 30 days

Baseline Characteristics

  • Mean age: 51.5 years
  • Sex: Female (40.5%)
  • Ethnicity:
    • White: 73%
    • Black: 17.5%
    • Hispanic: 6%
  • APACHE III score: 82.5
  • Mean PaO2:FiO2: 136
  • Mean tidal volume: 670 mL
  • Mean minute ventilation: 13.4 vs. 12.7 L/min (P=0.01)

Interventions

Patients randomly assigned to receive mechanical ventilation (volume-assist-control mode) with following strategies for tidal volume:

  • Low tidal volumes (lung protective strategy): Starting at 6ml/kg PBW to maintain plateau pressure ≤30cm H2O (n=432)
  • Traditional tidal volumes: Starting at 12ml/kg to maintain plateau pressure of ≤50cm H2O (n=429)

Patients monitored until day 28 or death for signs of system failure:

  • Circulatory failure: SBP ≤90mmHg or need for vasopressor
  • Coagulation failure: Platelets ≤80,000 mm3
  • Hepatic failure: Bilirubin ≥2mg/dL
  • Renal failure: Creatinine ≥2mg/dL

Outcomes

Primary Outcomes

  • 180-day mortality
    • 31.0% vs. 39.8% (RR 0.78; P=0.007)
  • Ventilator-free days (Days 1-28)
    • 12 vs. 10 (P=0.007)
  • Breathing without assistance by day 28
    • 65.7% vs. 55.0% (P<0.001; NNT 9)

Secondary Outcomes

  • Days w/o non-pulmonary organ or system failure (Days 1 to 28)
    • 15 vs. 12 (P=0.006)
  • Days w/o circulatory failure
    • 19 vs. 17 (P=0.004)
  • Days w/o coagulation failure
    • 21 vs. 19 (P=0.004)
  • Days w/o renal failure
    • 20 vs. 18 (P=0.005)
  • Barotrauma (New PTX, pneumomediastinum, subcutaneous emphysema, pneumatocele)
    • 10% vs. 11% (P=0.43)
  • Mean tidal volumes (ml/kg PBW)
    • 6.2 vs. 11.8 (P<0.001)
  • Mean plateau pressures (cm H2O)
    • 25 vs. 33 (P<0.001)
  • Peak inspiratory pressures (cm H2O)
    • 32 vs. 39 (P<0.05)

Criticisms

  • Control group tidal volume (12 mL/kg) was higher than what many clinicians were already using at the time
  • Plateau pressures were not controlled independently of tidal volume, so it is unclear whether the benefit was from lower volume or lower pressure
  • PEEP levels were relatively low in both groups; higher PEEP strategies were not evaluated
  • Predicted body weight was used for calculations, which requires accurate height measurement
  • The trial was stopped early for efficacy, which may have overestimated treatment effect

Funding

The National Heart, Lung, and Blood Institute.

See Also

Mechanical Ventilation Pages

References