Turning clinical evidence into patient recovery

AeroPace® provides important clinical benefits versus standard-of-care1

From Atrophy to Recovery

43%

Faster weaning from mechanical ventilation (MV) over 30 days

3.2

Fewer days on MV in ICU

74%

Greater diaphragm strength (MIP)

96%

Greater breathing efficiency (RSBI)

47%

Lower risk of reintubation or reconnection

50%

Lower risk of tracheostomy after initiation

32%

Lower risk of mortality

0

Low risk of infection (zero CLABSI)

AeroPace Evidence In Action

The RESCUE-3 randomized controlled trial (RCT) was performed in a diverse, difficult to wean population with prolonged mechanical ventilation and marked diaphragm atrophy.

Results That Move Patients Off The Vent—Sooner

43%

Faster weaning from MV
over 30 days

3.2

Fewer days on MV

in ICU

Meaningful Improvement in Diaphragm Strength and Breathing Efficiency

74%

Improvement in diaphragm strength (MIP change from baseline)

96%

Improvement in breathing efficiency (RSBI change from baseline)

Patients Treated with AeroPace Experienced
Additional Likely Clinical Benefits

 

47%

Lower risk of reintubation
after weaning

50%

Lower risk of tracheostomy after initiation

32%

Lower risk of mortality

Strong Safety Profile

Infection risk similar to standard CVCs based on contemporary literature3,4

0

Reported
CLABSI

  • Safety profile for AeroPace patients in RESCUE-3 was inline with standard central venous catheters (CVCs)
  • Reduction in MV days and trend towards survival benefit reinforce strong safety profile
97%
of patients in RESCUE-3 trial would recommend AeroPace2

Explore Higher Weaning Success and Reduced Days on Ventilation Backed by:

 

103

Scientific Abstracts / Presentations

31

Peer Reviewed Publications

400+

Patients
Studied

2+

Randomized
Clinical Trials

References:

1. Dres, M. (2025) Am J Resp Crit Care Med: doi: 10.1164/rccm.202505-1056OC; Modified intention to treat (mTT) and per-protocol (PP; >50% of required stimulations) data for the AeroPace group relative to the standard-of-care group. In most clinical trial applications, a posterior probability greater than 95% or 97.5% is considered a strong indication of success.
2. Pu, H. (2023) BMC Pulm Med 2023 Sep 13;23(1):343. doi: doi.org/10.1186/s12890-023-02633-y
3. Becerra-Bolaños, A. (2025) Sci Rep; 15(1): 1642. doi: 10.1038/s41598-025-85836-z;
4. Teja, B. (2024) JAMA Intern Med.; 184(5): 474-482. doi:10.1001/jamainternmed.2023.8232.

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