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Adherence to Low Tidal Volume in the Transition to Spontaneous Ventilation in Patients With Acute Respiratory Failure

Adherence to Low Tidal Volume in the Transition to Spontaneous Ventilation Mode in Patients With Acute Respiratory Failure in ICUs in Latin America

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06042036
Acronym
SPIRAL
Enrollment
422
Registered
2023-09-18
Start date
2023-06-12
Completion date
2024-10-12
Last updated
2023-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Hypoxemic Respiratory Failure, Respiration, Artificial, Respiratory Insufficiency

Keywords

Adherence, Treatment, intensive care units

Brief summary

The goal of this observational study is to estimate the prevalence of the use of protective ventilation with low tidal volume ventilation in the transition of spontaneous ventilation modes in patients with hypoxemic acute respiratory failure in ICUs in Latin America and its association with patient outcomes. The main questions it aims to answer are: * what is the prevalence of the use of low tidal volume ventilation (VT \<8 mL/kg of predicted body weight) in the first 24 hours of spontaneous ventilation modes in patients with hypoxemic acute respiratory failure? * Is there an association between the rate of adherence to low tidal volume ventilation in spontaneous ventilation modes and the ability to stay off ventilatory support and mortality? Participants are patients with acute respiratory failure under mechanical ventilation. Investigators will collect data on the ventilatory parameters of participants * 24 hours before they begin to be ventilated with spontaneous modes of ventilation * during the first 24 hours of spontaneous ventilation Investigators will collect several patient-centered clinical outcomes at 28 days after study inclusion, including ventilator-free days and mortality

Detailed description

Investigators will conduct a cohort study in Intensive Care Units (ICUs) across Latin America, aiming to include 422 patients with Hypoxemic Acute Respiratory Failure (ARF) and under invasive mechanical ventilation. The goal of this observational study is to estimate the prevalence of the use of protective ventilation with low tidal volume ventilation in the transition of spontaneous ventilation modes in patients with hypoxemic acute respiratory failure in ICUs in Latin America The primary objectives are to determine the prevalence of low tidal volume ventilation (VT \< 8 mL/kg of predicted body weight) during the initial 24 hours of spontaneous ventilatory modes in patients diagnosed with hypoxemic ARF and its association with clinically important patient outcomes. Investigators are interested in assessing the rate of adherence to low tidal volume ventilation, defined as maintaining VT \< 8 mL/kg of predicted body weight during the first 24 hours of ventilation in spontaneous mode.They are also interested in measuring the number of days that patients are alive and not receiving ventilatory support and survival at 28 days. Investigators will also measure the proportion of patients experiencing significant asynchrony during the transition to spontaneous mechanical ventilation, who revert to sedation and controlled mechanical ventilation within the first 24 hours or at any point during mechanical ventilation.

Interventions

OTHERSpontaneous mode of mechanical ventilation

any mode of mechanical ventilation classified as spontaneous or proportional, mainly pressure support ventilation, but also CPAP, APRV, NAVA, PAV+

Sponsors

Brazilian Research In Intensive Care Network
CollaboratorNETWORK
Latin American Intensive Care Network (LIVEN)
CollaboratorUNKNOWN
University of Sao Paulo General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 110 Years
Healthy volunteers
No

Inclusion criteria

* Age \> 18 years * Patients with hypoxemic ARF, defined as a PaO2/FIO2 ratio \<300 mmHg, under controlled invasive mechanical ventilation, with an expected duration of MV of at least 24h. * Patients transitioning to spontaneous ventilation modes (PSV, PAV Plus, NAVA or APRV)

Exclusion criteria

* Tracheostomized patients. * Decision not to maintain or add life support measures on the day of assessment (palliative care). * Patient in ECMO. * Air fistula or barotrauma that prevents adequate tidal volume monitoring. * Severe injuries to the central nervous system that result in abolished or very high respiratory drive, for whom it is not possible to maintain protective tidal volume.

Design outcomes

Primary

MeasureTime frameDescription
Low tidal volume24 hoursLow tidal volume, defined as less or equal to 8 mLs per Kg of predicted body weight
Ventilator- free days28 daysnumber of days alive and not receiving invasive mechanical ventilation after transition to spontaneous ventilation

Secondary

MeasureTime frameDescription
Number of participants that return to controlled mechanical ventilation in the first 24 hours24 hoursreturn to controlled mechanical ventilation in the first 24 hours after transition to spontaneous ventilation
Number of participants that return to sedation in the first 24 hours24 hoursreturn to sedation in the first 24 hours after transition to spontaneous ventilation
Number of participants that return to controlled mechanical ventilation after transition to spontaneous ventilation28 daysreturn to controlled mechanical ventilation any time after transition to spontaneous ventilation
Hospital mortality28 daysmortality in the hospital
Number of participants with PEEP and FIO2 compatible with the ARDSnet PEEP/FIO2 table24 hoursadherence to ARDSnet low PEEP/FIO2 table after transition to spontaneous ventilation
Number of participants who were extubated28 daysExtubation and discontinuation of mechanical ventilation after the transition to spontaneous mode
Rate of reintubation28 daysReintubation after transition to spontaneous mode and extubation
Number of participants that return to sedation after transition to spontaneous ventilation28 daysreturn to sedation any time after transition to spontaneous ventilation
Rate of patient-ventilator asynchrony24 hourspresence of patient asynchrony 24h after transition to a spontaneous mode of mechanical ventilation

Countries

Argentina, Bolivia, Brazil, Chile, Colombia, Ecuador, Mexico, Paraguay, Peru, Uruguay

Contacts

Primary ContactFabia D Silva, PhD
fabiadiniz@usp.br34992484248
Backup ContactJuliana C FERREIRA, MD
juliana.ferreira@hc.fm.usp.br11983355876

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026