Mechanical Ventilation Clinical Trial
Official title:
Biphasic Intermittent Positive Airway Pressure Versus Airway Pressure Release Ventilation in Critically Ill Trauma Patients: Metabolic Demands and Respiratory Mechanics
Adequate supply of energy is an essential part of the overall treatment of critically ill patients and adjustment of energy requirements of patients is important clinical evolution .The adequate assessment of energy expenditure is the basis of effective nutri¬tional planning.
Inappropriate energy supply, may cause important complications that affect the progression of
the disease, especially in critically ill patients receiving mechanical ventilation.
Mechanically ventilated patients make a considerable respiratory muscle effort that is not
always decreased by intermittent positive pressure ventilation.
No work of breathing is observed in patients under controlled mechanical ventilation who are
receiving drugs for sedation and muscle paralysis. In this situation, the work of breathing
is carried out by the ventilator which initiates the ventilation cycle, and patients are
spared the inspiratory efforts. Conversely, in assisted ventilation modes, the patient has to
make a considerable inspiratory effort before a ventilation cycle initiates, and there is no
airflow up to the moment when the effective sensitivity threshold is reached by the
ventilator. Therefore, the choice of ventilation mode may determine differences in energy
expenditure.
Some studies found that in patients on mechanical ventilation, weight, height, body
temperature, type of mechanical ventilation, and type of medication received influenced the
REE Acute hypoxemic respiratory failure is a common reason for patients to be admitted to the
intensive care unit (ICU). An international study showed an incidence of acute respiratory
distress syndrome (ARDS) of 10.4% in ICU critically ill trauma patients with an hospital
mortality reaching 46.1% for most severe cases. A protective ventilation strategy using low
tidal vol-ume (LTV) and a plateau pressure lower than 30 cmH2O is widely accepted to limit
ventilator-induced lung injury, and it currently represents the intervention able to reduce
mortality supported by the strongest evidences. Airway pressure release ventilation (APRV)
was described for the first time by Stock and Downs and consists in a time-triggered,
pressure-limited and time-cycled ventilation mode in which the pressure was alternated from a
high level (Phigh) applied for a prolonged time (Thigh) to maintain adequate lung volume and
alveo-lar recruitment, to a low level (Plow) for a short period of time (Tlow) where most of
ventilation and CO2 removal occurs. In contrast to pressure-controlled inverse-ratio
ventilation, APRV uses a release valve that allows spontaneous breathing during any phase of
respiratory cycle. The rationale behind this approach is to maintain a pressure above the
closing pressure of recruitable alveoli for a sustained time, limiting the release time to
allow CO2 removal but avoiding de-recruitment. Another conceptual advantage to APRV over
controlled modes is the preservation of spontaneous breathing, which may pro-mote a
redistribution of aeration to the dependent lung regions, less need for neuromuscular
blockade and sedation, improved venous return and a better ventilation/perfusion (V/Q)
matching. For this reason, APRV has been considered a tempting mode of ventilation during
acute respiratory failure within the concept of open lung ventilation.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05921656 -
Construction and Evaluation of Airway Leakage Risk Model of Patients With Endotracheal Tube
|
||
Recruiting |
NCT03941002 -
Continuous Evaluation of Diaphragm Function
|
N/A | |
Withdrawn |
NCT04288076 -
The Brain and Lung Interaction (BALI) Study
|
N/A | |
Completed |
NCT03031860 -
Semi-quantitative Cough Strength Score (SCSS)
|
N/A | |
Completed |
NCT02312869 -
Local Assessment of Management of Burn Patients
|
N/A | |
Completed |
NCT02545621 -
A Role for RAGE/TXNIP/Inflammasome Axis in Alveolar Macrophage Activation During ARDS (RIAMA): a Proof-of-concept Clinical Study
|
||
Completed |
NCT01885442 -
TryCYCLE: A Pilot Study of Early In-bed Leg Cycle Ergometry in Mechanically Ventilated Patients
|
N/A | |
Completed |
NCT01204281 -
Proportional Assist Ventilation (PAV) in Early Stage of Critically Ill Patients
|
Phase 4 | |
Terminated |
NCT01059929 -
Dexmedetomidine Versus Propofol in the Medical Intensive Care Unit (MICU)
|
Phase 4 | |
Completed |
NCT00824239 -
Intermittent Sedation Versus Daily Interruption of Sedation in Mechanically Ventilated Patients
|
Phase 3 | |
Completed |
NCT00529347 -
Mechanical Ventilation Controlled by the Electrical Activity of the Patient's Diaphragm - Effects of Changes in Ventilator Parameters on Breathing Pattern
|
Phase 1 | |
Unknown status |
NCT00260676 -
Protective Ventilatory Strategy in Potential Organ Donors
|
Phase 3 | |
Terminated |
NCT00205517 -
Sedation and Psychopharmacology in Critical Care
|
N/A | |
Completed |
NCT03281785 -
Ultrasound of Diaphragmatic Musculature in Mechanically Ventilated Patients.
|
N/A | |
Recruiting |
NCT04110613 -
RCT: Early Feeding After PEG Placement
|
N/A | |
Completed |
NCT04410783 -
The Emergency Department Sedation Pilot Trial
|
N/A | |
Recruiting |
NCT04821453 -
NAVA vs. CMV Crossover in Severe BPD
|
N/A | |
Completed |
NCT03930147 -
Ventilation With ASV Mode in Children
|
N/A | |
Recruiting |
NCT05029167 -
REstrictive Versus LIberal Oxygen Strategy and Its Effect on Pulmonary Hypertension After Out-of-hospital Cardiac Arrest (RELIEPH-study)
|
N/A | |
Recruiting |
NCT04849039 -
Lung Microbiota and VAP Development (PULMIVAP)
|