2. INVASIVE VENTILATION
Invasive mechanical ventilation is defined as the delivery of positive
pressure to the lungs via an endotracheal or tracheostomy tube.
During mechanical ventilation, a predetermined mixture of air (ie,
oxygen and other gases) is forced into the central airways and then
into the alveoli.
As the lungs inflate, the intra-alveolar pressure increases
termination signal (usually flow or pressure) eventually causes the
ventilator to stop forcing air into the central airways central airway
pressure decreases Expiration follows passively, with air flowing
from the higher pressure alveoli to the lower pressure central
airways.
8. General Care Of Mechanically Ventilated
Patients
Sedation, analgesia, and delirium management
Hemodynamic monitoring
Nutritional support
Glycemic control
Measures to prevent ventilator-associated pneumonia
Venous thromboembolism prophylaxis
Gastrointestinal prophylaxis for stress ulcers
Venous or arterial access (eg. central venous access)
9. PATHOPHYSIOLOGIC CONSEQUENCES OF MECHANICAL VENTILATION :
Pulmonary Effects:
Barotrauma : pneumothorax, subcutaneous emphysema, pneumomediastinum, and
pneumoperitoneum.
Ventilator-associated lung injury
Auto-PEEP - Intrinsic PEEP
Heterogeneous ventilation
Ventilation/perfusion mismatch - worsen dead space but improve shunt.
Diaphragm : Diaphragmatic muscle atrophy, a phenomenon called ventilator induced
diaphragmatic dysfunction(VIDD)
Respiratory muscles : Respiratory muscle atrophy in (VIDD).
Mucociliary motility : Impair mucociliary motility retention of secretions and
pneumonia.
10. Hemodynamics — Decreases cardiac output hypotension.
Gastrointestinal :Gastrointestinal bleeding due to stress ulceration
Renal : Acute renal failure
Central nervous system :Increases intracranial pressure (ICP)
Weakness :Systemic muscular weakness
Immune system :Induce inflammation
Sleep : Disordered sleep "atypical sleep" or "pathological
wakefulness"
11. Discontinuing Mechanical Ventilation
Three step process:-
Readiness testing : During readiness testing , the clinical criteria
and weaning predictors are evaluated to determine whether a
patient is ready to begin weaning.
Weaning : Weaning is the process of decreasing ventilator support
and allowing patients to assume a greater proportion of their
ventilation.
Extubation : considered once the patient demonstrates the ability to
breathe without the ventilator and both airway patency and airway
12. Weaning :-
Weaning is the process of decreasing ventilator support and allowing patients
to assume a greater proportion of their ventilation.
It may involve either an immediate shift from full ventilatory support to a period
of breathing without assistance from the ventilator (ie, a spontaneous
breathing trial [SBT]) or a gradual reduction in the amount of ventilator
support.
Simple wean – Patients are considered to have undergone a simple wean when
they pass their first weaning trial, typically a spontaneous breathing trial (SBT).
Difficult-to-wean – Patients are considered difficult-to-wean if they fail their first
SBT and then require up to three SBTs or seven days to pass an SBT
Prolonged weaning – Patients are considered to have undergone prolonged
weaning if they fail at least three SBTs or require more than seven days to pass an
SBT
14. CHOOSING A WEANING METHOD
For patients who have been intubated for more than 24 hours and have
been deemed as ready to wean weaning trial.
Preferred method : Daily spontaneous breathing trials (SBTs) with
inspiratory pressure support : efficient, safe, and effective
Older methods : progressive decreases in the level of pressure support
during pressure support ventilation (PSV) and progressive decreases in
the number of ventilator-assisted breaths during intermittent mandatory
ventilation (IMV).
Newer weaning methods : computer-driven automated PSV weaning
and early extubation with immediate use of post extubation noninvasive
ventilation (NIV)
15. Daily spontaneous breathing trials (SBTs)
For patients with acute respiratory failure on mechanical ventilation - SBT preferred
as the initial weaning strategy.
Patient breaths spontaneously through the endotracheal tube (ETT) for a set
period of time, typically 30 minutes to two hours.
Choosing ventilatory support - SBT with some form of ventilatory support is
preferred (eg, low-level PSV, automatic tube compensation [ATC] or continuous
positive airway pressure [CPAP; eg, 5 cm H2O]) rather than no ventilatory support
(eg, using a T-piece).
Recommendations of the American College of Chest Physicians/American
Thoracic Society PSV (eg, inspiratory pressure augmentation of 5 to 8 cm
H2O), When using PSV-SBT, the positive end-expiratory pressure (PEEP) remains
at 5 cm H2O and the fraction of inspired oxygen (FiO2) at 0.4 or lower.
T-piece may be more appropriate in patients at risk for acute cardiogenic
pulmonary edema and patients with acute hypercapnia from obstructive lung
disease.
16.
17. Trial duration :-
Duration of MV <24 hours : Generally do not require an SBT,
although a 30-minute SBT is unlikely to be harmful (eg, following
surgery or for airway protection).
Duration of MV 1 to <10 days : Initial SBT of 30 minutes duration is
generally sufficient.
Duration of MV ≥10 days : Trials of 30 minutes may still be sufficient
.However, in many cases trials extended for up to two hours.
Subsequent SBTs after failed initial SBT : Longer than 30 minutes,
up to two hours
18. Alternative methods : no longer typically used as an initial weaning strategy.
Pressure support weaning : Pressure support may be initially set between 12
and 18 cm H2O (to target a spontaneous respiratory rate ≤25 breaths per
minute). PSV is then reduced, if possible, by 2 to 4 cm H2O at least twice a day
until a pressure support of 5 to 8 cm H2O is reached for two hours or more (ie,
typically over a 24 hour period). More rapid reductions in PSV weaning have
also been described. PEEP of up to 4 or 5 cm H2O is usually applied.
Intermittent mandatory ventilation : Ventilator rate may be initially set at 8 to
12 breaths per minute. The IMV rates is then decreased usually by 2 to 4
breaths per minute, if possible, at least twice a day until four or five breaths per
minute or less is reached for two hours or more.
Extubation to noninvasive ventilation — For selected patients who fail the
initial SBT (eg, patients with COPD or chronic hypercapnic respiratory failure).
19. ASSESSMENT OF WEANING SUCCESS OR FAILURE
Clinical assessment :
Monitor vital signs and ventilator parameters such as the tidal volume and
respiratory rate (ie, minute ventilation).
Assess for respiratory distress and mental status changes, and if alert and
responsive, ask about the presence of dyspnea and chest pain.
Telemetry monitors : ST changes
Electrocardiography to look for cardiac ischemia.
Arterial or venous blood gas (ABG, VBG) in those at risk of developing acute
hypercapnia during weaning (eg, patients with chronic obstructive pulmonary
disease [COPD], patients who underwent prolonged mechanical ventilation,
patients with known or suspected neuromuscular weakness).
20.
21. Weaning success :
When a patient successfully passes a weaning trial, they should be
evaluated for safety of extubation by assessment of the volume of
respiratory secretions as well as airway patency and protection (ie,
has a sufficient cough and adequate level of consciousness)
Weaning failure :
Patients who fail a weaning trial should be placed back on their
previous ventilator settings. No further attempts at weaning are
typically made for another 24 hours.