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VAP/HAP
Hospital-acquired
(or nosocomial) pneumonia (HAP) is pneumonia that occurs 48 hours or
more after admission and did not appear to be incubating at the time of
admission. Ventilator-associated pneumonia (VAP) is a type of HAP
that develops more than 48 to 72 hours after endotracheal intubation and
the initiation of mechanical ventilation. It is probably caused by
digestive tract colonization, followed by aspiration of contaminated
secretions into the lower airways.
Many of the risk factors for VAP increase the risk of colonization and
aspiration, while most of the interventions to prevent VAP reduce
colonization and aspiration.
Healthcare-associated pneumonia (HCAP)
is defined as pneumonia that occurs in a non-hospitalized patient
with extensive healthcare contact, as defined by one or more of the
following:
Intravenous therapy, wound
care, or intravenous chemotherapy within the prior 30 days, residence
in a nursing home or other long-term care facility, hospitalization in
an acute care hospital for two or more days within the prior 90 days, or
attendance at a hospital or hemodialysis clinic within the prior 30 days
The
guidelines can be accessed through the ATS web site at www.thoracic.org.
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PREVENTING
VAP
Nebulizers can
be incorporated into the ventilator circuit and used to deliver
medications. However, they frequently become
contaminated and might contribute to the development of VAP.
Use
of a metered-dose inhaler probably eliminates this risk. Like
a nebulizer, a metered-dose inhaler delivers aerosolized medication
directly into the ventilator circuit. However, metered-dose inhalers do
not become contaminated because they are not part of the ventilator
circuit. Metered-dose inhalers are also less expensive, easier to use,
and deliver a dose more reliably than nebulizers.
Decontamination
of the digestive tract has been shown to decrease the colonization of
bacteria in the upper respiratory tract. The methods used include
antiseptics in the oropharynx and nonabsorbable antibiotics taken orally
with or without systemic antibiotics.
Decontamination
of the oropharynx — Gingival
and dental plaque rapidly becomes colonized with aerobic pathogens in
ICU patients due to poor oral hygiene and lack of mechanical
elimination. A number of trials have evaluated the efficacy of
decontamination of the oropharynx.
·
Subglottic drainage.
·
Elevation of head.
·
Maintaining an
endotracheal tube airway cuff pressure that is adequate to prevent
aspiration of contaminated secretions.
·
Use of silver coated
endotracheal tubes.
·
Minimizing transport out
of the ICU — Patients who are transported out of the ICU have an
incidence of VAP that is three to four times that of patients who are
never transported out of the ICU.
·
Avoiding the need for
reintubation.
·
Use of Noninvasive
instead of invasive mechanical ventilation whenever possible.
(Positive end-expiratory pressure (PEEP) — The application of PEEP may
decrease the incidence of VAP. In a trial that randomly assigned 131
mechanically ventilated patients to receive no PEEP or 5 to 8 cm H2O of
PEEP, the PEEP group had a lower incidence of VAP (25-37%).
Positive tracheal pressure may act to oppose aspiration of
pharyngeal secretions around the cuff of the endotracheal tube.
·
Weaning protocols
— Weaning protocols are recommended by many organizations, in order to
reduce the duration of ventilation. This was illustrated by an
observational study that found that the rate of VAP decreased from 15
percent to 5 percent after a weaning protocol was instituted.
The
most significant risk factor for HAP is mechanical ventilation! In
fact, many authors use the terms HAP and VAP interchangeably. Intubation
increases the risk of pneumonia 6- to 21- fold. Other risk factors,
which have emerged from multivariate analyses, include:
·
Age >70 years
·
Chronic lung disease
·
Depressed consciousness
·
Aspiration
·
Chest surgery
·
The presence of an
intracranial pressure monitor or nasogastric tube
·
H2 blocker or antacid
therapy
·
Transport from the ICU for
diagnostic or therapeutic procedures
·
Previous antibiotic
exposure, particularly to third generation cephalosporins
·
Reintubation or prolonged
intubation
·
Hospitalization during the
fall or winter season
·
Mechanical ventilation for
acute respiratory distress syndrome
·
Frequent ventilator
circuit changes
·
Paralytic agents
·
Underlying illness
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