Ventilator-Associated
Pneumonia: Improved Clinical Outcomes
Keith DD, Garrett KM,
Hicko XG, Echols B, Comeau E. Improved Clinical Outcomes.
Journal of Nursing Care Quality. 2004;19(4):328-333.
Introduction
St. Joseph Hospital, a 235-bed Catholic
hospital in Augusta, GA, created a multidisciplinary Ventilator-Associated
Pneumonia
Performance Improvement Team to reduce ventilator associated
pneumonia (VAP). The institution’s VAP rate at the
beginning of the project was 24.1 incidences per thousand
ventilator
days, significantly higher than the national benchmark rate
at the time of 11.6.
Barriers
The initial response from the facility
included doubt about the data’s applicability based
on patient population and diagnosis methods. The team addressed
these concerns
by benchmarking against the CDC VAP data by type of ICU and
institution,
and by evaluating patient mix to ensure it was similar to
the benchmark group. The team also established a procedure
for
multi-disciplinary review of VAP diagnoses to ensure they
met the criteria for nosocomial VAP.
Implementation
The task force reviewed the CDC guidelines
and published literature. All team members reviewed the
literature relating
to their
field of expertise. The Infection Control Practitioner
(ICP) conducted continuous surveillance and tracking on all
patients
with VAP. The following interventions were initiated:
- A
new ventilator flow sheet was developed to ensure adherence
to practices of changing ventilator circuits
every 7
days, and changing both in-line suction devices and
heat and
moisture exchange filters every 24 hours.
- Endotracheal
cuff pressures were assessed regularly using new
devices and protocols.
- Single-use vials of normal saline for endotracheal
lavage were used.
- Oral suction tips were changed
every 24 hours and kept in their original package between
uses.
- A new antibacterial mouth care product
was introduced.
- Head of bed elevation was assessed and
the practices at the time were found to be adequate.
- A waterless
hand wash containing chlorhexidine gluconate was used
by all staff prior to
manipulation of the
ventilator tubing or devices.
- The last intervention
was a specialized endotracheal tube for continuous
aspiration of subglottic
secretions (CASS),
which was piloted in the third quarter
of 2001 and made available for use
in the Emergency
Department, ICU, and
Operating Room
in the second quarter of 2002.
Results
The performance team began its work
in 1999 and formally concluded in 2002.
The VAP rates
during
this time
period, including the
years before and after the project,
are as follows:
| |
1998 |
1999 |
2000 |
2001 |
2002 |
2003 |
| NNIS rate |
11.6 |
10.3 |
10.3 |
9.1 |
9.1 |
8.7 |
St. Joseph
VAP rate |
24.21 |
15.79 |
17.06 |
9.6 |
2.52 |
1.25 |
| VAP rate reduction vs. prior year |
|
35% |
-8% |
44% |
74% |
50% |
| Cumulative VAP rate reduction |
|
35% |
30% |
60% |
90% |
95% |
The largest VAP
rate reduction was a 74% reduction between 2001 and 2002,
which coincides with the addition of the last intervention,
subglottic secretions removal. At the conclusion of 2003,
St. Joseph had reduced their incidence rate by 95%. Additionally,
it is estimated that over four years, the project reduced
318 ICU days for an approximate savings of $349,164.
Lessons Learned
One critical factor to success
was the addition of a pulmonary intensivist to the group,
which improved the accuracy of
diagnosis and improved aggressive weaning of high-risk
patients from the ventilator. The team also learned
that this performance
improvement project was a long-term rather than short-term
project and that it was important to analyze long-term
trends in infection rates rather than focusing on monthly
data.
Conclusions
The accomplishments of the team
were significant, with a 95% reduction in ventilator-associated
pneumonia.
|