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Module 6 • Infectious Diseases
Infectious Diseases I
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Infectious Diseases I
Jacob Schwarz ~3 min read Module 6 of 20
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Infectious Diseases I

(c)The rate of MDR pathogens during a recurrent VAP episode was higher in patients in the

15-day group.

ii.

Two meta-analyses that included the results of the PneumA trial suggest limited benefit of

prolonged duration of definitive antibiotic therapy for treating VAP (Chest 2013;144:1759-67;

Cochrane Database Syst Rev 2015;8:CD007577). Synopsis includes:

(a)Any increase in VAP recurrence rate is small;
(b)Mortality and clinical cure do not appear to be affected by shorter durations;
(c)Evidence for recurrence from subgroup analyses has important limitations.

iii.

Guidelines acknowledge that situations may exist in which shorter or longer durations of

definitive antibiotic therapy may be indicated, depending on the rate of clinical and radiologic

improvement. A single-center, retrospective study suggested that patients with β€œpossible VAP”

who had minimal and stable ventilator settings at diagnosis are appropriate for short-course

therapy (i.e., 1-3 days) (Clin Infect Dis 2017;64:870-6). However, application of these findings

is limited, given that only 39% of short-course patients had an identified pathogen on tracheal

aspirate or BAL culture, bringing into question the likelihood of confirmed pneumonia.

iv.

The iDIAPASON Trial was a randomized, controlled, open-label trial that compared 8 versus

15 days of antibiotic therapy solely for the treatment of Pseudomonas aeruginosa ventillator-

associated pneumonia (PA-VAP). The primary noninferiority endpoint was a composite

outcome of death and PA-VAP recurrence during the ICU stay until day 90. Duration of therapy

was counted from the time of effective antibiotic therapy (Intensive Care Med 2022;48:841-9).

Major study findings were the following:

(a)Short duration was not associated with an increased mortality, longer duration of mechanical

ventilation, or length of ICU stay.

(b)While not significant, there was a trend toward higher proportion of recurrence in

the 8 days of therapy compared with 15 days (17% vs. 9.2%; confidence interval [CI],

–0.5% –16.8%).

5

Response to antibiotic therapy should be assessed serially using clinical signs and symptoms of infection

(e.g., oxygenation requirements, blood pressure, WBC, temperature) and status of VAP-related organ

dysfunction.

Lack of response in signs and symptoms of VAP beyond treatment day 3 necessitates reassessment

of diagnosis, causative pathogen(s), antibiotic regimen, and presence of pneumonia-related

complications (e.g., ARDS).

Patients thought to have persistent VAP should undergo repeat lower respiratory tract culture and

receive empiric antibiotic therapy considering previous pathogen(s) and antibiotic exposure.

Table 2. Summary of Key Changes in 2016 IDSA VAP Guidelines

Characteristic

2005 Guidelines

2016 Guidelines

Methodology

Expert opinion based on level of evidence

ranging from Level I (high) to III (low)

GRADE criteria to identify β€œrecommended”

(strong) or β€œsuggested” (weak) guidance based

on level of evidence categories β€œvery low,” β€œlow,”

β€œmoderate,” and β€œhigh quality”

Diagnosis

Clinical strategy or bacteriologic strategy

Suggest clinical suspicion with noninvasive

sampling and semiquantitative cultures

If invasive sampling is used, suggest that

antibiotics be withheld rather than continued

if quantitative culture results are below the

diagnostic threshold for VAP

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