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Published on: February 23, 2014
Defining Pathogen and Susceptibility Patterns for Early Versus Late Ventilator Associated Pneumonia in Trauma
Kaitlin M Alexander1, S Noelle Davis2, C Caleb Butts2
1College of Pharmacy, University of Florida, Gainesville, FL, USA.
Introduction:
Studies have demonstrated that trauma patients with early-ventilator associated pneumonia (early-VAP, < 7 days) have decreased risk of methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa infections. We hypothesize that routinely using broad-spectrum antibiotics is unnecessary to treat trauma patients with the diagnosis of early-VAP.
Methods:
This retrospective cohort study included adult trauma patients with the diagnosis of VAP. The primary outcome was the presence of MRSA and/or P. aeruginosa in patients with early- and late-VAP. Secondary outcomes included the bacterial susceptibility of pathogens to methicillin, ampicillin/sulbactam, ceftriaxone, piperacillin/tazobactam, and cefepime. Intensive care unit (ICU) and hospital length of stay (LOS), ventilator-free days, and in-hospital mortality were also collected.
Results:
164 patients met inclusion criteria, and 208 organisms (n = 90 early vs n = 118 late) were identified by respiratory culture. The incidence of MRSA and P. aeruginosa in early-VAP was 7.7% (7/90) and 5.6% (5/90), respectively. The susceptibility of bacteria causing early-VAP to ampicillin/sulbactam and ceftriaxone was 73.3% (66/90) and 83.3% (75/90), respectively. Ventilator-free days at 30 days was similar between groups (P = .649). Patients with late-VAP spent more time in the ICU (P = .040); however, in-hospital mortality was higher in the early-VAP group (P = .012).
Conclusions:
Ampicillin/sulbactam or ceftriaxone monotherapy did not provide reliable broad-spectrum coverage for early-VAP in our cohort. These findings highlight the importance of each institution performing a similar analysis to ensure adequate initial treatment of VAP.
Insights
Routine broad-spectrum antibiotics may not be necessary for early ventilator-associated pneumonia (VAP) in trauma patients. However, ampicillin/sulbactam or ceftriaxone monotherapy lacked reliable coverage for early VAP in this study.
Area of Science:
- Critical Care Medicine
- Infectious Diseases
- Trauma Surgery
Background:
- Early-onset ventilator-associated pneumonia (VAP) in trauma patients (< 7 days) is associated with a lower risk of specific resistant infections.
- Current practices often involve broad-spectrum antibiotics for early VAP, but their necessity is questioned.
Purpose of the Study:
- To evaluate the necessity of routine broad-spectrum antibiotics for trauma patients diagnosed with early-VAP.
- To compare the incidence of methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa in early- versus late-VAP.
- To assess the susceptibility of common pathogens to specific antibiotics in early-VAP.
Main Methods:
- Retrospective cohort study of adult trauma patients with VAP.
- Primary outcome: presence of MRSA and/or P. aeruginosa in early- and late-VAP.
- Secondary outcomes: bacterial susceptibility, ICU/hospital length of stay, ventilator-free days, and mortality.
Main Results:
- 164 patients included; 208 organisms identified (90 early VAP, 118 late VAP).
- MRSA incidence: 7.7% (early VAP), P. aeruginosa incidence: 5.6% (early VAP).
- Susceptibility to ampicillin/sulbactam: 73.3% (early VAP); ceftriaxone: 83.3% (early VAP). Late VAP had longer ICU stay (P=0.040), early VAP had higher mortality (P=0.012).
Conclusions:
- Monotherapy with ampicillin/sulbactam or ceftriaxone did not provide reliable broad-spectrum coverage for early-VAP in this cohort.
- Institutional analysis is crucial to ensure appropriate initial treatment for VAP.
- Findings suggest a need to re-evaluate antibiotic strategies for early VAP in trauma patients.
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