Elsevier

Journal of Critical Care

Volume 27, Issue 1, February 2012, Pages 18-25
Journal of Critical Care

Ventilator-Associated Pneumonia/Mechanical Ventilation
Ventilator-associated pneumonia is an important risk factor for mortality after major cardiac surgery,☆☆

https://doi.org/10.1016/j.jcrc.2011.03.008Get rights and content

Abstract

Purpose

Ventilator-associated pneumonia (VAP) is the main infectious complication in cardiac surgery patients and is associated with an important increase in morbidity and mortality. The aim of our study was to analyze the impact of VAP on mortality excluding other comorbidities and to study its etiology and the risk factors for its development.

Materials and Methods

This prospective cohort study included 1610 postoperative cardiac surgery patients' status post cardiopulmonary bypass (CPB) between July 2004 and January 2008. The primary outcome measures were the development of VAP and in-hospital mortality.

Results

Ventilator-associated pneumonia was observed in 124 patients (7.7%). Patients with VAP had a longer length of hospitalization (40.7 ± 35.1 vs 16.1 ± 30.1 days, P < .0001) and greater in-hospital mortality (49.2% [61/124] vs 2.0% [30/1486], P = .0001) in comparison with patients without VAP. After performing the Cox multivariant analysis adjustment, VAP was identified as the most important independent mortality risk factor (adjusted hazard ratio [HR], 8.53; 95% confidence interval, 4.21-17.30; P = .0001). Other independent risk factors of in-hospital mortality were chronic renal failure (HR, 2.56), diabetes mellitus (HR, 1.90), CPB time (HR, 1.51), respiratory failure (HR, 2.13), acute renal failure (HR, 2.39), and mediastinal bleeding of at least 1000 mL (HR, 1.81).

Conclusions

The development of VAP after CPB is the most important independent risk factor for in-hospital mortality. Identification of effective strategies for the prevention of VAP is needed.

Introduction

Ventilator-associated pneumonia (VAP) is the most frequent serious infection among patients undergoing heart surgery. The prevalence of VAP is estimated to be 7.8% to 21.6% [1], [2], [3] and is associated with prolonged hospitalization [4], [5], increased health care costs [6], and a 15% to 45% attributable mortality [7].

In patients admitted to the intensive care unit (ICU), the extra mortality due to VAP remains a controversial issue in the literature. Previous studies have reached conflicting conclusions regarding the impact of VAP on mortality [1], [8], [9], [10], [11], [12], [13], [14], [15], [16], [17]. Although the gross mortality rate is high, there are doubts as to whether the higher mortality rate is due to VAP itself or to the seriousness of the underlying illness.

Patients undergoing heart surgery are at a particularly high risk for the development of VAP due to the presence of multiple comorbidities, frequent postoperative use of invasive devices (eg, intraaortic balloon counterpulsation, pulmonary artery catheter), and the common use of cardiopulmonary bypass (CPB). At the same time, in-hospital patients are also at risk for multiple postoperative events (eg, myocardial infarction [MI], congestive heart failure, acute renal failure, strokes) [1], [2], [3], [4], [16], [18], [19]. These comorbidities complicate the evaluation of the impact of VAP on mortality [17]. The repercussions of VAP on in-hospital mortality have not been adequately studied in the area of cardiac surgery.

Our working hypothesis was that VAP is the most important independent risk factor of in-hospital mortality in cardiac surgery patients. Our main objective was to assess whether the development of VAP during the postoperative period after cardiac surgery for patients undergoing CPB is associated with an excess of in-hospital mortality not attributable to the underlying severity of the illness or to the intraoperative and postoperative events. The secondary aim was to establish risk factors of in-hospital mortality.

Section snippets

Hospital setting and patients

This prospective observational study was carried out in the “Hospital Clínico Universitario,” a tertiary-level medical center with 800 beds in Valladolid, Spain. The Department of Cardiac Surgery annually performs approximately 550 open cardiac operations with extracorporeal circulation in adult patients. Two operating rooms were routinely used. There was an ICU with 10 beds dedicated exclusively to the postoperative care of patients who had undergone cardiac surgery. During a 3.5-year period

Patient and disease characteristics

During the period of the study, a total of 1610 patients were included. Mean patient age was 67.8 ± 10.3 years. There were 60.9% (980/1610) men and 39.1% (630/1610) women. Ventilator-associated pneumonia after cardiac surgery developed in 124 (7.7%) of patients, and the mean interval from surgery to presentation of VAP was 5.7 ± 5.8 days. In 80 (64%) patients, the antibiotic therapy was appropriate.

Patients with VAP (Table 1) had more comorbid conditions, longer aortic cross-clamp time (P <

Discussion

This prospective cohort study was designed to examine any potential effect of VAP on the in-hospital mortality of patients undergoing cardiac surgery with CPB and to differentiate this from the contributing factors concerning preoperative, intraoperative, and postoperative complications. In this context, the most relevant findings were that (1) the development of VAP during postoperative cardiac surgery is an important factor in determining in-hospital mortality, increasing the risk of death by

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    Funding sources: This work was supported in part by a grant from the “Gerencia de Salud, Consejería de Sanidad, Junta de Castilla y Leon” (GRS 143/A/07) and the Ministry of Health (RD06/0001/0020). All the authors carefully read the manuscript and fully approved it. The manuscript is original, and it is not submitted anywhere other than your journal. The authors declare not having conflict of interest regarding this study.

    ☆☆

    Contribution of authors: ET and FJA conceived the idea, designed the protocol, and supervised the analysis of the results. JB and BMR contributed to obtain the funding, oversaw the study, and acted as guarantors for the report. BMR, JB, JFBM, JC, JME, FJA, ET, JC, and JIGH helped in the conception of the study and the design of the protocol, supervised the recruitment of patients, collected the clinical material, and were responsible for statistical analysis. ET, IF, MH, FJA, and JB developed and supervised all work and analyzed the results. ET wrote the report in collaboration with FJA, JIGH, JB, and the other authors.

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