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Kardiochirurgia i Torakochirurgia Polska/Polish Journal of Thoracic and Cardiovascular Surgery
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Anaesthesiology and intensive care
Possibilities of modification of risk factors for ventilator-associated pneumonia in cardiac surgery patients

Marta Wróblewska
,
Agata Stępniak
,
Zbigniew Burnos
,
Marta Kania-Pudło
,
Piotr Leszczyński
,
Piotr Hendzel

Kardiochirurgia i Torakochirurgia Polska 2013; 10 (4): 389–396
Online publish date: 2013/12/27
Article file
- 12 Wroblewska.pdf  [0.76 MB]
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Introduction

Patients undergoing cardiac surgery procedures are subject to enormous operative trauma, intensified further by the large size of the operated surface area. Early postoperative care in a cardiac surgery intensive care unit is aimed at minimizing the effects of trauma, broadly defined, which leads to weakening of the body’s immune mechanisms and increases the risk of nosocomial infection.

Nosocomial infection is an infection that is acquired in a healthcare setting. Its definition is broad and includes not only patients, but also medical professionals and hospital domestic staff, as well as persons visiting the patient in the hospital. With regard to the patient, nosocomial infection is an infection which was not in its incubation period at the time of the patient’s admission. It has been established arbitrarily that the symptoms of nosocomial infection appear at least 48 hours after the start of hospitalization, during the hospitalization, and within 10 days after the patient’s discharge. In patients undergoing surgery, the latter period is extended to 30 days after the procedure, and in the case of biomaterial implantation, up to 1 year after the implantation.

Definition of pneumonia

Pneumonia is a pathological condition of the respiratory system involving the presence of inflammatory cells in the lung parenchyma and/or effusion in the pulmonary alveoli. These changes significantly inhibit gas exchange and impair breathing, leading to dyspnea and increased breathing frequency. Types and classification criteria of pneumonia occurring in hospitalized patients are presented in Table I.

Hospital-acquired pneumonia (HAP) is defined as pneumonia in which symptoms appear in a patient at least 48 hours after his/her admission to the hospital, and the existence of an inflammatory process in the lungs at the start of hospitalization is excluded [1].

According to the American Thoracic Society (ATS), pneumonia in patients undergoing mechanical ventilation is known as ventilator-associated pneumonia (VAP). This form of pneumonia appears more than 48-72 hours after the start of mechanical ventilation [1, 2]. Two types of HAP can be distinguished in this group, taking into account the time of symptom appearance [1]. Early-onset VAP appears within the first 4 days after intubation and is typically caused by the endogenous flora of the patient; late-onset VAP occurs ? 5 days after intubation, and is caused by exogenous (hospital) bacteria [1]. Current ATS guidelines also distinguish healthcare-associated pneumonia (HCAP) [1]. The CDC definition of VAP diagnosis is presented in Table II [3].

Modification of VAP risk factors

Among many risk factors which favor the development of VAP, there are those that can be modified by altering procedures of providing healthcare to the patient. They include intubation and mechanical ventilation, body position, enteral nutrition, prevention of oropharyngeal colonization and pharmacological intervention aimed at neutralizing gastric acid. Modifying these factors is the fundamental measure that can be taken in order to prevent VAP. This issue was described in detail in the guidelines of the American Thoracic Society (ATS) pertaining to the management of adult patients suffering from hospital-acquired pneumonia [1].

It should be stressed that maintaining hand hygiene and conducting regular training constitute important aspects of nosocomial infection prophylaxis [4-6]. An educational program should be offered especially to students and persons visiting the patient. The most recent scientific studies related to prophylaxis of hospital-acquired infections (including VAP) emphasize the significance of adhering to nursing staff employment norms. It is recommended that patients at high risk of lung infection be attended by nurses in a 1 : 1 ratio and if no such risk is present, two patients may be assigned to one nurse [5].

In VAP prophylaxis, the efficacy of the so-called ventilator bundle has been demonstrated; this grouping of practices includes the semirecumbent position of the mechanically ventilated patient, deep vein thromboembolism prophylaxis, prevention of stress-related gastric ulceration, daily “sedation vacations” and the assessment of the patient’s readiness for extubation [2]. Morris et al. demonstrated that even employing a care bundle consisting of only four elements – head-of-bed elevation, local application of chlorhexidine gel in the oral cavity, daily sedation holds, and assessment of the patient’s readiness for extubation – may reduce infection rates [7].

Intubation and mechanical ventilation

The use of non-invasive ventilation with a face mask is sometimes impossible and often ineffective. Therefore, in clinical practice it is often necessary to intubate the patient and employ mechanical ventilation, even though it is known that these procedures increase the risk of VAP by 6-21 times [1]. VAP prophylaxis requires careful selection of the intubation tube. Its size should be adjusted to the anatomical properties of the patient’s upper airway, in order to ensure proper and easy clearance of the bronchial tree and provide the possibility of maintaining tube cuff pressure > 20 cm H2O, in order to prevent the transfer of bacteria from the oropharyngeal cavity to the lower respiratory tract [8]. The pressure inside the tube cuff should not, however, exceed 30 cm H2O, as this may impair the flow of blood and damage the tracheal mucous membrane [8].

Careful suctioning of secretion from the subglottic region of the intubated patient is an efficacious method of preventing VAP [4, 9, 10]. Kollef et al. studied the influence of this procedure on VAP prophylaxis in cardiac surgery patients and observed that the time period before VAP onset was increased from 2.9 to 5.9 days [11]. A meta-analysis encompassing almost 2500 patients has recently demonstrated the efficiency of endotracheal tubes equipped with a system enabling the drainage of secretions from the subglottic region in providing VAP prophylaxis, shortening the ICU stay of the patient and reducing the number of days of assisted ventilation [12].

The route through which the tube is introduced is also significant. Oral intubation is recommended, as nasotracheal intubation is associated with the risk of sinusitis, which entails an increased presence of pathogens in the oropharyngeal cavity and an increased risk of VAP [4]. It should be remembered, however, that the endotracheal tube establishes a direct connection between the oropharyngeal cavity (colonized by bacterial flora) and the lower respiratory tract. For this reason, some authors believe that performing early tracheostomy (6-8 days after intubation), in comparison to late tracheostomy (14 days after intubation), may reduce the risk of VAP; however, this has not yet been unequivocally confirmed by clinical studies [13-16]. The intubation tube should be prevented from being accidentally removed, as reintubation further increases the risk of pneumonia [4, 14 17].

A mechanically ventilated patient is connected to the ventilator through a system of tubes providing gas flow. Studies have demonstrated that frequent exchange of these tubes does not significantly reduce the frequency of lower airway infection; therefore, they should be replaced only when they are soiled with the secretion from the patient’s airway [4, 18]. The colonization of the tube system by the so-called contaminated breath condensate may result in a respiratory system infection. Use of disposable tubes is currently recommended in clinical practice.

Moisteners and heat exchangers, used until recently in ventilators, may serve as reservoirs of bacteria. Currently, in order to eliminate this cause of VAP, single-use filters with heat and moisture exchangers are often employed; however, guidelines concerning their use are sometimes ambivalent [15]. The most recent guidelines, published in the USA in 2012, describe in detail the indications and contraindications for both the active and passive humidification of air exhaled by the ventilated patient [with heated humidifiers (HHs) and heat and moisture exchangers (HMEs), respectively] [19]. It should be noted that no significant difference in VAP incidence has been demonstrated between the two methods, indicating, however, that HMEs should be used in the case of mechanical ventilation lasting ? 96 hours and during the patient’s transport, whereas HHs should be employed when the use of HMEs is contraindicated [19].

Shortening the duration of mechanical ventilation is also an efficacious method of preventing pneumonia. In order to achieve this, the patient should be weaned from ventilatory support by decreasing the dose of sedatives [5]. The intubation tube should be prevented from being accidentally removed, as reintubation further increases the risk of pneumonia [4, 14, 17].

The evaluation of the patient’s condition by means of proper scales, with regard to both analgesic efficacy and sedation depth, is key for achieving this goal. Without efficacious analgesic treatment, it is extremely difficult, if not impossible, to achieve adequate sedation. The purpose of pain monitoring is served by the appropriate scales: the Visual Analogue Scale (VAS), the Numeric Rating Scale (NRS), the Behavioral Pain Scale (BPS) and the Critical-Care Pain Observation Tool (CPOT). The VAS and NRS require the cooperation of the patient, while the BPS and CPOT may be used regardless of the level of patient cooperation. Several scales are also available for monitoring sedation: the Ramsay Scale, the Cook Scale, the Sedation Agitation Scale (SAS) and the increasingly popular Richmond Agitation Sedation Scale (RASS) [4, 5]. Healthcare professionals should strive to evaluate the condition of the patient every two hours, or even more often, in order to select adequate doses of analgesic and sedative agents [1]. An adequate protocol may also include the modification of medication by the nurse, depending on the level of analgesia and sedation.

In recent years, thanks to the “Pain-free hospital” campaign, the scheme of treating and monitoring pain has been popularized in Poland. The obligation to record documentation concerning the monitoring and treatment of pain was included in the regulation of the Health Ministry of December 21, 2010, pertaining to the types, extent, and methods of processing medical documentation. However, the monitoring of sedation depth is still not performed in many hospitals. The RASS scale is very useful for this purpose (Table III).

Another method of reducing VAP incidence among intubated patients may be the use of endotracheal tubes, in which the internal lumen is coated with a thin layer of antibacterial substance (e.g. silver ions), which prevents the formation of bacterial biofilm inside the tube [13, 17, 20-22]. However, the recommendations included in the guidelines are not unequivocal in this respect [15]. It appears that using such tubes is warranted in patients in whom ventilatory support is expected to last longer than 48 hours, as such patients are at high risk of VAP occurrence [23].

The search for new methods or procedures for VAP prevention includes the evaluation of the potential significance of new technological solutions, such as endotracheal tubes with ultrathin or modified (low-volume/low-pressure) cuffs, as well as the maintenance of constant pressure in the tube cuff, the removal of biofilm from the tube lumen with mucus shavers and the routine administration of physiological saline before suctioning of secretions from the trachea [13, 15, 22, 24-26]. It may also be beneficial to employ tubes with cuffs made of polyurethane or other materials (elastane, silicone, latex) instead of PVC, as well as tubes with different cuff shapes, in order to ensure better leak tightness [27-29]. The efficacy of these methods, however, must be confirmed by clinical studies.

Body position

In order to reduce the risk of gastric aspiration, the patient should be maintained in a semirecumbent position, with the chest and head raised (30-45°); a flat dorsal position should be avoided [1, 4, 9, 13, 30]. According to the literature, VAP is 3 times more likely to occur in patients lying in a flat dorsal position than in those placed in a semirecumbent position [31].

Some recent reports suggest that placing the patient in a lateral position may be more effective in preventing the aspiration of secretion from the subglottic area and VAP development than placing them in a semirecumbent position [13, 22, 32]. Clinical studies are currently being conducted in order to explain this issue and, perhaps, modify the recommendations. It should, however, be noted that, in the case of cardiac surgery patients, the lateral position could only be considered with regard to patients undergoing modern, minimally invasive procedures that do not involve sternotomy.

Enteral nutrition

Parenteral nutrition constitutes a significant risk factor of VAP development; therefore, as part of VAP prophylaxis, implementing enteral nutrition is recommended in spite of the risk of gastric content aspiration into the respiratory system [33]. Administering nutrition through a gastric feeding tube prevents intestinal villi atrophy, thus decreasing the risk of bacterial translocation. It should, however, be stressed that although this feeding method is preferred, introducing enteral nutrition too early in intubated patients (within the first two days of ventilation) may increase the risk of VAP in comparison to employing this feeding mode at a later time [34]. It has recently been suggested that feeding the patients with post-pyloric feeding tubes reduces the risk of gastric content aspiration and VAP. Nevertheless, none of the clinical studies conducted so far have confirmed this relationship; therefore, the method is not currently recommended [13].

Preventing oropharyngeal colonization

Colonization of the oropharyngeal cavity by microorganisms is considered to be an independent risk factor of VAP [35, 36]. One of the methods of reducing this risk is the local use of antiseptics or antibiotics; it should, however, be emphasized that these measures, while reducing VAP incidence, facilitate patient colonization by multidrug-resistant (MDR) pathogens [8, 37]. On the other hand, studies conducted among patients, including cardiac surgery patients, demonstrated the positive significance of modulating the bacterial composition of the oral cavity by the local use of chlorhexidine [35, 38]. This measure had a preventive effect with regard to VAP development among the studied patients. An alternative measure consists of preventing oropharyngeal cavity secretions from reaching the lower airway by minimizing sedation and muscle relaxant administration, thus activating the cough reflex and other defense mechanisms of the respiratory system.

Current guidelines concerning VAP prophylaxis highlight the great importance of the patient’s oral hygiene [4]. Regular brushing of the teeth, gums and tongue with the use of toothpaste (every 2-4 hours), followed by moistening of the patient’s lips, is recommended [39]. The aim of these actions is to remove the proliferated bacterial flora from the oral cavity of the mechanically ventilated patient. These nursing activities may be conducted using commercially available accessories, which can facilitate the performance of this procedure and enhance its efficacy.

Doing this systematically is very efficient with regard to the prevention of bacterial colonization in the patient’s oral cavity without the need for the local use of antibiotics or antiseptics, which reduces the selection of MDR bacterial strains. Therefore, the above procedure of regular oral hygiene should be implemented in the patient’s daily care plan instead of using local antibiotics or antiseptics.

Pharmacological intervention aimed at neutralizing gastric acid

In patients hospitalized in intensive care units (ICU) pharmacological prophylaxis of stress-related gastric ulceration is implemented in the form of antacids (H2 receptor antagonists or proton-pump inhibitors). Unfortunately, pH elevation in the stomach creates favorable conditions for bacterial proliferation, eliminates the natural barrier and enables the bacteria to ascend into the upper segments of the gastrointestinal tract and, in the case of gastric content aspiration, also into the bronchial tree [4]. Although such treatment contributes to an increase in VAP incidence, it is still recommended in the current prophylaxis guidelines for this disorder [2, 13, 40]. According to some authors, using sucralfate instead of H2 receptor antagonists may reduce VAP incidence in mechanically ventilated patients [9].

Other options of VAP prophylaxis

Using the aforementioned procedures and guidelines reduces the risk of VAP, but does not eliminate it completely. Therefore, the search for additional methods of minimizing VAP incidence in patients with ventilation support continues [13, 15, 22].

Some authors claim that the functioning of the mechanisms of mucociliary clearance and airway secretion clearance may be improved by physical therapy consisting of rotating the patient mechanically by 40o instead of the regular rotation performed every 2 hours [13]. A meta-analysis of 10 clinical studies indicated that, although this measure reduces VAP incidence, it does not reduce the duration of mechanical ventilation or ICU stay, does not decrease patient mortality, and cannot currently be recommended [41]. Furthermore, it is associated with a risk of complications, such as unplanned extubation or cardiac dysrhythmias. The procedure may also be impossible to apply to patients after cardiac surgery procedures involving sternotomy.

A meta-analysis of prospective controlled studies pertaining to the use of probiotics in VAP prophylaxis indicates that they may be useful in reducing the incidence of this disease [42]. This may be related to the immunomodulatory properties of these agents and the fact that they inhibit the development of pathogenic bacterial flora in the oropharyngeal cavity and the stomach.

Hand hygiene of healthcare staff

Adhering to the protocols concerning hand hygiene of healthcare professionals is the simplest, and, at the same time, most efficacious and least expensive method of preventing nosocomial infections [9, 17]. This association was already noted in 1847 by Semmelweis, who ordered the staff of his hospital to regularly disinfect their hands, which reduced the mortality rate among postpartum mothers from 10% to 1%, proving that the hands of the medical personnel play a fundamental role in the transmission of nosocomial infections. Adherence to hand hygiene protocols by staff attending an intubated patient is crucial in VAP prophylaxis [6].

Hands of medical professionals may be colonized not only by their own physiological flora, but also by pathogens residing in the hospital environment, often equipped with genes of resistance to various antibiotic groups. If the medical staff fails to adhere to hand hygiene protocols, these microorganisms are then transferred to patients, in whom they may cause life-threatening infections. The only efficient method of pathogen removal is to thoroughly wash the hands, dry them, and disinfect them. In clinical practice, disinfection of hands without prior washing them is permitted (or, lately, even recommended) if they are visibly clean. An exception to this rule occurs if the patient is infected or colonized by Clostridium difficile. This bacterium produces spores that are unaffected by alcohol-based hand disinfectants; in the case of contact with a patient infected with this pathogen, washing of the hands is required in order to mechanically remove the spores.

Despite being considered the simplest and most important method in the prevention of nosocomial infections (including VAP), handwashing and hand disinfection protocols are not always adhered to by hospital staff. Studies conducted in the 1990s in American hospitals indicated that only 14-59% of physicians and nurses comply with the procedure [43]. In spite of the passage of time, these data still remain unsatisfactory – compliance with hand hygiene protocols among healthcare professionals on average does not exceed 50% [44]. Many reports emphasize that these numbers are lower with regard to physicians in comparison to nursing personnel. The most important element of motivating hospital staff to properly wash and/or disinfect their hands should be the awareness that this practice prevents the transmission of nosocomial infections, reduces treatment costs, and, most importantly, saves patients from suffering or death.

Besides being required to maintain proper hand hygiene, medical professionals are also obliged to use protective clothing, such as gloves, aprons, and masks. Using gloves does not obviate the obligation to wash and/or disinfect one’s hands after each use. Gloves should be changed not only before approaching a new patient, but also in between different nursing procedures performed on the same patient. Protective aprons should also be changed regularly, because during patients’ care they become contaminated with microorganisms. In order to prevent the transmission of pathogens from one patient to another, protective clothing should be changed daily, or even more frequently if necessary.

The role of nursing staff in VAP prophylaxis – procedural protocols

Bronchial clearance is an important element of nursing care provided to intubated patients or patients with tracheotomy tubes, which also reduces the risk of VAP. It should be performed as often as required. The process begins with informing the patient about the necessity of performing this procedure, regardless of the level of the patient’s awareness. In order to facilitate the evacuation of secretions from the bronchial tree, the suctioning procedure should be preceded by the administration of mucolytic inhalation, followed by pulmonary alveoli expansion using the ventilator.

Tables IV and V present the basic rules and procedural protocols with regard to bronchial clearance, while Tables VI-VIII present the rules concerning the proper use of equipment (ventilator and oxygen dispenser) in order to minimize VAP risk in mechanically ventilated patients.

Conclusions

Awareness of hazards associated with nosocomial infections and their consequences, combined with the knowledge about their causes, epidemiology, risk factors and symptoms, forms the foundation for the efficient control and prevention of such infections.

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