Introduction
Nosocomial pneumonia (NP) is a common complication in critically ill patients, particularly in patients who are intubated for more than 48 hours, and NP is responsible for significant in-hospital morbidity and mortality [
1‐
3]. When mechanically ventilated patients develop NP, it is known as ventilator-associated pneumonia (VAP) [
1,
2]. Multiple hospital-associated risk factors for NP have been identified. These risk factors are thought to contribute to increased bacterial colonization of the aerodigestive tract and facilitate the entry of pathogenic bacteria into the lower respiratory tract [
4].
Considerable efforts have been made to evaluate methods for reducing NP. For example, selective digestive tract decontamination in critically ill patients has been shown to reduce the occurrence of NP; however such decontamination has also been associated with increased rates of antimicrobial resistance [
5,
6]. Several experimental and clinical studies have suggested a promising effect of probiotics on preventing NP in critically ill patients [
7‐
10].
Probiotics are commercially available microorganisms that when ingested as individual strains or in combination may offer potential health benefits to the host [
11]. Prebiotics are non-digestible sugars that selectively stimulate the growth of certain bacteria colonies. The combination of pre- and probiotics has been designated as synbiotics. It is hypothesized that probiotics could potentially reduce the incidence of NP in critically ill patients through various local and systemic effects that minimize colonization by more virulent species or optimize host immune defenses. These effects include reducing overgrowth of potentially pathogenic microorganisms, enhancing gut barrier function, reducing bacterial translocation, and up-regulation of immune functions [
12‐
19].
To date, clinical research concerning the effects of probiotics in critically ill patients have provided conflicting results, with some suggesting clinical benefit [
20‐
29], and others showing no benefit [
30‐
33]. More recently, one study showed that probiotics therapy led to a significant reduction in VAP rates among treated patients [
22]. However, another study showed that daily prophylactic administration of probiotics was not effective for critically ill patients, notably for those with non-severe sepsis [
30].
Therefore, we performed a systematic literature review and meta-analysis to investigate the effects of probiotics in critically ill patients using incidence of NP as the primary outcome, and mortality, length of stay in the ICU and in hospital, and adverse outcomes as secondary outcomes.
Materials and methods
Data sources and search strategy
To identify studies for inclusion in this review, two authors independently searched PubMed, the Cochrane Central Database of Controlled Trials, and EMBASE for relevant studies published up to January 2012. The search was limited to studies conducted in humans. No language restriction was imposed. Search terms were individualized for each database. Search terms used included: ['pneumonia' OR 'critically ill' OR 'intensive care' OR 'trauma' OR 'pancreatitis' OR 'surgical patients'] AND ['probiotics' OR 'prebiotics' OR 'synbiotics' OR 'lactobacillus' OR 'bifidobacterium']. We also searched the proceedings of major relevant conferences, trial databases, the reference lists of identified trials, and major reviews.
Study selection
Two reviewers (KXL and YGZ) independently screened studies for inclusion, retrieved potentially relevant studies, and determined study eligibility. Any discrepancies were resolved by consensus. Analysis was restricted to double-blind, randomized controlled trials (RCTs). For this meta-analysis, we considered those RCTs that compared administration of probiotics vs. placebo in critically ill patients (such as those admitted to an ICU or having recently undergone abdominal or another major surgical procedure), and that reported the incidence of NP or VAP. Probiotics could be administered either alone or in combination with prebiotics.
Two authors independently extracted data from all of the enrolled studies. Extracted data included study design (for example, year conducted, sample size), patient characteristics, study methodology (for example, eligibility criteria, method of randomization and blinding), intervention (for example, type of probiotic agent, dose, route of its administration and duration), and clinical outcomes. The primary outcome was the incidence of NP. We used the authors' definitions for NP if they included clinical and radiological criteria. Secondary outcomes were mortality, length of stay in ICU and in hospital, and reports of adverse outcomes.
Quality assessment
We formally assessed the methodological quality of each trial using the Jadad score [
34], which incorporates randomization, blinding, and attrition to derive a score of 0 to 5; higher scores indicate higher quality. Two reviewers (KXL and YGZ) independently appraised the quality of the included trials. Studies were considered to be of low quality if the Jadad score was ≤ 2 and high quality if the score was ≥ 3.
Statistical analysis
The meta-analysis was performed using Review Manager 5.0 (Cochrane Collaboration, Oxford, UK). We computed pooled odds ratios (ORs) and 95% confidence intervals (CIs) from the adjusted ORs and 95% CIs reported in the observational studies. We used Cochrane Q and I
2
statistics to assess the heterogeneity of study results. We predefined heterogeneity as low, moderate or high with I
2
values above 25%, 50%, and 75%, respectively. In the analysis of heterogeneity, we considered a P- value < 0.10 statistically significant. Study-level data were pooled using a random-effects model when I
2
was > 50% or a fixed-effects model when I
2
was < 50%. Publication bias was assessed by a funnel plot using the occurrence of NP as an endpoint.
Discussion
Our meta-analysis found that probiotics administration was associated with statistically significant reduction in the incidence of NP in critically ill patients. However, the pooled results showed that probiotics did not affect overall mortality, or length of stay in the hospital and the ICU, which were the secondary endpoints of the study.
The current meta-analysis is different from previous reviews in several aspects. Although three recent reviews addressed somewhat similar questions, our meta-analysis identified and included more eligible studies than the previous reviews [
35‐
37]. These previous reviews on probiotics administration included studies that recruited patients requiring MV only [
35] or studies of surgical patients only [
36]. Thus, those meta-analyses were limited to selected populations. Trials of any type of critically ill patients were eligible for our study, and therefore our results are applicable across a wide range of clinical situations that are encountered with critically ill patients. In order to diminish the number of confounding factors, we excluded two studies using chlorhexidine and antibiotic decontamination as control groups, because the use of chlorhexidine in oral care procedures and antibiotic decontamination of the digestive tract were considered to be effective in preventing NP [
6,
21]. The review by Siempos
et al. used the data from one trial on the rate of respiratory tract infection as the rate of VAP [
35], which may have contributed to an overestimation of the VAP rate and a greater observed treatment effect. This trial has been recently published in a separate study [
23] and confirms that there are fewer patients with VAP than with respiratory tract infections. Accordingly, we included the latter study in our meta-analysis. Our results appear similar to the previous reviews by Siempos
et al. [
35] and Pitsouni
et al. [
36], but inconsistent with the results of the systematic review by Watkinson
et al. [
37]. Siempos
et al. found that administration of probiotics was beneficial in the incidence of both VAP and NP, length of stay in the ICU and colonization rates of
Pseudomonas aeruginosa in the respiratory tract [
35]. Similarly, the meta-analysis by Pitsouni
et al. demonstrated that probiotics significantly reduced the occurrence of postoperative pneumonia and any infectious complications, as well as the duration of postoperative hospital stay [
36]. While we restricted our subgroup analysis to patients in surgical populations, a pooled analysis showed a marginally non-significant reduction in NP in favor of probiotics. In contrast, Watkinson
et al. pooled eight trials and found that pre- pro- or synbiotics were not associated with any significant change in the outcomes studied, that is, length of ICU stay, hospital mortality and the incidence of nosocomial infection and more specifically incidence of pneumonia [
37]. Although there was no statistically significant effect on the incidence of NP in all subgroups, the risk reduction associated with probiotics use was substantial. The reasons for these inconsistent results may partly be due to differences in focus on clinical outcomes.
The results of this meta-analysis should be interpreted carefully based on other considerations. As the diagnosis of pneumonia is a more subjective outcome than mortality or length of stay in the ICU, it may be more subject to bias, and this may in part explain the marked reduction in pneumonia found in these studies. In addition, the definitions of pneumonia varied among different studies, which will affect the true nature of clinical outcomes. In addition, the absence of an effect on secondary outcomes may be from the small number of pooled RCTs and total patients. And lastly, the treatment durations in some studies were likely too short to demonstrate maximal benefits. Consequently, a lack of standard protocols and insufficient numbers of patients may make it difficult to derive conclusive results based on the current meta-analysis.
The potential harm due to probiotics therapy also warrants comment. The numbers of patients with diarrhea or abdominal cramps did not differ between those patients who received probiotics and those who did not in our current meta-analysis. However, a particular concern in critically ill patients is whether their exposure to probiotics places them at risk for developing an invasive infection. There were no reports of bacteremia or sepsis due to probiotics in the studies included in our meta-analysis. In addition, Besselink
et al. found an increased rate of bowel ischemia and mortality in those patients treated with probiotics [
33]. However, a meta-analysis of four RCTs that included severe acute pancreatitis, including the study by Besselink
et al. [
38] demonstrated that probiotics did not significantly influence mortality either favorably or adversely. Accordingly, we should monitor the safety of probiotics as our research efforts move forward.
Our analysis has several limitations. First, as already mentioned, there was heterogeneity in the inclusion criteria, the populations studied, the probiotic agents used, doses, time points when therapy was initiated, durations of therapy, the routes of administration, and the diagnostic criteria used for establishing NP or VAP. These factors were not comparable in most of the trials and might have affected the clinical outcomes. These differences may explain the statistical heterogeneity in some of the secondary outcomes investigated. Second, even though we were able to pool results across all trials, the number of patients included in this meta-analysis may not be sufficient to exclude significant clinical benefit. Third, most trials were done in single centers and may have had inherent bias related to local practice habits and the populations served. Although we extensively searched for relevant studies using multiple databases and multiple search items, and no language restriction was placed on the search, a funnel plot suggested the possibility of publication bias. Finally, the quality of the included studies was not consistent. Some RCTs included in our analysis had major methodological flaws [
24,
28]. The quality of trials can affect the direction and magnitude of treatment effects when performing a meta-analysis.
Although the results have been encouraging, there is insufficient evidence to suggest to clinicians that administration of probiotics is associated with significant clinical benefit in critically ill patients. In addition, there is a lack of head-to-head comparative trials with different probiotics to investigate and clarify which probiotic bacterial strains were of most benefit to critically ill patients. Data regarding the superiority of different doses of probiotics and routes of administration are also lacking. The questions that remain to be evaluated in large-scale, randomized controlled trials of probiotics use in NP include the optimal type of probiotic preparation, administration route, dose intensity, timing and duration of administration, safety, patient eligibility, and contraindications.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
KXL and YGZ carried out the primary study search, extracted data, performed statistical analysis, and drafted and revised the manuscript. JZ drafted and revised the manuscript. LLT carried out statistical analysis and revised the manuscript. JWL revised the manuscript and modified the written English. XDW carried out statistical analysis and helped draft the manuscript. JMQ conceived the idea, participated in its design, and drafted and revised the manuscript. All authors read and approved the final manuscript.