Efficacy of adjunctive inhaled colistin and tobramycin for ventilator-associated pneumonia: systematic review and meta-analysis

Ventilator-associated pneumonia (VAP) poses a significant challenge in intensive care units (ICUs) [1]. The rise in drug-resistant gram-negative pathogens, such as extended-spectrum beta-lactamase (ESBL)-producing and carbapenem-resistant Enterobacteriaceae, has been associated with treatment failures and increased mortality in ICU patients [2]. To address this issue, the use of adjunctive inhaled antibiotics has emerged as a viable strategy [3]. Inhaled antibiotics offer the advantage of achieving higher drug concentrations in the pulmonary epithelial cells, which is particularly beneficial for treating gram-negative infections with aminoglycosides [4]. Current clinical guidelines recomended to use inhaled antibiotics in addition to intravenous therapy, especially for patients infected with colistin/aminoglycoside-sensitive pathogens or those who have shown a poor response to intravenous antibiotics [5]. This approach improves treatment success rates while minimizing systemic antibiotic doses and associated toxicities.

Colistin and tobramycin are the most commonly prescribed nebulized antibiotics [6]. Previous systematic reviews have examined the efficacy of adjunctive inhaled antibiotic therapy for VAP treatment [7‐10]. However, contrary to more recent studies, these systematic reviews did not find any advantages in utilizing adjunctive inhaled antibiotics, including in terms of clinical cure rates. Furthermore, differing opinions among experts have raised concerns regarding the appropriateness of prescribing inhaled antibiotics for patients with VAP [11]. This study presents a comprehensive systematic review and meta-analysis, offering updated insights on the effectiveness of adjunctive inhaled colistin and tobramycin.

The initial search yielded 106 records, which were subsequently reduced to 31 after removing duplicates. Following the screening of titles and abstracts, 59 records were excluded, as shown in Fig. 1. Consequently, only seven randomized controlled trials (RCTs) that met the predefined inclusion criteria were included in the meta-analysis [14‐20].

Comprehensive information regarding the included studies is provided in the Supplementary material. The studies range in design, with sample sizes varying from smaller studies like Hallal with 10 participants (5 treatment, 5 control) to larger studies such as Rattanaumpawan, which included 100 participants (51 treatment, 49 control) [14‐18, 20]. In these studies, a broad range of patient ages were included. Each study employed specific diagnostic criteria for VAP and reported a diverse distribution of bacterial species responsible for infections. For example, Rattanaumpawan focused on patients with Gram-negative bacteria isolated from an endotracheal tube aspirate, including Acinetobacter (50%) and Pseudomonas (26%), among others [19]. The distribution of various bacterial species causing VAP was also diverse across the studies, with Pseudomonas aeruginosa, Acinetobacter spp., and Klebsiella spp. being some of the most reported pathogens. Specific interventions included the use of tobramycin at dosages like 40 mg every 8 h in the case of Brown, and colistin nebulized at 75 mg every 12 h for a duration of 9 to 12 days in Rattanaumpawan. These interventions were compared against control groups that received placebo treatments or systemic antibiotics without the aerosolized form. The duration of the interventions varied, with some studies specifying the exact number of days the aerosolized antibiotics were administered and others not. For instance, Le Conte employed tobramycin for 5 days, whereas Nassar did not provide specific duration details for the use of colistin [17, 18].

Table 1 presents the biases observed in these studies, indicating that three studies exhibited attrition bias, one had reporting bias, two had detection bias, and one had performance bias. The GRADE results, as depicted in Table 2, indicated a “very low quality” of evidence for both clinical cure and adverse events. Due to the limited number of studies, the interpretation of the results is constrained, and it is difficult to ascertain the risk of publication bias with sufficient confidence.

The present systematic review and meta-analysis provide valuable insights into the efficacy and safety of adjunctive inhaled antibiotics for the treatment of ventilator-associated pneumonia (VAP). The findings suggest that the use of tobramycin or colistin as adjunctive inhaled antibiotics may have a positive impact on both the clinical and microbiological cure rates of VAP. The meta-analysis demonstrated a higher probability of clinical cure and a greater likelihood of achieving microbiological eradication in the groups receiving adjunctive inhaled antibiotics compared to the control group. However, it is important to note that the quality of evidence supporting these findings is rated as “very low” and “moderate,” indicating a significant degree of uncertainty. Therefore, further research is required to strengthen the evidence base and establish more definitive conclusions.

The results of our study align with previous evidence in the field [7, 21]. However, a notable difference between our study and previous systematic reviews is the inclusion of the studies conducted by Angermain and Hallal [14, 16]. These studies evaluated the effectiveness of tobramycin and reported positive results in terms of microbiological eradication and the probability of clinical cure, without observing a reduction in mortality. It is worth mentioning that due to their small sample sizes, the weight of these studies in the meta-analysis is relatively low compared to other studies, and thus our conclusions align with previous systematic reviews.

Our work has limitations. First, the small sample size (seven RCTs) restricts generalizability and raises concerns about chance findings. Additionally, potential biases identified in the included studies (attrition, reporting, detection, performance) could generate doubt on the reliability of the results. Furthermore, the low quality of evidence (“very low” for clinical cure and adverse events) highlights the need for further research before definitive conclusions can be drawn. The limited exploration of adverse events (only three studies reporting) restricts understanding of potential risks. The possibility of publication bias, given the restricted sample size, warrants caution in interpreting findings. Additionally, further investigation is needed to determine optimal dosing regimens and treatment durations for inhaled antibiotics. Furthermore, the impact of adjunctive inhaled antibiotics on specific patient subgroups and the potential development of antibiotic resistance requires further exploration. Our study has several strengths. Our search was exhaustive including gray literature and clinical trial registries. We follow the recommendations of the Cochrane collaboration and use GRADE to assess the quality of the evidence.

While this study sheds light on the potential benefits of adjunctive inhaled colistin and tobramycin for VAP, further research is crucial to optimize their use and refine clinical practice. Several key areas demand exploration: 1. Dosing and Treatment Duration: The optimal dosing regimen and treatment duration for inhaled antibiotics remain unclear. Future studies should explore a wider range of doses and durations to identify the most effective and safe approach, considering factors like patient characteristics and pathogen susceptibility. 2. Subpopulation Analysis: The present analysis did not delve into potential differences in treatment response across diverse patient subgroups (e.g., specific pathogens, underlying comorbidities). Future research should stratify analyses by relevant subgroups to provide more nuanced insights on which patients benefit most from this intervention. 3. Delivery System Optimization: The impact of delivery systems on drug bioavailability in the lungs was not addressed. Investigating and optimizing delivery systems could significantly improve treatment efficacy and potentially reduce required doses, enhancing safety and minimizing antibiotic resistance concerns. 4. Long-Term Outcomes and Resistance: The long-term effects of inhaled antibiotics on lung function, antibiotic resistance development, and other relevant outcomes require further investigation. Additionally, exploring the potential for emergence of resistant strains specific to inhaled antibiotics is crucial for informing sustainable resistance management strategies.

Tobramycin or colistin may have a positive impact on the clinical and microbiological cure rates of ventilator-associated pneumonia. The quality of evidence is low indicating a high degree of uncertainty. This highlights the importance of conducting more rigorous and well-designed studies to improve the quality of evidence and inform clinical decision-making.