Fish oil and sepsis: we still need more trials

Pontes-Arruda and colleagues addressing eicosapenta enoic acid/γ-linolenic acid (EPA/GLA) use in septic patients [1]. First, I did not fi nd an adequate sample size calculation and we should know whether a type I error could have occurred. Another major concern is the inclusion imbalance among sites, which is not mentioned in the results or as a study limitation. Th e authors recognized that only fi ve sites included patients among the initial 12 selected sites. As the principal investigator of one of these centers without inclusion, I believe it would be important to mention that the fi rst author’s site included the vast majority of patients. Although this is undoubtedly a multicenter study, readers should analyze the results considering exactly how many patients were included from each site and how many were excluded thereafter. It is not necessary to state the number of patients per site in large, multicenter studies without imbalance. When an imbalance is too high, however, it is advisable to provide possible reasons and to assume that it is a limitation. Th e authors recognized a limitation only in the highly selected population: patients without organ dysfunction already in the ICU and under enteral nutrition. It is well known that Brazil has a shortage of ICU beds, mostly in public hospitals, so patients without organ dysfunction are not likely to be admitted. Th e patients’ baseline characteristics also draw attention, with high Sequential Organ Failure Assessment (SOFA) score, high Multiple Organ Dysfunction Score and hyperlactatemia. Organ dysfunction was one of the exclusion criteria, with quite similar defi nitions to the SOFA score. Th e authors should therefore have provided a possible expla nation for this fi nding. Th e development of organ dysfunction within the 48-hour window to the start of enteral feeding is a possibility. However, this could compromise the results, as organ dysfunction would be already present by the time the intervention took place. Th e strong criticism regarding the not yet published EDEN Omega trial is also unusual [2]. Th is trial will be the strongest evidence for EPA/GLA use and we should wait for a proper peer-review process. I disagree with the authors when they suggest that doctors do not use EPA/ GLA because of these unpublished results. I do believe that the medical community does not widely use fi sh oil because the available evidence is weak [3-6]. We will need another EPA/GLA trial – multicenter, doubleblinded and well sized for mortality – to fi nally defi ne its role in early or late sepsis management.