https://doi.org/10.5812/pedinfect.15320

Prophylactic Probiotics for Prevention of Necrotizing Enterocolitis (NEC) in Low Birth Weight Neonates; Quality of the Evidence

authors:

avatar Mario Augusto Rojas 1 , *

Wake Forest University School of Medicine, Winston-Salem, USA
Archives of Pediatric Infectious Diseases: Vol.2, issue 2; 231-232
published online: April 14, 2014
article type: Letter
received: October 8, 2013
accepted: October 11, 2013

how to cite: Rojas M A. Prophylactic Probiotics for Prevention of Necrotizing Enterocolitis (NEC) in Low Birth Weight Neonates; Quality of the Evidence. Arch Pediatr Infect Dis. 2014;2(2): 231-232. https://doi.org/10.5812/pedinfect.15320.

Dear Editor,

The study by Dashti et al. is a single center double-blinded placebo controlled trial that exposed infants≤ 1800 grams in the intervention group to a multi-species preparation of probiotics. The authors of this paper did not find a difference in the incidence of necrotizing enterocolitis (NEC) between the intervention and the placebo group, nor did they find a difference in any of their secondary outcomes. The paper does not describe the incidence of NEC in their institution and they do not describe how they calculated the sample size based on their historical incidence of NEC. I believe this to be the main weakness of this study and the major reason why the authors of this paper were not powered to find a difference in the primary outcome if in fact this difference did exist. Using the control group incidence of NEC of 1.49% (stage II and III Bell’s classification), a confidence level of 95%, a power of 80% and an expected decrease of 50% in the incidence rate of NEC (to 0.75%), the total sample size required for this study would have been 6,876 infants (3,438 infants in each group). Another possible explanation for the observed lack of efficacy may be due to the inclusion of infants > 1500 grams, a group that traditionally has a much lower incidence of NEC compared to infants born at≤ 1500 grams. Recruitment of this proportionally large number of more mature infants would tend to dilute the effect of the intervention. Also, the late administration of the probiotic preparation (mean age 4.36 days) when colonization with potential NICU pathogens may already be established could also add to the observed lack of efficacy. The main weaknesses highlighted in this study are not unique to this study but a major theme of the majority of studies included in the multiple meta-analyses published on the use of Probiotics in preterm infants (1-5). Although these meta-analyses have shown a decrease in the incidence of NEC with the use of different species of probiotics, the potential for publication and selection bias is of great concern because of the known tendency for journals to reject studies that do not show efficacy. From this perspective, I welcome Archives of Pediatric Infectious Diseases’s decision to publish this manuscript. Also, the poor quality of the design of many of the studies included in these meta-analyses makes their conclusions at the very least suspicious. Are we ready to start using probiotics for the prevention of NEC in premature infants? Although we understand the urgency of finding an intervention that prevents NEC due to the high mortality and morbidity associated with this outcome, wisdom dictates a more thorough evaluation of the bio-molecular characteristics of specific species, their dosing, quality, and safety. This is especially relevant in the extremely premature infant population where some published studies have demonstrated a higher incidence of sepsis when exposed to probiotics (6, 7). I do not believe that we have at the present time a probiotic species that fulfills all these basic requirements. An international consensus agreement that prioritizes and directs future efforts in this area of research is urgently needed to expedite fulfilling these goals. This fragile population of premature infants embraces and supports our coordinated efforts.

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