Necrotizing enterocolitis: current perspectives
Phani Kiran Yajamanyam,1 Shree Vishna Rasiah,1 Andrew K Ewer1,2
1Neonatal Unit, Birmingham Women's Hospital NHS Foundation Trust, 2School of Clinical and Experimental Medicine, University of Birmingham, Birmingham, UK
Abstract: Necrotizing enterocolitis is the most common gastrointestinal emergency in neonates, particularly in those born very preterm. It is a leading cause of morbidity and mortality, especially in extremely low birth weight infants. Despite extensive research, the pathophysiology of necrotizing enterocolitis remains unclear and therapeutic options are limited. Multiple risk factors have been reported, but most are associated with prematurity and its complications. This makes management very challenging in vulnerable preterm infants. In this review, we focus on the risk factors and some of the current research in this area, particularly studies aimed at early detection and potential preventive measures for this potentially lethal condition.
Keywords: necrotizing enterocolitis, preterm infants, prematurity, probiotics
Necrotizing enterocolitis (NEC) can be defined as an acute inflammatory disease occurring in the intestines of the newborn, particularly in preterm infants, and is characterized by hemorrhagic necrosis of intestinal tissue which may lead to perforation and destruction of the gut.
NEC is the most common neonatal gastrointestinal emergency, particularly in those born at <32 weeks’ gestation and/or <1,500 g birth weight. NEC remains a challenging condition for neonatologists worldwide, with unclear pathogenesis, treatment options that might prove inadequate, a mortality rate as high as 50%,1 and high morbidity among survivors of significant disease, including short gut syndrome and significantly increased hospitalization.1 Even though it was first described more than a century ago,2 and although significant recent advances have been achieved in other complications of prematurity, such as respiratory distress syndrome, NEC remains a major cause of death. The main difficulties are predicting which babies will develop the disease and establishing the diagnosis before fulminant disease has occurred.
Numerous epidemiological studies have attempted to describe the incidence and prevalence of NEC based on either gestational age at birth or birth weight. Table 1 shows the reported incidence in a number of developed countries for periods between 1994 and 2009.3–9 Although there are minor differences in both the infants investigated and the incidence of NEC, an increase in the incidence of NEC among infants born <32 weeks’ gestation or <1,500 g has been reported,9 which may be linked to the increasing survival of infants born extremely preterm. Variation in the incidence of NEC between centers is well reported, and potential explanations include inherent population variability, differences in the local prevalence of microorganisms, and possible minor epidemics.10
Table 1 Epidemiological studies describing the incidence of necrotizing enterocolitis
NEC is characterized by a significant proinflammatory response involving a host of inflammatory mediators, including platelet-activating factor, interleukins (such as IL-1 and IL-6), and tumor necrosis factor-α.11 The mechanisms leading to clinically apparent NEC are unclear, although various causal factors have been proposed (Figure 1). The most well recognized causal factors are prematurity, hypoxia-ischemia, bacterial colonization, and enteral feeding.
Figure 1 Pathogenesis of NEC.
The vast majority of NEC occurs in infants born preterm,12,13 although up to 10% of all cases affect late preterm and term babies.14 The preterm gastrointestinal tract is potentially more susceptible to NEC as a result of immature barrier function of the intestinal mucosa,15 inadequate digestion of feeds,16 immature intestinal circulatory regulation,17 and immature innate immunity.
Hypoxia-ischemia as a primary causative factor in the pathogenesis of NEC18 has not been proven in clinical studies.19 However, in those full-term or near-term infants with comorbidities such as congenital heart disease (which may predispose to impaired systemic circulation), hypoxic-ischemic injury appears to have a much greater role in the pathogenesis of NEC.20
It is now recognized that abnormal microbial colonization of the preterm gut has a definitive role to play in the pathogenesis of NEC.21,22 Although no single organism has been identified as a causative agent for NEC, the well reported evidence of epidemics or clusters of NEC also strongly suggests the role of microorganisms in the origin of the disease.23
NEC predominantly occurs in babies who have been enterally fed,24 although it has occasionally been reported in completely unfed babies.25,26 Feeding with formula milk appears to increase the risk of NEC, whereas breast milk has a protective effect.27,28 The timing of initiation and speed of increase of enteral feeds is a subject of much debate. Sisk et al29 have reported a significant decrease in the risk of NEC with early breast milk feeding in preterm infants, while a recent Cochrane systematic review concluded that delaying the introduction of enteral feeds for up to 5–7 days did not increase the risk of developing NEC in very preterm infants.30
NEC was classified according to disease severity by Bell in 1978 (Table 2).31 A more recent classification was proposed by Gordon et al,32 encompassing other acquired neonatal gastrointestinal disorders in the preterm infant that might mimic NEC, such as feeding intolerance of prematurity, viral enteritis of infancy, spontaneous intestinal perforation, NEC caused predominantly by ischemia, and cow’s milk protein allergy.
Table 2 Modified Bell’s staging system
There have been several recent reviews on this topic.1,2,12,33 This review will focus mainly on the potential risk factors associated with NEC and some of the current research relating to prevention and early diagnosis of NEC.
Risk factors associated with NEC
Prematurity and low birth weight
The biggest single risk factor for NEC is prematurity,3–9 with more than 85% cases of NEC occurring in either very preterm infants (<32 weeks) or in very low birth weight infants (<1,500 g), and only around 10% of all cases of NEC are reported in either late preterm or term infants.14,34 Evidence is emerging that the age of onset of NEC is inversely proportional to the gestational age at birth, ie, the more immature the infant, the later the onset of NEC.34,35
The barrier function of the preterm gastrointestinal tract is immature, both in its structure and secretory activity.36–40 Mucosal permeability of the preterm gut is higher compared with that in term infants, and this could potentially play a role in the pathogenesis of NEC.36 The mucin layer lining the intestinal mucosa in the preterm gut is thinner than in term infants, and this may lead to increased bacterial adherence and increased mucosal permeability, both of which predispose to mucosal injury and development of NEC.37 In preterm infants affected by NEC, mucosal injury has been shown to lead to increased nitric oxide production which, in turn, accentuates epithelial injury, thus increasing the susceptibility to NEC.38 The preterm gut affected by NEC has also been shown to have fewer and immature Paneth cells15,39 (specialized crypt cells in the human intestine producing natural antimicrobials, such as lysozyme) with near absence of lysozyme.40
The immature nature of the preterm immune system is thought to play a major role in the development of NEC.41–44 Various toll-like receptors have been identified in the human intestinal epithelial cells which assist in strengthening the intestinal barrier function by identifying pathogens in the intestinal lumen.41 Changes in the expression of toll-like receptors (particularly TLR4 and TLR9) have been found to precede the development of NEC in a rat model.41 In experimental studies, suppression of inflammatory mediators such as platelet-activating factor and tumor necrosis factor-α resulted in a less severe disease.42,43 It is still unclear whether preterm infants lack the ability to suppress the exaggerated inflammatory response (which may arise as a result of normal stimuli such as colonization with commensal bacteria or the introduction of enteral feeds) or if preterm infants are unable to mount an adequate inflammatory response to pathogenic bacteria.44
The microbiota of preterm infants is significantly less diverse,45,46 possibly as a result of prolonged use of antibiotics and the adverse nosocomial environment of the neonatal intensive care unit. Studies have compared the gut microbiome of preterm infants with clinical NEC with matched controls by investigating stool samples, and demonstrated an increase in particular species of bacteria (eg, proteobacteria) days before the onset of disease.45,47 This change in bacterial colonization of the gut in preterm infants further suggests the causative role of bacteria in the pathogenesis of NEC.
Intrauterine growth restriction
Preterm infants with poor fetal growth may be at a greater risk of developing NEC.48–50 In a large retrospective analysis, Garite et al reviewed the outcomes of almost 30,000 premature infants born before 34 weeks of gestation.48 Infants were categorized into three groups: small for gestational age (birth weight below the 10th centile); antenatally diagnosed intrauterine growth restriction (IUGR) and small for gestational age; and antenatally diagnosed IUGR but a birth weight above the 10th centile. These groups were compared with controls matched for gestational age. After correction for antenatal steroid exposure, gender, and mode of delivery, infants with a birth weight below the 10th centile and infants who were diagnosed as IUGR and had a birth weight below the 10th centile were more likely to die or develop severe intraventricular hemorrhage, severe retinopathy of prematurity, and NEC. Infants who were diagnosed antenatally as IUGR but had a birth weight above the 10th centile had similar outcomes as controls. Manogura et al reviewed 404 infants affected by growth restriction due to placental disease.49 Thirty-nine developed NEC, giving an incidence of 9.7% across all gestations; in addition, birth weight <790 g remained a predominant risk factor for NEC. A recent meta-analysis investigating the outcomes of preterm infants affected by growth restriction compared with those without growth restriction found that the incidence of NEC was at least 2.5 times higher in preterm infants with growth restriction.50
However, some experimental studies in animals have not demonstrated an association between IUGR and NEC. Che et al compared the incidence of NEC in normal weight and IUGR preterm pigs51 divided into two broad groups, ie, one fed immediately and one where feeds were delayed for 2–3 days. The incidence of NEC was similar between the normal weight and IUGR preterm pigs, but was higher in those fed formula milk. The limitation of this study was that the preterm pigs were delivered at 91%–93% gestation, which may not be equivalent to the extreme preterm human neonates who are the most susceptible to NEC. Until further evidence from prospective studies is available for severe IUGR (below the 10th centile) preterm infants, this remains a potential risk factor for NEC.
IUGR and abnormal antenatal
Doppler ultrasound examination of fetal blood vessels has become part of routine antenatal surveillance, particularly when pregnancies are complicated by fetal growth restriction. It is suggested that in such fetuses, blood flow to the brain is preserved at the expense of blood flow to other organs, including the gastrointestinal tract.52 Whether this antenatal reduction in blood flow to the gut poses an additional risk factor for the development of NEC has remained a significant concern among neonatologists. A meta-analysis of 14 observational studies examining fetuses with absent or reversed end diastolic flow in the umbilical arteries concluded that there is an increased risk of developing NEC among these infants, with an OR of 2.13 (95% confidence interval [CI] 1.49–3.03).53 ADEPT (the Abnormal Doppler Enteral Prescription Trial)52 was a multicenter investigation conducted in the UK and Ireland to evaluate the effect of early introduction of enteral feeds in preterm infants born before 35 weeks’ gestation with birth weight below the 10th centile and abnormal antenatal umbilical Doppler wave forms. Feeds were introduced either on day 2 or day 6 of life. There was no difference in the incidence of NEC between the two groups, and the early fed group achieved full enteral feeds much earlier, with less dependence on parenteral nutrition and a lower incidence of cholestatic jaundice. Although the evidence suggests that babies with IUGR and abnormal antenatal Dopplers are at increased risk of developing NEC, early initiation of breast milk feeds does not appear to increase the incidence of NEC in this population.
Patent ductus arteriosus
Patent ductus arteriosus (PDA) is diagnosed in approximately one third of babies born before 30 weeks’ gestation and in more than 60% of babies born <28 weeks’ gestation.54 The presence of a large, hemodynamically significant PDA in preterm infants can lead to the “steal” phenomenon, compromising blood flow to organs distal to the PDA, including the gastrointestinal tract, potentially increasing the risk of developing NEC. Dollberg et al analyzed data from over 6,000 babies born between 24 and 34 weeks’ gestation from the national database in Israel.55 The overall incidence of NEC in these babies was comparable with that in other studies (5.5%), but in babies with PDA the incidence of NEC was significantly greater at 9.4% (OR 1.85). In a more recent study, Saldeno et al compared babies with a persistent PDA for >3 weeks with babies with a persistent PDA for <3 weeks.56 Twenty-nine percent of babies with PDA for >3 weeks developed NEC compared with only 5% of babies with a PDA that persisted for <3 weeks. Despite this, various trials that have targeted treatment of PDA have consistently failed to show any difference in the incidence of NEC.57,58 Because of the lack of conclusive evidence, further investigation, in the form of prospective randomized trials, is needed to establish a causative relationship between PDA and NEC. Until such evidence is available, we have to be aware that the presence of a hemodynamically significant PDA poses a potential risk for developing NEC.
In preterm infants, numerous short-term and long-term advantages of breast milk are well established.59 These include better feed tolerance, reduced infection rates, better neurodevelopmental outcomes, fewer hospital readmissions in childhood, and a reduction in incidence of NEC. In preterm babies, rightly so, no randomized controlled trials have been performed comparing maternal breast milk with formula and its effect on the incidence of NEC.60 However, in a prospective multicenter study, the incidence of NEC was 6–10 times higher in exclusively formula-fed infants when compared with exclusively breast milk-fed infants, and three times higher when compared with infants who received breast milk and formula.27 Donor milk was found to be as protective as maternal breast milk, and this risk persisted across all gestations. A Cochrane review analyzing the trials comparing donor breast milk versus formula feeds for preterm infants concluded that preterm babies who received formula milk were twice as likely to have NEC compared with preterm babies who received donor breast milk, thus highlighting the protective nature of donor breast milk.28 Studies have also looked at the minimum proportion of human milk that a preterm infant should receive to gain these benefits. Sisk et al found that, for every 25% increase in the proportion of human milk a preterm infant received, the odds of having NEC decreased by 38%.29 Therefore, the evidence strongly suggests that breast milk (maternal or donor) offers protection against NEC.
The optimum timing for initiation and advancement of enteral feeds in preterm infants remains an area where strong evidence is lacking, resulting in varying feeding practices among different neonatal units.61 Early initiation of enteral feeds in preterm infants with very small non-nutritive volumes (known as trophic feeding or minimal enteral nutrition) is thought to have several advantages over complete fasting as a result of “priming” the gastrointestinal tract and aiding in its maturation processes.62–64 Trophic feeds might achieve this by improving overall gut motility,62 secretion of certain digestive enzymes,63 and promoting colonization with commensal bacteria when maternal breast milk is used.64 Both animal and human studies have shown that starvation leads to mucosal atrophy,65 lack of stimulation of trophic hormones,66 increased intestinal translocation of bacteria, and sepsis.67 As a result, it is now common practice to commence enteral feeds at very small volumes, eg, 10–20 mL/kg/day at intervals of 2–6 hours. However, a Cochrane systematic review of all studies comparing trophic feeds with complete fasting in preterm infants concluded that there was no difference in terms of incidence of NEC, feed tolerance, or growth rates.68 Because of the lack of harm and the likely physiological benefits mentioned previously, it is routine practice to commence enteral feeds in very low birth weight infants as early as possible, preferably with maternal breast milk.
Once trophic feeds have been started, the timing of increasing enteral feeds is still unclear. A Cochrane systematic review compared the commencement of increasing enteral feeds (either within 4 days or later than 5–7 days),30 and found no differences in the incidence of NEC (relative risk [RR] 0.92, 95% CI 0.64–1.34) or all-cause mortality (RR 1.26, 95% CI 0.78–2.01) between these two groups. An additional concern is the rate of increase of enteral feeds in the most vulnerable preterm infants. A Cochrane review, which included nearly 600 infants, compared two feeding regimens (increasing feeds at 15–20 mL/kg/day or 30–35 mL/kg/day) and found no significant difference in the risk of NEC (RR 0.91, 95% CI 0.47–1.75) or mortality (RR 1.43, 95% CI 0.78–2.61).69 Currently, a large multicenter trial in the UK has just started recruiting patients to evaluate the effect of two speeds of daily increments of milk feeds (30 mL/kg/day versus 18 mL/kg/day) in very preterm and very low birth weight infants.70
There is evidence that use of standardized feeding regimens leads to decreased rates of NEC.71 A total of six observational studies were reviewed in a meta-analysis. These studies were conducted between 1978 and 2003, and feeding practices varied widely between the studies. The implementation of a standardized feeding protocol within a neonatal unit significantly decreased the incidence of NEC in all the studies (pooled risk ratio 0.13, 95% CI 0.03–0.5; or a reduction of NEC incidence by 87%), irrespective of the finer details of the protocol. This difference was independent of the use of trophic feeds or the use of exclusive breast milk. Whilst we await the results of the above UK trial, it would seem prudent that every neonatal unit should implement a standardized feeding regimen for babies at risk of NEC.
Given that maternal or donor breast milk often does not meet the nutrient requirements of preterm babies, supplementing breast milk with fortifier to provide additional protein, calcium, and phosphorus has been shown to improve weight gain, and linear and head growth.72,73 However, there are concerns that addition of fortifiers to human milk increases the risk of NEC. A Cochrane review evaluating the benefit of fortification of human breast milk showed no statistically significant increase in NEC in infants receiving fortified human milk (RR 1.33, 95% CI 0.7–2.5).74 Sullivan et al studied the effect of human milk-based fortifier compared with bovine milk-based fortifier on neonatal morbidity among preterm infants.75 The incidence of NEC was significantly lower in babies receiving human milk-based fortifier compared with those who received bovine milk-based fortifier (P=0.02), and the incidence of NEC requiring surgery was also significantly lower in the human milk-based fortifier group (P=0.007). Despite this, it is now common practice to fortify breast milk with cow’s milk-based fortifiers (because human milk-based fortifiers are not yet widely available in all countries) once preterm babies have established full enteral feeds.
The observation of NEC occurring within 36–72 hours after blood transfusion is increasingly common. In a meta-analysis of 11 retrospective case-control studies and one cohort study, Mohamed and Shah reported the association between blood transfusion and NEC.76 The total number of transfusion-associated NEC cases in the meta-analysis was 365. The OR of NEC being present after a recent blood transfusion was 2.01, indicating a significant association. However, the PINT (Premature Infants in Need of Transfusion) study, which compared low and high hemoglobin thresholds for blood transfusion in preterm infants, found no difference in the rates of NEC (8.5% in the low threshold arm versus 5.3% in the high threshold arm, P=0.2).77 There is some suggestion that withholding feeds during blood transfusion may decrease the risk of developing transfusion associated NEC;78 however, the evidence for this is not substantiated by prospective trials. The description of transfusion-associated NEC79 and/or transfusion-related acute gut injury80 are often used synonymously and have emerged only in the last few years, and because this is based mainly on evidence from retrospective studies, further prospective investigation is required to establish causation.
Prolonged use of initial empirical antibiotics in preterm infants has been shown to be associated with an increased incidence of NEC and late-onset sepsis.81,82 Alteration of the intestinal microbiota is hypothesized as the possible mechanism. Guillet et al studied the association between use of H2 blockers and incidence of NEC5 in a large cohort of very low birth weight infants (n=11,072). Antecedent H2 blocker use was associated with an increased incidence of NEC (P<0.0001). The potential effect of increasing gastric pH on the colonization of intestinal bacteria may explain this observation.
The vasoconstrictive effects of cyclooxygenase inhibitors like indomethacin and ibuprofen increase concerns about reducing gastrointestinal blood flow and therefore increasing the risk of NEC.83 Treatment of PDA with indomethacin is not associated with an increase in the incidence of NEC,57 although a Cochrane review comparing ibuprofen and indomethacin for the treatment of PDA concluded that ibuprofen use was associated with less NEC than indomethacin.58
Umbilical arterial catheters
There have been concerns that the position of umbilical arterial catheters may affect gastrointestinal blood flow by compromising the blood flow within the aorta.84 However, a Cochrane systematic review analyzed six trials (of which five were randomized controlled trials) evaluating the evidence supporting a high or low position.85 In a total of 1,569 infants included in the meta-analysis, there was no difference in the incidence of NEC between the two groups (risk ratio 1.34, 95% CI 0.79–2.25).
Given that the role of inflammation in the pathogenesis of NEC is increasingly recognized, it has been suggested that antenatal inflammatory processes like chorioamnionitis may increase the susceptibility of preterm infants to develop NEC.86 Numerous recent studies have investigated the association between chorioamnionitis and NEC.87–91 A recent systematic review by Been et al analyzed 33 studies examining the association between chorioamnionitis and NEC.92 Three distinct groups were identified, ie, clinical chorioamnionitis, histological chorioamnionitis, and histological chorioamnionitis with fetal involvement. Clinical chorioamnionitis and histological chorioamnionitis with fetal involvement were associated with an increased incidence of NEC (OR 1.24, 95% CI 1.01–1.52 and OR 3.29 (95% CI 1.87–5.78, respectively), whereas histological chorioamnionitis alone did not result in a statistically significant association (OR 1.39, 95% CI 0.95–2.04). The authors concluded that the meta-analysis provides evidence of an association between chorioamnionitis and NEC. However the authors also refer to the presence of potential confounders, such as the higher incidence of chorioamnionitis at lower gestation ages (which may partly explain the higher incidence of NEC in the chorioamnionitis group, with gestation acting as a major confounder) and a lower rate of breast feeding in the chorioamnionitis-affected mothers. Decreased intestinal mucosal thickness and increased mucosal permeability as a result of inflammatory mediators may explain this association.93
Treatment of NEC follows a stepwise approach depending on disease severity. Initial medical management (conservative treatment) involves immediate cessation of feeds and aspiration of gastric contents, regular aspiration, gastric decompression via a nasogastric tube, and broad spectrum antibiotics. The antibiotics used usually depend on local policy (which may be dependent on the local flora), but should cover all potential pathogens including anaerobes. Anaerobic cover is particularly important if there is suspicion of perforation or in severe disease with systemic signs.12,14 Confirmation of the diagnosis of NEC is limited to abnormal radiographs and histopathology, both of which indicate established disease.
Up to 40% of cases of NEC require surgical intervention,1,12 but the decision of when to intervene surgically in NEC remains unclear. Recognized indications for surgery include: pneumoperitoneum due to intestinal perforation; evidence of necrotic bowel; palpable abdominal mass; development of intestinal stricture; and when there is no improvement or deterioration (including persistent hematological and biochemical derangements such as progressive thrombocytopenia and worsening metabolic acidosis) despite maximal conservative therapy.94,95 Increasing abdominal distension causing difficulty in ventilation may also prompt surgical intervention, including peritoneal drainage (see below). A scoring system comprising metabolic acidosis, hypotension, thrombocytopenia, hyponatremia, positive blood culture, neutropenia, and left shift of neutrophils has been suggested as an adjunct to the clinical and radiological parameters to aid in the timing of surgical intervention,96 but application of this system is not widely practiced.
Primary peritoneal drainage can be used as an alternative to laparotomy in unstable preterm infants with NEC. Various investigators have explored the benefits of primary peritoneal drainage over laparotomy. A recent Cochrane review on this topic concluded that there was no difference in mortality, hospital stay, or dependence on total parenteral nutrition.97 However, there is some suggestion that infants who undergo laparotomy instead of primary peritoneal drainage have a better neurodevelopmental outcome at 18 months of age.98 A multicenter trial in the US is currently recruiting patients to compare the effectiveness of laparotomy versus primary peritoneal drainage in NEC.99 Based on current evidence, the surgical management of NEC remains at the discretion of the local surgical team.
Mortality among infants affected by NEC varies with disease severity and therefore the need for surgery. Reported mortality ranges from 20% to 50% and the risk of death increases with decreasing birth weight and gestation.1 The rates of surgical intervention vary widely among studies from 20% to 60%, and the mortality rates among infants needing surgery for NEC can be as high as 50%.100 There is concern that the mortality rates among infants affected by NEC may be increasing. Rees et al101 analyzed the national population registries for births and deaths in England and Wales between 1999 and 2005. They reported that although both total infant mortality and mortality among extremely low birth weight infants (<1,000 g) decreased significantly during this period, mortality from NEC increased significantly (0.11/1,000 to 0.17/1,000; P<0.001). This apparent increase in mortality from NEC may be attributable to increasing early survival of extremely low birth weight infants, which increases the number of infants potentially susceptible to NEC.
Current research focus
As previously discussed, it is now well established that abnormal intestinal colonization in preterm infants is associated with an increased incidence of NEC.21,22 Probiotics can be defined as living microorganisms that provide health benefits other than nutrition. Probiotics exert their beneficial effect in various ways, such as improving epithelial function, increasing secretory immunoglobulin A, and attenuation of proinflammatory pathways.102 Numerous studies have evaluated the use of probiotics to supplement colonization of the preterm gut with commensal flora, and thereby reducing the incidence of NEC.103–107 However, there has been wide variation in the timing, dose, and formulation of probiotics used in the various trials. A Cochrane systematic review evaluating the use of probiotics in the prevention of NEC showed a statistically significant reduction in the incidence of NEC and mortality in the probiotics group (NEC RR 0.35, 95% CI 0.24–0.52 and mortality RR 0.40, 95% CI 0.27–0.60).108 Another recent meta-analysis has reported similar results (NEC RR 0.35, 95% CI 0.23–0.55, P<0.00001; mortality RR 0.42, 95% CI 0.29–0.62, P<0.00001).109 However, the safety and efficacy of use of probiotics have not been fully evaluated, making some clinicians reluctant to start routine supplementation.110 Currently in the UK, a multicenter trial has recruited over 1,300 babies to evaluate the effect of a single bacterium (Bifidobacterium breve) on reducing NEC.111 Based on the most recent evidence,112 some neonatal units have introduced probiotics into routine management of preterm infants.
Lactoferrin is a multifunctional protein found in breast milk and is known to have antimicrobial and anti-inflammatory actions in the human intestine, promoting growth and proliferation of intestinal epithelium and helping in iron absorption.113 Animal experiments have shown that lactoferrin when given along with the commensal bacterium Lactobacillus rhamnosus GG (LGG) reduced translocation of bacteria across the intestine.113 Manzoni et al114 have conducted the only reported randomized controlled trial investigating the efficacy of lactoferrin alone and lactoferrin + LGG in very low birth weight infants in preventing late-onset sepsis and NEC. The incidence of stage 2 and stage 3 NEC was significantly reduced in infants who received lactoferrin + LGG (0/151 infants, P=0.002) compared with infants who received lactoferrin alone (3/153 infants) or the control group (10/168 infants). The incidence of overall late-onset sepsis was also reduced in both the lactoferrin group versus controls and the lactoferrin + LGG group versus controls. Further evidence is awaited before use of lactoferrin becomes part of routine care. A large, UK-based, multicenter, randomized, placebo-controlled trial evaluating the effect of prophylactic lactoferrin on late-onset sepsis, NEC, and other important neonatal morbidities like retinopathy of prematurity and bronchopulmonary dysplasia in very preterm infants, is due to begin recruiting later this year.115
Researchers have long suspected that a genetic predisposition to NEC might exist, and are focusing on various biomarkers for both predicting infants who are most susceptible to NEC and early identification of NEC.116 Genetic markers, such as a specific mannose binding lectin genotype117 and variations in the toll-like receptor pathway genes,118 may offer a way of predicting preterm infants who are most susceptible to developing NEC. Various other nonspecific biomarkers, including the widely used C-reactive protein, procalcitonin, and some of the “early warning” biomarkers like IL-6 and neutrophil CD64, have been studied to aid in early detection of NEC, but most of these biomarkers are nonspecific and do not differentiate NEC from other infectious/inflammatory conditions.116,119
More recently researchers have attempted to identify gut-specific biomarkers such as fatty acid binding protein120 and fecal calprotectin121 to diagnose NEC early. It is proposed that identification of fatty acid binding protein in the urine of preterm infants during the first few days of life can help in predicting the occurrence of NEC. A research trial will soon be recruiting patients in the US to evaluate the effectiveness of urinary fatty acid binding protein monitoring in reducing the incidence of NEC.122 Fecal volatile organic compounds (VOCs) are another potential gut-specific biomarker. VOCs are produced due to interaction of bacteria with the intestinal contents. Research has shown that the pattern of VOCs in adult gut disorders such as ulcerative colitis and Clostridium difficile infection is recognizably different compared with healthy subjects.123 VOCs can also be measured in preterm infants.124 In a pilot study reported in 2009, 58 babies born before 36 weeks’ gestation were recruited.125 Daily fecal samples were collected and analyzed for VOCs. Six infants developed NEC. After matching the cases to controls according to gestational age and birth weight, there remained a noticeable difference in the pattern of VOCs among infants who developed NEC. These differences were noted up to 4 days before NEC was diagnosed. To explore this further, a large multicenter trial is currently recruiting babies to evaluate the usefulness of VOC detection in early identification of NEC before clinical suspicion arises.126
Therapeutic hypothermia for NEC
Therapeutic hypothermia is a well-established treatment for hypoxic-ischemic brain injury.127 The potential for treating NEC in a similar way is currently being explored. In a nonrandomized feasibility trial, Hall et al administered therapeutic hypothermia to 15 infants with advanced NEC and multiorgan dysfunction.128 Median gestation at birth of babies in this trial was 27 weeks, with a median admission weight of 1.1 kg. All infants received hypothermia for 48 hours. Five infants were cooled to 35.5°C, five were cooled to 34.5°C, and five were cooled to 33.5°C. The control group comprised ten infants with advanced NEC and multiorgan dysfunction. Hypothermia was maintained within the target range for 90% of the time. There was no increase in mortality, bleeding, infection, or need for inotropes in the cooled group. Based on this, the CoolNEC (Therapeutic Controlled Hypothermia in the Treatment of Neonates With Severe Necrotizing Enterocolitis) trial is currently recruiting patients with NEC to evaluate the benefit of therapeutic hypothermia in NEC.129
Having recognized the therapeutic role of stem cells in inflammatory bowel conditions like Crohn’s disease, their use in NEC has been explored in a well-established rat model of NEC.130 Amniotic fluid stem cells injected intraperitoneally resulted in improved survival, decreased the incidence of NEC, and improved the macroscopic appearance and function of the gastrointestinal tract. Use of stem cells in clinical neonatology may not be very close, but is one of the therapeutic options with huge potential, and needs further trials to establish its safety and efficacy.
NEC continues to cause significant morbidity and mortality in large numbers of very vulnerable preterm infants. With its multifactorial pathogenesis, disease prevention remains a challenge. Awareness of the risk factors associated with NEC is important. Early initiation of breast milk feeds and a standardized feeding regimen have been shown to reduce the incidence of NEC. Current research is focused on prevention, early diagnosis, and treatment of NEC.
The authors report no conflicts of interest in this work.
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