Global incidence of Necrotizing Enterocolitis: a systematic review and Meta-analysis

Abstract

Background

Necrotizing Enterocolitis (NEC) is a major cause of morbidity and mortality in the Neonatal Intensive Care Unit (NICU), yet the global incidence of NEC has not been systematically evaluated. We conducted a systematic review and meta-analysis of cohort studies reporting the incidence of NEC in infants with Very Low Birth Weight (VLBW).

Methods

The databases searched included PubMed, MEDLINE, the Cochrane Library, EMBASE and grey literature. Eligible studies were cohort or population-based studies of newborns including registry data reporting incidence of NEC. Incidence were pooled using Random Effect Models (REM), in the presence of substantial heterogeneity. Additional, bias adjusted Quality Effect Models (QEM) were used to get sensitivity estimates. Subgroup analysis and meta-regression were used to explore the sources of heterogeneity. Funnel plots as appropriate for ratio measures were used to assess publication bias.

Results

A systematic and comprehensive search of databases identified 27 cohort studies reporting the incidence of NEC. The number of neonate included in these studies was 574,692. Of this 39,965 developed NEC. There were substantial heterogeneity between studies (I2 = 100%). The pooled estimate of NEC based on REM was 7.0% (95% CI: 6.0–8.0%). QEM based estimate (6.0%; 95% CI: 4.0–9.0%) were also similar. Funnel plots showed no evidence of publication bias. Although, NEC estimates are similar across various regions, some variation between high and low income countries were noted. Meta regression findings showed a statistically significant increase of NEC over time, quantified by the publication year.

Conclusion

Seven out of 100 of all VLBW infants in NICU are likely to develop NEC. However, there were considerable heterogeneity between studies. High quality studies assessing incidence of NEC along with associated risk factors are warranted.

Keywords: Necrotizing Enterocolitis, Incidence, Systematic review, Meta-analysis

Background

Last three decades have witnessed great improvements in the neonatal intensive care, in particular, with the introduction of surfactant therapy and the subsequent improvement in the care of respiratory distress syndrome (RDS) that reduced the mortality among preterm newborns [1]. With better survival of premature babies, Necrotizing Enterocolitis (NEC) became more common and its burden became more prominent [2].

Multiple population-based studies, some based on large cohort studies, have reported the incidence of NEC to vary from 2 to 13% in preterm and Very Low Birth Weight (VLBW) infants [2–6]. The variation in the incidence were attributed to differences in the risk factor profiles as well as differing population at risk, detection rate and inclusion and exclusion criteria. There is no pooled estimate of the incidence of NEC worldwide. Furthermore, there is no incidence data from some regions such as North Africa, the Middle East or the Arab Gulf region, apart from a single study from the UAE [7].

With the continuing improvement in survival of preterm newborns, the modifiable risk factors of NEC need to be studies and made use of in developing appropriate interventions to reduce the incidence and impact of NEC. In this context, clinicians and researchers have attempted to identify the factors associated with risk and prognosis of NEC. It was reported as early as the 1980’s, that there exist an association between rapid advancement of feeding and the onset of NEC [8]. Subsequent reports showed preterm birth [9, 10], small birth weight [9–11] and race [11] were also to be important risk factors. Contemporary reports confirm these initial reports and expand the list to include a few more. More recent studies have shown that preterm birth [3, 12]. low birth weight [2, 12], rapid advancement of feeding, race and ethnicity, use of glucocorticosteriods [2], maternal infection [13], indomethacin therapy [14], congenital pneumonia [14], meconium aspiration [15], asphyxia [15], blood transfusion [15] and hypotension within the first week of life [16] are also potential contributing factors.

This study aims to systematically review the incidence reported from different parts of the world to synthesize a global incidence of confirmed NEC in VLBW infants. The study also aims to explore the regional variability as well as other potential factors that can explain variability in the incidence.

Methods

The recommendations from the Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) served as the guide in collating and reporting this review [17].

Eligibility criteria

Eligible studies included cohort or population-based studies of newborns including registry data. Both prospective and retrospective studies were included. Studies reporting the number, frequency or incidence of confirmed NEC in preterm infants or VLBW infants along with appropriate denominator were included. Studies that reported data on subgroups of infants with specific exposures such as congenital heart disease, perinatal infections, preterm rupture of membrane, or sepsis were excluded when the incidence could not be extracted. Studies with unclear case definitions of NEC were also excluded. Randomized controlled trials had strict selection criteria therefore including them would have caused selection bias and reduced the external validity of our pooled estimate. Hence, experimental studies that were assessing the effect of an intervention on a selected group of neonates were excluded. Case series where there were no denominator data to compute the incidence were also excluded.

Incidence is used as opposed to prevalence because of the natural history of NEC and its short duration of disease. It is envisaged that findings form this study would provide clinically important baseline data as the starting point for studies that aim to reduce the incidence of NEC.

Population and outcome

The VLBW infants formed the population of this study and the outcome of was the incidence of NEC stage II or above according to Bells criteria.

Search data bases

The database search was started in September 2018 and last updated in December 2019. The databases searched were PUBMED, MEDLINE (Ovid), EMBASE, the Cochrane Library. Additional databases searched included: African Index Medicus Database, Latin America and Caribbean Center of Health Science International, Open Grey, IndMED, KoreaMED, Virtual Health Library, National Library of Australia and Social Care Online.. Further manual search included looking for relevant studies in the reference lists of the included papers.

Search strategy

The search strategy was developed by the authors to include a comprehensive database search using broader search terms such as: “Enterocolitis, Necrotizing”, “Epidemiology”, “Incidence”, “Cohort Studies”, and “population-Based studies”, “cohort studies”, “epidemiological data”, “prematurity”, “Very low birth weight”, “clinical study”, “cohort analysis”, and “‘human”. Additional MeSH (Medical Subject Heading) term based search complemented the above search. When appropriate using the above terms with a combination of ‘and’ and ‘or’ in accordance with search engine specifications were carried out. The search string used for PUBMED is given in Supplementary file S1 as an illustration.

Study selection

Two review authors (AA and NI) independently assessed the titles and abstracts of all citations retrieved by the search for relevance against the inclusion criteria. Then the full-text versions of studies considered potentially eligible were retrieved. The same two authors independently assessed the full papers for eligibility, with disagreements resolved through input of the third author. The duplicate records and those not eligible were eliminated and a PRISMA flow chart was created to depict the study selection process.

Data extraction

Data form the eligible studies were extracted and collated on to data tables. Name of the authors, year of publication, data on the time period covered by the study, location of the study, inclusion and exclusion criteria of the study (Table 1), the reported population at risk and whether it was VLBW infants or preterm infants, case definition, incidence or number on NEC cases and size of population at risk (Table 2) were collected. The data extraction process was performed by AA and checked by NI. Any discrepancies is resolved by discussion.

Risk of Bias assessment

All the included studies were assessed for internal and external validity using the criteria put forward by Hoy et al. that were specific for prevalence and incidence studies (Fig. 1). This tool was developed based on key domains they identified to be important in assessing the risk of bias in incidence and prevalence studies. The tool was subsequently validated and found to have good validity [30].

Fig. 1 The 10 criteria used to assess the risk of bias in each included studies (Figure not reproduced here; see the original article.)

Data synthesis

Pooling the incidence estimates was done after arcsine transformations of the data as it has been shown to stabilize variance and reduce bias [31]. Heterogeneity was assessed using the Cochrane Q test and Higgin’s I² value. Smaller p values and I² > 50% were indicative of significant heterogeneity [32, 33]. As Cochrane guidelines suggest use of Random Effect Models (REM) when significant heterogeneity is encountered [34] we employed REM models estimates to arrive at the main conclusion. Further, bias adjusted Quality Effect Models (QEM) [35] were used to obtain sensitivity estimates to check the robustness of the REM estimates. Quality scores obtained using Hoy’s criteria were used in fitting the QEM.

Forest plots were used to display the incidence of NEC with corresponding 95% confidence intervals. We used Hunter plots to assess the publication bias as Hunter et al. have shown the classical funnel plot to be in-appropriate for proportion studies such as prevalence or incidence [36].

A-priori planned meta-regression was performed to evaluate if the publication year has any impact on the variability of the incidence and as a possible cause of heterogeneity. This was also thought to be important to understand if the long term trend in incidence of NEC to see if they are on a rise or decline. Further subgroup analysis by region based on income category of the countries provided by World Bank and population at risk (VLBW or extremely premature) was also carried out [37]. This sub-group analysis was not an a-priori decision but an attempt to explain the variability in NEC due to substantial heterogeneity. Groups consisted of high income countries (HIC) and low middle-income countries (LMIC).

The meta analyses were carried out using MetaXL [31] and the subgroup analysis and meta regression were carried out using Comprehensive Meta-Analysis (CMA-V3) software [38].

Results

Study characteristics

The total number of publications identified for screening was 1694. The process of selection of eligible studies are depicted as a PRISMA flow chart (Fig. 2). A total of 27 studies were found to fulfill the eligibility criteria and included in the review (Table 1). The number of neonate included in these studies was 574,692. Of these, 39,965 neonates developed confirmed NEC (Table 2). The studies covered a broader geographical areas globally. Some regions had multiple studies other areas had none. A total of eight studies were reported from the United States covering a number of states including: California, Texas, Atlanta, Connecticut, and New York [3, 6, 9, 18, 19, 39–41]. Multiple studies were also reported from the Europe including Poland, Romania, Finland, Belgium, Sweden and Switzerland [12, 13, 23, 39, 42, 43]. Also, four studies were done in China, Korea, Singapore and Malaysia [14, 16, 44, 45]. Three studies from Australia [4, 21, 46], one from the Middle East [7] and one from India [24].

Fig. 2 Flow chart depicting the studies screened, selected and included based on PRISMA (Figure not reproduced here; see the original article.)

The publication year of the studies ranged from 1988 to 2019, but the majority were carried out after 2000. Some of the studies focused on evaluating a certain exposure [7, 9, 21, 43], however, the data presented in these papers were not limited to the exposure groups and data from the general population was extracted to compute the incidence (Table 2).

Qualitative review

Andersone et al. reviewed a cohort data from the California Office Statewide Health Planning And Development [OS HPD] [39]. Upon retrograde calculation of the number of NEC cases and dividing them by a total number of NICU preterm babies the incidence of NEC was 9.1%. Whilst, Patole et al. conducted a retrospective cohort study reviewing 1755 neonates who were less than 34 weeks of gestation [21]. The aim was to study the effect on the incidence of NEC. In the control group (prior to the initiation of probiotic), there were 835 babies. Among those 250 were preterm with gestational age less than 28 weeks. Stage II or above NEC was found in 16 cases (6% of preterm controls).

Stoll et al. [38] analyzed data on 9575 newborns with very low birthweight and extremely low gestational age. The incidence in this population was 11%. Llanos et al. [3] reported the incidence among VLBW infants therefore was 3.29%. They used a retrospectively conducted a population-based survey from six counties in New York State. Holeman et al. analyzed the hospital discharge data from the Kid’s Inpatient Database from the year 2000 [47]. Among those born with weight less than 1500 g, the number of cases was 2554 and the rate was 4342.8 per 100,000 live births annually with an incidence of 4.3%. Fanaroff et al. evaluated VLBW infants and compared three periods of time: 1987–1988, 1993–1994, and 1999–2000 [20]. The analysis aimed to compare the outcome across the time periods. They showed that the incidence of NEC did not change over time.

Bajwa et al. reviewed the data from the Swiss neonatal network that conatins comprehensive population-based data of all infants in Switzerland [23]. The analysis included 368,055 infants born between 2000 and 2004, Ahle et al. collected data from the Swedish National Board of Health and Welfare, the National Patient Register, the Swedish Medical Birth Register and The National Cause of Death Register between 1987 and 2009 [12]. The incidence of NEC in less than 750 g, 750–999 g, 1000–1499 g and 1500–2499 g were 5.31, 4.16, 1.52, and 0.007%, respectively.

Verstrate et al. based on a retrospective cohort of 5134 neonatal intensive care unit admissions from a single hospital Belgium found 973 cases were born with a very low birthweight of less than 1500 g [42]. The incidence of NEC with stage II or above, in this subgroup was 16.23%. Härkin et al. reviewed the data from the national Registry of preterm infants born between 2005 and 2013 in Finland [43]. The incidence of NEC among preterm babies was therefore 16.58%. Wójkowska-Mach et al. reviewed the Polish Neonatal Surveillance Network for all VLBW infants recorded in the national registry. They used clinical criteria for the definition of NEC and 79 of 910 babies developed NEC [13].

Suciu et al. reviewed data from three tertiary centers in Romania. The study included 480 preterm babies born before 28 weeks of gestation [22]. The incidence was estimated to be 16.6%. The Bell’s criteria were used to define cauterizing enterocolitis as stage II and above in this study. Agarwal et al. collected data from the single largest neonatal center in Singapore with a vitality threshold defined at 25 weeks of gestation [45]. The database included all neonates who are with VLBW and gestational age less than 29 weeks. Bell’s classification was used to define NEC. 50 babies among 835 developed NEC.

Qian et al. reported data extracted retrospectively from 95 major referral centers and hospitals in china covering a large area of 29 provinces [44]. VLBW infants were specified and the incidence of NEC according to Bell’s criteria was presented in 2011. The data included 46,686 infants of whom, 8727 were born with VLBW. The incidence of confirmed NEC in VLBW infants was 6.5 among a cohort of 8727 infants.

Youn et al. reported a large cohort from South Korea. Among a total of 2326 infant with VLBW, 145 (6.8%) were diagnosed with confirmed NEC stage II of above [16]. Boo et al. collected data retrospectively from 31 neonatal intensive care units around Malaysia on NEC defined by Bell’s criteria among VLBW infants. Among the 3601 babies included, 222 developed NEC. Of these 197 had NEC II and 25 were NEC III or above according to Bell’s staging criteria. The incidence was 6.2% [14]. Luig et al. reported data on all infants born between 24 to 28 weeks of gestation in New South Wales and England, over three different time periods: 1986–1987, 1992–1993, and 1998–1999 [4]. The population included 1655 cases from the three groups divided to 360, 622, and 673 cases in time periods 1986–1987, 1992–1993, and 1998–1999 respectively. Over the entire population the incidence was 7.67%.

Wong et al. conducted a retrospective cohort study reviewing 2549 neonates from 10 neonatal intensive care units serving New South Wales in Australia [46]. This study population accounted for all preterm infants in the region of Australia between 1998 and 2004. The conducted the analysis complaining those exposed to steroids and those who were not. The incidence of NEC was 7.8% as 199 cases developed necrotizing enterocolitis among 2549 preterm babies born before 29 weeks of gestation.

Narang et al. 1993, collected 2200 admissions to the NICU during the period January 1986to September 1990 [24]. Among them 33 developed NEC (Bell’s stage ≥2). The incidence was 1.5%. Chedid et al. reviewed 173 newborns from 1 Tertiary Referral Center in UAE, Al Ain. All the cohort were born with weight less than 1500 g [very low birthweight infants] [7]. NEC was diagnosed clinically. Among the study population, 10 babies developed confirmed NEC. The incidence of NEC was 5.8%.

Lodha et al. 2019, compared neonatal outcomes after deferred cord clamping and immediate cord clamping in extremely low-gestational-age neonates from tertiary neonatal intensive care units participating in theestimated incidence based on Canadian Neonatal Network in 2019 was 9% (43)9%.

Boghossaan et al. 2018, examined infants of gestational ages 22 to 29 weeks born between January 2006 and December 2016 at a Vermont Oxford Network center in the United States were. NEC developed in 18,129 among the 194,736 infants. The incidence of NEC was 9% [26]. Persson et al. 2018, conducted a retrospective cohort study at 7 national networks in high-income countries that are part of the International Neonatal Network for Evaluating Outcomes in Neonates and used prospectively collected data on 76,360 very preterm, singleton infants. 2077 infants developed NEC and the incidence was 3% [27].

Suzuki et al. 2018, retrospectively examined 8245 extremely preterm infants born between 2008 and 2012 using Neonatal Research Network database in Japan. They estimated incidence to be 4% [28]. Boghossian et al. 2018, collected 138,869 large for gestational age infant’s data from 852 US centers participating in the Vermont Oxford Network. The incidence of NEC was 7% (10,376 new cases) [29]. Beltempo et al. 2018, collected data about extremely preterm infants born from 22 to 28 weeks’ gestational age Canadian Neonatal Network. Study population was 9230 among them 778 developed NEC. The incidence of NEC was 8% [48].

Assessment of risk of Bias

The quality assessment of 27 individual studies carried out as per Hoy et al. [30] criteria are summarized graphically presented in Fig. 3. Studies performed very highly on components like use of consistent mode of data collection from all infants as well as sufficient follow up time required for the desired outcome to occur. However, only about 50% of the studies had a random selection of samples. Overall, most studies scored high and 17 out of 27 studies had a lower risk of bias based on a cut of 8/10 or more as suggested by the Hoy’s criteria.

Fig. 3 Risk of bias plot that shows the methodological quality assessment of the 27 studies included (Figure not reproduced here; see the original article.)

Quantitative analysis of incidence

There were significant heterogeneity between studies, as indicated by I² value of 100% and the Cochrane Q- statistics (value =7473; P < 0.0001). As such we used REM as the main model to obtain our conclusions. REM estimate were 7.0% (95% CI: 6.0–8.0%) (Fig. 4), and additional quality adjusted QEM provided a sensitivity estimate of 6.0% (95% CI: 4.0–9.0%) (Fig. 5).

Fig. 4 Forrest plot obtained using Random Effect Model (Figure not reproduced here; see the original article.)

Fig. 5 Forrest plot obtained using Quality Effect Model (Figure not reproduced here; see the original article.)

Publication bias

Hunter’s modified funnel Plot [36] as appropriate for the incidence data used to evaluate the publication bias appear to not to show a serious concern (Fig. 6). Further, the Eggers regression confirmed that publication bias was not statistically significant (two tailed p-value = 0.80). The Kendall’s Tau test statistics was also not statistically indicating less likely that these studies encountered publication bias (two tailed p-value = 0.936).

Fig. 6 Hunter’s plot used to assess the publication bias (Figure not reproduced here; see the original article.)

Subgroup analysis

There was no significant regional variation between North America, Western Europe and Australia as well as Asia (Table 3). There appear to be some variation between HIC and LMIC countries, although these differences were not statistically significant. No significant variation between VLBW infants and extreme prematurity was found.

Meta-regression

There was a statistically significant increase in the log event rate over time, quantified by the publication year (Fig. 7).

Fig. 7 Meta regression of incidence over time (Figure not reproduced here; see the original article.)

Discussion

This study is perhaps the first attempt to provide a pooled estimate of the incidence of Necrotizing Enterocolitis in VLBW infants. Seven out of 100 of all VLBW infants in NICU are likely to develop NEC as per our synthesis. However, there were considerable heterogeneity in the estimates across studies. Such important variability may be driven by myriad of factors including the variation in the quality of health care systems.

Subgroup analysis based on geographic regions did not reveal any differences (i.e. South East Asia versus Europe, North America and Australia). However, when countries reporting the data on NEC were re-classified based on income levels using Word Bank classifications the incidence in high income counties (HIC) varied from the low and mid income countries (LMIC), although, these differences were not statistically significant. Such variation may be attributed to the fewer published studies from LMIC and potential under power to detect any differences. However, it is also possible that slightly lower incidence reported in LMIC may be due to higher gestational age cutoff point for resuscitation used in case of extreme prematurity. It is also possible that the sicker babies in LMIC may have had higher risk of mortality. As a result the population of neonates in LMIC may appear healthier and at lesser risk of developing NEC.

The increase in the incidence of NEC over time that our study found using meta-regression maybe attributed to multiple factors. Improvement in neonatal care and better survival of premature infants are possible causes as well as improvement in diagnosis and reporting. Increase in incidence of NEC over time can also be attributed to lack of wide scale prevention strategies. Ahle et al. demonstrated a j-shaped distribution of incidence over time in Sweden. While the incidence was 150 per 10,000 live births among VLBW infants in the late 80s, it increased to approximately 800 per 10,000 live births in VLBW, a multiple fold increase in later decade [12]. This increase may be related to variations in local health services. However, findings from the analysis of the NICHD data base from the United States reported [20] showed a different picture. They reviewed VLBW infants from three epochs: 1987–1988, 1993–1994, and 1999–2000. Their analysis compared the incidence across these three periods and they demonstrated that the incidence of NEC did not change over time. The data presented in our analysis represents a wider time period and a set of more diverse healthcare settings. Due to paucity of data available from lower income countries, the pooled estimate may have limited external validity and not fully generalizable to all global settings and populations.

Our findings, however, should be understood in the light of some limitations that this study encountered. Only 12 out 26 studies could be considered to be of higher quality and this may be linked to the substantially heterogeneity that we encountered. Although, we employed quality effect models to adjust for variation in study qualities, substantial heterogeneity noted in this study does pose a threat to evidence synthesis. The diagnosis of NEC using Bell’s criteria or similar definitions schemes is a day to day clinical challenge. To a certain extent, two clinicians may justifiably disagree on labeling a baby as confirmed NEC versus suspected NEC.

Conclusions

Seven out of 100 infants admitted to NICU and are VLBW are likely to develop NEC. However, there are substantial variability in incidence reported from different parts of the world, likely be due to differences in clinical and health settings in addition to methodological variations. Larger and higher quality studies on incidence of NEC and associated factors, particularly form low and middle income countries are warranted.

Supplementary information

Acknowledgements

Not applicable.

Abbreviations

Authors’ contributions

AA and LT designed the study and developed the study protocol. AA did the searchers, data extraction and quality assessment under the supervision of LT. NI assisted AA in database search, data extraction and quality assessment. AA carried out the data synthesis and analyses. AA written the first draft of the manuscript that was critically revised by LT. All authors approved the final draft of the manuscript.

Funding

None declared.

Availability of data and materials

Input data for the analyses are available from the corresponding author on request.

Ethics approval and consent to participate

Not applicable given this is a systematic review.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Footnotes

Supplementary information

Supplementary information accompanies this paper at 10.1186/s12887-020-02231-5.

References

Associated Data

Supplementary Materials

Data Availability Statement

Input data for the analyses are available from the corresponding author on request.

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