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ERNICA Evidence-Based Guideline on Surgical Aspects of Necrotizing Enterocolitis in Premature Neonates
Topic overview
European evidence-based clinical practice guideline for surgical management of necrotizing enterocolitis in preterm neonates, developed by ERNICA using GRADE methodology. Provides seven recommendations covering surgical indications, peritoneal drainage, operative techniques, extensive disease management, feeding protocols, and neurodevelopmental outcomes for this high-mortality condition affecting infants under 1,500g birthweight.
Key Takeaways
- NEC mortality is 25% overall, rising to 30% in infants <1,500g birthweight and 35% in those requiring surgery.
- ERNICA guideline provides 7 recommendations and 3 good practice statements on surgical indications, drainage, technique, and feeding.
- Evidence certainty is very low for most recommendations; expert consensus balanced benefits/harms for clinical decision-making.
- Guideline covers peritoneal drainage, management of extensive NEC, enteral feeding timing, and neurodevelopmental outcomes.
- Multidisciplinary European expert panel with patient representatives developed recommendations using GRADE methodology.
Keywords
Hashtags
Full guideline text
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Neonatology
Guidelines
Neonatology
DOI: 10.1159/000542540
Received: July 19, 2024
Accepted: October 29, 2024
Published online: November 19, 2024
European Reference Network for Inherited and
Congenital Anomalies Evidence-Based
Guideline on Surgical Aspects of Necrotizing
Enterocolitis in Premature Neonates
Jan Hulscher a Willemijn Irvine b, c Andrea Conforti d Antonio Di Cesare e
Martina Ichino e Rony Sfeir f Omid Madadi Sanjani g Joanna Strohm h
Maria Hukkinen i Laura Moschino j Lorenzo Norsa k Alena Kokešovál
Roel Bakx m Elisabeth Kooi n Sylvia Obermann-Borst o Elena Palleri p
Marijn Vermeulen q Marie Spruce r Udo Rolle s Marc Miserez t
Irene de Haro Jorge u Claudia Keyzer-Dekker b Francesco Fascetti Leon v
Iris den Uijl b Simon Eaton w Carmen Mesas Burgos x
aDivision of Pediatric Surgery, Department of Surgery, University Medical Center, Groningen, The Netherlands;
bDepartment of Pediatric Surgery, Erasmus Medical Center Sophia Children’s Hospital, Rotterdam, The Netherlands;
cDepartment of Evidence Based Medicine and Methodology, Qualicura HealthcareSupport Agency, Breda, The
Netherlands;dDepartment of Pediatric Surgery, IRCCS Ospedale Pediatrico Bambino Gesù, Rome, Italy;eDepartment of
Pediatric Surgery, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milan, Italy;fDepartment of Pediatric
Surgery, Centre Hospitalier Universitaire de Lille, Lille, France;gDepartment of Pediatric Surgery, Universitätsklinikum
Hamburg-Eppendorf, Hamburg, Germany;hDepartment of Pediatric Surgery, Universitätsklinikum Bonn, Bonn,
Germany;iSection of Pediatric Surgery, New Children’s Hospital, University of Helsinkiand Helsinki University Hospital,
Helsinki, Finland;jDepartment of Neonatology, Azienda Ospedaliera di Padova, Padua, Italy;kPediatric Department,
Vittore Buzzi Children’s Hospital University of Milan, Milan, Italy;lDepartment of Pediatric Surgery, University Hospital
Motol, Prague, Czech Republic;mDepartment of Pediatric Surgery, Amsterdam Academic Medical Center, Amsterdam,
The Netherlands;nDepartment of Neonatology, University Medical Center, Groningen, The Netherlands;oCare4Neo,
Neonatal Patient and Parent Advocacy Organization, Rotterdam, The Netherlands;pDepartment of Neonatology,
Karolinska University Hospital, Solna, Sweden;qDepartment of Neonatal and Pediatric Intensive Care, Erasmus Medical
Center Sophia Children’s Hospital, Rotterdam, The Netherlands;rNEC UK Representative, Ruislip, UK;sDepartment of
Pediatric Surgery, Universitätsklinikum Frankfurt, Frankfurt, Germany;tDepartment of Abdominal Surgery, University
Hospital Gasthuisberg, Leuven, Belgium;uDepartment of Pediatric Surgery, Sant Joan de Déu Barcelona Children’s
Hospital, Barcelona, Spain;vDepartment of Pediatric Surgery, Azienda Ospedaliera di Padova, Padua, Italy;wDepartment
of Developmental Biology and Cancer, UCL GOS Institute of Child Health, London, UK;xDepartment of Pediatric
Surgery, Karolinska University Hospital, Solna, Sweden
Keywords
Guideline · Necrotizing enterocolitis · Premature · Surgical
management · European Reference Network for Inherited
and Congenital Anomalies
Abstract
Necrotizing enterocolitis (NEC) is a severe intestinal condi-
tion primarily affecting preterm neonates. It has a high
mortality rate, particularly in infants with a birthweight of
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© 2024 The Author(s).
Published by S. Karger AG, Basel
Correspondence to:
Jan Hulscher, j.b.f.hulscher @ umcg.nl
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below 1,500 g or for those requiring surgical intervention.
The European Reference Network for Inherited and Con-
genital Anomalies (ERNICA) has developed a clinical practice
guideline to aid clinical decision-making pertaining to the
surgical treatment and management of NEC in preterm
neonates. This guideline was developed in accordance with
the Guidelines 2.0 checklist and GRADE methodology. A
multidisciplinary group of Europe ’s top experts collaborated
with patient representatives to develop this guideline. After
selecting critical points in care for which recommendations
are required, a systematic review of the literature and critical
appraisal of the evidence was performed. The Evidence to
Decision framework was used as a guide to structure the
consensus meetings and draft the recommendations. The
panel developed seven recommendations and three good
practice statements on the following topics: indications for
surgery, peritoneal drainage, surgical technique, manage-
ment of extensive NEC, enteral feeding, and neuro-
developmental outcomes in premature neonates with NEC.
The certainty of evidence was graded as (very) low for most
recommendations. However, the panel weighed up the
benefits and harms in light of all relevant arguments and
expert opinion. This guideline provides recommendations
on caring for premature neonates with NEC. These rec-
ommendations can assist clinicians in their care decisions
and can inform families on treatment options and relevant
considerations. This guideline will be revised every 5 years to
ensure it remains up to date.
© 2024 The Author(s).
Published by S. Karger AG, Basel
Introduction
Necrotizing enterocolitis (NEC) is a severe intestinal
disease, with a mortality rate of around 25% for all patients
with confirmed NEC. Mortality rates are rising for patients
with a birthweight of below 1,500 g (30%) and for patients
requiring surgical intervention (35%) [1]. NEC mainly affects
very preterm infants and/or infants with an extremely low
birthweight. The lower the gestational age, the higher the risk
of both NEC and complicated NEC (de fined as NEC re-
quiring surgery for survival). About fifteen percent of all
neonates born with a gestational age <26 weeks develop
NEC [1].
The European Reference Network for Inherited and
Congenital Anomalies (ERNICA) is the ERN for rare
inherited and congenital digestive disorders, including
NEC. To the best of our knowledge, there are no sys-
tematically developed guidelines to assist clinical decision-
making for NEC. We therefore aimed to develop such a
guideline for the treatment of (surgical) NEC, speci fically
for preterm neonates with a confirmed diagnosis (based on
clinical symptoms and/or pneumatosis intestinalis on
imaging, Modified Bell’sc l a s s ification stage IIa and higher
[2]) This guideline aims to answer important questions
concerning the surgical treatment, management, and
prognosis of preterm neonates with a NEC diagnosis. In
doing so, it aims to support healthcare providers and
parents to make informed decisions about the care for
these babies while simultaneously highlighting evidence
gaps and promoting a research agenda. We aim to set a
standard for treatment and care pathways, to bene fit
preterm neonates with NEC requiring surgery, both in the
short and long term. NEC in neonates born at term is not
considered part of this guideline, nor is NEC prevention or
diagnosis.
Materials and Methods
This guideline was developed in accordance with the
Guidelines 2.0 checklist [3] and GRADE methodology
[4, 5]. The supplementary materials include a full de-
scription of the methods (online suppl. S1; for all online
suppl. material, see https://doi.org/10.1159/000542540)
that were applied to develop this guideline, as well as all
Evidence to Decision (EtD) tables (online suppl. S2). The
guideline development group (GDG) met on several
occasions to (1) prioritize and select questions and
critical outcomes, (2) discuss results of the literature
review and (3) discuss recommendations according to
the EtD framework. Using a shortened Delphi procedure
the GDG selected 8 key questions and outcomes of
interest to be addressed in this guideline, shown in
Table 1. The EtD framework was used as a guide to
structure a 2 day consensus meeting, with most mem-
bers of the GDG present. During this meeting, con-
siderations, recommendations, and research needs
emerging from the literature analysis were discussed. To
prepare for this meeting, a summary of findings from all
modules was distributed among GDG members. This
was accompanied by an electronic survey seeking input
on all aspects of the EtD framework (Panel Voice). The
GDG selected a recommendation strength between Strong
or Conditional and indicated whether they supported (for)
or opposed (against) an intervention (shown in Table 2). In
accordance with the GRADE methodology, a low “cer-
tainty” of evidence did not preclude a strong recommen-
dation, and a weak recommendation was also possible with
a high certainty of evidence. The strength of the recom-
mendation was always determined by weighing up all
relevant arguments.
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Results
All recommendations are shown in Table 3. Full EtD tables
can be found in the online supplementary materials (S2).
Revisions of this guideline will be scheduled every 5 years
following the ERNICA protocol for revising guidelines. All
recommendations can be considered valid until revised.
Module 1 – Indications for Surgery
Recommendation
The panel suggests not to interpret the presence of
a fixed bowel loop (as a single parameter) as an
absolute indication for surgery, but instead
consider the presence of a fixed bowel loop in
combination with other factors.
Evidence summary: One retrospective study on the
prevalence of fixed bowel loop in 38 NEC patients, and its
relationship with the type of treatment (surgical versus
conservative) and death was retrieved [6]. No signi ficant
differences between patients with or without a fixed bowel
loop were found and the certainty of evidence was rated
‘very low’. No articles were found eligible to analyze clinical
deterioration while receiving intensive medical care or the
presence of portal air as an indication for surgery.
Considerations and Justi fication: Despite the absence of
RCTs, the available evidence suggests that both the inter-
v e n t i o na n dt h ec o m p a r i s o ny i e l ds i m i l a ro u t c o m e s .H o w -
ever, given that surgery is more invasive and carries a higher
risk of side effects, the panel concluded that the balance of
effects likely favors the comparison. Based on the current
evidence, it appears that the presence of a fixed bowel loop
alone may not be a definitive indication for surgery. Issuing a
firm recommendation for the intervention is likely not
feasible due to varying expert experiences and the lack of
clear evidence favoring one approach over the other.
Module 2 – Peritoneal Drainage or Laparotomy
Recommendations
The panel suggests to choose either initial laparotomy
or initial drainage to treat patients with suspected or
confirmed perforation due to NEC, based on
preferences and experiences of the treatment center.
The panel suggests peritoneal drainage as a bridge
treatment in cases where early operation is not
possible or available.
The panel recommends that families of the patients
should always be adequately informed that if
drainage is chosen as the primary option, many
patients will not improve or will deteriorate and
subsequently require a laparotomy.
Good practice statement
As many patients will require subsequent laparotomy
if primary drainage is chosen, a pediatric surgeon
should be consulted and the patient should always be
transferred to an expert center.
Evidence summary: Two RCTs comparing initial
drainage to initial laparotomy with a total of 212 patients
Table 1. Key questions addressed in this guideline
Module Key question
1 Should (1) fixed bowel loop, (2) worsening clinical condition despite maximal conservative treatment, or (3) portal air
be considered an indication for surgery in premature neonates with NEC?
2 Should the patients with surgical NEC be treated with a peritoneal drain instead of a laparotomy?
Should peritoneal drain placement be used as a bridge to laparotomy in patients with surgical NEC?
3 Should preterm neonates with NEC in need of bowel resection be treated with primary anastomosis or enterostomy?
4 What are the (un)favorable effects of laparotomy with resection of all necrotic bowel in neonates with a large part of
the small bowel affected and ultrashort bowel remaining?
5 In preterm neonates with con firmed NEC treated surgically, what are the (un)favorable effects of early feeding (≤7 days
after surgery) compared to late feeding ( ≥8 days after surgery)?
6 Is surgical NEC in very preterm infants a prognostic factor for worse neurodevelopment?
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Table 2. Types of recommendations and their wording
Type of recommendation Wording
Strong recommendations against the intervention The panel recommends against, not to/to refrain
from
Conditional/weak recommendation against the intervention The panel suggests against, not to/to refrain from
Conditional/weak recommendation for either the intervention or the
comparison
The panel suggests either ... or...
Conditional/weak recommendation for the intervention The panel suggests ...
Strong recommendation for the intervention The panel recommends ...
Table 3. Summary of recommendations
Module Recommendation Type Certainty of
evidence
1 The panel suggests not to interpret the presence of a fixed bowel loop as single
parameter as an indication for surgery but to consider the presence of a fixed bowel
loop in combination with other factors
Conditional Very low
2 The panel suggests to choose either initial laparotomy or initial drainage to treat
patients with suspected or con firmed perforation due to NEC based on preferences
and experiences of the treatment center
Conditional Low
The panel suggests peritoneal drainage as a bridge treatment in cases where direct
operation is not possible or available
Conditional Low
Good practice statement ––
The panel recommends that families of the patients should always be adequately
informed that if drainage is chosen as the primary option, many patients will not
improve or will deteriorate and subsequently require a laparotomy
Good practice statement ––
As many patients will require subsequent laparotomy if primary drainage is chosen, a
pediatric surgeon should be consulted and the patient should always be transferred to
an expert center
3 The panel suggests to consider a primary anastomosis if the baby is stable and the
remaining bowel is either unaffected or perfused well enough to attempt primary
anastomosis, especially in the setting of a threatening short bowel
Conditional Very low
4 Good practice statement ––
The decision to continue surgical treatment or to offer comfort care, is up to the
treating team to decide but should not be based on the length of the bowel alone. All
important factors need to be taken into account, also that there are many uncertainties
concerning the long-term outcome of these patients
5 The panel suggests to start enteral feeding within 7 days after surgery for NEC in
patients without active signs of ongoing disease or obstruction, with or without stoma
Conditional Very low
6 The panel recommends to include information on the neurodevelopmental prognosis
alongside other factors relevant to the patient when counseling on care decisions such
as surgery for NEC in preterm infants
Strong Low
Extreme low birthweight and/or (need for) surgical intervention seem to be factors
that further increase the risk for neurodevelopmental disability and impaired quality of
life. This should be considered when providing information on neurodevelopmental
prognosis
Strong Low
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were included [7, 8]. Laparotomy seemed to result in fewer
deaths compared to primary drainage, but results were not
statistically signi ficant. No signi ficant differences were
found in complications or neurodevelopment. Despite the
inclusion of two RCTs, the certainty of evidence for
mortality was rated as low as there were strong concerns
regarding selection bias and imprecision. The certainty of
evidence for the other outcomes was rated as moderate.
Considerations and Justification: Starting the treatment
strategy with a peritoneal drainage seems to be as effective as
the laparotomy when it comes to survival of the patient. A
third trial which was initially excluded because of the
population included (NEC as well as spontaneous intestinal
perforation patients) was considered but also did not show a
significant difference [9]. The panel recognized both as
viable options for patients with NEC. However, it was
recognized that many of the patients who received primary
drainage had a subsequent laparotomy and a secondary
laparotomy was significantly more frequent in the primary
drainage group compared to the primary laparotomy group
[7]. However, drainage is less invasive, may have the ad-
vantage of immediate decompression, and may prevent
exposure to general anesthesia in at least some of the pa-
tients. No studies that explored drainage as a bridging
treatment could be included. The aim of these studies was to
compare drainage and laparotomy as primary interven-
tions. However, since the mortality rates do not seem to
differ, even after secondary laparotomy, these conclusions
could support the idea of peritoneal drain placement as
bridge treatment. The panel emphasized that the downsides
of a drain (high possibility of needing a second intervention
due to further deterioration of the patient or a lack of
improvement) should always be considered and discussed
with the family. As the analyzed studies only included
patients based on pneumoperitoneum or pneumatosis in-
testinalis, we did not gain any insight into the role of
drainage versus laparotomy in patients with a surgical in-
dication due to deteriorating clinical or biochemical status.
Module 3 – Surgical Technique
Recommendation
The panel suggests considering a primary
anastomosis if the baby is stable and the
remaining bowel is either unaffected or perfused
well enough to attempt primary anastomosis,
especially in the case of a threatening short bowel.
Evidence summary : Four studies with a total of 239
patients have been evaluated to explore the effect of bowel
resection and enterostomy versus resection and primary
anastomosis on mortality, NEC-related complications,
NEC recurrence, and neurodevelopmental outcomes
[10–13]. There were no signi ficant differences in mor-
tality or NEC recurrence, but intelligence at the age of
6–13 years was lower in children that were treated with
enterostomy. The panel could not draw a conclusion on
the effect of surgical techniques on the number of
complications as only two small retrospective studies
could be included, and their results were con flicting. The
certainty of evidence for all conclusions is very low,
mainly due to the retrospective design of the studies
included.
Considerations and Justi fication: Compared to pri-
mary anastomosis, enterostomy creation warrants a
second procedure for stoma closure. Undergoing only
one as opposed to two surgical procedures is bene ficial
in order to avoid possible (serious) adverse events, risks
related to anesthesia or prolonged hospital stay. The
choice of surgical method should occur during lapa-
rotomy and depends on the stability of the baby, bowel
viability, degree of contamination, and the extent of the
resection. In addition, the personal experience of the
operating surgeon may in fluence this decision. Primary
anastomosis may not be feasible for some patients, but
the panel concluded that if only one operation can
achieve similar or better long-term outcomes, this
probably has an advantage over two operations. Panel
members further discussed situations or factors that
could mean certain “subgroups ” of patients bene fit
more from the recommendation than others. Even
though we found no evidence to support this, experts
on the panel agreed that in the case of threatening short
bowel, considering primary anastomosis is highly
valuable (if feasible).
Module 4 – Extensive NEC
Good practice statement
The decision to continue surgical treatment or to
offer comfort care is up to the treating team to
decide, but should not be based on the length of the
bowel alone. All important factors need to be taken
into account, as well as the uncertainty concerning
the long-term outcomes for these patients.
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Evidence summary: No evidence could be included for
analysis.
Considerations and Justi fication:T h ep a n e lf o u n di t
difficult to de fine a grade of bowel affection severity in-
dicating a withdrawal of care. Ethical considerations arise
for disease progressions ranging from NEC-totalis or near-
totalis to <30 cm of remaining bowel [14 –16]. It remains
undetermined if there is also an association between the
length of the necrotic bowel and (neurodevelopmental)
outcome if the patient survives surgery. Evidence that
even <30 cm of the remaining small intestine may allow for
parenteral nutrition weaning is increasing, and some
authors suggest post-NEC patients have a greater weaning
potential than those with short bowel syndrome arising
from other causes [17]. Therefore, the panel agrees that the
bowel length cannot solely be used to make a decision on
whether to continue treatment.
Module 5 – Enteral Feeding
Recommendation
The panel suggests to start enteral feeding within
7 days after surgery for NEC in patients without
active signs of ongoing disease or obstruction, with
or without a stoma.
Evidence summary: Two studies with a total of 187
patients with surgical NEC were analyzed [18, 19]. There
are no differences in regard to mortality, NEC recurrence,
or strictures between groups that had an early re-
introduction and later reintroduction of enteral feeding.
Despite a very low certainty of evidence, we found indi-
cations that patients with surgical NEC that have an early
reintroduction of feeding are less likely to need parenteral
nutrition at 28 days and have shorter hospital stays.
Considerations and Justi fication: The possible bene fits
of early reintroduction of feeding after medical surgery
for NEC may be large, despite low evidence quality. Panel
members agree that adequate nutrition supports normal
brain development. Additionally, they also recognize that
earlier enteral feeding is possibly bene ficial for the de-
velopment of the bowel (even if via nasogastric tube) and
may prevent oral aversion. No undesirable effects of early
feeding were detected in the evaluation of evidence;
however, long-term effects were not considered in these
studies. The decrease length of hospital stay for the early
feeding groups could lead to large cost savings for hos-
pitals. If earlier feeding does not lead to any disadvantage,
a recommendation in favor of early feeding for medical
NEC could make it accessible for more patients, thereby
increasing equity.
Module 6 – Neurodevelopmental Outcomes
Recommendations
Extreme low birthweight and/or the (need for)
surgical intervention seem to be factors that
further increase the risk for neurodevelopmental
disability and impaired quality of life. This should
be considered when providing information on
neurodevelopmental prognosis.
The panel recommends to include information on
the neurodevelopmental prognosis alongside other
factors relevant to the patient when counseling on
care decisions such as surgery for NEC in preterm
infants.
Good practice statement
The panel recommends to closely follow-up these
patients with regard to their neurodevelopment.
Evidence summary: The panel analyzed six studies
reporting on neurodevelopment after surgery for NEC
[20–24] and performed a subgroup analysis for neonates
with a birthweight ≤750 g [25, 26]. Where possible,
surgical NEC patients were compared to peers with
medical NEC and premature neonates without NEC.
Compared to peers without NEC, surgical NEC patients
seem to have lower scores on mental development and
psychomotor development tests at 18 –24 months of age
and at cognitive tests at school age. It is unclear if patients
with surgical NEC have impaired mental and psycho-
motor development compared to peers with medical NEC
as the results of studies in the analysis were con flicting. It
is likely that neonates with a birthweight of ≤750 g who
survived surgery for NEC are at higher risk for any severe
or moderate neurodevelopmental disability, severe
mental developmental delay, and severe psychomotor
delay at 18 –24 months old compared to peers with
medical NEC and peers without a history of NEC.
Considerations and Justi fication: For the analysis
without weight as a cut-off, the overall certainty of evi-
dence is low. Evidence levels were rated as low because of
the inconsistency and lack of correction for important
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confounders, such as intra-ventricular hemorrhages
during NICU stay. The body of evidence for the subgroup
of neonates with a birthweight of ≤750 g was low due to
concerns regarding the correction for confounders; many
but not all important confounders were included in the
corrected analysis. Despite the limitations in regard to the
quality of this evidence, panel members believe that this
information on neurodevelopmental prognosis should be
part of providing complete information to families and
should not be left out. The importance families and
physicians attach to neurodevelopmental outcomes will
likely be different for different people in different
countries. This may be strongly in fluenced by personal,
cultural, social, and religious factors. Therefore, the panel
does not provide a recommendation on care decisions
based on this prognostic factor but wants to emphasize
the importance of taking this prognostic factor into
consideration during counseling.
Discussion
This guideline aimed to provide answers to seven
prominent clinical questions and form recommendations
to optimize the care for neonates with NEC. Seven rec-
ommendations and three good practice statements were
developed. These recommendations can assist clinicians
in their care decisions and can inform families on the
treatment options and relevant considerations.
As in other rare diseases, the available evidence on
NEC is scarce and of poor quality. Almost all of the
included studies have major methodological limitations.
Some of these may be induced by the context of the
disease, others by poor methodological design. As a
consequence, the average certainty of evidence of the
included studies is “low” to “very low. ” This leaves the
panel with very little certainty over the conclusion and
with minimal evidence-based input for recommenda-
tions. In five of our six modules, the evidence quality was
considered too low for the panel to be con fident enough
to make strong recommendations. This is recognized as a
limitation for the applicability of evidence-based guide-
line development methods in rare diseases.
Besides the aforementioned limitations, there are also
considerable strengths of this guideline, particularly
falling within the AGREE II domains “rigor of devel-
opment” and “stakeholder involvement. ” Despite little
available and low-quality evidence for most questions,
the EtD framework was applied and offered structure to
the discussion. The combination of digital surveys and
live discussion facilitated a critical assessment of the
available evidence and its possible implications for
clinical practice. As the digital surveys prior to the
consensus meeting enabled all panel members to
comment on the different aspects of the EtD, even those
who could not be present at the meeting. A large group
of Europe ’s top experts was closely involved in all steps
of the process and was composed of pediatric surgeons,
neonatologists, gastroenterologists, and patient/family
representatives. A draft version of this guideline was
circulated within ERNICA for peer review and key
experts beyond Europe were invited to participate in this
review as well. Altogether, this led to a set of balanced
recommendations which were validated by a large,
varied group of experts.
Despite a full systematic review of the literature and a
rigorous methodological approach to development, sev-
eral questions remain unanswered. To allow for con-
tinuous quality improvement in the care of premature
neonates with NEC, the panel identi fied research pri-
orities. Among other things, these research priorities
include reaching a formal consensus on the de finition of
clinical deterioration (despite maximum conservative
treatment) and the establishment of a European feeding
protocol for NEC patients. Supplement 3 contains an
overview of all identi fied knowledge gaps and research
priorities. To allow for continuous quality improvement
of NEC care, ERNICA will add NEC to the European
Pediatric Surgery Audit (EPSA).
Conclusion
This guideline provides recommendations on indica-
tions for surgery, peritoneal drainage, surgical techniques,
extensive NEC, enteral feeding and neurodevelopment in
premature neonates with NEC. These recommendations
can assist clinicians in their care decisions and can inform
families on treatment options and relevant consider-
ations. This guideline will be revised every 5 years to
ensure it remains up to date.
Acknowledgments
The authors want to acknowledge the Health Technology
Assessment (HTA) Unit at the Canary Islands (SESCS) for their
assistance with the systematic review and Neena Modi (Professor
in Neonatal Medicine, Imperial College London, UK), David
Hackam (Pediatric Surgeon, Johns Hopkins Children ’s Center,
Baltimore, MD, USA), Ruth Del Río Florentino (Neonatologist,
Hospital S Joan de Déu, Barcelona, Spain), Jordi Prat Ortells
(Pediatric Surgeon, Hospital S Joan de Déu, Barcelona, Spain),
Giovanna Verlato (Neonatologist, Hospital of Padova, Padova,
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Italy), and Michal Rygl (Professor of Pediatric surgery, Motol
University Hospital, Prague, Czech Republic) for proofreading the
draft manuscript during the peer review phase. Last, the authors
want to thank Olivia Spivack for her linguistic advice and im-
provements to this manuscript.
Conflict of Interest Statement
The authors have no con flicts of interest to declare.
Funding Sources
ERNICA has received funding of the European Committee for
this work. The HTA team from SESCS worked on this project as
part of the ERN Guidelines Project (SANTE/2018/B3/030). These
funders had no role in the design, data collection, data analysis,
and reporting of this guideline.
Author Contributions
Jan Hulscher, Carmen Mesas Burgos, and Willemijn Irvine
planned and guided the guideline development process and took
the lead in writing this executive summary. Iris den Uijl provided
logistic and organizational support before, during, and after
meetings of the guideline development group. The HTA team
from SECS performed the systematic review. Willemijn Irvine
summarized and critically appraised the literature and drafted
the EtD tables. Andrea Conforti, Antonio Di Cesare, Martina
I c h i n o ,R o n yS f e i r ,O m i dM a d a d i - S a n j a n i ,J o a n n aS t r o h m ,M a r i a
Hukkinen, Laura Moschino, Lorenzo Norsa, Alena Kokesova,
Roel Bakx, Elisabeth Kooi, Sylvia Obermann, Elena Palleri,
Marijn Vermeulen, Marie Spruce, Udo Rolle, Marc Miserez,
Irene De Haro, Claudia Keyzer-Dekker, Francesco Fascetti, and
Simon Eaton contributed to the interpretation of the results, the
forming of recommendations, and writing of the full version of
this guideline. All authors provided critical feedback to the
manuscript.
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Surgical NEC Guidelines Neonatology
DOI: 10.1159/000542540
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How to cite: GlobalCastMD. ERNICA Evidence-Based Guideline on Surgical Aspects of Necrotizing Enterocolitis in Premature Neonates. GlobalCastMD Medical Library. https://library.globalcastmd.com/guideline/9965
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