Abstract
Background
Adequate pain management for preterm born neonates suffering from the extremely painful disease necrotizing enterocolitis (NEC) is essential, since neonatal exposure to pain is related to negative short-term and long-term consequences. The aim of this study was to describe the current pain management and its effectiveness in NEC patients.
Methods
In this single-center, retrospective study, neonates (gestational age < 32 weeks and/or birth weight < 1500 g) with NEC Bell’s stage II or III were included. Information on pain (based on COMFORTneo and NRS scores) and analgesic therapy was collected and analyzed for the acute disease period.
Results
Of 79 patients included, 74 (94%) received intravenous analgesic therapy: most commonly morphine, fentanyl, and acetaminophen. The median COMFORTneo score was 11 (IQR 10–11), however, 49 patients had at least one COMFORTneo score ≥ 14 indicating pain. Nineteen patients had persistent high pain scores ≥ 14 with a median duration of 7.2 h (IQR 2.8–14.0).
Conclusions
This study showed that despite analgesic therapy, most NEC patients showed signs of pain, and in some, pain persisted for several hours. It suggests that current analgesic therapy frequently failed to prevent pain and existing pain was often insufficiently treated. This supports the urgent need for individualized pain management guidelines for NEC patients.
Impact
-
This study is unique in reporting on pain management in neonates suffering from necrotizing enterocolitis (NEC) during the full acute disease period.
-
Despite analgesic therapy, the majority of NEC patients experience pain, and in some patients, pain persists for several hours.
-
These findings highlight the need for improvement of neonatal pain management in NEC patients, including better pain monitoring and guidelines for individualized analgesic therapy.
-
Improved pain management guidelines may help to prevent short-term and long-term consequences of neonatal exposure to pain, as well as excessive exposure to opioids.
Similar content being viewed by others
Introduction
Necrotizing enterocolitis (NEC) is an extremely painful and life-threatening disease in preterm born neonates, which affects approximately 5–10% of very-low-birth-weight (VLBW, <1500 g) infants.1 It is characterized by a painful excessive inflammatory process in the intestine, which quickly spreads and can eventually have systemic effects with a negative impact on distant organs such as the brain.2 NEC is associated with high mortality, ranging from 15 to 50%, depending on birth weight and severity of NEC, and is particularly high in VLBW infants requiring surgical intervention.3 Among NEC survivors short-bowel syndrome and neurodevelopmental disabilities are common, resulting in significant long-term morbidity.3
Treatment of NEC primarily consists of medical treatment, including abdominal decompression, broad-spectrum intravenous antibiotics, no enteral feeding, and therefore total parenteral nutrition.2 Surgical intervention is required if the patient does not recover or in case of bowel perforation, and comprises resection of the affected intestinal parts, often with the placement of an enterostomy. An essential aspect of NEC treatment is adequate pain management, since it is a very painful disease due to the ongoing inflammation and ischemia in the intestine. In contrast to what clinicians once thought, preterm neonates can experience pain and it is important to adequately treat their pain in order to prevent discomfort and severe short-term metabolic and circulatory complications.4 Exposure to pain during the neonatal period not only threatens short-term comfort and recovery, but can also have negative long-term consequences by harming neurodevelopment.5 Rodent studies suggest that exposure to pain during the neonatal period affects brain development and induces long-term behavioral changes.6,7,8,9,10,11 In humans, neonatal exposure to pain has been associated with changes in brain morphology, impaired cognitive development, and altered pain sensitivity.12,13,14,15,16,17,18,19,20,21,22 These negative effects were already found in children who had been exposed to mild procedural pain during NICU admission. NEC, on the other hand, causes severe visceral pain, and is therefore expected to have even more negative long-term consequences.23 Additionally, NEC patients are often very preterm, which makes them specifically vulnerable to the negative effects of pain due to the immaturity of the developing nociceptive system. On top of that, seeing your vulnerable child experiencing pain is very stressful for parents.24
Opioids such as morphine and fentanyl are most commonly used for treating pain in neonates suffering from NEC.25 When treating neonates with opioids, caution is needed, as animal studies have shown that neonatal exposure to opioids could potentially harm neurodevelopment.8,9,10 However, these rodent studies found that exposure to opioids in the presence of pain has a neuroprotective effect.8,9,10 In humans, contradictory effects of neonatal opioid exposure on brain morphology and cognition have been suggested.5
Since both exposure to pain and to opioids during the neonatal period could have negative short-term and long-term effects, it is essential to adequately treat pain in NEC patients, while avoiding overtreatment and side effects. In other words: getting the balance right. Currently, it is unknown whether pain in neonates with NEC is treated adequately or whether these neonates are exposed to excessive pain or overtreatment with opioids. Importantly, it has been suggested that the current pain treatment of neonates suffering from NEC is not balanced yet. For instance, Van Ganzewinkel et al. found that NEC survivors had a decreased pain threshold and pain tolerance in adolescence, which may reflect the effects of neonatal exposure to excessive pain.26 To find out whether current pain management for NEC patients is well-balanced or if patients receive too little or too much analgesic therapy, this study aims to describe current pain management in preterm neonates suffering from NEC.
Methods
Study design and sample
In this single-center, retrospective study, all neonates diagnosed with NEC who were admitted to the level III-IV neonatal intensive care unit of the Erasmus MC—Sophia Children’s Hospital, Rotterdam, The Netherlands, between January 1, 2015, and December 31, 2020, were included. Only patients with NEC stage ≥ II, according to modified Bell’s criteria, were included.27 NEC diagnosis and staging according to these criteria was based on clinical symptoms, radiographic findings, surgical and pathology reports and decided on in expert consensus meetings. Infants with spontaneous intestinal perforation (SIP) were excluded. Surgical NEC was defined as NEC with a surgical indication within 7 days after NEC onset.
The Erasmus MC—Sophia Children’s Hospital is a teaching hospital with open-bay units and 24-h accessibility of the ward for parents, who participate in the care for their child and generally provide kangaroo care for a few hours daily if the child’s condition allows.
This study was embedded in the Risk NEC Study, an ongoing local cohort study on risk factors, treatment, and outcomes related to NEC in very preterm infants. The Risk NEC Study started in 2008 and includes patients with a birth weight < 1500 grams and/or a gestational age < 32 weeks who are admitted to the NICU of the Erasmus MC—Sophia Children’s Hospital. This study aims to assess risk factors and outcomes of NEC. The institutional medical ethical review board waived the need for specific approval for this study according to the Dutch law (MEC-2013-409), based on the observational nature of the study. No specific informed consent was deemed necessary for the use of the retrospective data in this study.
Data collection
Demographics were extracted from the existing database of the ongoing Risk NEC Study. Pain and pharmacological data were additionally retrieved from the electronic patient management systems HiX© (Chipsoft, Amsterdam, The Netherlands) and Picis© (Picis Clinical Solutions, Inc., Wakefield, Massachusetts) for each individual NEC disease period. The onset of the disease period was defined as the day of prescription and the start of antibiotic treatment as part of (suspected) NEC (e.g., Augmentin/Gentamicin). The last day of the NEC disease period was defined as the second day after the administration of intravenous analgesics had been discontinued or until death. If a patient had not received intravenous analgesic therapy, the NEC disease period ended on the second day after re-initiation of minimal enteral feeding (MEF).
The effectiveness of the analgesic therapy was determined using the neonates’ COMFORTneo, NRS pain, and NRS distress scores. These pain scores were collected for each patient for the total disease period. Patients were treated according to the local pain guideline (Supplement 2), which prescribes starting with acetaminophen and optionally combining this with morphine or fentanyl guided by the pain scores. Pharmacological data on dosage and duration of the analgesics acetaminophen, morphine and fentanyl, the sedative midazolam, the anesthetics ketamine and propofol, and the muscle relaxants rocuronium and cisatracurium were collected from the electronic patient management systems, which were used to calculate each patient’s daily cumulative doses during the disease period. The median daily cumulative dose and highest daily cumulative dose were calculated for each patient.
Measurement instruments
Nurses in our NICU have been trained to assess the COMFORTneo, NRS pain, and NRS distress score and enter these in the electronic patient management system. The COMFORTneo score (Supplement 1) ranges from 6 to 30 and has been validated for assessment of prolonged pain in preterm neonates.28 The COMFORTneo score has a good interrater reliability among trained nurses.28 A COMFORTneo score of 14 or higher indicates pain and a COMFORTneo score of 8 or lower indicates possible analgesic overtreatment. The NRS pain and NRS distress scores range from 0 to 10 (0 = no pain/distress, 10 = worst imaginable pain/distress) and represent a nurse’s subjective estimate of the patient’s pain and distress. An NRS pain score of 4 or higher indicates pain and an NRS distress score of 4 or higher indicates distress.
The local pain management protocol prescribes three measurements per day and additional measurements in case of suspected pain or oversedation and after a change of analgesic therapy (Supplement 2).29 A previous study in our center has shown that the compliance rate to these prescribed measurements is 60%.29
Statistical analyses
The pain scores and dosages of analgesics are presented as medians (interquartile ranges) or numbers (percentages). The number of patients with a COMFORTneo score ≤ 8 was calculated among patients who received intravenous analgesics. The median doses of analgesics were calculated among patients receiving those analgesics.
In order to evaluate the agreement between different pain scores used in our NICU, the positive and negative percent agreement between these scores were calculated. The positive percent agreement between the COMFORTneo score and the NRS pain and NRS distress score was calculated by dividing the number of times both scores indicated pain by the number of times the COMFORTneo score indicated pain. The negative percent agreement was calculated by dividing the number of times both scores indicated no pain by the number of times the COMFORTneo score indicated no pain.
To look further into different patterns of pain, a subgroup analysis was performed, based on three pain score patterns: persistent high scores, persistent low scores, and recurrent high scores. Persistent high scores were defined as at least two consecutive COMFORTneo scores ≥ 14 with at least 1 h between these scores. Recurrent high scores were defined as at least 3 COMFORTneo scores ≥ 14 with normal scores (i.e., 9–13) in between. Persistent low scores were defined as at least two consecutive COMFORTneo scores ≤ 8 with at least 1 h between these scores. The number of patients with persistent low scores was calculated among patients receiving analgesic therapy. The association between COMFORTneo score and analgesic therapy was visualized for the patient with the most illustrative pain patterns, selected based on an independent review of all patient plots by three neonatologists. Analyses were conducted using RStudio version 1.4.1106 (R Core Team, Vienna, Austria) and SPSS version 25.0 (IBM Corp., Armonk, New York).
Results
During the study period, 4074 neonates were primarily admitted to the NICU of the Erasmus MC—Sophia Children’s Hospital, of whom 1524 neonates were born at a gestational age < 32 weeks. Seventy-nine preterm neonates diagnosed with NEC were included, corresponding to a NEC rate of 5.2% among very preterm neonates. Table 1 shows the patients’ background and clinical characteristics. The median gestational age was 26 (IQR 25–28) weeks and the median postnatal age at diagnosis was 10 (IQR 7–20) days. Nineteen patients had NEC stage II and 60 patients had NEC stage III. Fifty-nine patients had surgical NEC (i.e., indication for surgery within a week), of whom 49 patients received surgery, since 10 surgical NEC patients were not stable enough to tolerate surgery and died. Two patients received surgery but were not classified as surgical NEC, since the indication for surgery was not within a week. Overall, 38 patients (48%) died during NICU admission, 33 deaths (42%) were directly related to NEC.
Assessment of pain scores
The duration of the NEC disease period ranged from 1 to 47 days (median 7, IQR 2–12) and the total number of pain score measurements per patient ranged from 0 to 195 (median 21, IQR 4–41). At least one COMFORTneo score, NRS pain score or NRS distress score was available for 76 patients (96%). In three patients, no pain score was available, likely because these patients died shortly after the diagnosis of NEC. Summary statistics for the pain scores are shown in Table 2. The overall median of the individual median COMFORTneo scores per patient was 11 (IQR 10–11) and the overall median of the highest COMFORTneo scores per patient was 15 (IQR 12–20). Forty-nine patients (62%) had at least one COMFORTneo score ≥ 14. Fifty patients (63%) had at least one COMFORTneo score ≤ 8 while treated with intravenous analgesics. In four cases (2.6%) of all COMFORTneo scores ≤ 8, the NRS pain or NRS distress score was ≥ 4, indicating that analgesic overtreatment was unlikely. Figure 1 shows the distribution of COMFORTneo scores during the first 21 NEC disease days and the number of patients in the cohort (i.e., still alive and suffering from NEC) per day. Figure 2 shows the distribution of COMFORTneo scores separately for medically and surgically treated patients. A cut-off of 21 days was chosen for both graphs, since only five patients had a longer disease duration than 21 days. The median of the individual median NRS pain and NRS distress scores was 0 (IQR 0–0), indicating that the median NRS pain and NRS distress scores in at least three-quarters of NEC patients equaled 0. The positive and negative percent agreement between the COMFORTneo score and NRS pain score were 31.8% and 98.6%, respectively, and the positive and negative percent agreement between the COMFORTneo score and NRS distress score were 32.9% and 99.6%, respectively.
Treatment with analgesics, sedatives, and anesthetics
The total cumulative doses and daily cumulative doses of the administered analgesics are shown in Table 3. Overall, 74 out of 79 patients (94%) with NEC were treated with analgesics. The five patients that did not receive analgesics were four stage II patients with a mild disease course and one stage III patient that died shortly after the diagnosis. The most commonly used analgesics were intravenous morphine, fentanyl, and acetaminophen. Sixty-six patients (84%) were treated with morphine and their median daily cumulative dose was 194 μg/kg (IQR 138–275) for a median of two (IQR 1–6) days. This corresponds to a median continuous dose of 8 μg/kg/h. Fentanyl was administered to 60 patients (76%) and their median daily cumulative dose was 22 μg/kg (IQR 10–44) for a median three (IQR 1–6) days. Forty-eight patients (61%) received acetaminophen and they received a median daily cumulative dose of 22 mg/kg (IQR 19–24) for a median seven (IQR 2–12) days. Midazolam was administered to 31 patients (39%) with a median daily cumulative dose of 0.24 mg/kg (IQR 0.08–0.74) for a median of one (IQR 1–3) day. No interruptions in analgesic therapy were observed during the disease period. Twenty-six patients (33%) were treated with propofol for endotracheal intubation. Methadone was administered to one patient (1%) in order to prevent withdrawal symptoms after prolonged treatment with morphine and fentanyl. Rocuronium and cisatracurium were administered pre-operatively to 25 (32%) and 20 patients (25%), respectively. Ketamine, phenobarbital, and clonidine were administered to one patient (1%) each.
Daily cumulative doses of morphine, fentanyl, acetaminophen, and midazolam and the percentage of patients receiving these analgosedatives are shown in Fig. 3.
Pain patterns
Persistent high COMFORTneo scores were found in 19 patients (24%), recurrent high scores in 24 patients (30%), and persistent low scores in 18 patients (23%) (Table 4). Some patients showed more than one pain pattern during their NEC episode, of whom six patients (8%) showed all three patterns. In 38 patients (48%), none of the described pain patterns were seen. In those with persistent high scores, the median duration of consecutive high pain scores was 7.2 h (IQR 2.8–14.0). In 62.5% of cases of persistent high scores, the analgesic therapy dosage was increased after the first high score. The median duration until an increase of dosage was 1.5 (IQR 0.5–3.6) h after the first high pain score. The median duration of consecutive low scores was 6.7 h (IQR 3.9–15.2). In 21.7% of cases of persistent low scores, the analgesic therapy dosage was decreased, which occurred a median duration of 3.2 (IQR 2.2–13.0) h after the first low score. The patients with recurrent high scores had a median number of six scores (IQR 4–15) above the pain threshold ≥ 14. In patients undergoing surgery, the three pain patterns (i.e., persistent high scores, persistent low scores, and recurrent high scores) were mostly seen during the entire post-operative period. In these patients, pain might be attributed to a prolonged post-operative course.
For the most illustrative patient with all pain patterns, pain scores and dosages of analgesics are shown over time (Fig. 4). Figure 4 shows that there was not only variation in pain level between patients, but also within a patient, with different pain patterns occurring over the disease course.
Discussion
This retrospective cohort study on pain management in NEC patients showed that even though most pain scores were acceptable, over half of NEC patients showed signs of pain during their disease course, as indicated by a COMFORTneo score ≥ 14. Although the variation between individuals was high, the overall distribution of COMFORTneo scores seemed constant over the disease period. In NEC patients, repeated intermittent moments of pain were more common than prolonged periods of pain. Various pain patterns were observed in spite of analgesic therapy in 94% of NEC patients. Therapy included morphine, fentanyl, and acetaminophen that were often combined. Surprisingly, treatment with acetaminophen was initiated less frequent and on average later than treatment with morphine, even though the local pain protocol prescribes starting with acetaminophen as the first step in the treatment of NEC. We speculate that the relatively infrequent use of acetaminophen is because physicians sometimes forgot the prescription of acetaminophen rather than deliberate non-use. Our data suggest that analgesic therapy was generally effective, but failed to prevent pain at times in the majority of patients. Furthermore, analysis of pain patterns has shown that persistent pain, with a median duration of 7 h, was prevalent in a quarter of NEC patients, indicating that pain was often not relieved promptly after a high pain score. The analgesic dosage was increased in 62.5% of cases of persistent high pain scores, after a median duration of 1.5 h. Thus, persistent pain often occurred despite a change of analgesic therapy.
The data additionally show that analgesic therapy might have been excessive at times, since 63% of NEC patients had at least one COMFORTneo score ≤ 8 and persistent low scores were common too. However, low COMFORTneo scores in NEC patients do not necessarily indicate overtreatment; they can also be the result of low consciousness and reduced reactivity related to the disease itself. Importantly, the level and pattern of pain varied significantly between patients, reflecting the need for individualized pain treatments. This heterogeneity complicates the development of an appropriate pain management protocol for NEC patients. More research is needed to predict which patients are at risk of having a highly painful disease course.
To our knowledge, this study is unique in longitudinally exploring pain and analgesic therapy during complete NEC disease episodes. Only two previous papers have been published on pain and analgesic therapy in NEC patients.25,30 The first study, by Gibbins et al., assessed procedural pain in 25 stage II NEC patients using the Premature Infant Pain Profile (PIPP).30 They found that NEC patients on average experienced 16 painful procedures per day. However, the pain scores were not presented in this paper and nurses’ compliance with the pain assessment was low. The other paper, from our own research group, studied pain scores and analgesic therapy of NEC patients around the surgical intervention and showed that the median COMFORTneo score was 10 pre-operatively and 11 post-operatively and that most patients had at least one high pain score.25 Our current study confirms the earlier findings that pain scores are overall acceptable, but that the majority of NEC patients at least once have a high pain score. The current study additionally shows that pain occurs during the entire disease course of NEC, not just in the first days or around surgery, and that pain often persists. Acknowledging that NEC is likely the most painful condition in neonatal care, it is disappointing that no further studies on pain management in NEC have been published. There is a gap in knowledge, and consequently lack of consensus, on adequate drugs, doses, and pain assessment for these vulnerable patients. Larger prospective multi-center studies are highly needed.
A strength of our study is the complete and comprehensive overview of pain and pain management during the entire NEC disease period, in a substantial cohort of preterm infants that suffer from the rare disease NEC. A limitation of our study is the retrospective design, with the number of pain measurements differing between patients. The number of measurements may not only be related to the disease duration, but also to the severity of pain, since pain scores tend to be measured more frequently after high scores. This reflects good clinical practice, but may have led to over-representation of the painful periods, and may therefore have biased our results. The retrospective design also limited our ability to evaluate effectiveness of specific therapeutic interventions. As systematic pre- and post-intervention pain scores were lacking, this study describes the overall effect of analgesic therapy on pain scores. Another limitation of our study is that the COMFORTneo score has been validated in preterm infants, but not specifically in NEC patients.28 Unfortunately, other scores for assessing prolonged pain, such as the EDIN scale (Échelle Douleur Inconfort Nouveau-Né) and the N-PASS scale (Neonatal Pain, Agitation and Sedation Scale), have not been validated specifically in NEC patients either.31,32 The validation studies of the COMFORTneo, EDIN, and N-PASS score all included too few NEC patients to assess validity in this group specifically.28,31,32 More research is needed to determine the validity of prolonged pain scores in NEC patients.
The COMFORTneo score might be less reliable in NEC patients, since NEC patients are often severely ill and therefore less reactive showing a blank face and few movements, which could result in a normal or low COMFORTneo score in presence of pain.31 Therefore, the NRS pain and NRS distress score were evaluated as well, which represent nurses’ subjective estimates of pain and distress. We found a poor positive percent agreement between the COMFORTneo score and the NRS pain and NRS distress score, with the COMFORTneo score indicating pain more frequently than the NRS scores. This contradicts the results from a previous validation study of the COMFORTneo score by Van Dijk et al., which found a good agreement between the COMFORTneo score and the NRS pain and NRS distress score.28 The low positive percent agreement compared with the negative percent agreement might reflect the difficulty of detecting pain in NEC patients. Perhaps a different approach is needed, which integrates pain scores and other clinical parameters such as heart rate. A bedside pain dashboard, as has been suggested by Vinks et al., might enable the integration of different sources of information regarding a patient’s real-time pain level and trends and might benefit the implementation of personalized pain management.33 Current pain scores being repeatedly outside the normal window, suggest that analgesic therapy was not adequately tailored to the individual patient’s needs. Furthermore, pain persisting for several hours suggests suboptimal adherence to the local pain guideline, which prescribes considering extra medication in case of a high pain score and reassessing the pain score within an hour. Pain measurements being missed could have resulted in delayed analgesic therapy and thereby higher pain scores.
The finding that most NEC patients experience pain is of clinical importance, since there is evidence that neonatal exposure to pain could have negative long-term consequences. For instance, rodent studies have shown that exposure to pain during the neonatal period causes neurodegeneration and has negative effects on adult behavior.7,8,9 In humans, exposure to procedural pain during NICU admission has been associated with impaired brain development and cognitive development and with altered pain sensitivity later in life.15,16,19 The long-term consequences of intense visceral pain, as is caused by NEC, are largely unknown. It has been shown that NEC survivors have a lower pain tolerance and pain threshold at adult age, which might be explained by their exposure to pain during the disease.26
Most NEC patients in our study were treated with opioids, which may also harm neurodevelopment. Studies in rodents have shown that neonatal exposure to morphine in absence of pain causes neuronal damage and learning impairment, while exposure to morphine in presence of pain does not.8,9,10 Thus, in rodents, both neonatal pain and neonatal opioid exposure solely could be harmful to the developing brain, but in the presence of pain, exposure to opioids could have a neuroprotective effect. Conflicting effects of neonatal opioid exposure have been found in humans regarding brain development and cognition.5 These conflicting results might reflect differences in the balance between exposure to pain and analgesics.
Thus, it is important to find the right balance in the pain management of NEC patients: on the one hand, pain should be prevented by adequate analgesic therapy and on the other hand, excessive exposure to opioids should be prevented. NEC patients’ pain level should be measured regularly, and physicians should pay attention to pain scores and adequately adapt the analgesic therapy based on the pain score.
Conclusion
Despite the use of acetaminophen and opioids, most NEC patients still experienced pain at some point. The analgesic therapy regimen often failed to relieve pain after a high pain score, resulting in pain persisting for hours in some patients. There is a lack of pain management guidelines for NEC patients. More research is needed to determine how the current analgesic therapy regimen can be adapted to improve the prevention and treatment of pain in NEC patients.
References
Thompson, A. M. & Bizzarro, M. J. Necrotizing enterocolitis in newborns: pathogenesis, prevention and management. Drugs 68, 1227–1238 (2008).
Neu, J. & Walker, W. A. Necrotizing enterocolitis. N. Engl. J. Med. 364, 255–264 (2011).
Jones, I. H. & Hall, N. J. Contemporary outcomes for infants with necrotizing enterocolitis-a systematic review. J. Pediatr. 220, 86–92 (2020).
Anand, K. J., Sippell, W. G. & Aynsley-Green, A. Randomised trial of fentanyl anaesthesia in preterm babies undergoing surgery: effects on the stress response. Lancet 1, 243–248 (1987).
van den Bosch, G. E., Dijk, M. V., Tibboel, D. & de Graaff, J. C. Long-term effects of early exposure to stress, pain, opioids and anaesthetics on pain sensitivity and neurocognition. Curr. Pharm. Des. 23, 5879–5886 (2017).
Anand, K. J., Coskun, V., Thrivikraman, K. V., Nemeroff, C. B. & Plotsky, P. M. Long-term behavioral effects of repetitive pain in neonatal rat pups. Physiol. Behav. 66, 627–637 (1999).
Bhutta, A. T. et al. Interactions of inflammatory pain and morphine in infant rats: long-term behavioral effects. Physiol. Behav. 73, 51–58 (2001).
Boasen, J. F., McPherson, R. J., Hays, S. L., Juul, S. E. & Gleason, C. A. Neonatal stress or morphine treatment alters adult mouse conditioned place preference. Neonatology 95, 230–239 (2009).
Dührsen, L. et al. Effects of repetitive exposure to pain and morphine treatment on the neonatal rat brain. Neonatology 103, 35–43 (2013).
McPherson, R. J. et al. A new model of neonatal stress which produces lasting neurobehavioral effects in adult rats. Neonatology 92, 33–41 (2007).
Ruda, M. A., Ling, Q. D., Hohmann, A. G., Peng, Y. B. & Tachibana, T. Altered nociceptive neuronal circuits after neonatal peripheral inflammation. Science 289, 628–631 (2000).
Brummelte, S. et al. Procedural pain and brain development in premature newborns. Ann. Neurol. 71, 385–396 (2012).
Doesburg, S. M. et al. Neonatal pain-related stress, functional cortical activity and visual-perceptual abilities in school-age children born at extremely low gestational age. Pain 154, 1946–1952 (2013).
Duerden, E. G. et al. Early procedural pain is associated with regionally-specific alterations in thalamic development in preterm neonates. J. Neurosci. 38, 878–886 (2018).
Grunau, R. E. et al. Neonatal Pain, parenting stress and interaction, in relation to cognitive and motor development at 8 and 18 months in preterm infants. Pain 143, 138–146 (2009).
Hermann, C., Hohmeister, J., Demirakça, S., Zohsel, K. & Flor, H. Long-term alteration of pain sensitivity in school-aged children with early pain experiences. Pain 125, 278–285 (2006).
Hohmeister, J. et al. Cerebral processing of pain in school-aged children with neonatal nociceptive input: an exploratory Fmri study. Pain 150, 257–267 (2010).
Ranger, M. et al. Neonatal pain-related stress predicts cortical thickness at age 7 years in children born very preterm. PLoS ONE 8, e76702 (2013).
Ranger, M. et al. Neonatal pain and infection relate to smaller cerebellum in very preterm children at school age. J. Pediatr. 167, 292–298 (2015).
Smith, G. C. et al. Neonatal intensive care unit stress is associated with brain development in preterm infants. Ann. Neurol. 70, 541–549 (2011).
Tortora, D. et al. Early pain exposure influences functional brain connectivity in very preterm neonates. Front. Neurosci. 13, 899 (2019).
Walker, S. M. et al. Long-term impact of neonatal intensive care and surgery on somatosensory perception in children born extremely preterm. Pain 141, 79–87 (2009).
Al-Chaer, E. D. & Hyman, P. E. Visceral pain in infancy. In Pain in Neonates and Infants (eds Anand, K. J., Stevens, B. J. & McGrath, P. J.) Ch. 14, 201–210 (Elsevier, 2007).
Franck, L. S., Cox, S., Allen, A. & Winter, I. Parental concern and distress about infant pain. Arch. Dis. Child Fetal Neonatal Ed. 89, F71–F75 (2004).
Meesters, N. J. et al. Infants operated on for necrotizing enterocolitis: towards evidence-based pain guidelines. Neonatology 110, 190–197 (2016).
van Ganzewinkel, C. et al. Pain threshold, tolerance and intensity in adolescents born very preterm or with low birth weight. Early Hum. Dev. 110, 31–38 (2017).
Kliegman, R. M. & Walsh, M. C. Neonatal necrotizing enterocolitis: pathogenesis, classification, and spectrum of illness. Curr. Probl. Pediatr. 17, 213–288 (1987).
van Dijk, M. et al. Taking up the challenge of measuring prolonged pain in (premature) neonates: the Comfortneo scale seems promising. Clin. J. Pain. 25, 607–616 (2009).
Aukes, D. I., Roofthooft, D. W. E., Simons, S. H. P., Tibboel, D. & van Dijk, M. Pain management in neonatal intensive care: evaluation of the compliance with guidelines. Clin. J. Pain. 31, 830–835 (2015).
Gibbins, S. et al. Pain assessment and pharmacologic management for infants with Nec: a retrospective chart audit. Neonatal Netw. 25, 339–345 (2006).
Debillon, T., Zupan, V., Ravault, N., Magny, J. F. & Dehan, M. Development and initial validation of the Edin scale, a new tool for assessing prolonged pain in preterm infants. Arch. Dis. Child Fetal Neonatal Ed. 85, F36–F41 (2001).
Hummel, P., Puchalski, M., Creech, S. D. & Weiss, M. G. Clinical reliability and validity of the n-pass: neonatal pain, agitation and sedation scale with prolonged pain. J. Perinatol. 28, 55–60 (2008).
Vinks, A. A. et al. Electronic health record-embedded decision support platform for morphine precision dosing in neonates. Clin. Pharm. Ther. 107, 186–194 (2020).
Acknowledgements
We would like to thank Robert Flint for providing pharmacological data and Annelies Ham for managing the data set of the Risk NEC Study.
Author information
Authors and Affiliations
Contributions
Substantial contributions to conception and design, acquisition of data, or analysis and interpretation of data: J.A.t.B., M.J.V., S.H.P.S., and G.E.v.d.B. Drafting the article: J.A.t.B. Revisiting the article critically for important intellectual content: M.J.V., S.H.P.S., and G.E.v.d.B. Final approval of the version to be published: J.A.t.B., M.J.V., S.H.P.S., and G.E.v.d.B.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Consent statement
Informed consent was not needed due to the retrospective nature of this study.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
ten Barge, J.A., Vermeulen, M.J., Simons, S.H.P. et al. Pain management for necrotizing enterocolitis: getting the balance right. Pediatr Res 92, 1423–1431 (2022). https://doi.org/10.1038/s41390-022-01968-2
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1038/s41390-022-01968-2
- Springer Nature America, Inc.
This article is cited by
-
Neonatal Necrotizing Enterocolitis: An Update on Pathophysiology, Treatment, and Prevention
Pediatric Drugs (2024)
-
Global cross-sectional survey on neonatal pharmacologic sedation and analgesia practices and pain assessment tools: impact of the sociodemographic index (SDI)
Pediatric Research (2024)
-
Current pain management practices for preterm infants with necrotizing enterocolitis: a European survey
Pediatric Research (2023)