To provide a process for prevention, assessment and management of pain in neonates admitted to the Neonatal Unit. The primary aim is to prevent the potentially damaging effects to the neonatal brain from both the pain experience and the sequelae of medications used to treat pain and agitation.
This guideline is applicable to all medical, nursing and midwifery staff caring for neonates and Infants in West of Scotland Neonatal Units.
Pain is defined as an unpleasant sensory and emotional experience associated with actual and potential tissue damage (IASP, 2003).
Neonates cannot verbally communicate their discomfort, however evidence suggests that neonates do experience pain but lack the adaptive mechanisms that modulate painful stimuli in older children. They express their vulnerability to pain and stress through specific behaviours and with physiological and biochemical responses to pain (Anand et al 2007).
Neonates are frequently exposed to acute, repetitive, and chronic pain within the NICU setting because of procedures, surgeries, and disease processes. Preterm neonates, especially those <30 weeks’ gestation, are exposed to 10-15 painful procedures per day at a time when pain is developmentally unexpected. Pain in the neonatal period is often unrecognised and undertreated. In infants born extremely preterm (gestational age ≤29 weeks) greater numbers of painful procedures have been associated with poor early neurodevelopment, altered brain development, delayed postnatal growth and higher cortical activation (Beatriz et al. 2015).
It has also been reported that in toddlers born very preterm (gestational age ≤32 weeks) bio-behavioral pain reactivity-recovery scores have been associated with negative affectivity temperament. Furthermore high numbers of painful experiences in the neonatal period have been associated with a poor quality of cognitive and motor development at 1 year of age and changes in cortical rhythmicity and cortical thickness in children at 7 years of age (Beatriz et al. 2015). Few longitudinal studies have examined the impact of neonatal pain in the long-term development of children born preterm, however neonatal pain-related stress is associated with alterations in both early and in later developmental outcomes (Beatriz et al. 2015).
It is therefore recommended that appropriate methods of assessing pain are applied, such as a validated pain assessment scale NPASS (Neonatal Pain Agitation and Sedation Scale) and appropriate interventions implemented.
There are a wide range of causes of pain to the neonate. It is important that each procedure/event is assessed and appropriate analgesia/support is given.
Summary of Pain Relieving Interventions for Neonatal Procedures
Procedure |
Interventions |
Comments |
|
|
Non-pharmacological |
Pharmacological |
|
NGT/OGT insertion |
Breast milk |
|
|
Urinary catheter placement |
Breast milk |
|
|
Tape removal |
Breast milk |
|
|
Intramuscular injections Immunisations |
Breast milk
|
Paracetamol |
|
ROP /indirect opthalmoscopy |
Breast milk |
Local analgesic eye drops |
Prior to exam |
Supra pubic aspiration |
Breast milk |
|
|
Heel stick |
Breast milk |
|
|
PICC line placement |
Breast milk
|
Morphine |
For intubated patients |
Lumbar puncture |
Breast milk |
|
|
Chest drain |
|
Lidocaine |
For intubated patients |
Intubation |
|
Fentanyl
Ketamine |
Slow bolus to avoid chest wall rigidity Neonates with hypoplastic left heart syndrome/unstable circulation |
Starting doses for each medication are as per the MCN for West of Scotland Guideline, but dosing and weaning should be individualised
Acute pain- Consequences of acute pain which may be experienced by the neonate include; acute increases in heart rate, blood pressure, intracranial pressure and decreases in oxygen saturations. These changes in cerebral blood flow may be associated with an increased risk of IVH and PVL. It has also been suggested that acute pain episodes experienced within the neonatal period may have long-lasting effects on future behavioural pain responses (Taddio et al 1997).
Repetitive pain - Consequences of repetitive or prolonged pain during the neonatal period may result in developmental alterations of the immature nervous system. Preterm infants may have specific learning deficits, poor adaptive behaviour and decreased pain threshold which can alter their response to future episodes to painful or non-painful stimuli. Exposure to repeated painful stimuli early in life is known to have short and long-term adverse sequelae. These sequelae include physiologic instability, altered brain development, and abnormal neurodevelopment (Vinall and Grunau 2014).
Chronic pain- Chronic pain has been described as a pathological pain state without apparent biological value that has persisted beyond the normal tissue healing time (Jovey 2002) suggesting that the end of the pain state is not known. Chronic disease conditions such as bronchopulmonary dysplasia (BPD) and some surgical conditions can produce chronic repetitive pain and stress on the neonate. However there are no working definitions or validated assessment scales which can assess an extended period of chronic pain in the neonate and is an area for future study.
It is important to consider each procedure/event and avoid or limit where possible.
Limitation or avoidance of skin-breaking or other painful procedures
Limit environmental stressors by reducing noise and light levels.
Interventions may include:
a) Cluster nursing care and interventions where appropriate and limit handling of the infant to allow undisturbed rest.
b) Pain and stress may also be alleviated by providing boundaries, swaddling, positioning infants with flexion of extremities, and using pacifiers/encouraging non-nutritive sucking.
c) Parental involvement and interaction should be actively encouraged and should be an integral part of the baby’s care
Interventions may include:
For further information on Developmental Care please refer to the WoS Developmental Care Guideline
Central Line Access
In the first few days of life an umbilical arterial catheter (UAC) / umbilical venous catheter (UVC) may be required for blood sampling, blood pressure monitoring and administration of intravenous fluids. This may prevent frequent heel stabs for blood sampling and excessive handling. However, the benefits of central access lines should be carefully balanced with the risks e.g. infection.
Identify actual or potential sources of pain/irritability.
Suggestions for frequency of pain assessment:
Assessment of Sedation
There are a plethora of neonatal pain assessment scales in the literature (Appendix 1). Each Neonatal Unit should select a validated pain assessment scale and become experienced in its use for pain measurement.
Within the West of Scotland MCN the N-PASS (Neonatal Pain Agitation and Sedation Scale) is recommended for use. The N-PASS is a validated pain assessment scale developed in North America for the assessment of pain (page 12) and sedation (page 13) in both term, preterm and surgical neonates utilising multidimensional indicators of neonatal pain. It is crucial that all staff using the N-PASS are trained in use of the scale in order to ensure appropriate pain assessment.
When using the N-PASS pain and sedation are scored SEPARATELY.
It is recommended that pain levels should be assessed using the N-PASS:
More frequent pain assessment indications:
Premature Neonates: + 1 if <30 weeks gestation / corrected age
Assessment of Pain/Agitation
Post-operative → at least every 2 hours for 24-48 hours, then every 4 hours until off
Muscle Relaxed
Assessment of Sedation
Muscle Relaxant
The following information relays the assessment criteria used to score the N-PASS pain assessment scale.
N-PASS Assessment Criteria
Crying / Irritability
-2 → No response to painful stimuli, e.g.:
-1 → Moans, sighs, or cries (audible or silent) minimally to painful stimuli, e.g. needle sticks, ETT or nares suctioning, care giving
0 → Not irritable – appropriate crying
+1 → Infant is irritable/crying at intervals – but can be consoled
+2 → Any of the following:
Behavior / State
-2 → Does not arouse or react to any stimuli:
-1 → Little spontaneous movement, arouses briefly and/or minimally to any stimuli:
0 → Behavior and state are gestational age appropriate
+1 → Any of the following:
+2 → Any of the following:
Facial Expression
-2 → Any of the following:
-1 → Minimal facial expression with stimuli
0 → Face is relaxed at rest but not lax – normal expression with stimuli
+1 → Any pain face expression observed intermittently
+2 → Any pain face expression is continual
Extremities / Tone
-2 → Any of the following:
-1 → Any of the following:
0 → Relaxed hands and feet – normal palmar or sole grasp elicited – appropriate tone for gestational age
+1 → Intermittent (<30 seconds duration) observation of toes and/or hands as clenched or fingers splayed
+2 → Any of the following:
Vital Signs: HR, BP, RR, & O2 Saturations
-2 → Any of the following:
-1 → Vital signs show little variability with stimuli – less than 10% from baseline
0 → Vital signs and/or oxygen saturations are within normal limits with normal variability – or normal for gestational age
+1 → Any of the following:
+2 → Any of the following:
1) The best approach to management of neonatal pain is prevention.
2) Non-pharmacological Interventions
3) Pharmacological Interventions- Oral and Topical
Oral Analgesics
Topical or Local Anaesthetics
Local anaesthetics may be applied to the skin before clinical procedures. The cream should be applied to no more than three areas at the same time.
There are two types of local anaesthetic cream: Ametop Gel and EMLA cream.
EMLA cream is licenced for infants over one year of age and therefore not frequently used within neonatal units.
Potential Side Effects of the Creams
There can be allergic reactions to the creams, causing itching, swelling or bruising where it is applied. Some changes in skin colour may occur where it is applied however this is normal.
Local anaesthetics should NOT be used on:
IV Pharmacological Interventions:
i) Morphine
ii) Fentanyl
iii) Paracetamol
4) Sedatives for the treatment of stress/anxiety
Benzodiazepines may be given for associated anxiety/stress but are not appropriate for the treatment or prevention of pain and not recommended for use in the preterm neonate.
5) Nurse Controlled Analgesia (NCA)
Nurse controlled analgesia (NCA) refers to a modified morphine infusion using technology which permits more flexibility to manage breakthrough pain than a simple continuous infusion. It is used in limited clinical areas in the West of Scotland generally in the immediate post- operative period. The nurse caring for the patient may press a button to give a bolus dose on the basis of a request for analgesia, pain severity scoring or in anticipation of pain.
Nurse Controlled Analgesia (NCA) is a technique of morphine administration appropriate for some neonates. NCA is delivered through a specifically designed locked pump which allows for programming of a bolus dose to be delivered by nursing staff on the press of the NCA button. Commonly the bolus is 10 – 20 micrograms/kg with a 20-30 minute lockout period. A low rate of background infusion may also be used alongside the bolus, and is set from 4micrograms/kg/hr upwards.
Although this technique potentially allows for larger doses of opiates to be administered, experience shows that the same level of background pain relief is achieved with much reduced total opiate dose. This is because of the dynamic nature of the administration which allows for doses to be given exactly at the moment the patient is experiencing pain or to pre-empt painful/ distressing procedures such as endotracheal suction.
At its most effective, when used in tandem with regular pain scoring NCA will tend to wean itself. For example, as the patient recovers from the pain of surgery their pain scores will improve and the NCA will require fewer presses. Reduction in total opiate load has the potential advantages of reduced respiratory support and more rapid return of GI function post-surgery.
Patient Selection
Patients selected for NCA usually have (or are expected to have) severe acute pain for whom the oral route is not appropriate, such as during the immediate post-operative period. Prior to setting up the infusion the anaesthetist or acute pain service staff will consider the suitability of NCA for each individual patient and the anticipated effectiveness of NCA for the type of surgery / pain.
Absolute contraindications to NCA are:
Extra caution is advised when using a NCA in patients with certain medical conditions:
6) Neonatal Regional Techniques
Neonates can present a unique challenge in the management of post-operative pain. Regional techniques are being increasingly used to minimize post-operative pain.
Epidural
The most commonly used technique is a single dose administration of local anaesthetic agent into the caudal (epidural) space for operations such as inguinal hernia repair. This provides adequate pain relief during the surgery itself, and for up to four hours afterwards.
Another commonly used regional technique involves placement of an epidural catheter in the epidural space in theatre for prolonged pain management. The epidural catheter may have been inserted into the caudal space and advanced to a level in the back that corresponds to the level of surgical incision, or may have been inserted higher up the back at this level. For surgery, where significant pain may be a predicted problem post-operatively, for example laparotomy, a local anaesthetic infusion pump is attached to the catheter to provide ongoing pain relief. Strict monitoring of the patient and pump infusion rates is in accordance with local Acute Pain Team guidelines and protocols. Epidural infusions would normally run for 2 to 3 days post operatively. Observed benefits from this technique are potentially earlier extubation, early return of bowel function, and a reduction in morphine requirement.
More recently single shot spinal anaesthesia, combined with a single shot caudal injection in ex-premature neonates is being performed for surgery below the umbilicus. This is perceived to be beneficial in reducing the risk of post-operative apnoea’s in this group of patients by avoiding the need for general anaesthesia, and can result in earlier return to feeding. This technique will result in the neonate not being able to move their legs for about an hour after the local anaesthetic injection. Movement of their legs should be observed to return to normal after this time period.
Extrapleural Catheters
Extrapleural catheters are placed by the surgeons in neonates undergoing cardiac or thoracic surgery. Local anaesthetic infusion pumps will be used in a similar way to epidural pumps to provide ongoing pain relief.
Pain Measure |
Age |
Pain |
Indicator |
Psychometric Properties |
Pain Assessment Tool (PAT) (Hodgkinson et al. 1994)
|
< 3 years of age unable to verbalise pain |
Prolonged (post-operative) |
Sleep pattern |
Content validity |
Neonatal Pain Agitation and Sedation Scale (N-PASS) (Hummel et al. 2003) |
<28 weeks -Term Corrected for prematurity |
Prolonged Mechanical ventilation or postoperative |
Behavioural state |
Preliminary reliability and validity in progress. |
Neonatal Infant Pain Scale (NIPS) (Lawrence et al 1993) |
Preterm and term |
Procedural |
Cry |
Content validity |
Premature Infant Pain Profile (PIPP) Stevens et al. 1996) |
Preterm and term |
Procedural |
Behavioural state |
Content validity |
IV Morphine → Oramorph
I.e. Current dose in mcg/kg/hr X working weight X 24
Weaning Oramorph
Anand K.J, Hall R.W, Desai N, Shephard B, et al. (2004). Effects of morphine analgesia in ventilated preterm neonates: primary outcomes from the NEOPAIN randomised trial. Lancet: 363(9422)1673-82.
Anand KJ, Aranda JV, Berde CB, Buckman S, et al. (2006) Summary proceedings from the neonatal pain control group. Pediatrics ;117:S9-S22.
Anand KJ (2001) International Evidence-Based Group for Neonatal P. Consensus statement for the prevention and management of pain in the newborn. Arch Pediatr Adolesc Med 155:173-80.
Anand K.J.S, Stevens B.J and McGrath P.J (2007) Pain in Neonates and Infants (3rdEdition). London: Elsevier
Barker D.P, Rutter N. (1995) Exposure to invasive procedures in neonatal intensive care unit admissions. Arch Dis Child Fetal Neonatal Ed, 72(1):F47-8.
Barr RG (1998) Reflections on measuring pain in infants: dissociation in responsive systems and “honest signalling”. Archive of Diseases in Childhood Fetal and Neonatal Edition 79 (1): 152-156.
Beatriz, V.O., Holsti, L., Linhares, M. (2015) Neonatal Pain and Developmental Outcomes in Children Born Preterm: A Systematic Review. Clinical Journal of Pain. 31(4) pp355-362
Bellú R, de Waal K, Zanini, R. (2010) Opioids for neonates receiving mechanical ventilation: a systematic review and meta-analysis. Arch Dis Child Fetal Neonatal Ed; 95(4):F241-51.
Craig KD, Whitfield MF, Grunau RVE, Linton J and Hajistavropoulos HD (1993) Pain in the preterm neonate: behavioural and physiological indices. Pain 52(3): 287-299
Duhn L and Medves J (2004) A systematic integrative review of infant pain assessment tools. Advances in Neonatal Care 4 (3): 126-140
Elserafy F, Alsaedi SA, Louwrens J, Bin Sadiq B, et al. (2009) Oral sucrose and a pacifier for pain relief during simple procedures in preterm infants: a randomized controlled trial. Ann Saudi Med, 29(3):184-8.
Gibbons S, Stevens B, Hodnett E, Pinelli J, Ohlsson A and Darlington G (2002) Efficacy and safety of sucrose for procedural pain relief in preterm and term neonates. Nursing Research 51(6): 378-382
Grunau RE and Tu MT (2007) Long- term consequences of pain in human neonates IN: Anand KJS, Stevens BJ and McGrath PJ (eds) Pain in Neonates and Infants. London: Elsevier 45-55
Hall RW, Huitt TW, Thapa R, Williams DK, Anand KJ, Garcia-Rill E. (2008) Long-term deficits of preterm birth: evidence for arousal and attentional disturbances. ClinNeurophysiol,19:1281-91.
Hall RW. (2012) Anesthesia and analgesia in the NICU. Semin Perinatol, 39(1):239-54.
Hamers JHP, Abu Saad HH, van den Hout MA, Halfens RJG and Kester ADM (1994) The influence of childrens vocal expression, age, medical diagnosis and information obtained from parents on nurses’ pain assessments and decisions regarding interventions. Pain 65(1): 53-61
Holsti L, Grunau RE. (2010) Considerations for using sucrose to reduce procedural pain in preterm infants. Pediatrics,125(5):1042-7.
Hudson-Barr DC, Duffey MA and Holditch-Davis D (1998) Pediatric Nurses use of behaviours to make medication administration decisions in infants recovering from surgery. Research in Nursing Health 21(1): 3-13
Hummel P, Puchalski M, Creech SD, Weiss MG. (2008) Clinical reliability and validity of the N-PASS: neonatal pain, agitation and sedation scale with prolonged pain. J Perinatol, 28(1):55-60.
IASP Task Force on Taxonomy (2003) IASP Pain terminology. Available from: http://www.iasp-pain.org/terms-p.html
Jovey RD (2002) Opioids, pain and addiction. In: Jovey RD (ed) Managing pain: the Canadian Healthcare Professionals Reference, pp63-77. Rogers Media, Toronto, Canada
McGrath PJ (1996) There is more to pain measurement in children than “ouch”. Canadian Psychology 37 (2): 63-75
Merskey M and Bogduk N (1994) Classifications of Chronic Pain: Descriptions of Chronic Pain Syndromes and Definitions of Pain Terms. Seattle: (IASP) Press
Mokhnach L, Anderson M, Glorioso R, Loeffler K, et al.(2010) NICU procedures are getting sweeter: development of a sucrose protocol for neonatal procedural pain. Neonatal Netw 29(5):271-9.
Ng E., Taddio A., Ohissin A. (2017) Intravenous midazolam infusion for sedation of infants in the neonatal intensive care unit. Cochrane Database of Systematic Reviews Issue 1 Art No CD 002052. DOI: 10. 1002/14651858. CD002052 pub 3
O'Sullivan A, O’Connor M, Brosnahan D, McCreery K, et al. (2010) Sweeten, soother and swaddle for retinopathy of prematurity screening: a randomised placebo controlled trial. Arch Dis Child Fetal Neonatal Ed, 95(6):F419-22
Owens ME and Todt EH (1984) Pain in infancy: neonatal reactions to heel lance. Pain 20 (1): 77-86
Ramsay M (2000) Measuring level of sedation in the intensive care unit. Journal of the American Medical Association 294: 441-442
Stevens BJ and Johnston C (1994) Physiological responses of premature infants of painful stimulus. Nursing Research 43 (4): 226-231
Stevens BJ, Johnson CC and Grunau RVE (1995) Issues of assessment of pain and discomfort in neonates. JOGNN 24 (9):849-854
Stevens BJ, Riddell RRP, Oberlander TE and Gibbins S (2007) Assessment of Pain in Neonates and Infants IN: Anand KJS, Stevens BJ and McGrath PJ (eds) Pain in Neonates and Infant. London: Elsevier 67-86
Streiner DL and Norman GR (2006) Health Measurement Scales (3rd Edition) Oxford: Oxford University Press
Taddio A, Katz J, Ilersich A and Koren G (1997) Effect of Circumcision on Pain Response during Subsequent Routine Vaccination. The Lancet 349:599-603.
Van Dijk M, Peters J and Bowmeester N (2002) Are postoperative pain instruments useful for specific groups of vulnerable infants? Clinics in Perinatology 29 (3): 469-491
Van Howe RS (1999) Pain relief for neonatal circumcision: serious design flaws? Pediatrics 103 (1):196-197
Vinall J and Grunau RE (2014) Impact of repeated procedural pain-related stress in infants born very preterm. Pediatric Research 2014; 75(5):584–587
Wasz-Hockert O, Michelsson K and Lind J (1987) Cry in various diseases. IN: Lester BM, Boukydis CFZ (eds) Infant Crying: Theoretical and Research Perspectives. New York: Plenum Press
Additional Resources for Assessment Tools
N-PASS. Hummel PA et al. Clinical reliability and validity of the N-PASS: neonatal pain, agitation and sedation scale with prolonged pain. J Perinatol 2007; 28: 55-60.
Pain Assessment Tool (PAT) Hodgkinson K, Bear M, Thorn J, Blaricum S. Measuring pain in neonates: Evaluating an instrument and developing a common language. J Adv Nurs 1994;12(1):17-22.
The Distress Scale for Ventilated Newborn Infants (DSVNI) Sparshott M. The development of a clinical distress scale for ventilated newborn infants: identification of pain and distress based on validated behavioural scores. J Neonatal Nurs 1996;2:5- 11.
The Neonatal Infant Pain Scale (NIPS) Lawrence J, Alcock D, McGrath J, Kay S, et al. The development of a tool to assess neonatal pain. Neonatal Network, 1993;12(6):59-66.
Last reviewed: 22 December 2021
Next review: 01 December 2024
Author(s): L Raeside, ANNP, NICU, RHC; K. Reilly, Specialist in Pain Management, RHC
Co-Author(s): Other Professionals Consulted: Dr L Jackson, Neonatal Consultant, NICU, RHC; Dr Joyce O’Shea, Neonatal Consultant, NICU RHC; Anisa Patel, Neonatal Pharmacist, NICU, RHC
Approved By: West of Scotland Neonatology MCN