Sammanfattning/ Abstract
Our knowledge of pain in neonates has increased significantly
during the last fifteen years. We now have an improved understanding of the pain
system and of the negative effects of untreated pain. Advances in neonatal care
have increased the number of preterm and severely ill infants who are treated in
neonatal intensive care units (NICU). These infants are subjected to a variety
of painful procedures as part of their management. Sufficient pain relief is
needed and for this, valid pain assessment is one prerequisite.
The aim of this research was to improve the management of procedural pain and to
examine the assessment of neonatal pain in clinical practice.
In an earlier study, oral glucose was found to reduce pain during blood
sampling. To further evaluate the pain-reducing effect of oral glucose and to
compare this effect with different blood sampling techniques, a trial was
performed. The pain score was lower and crying time shorter in the venipuncture
group than in the heel stick group when no glucose was given. When glucose was
administered, the pain score was lower in both glucose groups than in the groups
not receiving glucose (paper I).
In a randomized, controlled study, the effect of oral glucose was compared with
that of a topical local anaesthetic, EMLA, during venipuncture. The pain scores
were found to be lower in the glucose group and fewer infants were scored as
having pain. Crying time was also shorter in the glucose group (paper II).
To compare the pain-reducing effect of oral glucose with that of breast-feeding
shortly before venipuncture, a new trial was performed. The pain score was
significantly lower in the infants receiving glucose than in those not given
glucose. There was no significant difference in pain score between the infants
who were fed and the fasting infants (paper III).
In a previous study we found an increase in heart rate in newborns when they
received glucose as pain relief. We therefore investigated whether oral glucose
in itself could cause an increase in heart rate in healthy infants. In a trial,
infants were randomized to receive oral glucose or placebo without undergoing
any painful procedure. The heart rate was significantly higher in the glucose
than in the placebo group (paper IV).
Activation of endogenous opioids is suggested as one possible mechanism
underlying the pain-reducing effect of oral glucose. We therefore investigated
whether administration of an opioid antagonist would reduce the effect of oral
glucose at heel stick in full-term newborns. There were no significant
differences in pain score or crying between the group receiving an opioid
antagonist before oral glucose and the group receiving placebo before oral
glucose during heel stick (paper V).
To document whether pain is assessed in Swedish neonatal units and by what
methods, a questionnaire was distributed to all neonatal departments in Sweden
in 1993, and again in 1998. Only a small proportion of neonatal units in Sweden
attempted to assess pain, but a slow increase was seen. There was a minor
increase in the number of departments that used a structured method for pain
scoring. Documentation of pain is still inadequate and needs to be improved (paper
VI). We compared parental assessment during blood sampling with measurement of
the pain score with a multidimensional tool and crying. There was low agreement
between these variables during the procedure (paper III).
In conclusion, we found that oral glucose reduces signs of pain from both heel
stick and venipuncture blood sampling. Oral glucose reduces pain better than
does EMLA cream and better than if the infant is breast-fed shortly before the
procedure. Oral glucose increases the heart rate in infants and the
pain-reducing effect of oral glucose in newborns was not diminished by injection
of an opioid antagonist. Parental assessment of an infants pain cannot replace
measurement by pain scores. The pain assessment at neonatal units in Sweden
needs to be improved.