Distinguishing between Emergence Delirium and Pain in Early Post-Operative Period among Paediatric Patients: A Prospective Observational Study

Abstract:
Emergence delirium (ED) and postoperative pain are
common and significant concerns in paediatric anaesthesia. Both conditions can
occur early in the postoperative period and are challenging to distinguish due
to overlapping clinical presentations. ED is characterized by confusion,
agitation, and disorientation after anaesthesia, often leading to distress in
the child and anxiety among caregivers. Postoperative pain can similarly
present with agitation and crying, making differentiation critical for effective
management. This study aimed to prospectively observe paediatric patients to
identify distinguishing characteristics between ED and pain, thereby improving
postoperative care and reducing misdiagnosis. This prospective observational
study included 100 paediatric patients aged 2 to 6 years. All participants were
ASA physical status 1 or 2 and underwent elective surgeries requiring general
anaesthesia. Postoperative behaviour was assessed using the PAED score for ED
and the FLACC scale for pain. Two trained observers, blinded to the study
hypothesis, evaluated the children at multiple time points during and after
surgery. The primary outcomes were the incidence of ED and pain, and the
relationship between sevoflurane exposure time and these outcomes. The majority
of patients (89.375%) exhibited normal postoperative behaviour, while 10.5%
experienced ED, and 3.75% experienced pain without ED. A smaller subset (3.5%)
experienced both ED and pain. Patients with sevoflurane exposure greater than
100 minutes had a significantly higher risk of ED, with a risk ratio of 4.5
compared to those with less exposure. ED was most prevalent at awakening and
rapidly decreased, while pain became more prominent later in the recovery
period. While most paediatric patients recover from anaesthesia without issues,
a notable group remains at risk for ED, especially with longer sevoflurane
exposure.
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