Mucositis Pain and Its Temporal Relationship to White Cell Count
Claire Douglas1, James D Morse2,3, Brian J Anderson1,2
1Department of Anaesthesia, Starship Children's Hospital, Auckland, New Zealand.
Insights
Pain in children with mucositis improves as white blood cell counts rise, with a noticeable delay in pain relief. This natural recovery offers more pain reduction than opioids or ketamine.
Area of Science:
- Pediatric Oncology
- Pain Management
- Immunology
Background:
- Children undergoing chemotherapy/radiotherapy can develop neutropenia, leading to painful mucositis.
- This study investigates pain and white cell count in pediatric mucositis patients.
Purpose of the Study:
- To explore the relationship between pain score and white cell count in pediatric mucositis.
- To assess the efficacy of opioid and ketamine analgesia in this patient group.
Main Methods:
- Observational study of 50 children with mucositis referred for intravenous analgesia.
- Analysis using nonlinear mixed effects models with a sigmoid EMAX model and delayed effect model.
- Daily recording of pain scores, white cell count, neutrophil count, and analgesia requirements.
Main Results:
- A delay of 0.29 days was observed between rising white cell count and pain response.
- Initial pain scores averaged 6.3/10, with a maximum reduction of 59% attributed to rising white cell counts.
- Opioids reduced pain by 38%, and ketamine by 11%.
Conclusions:
- Increased white cell count, a surrogate for neutrophils, correlates with pain relief in pediatric mucositis.
- Analgesic response to rising white cell count is delayed by approximately 1 day.
- The natural increase in white cell count provided greater pain relief than opioid or ketamine analgesia.
Background:
Children who have received chemotherapy and/or radiotherapy treatment resulting in neutropenia can suffer painful mucositis. We explored the relationship between pain score and white cell count in children with mucositis due to immunosuppression and assessed the influence of opioid and ketamine analgesia.
Methods:
Children with mucositis nursed in the pediatric oncology and hematology ward were invited to partake in this observational study following referral to the pediatric pain service for intravenous analgesia. Pain scores, white cell count, neutrophil count, and analgesia requirements were recorded daily until intravenous analgesia was either stopped or transitioned to oral analgesia. Data were analyzed using nonlinear mixed effects models that sought a relationship between white cell count and pain score using a sigmoid maximal effect (EMAX) model. The impact of analgesic use on pain score was determined. The temporal relationship between white cell count and pain score was characterized by using a delayed effect model with an equilibration half-time.
Results:
Fifty children were enrolled in the study from January 2022 to December 2023. The equilibration half-time relating the rise in white cell count and pain response was 0.29 days. The initial pain score (estimated in those children already started on treatment with paracetamol and tramadol) was 6.3 (maximum pain 10). The maximum pain reduction was 59% of that initial pain score. Morphine and ketamine further reduced pain; the maximum response for opioids was 38% reduction and that for ketamine was 11%.
Conclusion:
Pain relief from mucositis is related to an increase in white cell count after a period of severe neutropenia, where white cell count is a surrogate for neutrophil count. There is a delay in analgesic response of approximately 1 day. This analgesic response to increasing white cell count had greater dominance than analgesia achieved using either opioids or ketamine.
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