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February 8, 2026Palliative & Supportive Care0 citationsOpen Access

Development and implementation of a cancer pain intervention registry: An Australian pilot study with preliminary outcome evaluation from 2 tertiary centers

YLYi-Ching LeeEZEmma ZhaoTBTimothy Brake

Key Points

  • Evaluate the effectiveness of a registry for interventional cancer pain management in Australia.
  • Created a longitudinal clinical registry capturing patient demographics and pain information at 2 hospitals.
  • Collected data on interventional procedures, including type and site of treatment.
  • Used patient-reported outcomes and quality of life surveys pre- and post-procedure.
  • A total of 48 patients underwent 55 procedures, with celiac plexus neurolysis being the most common.
  • There was a significant trend toward reduced pain intensity post-procedure.
  • Patients reported decreased opioid use and improved quality of life following interventions.

Abstract

Abstract Objectives To pilot a registry to evaluate the use and effectiveness of interventional cancer pain management. Methods Upon interventional pain procedure scheduling, patient demographics, cancer, and pain information were entered into the longitudinal clinical registry in 2 tertiary hospitals in Sydney, Australia (Royal Prince Alfred Hospital and Chris O’Brien Lifehouse). Details of the procedure (including proceduralist, nature of the intervention, and site of treatment), post-procedure patient-reported outcomes and quality of life surveys, adverse events, and mortality data (when known) were collected longitudinally. Results Between October 2021 and March 2023, 48 patients underwent 55 procedures. Procedures included treatment targeting autonomic plexuses, peripheral nerves, fascial planes, and neuraxial structures. Celiac plexus neurolysis was the most frequently reported procedure (33.3%). Post-procedure, there was a trend in reduction in pain intensity on the Patient-Reported Outcome Measurement Information System ( p < 0.01), reduction in opioid consumption, and improvement in quality of life on the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core-15-Palliative Care. Significance of results This is a vital first step in creating a more widely applicable registry evaluating cancer pain intervention. It provided valuable information on the range of available pain intervention procedures and data on patient-reported outcome measures using validated instruments. This will facilitate a timely review of clinical practice to improve future patient care. An Australian-wide database of cancer pain will be a valuable next step in the improvement of cancer pain management. Trial registration Clinical trial number: not applicable.

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Cite This Study

Lee et al. (2026) studied this question.

synapsesocial.com/papers/698829520fc35cd7a88498c0https://doi.org/10.1017/s1478951526101631
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