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Predictors of pain response after endoscopic ultrasound-guided celiac plexus neurolysis for abdominal pain caused by pancreatic malignancy. | LitMetric

Predictors of pain response after endoscopic ultrasound-guided celiac plexus neurolysis for abdominal pain caused by pancreatic malignancy.

World J Gastroenterol

Division of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, Hubei Province, China.

Published: January 2021

AI Article Synopsis

  • EUS-CPN is an effective and safe treatment option for managing pain in patients with inoperable pancreatic cancer, demonstrating good pain relief in 74.1% at one week and 67.2% at four weeks post-treatment.
  • Factors influencing treatment effectiveness include tumor location, bilateral treatment, and most notably, the presence of invisible ganglia and distant metastasis, which predict poorer pain response.
  • The study highlights the need for careful consideration of these predictors to optimize EUS-CPN outcomes for patients with advanced pancreatic cancer-related pain.

Article Abstract

Background: Endoscopic ultrasound-guided celiac plexus neurolysis (EUS-CPN) has gained popularity as a minimally invasive approach and is currently widely used to treat pancreatic cancer-associated pain. However, response to treatment is variable.

Aim: To identify the efficacy of EUS-CPN and explore determinants of pain response in EUS-CPN for pancreatic cancer-associated pain.

Methods: A retrospective study of 58 patients with abdominal pain due to inoperable pancreatic cancer who underwent EUS-CPN were included. The efficacy for palliation of pain was evaluated based on the visual analog scale pain score at 1 wk and 4 wk after EUS-CPN. Univariable and multivariable logistic regression analyses were performed to explore predictors of pain response.

Results: A good pain response was obtained in 74.1% and 67.2% of patients at 1 wk and 4 wk, respectively. Tumors located in the body/tail of the pancreas and patients receiving bilateral treatment were weakly associated with a good outcome. Multivariate analysis revealed patients with invisible ganglia and metastatic disease were significant factors for a negative response to EUS-CPN at 1 wk and 4 wk, respectively, particularly for invasion of the celiac plexus (odds ratio (OR) = 13.20, = 0.003 for 1 wk and OR = 15.11, = 0.001 for 4 wk). No severe adverse events were reported.

Conclusion: EUS-CPN is a safe and effective form of treatment for intractable pancreatic cancer-associated pain. Invisible ganglia, distant metastasis, and invasion of the celiac plexus were predictors of less effective response in EUS-CPN for pancreatic cancer-related pain. For these patients, efficacy warrants attention.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789068PMC
http://dx.doi.org/10.3748/wjg.v27.i1.69DOI Listing

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