EUS visualization and direct celiac ganglia neurolysis predicts better pain relief in patients with pancreatic malignancy (with video)

Background EUS-guided celiac plexus neurolysis (EUS-CPN) improves pain control in patients with pancreatic cancer. EUS allows visualization of the celiac ganglion. Objective To determine predictors of response to EUS-CPN in a cohort of 64 patients with pancreatic malignancy. Design Retrospective ana...

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Veröffentlicht in:Gastrointestinal endoscopy 2011-02, Vol.73 (2), p.267-274
Hauptverfasser: Ascunce, Gil, MD, Ribeiro, Afonso, MD, Reis, Isildinha, DrPH, Rocha-Lima, Caio, MD, Sleeman, Danny, MD, Merchan, Jaime, MD, Levi, Joe, MD
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Sprache:eng
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Zusammenfassung:Background EUS-guided celiac plexus neurolysis (EUS-CPN) improves pain control in patients with pancreatic cancer. EUS allows visualization of the celiac ganglion. Objective To determine predictors of response to EUS-CPN in a cohort of 64 patients with pancreatic malignancy. Design Retrospective analysis of prospective database. Setting Academic medical center. Patients Sixty-four patients with pancreatic cancer referred for EUS between March 2008 and January 2010. Interventions EUS-CPN injected directly into celiac ganglia when visible by linear EUS or bilateral injection at the celiac vascular trunk. Main Outcome Measurements Predictors of pain improvement at week 1 by univariate and multivariate analysis. Results At week 1, 32 patients (50%) had a symptomatic response. In a multivariate model with 8 potential predictors, visualization of the ganglia was the best predictor of response; patients with visible ganglia were >15 times more likely to respond (odds ratio 15.7; P < .001). Tumors located outside the head of the pancreas and patients with a higher baseline pain level were weakly associated with a good response. Limitations Retrospective design and lack of blinding. Conclusions Visualization of celiac ganglia with direct injection is the best predictor of response to EUS-CPN in patients with pancreatic malignancy.
ISSN:0016-5107
1097-6779
DOI:10.1016/j.gie.2010.10.029