98%
921
2 minutes
20
Background: Studies have shown that oral oxycontin tablets can be used for opioid titration. The European Society for Medical Oncology (ESMO) guidelines for adult cancer pain recommend opioid titration through the parenteral route, usually the intravenous or subcutaneous route. Patient-controlled subcutaneous analgesia (PCSA) with hydromorphone needs further evaluation for opioid titration. This prospective multicenter study was designed to compare the efficacy and safety of hydromorphone PCSA with oral oxycontin tablets for opioid titration of cancer pain.
Patients And Methods: Eligible patients with cancer pain were randomly assigned in a 1:1 ratio to the PCSA group or the oxycontin group for dose titration. Different titration methods were given in both groups depending on whether the patient had an opioid tolerance. The primary endpoint of this study was time to successful titration (TST).
Results: A total of 256 patients completed this study. The PCSA group had a significantly lower TST compared with the oxycontin group (median [95% confidence interval (CI)], 5.5[95% CI:2.5-11.5] hours vs.16.0 [95% CI:11.5-22.5] hours; <0.001). The frequency (median; interquartile) of breakthrough pain (Btp) over 24 hours was significantly lower in the PCSA group (2.5;2.0-3.5) than in the oxycontin group.(3.0; 2.5-4.5) (=0.04). The pain was evaluated by numeric rating scale (NRS) score at 12 hours after the start of titration. The pain score (median; interquartile) was significantly lower in the PCSA versus the oxycontin group (2.5;1.5-3.0) vs 4.5;3.0-6.0) (=0.02). The equivalent dose of oral morphine (EDOM) for a successful titration was similar in both groups (=0.29), but there was a significant improvement in quality of life (QoL) in both groups (=0.03). No between-group difference in the incidence of opioid-related adverse effects was observed (=0.32).
Conclusion: Compared with oral oxycontin tablet, the use of PCSA with hydromorphone achieved a shorter titration duration for patients with cancer pain (<0.001), without significantly increasing adverse events (=0.32).
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11020333 | PMC |
http://dx.doi.org/10.2147/JPR.S451698 | DOI Listing |
Pain
September 2025
Department of Biostatistics, Epidemiology, and Informatics, University of Pennsylvania, Philadelphia, PA, United States.
This study aims to identify predictors of success in treating chronic pain patients with full agonist opioids by analyzing harmonized individual patient data from 5594 participants in 9 enriched enrollment randomized withdrawal clinical trials available in the Food and Drug Administration data repository. We analyzed both the participants' success with titration and continued success in the 84-day maintenance phases after randomization for those maintained on the drug. We used the full data set to assess participant demographics and subsets of data containing participant reported outcomes at baseline.
View Article and Find Full Text PDFJ Palliat Med
September 2025
Division of Palliative Medicine, UConn Health, Farmington, Connecticut, USA.
Despite guidelines advocating that patients with advanced cancer receive dedicated palliative care (PC) services, many patients lack access. Improved training in PC for hematology-oncologists could help, yet studies have shown deficits in PC knowledge and education. We designed a novel longitudinal, PC continuity rotation for hematology-oncology (H/O) fellows and assessed feasibility, acceptability, value, and impact.
View Article and Find Full Text PDFJ Pain Symptom Manage
August 2025
Department of Pain Medicine, University of Texas MD Anderson Cancer Center, Houston, United States. Electronic address:
Context: Low dose naltrexone (LDN) has been utilized off-label for chronic non-cancer pain; its benefits in treating cancer-related pain remain unclear.
Objectives: We describe the safety and effectiveness of LDN therapy from initiation to the first two follow-up visits in treating refractory cancer-pain.
Methods: Medical charts of cancer patients seen in the Pain Management Center who were prescribed LDN between 2022 and 2023 were reviewed.
Ann Med
December 2025
Department of Anesthesiology, First Affiliated Hospital of Soochow University, Suzhou, China.
Background: Same-visit bidirectional endoscopic procedures under sedation are frequently performed in elderly patients. However, the optimal sedation regimen for elderly patients remains uncertain. This study seeks to evaluate the hypothesis that intravenous lidocaine, when used as an adjunct to propofol sedation, reduces the incidence of sedation-related adverse events during these procedures.
View Article and Find Full Text PDFJAMA Netw Open
August 2025
ICES, Toronto, Ontario, Canada.
Importance: The increased potency of the fentanyl-dominated drug supply has precipitated a shift in patient-reported opioid tolerance and methadone prescribing guidance. However, adoption of new methadone prescribing approaches remains unknown.
Objective: To examine methadone initiation trends within the context of changing prescribing guidance and an increasingly volatile unregulated drug supply.