Oxycodone Extended-Release Capsule Utilization for Pain Management in a Cancer Palliative Care Clinic: A Retrospective Review.

IF 0.9 Q3 ANESTHESIOLOGY
Jordan Fortunato, Justin Kullgren, Gary Houchard, Jessica Hirsch, Nicole Shirilla, Meridith Bumb, Junan Li
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引用次数: 0

Abstract

Xtampza ER™, an oxycodone extended-release capsule (OERC), was the first long-acting opioid to feature abuse-deterrent properties and various routes of administration without pharmacokinetic alterations. The primary objective of this study was to evaluate changes in reported pain scores after initiation of or rotation to OERC from a previous opioid.  Baseline scores were from patients' outpatient visits immediately before starting OERC and were compared to those at the next two follow-up visits. Secondary objectives identified variables that influenced pain scores. Methods included screening for cancer patients with outpatient OERC prescriptions seen in the palliative care clinic. Eighty-two charts were reviewed with 66 included. Overall mean pain scores at both follow-ups were lower than those at baseline (-0.7 ± 2.1; -1.1 ± 2.4). Results were statistically significant between first and second-reported pain scores versus baseline (p = 0.009; 0.012) but clinically insignificant, defined as a ≥ 2-point change in numeric pain scores. Most patients discontinued OERC at the first or second follow-up (35; 53%), and 12.1% of patients who started OERC were prescribed OERC at the end of the study. There were no significant variables identified to influence pain scores either statistically or clinically. Further studies are needed to determine the long-term efficacy and safety in cancer palliative-care patients.

羟考酮缓释胶囊用于癌症姑息治疗临床疼痛管理:回顾性回顾。
Xtampza ER™是一种羟考酮缓释胶囊(OERC),是第一个具有滥用威慑特性和多种给药途径而不改变药代动力学的长效阿片类药物。本研究的主要目的是评估从先前的阿片类药物开始或轮换到OERC后报告的疼痛评分的变化。 基线评分来自患者在开始OERC之前的门诊就诊,并与接下来两次随访的结果进行比较。次要目标确定影响疼痛评分的变量。 方法包括筛查姑息治疗诊所门诊OERC处方的癌症患者。回顾了82张图表,其中包括66张。两组随访时的总体平均疼痛评分均低于基线时(-0.7±2.1;-1.1±2.4)。第一次和第二次报告的疼痛评分与基线相比,结果具有统计学意义(p = 0.009;0.012),但临床不显著,定义为数值疼痛评分变化≥2点。大多数患者在第一次或第二次随访时停止OERC治疗(35;53%), 12.1%开始OERC的患者在研究结束时处方OERC。无论在统计学上还是临床上,都没有发现影响疼痛评分的显著变量。需要进一步的研究来确定癌症姑息治疗患者的长期疗效和安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.60
自引率
9.10%
发文量
40
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