Harvard Medical School, Beth Israel Deaconess Medical Center, Brookline, Massachusetts, USA.
Department of Gastroenterology.
Pain Med. 2018 Feb 1;19(2):336-347. doi: 10.1093/pm/pnx064.
Interventional pain management procedures have an important role in the management of chronic pain. The present study seeks to identify the proportion of patients who experience severe pain during pain procedures either with or without sedation. There is then an attempt to identify any association of high pain levels with factors such as age, gender, ethnicity, preprocedure pain level, procedure type, tobacco use, and baseline pharmaceuticals taken for both pain and/or mood disorder management.
This is a prospective survey study evaluating patients' discomfort during interventional pain procedures in an outpatient academic facility. Patient discomfort was assessed by the PROcedural Sedation Assessment Survey (PROSAS) and modified for nonsedation cases.
There were 155 patients in the survey, with 20 of these receiving nonspinal injections. Of the remaining 135 patients who underwent spinal injections, only 10 received conscious sedation. On average, 14.2% experienced severe pain during spinal injections, whereas 20% experienced severe pain with nonspinal injections. Though few patients received conscious sedation, most of these (60%) experienced high levels of pain. There was no correlation between level of procedural pain with age, gender, ethnicity, preprocedure pain level, procedure type, tobacco use, or medication type used.
The majority of patients who undergo nonsedated interventional pain management procedures do not experience severe pain. There is a small but appreciable group of subjects who seem to experience severe pain that cannot be correlated to any particular clinical characteristic in a standard patient evaluation. Even with standard conscious sedation, there is no clear best method to ensure patient comfort for this high-pain level group.
介入性疼痛管理程序在慢性疼痛管理中具有重要作用。本研究旨在确定在有或没有镇静的情况下,在疼痛程序中经历严重疼痛的患者比例。然后,试图确定高疼痛水平与年龄、性别、种族、术前疼痛水平、程序类型、吸烟以及用于疼痛和/或情绪障碍管理的基础药物等因素之间的任何关联。
这是一项前瞻性调查研究,评估了在门诊学术机构中接受介入性疼痛程序的患者的不适。患者的不适通过 PROcedural Sedation Assessment Survey(PROSAS)进行评估,并针对非镇静病例进行了修改。
该调查共纳入 155 例患者,其中 20 例接受非脊柱注射。在其余 135 例接受脊柱注射的患者中,只有 10 例接受了清醒镇静。平均而言,14.2%的患者在脊柱注射过程中经历严重疼痛,而 20%的患者在非脊柱注射过程中经历严重疼痛。尽管少数患者接受了清醒镇静,但大多数(60%)患者经历了高水平的疼痛。手术疼痛程度与年龄、性别、种族、术前疼痛水平、手术类型、吸烟或使用的药物类型之间没有相关性。
大多数接受非镇静介入性疼痛管理程序的患者不会经历严重疼痛。有一小部分患者似乎经历了严重的疼痛,但无法用标准患者评估中的任何特定临床特征来解释。即使使用标准的清醒镇静,对于这组高疼痛水平的患者,也没有明确的最佳方法来确保患者的舒适度。