Department of Anesthesiology, University of Utah, School of Medicine, Salt Lake City, UT, USA.
University of Utah, School of Medicine, Salt Lake City, UT, USA.
Neuromodulation. 2021 Oct;24(7):1204-1208. doi: 10.1111/ner.13372. Epub 2021 Feb 23.
Radiation therapy (RT) and intrathecal drug delivery systems (IDDS) are often used concurrently to optimize pain management in patients with cancer. Concern remains among clinicians regarding the potential for IDDS malfunction in the setting of RT. Here we assessed the frequency of IDDS malfunction in a large cohort of patients treated with RT.
Cancer patients with IDDS and subsequent RT at our institution from 2011 to 2019 were eligible for this study. Patients were excluded in the rare event that their IDDS was managed by an outside clinic and follow-up documentation was unavailable. Eighty-eight patients aged 22-88 years old (43% female, 57% male) representing 106 separate courses of RT were retrospectively identified. Patients received varying levels of radiation for treatment of cancer and cumulative dose to the IDDS was calculated. IDDS interrogation was subsequently performed by a pain specialist. Malfunction was recorded as deviation from the expected drug volume and/or device errors reported upon interrogation as defined by the manufacturer.
Total measured RT dose to the IDDS ranged from 0 to 18.0 Gy (median = 0.2 Gy) with median dose of 0.04 Gy/fraction (range, 0-3.2 Gy/fraction). Ten pumps received a total dose >2 Gy and three received ≥5 Gy. Eighty-two percentage of patients had follow-up with a pain specialist for IDDS interrogation and all patients underwent follow-up with a healthcare provider following RT. There were zero incidences of IDDS malfunction related to RT. No patient had clinical evidence of radiation related pump malfunction at subsequent encounters.
We found no evidence that RT in patients with IDDS led to device failure or dysfunction. While radiation oncologists and pain specialists should coordinate patient care, it does not appear that RT dose impacts the function of the IDDS to warrant significant clinical concern.
放射治疗(RT)和鞘内药物输送系统(IDDS)常被同时用于优化癌症患者的疼痛管理。临床医生仍然担心 IDDS 在 RT 治疗中可能会出现故障。在这里,我们评估了在接受 RT 治疗的大量患者中 IDDS 出现故障的频率。
本研究纳入了 2011 年至 2019 年在我院接受 IDDS 和随后 RT 治疗的癌症患者。如果患者的 IDDS 由外部诊所管理且随访记录不可用,则将其排除在罕见情况下。最终确定了 88 名年龄在 22-88 岁(43%女性,57%男性)的患者,共涉及 106 例单独的 RT 治疗。患者接受了不同程度的放射治疗以治疗癌症,计算了 IDDS 的累积剂量。随后由疼痛专家对 IDDS 进行了检测。故障被记录为与预期药物量的偏差和/或制造商定义的设备故障。
IDDS 接受的总 RT 剂量范围为 0 至 18.0Gy(中位数为 0.2Gy),中位剂量为 0.04Gy/分次(范围 0-3.2Gy/分次)。10 个泵接受的总剂量超过 2Gy,3 个泵接受的剂量超过 5Gy。82%的患者接受了 IDDS 检测的疼痛专家随访,所有患者在接受 RT 治疗后都接受了医疗保健提供者的随访。没有与 RT 相关的 IDDS 故障的发生。在随后的就诊中,没有患者出现与辐射相关的泵故障的临床证据。
我们没有发现 IDDS 患者接受 RT 会导致设备故障或功能障碍的证据。虽然放射肿瘤学家和疼痛专家应协调患者的护理,但 RT 剂量似乎不会影响 IDDS 的功能,不需要引起严重的临床关注。