Department of Pharmacy, Burnaby Hospital, Burnaby, British Columbia, Canada.
Department of Pharmacy, Abbotsford Regional Hospital and Cancer Centre, Abbotsford, British Columbia, Canada.
PLoS One. 2023 Sep 27;18(9):e0292016. doi: 10.1371/journal.pone.0292016. eCollection 2023.
Patients seen by the palliative care team often have difficult and intractable symptoms. The current standard of practice to manage these symptoms is the deeply sedating midazolam continuous subcutaneous infusion for patients who are expected to expire within hours to days. Dexmedetomidine provides sedation but lacks evidence in palliative care use. This study describes continuous subcutaneous infusion of dexmedetomidine's effect on refractory pain and delirium. Retrospective, observational chart review and conducted in accordance with SQUIRE (quality improvement study). Twenty adult patients (18 years of age or older) with metastatic cancer disease admitted to three palliative complex care units of Fraser Health who received continuous subcutaneous infusion of dexmedetomidine between January 2017 to August 31, 2019. Average length of dexmedetomidine use was 9 days (1/3 length of stay). Eight of the 13 patients with pain symptoms exhibited an overall decline in pain. Four of the 6 patients with delirium had an initial decrease in delirium, but it did not last beyond the first day. Despite progressive clinical deterioration, adjunctive medications decreased or remained the same for 53% of as needed medications and 65% for regularly scheduled medications. Forty-five percent of patients had ≥50% days of rousable sedation. Hypotension occurred in 85% of patients. Dexmedetomidine provided benefit in managing intractable pain while allowing patients to remain rousable, but only had a short effect on delirium symptoms.
接受姑息治疗团队治疗的患者通常存在严重和难以控制的症状。目前,预计在数小时至数天内死亡的患者,管理这些症状的标准做法是使用深度镇静咪达唑仑持续皮下输注。右美托咪定可提供镇静作用,但在姑息治疗中缺乏证据。本研究描述了持续皮下输注右美托咪定对难治性疼痛和谵妄的影响。回顾性观察性图表审查,并按照 SQUIRE(质量改进研究)进行。20 名成年患者(年龄在 18 岁或以上)患有转移性癌症疾病,在弗雷泽健康的三个姑息性综合护理病房入院,他们在 2017 年 1 月至 2019 年 8 月 31 日期间接受了右美托咪定持续皮下输注。右美托咪定的平均使用时间为 9 天(住院时间的 1/3)。在有疼痛症状的 13 名患者中,有 8 名患者的疼痛总体有所缓解。在有谵妄症状的 6 名患者中,有 4 名患者的谵妄最初有所减轻,但持续不到第一天。尽管临床情况逐渐恶化,但 53%的按需药物和 65%的定期药物的辅助药物减少或保持不变。45%的患者有≥50%的可唤醒镇静天数。85%的患者出现低血压。右美托咪定在管理难治性疼痛方面有效,同时使患者保持可唤醒状态,但对谵妄症状只有短暂的影响。