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评估针对神经科患者的个体化皮下免疫球蛋白治疗方案。

Evaluation of a Personalized Subcutaneous Immunoglobulin Treatment Program for Neurological Patients.

机构信息

Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.

Division of Infectious Diseases, Department of Medicine, The Ottawa Hospital, Ottawa, Ontario, Canada.

出版信息

Can J Neurol Sci. 2019 Jan;46(1):38-43. doi: 10.1017/cjn.2018.363.

Abstract

BACKGROUND

Subcutaneous immunoglobulin (SCIg) treatment has been shown to control symptoms and improve overall satisfaction in patients with neurological disorders. However, a large injection volume can be overwhelming and a barrier to successful SCIg treatment. We established a nurse-led individualized approach program to facilitate a smooth and successful treatment transition from intravenous immunoglobulin (IVIg) to SCIg. The program involved a lead nurse to provide two or more individual educational sessions on SCIg administration, establish a written transition plan, and liaise care with physicians.

OBJECTIVES

We aimed to evaluate the impact of our program to a successful transition defined as SCIg retention or adherence without a need to restart IVIg by six or twelve months.

METHODS

We reviewed medical charts of all patients with immune-mediated neuromuscular disorders who were in our program during January 2010 to Dec 2016.

RESULTS

Nineteen patients were identified. Mean IVIg treatment duration was 31.5 months (range 4-98) before the transition. Mean steady state SCIg dosage was 26.2 g/week (SD 10.3). All patients were initially able to switch to SCIg, with a retention rate of 17/19 (89.5%) at six months and 15/19 (78.9%) at twelve months. Two patients reverted back to IVIg treatment due to worsening of their symptoms at two and three months, while two required supplemental IVIg infusions. There were no major adverse events reported during the twelve-month period, but one minor cutaneous adverse event (redness around the injection site).

CONCLUSIONS

Successful treatment transition may be achieved with the nurse led individualized approach program.

摘要

背景

皮下免疫球蛋白(SCIg)治疗已被证明可控制症状并提高神经疾病患者的总体满意度。然而,大剂量注射可能会让人难以接受,成为 SCIg 治疗成功的障碍。我们建立了一个护士主导的个体化方法计划,以促进从静脉注射免疫球蛋白(IVIg)顺利过渡到 SCIg。该计划包括一名主管护士提供两次或更多次关于 SCIg 给药的个体教育课程,制定书面过渡计划,并与医生沟通协调。

目的

我们旨在评估我们的方案对成功过渡的影响,成功过渡定义为在六个月或十二个月内无需重新开始 IVIg 治疗即可保留或坚持使用 SCIg。

方法

我们回顾了 2010 年 1 月至 2016 年 12 月期间参加我们计划的所有免疫介导性神经肌肉疾病患者的病历。

结果

确定了 19 名患者。过渡前 IVIg 治疗的平均持续时间为 31.5 个月(范围为 4-98)。平均稳态 SCIg 剂量为 26.2 g/周(标准差 10.3)。所有患者最初均能成功转换为 SCIg,六个月时的保留率为 17/19(89.5%),十二个月时为 15/19(78.9%)。两名患者因症状恶化在两个月和三个月时重新开始 IVIg 治疗,两名患者需要补充 IVIg 输注。在十二个月期间没有报告重大不良事件,但有一例轻微皮肤不良事件(注射部位发红)。

结论

通过护士主导的个体化方法计划可以实现成功的治疗过渡。

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