Immunoglobulin utilization in Canada: a comparative analysis of provincial guidelines and a scoping review of the literature.

Megan Harmon, Kiarash Riazi, Jeannie Callum, Donald M Arnold, Rebecca Barty, Davinder Sidhu, Nancy M Heddle, Laurie MacLeod, Na Li
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Abstract

Background: Canada has high immunoglobulin (IG) product utilization, raising concerns about appropriate utilization, cost and risk of shortages. Currently, there is no national set of standardized IG guidelines, and considerable variations exist among the existing provincial guidelines. The aims of this study were: (1) to compare the existing Canadian provincial guidelines on the use of IG products to identify their consistencies and differences and (2) to examine the existing research in Canada on IG supply and utilization following the establishment of IG guidelines to understand the scope of research and pinpoint the gaps.

Methods: A comparative analysis accounted for the differences across provincial IG guidelines. We highlighted similarities and differences in recommendations for medical conditions. A scoping review of citations from MEDLINE, PubMed, Scopus and Embase databases was conducted for studies published from January 01, 2014, to April 12, 2023.

Results: While provincial guidelines represented a considerable overlap in the medical conditions delineated and relatively uniform dose calculations, numerous differences were observed, including in recommendation categories, provision of pediatric dosing, and divergent recommendations for identical conditions based on patient demographics. The scoping review identified 29 studies that focused on the use of IG in Canada. The themes of the studies included: IVIG utilization and audits, the switch from IVIG to SCIG, patient satisfaction with IVIG and/or SCIG, the economic impact of self-administered SCIG versus clinically administered IVIG therapy, and the efficacy and cost-effectiveness of alternative medications to IG treatment.

Conclusion: The differences in guidelines across provinces and the factors influencing IVIG/SCIG use, patient satisfaction, and cost savings are highlighted. Future research may focus on clarifying costs and comparative effectiveness, exploring factors influencing guideline adherence, and evaluating the impact of updated guidelines on IG use and patient outcomes.

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Abstract Image

免疫球蛋白的使用在加拿大:省级指南的比较分析和文献的范围审查。
背景:加拿大免疫球蛋白(IG)产品利用率高,引起了人们对适当利用、成本和短缺风险的关注。目前,没有一套标准化的全国性IG指南,现有的省级指南之间存在相当大的差异。本研究的目的是:(1)比较现有的加拿大省级IG产品使用指南,以确定其一致性和差异;(2)检查IG指南建立后加拿大关于IG供应和利用的现有研究,以了解研究范围并找出差距。方法:对各省IG指南的差异进行比较分析。我们强调了医疗条件建议的异同。对2014年1月1日至2023年4月12日期间发表的研究进行了MEDLINE、PubMed、Scopus和Embase数据库的引用范围评估。结果:虽然各省指南在描述的医疗条件和相对统一的剂量计算方面有相当大的重叠,但观察到许多差异,包括推荐类别、儿科剂量的提供以及基于患者人口统计学的相同条件的不同建议。范围审查确定了29项研究,重点关注IG在加拿大的使用。这些研究的主题包括:IVIG的使用和审计,从IVIG到SCIG的转换,患者对IVIG和/或SCIG的满意度,自我给药SCIG与临床给药IVIG治疗的经济影响,以及替代IG治疗的疗效和成本效益。结论:各省指南的差异,以及影响IVIG/SCIG使用、患者满意度和成本节约的因素。未来的研究可能侧重于澄清成本和比较有效性,探索影响指南依从性的因素,并评估更新指南对IG使用和患者预后的影响。
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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