Champagne Jean-Nicolas, Desilets Antoine, Roy Guillaume, Landon-Cardinal Océane, Chapdelaine Hugo, Matte Geneviève, Bouchard Claudia, Rioux-Massé Benjamin, Lemay Anne-Sophie
Université de Montréal, Montreal, Quebec, Canada.
Division of Hematology and Oncology, Department of Medicine, Centre Hospitalier de l'Université de Montréal (CHUM), Montreal, Quebec, Canada.
Transfusion. 2024 Dec;64(12):2286-2295. doi: 10.1111/trf.18031. Epub 2024 Oct 17.
Intravenous immunoglobulin (IVIG) shortage represents an emerging issue in transfusion medicine. Limited data are available to determine effective strategies for optimal use. The objective of this retrospective observational study was to determine the impact of institutional measures on IVIG use at a large academic center.
IVIG infusions from November 26, 2018 to September 25, 2022 were categorized according to their appropriateness (Recommended, Option of treatment, or Unrecommended), based on provincial guidelines, and separated into three phases: Reference, Transition, and Post-Implementation phases, the latter following the adoption of restrictive measures, including mandatory standardized order forms, a blood bank gatekeeping strategy, and the creation of a stewardship committee.
A total of 5431 IVIG infusions were administered to 544 patients, accounting for 295,033 g. The most common indication categories were neurology (30.4%), immunology (29.0%), and hematology (17.4%). From Reference to Post-Implementation phase, IVIG infusions decreased from 2275 to 2000 with unrecommended indications dropping from 9.5% to 7.4% (p = 0.01), and a global reduction of 23.0% (from 131,163 g to 100,936 g of IVIG). Decrease in chronic immunomodulation accounted for 48.3% of total reduction (14,610 g of 30,227 g), whereas single-use immunomodulation, 40.5% (12,237 g of 30,227 g). Moreover, an absolute reduction of 16.9% was observed in orders exceeding the recommended doses (20.8% to 3.9%; p < 0.0001). Together, the unrecommended and excessive IVIG doses decreased from 19,975 g (15.2%) to 6670 g (6.6%).
A global reduction in IVIG use and a preferential decrease in the unrecommended orders were observed, most likely attributable to the bundle of restrictive strategies implemented.
静脉注射免疫球蛋白(IVIG)短缺是输血医学中一个新出现的问题。目前可用于确定最佳使用有效策略的数据有限。这项回顾性观察研究的目的是确定机构措施对一家大型学术中心IVIG使用的影响。
根据省级指南,将2018年11月26日至2022年9月25日的IVIG输注按照其适用性(推荐、治疗选择或不推荐)进行分类,并分为三个阶段:参考阶段、过渡阶段和实施后阶段,后者是在采取了包括强制使用标准化订单、血库把关策略以及设立管理委员会等限制性措施之后。
共对544例患者进行了5431次IVIG输注,总量为295,033克。最常见的适应证类别为神经科(30.4%)、免疫科(29.0%)和血液科(17.4%)。从参考阶段到实施后阶段,IVIG输注次数从2275次降至2000次,不推荐适应证的比例从9.5%降至7.4%(p = 0.01),IVIG总量整体减少了23.0%(从131,163克降至100,936克)。慢性免疫调节减少占总减少量的48.3%(30,227克中的14,610克),而一次性免疫调节减少占40.5%(30,227克中的12,237克)。此外,超过推荐剂量的订单绝对减少了16.9%(从20.8%降至3.9%;p < 0.0001)。不推荐和过量的IVIG剂量合计从19,975克(15.2%)降至6670克(6.6%)。
观察到IVIG使用总体减少,不推荐订单优先减少,这很可能归因于所实施的一系列限制性策略。