Department of Internal Medicine, Division of Gastroenterology and Hepatology, Maastricht University Medical Center+, Maastricht, The Netherlands.
NUTRIM - School for Nutrition and Translational Research in Metabolism, Maastricht University Medical Center, Maastricht, The Netherlands.
J Gastroenterol Hepatol. 2018 Feb;33(2):426-430. doi: 10.1111/jgh.13920.
Biologicals are potent drugs for immune-mediated inflammatory diseases. After discontinuation or switch of therapy, many patients have unused biological injectors left. This study aimed to evaluate potential redistribution of unused injectors to prevent spillage of these costly drugs by assessing (i) the quality of transport and home storage through the proportion of injectors stored within the recommended temperature range (2-8 °C) and (ii) acceptance of redistribution by patients.
All golimumab users, irrespective of the indication, at Maastricht University Medical Center were eligible for inclusion. Patients received golimumab in a sealed bag containing a validated temperature sensor, measuring temperature every 5 min. Patients were asked to store their medication as usual. Deviations from the recommended range were defined as any duration below 0 °C and > 30 min below 2 °C or above 8 °C. After 3 months, patients completed a questionnaire on their opinion towards potential redistribution of unused biologicals.
Fifty patients (42.0% male, mean age 53.2 ± 14.3 years) received 276 injectors. The mean storage time was 30.9 ± 33.1 days. Only 11.6% of the injectors were stored within the recommended temperature range. In addition, 11.2% were stored > 30 min below 0 °C and 33.2% were stored > 1 week above 8 °C. Of all patients, 95% would accept redistributed medication when product quality is ensured.
During transport and home storage, only one in eight biological injectors was stored within the recommended temperature range. This hinders redistribution of unused injectors but also raises concern regarding drug effectiveness in immune-mediated inflammatory disease patients.
生物制剂是治疗免疫介导性炎症性疾病的强效药物。在停止治疗或换药后,许多患者仍有未使用的生物制剂注射器。本研究旨在评估未使用注射器的潜在再分配情况,以防止这些昂贵药物的浪费,并通过以下两种方法来实现:(i)通过处于推荐温度范围(2-8°C)内的注射器比例来评估运输和家庭储存的质量,(ii)评估患者对再分配的接受程度。
所有在马斯特里赫特大学医学中心使用戈利木单抗的患者(无论适应证如何)均符合纳入标准。患者使用的戈利木单抗装在一个密封袋中,其中包含一个经过验证的温度传感器,每 5 分钟测量一次温度。患者被要求按常规方式储存药物。任何低于 0°C 的持续时间以及低于 2°C 或高于 8°C 的持续时间超过 30 分钟均被定义为偏离推荐范围。3 个月后,患者完成一份关于他们对未使用生物制剂潜在再分配意见的问卷。
50 名患者(42.0%为男性,平均年龄 53.2±14.3 岁)共接受了 276 个注射器。平均储存时间为 30.9±33.1 天。只有 11.6%的注射器处于推荐温度范围内。此外,11.2%的注射器在 0°C 以下储存超过 30 分钟,33.2%的注射器在 8°C 以上储存超过 1 周。所有患者中,95%的患者在确保产品质量的情况下会接受再分配的药物。
在运输和家庭储存过程中,只有八分之一的生物制剂注射器处于推荐的温度范围内。这不仅阻碍了未使用注射器的再分配,还引起了人们对免疫介导性炎症性疾病患者药物疗效的担忧。