Brandenburg Nancy A, Bwire Robert, Freeman John, Houn Florence, Sheehan Paul, Zeldis Jerome B
Celgene Corporation, 556 Morris Ave, Summit, NJ, 07901, USA.
Drug Saf. 2017 Apr;40(4):333-341. doi: 10.1007/s40264-016-0501-2.
The effectiveness of patient education activities conducted within the lenalidomide and thalidomide risk evaluation and mitigation strategies (REMS) programs was evaluated by measuring understanding of serious risk and safe-use messages.
Results from mandatory knowledge, attitude, and behavior surveys and voluntary patient surveys completed between June 2012 and June 2013 were analyzed, and responses to questions relating to compliance with birth control measures and understanding of safe-use messages are presented by patient risk category.
In total, 73,645 patients were enrolled into the REMS programs for lenalidomide and thalidomide and completed mandatory surveys prior to medication dispense. Of these, 2790 (3.8%) completed an additional voluntary survey. Among voluntary survey participants, for all patient pregnancy risk categories, reported compliance with birth control requirements was above 90% when starting therapy and at follow-up. At the beginning of therapy, complete compliance was 96.3%; 3 months later it was 96.4%. Patient understanding of safe-use messages was very high in all pregnancy risk groups, notably for messages repeated at each physician visit. Overall, 98.2% of patients knew that lenalidomide and thalidomide could cause birth defects, which is part of the repeated educational messaging. In contrast, 87.1% recalled that unused product should be returned to their healthcare professional, which is not included in repeated messaging.
The lenalidomide and thalidomide REMS programs enhance patient understanding of safe-use messages, resulting in high levels of compliance with the birth control precautions essential to prevent fetal exposure to these known and potential human teratogens. Overall compliance was maintained after 3 months of follow-up and throughout therapy.
通过衡量对严重风险和安全用药信息的理解,对在来那度胺和沙利度胺风险评估与降低策略(REMS)项目中开展的患者教育活动的有效性进行了评估。
分析了2012年6月至2013年6月期间完成的强制性知识、态度和行为调查以及自愿性患者调查的结果,并按患者风险类别呈现了与遵守避孕措施及对安全用药信息的理解相关问题的回答。
共有73645名患者纳入来那度胺和沙利度胺的REMS项目,并在配药前完成了强制性调查。其中,2790名(3.8%)完成了额外的自愿性调查。在自愿性调查参与者中,对于所有患者妊娠风险类别,在开始治疗时及随访时报告的遵守避孕要求情况均高于90%。在治疗开始时,完全遵守率为96.3%;3个月后为96.4%。在所有妊娠风险组中,患者对安全用药信息的理解程度都很高,尤其是每次医生就诊时重复提及的信息。总体而言,98.2%的患者知道来那度胺和沙利度胺可导致出生缺陷,这是重复教育信息的一部分。相比之下,87.1%的患者记得未使用的产品应返还给其医疗保健专业人员,这并未包含在重复信息中。
来那度胺和沙利度胺REMS项目增强了患者对安全用药信息的理解,从而使患者高度遵守预防胎儿接触这些已知及潜在人类致畸剂所必需的避孕预防措施。在随访3个月及整个治疗过程中,总体遵守情况得以维持。