Knowing Your Target: Altered Mental Status From an Unsuspected Source

Sarah Hemstetter, MSN, CRNP, AOCNP
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Abstract

Daratumumab is a human monoclonal antibody targeting CD38 that is used in the treatment of multiple myeloma. In addition to being a target for cancer-related treatment, CD38 also plays a significant role in the immune response to infection. CD38 deficiency can increase susceptibility to several bacterial infections. This article discusses the case of a 52-year-old female with a history of IgG multiple myeloma status post autologous stem cell transplant with relapse who was receiving therapy with daratumumab, lenalidomide, and dexamethasone. She presented to the emergency department with a history of 3 to 4 days of generalized weakness, poor appetite, nausea, vomiting, watery stools, and fevers. Her symptoms did not improve with initial fluid resuscitation and broad-spectrum antimicrobials; instead, she experienced progressive neurological decline. This case illustrates how utilizing targets for cancer-directed treatments can also affect immune function, which may leave patients susceptible to unique infections that may not otherwise be commonly encountered. Therefore, advanced practitioners must understand the functional role of these targets and the sequelae that could occur when expression is altered by pharmacological therapies to allow for expeditious recognition and management.
了解你的目标:从一个未知的来源改变精神状态
Daratumumab是一种靶向CD38的人单克隆抗体,用于多发性骨髓瘤的治疗。除了作为癌症相关治疗的靶点外,CD38在感染的免疫反应中也起着重要作用。CD38缺乏会增加对几种细菌感染的易感性。本文讨论了一例52岁女性,自体干细胞移植后IgG多发性骨髓瘤复发病史,接受达拉单抗、来那度胺和地塞米松治疗。她以3至4天的全身性虚弱、食欲不振、恶心、呕吐、水样便和发烧病史就诊于急诊科。她的症状在最初的液体复苏和广谱抗菌素治疗后没有改善;相反,她的神经功能出现了进行性衰退。这个案例说明了利用癌症靶向治疗也会影响免疫功能,这可能会使患者容易受到原本不常见的独特感染。因此,高级从业者必须了解这些靶点的功能作用,以及当药物治疗改变表达时可能发生的后遗症,以便快速识别和管理。
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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