Hamed Eman Mostafa, Meabed Mohamed Hussein, Ibrahim Ahmed R N, Khalaf Ahmed M, El Demerdash Doaa Mohamed, Elgendy Marwa O, Saeed Haitham, Mahmoud Tamer M, Salem Heba F, Rabea Hoda
Department of Clinical Pharmacy, Faculty of Pharmacy, Nahda University (NUB), Beni-Suef 62521, Egypt.
Department of Pediatrics and Hematology, Faculty of Medicine, Beni-Suef University, Beni-Suef 62521, Egypt.
Medicina (Kaunas). 2023 Sep 11;59(9):1645. doi: 10.3390/medicina59091645.
Immune thrombocytopenia (ITP) is an autoimmune bleeding disorder caused by antigen-specific T cells and antiplatelet autoantibodies that inhibit platelet production in the bone marrow or destroy platelets in the spleen. ITP is a form of autoimmunity and is closely associated with inflammation. Corticosteroids are the first-line therapy for ITP, with a total response rate of 53-80%. However, corticosteroid therapy is associated with significant side effects and is often ineffective in patients with corticosteroid-resistant or -intolerant disease. Eltrombopag has been validated as a second-line option in ITP therapy. Despite several studies demonstrating the efficacy and safety of Eltrombopag in immune thrombocytopenia patients, the prevalence of Eltrombopag-induced acute kidney injury has been observed. This case report describes a patient who experienced acute kidney injury during Eltrombopag therapy. A sudden increase in serum creatinine to 6.7 mg/dL and metabolic acidosis occurred after eight weeks of Eltrombopag. The patient's renal failure had worsened, proteinuria was detected, and emergency hemodialysis was initiated. With vigilant kidney function screening and prompt treatment, the patient's renal function improved remarkably following cessation of Eltrombopag and initiation of hemodialysis. This case highlights the importance of comprehensive medication history-taking and vigilant kidney function screening in patients receiving Eltrombopag.
免疫性血小板减少症(ITP)是一种自身免疫性出血性疾病,由抗原特异性T细胞和抗血小板自身抗体引起,这些抗体抑制骨髓中的血小板生成或破坏脾脏中的血小板。ITP是自身免疫的一种形式,与炎症密切相关。皮质类固醇是ITP的一线治疗药物,总有效率为53%-80%。然而,皮质类固醇治疗伴有显著的副作用,并且在皮质类固醇抵抗或不耐受的患者中往往无效。艾曲泊帕已被证实是ITP治疗的二线选择。尽管多项研究证明了艾曲泊帕在免疫性血小板减少症患者中的疗效和安全性,但已观察到艾曲泊帕引起急性肾损伤的情况。本病例报告描述了一名在接受艾曲泊帕治疗期间发生急性肾损伤的患者。服用艾曲泊帕八周后,血清肌酐突然升至6.7mg/dL,并出现代谢性酸中毒。患者的肾衰竭加重,检测到蛋白尿,并开始进行紧急血液透析。通过对肾功能的密切筛查和及时治疗,在停用艾曲泊帕并开始血液透析后,患者的肾功能显著改善。本病例强调了在接受艾曲泊帕治疗的患者中全面记录用药史和密切筛查肾功能的重要性。