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Replacement of Mycophenolate Acid With Everolimus in Patients Who Became Neutropenic After Renal Transplant

机译:肾移植后中性粒细胞减少的患者用依维莫司替代霉酚酸

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Objectives: Neutropenia after kidney transplant is an adverse event usually treated with a dosage reduction of mycophenolic acid. We evaluated the efficacy and safety of substituting mycophenolic acid with everolimus in patients with persistent neutropenia after kidney transplant. Materials and Methods: This study was a retrospective analysis. A total of 17 patients who were initially treated with mycophenolic acid (1912 ± 196 mg/d), calcineurin inhibitors, and methylprednisolone for kidney transplant were included. Results: In 15 patients, neutropenia occurred within the first 3 months (during valganciclovir administration), and in 2 patients between the fourth and sixth month after transplant. One hundred eighteen episodes of neutropenia were recorded, originally treated by reducing the dosage of mycophenolic acid (765 ± 390 mg/d) and administering granulocyte colony-stimulating factor. Three patients experienced acute rejection 5 to 10 days after reducing the dosage of mycophenolic acid, and they were successfully treated with pulse steroids. Five patients developed cytomegalovirus infection 108 ± 65 days after the onset of neutropenia. After replacing mycophenolic acid with everolimus, episodes of neutropenia were observed in 6 patients. In 1 patient, discontinuing everolimus was necessary after 1.5 months of treatment. In 5 patients with cytomegalovirus infection, neutropenia subsided after termination of valganciclovir treatment. In the remaining 11 patients, no episodes of neutropenia were observed. No episodes of acute rejection occurred, and renal function remained stable during a follow-up of 47 ± 30 months (estimated glomerular filtration rate [eGFR MDRD6 ]: 45 ± 14 mL/min/1.73 m 2 → 47 ± 22 mL/min/1.73 m 2 ]. Conclusions: Replacing mycophenolic acid with everolimus appears to be a safe and effective alternative treatment in neutropenic renal transplant recipients.
机译:目的:肾移植后的中性粒细胞减少是一种不良事件,通常可通过减少麦考酚酸的剂量治疗。我们评估了依维莫司替代麦考酚酸在肾移植术后持续中性粒细胞减少症患者中的疗效和安全性。材料与方法:本研究为回顾性分析。总共包括最初接受麦考酚酸(1912±196 mg / d),钙调神经磷酸酶抑制剂和甲基强的松龙用于肾脏移植的17位患者。结果:在15例患者中,中性粒细胞减少症发生在前3个月内(缬更昔洛韦给药期间),而2例患者在移植后的第四个月至第六个月之间发生。记录了118例中性粒细胞减少症,最初是通过减少霉酚酸的剂量(765±390 mg / d)和给予粒细胞集落刺激因子来治疗的。 3例患者在降低麦考酚酸剂量后5至10天出现了急性排斥反应,并成功接受了脉冲类固醇治疗。中性粒细胞减少症发作后108±65天,有五名患者发生巨细胞病毒感染。用依维莫司代替麦考酚酸后,有6例患者出现中性粒细胞减少症。 1名患者在治疗1.5个月后必须停用依维莫司。在5例巨细胞病毒感染患者中,缬更昔洛韦治疗终止后中性粒细胞减少症消退。在其余11例患者中,未观察到中性粒细胞减少症发作。在47±30个月的随访中,没有发生急性排斥反应,并且肾功能保持稳定(估计肾小球滤过率[eGFR MDRD6]:45±14 mL / min / 1.73 m 2→47±22 mL / min / 1.73 m 2]。结论:用依维莫司代替麦考酚酸似乎是中性粒细胞减少性肾移植受者的一种安全有效的替代疗法。

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