糖皮质激素治疗阵发性夜间血红蛋白尿的局限性和挑战。

Q3 Medicine
B Han
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引用次数: 0

摘要

阵发性夜间血红蛋白尿(Paroxysmal nocturnal hemoxybinuia, PNH)是一种罕见的获得性造血干细胞疾病,主要发生于青壮年,以骨髓衰竭、持续性血管内溶血和血栓形成为特征,均可造成严重的终末器官损害,增加早期死亡的风险,给患者带来严重的疾病负担。在中国,由于历史原因,糖皮质激素在许多地方仍被常规使用。然而,糖皮质激素对PNH溶血的影响尚不确定。目前尚缺乏糖皮质激素治疗PNH的循证医学数据和临床益处,但长期使用糖皮质激素会显著增加患者不良反应的风险。由于PNH需要终身随访和管理,长期糖皮质激素治疗不可避免地会严重损害患者的健康。因此,无论是国内外指南还是专家共识,糖皮质激素都不推荐用于PNH的治疗。本文阐述了糖皮质激素治疗PNH的局限性和挑战,以鼓励更有效和安全的治疗策略在中国被接受。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Limitations and challenges of glucocorticoids in the treatment of paroxysmal nocturnal hemoglobinuria].

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare acquired hematopoietic stem cell disease that mainly occurs in young adults and is characterized by bone marrow failure, persistent intravascular hemolysis and thrombosis, all of which can cause severe end-organ damage, increase the risk of early death, and cause a severe disease burden in patients. In China, based on the historic reasons, glucocorticoids are still routinely used in many places. However, the effects of glucocorticoids on PNH hemolysis are uncertain. Evidence-based medical data and clinical benefits for glucocorticoid on PNH are missing, but the long-term use of glucocorticoids significantly increases the risk of adverse reactions in patients. Since PNH needs a lifelong follow-up and management, long-term glucocorticoid therapy will unavoidably seriously damage the health of patients. Therefore, glucocorticoids are not recommended for the treatment of PNH, either from domestic or overseas guidelines, or expert consensus. In this article, the limitations and challenges of glucocorticoids in the treatment of PNH were expounded upon, in order to encourage more effective and safe strategies to be accepted in China.

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CiteScore
0.80
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