Suppr超能文献

无症状原发性胆汁性肝硬化。临床表现、组织学及青霉胺治疗结果

Asymptomatic primary biliary cirrhosis. Presentation, histology, and results with D-penicillamine.

作者信息

Fleming C R, Ludwig J, Dickson E R

出版信息

Mayo Clin Proc. 1978 Sep;53(9):587-93.

PMID:355732
Abstract

Of 103 patients with the syndrome of primary biliary cirrhosis (chronic, nonsuppurative destructive cholangitis) who entered a double-blind, randomized, controlled treatment trial with either D-penicillamine or placebo, 21 (20%) were asymptomatic with respect to their liver disease. Study of these 21 patients revealed that (1) 43% of patients with asymptomatic primary biliary cirrhosis had advanced histologic lesions (fibrosis or cirrhosis); (2) asymptomatic patients with advanced histologic lesions likely have had their disease for 10 years or more; (3) stage of primary biliary cirrhosis may remain unchanged for years; and (4) most asymptomatic patients receiving D-penicillamine, when compared with patients given placebo, had improved liver function tests at 1-year follow-up. However, the incidence of major toxicity with D-penicillamine for primary biliary cirrhosis in a maintenance dose of 1 g approximates 20%. Furthermore, one of our patients who was asymptomatic but who had advanced histologic changes died recently from D-penicillamine-associated bone marrow suppression. It remains to be determined whether the benefit-to-risk ratio of D-penicillamine in primary biliary cirrhosis justifies its use.

摘要

在103例原发性胆汁性肝硬化综合征(慢性、非化脓性破坏性胆管炎)患者中,有21例(20%)在肝脏疾病方面无症状,这些患者参与了一项双盲、随机、对照治疗试验,分别接受D-青霉胺或安慰剂治疗。对这21例患者的研究发现:(1)43%的无症状原发性胆汁性肝硬化患者存在组织学高级别病变(纤维化或肝硬化);(2)存在组织学高级别病变的无症状患者可能患病已达10年或更长时间;(3)原发性胆汁性肝硬化的阶段可能多年保持不变;(4)与接受安慰剂的患者相比,大多数接受D-青霉胺治疗的无症状患者在1年随访时肝功能检查有所改善。然而,维持剂量为1g的D-青霉胺用于原发性胆汁性肝硬化时,严重毒性的发生率约为20%。此外,我们有一名无症状但存在组织学高级别改变的患者最近死于与D-青霉胺相关的骨髓抑制。D-青霉胺用于原发性胆汁性肝硬化的利弊比是否合理仍有待确定。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验