Suppr超能文献

进行性系统性硬化症中的高血压与肾衰竭(硬皮病肾危象)。25年68例病例回顾。

Hypertension and renal failure (scleroderma renal crisis) in progressive systemic sclerosis. Review of a 25-year experience with 68 cases.

作者信息

Traub Y M, Shapiro A P, Rodnan G P, Medsger T A, McDonald R H, Steen V D, Osial T A, Tolchin S F

出版信息

Medicine (Baltimore). 1983 Nov;62(6):335-52. doi: 10.1097/00005792-198311000-00001.

Abstract

This paper reports the experiences of our group with 68 patients with progressive systemic sclerosis (PSS) admitted to hospitals of the University of Pittsburgh Health Center between 1955 and 1981 with scleroderma renal crisis (SRC). The onset of SRC was characterized by four features, namely, onset or aggravation, usually abrupt, of arterial hypertension; appearance of Grade III or IV retinopathy; elevations of peripheral renin activity to at least twice the upper limit of normal; and rapid deterioration of renal function within a period of less than one month. Over 90% of our patients in whom these criteria could be determined had at least three of them present with the onset of SRC. Management of these patients during the first 15 years of this period was uniformly ineffective. Before 1971, no patients lived longer than a year; usual survival ranged from 1 to 3 months. With the advent of renal dialysis and the more effective treatment of severe hypertension, along with the utilization of bilateral nephrectomy in selected anuric patients, some improvement in longevity was achieved. However, only in the past few years have we accumulated a group of 11 patients who have survived for longer than one year. The clinical characteristics of the onset and progression of SRC suggest the sudden imposition of severe stress such as cold or an autoimmune insult affecting vulnerable arteries and arterioles. The renal damage becomes self-perpetuating with extremely high renin activity causing further rise in blood pressure and additional renal and systemic vascular damage. Progress in the last few years seems to have been achieved primarily by the advent of pharmacologic agents that specifically block the effect of angiotensin II by inhibiting the angiotensin I converting enzyme. When diagnosis is prompt and the condition is treated as an emergency with these compounds, we and others have found that normal renal function can be restored in a number of patients. The result is a considerably brighter outlook for patients with this previously rapidly fatal complication of progressive systemic sclerosis.

摘要

本文报告了我们小组对1955年至1981年间收治于匹兹堡大学健康中心医院的68例进行性系统性硬化症(PSS)合并硬皮病肾危象(SRC)患者的治疗经验。SRC的发病具有四个特征,即动脉高血压通常突然发作或加重;出现III级或IV级视网膜病变;外周肾素活性升高至至少正常上限的两倍;以及在不到一个月的时间内肾功能迅速恶化。在我们能够确定这些标准的患者中,超过90%在SRC发作时至少出现其中三项特征。在此期间的前15年,对这些患者的治疗均无效。1971年以前,没有患者存活超过一年;通常的存活时间为1至3个月。随着肾透析的出现以及对重度高血压更有效的治疗,再加上对某些无尿患者采用双侧肾切除术,患者的寿命有了一定改善。然而,直到最近几年,我们才积累了一组11例存活超过一年的患者。SRC发作和进展的临床特征表明,突然遭受严重应激,如寒冷或自身免疫性损伤,影响了脆弱的动脉和小动脉。肾损伤会因极高的肾素活性而自我持续,导致血压进一步升高以及额外的肾和全身血管损伤。过去几年的进展似乎主要得益于出现了通过抑制血管紧张素I转换酶来特异性阻断血管紧张素II作用的药物。当诊断及时且用这些药物将病情作为紧急情况进行治疗时,我们和其他人发现许多患者的肾功能可以恢复。对于这种以前进展性系统性硬化症的快速致命并发症患者来说,结果是前景大为光明。

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