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2例成年溶血尿毒综合征患者的6-酮-前列环素F1α水平及前列环素治疗

6-keto-PGF1 alpha levels and prostacyclin therapy in 2 adult patients with hemolytic-uremic syndrome.

作者信息

Hautekeete M L, Nagler J M, Cuykens J J, Parizel G, Laekeman G M, Herman A G

出版信息

Clin Nephrol. 1986 Sep;26(3):157-9.

PMID:3533335
Abstract

Evidence supports the hypothesis that plasma prostacyclin activity is deficient in hemolytic-uremic syndrome (HUS). We studied 2 adult patients with HUS. Plasma levels of 6-keto-PGF1 alpha, the stable metabolite of prostacyclin, were measured by radioimmunoassay. Both patients were found to have elevated 6-keto-PGF1 alpha levels. These findings are in contradiction with the prostacyclin deficiency hypothesis and with earlier reports of low or undetectable plasma levels of this metabolite. The patients were treated with IV prostacyclin after a single plasma exchange. The first patient, admitted with advanced renal failure, obtained a rapid remission but renal function did not recover; the second patient, admitted with a less pronounced degree of renal failure, reacted slowly to therapy but renal function partially recovered. We believe that, if any benefit is to be expected from prostacyclin therapy in HUS, it should be started early in the course of the disease.

摘要

有证据支持这样的假说,即溶血尿毒综合征(HUS)患者存在血浆前列环素活性不足。我们研究了2例成年HUS患者。通过放射免疫分析法测定了前列环素的稳定代谢产物6-酮-前列腺素F1α的血浆水平。结果发现两名患者的6-酮-前列腺素F1α水平均升高。这些发现与前列环素缺乏假说以及此前关于该代谢产物血浆水平低或检测不到的报道相矛盾。在进行单次血浆置换后,对这两名患者使用静脉注射前列环素进行治疗。第一名患者入院时已处于晚期肾衰竭,病情迅速缓解,但肾功能未恢复;第二名患者入院时肾衰竭程度较轻,对治疗反应缓慢,但肾功能部分恢复。我们认为,如果要从前列环素治疗HUS中获得任何益处,应该在疾病病程早期开始治疗。

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