Bahrami Simin, Raman Steven S, Sauk Steven, Salehmoghaddam Saleh, Villablanca Juan Pablo, Finn J Paul, Lu David S K
Department of Radiological Sciences, Ronald Reagan UCLA Medical Center, Los Angeles, CA 90095-7437, USA.
J Comput Assist Tomogr. 2009 Nov-Dec;33(6):819-23. doi: 10.1097/RCT.0b013e31819d68ed.
To analyze all cases of nephrogenic systemic fibrosis (NSF) at our institution and to compare them with controls.
After the institutional review board approval, 13 biopsy-proven NSF cases were identified. Ten cases had complete records and were compared in a case-control format with 10 age- and sex-matched, dialysis-dependent controls. Analyzed risk factors included single and cumulative gadolinium dose, medication and transplant history, and serum electrolytes at the time of gadolinium exposure.
There were 1.9% of dialysis-dependent, gadolinium-exposed patients who developed NSF. There was no difference in gadolinium dose, transplant history, or serum electrolytes. Seven of 10 cases and 3 of 10 controls were treated with erythropoietin (P = 0.13). At the time of NSF diagnosis, 7 of 10 cases were on immunosuppressive therapy. Two of 7 cases developed NSF only after immunosuppressive therapy was initiated. Two of 10 controls were on immunosuppressive therapy (P = 0.06).
All cases of NSF occurred in dialysis-dependent, gadolinium-exposed patients. Associations between immunosuppressive and erythropoietin therapies and NSF need further investigation.
分析我院所有肾源性系统性纤维化(NSF)病例,并与对照组进行比较。
经机构审查委员会批准后,确定了13例经活检证实的NSF病例。其中10例有完整记录,并与10例年龄和性别匹配、依赖透析的对照者以病例对照形式进行比较。分析的危险因素包括钆的单次和累积剂量、用药及移植史,以及钆暴露时的血清电解质。
依赖透析且暴露于钆的患者中,NSF发病率为1.9%。钆剂量、移植史或血清电解质方面无差异。10例病例中有7例、10例对照中有3例接受了促红细胞生成素治疗(P = 0.13)。在NSF诊断时,10例病例中有7例正在接受免疫抑制治疗。7例病例中有2例仅在开始免疫抑制治疗后才发生NSF。10例对照中有2例正在接受免疫抑制治疗(P = 0.06)。
所有NSF病例均发生在依赖透析且暴露于钆的患者中。免疫抑制治疗和促红细胞生成素治疗与NSF之间的关联需要进一步研究。