首页> 外文期刊>International journal of clinical pharmacology and therapeutics >Different time courses of nephrogenic systemic fibrosis: Is there a role for pharmacokinetic aspects in explaining a new clinical entity?
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Different time courses of nephrogenic systemic fibrosis: Is there a role for pharmacokinetic aspects in explaining a new clinical entity?

机译:肾源性系统纤维化的不同时程:药代动力学方面在解释新的临床实体方面是否有作用?

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OBJECTIVE: To report 3 cases of nephrogenic systemic fibrosis (NSF) focussing on the time course of clinical symptoms after exposure to gadolinium based contrast agents (GBCA) and to discuss pharmacokinetic aspects of commercially available GBCA. PATIENTS' DETAILS: All 3 patients (2 men, 1 woman, aged 51 - 54 years) suffered from end-stage renal disease (ESRD) and were on long-term dialysis. Linear GBCA compounds were given to all patients and NSF symptoms started 6 months, 1 and 4 years after the last GBCA exposure. In 2 patients, GBCA was administered after the occurrence of (unrecognized) NSF symptoms leading to worsening of clinical courses. 1 of the patients received multiple therapies (e.g. UV-A1 treatment, physical therapy) without significant improvement, 2 patients died from cardiac complications shortly after the diagnosis of NSF. CONCLUSION: NSF may develop after a longer period of time than generally reported and GBCA administration may aggravate or accelerate chronic, subclinical NSF symptoms.
机译:目的:报告3例肾源性系统性纤维化(NSF)病例,重点是暴露于g基造影剂(GBCA)后的临床症状时程,并讨论市售GBCA的药代动力学方面。患者详细信息:所有3例患者(2例男性,1例女性,年龄51-54岁)均患有终末期肾病(ESRD),并接受长期透析。所有患者均接受线性GBCA化合物,并且在最后一次GBCA暴露后6个月,1年和4年开始出现NSF症状。在2例患者中,发生(无法识别的)NSF症状导致临床病情恶化后,给予了GBCA。其中1例患者接受了多种疗法(例如UV-A1治疗,物理疗法),但无明显改善; 2例患者在NSF诊断后不久因心脏并发症死​​亡。结论:NSF可能在比一般报道更长的时间后发展,并且GBCA给药可能加重或加速慢性亚临床NSF症状。

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