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An unusual case of acute kidney injury due to vancomycin lessons learnt from reliance on eGFR.

机译:因依赖eGFR而吸取的万古霉素教训,导致一例罕见的急性肾损伤。

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We present a case of renal impairment in an emaciated HIV-infected male that initially went unrecognized because of reliance on serum creatinine and estimated glomerular filtration rate (eGFR). Inaccurate vancomycin dosing led to toxic drug levels (66 mg/l), associated with acute and severe worsening of kidney function. This occurred in the context of escalating doses of vancomycin given in the presence of changing kidney function, albeit kidney function that always remained well within the normal range (serum creatinine 29 - 42 mumol/l). In the absence of other plausible explanations, a presumptive diagnosis of vancomycin nephrotoxicity was made. Given the rarity of this diagnosis in the current era, we discuss the pathophysiology of vancomycin nephrotoxicity. We also explore the potential reasons for inaccuracy of GFR prediction equations in the HIV population, and discuss the potential pitfalls associated with application of eGFR or even serum creatinine without appropriate understanding of their limitations. We believe our case highlights a number of important teaching points:Vancomycin nephrotoxitiy is rare but can occur in the setting of kidney dysfunction. Current assessment of kidney function using creatinine and eGFR requires awareness of the clinical caveats in which these measures may be misleading. Acute changes in kidney function, irrespective of the test used, should be contextualized to the individual situation. Persons with HIV and low muscle mass constitute a specific subgroup in whom assessment of kidney function may be problematic using creatinine. We support ongoing efforts to develop or refine equations for specific unique and easily identifiable populations.
机译:我们提出了一个瘦弱的艾滋病毒感染的男性肾功能损害的案例,该患者最初由于依赖血清肌酐和估计的肾小球滤过率(eGFR)而无法识别。万古霉素剂量不正确会导致毒性药物水平(66 mg / l),与肾功能的急性和严重恶化有关。这是在肾脏功能改变的情况下,万古霉素剂量不断增加的情况下发生的,尽管肾脏功能始终保持在正常范围内(血清肌酐为29-42摩尔/升)。在没有其他合理解释的情况下,作出万古霉素肾毒性的推定诊断。鉴于当前这一诊断的罕见性,我们讨论了万古霉素肾毒性的病理生理学。我们还探讨了HIV人群中GFR预测方程式不准确的潜在原因,并讨论了与eGFR甚至血清肌酐应用相关的潜在陷阱,而没有适当了解它们的局限性。我们认为我们的病例突出了许多重要的教学要点:万古霉素肾毒性罕见,但可能在肾功能不全的情况下发生。当前使用肌酐和eGFR评估肾功能需要了解可能会引起误解的临床注意事项。不论使用哪种测试,肾脏功能的急性变化都应根据具体情况而定。艾滋病毒和低肌肉量人群是一个特定的亚组,使用肌酐可能无法评估肾脏功能。我们支持为特定或易于识别的特定人群开发或完善方程式的持续努力。

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