Severe MTX Toxicity in Rheumatic Diseases - Analysis of 22 Cases

R. Bergner, D. Wadsack, C. Löffler
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引用次数: 1

Abstract

Background: Severe MTX (methotrexate) toxicity due to low dose MTX used in rheumatic diseases is rare but linked with a high mortality ranging from 13 to 44%. We analyzed 22 cases with a minimum toxicity of CTC (common toxicity criteria) grade 2, that were admitted to our hospital. Methods: We retrospectively analyzed epidemiological data, the weekly MTX dosage, renal function before and at the beginning of the adverse event, co-medication with influence on MTX toxicity or on renal function and potential other co-factors like infections, as well as the outcome, respectively. Results: 22 patients were involved in the study. Three patients died due to pneumonia, all other patients recovered. The main reason for toxicity was an impaired renal function (82%), either from acute renal failure or from acute on chronic renal failure or chronic renal disease stage 4. In 5 cases a dosing error, mainly with daily instead of weekly MTX intake, was the reason. Only in one case the reason remains unclear. Discussion: An impaired renal function with an estimated glomerular filtration rate (eGFR) of 11-54 ml/min was the main cause for MTX toxicity with dosage errors being the second numerous reasons. Our data are in accordance with previous case series, but the influence of reduced renal function is still higher than in the most reports. One reason might be that most case series took only into account the serum creatinine but not a calculated GFR. Serum creatinine alone underestimates the stage of renal failure in patients with lower muscle mass.
甲氨蝶呤在风湿病中的严重毒性22例分析
背景:由于用于风湿病的低剂量甲氨蝶呤引起的严重甲氨蝶呤毒性很少见,但与13%至44%的高死亡率相关。我们分析了22例最低毒性为CTC(常见毒性标准)2级的住院患者。方法:回顾性分析流行病学资料、不良事件发生前和开始时甲氨喋呤周剂量、肾功能、联合用药对甲氨喋呤毒性或肾功能的影响以及感染等潜在的其他辅助因素以及结局。结果:22例患者纳入研究。3名患者死于肺炎,其余患者均已康复。毒性的主要原因是肾功能受损(82%),无论是急性肾功能衰竭还是急性或慢性肾功能衰竭或慢性肾脏疾病4期。在5例病例中,剂量错误是主要原因,主要是每天而不是每周服用MTX。只有一个案例的原因尚不清楚。讨论:估计肾小球滤过率(eGFR)为11-54 ml/min的肾功能受损是MTX毒性的主要原因,剂量错误是第二个众多原因。我们的数据与以前的病例系列一致,但肾功能下降的影响仍然高于大多数报道。一个原因可能是大多数病例序列只考虑了血清肌酐而没有计算GFR。血清肌酐单独低估了低肌肉量患者肾功能衰竭的分期。
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