甲氨蝶呤毒性——敲响警钟!

Pooja Agarwal, Snehal V. Chaudhari, Kalgi Baxi, Sabha Neazee, Sohini Soneji, Malhar J. Shah
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摘要

自1951年问世以来,甲氨蝶呤(MTX)被广泛用作抗银屑病的主要药物。然而,患者在无监督的情况下给药或同时使用过量的非甾体抗炎药(NSAIDs)可导致毒性。胃肠道症状是最常见的表现,其次是皮肤毒性。在古吉拉特邦的一家三级医疗中心进行的这项回顾性研究中,分析了2017年4月至2019年12月期间因MTX毒性入院的患者的数据。收集和评估详细的病史,包括剂量、持续时间、体征和症状、调查、治疗和结果。该研究包括12例MTX毒性住院患者(年龄35-70岁)。其中银屑病10例,银屑病关节炎1例,类风湿性关节炎合并盘状红斑狼疮1例。11名患者在服用止痛药的同时每天服用口服甲氨蝶呤,持续一周,而一名患者在没有接受任何调查的情况下服用了数量不详的甲氨蝶呤。所有病例均出现粘膜溃疡,2例出现皮肤坏死。血液学检查显示所有患者骨髓抑制,1例患者肾功能改变。所有患者均给予亚叶酸素(15mg /ml)治疗,10例患者出现改善,但2例患者出现持续的骨髓抑制并因毒性而死亡。本研究强调治疗前调查、适当监测和严格避免使用甲氨蝶呤时自我给药的重要性。此外,非甾体抗炎药等药物的联合用药应谨慎管理。亚叶酸在甲氨蝶呤中毒和过量的情况下显示有用。总之,这项研究强调了谨慎给药和监测MTX的重要性,同时避免自行给药。它强调了审慎使用联合用药的必要性,并强调了亚叶酸在MTX毒性和用药过量管理中的作用。
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Methotrexate toxicity-an alarming bell!
Since its introduction in 1951, methotrexate (MTX) has been widely used as the primary anti-psoriatic agent. However, unsupervised dosing by patients or concurrent use of excessive nonsteroidal anti-inflammatory drugs (NSAIDs) can lead to toxicity. Gastrointestinal symptoms are the most commonly observed manifestations, followed by cutaneous toxicity. In this retrospective study conducted at a tertiary care center in Gujarat, data from patients admitted for MTX toxicity between April 2017 and December 2019 were analyzed. A detailed history, including dosage, duration, signs and symptoms, investigations, treatment, and outcomes, was collected and evaluated. The study included 12 hospitalized patients (aged 35-70 years) with MTX toxicity. Among them, 10 patients had psoriasis, 1 had psoriatic arthritis, and 1 had rheumatoid arthritis with discoid lupus erythematosus. Eleven patients had taken daily oral MTX for one week along with painkillers, while one patient had taken an unknown amount without undergoing any investigations. Mucosal ulceration was observed in all cases, and skin necrosis was seen in 2 patients. Hematological investigations revealed myelosuppression in all patients, with altered renal function in 1 patient. Leucovorin (15 mg/ml) was administered to all patients, resulting in improvement for 10 patients, but 2 patients experienced persistent myelosuppression and succumbed to the toxicity. This study emphasizes the importance of pre-treatment investigations, proper monitoring, and strict avoidance of self-administration when administering MTX. Additionally, the co-administration of drugs such as NSAIDs should be judiciously managed. Folinic acid has shown usefulness in cases of MTX toxicity and overdose. In summary, this study underscores the significance of careful administration and monitoring of MTX, along with the avoidance of self-dosing. It highlights the need for judicious use of co-administered medications, and emphasizes the utility of folinic acid in managing MTX toxicity and overdose.
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