{"title":"不良临床事件报告","authors":"J. Dill, T. Mcevoy","doi":"10.1177/00694770211007805","DOIUrl":null,"url":null,"abstract":"A 68-year-old woman developed a diffuse rash and a fever approximately 1 month after starting atorvastatin (20 mg nightly) following mitral valve replacement. Concurrent medications included digoxin (0.125 mg daily), furosemide (20 mg twice daily), potassium chloride (1 g twice daily), and warfarin (0.625 mg nightly). Laboratory findings included albumin (34.6 g/L), -glutamyl transpeptidase (45 units/L), glucose (13.24 mmol/L), creatine kinase MB subtype (18.0 units/L), creatine kinase (20 units/L), lactic dehydrogenase (398 units/L), sodium (135.9 mmol/L), leukocyte count (5.19 10/L), hemoglobin (98.0 g/L), platelet count (267 g/L), procalcitonin (0.130 ng/mL), and fibrinogen (4.35 g/L). Treatment included discontinuation of all drugs used prior to admission and administration of loratadine (10 mg daily), cetirizine (10 mg daily), vitamin C (100 mg 3 times daily), methylprednisolone (120 mg every 12 hours), intravenous omeprazole (40 mg every 12 hours), calamine, and ethacridine. A large number of blisters covering greater than 30% of the body appeared the next day, accompanied by fever. Additional treatment included administration of intravenous human immunoglobulin. The facial skin began to peel, and the trunk blisters ruptured. Mupirocin was applied topically. A new red patchy rash appeared on the lower extremities. On day 17, the face of the skin and trunk was mostly healed. After 60 days, the skin had regrown. HLA allele detection revealed the HLA-A*2:07, HLA-A*11:01, HLAB*15:02, HLA-B*40:01, HLA-C*3:04, and HLA-C*08:01 alleles. The authors concluded that this case described toxic epidermal necrolysis associated with atorvastatin. They proposed that the mutant HLA genotypes carried may have a correlation with Stevens-Johnson syndrome and toxic epidermal necrolysis. Atorvastatin [“Lipitor”] Lv M et al (J Zhang, Department of Pharmacy, Fujian Medical University Union Hospital, #29 Xinquan Rd, Fuzhou 350001, China; e-mail: pollyzhang2006@126.com) Toxic epidermal necrolysis in a patient on atorvastatin expressing human leukocyte antigen alleles: a case report. Medicine (Baltimore) 100:e24391 (Jan) 2021","PeriodicalId":102871,"journal":{"name":"Clin-Alert®","volume":"41 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reporting on Adverse Clinical Events\",\"authors\":\"J. Dill, T. Mcevoy\",\"doi\":\"10.1177/00694770211007805\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A 68-year-old woman developed a diffuse rash and a fever approximately 1 month after starting atorvastatin (20 mg nightly) following mitral valve replacement. Concurrent medications included digoxin (0.125 mg daily), furosemide (20 mg twice daily), potassium chloride (1 g twice daily), and warfarin (0.625 mg nightly). Laboratory findings included albumin (34.6 g/L), -glutamyl transpeptidase (45 units/L), glucose (13.24 mmol/L), creatine kinase MB subtype (18.0 units/L), creatine kinase (20 units/L), lactic dehydrogenase (398 units/L), sodium (135.9 mmol/L), leukocyte count (5.19 10/L), hemoglobin (98.0 g/L), platelet count (267 g/L), procalcitonin (0.130 ng/mL), and fibrinogen (4.35 g/L). Treatment included discontinuation of all drugs used prior to admission and administration of loratadine (10 mg daily), cetirizine (10 mg daily), vitamin C (100 mg 3 times daily), methylprednisolone (120 mg every 12 hours), intravenous omeprazole (40 mg every 12 hours), calamine, and ethacridine. A large number of blisters covering greater than 30% of the body appeared the next day, accompanied by fever. Additional treatment included administration of intravenous human immunoglobulin. The facial skin began to peel, and the trunk blisters ruptured. Mupirocin was applied topically. A new red patchy rash appeared on the lower extremities. On day 17, the face of the skin and trunk was mostly healed. After 60 days, the skin had regrown. HLA allele detection revealed the HLA-A*2:07, HLA-A*11:01, HLAB*15:02, HLA-B*40:01, HLA-C*3:04, and HLA-C*08:01 alleles. The authors concluded that this case described toxic epidermal necrolysis associated with atorvastatin. They proposed that the mutant HLA genotypes carried may have a correlation with Stevens-Johnson syndrome and toxic epidermal necrolysis. Atorvastatin [“Lipitor”] Lv M et al (J Zhang, Department of Pharmacy, Fujian Medical University Union Hospital, #29 Xinquan Rd, Fuzhou 350001, China; e-mail: pollyzhang2006@126.com) Toxic epidermal necrolysis in a patient on atorvastatin expressing human leukocyte antigen alleles: a case report. 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引用次数: 0
摘要
一名68岁女性在二尖瓣置换术后开始阿托伐他汀(每晚20毫克)约1个月后出现弥漫性皮疹和发烧。同时使用的药物包括地高辛(0.125 mg /天)、速尿(20 mg /天2次)、氯化钾(1 g /天2次)和华法林(0.625 mg /天)。实验室检查结果包括白蛋白(34.6 g/L)、-谷氨酰转肽酶(45单位/L)、葡萄糖(13.24 mmol/L)、肌酸激酶MB亚型(18.0单位/L)、肌酸激酶(20单位/L)、乳酸脱氢酶(398单位/L)、钠(135.9 mmol/L)、白细胞计数(5.1910/L)、血红蛋白(98.0 g/L)、血小板计数(267 g/L)、降钙素原(0.130 ng/mL)、纤维蛋白原(4.35 g/L)。治疗包括停用入院前使用的所有药物,并给予氯雷他定(每日10毫克)、西替利嗪(每日10毫克)、维生素C(100毫克,每日3次)、甲基强的松龙(每12小时120毫克)、静脉注射奥美拉唑(每12小时40毫克)、炉甘石和乙沙啶。第二天出现大量水泡,覆盖全身30%以上,并伴有发热。其他治疗包括静脉注射人免疫球蛋白。面部皮肤开始剥落,躯干的水泡破裂。局部应用莫匹罗星。下肢出现新的红色斑疹。第17天,面部皮肤和躯干基本愈合。60天后,皮肤再生了。HLA等位基因检测结果为HLA- a *2:07、HLA- a *11:01、HLAB*15:02、HLA- b *40:01、HLA- c *3:04、HLA- c *08:01等位基因。作者得出结论,该病例描述了与阿托伐他汀相关的中毒性表皮坏死松解。他们提出携带的突变HLA基因型可能与Stevens-Johnson综合征和中毒性表皮坏死松解有关。350001福州新泉路29号福建医科大学协和医院药剂科;表达人白细胞抗原等位基因的阿托伐他汀患者中毒性表皮坏死松解一例报告。医学(巴尔的摩)100:e24391 (Jan) 2021
A 68-year-old woman developed a diffuse rash and a fever approximately 1 month after starting atorvastatin (20 mg nightly) following mitral valve replacement. Concurrent medications included digoxin (0.125 mg daily), furosemide (20 mg twice daily), potassium chloride (1 g twice daily), and warfarin (0.625 mg nightly). Laboratory findings included albumin (34.6 g/L), -glutamyl transpeptidase (45 units/L), glucose (13.24 mmol/L), creatine kinase MB subtype (18.0 units/L), creatine kinase (20 units/L), lactic dehydrogenase (398 units/L), sodium (135.9 mmol/L), leukocyte count (5.19 10/L), hemoglobin (98.0 g/L), platelet count (267 g/L), procalcitonin (0.130 ng/mL), and fibrinogen (4.35 g/L). Treatment included discontinuation of all drugs used prior to admission and administration of loratadine (10 mg daily), cetirizine (10 mg daily), vitamin C (100 mg 3 times daily), methylprednisolone (120 mg every 12 hours), intravenous omeprazole (40 mg every 12 hours), calamine, and ethacridine. A large number of blisters covering greater than 30% of the body appeared the next day, accompanied by fever. Additional treatment included administration of intravenous human immunoglobulin. The facial skin began to peel, and the trunk blisters ruptured. Mupirocin was applied topically. A new red patchy rash appeared on the lower extremities. On day 17, the face of the skin and trunk was mostly healed. After 60 days, the skin had regrown. HLA allele detection revealed the HLA-A*2:07, HLA-A*11:01, HLAB*15:02, HLA-B*40:01, HLA-C*3:04, and HLA-C*08:01 alleles. The authors concluded that this case described toxic epidermal necrolysis associated with atorvastatin. They proposed that the mutant HLA genotypes carried may have a correlation with Stevens-Johnson syndrome and toxic epidermal necrolysis. Atorvastatin [“Lipitor”] Lv M et al (J Zhang, Department of Pharmacy, Fujian Medical University Union Hospital, #29 Xinquan Rd, Fuzhou 350001, China; e-mail: pollyzhang2006@126.com) Toxic epidermal necrolysis in a patient on atorvastatin expressing human leukocyte antigen alleles: a case report. Medicine (Baltimore) 100:e24391 (Jan) 2021