Juan A Vasquez Vasquez, Kyle D Pires, Belbina J Pereira, Kimberly M Brown, James A Langston, Charles E Langs, Robert S Hoffman
{"title":"缬昔洛韦剂量过大对5期慢性肾病老年妇女的神经毒性","authors":"Juan A Vasquez Vasquez, Kyle D Pires, Belbina J Pereira, Kimberly M Brown, James A Langston, Charles E Langs, Robert S Hoffman","doi":"10.1002/bcp.70138","DOIUrl":null,"url":null,"abstract":"<p><p>Unadjusted doses of valacyclovir can cause neurotoxicity in patients with chronic kidney disease. There are no well documented reports of valacyclovir or acyclovir toxicity providing pre- and postdialysis concentrations of acyclovir in the blood, dialysate and urine of acutely neurotoxic patients. We report an elderly woman with stage 5 chronic kidney disease who developed neurotoxicity after being prescribed unadjusted doses of valacyclovir and provide measurements of the amount of the drug eliminated through haemodialysis vs. native renal clearance. The patient's estimated body-burden of drug before the first session of dialysis was estimated at 580.3 mg. During the first haemodialysis session acyclovir plasma concentrations decreased from 8.8 to 3.2 mg/L (63.6%). Her body-burden of drug before the second session of haemodialysis was estimated as 131.9 mg. During the 2.5 h of the second dialysis session a total of 66.6 mg was eliminated based on measured dialysate concentrations. Urinary elimination was 17.7 mg over 30 h. Despite minimal urinary elimination her blood concentration fell from 8.8 to 0.88 mg/L with a total of 4.5 h of haemodialysis. Haemodialysis appears to be an effective method of eliminating acyclovir, especially in patients with advanced kidney disease.</p>","PeriodicalId":9251,"journal":{"name":"British journal of clinical pharmacology","volume":" ","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Neurotoxicity from inordinate valacyclovir dosage in an elderly woman with stage 5 chronic kidney disease.\",\"authors\":\"Juan A Vasquez Vasquez, Kyle D Pires, Belbina J Pereira, Kimberly M Brown, James A Langston, Charles E Langs, Robert S Hoffman\",\"doi\":\"10.1002/bcp.70138\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Unadjusted doses of valacyclovir can cause neurotoxicity in patients with chronic kidney disease. There are no well documented reports of valacyclovir or acyclovir toxicity providing pre- and postdialysis concentrations of acyclovir in the blood, dialysate and urine of acutely neurotoxic patients. We report an elderly woman with stage 5 chronic kidney disease who developed neurotoxicity after being prescribed unadjusted doses of valacyclovir and provide measurements of the amount of the drug eliminated through haemodialysis vs. native renal clearance. The patient's estimated body-burden of drug before the first session of dialysis was estimated at 580.3 mg. During the first haemodialysis session acyclovir plasma concentrations decreased from 8.8 to 3.2 mg/L (63.6%). Her body-burden of drug before the second session of haemodialysis was estimated as 131.9 mg. During the 2.5 h of the second dialysis session a total of 66.6 mg was eliminated based on measured dialysate concentrations. Urinary elimination was 17.7 mg over 30 h. Despite minimal urinary elimination her blood concentration fell from 8.8 to 0.88 mg/L with a total of 4.5 h of haemodialysis. Haemodialysis appears to be an effective method of eliminating acyclovir, especially in patients with advanced kidney disease.</p>\",\"PeriodicalId\":9251,\"journal\":{\"name\":\"British journal of clinical pharmacology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-06-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"British journal of clinical pharmacology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1002/bcp.70138\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"British journal of clinical pharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/bcp.70138","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
Neurotoxicity from inordinate valacyclovir dosage in an elderly woman with stage 5 chronic kidney disease.
Unadjusted doses of valacyclovir can cause neurotoxicity in patients with chronic kidney disease. There are no well documented reports of valacyclovir or acyclovir toxicity providing pre- and postdialysis concentrations of acyclovir in the blood, dialysate and urine of acutely neurotoxic patients. We report an elderly woman with stage 5 chronic kidney disease who developed neurotoxicity after being prescribed unadjusted doses of valacyclovir and provide measurements of the amount of the drug eliminated through haemodialysis vs. native renal clearance. The patient's estimated body-burden of drug before the first session of dialysis was estimated at 580.3 mg. During the first haemodialysis session acyclovir plasma concentrations decreased from 8.8 to 3.2 mg/L (63.6%). Her body-burden of drug before the second session of haemodialysis was estimated as 131.9 mg. During the 2.5 h of the second dialysis session a total of 66.6 mg was eliminated based on measured dialysate concentrations. Urinary elimination was 17.7 mg over 30 h. Despite minimal urinary elimination her blood concentration fell from 8.8 to 0.88 mg/L with a total of 4.5 h of haemodialysis. Haemodialysis appears to be an effective method of eliminating acyclovir, especially in patients with advanced kidney disease.
期刊介绍:
Published on behalf of the British Pharmacological Society, the British Journal of Clinical Pharmacology features papers and reports on all aspects of drug action in humans: review articles, mini review articles, original papers, commentaries, editorials and letters. The Journal enjoys a wide readership, bridging the gap between the medical profession, clinical research and the pharmaceutical industry. It also publishes research on new methods, new drugs and new approaches to treatment. The Journal is recognised as one of the leading publications in its field. It is online only, publishes open access research through its OnlineOpen programme and is published monthly.