Optimal regimen of levetiracetam for prevention of busulfan-induced seizure in patients undergoing hematopoietic stem cell transplantation: A review of available evidence

被引:0
|
作者
Tavajohi, Rayeheh [1 ]
Shahrami, Bita [1 ,2 ,3 ]
Rostami, Tahereh [2 ]
Kiumarsi, Azadeh [2 ]
Honarmand, Hooshyar [1 ]
Hadjibabaie, Molouk [1 ]
机构
[1] Univ Tehran Med Sci, Sch Pharm, Dept Clin Pharm, Tehran, Iran
[2] Univ Tehran Med Sci, Res Inst Oncol, Oncol & Stem Cell Transplantat Res Ctr, Hematol, Tehran, Iran
[3] Univ Tehran Med Sci, Dept Clin Pharm, 16 Azar St, Enghelab Ave, Tehran 1417614418, Iran
关键词
Antiepileptic; prophylactic seizure therapy; loading dose; high-dose busulfan; bone marrow transplantation; HIGH-DOSE BUSULFAN; CHILDREN; EPILEPSY;
D O I
10.1177/10781552231159056
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective This review aimed to summarize the available data and offer a practical recommendation regarding the optimal regimen of levetiracetam (LEV) for the prevention of busulfan-induced seizure (BIS) in patients undergoing hematopoietic stem cell transplantation (HSCT). Data Sources Published articles by searching databases (PubMed, Google Scholar, Cochrane Library, ScienceDirect) were reviewed. All types of original studies performed in pediatric and adult populations have been investigated and required data was extracted. Data Summary Eleven articles were eligible to be included in this review. A loading dose was not used in any of the studies. LEV had been started from 6 to 48 h before busulfan (Bu) initiation and continued up to 24 to 48 h after its termination. The dose range of LEV was 10 to 20 mg/kg/day divided every 12 h in pediatrics and 500 to 1000 mg twice daily in adults. Both oral and intravenous (IV) routes of administration were used. Except for three studies, no seizure had occurred in patients who had received LEV. Conclusions Considering the available evidence, LEV with the dose range from 500 to 1000 mg twice daily in adults and 10 mg/kg twice daily (20 mg/kg/day in 2 divided doses) in children orally or IV started from 6 to 24 h before Bu initiation up to 24 to 48 h after the last dose of Bu seems to prevent BIS appropriately. More prospective clinical trials with a larger population are needed to validate the optimal dosing of LEV for BIS prophylaxis in patients undergoing HSCT.
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收藏
页码:927 / 933
页数:7
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