首页|膝骨关节炎患者口服艾瑞昔布血药浓度与药品不良反应的关联性研究

膝骨关节炎患者口服艾瑞昔布血药浓度与药品不良反应的关联性研究

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目的 探索艾瑞昔布治疗膝骨关节炎的血药浓度监测及药品不良反应(ADR)分析.方法 回顾性分析2020年3月至2023年9月湖北省第三人民医院和湖北省汉川市人民医院收治的124例采用艾瑞昔布治疗并进行治疗药物监测的膝骨关节炎患者,收集临床资料,根据ADR发生情况分为ADR组(n=30)与无ADR组(n=94),分析膝骨关节炎患者艾瑞昔布血药浓度与ADR发生的关系,采用Logistic回归分析影响ADR发生的危险因素.结果 ADR组天冬氨酸氨基转移酶(AST)、尿素氮(BUN)、艾瑞昔布稳态谷浓度(Cssmin)[分别为(21.58±3.21)U·L-1、(5.32±0.51)mmol·L-1、(46.57±15.98)μg·L-1]高于无ADR组[分别为(19.93±3.11)U·L-1、(5.07±0.58)mmol·L-1、(37.39±9.75)μg·L-1](均P<0.05);发生胃肠道反应、下肢水肿、皮疹的Cssmin[分别为(40.13±10.98)U·L-1、(37.94±6.31)mmol·L-1、(35.67±4.35)μg·L-1]均高于无ADR组[分别为(19.93±3.11)U·L-1、(5.07±0.58)mmol·L-1、(37.39±9.75)μg·L-1](均P<0.05);AST、BUN、艾瑞昔布Cssmin是导致患者发生ADR的危险因素(OR=1.642,1.487,2.365,95%CI为1.241~2.173,1.185~1.867,1.598~3.501,均P<0.05).结论 随着Cssmin水平的增加,膝骨关节炎患者发生ADR的概率逐渐增高.AST、BUN、艾瑞昔布Cssmin是导致ADR发生的危险因素.
A study on correlation between plasma concentration of imrecoxib and adverse drug reactions in patients with knee osteoarthritis
Objective To explore the correlation between blood drug concentration and adverse drug reaction(ADR)of imrecoxib in the treatment of knee osteoarthritis.Methods The clinical data of 124 patients receiving imrecoxib therapy for knee osteoarthritis who were routinely monitored in the Third People's Hospital of Hubei Province and Hanchuan People's Hospital from March 2020 to September 2023 were retrospectively analyzed.Patients were divided into the ADR group(n=30)and non-ADR group(n=94)according to the occurrence of ADR.The correlation between plasma concentration of imrecoxib and ADR occurrence in all the patients was investigated.Logistic regression analysis was used to identify the risk factors of ADR.Results The levels of aspartate aminotransferase(AST),blood urea nitrogen(BUN)and steady state trough concentration(Cssmin)in the ADR group were(21.58±3.21)U·L-1,(5.32±0.51)mmol·L-1 and(46.57±15.98)μg·L-1,respectively,which were higher than those of((19.93±3.11)U·L-1,(5.07±0.58)mmol·L-1 and(37.39±9.75)μg·L-1)in the non-ADR group(all P<0.05).Cssmin for gastrointestinal reactions,lower limb edema and rash was(40.13±10.98)U·L-1,(37.94±6.31)mmol·L-1 and(35.67±4.35)μg·L-1,which was higher than that of((19.93±3.11)U·L-1,(5.07±0.58)mmol·L-1 and(37.39±9.75)μg·L-1)in those patients without the disease(all P<0.05).AST,BUN and Cssmin of imrecoxib were risk factors for ADR(OR=1.642,1.487,2.365,95%CI=1.241-2.173,1.185-1.867,1.598-3.501,all P<0.05).Conclusion The incidence of ADR in patients gradually increases as the level of Cssmin is elevated.AST,BUN and Cssmin are risk factors for the occurrence of ADR.

Knee osteoarthritisImrecoxibDrug monitoringPlasma drug concentrationAdverse drug reaction

李思锐、吕雷、王显勋、李志华

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湖北省第三人民医院骨外科,武汉 430030

湖北省汉川市人民医院骨科,孝感 432300

膝骨关节炎 艾瑞昔布 药物监测 血药浓度 药品不良反应

2024

中国药物应用与监测
中国人民解放军总医院

中国药物应用与监测

CSTPCD
影响因子:1.983
ISSN:1672-8157
年,卷(期):2024.21(3)
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