海峡药学
海峽藥學
해협약학
STRAIT PHARMACEUTICAL JOURNAL
2014年
7期
170-172
,共3页
段自皞%沈炳香%刘铖%聂松柳
段自皞%瀋炳香%劉鋮%聶鬆柳
단자호%침병향%류성%섭송류
高效液相色谱法( HPLC)%急性淋巴细胞白血病( ALL)%大剂量甲氨蝶呤(HD-MTX)%血药浓度监测( TDM)%个体化给药
高效液相色譜法( HPLC)%急性淋巴細胞白血病( ALL)%大劑量甲氨蝶呤(HD-MTX)%血藥濃度鑑測( TDM)%箇體化給藥
고효액상색보법( HPLC)%급성림파세포백혈병( ALL)%대제량갑안접령(HD-MTX)%혈약농도감측( TDM)%개체화급약
High performance liquid chromatography ( HPLC )%Acute lymphoblastic leukemia ( ALL )%Large dose methotrexate ( HD-MTX)%Therapeutic drug monitoring ( TDM)%Individualized drug administration
目的:通过监测甲氨蝶呤血药浓度指导急性淋巴细胞白血病(ALL)患者的大剂量甲氨蝶呤(HD-MTX)化疗和解救方案,保证用药合理、有效、安全。方法①将30例次HD-MTX化疗的ALL患者按甲氨蝶呤剂量不同分组,每组15例次,Ⅰ组3g/m2,Ⅱ组5g/m2。用高效液相色谱法( HPLC法)测定化疗结束后0、20、44h(必要时追加68h、92h采血点)所测得的血药浓度监测,指导亚叶酸钙( CF)解救,同时观察患者不良反应和Ⅰ组、Ⅱ组两组化疗前后患者肝肾功能各项指标的变化。②按照①中HPLC法所测得的甲氨蝶呤血药浓度将30例ALL患者分为排泄延迟组和非排泄延迟组,并分析甲氨蝶呤排泄延迟与不良反应之间的联系。结果①于0、20和44h时,高剂量Ⅱ组的血药浓度均比低剂量Ⅰ组血药浓度高。相应的是,高剂量Ⅱ组各种不良反应发生率也较低剂量Ⅰ组高;②排泄延迟组肝肾功能异常的比例明显比非排泄延迟组高。结论甲氨蝶呤的血药浓度监测可提高治疗用药安全性和有效性,对CF个体化解救、减少不良反应的发生具有十分重要的意义。
目的:通過鑑測甲氨蝶呤血藥濃度指導急性淋巴細胞白血病(ALL)患者的大劑量甲氨蝶呤(HD-MTX)化療和解救方案,保證用藥閤理、有效、安全。方法①將30例次HD-MTX化療的ALL患者按甲氨蝶呤劑量不同分組,每組15例次,Ⅰ組3g/m2,Ⅱ組5g/m2。用高效液相色譜法( HPLC法)測定化療結束後0、20、44h(必要時追加68h、92h採血點)所測得的血藥濃度鑑測,指導亞葉痠鈣( CF)解救,同時觀察患者不良反應和Ⅰ組、Ⅱ組兩組化療前後患者肝腎功能各項指標的變化。②按照①中HPLC法所測得的甲氨蝶呤血藥濃度將30例ALL患者分為排洩延遲組和非排洩延遲組,併分析甲氨蝶呤排洩延遲與不良反應之間的聯繫。結果①于0、20和44h時,高劑量Ⅱ組的血藥濃度均比低劑量Ⅰ組血藥濃度高。相應的是,高劑量Ⅱ組各種不良反應髮生率也較低劑量Ⅰ組高;②排洩延遲組肝腎功能異常的比例明顯比非排洩延遲組高。結論甲氨蝶呤的血藥濃度鑑測可提高治療用藥安全性和有效性,對CF箇體化解救、減少不良反應的髮生具有十分重要的意義。
목적:통과감측갑안접령혈약농도지도급성림파세포백혈병(ALL)환자적대제량갑안접령(HD-MTX)화료화해구방안,보증용약합리、유효、안전。방법①장30례차HD-MTX화료적ALL환자안갑안접령제량불동분조,매조15례차,Ⅰ조3g/m2,Ⅱ조5g/m2。용고효액상색보법( HPLC법)측정화료결속후0、20、44h(필요시추가68h、92h채혈점)소측득적혈약농도감측,지도아협산개( CF)해구,동시관찰환자불량반응화Ⅰ조、Ⅱ조량조화료전후환자간신공능각항지표적변화。②안조①중HPLC법소측득적갑안접령혈약농도장30례ALL환자분위배설연지조화비배설연지조,병분석갑안접령배설연지여불량반응지간적련계。결과①우0、20화44h시,고제량Ⅱ조적혈약농도균비저제량Ⅰ조혈약농도고。상응적시,고제량Ⅱ조각충불량반응발생솔야교저제량Ⅰ조고;②배설연지조간신공능이상적비례명현비비배설연지조고。결론갑안접령적혈약농도감측가제고치료용약안전성화유효성,대CF개체화해구、감소불량반응적발생구유십분중요적의의。
OBJECTIVE To ensure the use of medication reasonable ,offective and safe by therapeutic drug mo-nitoring of high-dose methotrexate in pediatric acute lymphoblastic leukemia and assessing the clinical signifi -cance.METHODS ①30 acute lymphoblastic leukemia patients were grouped according to the dosage of methotrex-ate:the high dosage group received MTX 5.0g/m2 and the low dosage group received MTX 3.0g/m2.The MTX con-centration in serum at 0,20,44(68h,92h p.r.n) were detected by high performance liquid chromatography (HPLC).Then adjust the dosage of CF according to MTX concentration and observe the adverse effects of MTX in patients .②patients were grouped elimination delay group and no-elimination delay group according to MTX concentration by high performance liquid chromatography (HPLC) from①,then analyze the relationship between elimination delay of methotrexate and adverse reaction.RESULTS ①The concentration of MTX at 20 ,44 of high dosage group were higher than the concentration of MTX at 20,44 of low dosage group,respectively.And,the occurrence of adverse re-actions of high dosage group is also higher than low dosage group;②The proportion of abnormity of hepatorenal func-tion in elimination delay group is obviously higher than no-elimination delay group.CONCLUSION To Monitoring the concentration of MTX can enhance safety and effectiveness of medication use ,which has clinical significance.For CF individual rescueing and the occurrence of adverse reactions reducing.