浙江临床医学
浙江臨床醫學
절강림상의학
ZHEJIANG CLINICAL MEDICAL JOURNAL
2015年
6期
892-893,896
,共3页
重组人血小板生成素%环孢素A%难治性免疫性血小板减少症
重組人血小闆生成素%環孢素A%難治性免疫性血小闆減少癥
중조인혈소판생성소%배포소A%난치성면역성혈소판감소증
Recombinant human thrombopoietin%cyclosporin A%refractory immune%thrombocytopenia
目的:观察重组人血小板生成素(rhTPO)联合环孢素A(CsA)治疗难治性免疫性血小板减少症(ITP)的疗效及安全性。方法26例难治性ITP患者采用rhTPO(15000U/d,d1-14)联合口服CsA[剂量2~3mg/(kg.d)]。观察治疗前后血小板数及T淋巴细胞亚群,并观察药物的毒副反应。结果经1周、2周及1个月治疗后总有效率分别为61.6%、92.3%和84.6%;而1、2、3个月治疗后复发率分别为7.7%、19.2%和26.9%。治疗后ITP患者血小板数明显升高,与治疗前比较差异有显著性(P<0.05)。CD4/CD8比值明显升高,与治疗前比较差异有显著性(P<0.05)。毒副反应轻微。结论 rhTPO联合CsA治疗难治性ITP效果确切。其可能主要通过调节T细胞起治疗作用。
目的:觀察重組人血小闆生成素(rhTPO)聯閤環孢素A(CsA)治療難治性免疫性血小闆減少癥(ITP)的療效及安全性。方法26例難治性ITP患者採用rhTPO(15000U/d,d1-14)聯閤口服CsA[劑量2~3mg/(kg.d)]。觀察治療前後血小闆數及T淋巴細胞亞群,併觀察藥物的毒副反應。結果經1週、2週及1箇月治療後總有效率分彆為61.6%、92.3%和84.6%;而1、2、3箇月治療後複髮率分彆為7.7%、19.2%和26.9%。治療後ITP患者血小闆數明顯升高,與治療前比較差異有顯著性(P<0.05)。CD4/CD8比值明顯升高,與治療前比較差異有顯著性(P<0.05)。毒副反應輕微。結論 rhTPO聯閤CsA治療難治性ITP效果確切。其可能主要通過調節T細胞起治療作用。
목적:관찰중조인혈소판생성소(rhTPO)연합배포소A(CsA)치료난치성면역성혈소판감소증(ITP)적료효급안전성。방법26례난치성ITP환자채용rhTPO(15000U/d,d1-14)연합구복CsA[제량2~3mg/(kg.d)]。관찰치료전후혈소판수급T림파세포아군,병관찰약물적독부반응。결과경1주、2주급1개월치료후총유효솔분별위61.6%、92.3%화84.6%;이1、2、3개월치료후복발솔분별위7.7%、19.2%화26.9%。치료후ITP환자혈소판수명현승고,여치료전비교차이유현저성(P<0.05)。CD4/CD8비치명현승고,여치료전비교차이유현저성(P<0.05)。독부반응경미。결론 rhTPO연합CsA치료난치성ITP효과학절。기가능주요통과조절T세포기치료작용。
Objective To observe the efficacy and safety of recombinant human thrombopoietin (rhTPO) in combination with cyclosporin A (CsA) for the treatment of patients with refractory immune thrombocytopenia (RITP). Methods Twenty-six patients with RITP received subcutaneous injection of rhTPO at a dose of 15000U once daily up to day 14. Simultaneously they also received oral CsA at a dose of 2-3mg·kg-1·d-1 for three months. Platelet counts and T cell subsets were monitored before and after treatment. Also the side effects were observed. Results The total effective rate was 61.6%,92.3% and 84.6% respectively after one-week,two-week and one-month treatment. The relapse rate was 7.7%, 19.2% and 26.9% respectively after one-month,two-month and three-month treatment. Platelet counts after treatment were significantly higher than before (P<0.05). The specific value of CD4/CD8 was also increased significantly (P<0.05). All the adverse events were generally mild. Conclusion Combination therapy with rhTPO and CsA was effective and well tolerated in the management of patients with RITP. The efficacy may be related with regulation of T cell.