南方医科大学学报
南方醫科大學學報
남방의과대학학보
JOURNAL OF SOUTHERN MEDICAL UNIVERSITY
2009年
10期
2124-2127
,共4页
蔡晓斌%朱治山%张明之%郭瑾%王辉兰
蔡曉斌%硃治山%張明之%郭瑾%王輝蘭
채효빈%주치산%장명지%곽근%왕휘란
降纤酶%急性脑梗死%治疗%个体化
降纖酶%急性腦梗死%治療%箇體化
강섬매%급성뇌경사%치료%개체화
defibrase%acute cerebral infarction%individualized therapy
目的 根据血浆纤维蛋白原(FIB)水平给予不同剂量降纤酶治疗,探讨降纤酶个体化剂量治疗急性脑梗死(ACI)的疗效.方法 60例急性脑梗死(发病72 h内)患者随机分为2组,降纤酶组30例,对照组30例.降纤酶治疗组根据治疗前血浆Fm水平>4 g/L,2-4 g/L,1.3~2 g/L分别给予首剂降纤酶15 U,10 U,5 U,给药后每12 h监测一次血浆FIB水平,当血浆FIB水平>1.3g/L时再次给予降纤酶5U,维持患者血浆FIB水平在0.7-1.3 g/L之间达7 d时间,检测治疗前及治疗7d后血浆凝血酶原时间(PT)、血浆活化部分凝血激酶时间(APTT)、血浆纤维蛋白原(Fg)水平,并在治疗14d后进行神经功能缺损程度评分(CSS)和3个月后日常生活活动(ADL)量表评分,评价临床疗效.结果 (1)治疗7 d降纤酶组血浆PT、APTT延长,Pg下降,与治疗前及对照组比较,差异均有显著性.(2)治疗14 d降纤酶组神经功能缺损程度评分改善,与治疗前及对照组比较,差异均有显著性.(3)临床疗效降纤酶组总有效率80%,对照组总有效率50%,两组比较差异有显著性.(4)治疗后3个月日常生活活动量表评分,两组比较差异无显著性,但(独立+轻度依赖)比例降纤酶组为93.3%,对照组为70.0%,两组比较差异有显著性.(5)治疗期间降纤酶组无颅内外出血,随访3个月无死亡病例发生.结论 基于血浆纤维蛋白原水平,应用降纤酶治疗急性脑梗死能快速平稳降低患者血浆纤维蛋白原水平,减少神经功能缺损.提高生活质量.个体化降纤酶治疗安全有效.
目的 根據血漿纖維蛋白原(FIB)水平給予不同劑量降纖酶治療,探討降纖酶箇體化劑量治療急性腦梗死(ACI)的療效.方法 60例急性腦梗死(髮病72 h內)患者隨機分為2組,降纖酶組30例,對照組30例.降纖酶治療組根據治療前血漿Fm水平>4 g/L,2-4 g/L,1.3~2 g/L分彆給予首劑降纖酶15 U,10 U,5 U,給藥後每12 h鑑測一次血漿FIB水平,噹血漿FIB水平>1.3g/L時再次給予降纖酶5U,維持患者血漿FIB水平在0.7-1.3 g/L之間達7 d時間,檢測治療前及治療7d後血漿凝血酶原時間(PT)、血漿活化部分凝血激酶時間(APTT)、血漿纖維蛋白原(Fg)水平,併在治療14d後進行神經功能缺損程度評分(CSS)和3箇月後日常生活活動(ADL)量錶評分,評價臨床療效.結果 (1)治療7 d降纖酶組血漿PT、APTT延長,Pg下降,與治療前及對照組比較,差異均有顯著性.(2)治療14 d降纖酶組神經功能缺損程度評分改善,與治療前及對照組比較,差異均有顯著性.(3)臨床療效降纖酶組總有效率80%,對照組總有效率50%,兩組比較差異有顯著性.(4)治療後3箇月日常生活活動量錶評分,兩組比較差異無顯著性,但(獨立+輕度依賴)比例降纖酶組為93.3%,對照組為70.0%,兩組比較差異有顯著性.(5)治療期間降纖酶組無顱內外齣血,隨訪3箇月無死亡病例髮生.結論 基于血漿纖維蛋白原水平,應用降纖酶治療急性腦梗死能快速平穩降低患者血漿纖維蛋白原水平,減少神經功能缺損.提高生活質量.箇體化降纖酶治療安全有效.
목적 근거혈장섬유단백원(FIB)수평급여불동제량강섬매치료,탐토강섬매개체화제량치료급성뇌경사(ACI)적료효.방법 60례급성뇌경사(발병72 h내)환자수궤분위2조,강섬매조30례,대조조30례.강섬매치료조근거치료전혈장Fm수평>4 g/L,2-4 g/L,1.3~2 g/L분별급여수제강섬매15 U,10 U,5 U,급약후매12 h감측일차혈장FIB수평,당혈장FIB수평>1.3g/L시재차급여강섬매5U,유지환자혈장FIB수평재0.7-1.3 g/L지간체7 d시간,검측치료전급치료7d후혈장응혈매원시간(PT)、혈장활화부분응혈격매시간(APTT)、혈장섬유단백원(Fg)수평,병재치료14d후진행신경공능결손정도평분(CSS)화3개월후일상생활활동(ADL)량표평분,평개림상료효.결과 (1)치료7 d강섬매조혈장PT、APTT연장,Pg하강,여치료전급대조조비교,차이균유현저성.(2)치료14 d강섬매조신경공능결손정도평분개선,여치료전급대조조비교,차이균유현저성.(3)림상료효강섬매조총유효솔80%,대조조총유효솔50%,량조비교차이유현저성.(4)치료후3개월일상생활활동량표평분,량조비교차이무현저성,단(독립+경도의뢰)비례강섬매조위93.3%,대조조위70.0%,량조비교차이유현저성.(5)치료기간강섬매조무로내외출혈,수방3개월무사망병례발생.결론 기우혈장섬유단백원수평,응용강섬매치료급성뇌경사능쾌속평은강저환자혈장섬유단백원수평,감소신경공능결손.제고생활질량.개체화강섬매치료안전유효.
Objectives To evaluate the therapeutic effect of individualized defibrase therapy according to the level of plasma fibrinogen (FIB) in patients with acute cerebral infarction (ACI). Methods Sixty patients with ACI (within 72 h after onset) were randomly divided into defibrase group (n=30) and control group (n=30). The patients in defibrase group received intravenous defibrase infusion at different first doses (15, 10, and 5 U) according to plasma FIB level (>4 g/L, 2~4 g/L, and 1.3~2 g/L) before treatment. Plasma FIB was measured every 12 h after the first dose of defibrase, and when plasma FIB was over 1.3 g/L, intravenous infusion of 5 U defibrase was given to maintain plasma FIB within the range of 0.70~1.13 g/L over a period of 7 days. The plasma prothrombin time (PT), activated partial thromboplastin time (APTT) and FIB before and after the 7-day treatment were measured, and the scores of Chinese stroke scale (CSS) after 14 days of treatment and Activity of Daily Living (ADL) after 3 months were recorded. Results After 7 days of treatment, plasma PT and APTT were significantly prolonged lengthened and plasma FIB was lowered in defibrase group. The scores of CSS improved in defibrase group after 14 days of treatment, showing significant difference from those of the control group. The clinical effective rate was 80% in defibrase group, significantly higher than that in the control group (50%). The scores of ADL after 3 months were similar between the 2 groups, but the percentage of independent living and mild dependency was significantly higher in defibrase group (93.3% vs 70.0%). No intracerebral and extracerebral hemorrhage occurred in defibrase group the during treatment, no did death occur after 3 months of treatment. Conclusion Defibrase therapy based on plasma FIB level can rapidly and effectively lower plasma FIB, reduce neurological impairment and improve the quality of life in patients with ACI.