实验与检验医学
實驗與檢驗醫學
실험여검험의학
EXPERIMENTAL AND LABORATORY MEDICINE
2014年
3期
264-266,284
,共4页
钟青%许业栋%吴永国%刘文毅%肖静%胡国刚
鐘青%許業棟%吳永國%劉文毅%肖靜%鬍國剛
종청%허업동%오영국%류문의%초정%호국강
血液分析仪%血小板计数%小红细胞%裂红细胞%血小板参数
血液分析儀%血小闆計數%小紅細胞%裂紅細胞%血小闆參數
혈액분석의%혈소판계수%소홍세포%렬홍세포%혈소판삼수
Hematology analyzer%Platelet count%Microcyte%Schistocyte%Platelet parameters
目的:探讨XS1000i血细胞分析仪部分血小板参数缺失时小红细胞/裂红细胞对血小板计数的影响。方法对XS1000i血细胞分析仪分析后MCV<80fl且部分血小板参数缺失的标本再使用PENTRA120Retic血细胞分析仪计数血小板、显微镜计数血小板及瑞氏染色镜检。结果 PLT>100×109/L时,XS1000i与PENTRA120Retic、显微镜计数血小板的差异有统计学意义(P<0.01),PLT<100×109/L时, XS1000i与PENTRA120Retic、显微镜计数血小板的结果差异无统计学意义(P>0.01);当MCV分别为70~80fl,60~70fl,<60fl时,XS1000i均高于显微镜计数血小板的结果,差异有统计学意义(P<0.01)。显微镜检查结果发现:101例标本均检出小红细胞或(和)裂红细胞,其中60例伴有大血小板或(和)巨血小板,4例伴有大血小板和血小板聚集。结论对于电阻抗血细胞分析仪,当MCV<80fl且部分血小板参数缺失时的标本应用显微镜或ICSH推荐的参考方法计数血小板,同时染色镜检异常血细胞的形态、数量及分布。
目的:探討XS1000i血細胞分析儀部分血小闆參數缺失時小紅細胞/裂紅細胞對血小闆計數的影響。方法對XS1000i血細胞分析儀分析後MCV<80fl且部分血小闆參數缺失的標本再使用PENTRA120Retic血細胞分析儀計數血小闆、顯微鏡計數血小闆及瑞氏染色鏡檢。結果 PLT>100×109/L時,XS1000i與PENTRA120Retic、顯微鏡計數血小闆的差異有統計學意義(P<0.01),PLT<100×109/L時, XS1000i與PENTRA120Retic、顯微鏡計數血小闆的結果差異無統計學意義(P>0.01);噹MCV分彆為70~80fl,60~70fl,<60fl時,XS1000i均高于顯微鏡計數血小闆的結果,差異有統計學意義(P<0.01)。顯微鏡檢查結果髮現:101例標本均檢齣小紅細胞或(和)裂紅細胞,其中60例伴有大血小闆或(和)巨血小闆,4例伴有大血小闆和血小闆聚集。結論對于電阻抗血細胞分析儀,噹MCV<80fl且部分血小闆參數缺失時的標本應用顯微鏡或ICSH推薦的參攷方法計數血小闆,同時染色鏡檢異常血細胞的形態、數量及分佈。
목적:탐토XS1000i혈세포분석의부분혈소판삼수결실시소홍세포/렬홍세포대혈소판계수적영향。방법대XS1000i혈세포분석의분석후MCV<80fl차부분혈소판삼수결실적표본재사용PENTRA120Retic혈세포분석의계수혈소판、현미경계수혈소판급서씨염색경검。결과 PLT>100×109/L시,XS1000i여PENTRA120Retic、현미경계수혈소판적차이유통계학의의(P<0.01),PLT<100×109/L시, XS1000i여PENTRA120Retic、현미경계수혈소판적결과차이무통계학의의(P>0.01);당MCV분별위70~80fl,60~70fl,<60fl시,XS1000i균고우현미경계수혈소판적결과,차이유통계학의의(P<0.01)。현미경검사결과발현:101례표본균검출소홍세포혹(화)렬홍세포,기중60례반유대혈소판혹(화)거혈소판,4례반유대혈소판화혈소판취집。결론대우전조항혈세포분석의,당MCV<80fl차부분혈소판삼수결실시적표본응용현미경혹ICSH추천적삼고방법계수혈소판,동시염색경검이상혈세포적형태、수량급분포。
Objective To investigate the effect of microcytes/schistocytes on platelet count when deficiency of portion platelet parameters measured by XS1000i hematology analyzer. Methods After analyzed by XS1000i hematology analyzer, the samples which have MCV<80fl and loss partial platelet parameters were re-measured with the PENTRA120Retic hematology analyzer, mi-croscopic platelet count and,Wright staining for platelets. Results When PLT>100×109/L, there were statistically significant differ-ences in the platelet counts among XS1000i, PENTRA120Retic and microscopic counting (P<0.01); when PLT<100×109/L, there were no statistically significant differences in the platelet counts among XS1000i PENTRA120Retic and microscopic counting (P>0.01). When MCV was 70~80fl, 60~70fl and<60fl, respectively, the platelet counts of XS1000i were higher than those of micro-scopic counting , the difference was statistically significant(P<0.01). The results of microscope examination were as follows:all 101 specimens were detected and had microcytes or (and) schistocytes, of which 60 cases were accompanied with large platelets and/or giant platelets, and 4 cases were accompanied with large platelets and platelet aggregation. Conclusions The samples with MCV<80fl and missing partial platelet parameters when analyzed by impedance hematology analyzer should be re-measured with the reference method recommended by ICSH or microscopic platelet counting, meanwhile, detect the morphology, number and distribu-tion of abnormal blood cells by staining and microscopic examination.