A multicenter laboratory assessment of a new automated chemiluminescent assay for ADAMTS13 activity

被引:24
作者
Favaloro, Emmanuel J. [1 ,2 ,3 ]
Mohammed, Soma [1 ,2 ]
Chapman, Kent [2 ,4 ]
Swanepoel, Priscilla [2 ,4 ]
Zebeljan, Diane [2 ,5 ]
Sefhore, Opelo [2 ,5 ]
Malan, Erica [6 ]
Clifford, Joanne [6 ]
Yuen, Agnes [6 ]
Donikian, Dea [2 ,7 ]
Kondo, Mayuko [2 ]
Duncan, Elizabeth [7 ,8 ]
Abraham, Sunil [8 ]
Beggs, Joanne [9 ]
Chatrapati, Ritesh [9 ]
Perel, Joanne [9 ]
Coleman, Robyn [10 ]
Klose, Nathan [10 ]
Hsu, Danny [2 ,5 ]
Motum, Penelope [2 ,5 ]
Tan, Chee Wee [8 ,11 ]
Brighton, Timothy [2 ,7 ]
Pasalic, Leonardo [1 ,2 ,3 ]
机构
[1] NSW Hlth Pathol, Westmead Hosp, Inst Clin Pathol & Med Res ICPMR, Dept Haematol, Westmead, NSW, Australia
[2] NSW Hlth Pathol, Westmead, NSW, Australia
[3] Sydney Ctr Thrombosis & Haemostasis, Westmead, NSW, Australia
[4] NSW Hlth Pathol, John Hunter Hosp, Newcastle, NSW, Australia
[5] NSW Hlth Pathol, Liverpool Hosp, Liverpool, NSW, Australia
[6] Monash Hlth, Melbourne, Vic, Australia
[7] NSW Hlth Pathol, Prince Wales Hosp, Randwick, NSW, Australia
[8] SA Pathol, Adelaide, SA, Australia
[9] Queensland Hlth, Brisbane, Qld, Australia
[10] Sullivan Nicolaides Pathol, Brisbane, Qld, Australia
[11] Royal Adelaide Hosp, Adelaide, SA, Australia
关键词
ADAMTS13; activity; inhibitors; laboratory testing; thrombotic thrombocytopenic purpura; TTP; VON-WILLEBRAND-FACTOR; THROMBOTIC THROMBOCYTOPENIC PURPURA; FACTOR-CLEAVING PROTEASE; FACTOR-VIII; PLASMA; MICROANGIOPATHY; DEFICIENCY; DIAGNOSIS;
D O I
10.1111/jth.15157
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Thrombotic thrombocytopenic purpura (TTP) is a rare but potentially fatal disorder caused by ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13) deficiency. Prompt identification/exclusion of TTP can thus be facilitated by rapid ADAMTS13 testing. The most commonly utilized (enzyme-linked immunosorbent assay [ELISA]-based) assay takes several hours to perform and so does not generally permit rapid testing. Objectives To evaluate the utility of a new automated test for ADAMTS13 activity, the HemosIL AcuStar ADAMTS13 Activity assay, based on chemiluminescence and able to be performed on an ACL AcuStar instrument within 33 minutes. Patients/Methods This multicenter (n = 8) assessment included testing of more than 700 test samples, with similar numbers of prospective (n = 348) and retrospective (n = 385) samples. The main comparator was the Technozym ADAMTS13 Activity ELISA. We also assessed comparative performance for detection of ADAMTS13 inhibitors using a Bethesda assay. Results Overall, the chemiluminescent assay yielded similar results to the comparator ELISA, albeit with slight negative bias. ADAMTS13 inhibitor detection was also comparable, albeit with slight positive bias with the AcuStar assay. Assay precision was similar with both assays, and we also verified assay normal reference ranges. Conclusions The HemosIL AcuStar ADAMTS13 Activity assay provided results rapidly, which were largely comparable with the Technozym ADAMTS13 Activity ELISA assay, albeit lower on average. Conversely, inhibitor levels tended to be identified at a higher level on average. Thus, the HemosIL AcuStar ADAMTS13 Activity assay provides a fast and accurate means to quantitate plasma levels of ADAMTS13 for TTP/ADAMTS13 identification/exclusion, and potentially also for other applications.
引用
收藏
页码:417 / 428
页数:12
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