Joan Cid, N ú ria Nogués, Rosa Montero, Marta Hurtado, Albert Briega and Rafael Parra. Blood and Tissue Bank. Barcelona, Spain. INTRODUCTION
Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author.While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server.
Joan Cid, Núria Nogués, Rosa Montero, Marta Hurtado, Albert Briega and Rafael Parra.
Blood and Tissue Bank. Barcelona, Spain.
Antibody screening is performed to detect clinically relevant red blood cell (RBC) antibodies in transfusion recipients and blood donors. The classical low-ionic-strength-solution (LISS) tube indirect antiglobulin test (IAT) for detecting clinically significant antibodies has been replaced in many countries by microtube column agglutination systems, described for first time in 1988 and published in 1990 (1). The first microtube system was manufactured and distributed by DiaMed-ID (Switzerland), followed by Otho BioVue (Otho Diagnostic GmBH, Germany). Recently, a new microtube column agglutination system has been launched on the market by Diagnostic Grifols, S.A. (Barcelona, Spain) with the name of DG Gel.
The aim of the present study was to evaluate the diagnostic accuracy of this new system, to analyze the antibody reactivity and to compare the data with the two cited well-established methods.
Samples. We collected 3,024 specimens: 2,408 (79.6%) were plasma samples obtained from EDTA tubes and 616 (20.4%) were serum samples. We obtained 2,422 (80.1%) samples from blood donors in our blood bank; 382 (12.6%) samples from transfusion recipients and 220 (7.3%) from pregnant women in Hospital Vall d’Hebron (Barcelona, Spain). We stored all these samples in the refrigerator at 2-8 ºC and we processed them before 72 hours from extraction. We additionally obtained 100 samples containing antibodies of known specificity from the immunohematology laboratory of our blood bank. These samples had been stored in a frozen state at -30 ºC and were thawed immediately before processing.
Test RBCs. The RBCs used for the antibody screening and for the panel identification were obtained from our selected blood donors. These RBCs were suspended to final concentration 0.8 % in the corresponding modified LISS provided by the manufacturers according to their instructions as follows. We calculated the conductivity of these solutions.
DG Gel:50 µL of RBCs in diluent provided by Diagnostic Grifols (Cond.: 5.09 mS/cm) + 25 µL of sample. Incubation: 15 min, 37 ºC. Centrifugation: 9 min.
DiaMed-ID: 50 µL of RBCs in ID-CellStab (Cond.: 5.89 mS/cm) + 25 µL of sample.Incubation: 15 min, 37 ºC. Centrifugation: 10 min.
Ortho BioVue: 50 µL of RBCs in Ortho BLISS (Cond.: 3.03 mS/cm) + 40 µL of sample.Incubation: 10 min, 37 ºC. Centrifugation: 5 min.
We performed the antibody screening of 3,024 fresh samples with the three microtube systems and we obtained concordant results in 3,019 (99.83%) and discrepant results in 5 (0.17%). Table 1 shows the specificities of the antibody after the identification steps using 11-cell panel and additional techniques, e.g. papain-treated reagent RBCs and IAT with polyethylenglycol (PEG) tube technique (2).
We titrated 100 frozen samples containing antibodies with known specificities. The score mean and standard desviation of the antibody titration for each microtube system were the 34.31±26.7 for DG Gel, 30.3±27.76 for Diamed-ID, and 37.38±28.68 for Ortho BioVue (see Table 2).
The antibody titration score was higher with the DG Gel when compared with DiaMed-ID in samples containing anti-K (46.23 vs. 44.38; p<0.05) and in samples containing anti-M (11.88vs. 5.38; p<0.05). No significant differences were seen in other antibodies specificities.
Table 1. Antibody detected by the three systems using 2 screening cells.
Sensitivity and Specificity
In order to obtain a comparative value between the new test and the other two we calculated the estimated diagnostic accuracy for each system (see Table 3). For calculating estimates of these statistical measures we include the 100 positive samples and we reported the confidence intervals (CI) for a sample size of 3,124.
Table 3. Estimated diagnostic accuracy. In parenthesis the 95 % CI. (a) PPV: predictive positive value, (b) PNV: predictive negative value.
All three microtube column agglutination systems work well showing a high estimated sensitivity and specificity.
1. Lapierre, Y. Rigal, D., Adam, J. Josef, D., Meyer, F., Greber, S. andDrot, C. (1990)Transfusion, 30, 109-113.
2.AABB (2002) Technical Manual, 14 th edition, Beshesda.
Table 2. Samples containing antibodies of known specificities used forantibody titration.