A North American multilaboratory study of CD4 counts using flow cytometric panleukogating (PLG): A NIAID-DAIDS Immunology Quality Assessment Program Study

التفاصيل البيبلوغرافية
العنوان: A North American multilaboratory study of CD4 counts using flow cytometric panleukogating (PLG): A NIAID-DAIDS Immunology Quality Assessment Program Study
المؤلفون: Alan L. Landay, Thomas N. Denny, Lee Lam, Thomas J. Spira, Cindy Wilkening, Rebecca Gelman, Frank Mandy, John L. Schmitz, Raul Louzao, Michèle Bergeron, Deborah K. Glencross
المصدر: Cytometry Part B: Clinical Cytometry. :S52-S64
بيانات النشر: Wiley, 2008.
سنة النشر: 2008
مصطلحات موضوعية: Histology, Quality Assurance, Health Care, Coefficient of variation, Human immunodeficiency virus (HIV), medicine.disease_cause, Specimen Handling, Pathology and Forensic Medicine, Bias, Leukocytes, medicine, Humans, Cd4 t cell, Quality assessment, business.industry, Cell Biology, Flow Cytometry, Blood Cell Count, CD4 Lymphocyte Count, Cost savings, North America, Immunology, CD4 Lymphocyte, Laboratories, business, Aids pandemic, Healthcare system
الوصف: Background The global HIV/AIDS pandemic and guidelines for initiating anti-retroviral therapy (ART) and opportunistic infection prophylaxis demand affordable, reliable, and accurate CD4 testing. A simple innovative approach applicable to existing technology that has been successfully applied in resource-challenged settings, PanLeukogated CD4 (PLG), could offer solutions for cost saving and improved precision. Methods Day-old whole blood from 99 HIV+ donors was simultaneously studied in five North-American laboratories to compare the performance of their predicate methods with the dual-platform PLG method. The predicate technology included varying 4-color CD45/CD3/CD4/CD8 protocols on different flow cytometers. Each laboratory also assayed eight replicate specimens of day-old blood from 10 to 14 local donors. Bias and precision of predicate and PLG methods was studied between- and within-participating laboratories. Results Significantly (P < 0.0001) improved between-laboratory precision/coefficient of variation (CV%) was noted using the PLG method (overall median 9.3% vs. predicate median CV 13.1%). Within-laboratory precision was also significantly (P < 0.0001) better overall using PLG (median 4.6% vs. predicate median CV 6.2%) and in 3 of the 5 laboratories. PLG counts tended to be 11% smaller than predicate methods (P < 0.0001) for shipped (median of predicate—PLG = 31) and local specimens (median of predicate—PLG = 23), both overall and in 4 of 5 laboratories (median decreases of 4, 16, 20, and 21% in shipped specimens); the other laboratory had a median increase of 5%. Conclusion Laboratories using predicate CD4 methods similar to those in this study could improve their between-laboratory and their within-laboratory precision, and reduce costs, by switching to the PLG method after adequate training, if a change (usually, a decrease) in CD4 counts is acceptable to their health systems. © 2008 Clinical Cytometry Society
تدمد: 1552-4957
1552-4949
DOI: 10.1002/cyto.b.20417
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff33195d2806642e7e94d05cd1d580e7
https://doi.org/10.1002/cyto.b.20417
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....ff33195d2806642e7e94d05cd1d580e7
قاعدة البيانات: OpenAIRE
الوصف
تدمد:15524957
15524949
DOI:10.1002/cyto.b.20417