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Field evaluation of a prototype paper-based point-of-care fingerstick transaminase test.
Pollock, Nira R; McGray, Sarah; Colby, Donn J; Noubary, Farzad; Nguyen, Huyen; Nguyen, The Anh; Khormaee, Sariah; Jain, Sidhartha; Hawkins, Kenneth; Kumar, Shailendra; Rolland, Jason P; Beattie, Patrick D; Chau, Nguyen V; Quang, Vo M; Barfield, Cori; Tietje, Kathy; Steele, Matt; Weigl, Bernhard H.
Afiliação
  • Pollock NR; Division of Infectious Diseases, Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States of America ; Department of Laboratory Medicine, Boston Children's Hospital, Boston, Massachusetts, United States of America.
PLoS One ; 8(9): e75616, 2013.
Article em En | MEDLINE | ID: mdl-24098705
ABSTRACT
Monitoring for drug-induced liver injury (DILI) via serial transaminase measurements in patients on potentially hepatotoxic medications (e.g., for HIV and tuberculosis) is routine in resource-rich nations, but often unavailable in resource-limited settings. Towards enabling universal access to affordable point-of-care (POC) screening for DILI, we have performed the first field evaluation of a paper-based, microfluidic fingerstick test for rapid, semi-quantitative, visual measurement of blood alanine aminotransferase (ALT). Our objectives were to assess operational feasibility, inter-operator variability, lot variability, device failure rate, and accuracy, to inform device modification for further field testing. The paper-based ALT test was performed at POC on fingerstick samples from 600 outpatients receiving HIV treatment in Vietnam. Results, read independently by two clinic nurses, were compared with gold-standard automated (Roche Cobas) results from venipuncture samples obtained in parallel. Two device lots were used sequentially. We demonstrated high inter-operator agreement, with 96.3% (95% C.I., 94.3-97.7%) agreement in placing visual results into clinically-defined "bins" (<3x, 3-5x, and >5x upper limit of normal), >90% agreement in validity determination, and intraclass correlation coefficient of 0.89 (95% C.I., 0.87-0.91). Lot variability was observed in % invalids due to hemolysis (21.1% for Lot 1, 1.6% for Lot 2) and correlated with lots of incorporated plasma separation membranes. Invalid rates <1% were observed for all other device controls. Overall bin placement accuracy for the two readers was 84% (84.3%/83.6%). Our findings of extremely high inter-operator agreement for visual reading-obtained in a target clinical environment, as performed by local practitioners-indicate that the device operation and reading process is feasible and reproducible. Bin placement accuracy and lot-to-lot variability data identified specific targets for device optimization and material quality control. This is the first field study performed with a patterned paper-based microfluidic device and opens the door to development of similar assays for other important analytes.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise Química do Sangue / Monitoramento de Medicamentos / Sistemas Automatizados de Assistência Junto ao Leito / Alanina Transaminase / Doença Hepática Induzida por Substâncias e Drogas / Testes de Função Hepática Tipo de estudo: Evaluation_studies / Prognostic_studies Limite: Humans País como assunto: Asia Idioma: En Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise Química do Sangue / Monitoramento de Medicamentos / Sistemas Automatizados de Assistência Junto ao Leito / Alanina Transaminase / Doença Hepática Induzida por Substâncias e Drogas / Testes de Função Hepática Tipo de estudo: Evaluation_studies / Prognostic_studies Limite: Humans País como assunto: Asia Idioma: En Ano de publicação: 2013 Tipo de documento: Article