Evaluation of a point-of-care rapid diagnostic test kit (SICKLECHECK) for screening of sickle cell diseases.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 06 02 2024
accepted: 05 08 2024
medline: 16 8 2024
pubmed: 16 8 2024
entrez: 16 8 2024
Statut: epublish

Résumé

Sickle cell diseases (SCD) are the most common genetic disorders with significant morbidity and mortality worldwide, including in India. The high prevalence of this disorder in many geographical regions calls for the use of a point-of-care rapid diagnostic test (RDT) for early screening and management of the diagnosed cases to reduce the allied clinical severity. In view of this, the present study was undertaken for the validation of a point-of-care RDT kit (SICKLECHECKTM) for the screening of SCD. This validation and diagnostic accuracy study was conducted among the cases advised for screening of SCD. For validation, all the recruited cases were investigated for both the SICKLECHECKTM RDT kit and HPLC (Variant-II) considering HPLC as a gold standard. A total of 400 cases were screened for both tests. For the presence and absence of sickle cell hemoglobin in the samples, SICKLECHECKTM RDT kit results showed a sensitivity and specificity of 99.39% and 98.73% respectively with references to HPLC findings. For the detection of the 'AS' pattern, the SICKLECHECKTM RDT kit has shown a sensitivity and specificity of 99.07% and 98.81% respectively. For the detection of the 'SS' pattern, the SICKLECHECKTM RDT kit has shown a sensitivity and specificity of 97.92% and 100.0% respectively. Cases with β thalassemia trait, hemoglobin E trait, hemoglobin Lepore trait and trait for hereditary-persistence-of-fetal-hemoglobin (high HbF %) diagnosed in HPLC were resulted with 'AA' pattern in SICKLECHECKTM RDT kit. The high sensitivity and specificity of the SICKLECHECKTM RDT kit insist on its use as a point-of-care screening tool for SCD especially where there is a lack of laboratory facilities as well as in hospital-based set-up requiring immediate diagnosis and management of SCD. However, for further confirmation, the samples should be analyzed with other gold standard techniques like HPLC.

Identifiants

pubmed: 39150948
doi: 10.1371/journal.pone.0309045
pii: PONE-D-24-04629
doi:

Substances chimiques

Reagent Kits, Diagnostic 0
Hemoglobin, Sickle 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0309045

Informations de copyright

Copyright: © 2024 Purohit et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Prasanta Purohit (P)

Multi-Disciplinary Research Unit, Maharaja Krishna Chandra Gajapati (M.K.C.G) Medical College, Berhampur, Odisha, India.

Chinmayee Parida (C)

Multi-Disciplinary Research Unit, Maharaja Krishna Chandra Gajapati (M.K.C.G) Medical College, Berhampur, Odisha, India.

Tapan Kumar Martha (TK)

Multi-Disciplinary Research Unit, Maharaja Krishna Chandra Gajapati (M.K.C.G) Medical College, Berhampur, Odisha, India.

Snehal Bholo (S)

Multi-Disciplinary Research Unit, Maharaja Krishna Chandra Gajapati (M.K.C.G) Medical College, Berhampur, Odisha, India.

Aparupa Naik (A)

Multi-Disciplinary Research Unit, Maharaja Krishna Chandra Gajapati (M.K.C.G) Medical College, Berhampur, Odisha, India.

Samira Kumar Behera (SK)

Multi-Disciplinary Research Unit, Maharaja Krishna Chandra Gajapati (M.K.C.G) Medical College, Berhampur, Odisha, India.
Department of Pathology, Maharaja Krishna Chandra Gajapati (M.K.C.G) Medical College, Berhampur, Odisha, India.

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