Literature DB >> 28617057

Preliminary Evaluation of a Point-of-Care Testing Device (SickleSCAN™) in Screening for Sickle Cell Disease.

Maxwell M Nwegbu1,2, Hezekiah A Isa3,2, Biyaya B Nwankwo4,2, Chinedu C Okeke3,2, Uduak J Edet-Offong2, Norah O Akinola5, Adekunle D Adekile6, John C Aneke7, Emmanuel C Okocha7, Thomas Ulasi7, Usman Abjah8, Ngozi I Ugwu9, Angela A Okolo10,11, Anazoeze Madu11, Ifeoma Emodi11, Ahmed Girei12, Taiwo M Balogun13, Ijeoma N Diaku-Akinwumi13, Chinatu Ohiaeri14, Biobele J Brown15, John A Olaniyi15, Abdulaziz Hassan16, Sani Awwalu16, Dorothy A Okoh17, Obiageli E Nnodu3,2.   

Abstract

Sickle cell disease affects about 150,000 births annually in Nigeria. Early diagnosis is hampered by factors such as centralized and urban localization of laboratories, high cost of diagnostic equipment and inadequate skilled manpower to operate them. The need for a low-cost, portable, easy-to-use diagnostic test for sickle cell disease is critical, especially in resource-poor countries. In this study, we evaluated the performance characteristics of a novel point-of-care testing device (SickleSCAN™), and its acceptability and feasibility, as a possible screening tool for sickle cell disease. In the first phase, we assessed the performance characteristics of SickleSCAN™ by evaluating 57 subjects comprising both children and adults attending a primary health center, for Hb SS (βS/βS; HBB: c.20A>T), Hb SC (βS/βC; HBB: c.19G>A) and Hb AS (βA/βS) using SickleSCAN™, cellulose acetate electrophoresis (CAE) and high performance liquid chromatography (HPLC). Performance characteristics such as diagnostic sensitivity and specificity were compared to HPLC as a standard method. We subsequently undertook a second phase wherein the acceptability and feasibility of the device for sickle cell disease screening, was evaluated using semi-structured and structured questionnaires among 197 healthcare personnel and 221 subjects, respectively. Sickle cell disease was carried by 3.4% of the subjects. The diagnostic sensitivity, specificity and test efficiency of SickleSCAN™ for sickle cell disease (Hb SS and Hb SC), were 100.0, 98.2 and 98.2%, respectively. Findings from this study showed SickleSCAN™ to be a viable screening tool that can easily be applied in community-based screening for early diagnosis of sickle cell disease with little expertise and low cost.

Entities:  

Keywords:  Point-of-care; screening; sensitivity; sickle cell disease; specificity

Mesh:

Substances:

Year:  2017        PMID: 28617057     DOI: 10.1080/03630269.2017.1329151

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  4 in total

1.  Simultaneous point-of-care detection of anemia and sickle cell disease in Tanzania: the RAPID study.

Authors:  Luke R Smart; Emmanuela E Ambrose; Kevin C Raphael; Adolfine Hokororo; Erasmus Kamugisha; Erika A Tyburski; Wilbur A Lam; Russell E Ware; Patrick T McGann
Journal:  Ann Hematol       Date:  2017-11-16       Impact factor: 3.673

2.  Empowering newborn screening programs in African countries through establishment of an international collaborative effort.

Authors:  Bradford L Therrell; Michele A Lloyd-Puryear; Kwaku Ohene-Frempong; Russell E Ware; Carmencita D Padilla; Emmanuela E Ambrose; Amina Barkat; Hassan Ghazal; Charles Kiyaga; Tisungane Mvalo; Obiageli Nnodu; Karim Ouldim; Mohamed Chérif Rahimy; Brígida Santos; Léon Tshilolo; Careema Yusuf; Guisou Zarbalian; Michael S Watson
Journal:  J Community Genet       Date:  2020-05-15

3.  Diagnostic accuracy in field conditions of the sickle SCAN® rapid test for sickle cell disease among children and adults in two West African settings: the DREPATEST study.

Authors:  Akueté Yvon Segbena; Aldiouma Guindo; Romain Buono; Irénée Kueviakoe; Dapa A Diallo; Gregory Guernec; Mouhoudine Yerima; Pierre Guindo; Emilie Lauressergues; Aude Mondeilh; Valentina Picot; Valériane Leroy
Journal:  BMC Hematol       Date:  2018-09-17

4.  HemoTypeSC, a low-cost point-of-care testing device for sickle cell disease: Promises and challenges.

Authors:  Obiageli Nnodu; Hezekiah Isa; Maxwell Nwegbu; Chinatu Ohiaeri; Samuel Adegoke; Reuben Chianumba; Ngozi Ugwu; Biobele Brown; John Olaniyi; Emmanuel Okocha; Juliet Lawson; Abdul-Aziz Hassan; Ijeoma Diaku-Akinwumi; Anazoeze Madu; Osita Ezenwosu; Yohanna Tanko; Umar Kangiwa; Ahmed Girei; Yetunde Israel-Aina; Adama Ladu; Perpetua Egbuzu; Usman Abjah; Angela Okolo; Nagihan Akbulut-Jeradi; Maria Fernandez; Frédéric B Piel; Adekunle Adekile
Journal:  Blood Cells Mol Dis       Date:  2019-02-08       Impact factor: 3.039

  4 in total

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