# Addressing Barriers to the Development and Adoption of Rapid Diagnostic Tests in Global Health

**Authors:** Eric Miller, Hadley D. Sikes

PMC · DOI: 10.5772/61114 · Nanobiomedicine · 2015-11-19

## TL;DR

This paper explores the challenges in developing and adopting rapid diagnostic tests for global health and suggests ways to overcome them.

## Contribution

The paper identifies and discusses barriers to the broader adoption of RDTs beyond malaria and proposes a path forward.

## Key findings

- RDTs for malaria have achieved high maturity and market penetration.
- Adoption of RDTs for other diseases is hindered by technical, social, and economic challenges.
- Addressing these barriers could improve global health outcomes through broader RDT use.

## Abstract

Immunochromatographic rapid diagnostic tests (RDTs) have demonstrated significant potential for use as point-of-care diagnostic tests in resource-limited settings. Most notably, RDTs for malaria have reached an unparalleled level of technological maturity and market penetration, and are now considered an important complement to standard microscopic methods of malaria diagnosis. However, the technical development of RDTs for other infectious diseases, and their uptake within the global health community as a core diagnostic modality, has been hindered by a number of extant challenges. These range from technical and biological issues, such as the need for better affinity agents and biomarkers of disease, to social, infrastructural, regulatory and economic barriers, which have all served to slow their adoption and diminish their impact. In order for the immunochromatographic RDT format to be successfully adapted to other disease targets, to see widespread distribution, and to improve clinical outcomes for patients on a global scale, these challenges must be identified and addressed, and the global health community must be engaged in championing the broader use of RDTs.

## Linked entities

- **Diseases:** malaria (MONDO:0005136)

## Full-text entities

- **Genes:** IVNS1ABP (influenza virus NS1A binding protein) [NCBI Gene 10625] {aka ARA3, FLARA3, HSPC068, IMD70, KLHL39, ND1}, HDGFL2 (HDGF like 2) [NCBI Gene 84717] {aka HDGF-2, HDGF2, HDGFRP2, HRP-2, HRP2}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, RNF130 (ring finger protein 130) [NCBI Gene 55819] {aka G1RP, G1RZFP, GOLIATH, GP}
- **Diseases:** syphilis (MESH:D013587), resistance (MESH:D060467), visceral leishmaniasis (MESH:D007898), infectious disease (MESH:D003141), febrile symptoms (MESH:D012816), influenza (MESH:D007251), P. falciparum malaria (MESH:D016778), infected (MESH:D007239), TB (MESH:D014376), leptospirosis (MESH:D007922), febrile illness (MESH:D005334), chikungunya (MESH:D065632), dengue (MESH:D003715), RDT (MESH:C563738), febrile (MESH:D000071072), sexually transmitted infections (MESH:D012749), rheumatoid factors (MESH:D001171), HIV (MESH:D015658), enteric fever (MESH:D014435), dengue haemorrhagic fever (MESH:D019595), deaths (MESH:D003643), yellow fever (MESH:D015004), brucellosis (MESH:D002006), tumour (MESH:D009369), -borne (MESH:D017282), Malaria (MESH:D008288), tropical diseases (MESH:D015493), bacterial, viral or parasitic infections (MESH:D014777), cholera (MESH:D002771), pneumonia (MESH:D011014)
- **Chemicals:** lipopolysaccharide (MESH:D008070), cephalosporin (MESH:D002511), sucrose (MESH:D013395), carbon (MESH:D002244), mannan (MESH:D008351), Coartem (MESH:D000077611), haem (MESH:D006418), silver (MESH:D012834), sugar (MESH:D000073893), disaccharide (MESH:D004187), cellulose (MESH:D002482), LAM (MESH:C050016), Au (MESH:D006046), artemisinin (MESH:C031327), silica (MESH:D012822), oligonucleotide (MESH:D009841), polymer (MESH:D011108), trehalose (MESH:D014199), AgNPs (-), cobalt dichloride (MESH:C018021), methyl violet (MESH:D005840), iron salts (MESH:C000499), phenolphthalein (MESH:D020113)
- **Species:** Ebola virus (no rank) [taxon 1570291], EV [taxon 2844103], Komagataella pastoris (species) [taxon 4922], Escherichia coli (E. coli, species) [taxon 562], Gallus gallus (bantam, species) [taxon 9031], Plasmodium vivax (malaria parasite P. vivax, species) [taxon 5855], Plasmodium falciparum (malaria parasite P. falciparum, species) [taxon 5833], Mus musculus (house mouse, species) [taxon 10090], Dengue virus (no rank) [taxon 12637], Human immunodeficiency virus 1 (no rank) [taxon 11676], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Homo sapiens (human, species) [taxon 9606], Mycobacterium tuberculosis (species) [taxon 1773]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC4652944/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC4652944/full.md

## References

137 references — full list in the complete paper: https://tomesphere.com/paper/PMC4652944/full.md

---
Source: https://tomesphere.com/paper/PMC4652944