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  • Sickle Cell Disorder: How wrong diagnosis has ruined lives, families – Expert
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Sickle Cell Disorder: How wrong diagnosis has ruined lives, families – Expert

Admin January 7, 2020

Fingers affected by sickle cell

Fingers affected by sickle cell

The Sickle Cell Hope Alive Foundation (SCHAF) says wrong genotype diagnosis is a major contributing factor to the high prevalence rate of Sickle Cell Disease (SCD) in Nigeria.

Its President, Prof. Adeyinka Falusi, made this known at a news conference on Monday in Ibadan.

The news conference was held to kick start the annual “Know Your Genotype (KYG) Workshop” organised by the NGO for school-age children and parents.

The workshop has the tagline: “Changing the Dynamics to Reduce the Burden of SCD in Nigeria.”

Falusi, a Professor of Haematology and Genetics, said that the most commonly used diagnostic tests for genotype was costly and might take weeks, which could result in misdiagnosis.

“SCD is the commonest genetic inherited blood disorder in Nigeria affecting over four million individuals and with about 40 million sickle cell trait carriers.

“In Nigeria, genotype testing is very difficult and sometimes inaccurate; we cannot talk about awareness of SCD without accessible and affordable genotype testing methods.

“Genotype wrong diagnosis has resulted in people choosing incompatible partners and spouses, thus resulting in more children being born with SCD.

“SCHAF is stepping in to support the government to fashion out ways in which we can reduce the public health burden of SCD through accurate diagnosis and awareness, which are hallmarks of prevention strategy,” she said.

According to her, the foundation has started making use of a fast, inexpensive diagnostic tool for SCD screening called HemoType SC to facilitate accessible and affordable access to genotype screening in the country.

“The diagnostic test ‘HemoTypeSC’ is a point of care rapid test kit that has been approved by the World Health Organisation (WHO).

“The kit, which is being used in countries like Canada, Uganda and Ghana, is a viable option for the highly sensitive rapid diagnosis of sickle cell disease.

“The HemoTypeSC tool is for accurate and on the spot result for blood genotype.

“It is affordable and easy to use on the field, especially in hard to reach areas like the rural settings and low-income communities.

“It requires no special facilities, only a small amount of blood is needed and the results are available within 15 minutes window of operation with 99.9 per cent accuracy when compared to other standard diagnostic methods.

“The quick and accurate testing can inform parental choices and reduce the incidence of SCD births on the country,” she said.

Falusi, however, appealed to the government to have a robust Sickle Cell Disease Prevention programmes like those available for diseases like HIV and polio in order to reduce the prevalence rate.

In her remarks, Dr Chinedum Babablola, said that government should also subsidise the drugs used in SCD treatment like that of HIV.

Bablola, also Vice-Chancellor, Chrisland University, Abeokuta, said that subsidised and affordable treatment of SCD would help reduce its attendant morbidity and mortality rate.

“Government and corporate organisations have done a lot to reduce the cost of HIV treatment in the country, they can do same for SCD and have programmes that support sickle cell prevention and early detection.

“There should also be concerted effort to make the point of care test kit widely available in the country, for early detection and accurate diagnosis.

“This is to improve the outcomes of individuals with SCD and reduce its public health burden,” she said. (NAN)

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Tags: Genotype HemoTypeSC Prof. Adeyinka Falusi Sickle Cell Disease Sickle Cell Hope Alive Foundation (SCHAF)

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