Children in the resource-challenged sub-Saharan African region living with the painful and deadly blood disease sickle cell anemia (SCA) can now be cured with a daily dosage of hydroxyurea pill. The disease is known to be prevalent in the region and the healthcare availability is poor.
This is what a large multinational clinical trial called REACH discovered when it tested daily hydroxyurea treatment in 606 children between the ages of 1 and 10 years old. The children took a pill each day for six months, followed by increases in the daily dosages based on their health status and weight. Initial doses varied between 15-20 mg/kg a day.
Sickle Cell Anemia
Sickle cell anemia (SCA) is a genetic blood disorder caused by abnormal inherited hemoglobin. Sickle cell anemia is the most common form of sickle cell disease.
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‘Hydroxyurea is safe to use and is effective in improving anemia, reducing sickle cell pain events and malaria and better survival for the patients.’
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The treatment improved their health by controlling SCA symptoms and, in an expected finding, giving them some protection from malaria that is also prevalent in the region, according to the study's lead physicians at Cincinnati Children's Hospital Medical Center and Centre Hospitalier Monkole in Kinshasa, in the Democratic Republic of the Congo.
Study results are published today online by The New England Journal of Medicine in conjunction with being presented at the American Society of Hematology's annual meeting in San Diego.
![Hemolytic Anemia]( "Hemolytic Anemia")
Hemolytic anemia, also known as hemolysis, is a condition where the destruction of red blood cells outpaces its production. It occurs both in infants and adults.
The clinical trial determined that hydroxyurea therapy is feasible to use and safe for children in sub-Saharan Africa. Compared to pre-treatment levels, hydroxyurea use was linked to reduced rates of sickle cell pain by an average of 55 percent, infections by 38 percent, malaria by 51 percent, transfusions by 67 percent, and death by 70 percent.
"Hydroxyurea was safe and offered many benefits to these young patients, including improved anemia, fewer sickle cell pain events, less malaria, and better survival," said Russell Ware, MD, PhD, the study's senior investigator and a physician-scientist at the Cincinnati Children's Cancer and Blood Diseases Institute.
Also leading the clinical trial was Leon Tshilolo, MD, PhD, at the Centre Hospitalier Monkole. Investigators named the study REACH, an acronym for Realizing Effectiveness Across Continents with Hydroxyurea. According to Tshilolo, the clinical trial lived up to its name.
"The study shows the importance of research partnerships between the US and Africa to improve clinical care," he said. "Even in an African setting hydroxyurea is feasible to use, accepted by patients and families, well-tolerated, and safe for children with sickle cell anemia. Almost all of the children had clinical improvements, and the older patients were well enough to attend school."
SCA's Heavy Burden
Caused by a genetic mutation and most prevalent in people of African ancestry, SCA is a painful disease where blood cells turn sickle-shaped and become stuck in the vascular system where they block blood flow. This can damage vital organs and cause death. Hydroxyurea works by significantly increasing both hemoglobin and fetal hemoglobin in the blood, which helps reduce sickling, anemia and other impacts on patients.
Available therapies to treat SCA effectively are limited, although numerous studies in recent years--almost all in developed countries--show that hydroxyurea is a safe and effective drug for managing the disease and improving quality of life.
SCA affects more than 90,000 people in the United States and millions of people worldwide, with 75 percent of the disease's burden in sub-Saharan Africa. Other nations with high incidence rates are India, nations in the Caribbean, Central America, and South America.
Because of the lack of detailed medical records, the best available estimates are that 50 to 90 percent of infants with SCA born in sub-Saharan Africa die before the age of 5, according to a 2017 paper published by Cincinnati Children's researchers that included Ware. The paper also reported that efforts to help people in the region with SCA have been stagnant because most affected people lack access to basic diagnostics and clinical care.
Institutions like Cincinnati Children's are working with ASH and the National Heart, Lung, and Blood Institute (part of NIH) to invest in research and clinical programs and address the global burden of SCA in limited-resource settings, especially sub-Saharan Africa.
The Phase 1-2 multi-center open-label REACH clinical trial treated children in four sub-Saharan countries: the Democratic Republic of Congo, Uganda, Kenya and Angola. Researchers plan to follow children in the study long-term to get additional data about growth and development and to look for any possible effects on organ function and fertility.
Source: Eurekalert
Hemolytic Anemia
Hemolytic anemia, also known as hemolysis, is a condition where the destruction of red blood cells outpaces its production. It occurs both in infants and adults.
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The clinical trial determined that hydroxyurea therapy is feasible to use and safe for children in sub-Saharan Africa. Compared to pre-treatment levels, hydroxyurea use was linked to reduced rates of sickle cell pain by an average of 55 percent, infections by 38 percent, malaria by 51 percent, transfusions by 67 percent, and death by 70 percent.
"Hydroxyurea was safe and offered many benefits to these young patients, including improved anemia, fewer sickle cell pain events, less malaria, and better survival," said Russell Ware, MD, PhD, the study's senior investigator and a physician-scientist at the Cincinnati Children's Cancer and Blood Diseases Institute.
Also leading the clinical trial was Leon Tshilolo, MD, PhD, at the Centre Hospitalier Monkole. Investigators named the study REACH, an acronym for Realizing Effectiveness Across Continents with Hydroxyurea. According to Tshilolo, the clinical trial lived up to its name.
"The study shows the importance of research partnerships between the US and Africa to improve clinical care," he said. "Even in an African setting hydroxyurea is feasible to use, accepted by patients and families, well-tolerated, and safe for children with sickle cell anemia. Almost all of the children had clinical improvements, and the older patients were well enough to attend school."
SCA's Heavy Burden
Caused by a genetic mutation and most prevalent in people of African ancestry, SCA is a painful disease where blood cells turn sickle-shaped and become stuck in the vascular system where they block blood flow. This can damage vital organs and cause death. Hydroxyurea works by significantly increasing both hemoglobin and fetal hemoglobin in the blood, which helps reduce sickling, anemia and other impacts on patients.
Available therapies to treat SCA effectively are limited, although numerous studies in recent years--almost all in developed countries--show that hydroxyurea is a safe and effective drug for managing the disease and improving quality of life.
SCA affects more than 90,000 people in the United States and millions of people worldwide, with 75 percent of the disease's burden in sub-Saharan Africa. Other nations with high incidence rates are India, nations in the Caribbean, Central America, and South America.
Because of the lack of detailed medical records, the best available estimates are that 50 to 90 percent of infants with SCA born in sub-Saharan Africa die before the age of 5, according to a 2017 paper published by Cincinnati Children's researchers that included Ware. The paper also reported that efforts to help people in the region with SCA have been stagnant because most affected people lack access to basic diagnostics and clinical care.
Institutions like Cincinnati Children's are working with ASH and the National Heart, Lung, and Blood Institute (part of NIH) to invest in research and clinical programs and address the global burden of SCA in limited-resource settings, especially sub-Saharan Africa.
The Phase 1-2 multi-center open-label REACH clinical trial treated children in four sub-Saharan countries: the Democratic Republic of Congo, Uganda, Kenya and Angola. Researchers plan to follow children in the study long-term to get additional data about growth and development and to look for any possible effects on organ function and fertility.
Source: Eurekalert
Nodding Syndrome / Nodding Disease
Nodding syndrome or nodding disease is a neurological illness that affects children in the African countries of Sudan, Uganda and Tanzania.
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