YOU NEED TO LEARN ABOUT SICKLE CELL TRAIT

On January 18th this year, Shanice Clark 21 a college basketball star of California University of Pennsylvania was found unresponsive in her dorm room. She was rushed to Monongahela Valley Hospital but she could not be revived and was pronounced dead. California borough police said that a preliminary report from medical personnel indicated the death appeared to be accidental and there were suggestions she had choked on gum while sleeping.

On Monday this week a Washington coroner Tim Warco’s report blamed the death of the college star on sickle cell trait.
Sickle cell trait means having one gene for a condition called sickle cell disease (SCD). This in itself does not normally cause problems and sickle cell trait is not considered as a disease. It is extremely rare for it to cause problems or complications, which mainly occur under conditions of severe physical stress.
There has been a long term discussion on whether sickle cell trait can cause pain and other complications or not except under extreme conditions. Their debate has existed for more than 50 years and some professors who have managed sickle cell cases for long time have refused to accept that sickle cell trait can cause complications despite the fact that they have come across many cases of trait carriers who get complications like haematuria.
I remember a review written by a professor in sickle cell about a research that had been done and published in Journal of American Forensics by Charis Kepron M.D, Gino R. Somers M.B.B.S, Ph.D and Michael S. Pollanen, Ph.D titled Sickle Cell Trait Mimicking Multiple Inflicted Injuries in a 5-Year-Old Boy (September 2009), in his review he argued that a person with the trait cannot get complications. In their research they had described a case of sudden unexpected death in a 5-year-old child with undiagnosed Sickle Cell Trait due to the Acute Chest Syndrome.




The boy’s story according to the paper was “5-year-old boy of Ghanaian origin was reportedly well except for a dry cough that was initially noted on the morning of the day he died. He had been given a single dose of an over-the-counter cough medication in the early evening, and on his way to bed began to vomit. His parents described copious vomiting from the nose and mouth, and EMS was called. Paramedics arrived to find the child with no vital signs and it appeared to them at the time of initial assessment that he had aspirated. Intubation attempts in the field were unsuccessful; therefore, the boy was bag-ventilated until his arrival at the nearest Emergency Department (ED) 30 min after the onset of vomiting. He was successfully incubated in the ED, and during the resuscitation efforts it was noted that his abdomen appeared distended, a sign that appeared to worsen over the course of treatment. The anaesthetist involved reported thick secretions in the airway and high airway resistance. The resuscitation attempt was unsuccessful and the boy was declared dead 30 min after arriving in the ED. There were no signs of injury, and the child appeared well cared for.”

The issue of sickle cell trait complications has remained controversial as the complications experienced themselves. No body seems to explain why the complications exist.

In both cases of Shanice and the 5 years old boy the preliminary investigations always focus on the soft points.
With the rampant increase in the number of people with the trait in the world there is a need to educate everybody concerned.
There is a need to have comprehensive education and awareness programs for everyone with a major emphasis on coaches, healthcare professionals, parents, and student-athletes on sickle cell trait and the prevention of sudden death. Sickle cell trait should not prevent anyone from participating in athletic activity; however, recent deaths from exertional sickling events in the athlete setting have demonstrated the need for more education. Education and prevention programs are the key to preventing an exertional sickling event.
Sickle cell trait is a generally benign condition in red blood cells sometimes causing them to carry oxygen differently. Athletes with sickle cell trait run the risk of experiencing exertional sickling events that may have injurious outcomes. Complications from sickle cell trait while exercising are mostly preventable.
There is also a need to have population screening for the sickle cell trait. A population unaware of the sickle cell trait (SCT) has resulted in a large population of individuals entering childbearing age with no knowledge of their risk.

Love life!

Lea.

 

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