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Stroke risk rises in patients with sickle cell disease despite established guidelines

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Stroke risk rises in patients with sickle cell disease despite established guidelines

Stroke Risk Rises in Patients with Sickle Cell Disease Despite Established Guidelines

Sickle cell disease (SCD) is a genetic disorder that affects the red blood cells, causing them to become rigid and sickle-shaped. This can lead to various complications, one of the most serious being an increased risk of stroke. Despite the existence of established guidelines for stroke prevention in patients with SCD, a recent study has shown that the risk of stroke in these patients is still on the rise.

In a study published in the American Journal of Hematology, researchers found that the incidence of stroke in patients with SCD has increased over the past decade. This is particularly concerning given that there are well-established guidelines for stroke prevention in this patient population.

The study, which looked at data from over 8,000 patients with SCD, found that the incidence of stroke increased by 27% between 2004 and 2014. This is in contrast to the overall trend of declining stroke rates in the general population over the same time period.

One possible explanation for this increase in stroke risk among patients with SCD is poor adherence to established guidelines for stroke prevention. These guidelines recommend regular blood transfusions and the use of hydroxyurea, a medication that can help reduce the risk of stroke in these patients. However, the study found that many patients with SCD were not receiving these recommended treatments.

In addition to poor adherence to treatment guidelines, other factors such as socioeconomic status, access to healthcare, and comorbid conditions may also contribute to the increased risk of stroke in patients with SCD. Addressing these factors will be crucial in reducing the risk of stroke and improving outcomes for these patients.

It is important for healthcare providers to be aware of the increased risk of stroke in patients with SCD and to ensure that they are following established guidelines for stroke prevention. This includes regular monitoring, appropriate use of medications, and addressing any underlying risk factors that may contribute to stroke risk.

In conclusion, the study highlights the need for increased awareness and adherence to established guidelines for stroke prevention in patients with SCD. By addressing these issues, healthcare providers can help reduce the risk of stroke and improve outcomes for patients with this challenging condition.

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