Fatal Factors of Sickle Cell Trait

When:  Oct 22, 2025 from 13:00 to 14:00 (ET)

2025 NSH Laboratory Webinar Series

Laboratory Webinars are a great, inexpensive way to provide continuing education to a large number of employees.  You have access to the live session AND the recordings for one year.  The cost for each session is the same regardless of the number of attendees!

Webinar Description

Sickle Cell Trait (SCT) affects nearly 300 million people worldwide. Awareness that SCT is not an entirely benign condition is growing, but many pathologists and clinicians overlook the fact that sickling may become fatal under certain conditions in patients with the trait. At autopsy, micro-occlusive sickling is identified and SCT is confirmed by postmortem hemoglobin fractionation which proves the trait to be a contributory factor to the cause of death.   This workshop discusses the controversy of SCT as a contributory cause of death, and explores autopsy findings in hospitalized patients with SCT dying of natural disease. Participants will get an understanding of the difference between the trait and the actual disease. We will also take a glimpse at S/E hemoglobinopathy, a rare form of sickle disease.

Webinar Pricing

Full Series Subscription -  $899.00
Individual Webinars  - $99.00

Registration

Register for individual webinars by topic or for the full series (best value).  Click here to register today.


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Contact

Debra Grandy
(443) 535-4060
debra@nsh.org