Sickle Cell Trait

Overview

4.8 out of 5 (9 Reviews)

Credits

1.00

Post Assessment Questions

5

Start Date

1 Sep 2023

Last Review Date

25 Feb 2024

Expiration Date

31 Aug 2026

Estimated Time To Finish

60 Minutes


 
Need Help?  If you have a system or content concerns, please contact support@statpearls.com

Activity Description

Sickle cell trait is a genetic condition that results when an individual inherits a gene for normal hemoglobin (A) and a gene for sickle hemoglobin (S) that results in the genotype (AS). Conversely, sickle cell disease occurs when an individual inherits 2 abnormal sickle genes (SS). Unlike individuals with SCD, those with SCT do not have symptoms related to sickling and consequently tend to have a better quality of life than patients who have SCD. Sickle cell disease results in lifelong debilitation and early mortality due to chronic anemia and organ damage, leading to poor quality of life. Sickle cell trait, on the other hand, is relatively benign because patients do not have vaso-occlusive crises as individuals with sickle cell disease do; they have a better quality of life, and mortality is the same as the rest of the general population.

Sickle cell trait is generally diagnosed through screening tests followed by confirmatory testing or genetic analysis. Since the Sickle Cell Anemia Act was established in 1972, there has been increased screening for sickle cell trait and disease. Furthermore, each state in the US now offers universal newborn screening before discharge from the hospital. This activity for healthcare professionals is designed to enhance the learner's competence when managing sickle cell trait, equipping them with updated knowledge, skills, and strategies for timely identification, effective interventions, and improved care coordination, leading to better patient outcomes and reduced morbidity.


Target Audience

This activity has been designed to meet the educational needs of physicians, physician associates, nurses, pharmacists, and nurse practitioners.

Learning Objectives

At the conclusion of this activity, the learner will be better able to:

  • Identify characteristic features of sickle cell trait, distinguishing them from other hemoglobinopathies.

  • Screen individuals for sickle cell trait, considering familial history and genetic factors.

  • Differentiate between sickle cell trait and sickle cell disease, ensuring accurate diagnosis and appropriate counseling.

  • Collaboration with the interprofessional team members to prevent or manage complications so patients with sickle cell trait have improved quality of life and outcomes. 

Disclosures

StatPearls, LLC requires everyone who influences the content of an educational activity to disclose relevant financial relationships with ineligible companies that have occurred within the past 24 months. Ineligible companies are organizations whose primary business is producing, marketing, selling, re-selling, or distributing healthcare products used by or on patients. All relevant conflict(s) of interest have been mitigated. Hover over contributor names for financial disclosures. Others involved in planning this educational activity have no relevant financial relationships to disclose.

Commercial Support: This activity has received NO commercial support.

Continuing Education Accreditation Information

In support of improving patient care, StatPearls, LLC is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC) to provide continuing education for the healthcare team.

 

Nurses: StatPearls designates this activity for 1.00 ANCC contact hour(s). Nurses should only claim credit commensurate with the extent of their participation in the activity.

Please consult your professional licensing board for information on the applicability and acceptance of continuing education credit for this activity.

Method of Participation and Credit

  1. Register for the activity.    
  2. Review the target audience, learning objectives, and disclosure information.
  3. Study the educational content of the enduring material.
  4. Choose the best answer to each activity test question. To receive credit and a certificate, you must pass the test questions with a minimum score of 100%.
  5. Complete the post-activity assessment survey.

If you have concerns regarding the CE/CME system, please contact support@statpearls.com.

Disclaimer

This educational activity was planned and produced in accordance with the ACCME Standards for Integrity and Independence in Accredited Continuing Education. Faculty may discuss investigational products or off-label uses of products regulated by the US Food and Drug Administration. Readers should verify all information before employing any therapies described in this educational activity.

The information provided for this activity is for continuing education purposes only and is not meant to substitute for the independent medical/clinical judgment of a healthcare provider relative to diagnostic and treatment options of a specific patient’s medical condition. The information presented does not necessarily reflect the views of StatPearls or any commercial supporters of educational activities on statpearls.com. StatPearls expressly disclaims responsibility for any adverse consequences resulting directly or indirectly from information in the course, for undetected error, or through a participant's misunderstanding of the content.

Unapproved Uses of Drugs/Devices: In accordance with FDA requirements, the audience is advised that information presented in this continuing education activity may contain references to unlabeled or unapproved uses of drugs or devices. Please refer to the FDA-approved package insert for each drug/device for full prescribing/utilization information.

Cancellation Policy: Please see the cancellation policy. StatPearls, LLC reserves the right to cancel any course due to unforeseen circumstances.

 

 
 

Reviews

Jennifer K. on 3/6/2022

Dr.Ayodhyaprasad S. on 7/11/2022

Michael F. on 12/13/2022

Khelsea C. on 12/15/2022

Gautam P. on 3/27/2023

Dr Sruthi G. on 6/17/2023

Michael L. on 11/1/2023

nduka-obi o. on 12/28/2023

Mary K. on 4/11/2024

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