Sickle Cell Disease by V. Tran, N. Archer | OPENPediatrics

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  • เผยแพร่เมื่อ 15 มิ.ย. 2024
  • By the end of this video, the learner will be able to describe the fundamental elements of sickle cell disease, including pathophysiology, potential complications, and management strategies.
    0:00 Introduction
    3:18 Pathophysiology
    5:06 Complications
    9:13 Management
    15:13 Summary
    LEARNING OBJECTIVES
    By the end of this video, the learner will be able to:
    • Describe the fundamental elements of sickle cell disease
    • Discuss the pathophysiology of sickle cell disease
    • Identify the common complications seen in this condition
    • Describe the management options for sickle cell disease and its complications
    AUTHORS
    Virginia Tran, BS
    Harvard Medical School
    Natasha Archer, MD
    Physician
    Dana Farber/Boston Children's Cancer and Blood Disorders Center
    Assistant Professor of Pediatrics
    Harvard Medical School
    DATES
    Initial publication: June 9, 2023
    A multilingual transcript is available for this video, thanks to the generous support of our community members who volunteered their time to translate our content. Learn more about our OPENPediatrics translation campaign here: www.openpediatrics.org/conten...
    Please visit: www.openpediatrics.org

    OPENPediatrics™ is an interactive digital learning platform for healthcare clinicians sponsored by Boston Children's Hospital and in collaboration with the World Federation of Pediatric Intensive and Critical Care Societies. It is designed to promote the exchange of knowledge between healthcare providers around the world caring for critically ill children in all resource settings. The content includes internationally recognized experts teaching the full range of topics on the care of critically ill children. All content is peer-reviewed and open-access and thus at no expense to the user.
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    CITATION
    Tran V, Callas C, Moulton H, Fantasia K, McFee AM, Wolbrink TA, Archer N. Sickle Cell Disease. 06/2023. OPENPediatrics. • Sickle Cell Disease by... .
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ความคิดเห็น • 6

  • @DrMohamedAyyedi
    @DrMohamedAyyedi ปีที่แล้ว +1

    Very common in Tunisia 🇹🇳🇹🇳🌶️🌶️

  • @Rene-uz3eb
    @Rene-uz3eb 5 หลายเดือนก่อน

    6:45 a higher calcium diet in rats delayed hypertrophy. Bp medication made it worse.
    Careful though: large intake will result in more urinary calcium, effected by calcitonin, and the precalcitonin levels are used to diagnose serious infections. So calcium intake right before a blood test should be avoided

  • @teanikahoffman1189
    @teanikahoffman1189 8 หลายเดือนก่อน +1

    Please stop telling providers the genotype HbSC is “ milder” by the time a person reaches adulthood it all becomes severe

  • @Praise_ye_Yahweh
    @Praise_ye_Yahweh 7 หลายเดือนก่อน

    I find the video very helpful, but the mutation occurs on the 11th chromosome, not the 6th chromosome.

    • @rukayarasheed5421
      @rukayarasheed5421 6 หลายเดือนก่อน

      Its 6 chromosome not 11

    • @Praise_ye_Yahweh
      @Praise_ye_Yahweh 6 หลายเดือนก่อน

      ​@@rukayarasheed5421I don't know everything, but I see the 11th in what I have read, if it would be easy for you, could you please provide me a source to check?
      Here are some sources that state the 11th: www.genome.gov/Genetic-Disorders/Sickle-Cell-Disease#:~:text=Sickle%20cell%20disease%20is%20caused,and%20glide%20through%20blood%20vessels.
      www.cdc.gov/genomics/about/basics.htm