治疗4Kids的转型:扩大知识转移能力
Fair Berg1, Kristy Conger1, Meghana Avula1
1Department of Global Pediatric Medicine, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Pediatric blood & cancer
|May 30, 2024
概括
儿童癌症患者的全球生存率差异很大. Cure4Kids为全球的医疗保健专业人员提供免费的在线儿科血液学/瘤学教育,旨在弥合这一差距.
科学领域:
- 儿科瘤学 儿科瘤学
- 医学教育 医学教育
- 全球卫生公平性全球卫生公平性
背景情况:
- 对于患有癌症和灾难性疾病的儿童而言,全球存在显著的生存差异.
- 医疗保健专业人员需要可访问的专业教育来解决这些差异.
- Cure4Kids旨在提供免费的,基于网络的儿科血液学/瘤学培训.
研究的目的:
- 重新设计Cure4Kids以满足医疗保健专业人员不断变化的需求.
- 提供免费的,基于网络的儿科血液学/瘤学教育.
- 介绍转型平台的设计和开发过程.
主要方法:
- 关于Cure4Kids平台转型的设计和开发阶段的概述.
- 描述了重新设计的Cure4Kids网站中包含的关键功能.
- 确定教育资源的未来扩展机会.
主要成果:
- 现在可以使用重新设计的Cure4Kids平台.
- 该平台提供免费的,基于网络的儿科血液学/瘤学教育.
- 已经确定了关键特征和未来的扩张机会.
结论:
- 经过重新设计的Cure4Kids平台解决了儿童瘤学教育的需求.
- 持续的发展和扩张将提高全球影响力和影响力.
- 提高医疗保健专业知识对于减少儿童癌症存活率差异至关重要.
相关概念视频
Methods Of Healthcare Delivery System
3.2K
At the different levels of the healthcare system, we see varying methods of healthcare used. These methods include managed care systems, case management, and primary healthcare.
Managed Care System:
The managed care system is designed to control the cost while maintaining the quality of care. The patient's care from admission to discharge is planned by the primary care provider or the case manager, also known as the gatekeeper. In a managed care system, the number of care providers is...
Managed Care System:
The managed care system is designed to control the cost while maintaining the quality of care. The patient's care from admission to discharge is planned by the primary care provider or the case manager, also known as the gatekeeper. In a managed care system, the number of care providers is...
3.2K
Methods of Nuclear Reprogramming
1.8K
Nuclear reprogramming is a process of transforming one cell type into an unrelated cell type by epigenetic changes that alter the cell’s original gene expression pattern. Such epigenetic changes force cells to express a different set of genes, which play a significant role in inducing transformation into other cell types. Nuclear reprogramming offers applications in reproductive cloning for livestock propagation and regenerative medicine — developing patient-specific cells for...
1.8K
Forced Transdifferentiation
1.9K
Transdifferentiation, also known as lineage reprogramming, was first discovered by Selman and Kafatos in 1974 in silkmoths. They observed that the moths’ cuticle-producing cells transformed into salt-producing cells. Many such cases of natural transdifferentiation occur in organisms. In humans, pancreatic alpha cells can become beta cells. In newts, the loss of the eye’s lens causes the pigmented epithelial cells to transdifferentiate into the lens cells.
Artificial...
Artificial...
1.9K
Nursing Clinical Information System
765
Nursing Clinical Information System (NCIS)
A Nursing Clinical Information System (NCIS) is a specialized type of healthcare information system tailored to meet the unique needs of nursing practice. It incorporates the principles of nursing informatics to streamline information management and improve the quality of care delivery.
Critical attributes of NCIS include:
A Nursing Clinical Information System (NCIS) is a specialized type of healthcare information system tailored to meet the unique needs of nursing practice. It incorporates the principles of nursing informatics to streamline information management and improve the quality of care delivery.
Critical attributes of NCIS include:
765
Somatic to iPS Cell Reprogramming
2.2K
Reprogramming alters the gene expression in somatic cells, transforming them into induced pluripotent stem (iPS) cells over several generations. Scientists can reprogram cells by introducing genes for four transcription factors—Oct4, Sox2, Klf4, and c-Myc (OSKM) by viral or non-viral methods. These factors are also known as Yamanaka factors after Shinya Yamanaka, who first generated iPS cells using mouse skin cells. Yamanaka was awarded the Nobel Prize in Physiology or Medicine in 2012...
2.2K
CRISPR
50.6K
Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
50.6K


