In recent years, national policies on rare diseases has been issued frequently, and great emphasis has been placed on the registration and related processing of rare disease diagnostic and treatment information.
The establishment of an information system to collect relevant data facilitates the understanding of the epidemiology, clinical diagnosis and treatment, and also the status of medical insurance of rare diseases in China. The information system also provides scientific basis for formulating population intervention strategy, improving the system of diagnosis and treatment services, improving the standards of medical insurance of patients, and improving drug accessibility.
Difficulties in the clinical diagnosis, treatment and scientific research of rare diseases
Detection
It's not uncommon
But it's hard to find out
Often overlooked
Diagnosis
It is difficult to diagnose due to the involvement of many disciplines
There is a general lack of professional knowledge of rare diseases
High rate of misdiagnosis and missed diagnosis
Treatment
It is difficult to use drugs accurately
More than 7000 rare diseases are known, but only 10% of them have a treatment plan
More than 700 rare diseases have been well-defined, yet 95% of them have no specific drugs
Research
Registration of rare diseases started later than foreign countries
There is a severe lack of data for research
The research is of great value
Background
In recent years, national policies on rare diseases has been issued frequently, and great emphasis has been placed on the registration and related processing of rare disease diagnostic and treatment information.
The establishment of an information system to collect relevant data facilitates the understanding of the epidemiology, clinical diagnosis and treatment, and also the status of medical insurance of rare diseases in China. The information system also provides scientific basis for formulating population intervention strategy, improving the system of diagnosis and treatment services, improving the standards of medical insurance of patients, and improving drug accessibility.
Difficulties in the clinical diagnosis, treatment and scientific research of rare diseases
Detection
It's not uncommon But it's hard to find out Often overlooked
Diagnosis
It is difficult to diagnose due to the involvement of many disciplines There is a general lack of professional knowledge of rare diseases High rate of misdiagnosis and missed diagnosis
Treatment
It is difficult to use drugs accurately More than 7000 rare diseases are known, but only 10% of them have a treatment plan More than 700 rare diseases have been well-defined, yet 95% of them have no specific drugs
Research
Registration of rare diseases started later than foreign countries There is a severe lack of data for research The research is of great value
Solution
Based on the advantages of data and intelligent application platform knowledge base system, BaseBit has launched an intelligent solution for the integration of clinical research on rare diseases. It is a multimodal and multidimensional AI solution integrating diagnosis and treatment registration of rare diseases, data mining, research and analysis, output of scientific research value and diagnosis and treatment plan. This solution highly conforms to the needs of medical workers, government departments and researchers to perform their jobs, thus providing research value, sharing value and clinical value.
Solution
Based on the advantages of data and intelligent application platform knowledge base system, BaseBit has launched an intelligent solution for the integration of clinical research on rare diseases. It is a multimodal and multidimensional AI solution integrating diagnosis and treatment registration of rare diseases, data mining, research and analysis, output of scientific research value and diagnosis and treatment plan. This solution highly conforms to the needs of medical workers, government departments and researchers to perform their jobs, thus providing research value, sharing value and clinical value.
Program Advantages
Improve the standards of diagnosis and treatment of rare diseases
Support the decision-making power of health management
Improve the ability of sequencing analysis
Improve the ability of report interpretation
Enhance academic influence
Deliver scientific research value
Program Advantages
Improve the standards of diagnosis and treatment of rare diseases
Support the decision-making power of health management
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