Objectives of Study:
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The purpose of this research project is to comprehensively apply advanced computer engineering, artificial intelligence, data analysis and mining technologies, and combine the Chinese medical texts on aplastic anaemia, diagnostic and therapeutic norms, the experience of famous Chinese medicine practitioners, as well as the current situation of domestic and international development, etc., and, relying on the existing Chinese medicine four-diagnostic and objective collection and analysis equipment and Chinese medicine scientific research and inheritance platform, collect the data of aplastic anaemia patients' symptoms and evidence databases by means of multi-centre real-world studies (RWS). Through multi-centre real-world research (RWS), we collect the data of patients with aplastic anaemia from the four objective TCM diagnoses of looking, smelling, questioning and cutting, Western medicine test and examination data, and evidence identification data, etc., to form a database of the four TCM specialties of diagnosis and evidence; we apply data mining technology to analyse the correlation between the data of the four diagnoses, the data of test and examination and the data of the results of the evidence identification, so as to excavate the specific indicators of the data of the four diagnoses of patients with aplastic anaemia; and we should use the deep learning technology to research and develop an AI model, form the Chinese medicine evidence diagnosis equipment with high sensitivity, and put it into more than 10 medical institutions for demonstration and application, so as to provide strong support for clinicians to collect and analyse the four diagnostic information of Chinese medicine characteristics of patients with aplastic anaemia, as well as to identify and prescribe evidence and prescriptions more accurately
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Inclusion criteria
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① Meet the diagnostic criteria for aplastic anaemia;
② The patient's age range is 16 to 80 years old;
③No standard regimen has been used for treatment after the first diagnosis, or the current regimen has been maintained for more than 3 months;
④ Sound liver and kidney function (creatinine ≦1.5*ULN, BUN ≦1.5*ULN, ALT ≦2*ULN, AST ≦2*ULN, total bilirubin ≦1.5*ULN);
⑤ Able to comply with the study visit schedule and understand and comply with all trial protocol requirements;
⑥ Able to understand and voluntarily sign the written informed consent.
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Exclusion criteria:
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① Combination of PNH clones;
② Allergy to herbal medicinal tablets;
(iii) Severe cardiac disease, including New York Heart Association (NYHA) class III or IV congestive heart failure, uncontrolled hypertension or hypotension, or severe valvular or endocardial disease resulting in a risk of thromboembolism in the subject;
④ Clinically significant or uncontrolled persistent inflammatory/autoimmune disease (e.g., rheumatoid arthritis, Crohn's disease, ulcerative colitis, celiac disease, systemic lupus erythematosus, etc.);
⑤ Anticipated haematopoietic stem cell transplantation within 3 months.
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