(a) to assist in the development of national clinical blood related systems, technical specifications and standards;
(b) to assist in guiding the national management and quality evaluation of clinical blood use, and to promote the improvement of rational clinical use of blood;
(c) to assist in the investigation and analysis of major clinical blood use safety incidents, and to propose ways to deal with the situation. (C) assisting in the investigation and analysis of major clinical blood safety incidents, and proposing treatment opinions;
(D) undertaking other tasks related to clinical blood management assigned by the Ministry of Health.
The Ministry of Health establishes a coordinating mechanism for the management of clinical blood use, improves the level of rational clinical use of blood, and ensures the quality of blood transfusion treatment. Article VI Provinces, autonomous regions, municipalities directly under the Central People's Government health administrative departments set up provincial clinical blood quality control center, responsible for the jurisdiction of the medical institutions of clinical blood management guidance, evaluation and training. Article VII medical institutions should strengthen the organization and management, clear job responsibilities, improve the management system.
The legal representative of the medical institutions for clinical blood management of the first responsible person. Article VIII above the second level hospitals and maternal and child health centers should be set up clinical blood management committee, responsible for the organization's clinical management of reasonable use of blood. Chairman of the president or vice president in charge of medical care, members of the medical department, blood transfusion, anesthesiology, to carry out blood transfusion treatment of the main clinical departments, nursing departments, operating rooms and other departments responsible for the composition. Medical and blood transfusion department **** the same responsible for clinical rational use of blood daily management.
Other medical institutions should set up clinical blood management working group, and designate a full-time (part-time) staff responsible for the daily management. Article IX clinical blood management committee or clinical blood management working group shall perform the following duties:
(1) conscientiously implement the clinical blood management of relevant laws, regulations, rules, technical specifications and standards, formulate the institution's clinical blood management rules and regulations and supervise the implementation of;
(2) assessment to determine the key departments of clinical blood use, the key links and processes;
(3) regular monitoring, monitoring, clinical blood use, and monitoring of the clinical blood use, and monitoring of the clinical blood use. p>(3) regularly monitor, analyze and evaluate clinical blood use, carry out quality evaluation of clinical blood use, and improve the level of rational clinical blood use;
(4) analyze the adverse events of clinical blood use, and put forward measures for treatment and improvement;
(5) provide guidance and promote the development of autologous transfusion and other blood protection and blood transfusion technology;
(6) undertake other tasks relating to clinical blood use assigned by the healthcare institutions. (f) To undertake other tasks related to clinical blood use assigned by the medical institutions. Article 10 Medical institutions shall set up blood transfusion departments or blood banks in accordance with the relevant provisions and clinical blood demand, and shall be equipped with professional and technical personnel, facilities and equipments suitable for blood transfusion work according to their own functions, tasks and scales.
The medical institutions that do not have the conditions to set up blood transfusion or blood bank, shall arrange for full-time (part-time) personnel responsible for clinical blood work. Article 11 The main duties of the Blood Transfusion Department and the blood bank are:
(1) to establish a quality management system for clinical blood use, and to promote the rational use of blood in the clinic;
(2) to be responsible for formulating a reserve plan for clinical blood use, and to coordinate the use of blood in clinic based on the early warning information of blood supply from the blood station and the blood inventory of the hospital;
(3) to be responsible for the work of booking, warehousing, storing, and distributing of blood;
(4) Responsible for transfusion-related immunohematology testing;
(5) Participate in the promotion of autologous transfusion and other blood protection and new technology of blood transfusion;
(6) Participate in the consultation of special transfusion therapy cases, and provide counseling on rational use of blood in the clinic;
(7) Participate in the investigation of adverse events of clinical use of blood;
(8) Participate in developing blood therapy-related technology according to the needs of clinical treatment (h) According to the clinical treatment needs, to participate in the development of blood treatment-related technologies;
(ix) Undertake other tasks assigned by the medical institutions related to clinical blood. Chapter III Clinical blood management Article XII of the medical institutions shall strengthen the management of clinical blood, establish and improve the management system and work standards, and ensure the implementation. Article XIII of the medical institutions shall use the health administrative department designated blood station to provide blood.
Medical institutions research blood by the local provincial health administrative department is responsible for approval.
Medical institutions should cooperate with the blood station to establish a blood inventory dynamic early warning mechanism to protect clinical blood demand and normal medical order. Article XIV of the medical institutions shall scientifically formulate clinical blood plan, the establishment of clinical rational use of blood evaluation system to improve the level of clinical rational use of blood. Article 15 Medical institutions shall manage the booking, reception, warehousing, storage, discharge and stock warning of blood, and ensure that the storage and delivery of blood meet the relevant national standards and requirements. Article 16 After receiving the blood sent by the blood station, the medical institutions shall check the label of the blood bag. The blood that meets the relevant state standards and requirements is put into storage and registered; and according to the different varieties, blood types and date of blood collection (or expiration date), are stored in special storage facilities in an orderly manner.
The main contents of the blood bag label checking are:
(a) the name of the blood station;
(b) the blood donation number or bar code, blood type;
(c) the blood varieties;
(d) the date and time of the blood collection or the preparation date and time;
(e) validity date and time;
(f) storage conditions.
It is prohibited to store blood with substandard bag labels.