(1) Medical institutions to carry out artificial hip replacement technology should be compatible with its functions and tasks.
(2) In principle, it should be carried out in tertiary hospitals.
(C) there are health administrative department approved registration of orthopedic diagnosis and treatment subjects and other related departments and equipment.
1. Orthopedics.
(1) to carry out orthopedic clinical diagnosis and treatment work for more than 8 years, with not less than 50 beds, with joint surgery specialized wards or specialized groups, joint surgery beds of not less than 10.
(2) Can independently complete hip trauma and hip joint orthopedic surgery, the annual volume of various types of hip surgery is not less than 200 cases, of which more than 50 cases of artificial hip joint replacement.
2. The operating room that carries out artificial hip joint replacement surgery.
(1) At least one operating room meets the standard of Class I clean operating room (100 levels of laminar flow in the operating area and 1000 levels in the peripheral area).
(2) Operating room use area of 30 square meters or more, reasonable layout.
(3) equipped with surgical equipment approved by the State Food and Drug Administration to meet the needs of artificial hip replacement surgery.
(4) Equipped with C-arm X-ray machine that meets the conditions of radiation protection.
3. Other related sections and equipment.
(1) There are anesthesiology, intensive care unit, cardiovascular medicine, respiratory medicine, endocrinology and rehabilitation and other specialized departments or specialized physicians, with comprehensive treatment of systemic comorbidities and complications and the ability to rescue.
(2) Possess CT, bedside X-ray camera, and postoperative functional rehabilitation system.
(4) It has a professional orthopedic physician team, including at least two physicians with professional and technical qualifications of associate director or above, and a reasonable personnel echelon structure.
(E) Level 2A hospitals meeting the following conditions are limited to carry out the initial artificial hip replacement technology:
1. The conditions of personnel, departments, equipment and facilities in accordance with the provisions of this specification.
2. In line with the relevant provisions of the health administrative department of the municipal level above the district medical technology management.
3. Artificial hip replacement diagnosis and treatment needs. Cities with districts as a unit, there are no qualified medical institutions for artificial hip replacement technology within the region; when the county needs to carry out emergency surgery for artificial hip replacement, it is impossible to reach the qualified medical institutions for artificial hip replacement technology in time.
4. Tertiary hospitals qualified in artificial hip joint replacement technology will provide assistance for at least one year.
5. Pass the clinical application ability assessment organized by the provincial health administrative department after 1 year of support.
(F) to carry out artificial hip replacement technology of the new or new orthopedic medical institutions, should be consistent with the norms of the personnel, departments, equipment, facilities conditions, and to the provincial health administrative departments to apply, through the provincial health administrative department organized by the clinical application of capacity assessment before carrying out.