Basic requirements of medical institutions in Technical Management Specification for Artificial Hip Replacement (20 12 Edition)

(a) medical institutions to carry out artificial hip replacement technology should be adapted to its functions and tasks.

(two) in principle, to carry out in tertiary hospitals.

(three) there are orthopedic diagnosis and treatment subjects and equipment approved and registered by the health administrative department and other relevant departments.

1. Orthopedics.

(1) has been engaged in clinical diagnosis and treatment of orthopedics for more than 8 years, and has no less than 50 beds, and there are no less than 10 beds in joint surgery wards or professional groups.

(2) can independently complete hip trauma and hip osteopathy surgery, each year to complete all kinds of hip surgery volume of not less than 200 cases, including more than 50 cases of artificial hip replacement.

2. Artificial hip replacement operating room.

(1) At least 1 operating rooms meet the first-class clean operating room standard (laminar flow in operating area 100, laminar flow in peripheral area 1000).

(2) The operating room covers an area of over 30 square meters and has a reasonable layout.

(3) Equipped with surgical equipment approved by the US Food and Drug Administration to meet the needs of artificial hip replacement surgery.

(4) Equipped with a C-arm X-ray machine that meets the radiation protection conditions.

3. Other relevant departments and equipment.

(1) has specialized departments or doctors such as anesthesiology, intensive care unit, cardiovascular medicine, respiratory medicine, endocrinology, rehabilitation, etc., and has comprehensive treatment and rescue capabilities for systemic complications and complications.

(2) Have CT, bedside X-ray and postoperative functional rehabilitation system.

(4) Having a team of orthopedic professional doctors, including at least two doctors with professional and technical post qualifications above deputy chief physician, and the personnel echelon structure is reasonable.

(five) the second-level hospitals that meet the following conditions are limited to the first artificial hip replacement technology:

1. Personnel, departments, equipment and facilities that meet the requirements of this specification.

2 in accordance with the relevant provisions of the administrative department of health at or above the municipal level.

3. There is a need for diagnosis and treatment of artificial hip replacement. The city divided into districts is a medical institution without the technical qualification of artificial hip replacement in the region; When the emergency operation of artificial hip replacement is needed in the county, it is impossible to reach the medical institution with the technical qualification of artificial hip replacement in time.

4. Help from a tertiary hospital with at least 1 year technical qualification of artificial hip replacement.

5. With the aid of 1 year, it passed the evaluation of clinical application ability organized by the provincial health administrative department.

(VI) Newly-built or newly-built orthopedic medical institutions that intend to carry out artificial hip replacement technology shall have the personnel, departments, equipment and facilities of this specification, and apply to the provincial health administrative department, and can only be carried out after the provincial health administrative department organizes the evaluation of clinical application ability.