Desenvolvimento de um procedimento operacional padrão para manutenção preventiva anual dos aparelhos de Raio X móvel Aquilla Plus 300 VMI do Hospital De Clínicas Da Universidade Federal de Uberlândia

Abstract

Radiographic images are extremely important in the analysis of bone trauma and in the analysis of structures of the thoracic cavity. For this purpose, x-ray machines are used in hospitals as a technical tool to acquire the medical image of interest. Being classified, by ANVISA, as a high risk equipment, it is necessary to ensure the quality, precision and safety of this equipment, since it causes the exposure of patients and health professionals to ionizing radiation. It is through annual preventive maintenance that this set of checks is carried out. Thus, we note the relevance of this activity to ensure the usability of the equipment in question. Procedures like this, must be registered in a document called Standard Operating Procedure (SOP), which will clearly and objectively instruct the sequence of activities to be performed, so that the preventive maintenance of any equipment of the same model is carried out in a standardized manner. and qualitative. The cClinical Hospital of the Federal University of Uberlândia (HC-UFU) has 11 mobile X-ray equipment of the VMI brand, model Aquilla Plus 300. Thus, the manufacture of the POP for this equipment was chosen, as the document had not yet existed. been made. In this way, a bibliographic research was carried out to deepen knowledge on the subject, as well as the principle of operation of this technology. In addition, some conventional preventive maintenance was monitored in the Bioengineering sector, which is in charge of keeping HC-UFU technologies in good working order. Therefore, with these tools, and with the reading of the technical service manual of the equipment, the POP of preventive maintenance was elaborated, that is, the set of instructions to be performed to ensure the quality, precision and safety in the equipment's functionalities. It is hoped that, with the completion of this work, good practices in Clinical Engineering will become effective and that the document will contribute to the dissemination of the necessary knowledge for the training of professionals, in order to make them able to perform the proper service.