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(Y77.0) Ophthalmic devices associated with adverse incidents : diagnostic and monitoring devices
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7 044 in individuals diagnosis ophthalmic devices associated with adverse incidents : diagnostic and monitoring devices confirmed
Diagnosis ophthalmic devices associated with adverse incidents : diagnostic and monitoring devices is diagnosed Men are 60.70% more likely than Women
5 660
Men receive the diagnosis ophthalmic devices associated with adverse incidents : diagnostic and monitoring devices
0 (less than 0.1%)Died from this diagnosis.
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1 384
Women receive the diagnosis ophthalmic devices associated with adverse incidents : diagnostic and monitoring devices
0 (less than 0.1%)Died from this diagnosis.
Risk Group for the Disease ophthalmic devices associated with adverse incidents : diagnostic and monitoring devices - Men aged 5-9 and Women aged 70-74
In Men diagnosis is most often set at age 5-9, 55-59, 65-74, 80-84
Less common in men the disease occurs at Age 0-5, 10-54, 60-64, 75-79, 85-95+Less common in women the disease occurs at Age 0-69, 75-95+
In Women diagnosis is most often set at age 70-74
Disease Features ophthalmic devices associated with adverse incidents : diagnostic and monitoring devices
Absence or low individual and public risk
Ophthalmic devices associated with adverse incidents : diagnostic and monitoring devices - what does this mean
Ophthalmic diagnostic and monitoring devices are associated with adverse incidents when they are used incorrectly, when the device is not maintained properly, or when the device is not used in accordance with manufacturer instructions. adverse incidents may include eye injury, infection, or other harm.
What happens during the disease - ophthalmic devices associated with adverse incidents : diagnostic and monitoring devices
The pathogenesis of ophthalmic devices associated with adverse incidents is multi-factorial. poor design, manufacturing, and maintenance of the device, as well as inadequate user training and education, can all contribute to an increased risk of adverse incidents. additionally, the device may be used inappropriately or in a manner inconsistent with its intended use, leading to an increased risk of harm.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Visual acuity test
- Slit lamp examination
- Tonometry
- Fundus examination
- Pupil examination
- Intraocular pressure measurement
- Corneal topography
- Optical coherence tomography
- Ultrasound biomicroscopy
- Confocal microscopy
- Electrophysiology
- Ultrasound imaging
- CT scan
- MRI scan
- Blood tests
Treatment and Medical Assistance
Main Goal: Treating Ophthalmic Devices Associated with Adverse Incidents
- Perform a thorough risk assessment of the device
- Identify potential sources of adverse incidents
- Develop a plan for monitoring and diagnosing adverse incidents
- Implement safety protocols to reduce the risk of adverse incidents
- Provide ongoing training to staff on the use of the device
- Educate patients on the proper use and safety of the device
- Ensure the device is regularly serviced and maintained
- Conduct regular audits of the device's performance
- Implement corrective action measures to address any adverse incidents
- Provide feedback to the manufacturer on device performance
9 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Ophthalmic devices associated with adverse incidents : diagnostic and monitoring devices - Prevention
The best way to prevent ophthalmic devices associated with adverse incidents is to ensure that they are regularly maintained and serviced according to manufacturer guidelines. additionally, users should be made aware of the potential risks associated with these devices and the importance of following safety protocols. proper training and education of both users and technicians is essential to ensure the safety and efficacy of these devices.