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(Y75) Neurological devices associated with adverse incidents
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4 201 in individuals diagnosis neurological devices associated with adverse incidents confirmed
1 384 deaths with diagnosis neurological devices associated with adverse incidents
33% mortality rate associated with the disease neurological devices associated with adverse incidents
Diagnosis neurological devices associated with adverse incidents is diagnosed Women are 31.73% more likely than Men
1 434
Men receive the diagnosis neurological devices associated with adverse incidents
0 (less than 0.1%)Died from this diagnosis.
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2 767
Women receive the diagnosis neurological devices associated with adverse incidents
1 384 (50.0 %)Died from this diagnosis.
Risk Group for the Disease neurological devices associated with adverse incidents - Men and Women aged 0-5
In Men diagnosis is most often set at age 0-5
Less common in men the disease occurs at Age 0-1, 5-95+Less common in women the disease occurs at Age 0-1, 5-69, 75-95+
In Women diagnosis is most often set at age 0-5, 70-74
Disease Features neurological devices associated with adverse incidents
Absence or low individual and public risk
Neurological devices associated with adverse incidents - what does this mean
Neurological devices associated with adverse incidents occur when a device used in a medical procedure causes unintended harm to a patient. this can be due to a malfunctioning device, incorrect use of the device, or a lack of knowledge about the device. the adverse events can range from minor to serious, and can include infection, nerve damage, and even death.
What happens during the disease - neurological devices associated with adverse incidents
Neurological devices associated with adverse incidents can be caused by a variety of factors, including improper use, device design flaws, inadequate training, and inadequate maintenance. these factors can lead to electrical shocks, device malfunctions, and other medical complications that can cause serious injury or death.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical exam to assess the patient's neurological functioning
- Neurological imaging such as MRI, CT, or EEG
- Blood tests to identify any underlying infections
- Neuropsychological testing to assess cognitive functioning
- Neurological examination to identify any abnormalities
- Neurological monitoring to track any changes in the patient's condition
- Neurological consultation to evaluate the patient's symptoms
Treatment and Medical Assistance
Main goal of the treatment: To reduce the number of neurological device-related adverse incidents.
- Implementing a comprehensive risk management system for neurological devices
- Developing standardized protocols for monitoring and reporting of neurological device-related adverse incidents
- Conducting regular reviews of neurological device-related incidents
- Educating healthcare professionals on the proper use of neurological devices
- Developing evidence-based guidelines for neurological device use
- Improving the design and manufacturing processes of neurological devices
- Creating a system for tracking and reporting of patient outcomes
- Conducting research on neurological device safety and efficacy
42 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Neurological devices associated with adverse incidents - Prevention
Neurological devices associated with adverse incidents can be prevented through careful selection of the device, proper maintenance and calibration, and regular monitoring of the device's performance. additionally, healthcare providers should be trained on the proper use and maintenance of the device, and any changes to the device should be evaluated for potential risks.