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(Y75.1) Neurological devices associated with adverse incidents : therapeutic (nonsurgical) and rehabilitative devices
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4 201 in individuals diagnosis neurological devices associated with adverse incidents : therapeutic (nonsurgical) and rehabilitative devices confirmed
1 384 deaths with diagnosis neurological devices associated with adverse incidents : therapeutic (nonsurgical) and rehabilitative devices
33% mortality rate associated with the disease neurological devices associated with adverse incidents : therapeutic (nonsurgical) and rehabilitative devices
Diagnosis neurological devices associated with adverse incidents : therapeutic (nonsurgical) and rehabilitative devices is diagnosed Women are 31.73% more likely than Men
1 434
Men receive the diagnosis neurological devices associated with adverse incidents : therapeutic (nonsurgical) and rehabilitative devices
0 (less than 0.1%)Died from this diagnosis.
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Women receive the diagnosis neurological devices associated with adverse incidents : therapeutic (nonsurgical) and rehabilitative devices
1 384 (50.0 %)Died from this diagnosis.
Risk Group for the Disease neurological devices associated with adverse incidents : therapeutic (nonsurgical) and rehabilitative devices - 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 : therapeutic (nonsurgical) and rehabilitative devices
Absence or low individual and public risk
Neurological devices associated with adverse incidents : therapeutic (nonsurgical) and rehabilitative devices - what does this mean
Neurological devices associated with adverse incidents typically occur when therapeutic or rehabilitative devices are used incorrectly or malfunction due to a manufacturing defect, improper use, or inadequate maintenance. these incidents can cause serious injury or even death in some cases.
What happens during the disease - neurological devices associated with adverse incidents : therapeutic (nonsurgical) and rehabilitative devices
The pathogenesis of neurological devices associated with adverse incidents is multifactorial. factors such as inadequate patient selection, inadequate device design, inadequate training of the medical staff, and inadequate maintenance and monitoring of the device can all contribute to adverse incidents. additionally, the patient's individual physiology and underlying medical conditions can also play a role in the development of adverse incidents.
Clinical Pattern
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How does a doctor diagnose
- Perform a physical examination
- Order laboratory tests and imaging studies
- Conduct a neurological evaluation
- Administer a battery of neuropsychological tests
- Perform an electrodiagnostic study
- Conduct an electromyography (EMG) or nerve conduction study
- Conduct an evoked potential study
- Perform a brainstem auditory evoked response (BAER) test
- Conduct a visual evoked potential (VEP) study
- Perform a transcranial magnetic stimulation (TMS) study
- Administer a transcranial doppler (TCD) test
- Conduct a magnetic resonance imaging (MRI) scan
- Perform a computed tomography (CT) scan
- Administer a positron emission tomography (PET) test
- Perform a single photon emission computed tomography (SPECT) scan
Treatment and Medical Assistance
The main goal of the treatment is to reduce the risk of adverse incidents associated with neurological devices.
- Educating patients and medical professionals about proper use of neurological devices
- Regularly monitoring and inspecting neurological devices
- Developing and implementing safety protocols for neurological devices
- Providing training on proper use of neurological devices
- Performing regular maintenance on neurological devices
- Using protective equipment when using neurological devices
- Using the most up-to-date neurological devices
- Using the appropriate device for the patient’s condition
- Using the appropriate device settings for the patient’s condition
- Developing and implementing protocols for reporting adverse incidents
- Developing and implementing protocols for responding to adverse incidents
- Developing and implementing protocols for preventing adverse incidents
- Developing and implementing protocols for monitoring adverse incidents
- Developing and implementing protocols for evaluating adverse incidents
- Developing and implementing protocols for treating adverse incidents
- Developing and implementing protocols for rehabilitation after adverse incidents
42 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Neurological devices associated with adverse incidents : therapeutic (nonsurgical) and rehabilitative devices - Prevention
The best way to prevent neurological devices associated with adverse incidents is to ensure that the device is properly installed and maintained. this includes proper training of personnel who will be using the device, regular inspections of the device to ensure it is functioning properly, and regular maintenance of the device to ensure it is in good working order. additionally, patients should be informed of the risks associated with the device and should be monitored closely for any adverse reactions or incidents.