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(Y70) Anaesthesiology devices associated with adverse incidents
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62 682 in individuals diagnosis anaesthesiology devices associated with adverse incidents confirmed
4 112 deaths with diagnosis anaesthesiology devices associated with adverse incidents
7% mortality rate associated with the disease anaesthesiology devices associated with adverse incidents
Diagnosis anaesthesiology devices associated with adverse incidents is diagnosed Men are 18.95% more likely than Women
37 280
Men receive the diagnosis anaesthesiology devices associated with adverse incidents
2 728 (7.3 %)Died from this diagnosis.
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25 402
Women receive the diagnosis anaesthesiology devices associated with adverse incidents
1 384 (5.4 %)Died from this diagnosis.
Risk Group for the Disease anaesthesiology devices associated with adverse incidents - Men and Women aged 65-69
In Men diagnosis is most often set at age 0-9, 15-19, 35-39, 50-89
Less common in men the disease occurs at Age 0-1, 10-14, 20-34, 40-49, 90-95+Less common in women the disease occurs at Age 0-34, 85-95+
In Women diagnosis is most often set at age 35-84
Disease Features anaesthesiology devices associated with adverse incidents
Absence or low individual and public risk
Anaesthesiology devices associated with adverse incidents - what does this mean
Anaesthesiology devices associated with adverse incidents occur when a device fails to perform as expected, leading to an unexpected medical outcome. this can be caused by a malfunction of the device, improper use of the device, or a lack of proper training in the use of the device.
What happens during the disease - anaesthesiology devices associated with adverse incidents
Anaesthesiology devices associated with adverse incidents can be caused by a number of factors, including user error, equipment malfunction, and improper selection of the device for the procedure. poorly maintained devices, inadequate training of the anaesthesiologist, and inadequate monitoring of the patient during the procedure can also contribute to the occurrence of adverse incidents. in some cases, the device itself may be faulty or not properly calibrated, resulting in a malfunction that can lead to serious patient injury or death.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Review of patient medical records
- Review of anaesthesiology devices used
- Interview of anaesthesiologist and other medical personnel
- Review of anaesthesiology device manufacturer’s instructions
- Review of the anaesthesiology device’s safety history
- Review of the anaesthesiology device’s design and operation
- Review of the anaesthesiology device’s maintenance and repair history
- Review of the anaesthesiology device’s quality control records
- Review of the anaesthesiology device’s testing and certification records
- Review of the anaesthesiology device’s user training records
- Review of the anaesthesiology device’s user feedback records
- Review of the anaesthesiology device’s incident reports
Treatment and Medical Assistance
Main Goal: Treating Anaesthesiology devices associated with adverse incidents.
- Assess the risk factors associated with the use of anaesthesiology devices.
- Develop strategies to reduce the risk of adverse incidents.
- Provide education and training to clinicians on the effective use of anaesthesiology devices.
- Develop protocols for the safe use of anaesthesiology devices.
- Implement systems to monitor and evaluate the use of anaesthesiology devices.
- Conduct regular reviews of anaesthesiology devices.
- Ensure that anaesthesiology devices are properly maintained and serviced.
- Monitor the performance of anaesthesiology devices.
- Develop and implement strategies to reduce the incidence of adverse incidents.
- Ensure that anaesthesiology devices are used in accordance with best practice guidelines.
29 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Anaesthesiology devices associated with adverse incidents - Prevention
The best way to prevent anaesthesiology devices associated with adverse incidents is to ensure that all medical staff are properly trained in the use of the equipment and that all anaesthesiology devices are regularly inspected and maintained in accordance with manufacturer guidelines. additionally, the use of safety protocols and checklists should be implemented to ensure that all devices are functioning correctly prior to use.