(Y81) General- and plastic-surgery devices associated with adverse incidents

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106 033 in individuals diagnosis general- and plastic-surgery devices associated with adverse incidents confirmed
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2 403 deaths with diagnosis general- and plastic-surgery devices associated with adverse incidents
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2% mortality rate associated with the disease general- and plastic-surgery devices associated with adverse incidents

Diagnosis general- and plastic-surgery devices associated with adverse incidents is diagnosed Men are 1.73% more likely than Women

53 935

Men receive the diagnosis general- and plastic-surgery devices associated with adverse incidents

321 (0.6 %)

Died from this diagnosis.

100
95
90
85
80
75
70
65
60
55
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15
10
5
0
52 098

Women receive the diagnosis general- and plastic-surgery devices associated with adverse incidents

2 082 (4.0 %)

Died from this diagnosis.

Risk Group for the Disease general- and plastic-surgery devices associated with adverse incidents - Men aged 55-59 and Women aged 60-64

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In Men diagnosis is most often set at age 10-14, 20-89
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Less common in men the disease occurs at Age 0-9, 15-19, 90-95+Less common in women the disease occurs at Age 0-14, 90-95+
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In Women diagnosis is most often set at age 15-89

Disease Features general- and plastic-surgery devices associated with adverse incidents

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Absence or low individual and public risk
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General- and plastic-surgery devices associated with adverse incidents - what does this mean

General- and plastic-surgery devices associated with adverse incidents occur when medical devices are used in a medical procedure that have not been properly tested and/or approved by the appropriate regulatory body. these devices can cause serious injury or death, and can also lead to medical complications. in some cases, the device may be defective or the medical procedure may be performed incorrectly.

What happens during the disease - general- and plastic-surgery devices associated with adverse incidents

The pathogenesis of the disease associated with general and plastic surgery devices is complex and multifactorial. it is thought to be caused by a combination of factors including device design, manufacturing defects, improper use, and inadequate training of medical personnel. in addition, inadequate sterilization and maintenance of the device can also contribute to adverse incidents.

Clinical Pattern

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How does a doctor diagnose

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Treatment and Medical Assistance

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20 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

General- and plastic-surgery devices associated with adverse incidents - Prevention

To prevent adverse incidents associated with general- and plastic-surgery devices, healthcare providers should ensure that all devices are properly maintained and sterilized, and that staff are trained in the proper use and handling of these devices. additionally, manufacturers should ensure that their products meet safety standards and are regularly inspected for any defects or malfunctions.