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(J84.1) Other interstitial pulmonary diseases with fibrosis
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2 362 202 in individuals diagnosis other interstitial pulmonary diseases with fibrosis confirmed
381 524 deaths with diagnosis other interstitial pulmonary diseases with fibrosis
16% mortality rate associated with the disease other interstitial pulmonary diseases with fibrosis
Diagnosis other interstitial pulmonary diseases with fibrosis is diagnosed Men are 4.97% more likely than Women
1 239 803
Men receive the diagnosis other interstitial pulmonary diseases with fibrosis
230 201 (18.6 %)Died from this diagnosis.
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1 122 399
Women receive the diagnosis other interstitial pulmonary diseases with fibrosis
151 323 (13.5 %)Died from this diagnosis.
Risk Group for the Disease other interstitial pulmonary diseases with fibrosis - Men aged 65-69 and Women aged 60-64
In Men diagnosis is most often set at age 0-95+
in in men, the disease manifests at any agein in women, the disease manifests at any age
In Women diagnosis is most often set at age 0-95+
Disease Features other interstitial pulmonary diseases with fibrosis
Absence or low individual and public risk
Other interstitial pulmonary diseases with fibrosis - what does this mean
Other interstitial pulmonary diseases with fibrosis are caused by a range of environmental and genetic factors, such as exposure to certain toxins, radiation, and certain medications. these diseases cause scarring of the lungs, leading to difficulty breathing and other respiratory symptoms.
What happens during the disease - other interstitial pulmonary diseases with fibrosis
Other interstitial pulmonary diseases with fibrosis are caused by a variety of factors, including exposure to environmental toxins, certain medications, radiation therapy, and autoimmune diseases. in some cases, the exact cause is unknown. the disease is characterized by inflammation and scarring of the lung tissue, which can lead to difficulty breathing, coughing, and other respiratory symptoms. treatment options vary depending on the cause and severity of the condition.
Clinical Pattern
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How does a doctor diagnose
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Treatment and Medical Assistance
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18 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Other interstitial pulmonary diseases with fibrosis - Prevention
The primary goal of prevention is to reduce exposure to environmental risk factors that can lead to the development of other interstitial pulmonary diseases with fibrosis. this includes avoiding exposure to workplace hazards, such as dust, fumes, and chemicals, as well as avoiding smoking and other forms of air pollution. it is also important to receive regular medical check-ups to detect any early signs of the disease.