(J84) Other interstitial pulmonary diseases

More details coming soon

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2 362 202 in individuals diagnosis other interstitial pulmonary diseases confirmed
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381 524 deaths with diagnosis other interstitial pulmonary diseases
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16% mortality rate associated with the disease other interstitial pulmonary diseases

Diagnosis other interstitial pulmonary diseases is diagnosed Men are 4.97% more likely than Women

1 239 803

Men receive the diagnosis other interstitial pulmonary diseases

230 201 (18.6 %)

Died from this diagnosis.

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1 122 399

Women receive the diagnosis other interstitial pulmonary diseases

151 323 (13.5 %)

Died from this diagnosis.

Risk Group for the Disease other interstitial pulmonary diseases - Men aged 65-69 and Women aged 60-64

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In Men diagnosis is most often set at age 0-95+
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in in men, the disease manifests at any agein in women, the disease manifests at any age
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In Women diagnosis is most often set at age 0-95+

Disease Features other interstitial pulmonary diseases

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Absence or low individual and public risk
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Other interstitial pulmonary diseases - what does this mean

Other interstitial pulmonary diseases refer to a group of lung diseases which cause inflammation and scarring of the lungs, leading to difficulty in breathing. these diseases are caused by a variety of factors, including environmental exposures, infections, and genetic factors. symptoms can include shortness of breath, coughing, and fatigue. treatment for these diseases is aimed at managing symptoms and slowing the progression of the disease.

What happens during the disease - other interstitial pulmonary diseases

Other interstitial pulmonary diseases refer to a group of chronic, progressive pulmonary disorders that involve inflammation and scarring of the lung tissue. these disorders are caused by a variety of environmental, genetic, and immunologic factors, and may lead to difficulty breathing, coughing, and wheezing. the scarring of the lung tissue can cause the air sacs to become stiff and inflexible, and the walls of the airways can become thick and narrowed, leading to obstruction of airflow. this can cause a decrease in oxygen levels in the bloodstream and lead to symptoms such as fatigue, shortness of breath, and even respiratory failure.

Clinical Pattern

More details coming soon

How does a doctor diagnose

  • Physical examination
  • Chest X-ray
  • CT scan
  • Pulmonary function tests
  • Bronchoscopy
  • Sputum cytology
  • Lung biopsy
  • Blood tests

Treatment and Medical Assistance

Main Goal: To reduce symptoms and improve quality of life for people with other interstitial pulmonary diseases.
  • Medication to reduce inflammation and other symptoms
  • Oxygen therapy
  • Pulmonary rehabilitation
  • Surgery to remove damaged tissue
  • Lung transplant
  • Nutritional counseling
  • Counseling for emotional support
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18 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

Other interstitial pulmonary diseases - Prevention

The best way to prevent other interstitial pulmonary diseases is to avoid risk factors such as smoking, air pollution, and exposure to certain chemicals. additionally, regular exercise, healthy eating habits, and maintaining a healthy weight can help to reduce the risk of developing these diseases.

Specified forms of the disease

(J84.0) Alveolar and parietoalveolar conditions
(J84.1) Other interstitial pulmonary diseases with fibrosis
(J84.8) Other specified interstitial pulmonary diseases
(J84.9) Interstitial pulmonary disease, unspecified