Interstitial (Nonidiopathic) Pulmonary Fibrosis Follow-up
- Author: Eleanor M Summerhill, MD, FACP, FCCP; Chief Editor: Zab Mosenifar, MD more...
Further Inpatient Care
- Patients with interstitial lung disease generally are treated in an outpatient setting.
- With advancing disease, progressive respiratory failure, pneumonia, pulmonary embolism, and cor pulmonale may all occur and require hospital admission.
- Bronchogenic cancer occurs with increased frequency.[17]
Further Outpatient Care
- See patients with diffuse interstitial lung disease every 3-6 months.
- Order pulmonary function testing every 3-6 months to assess disease progression and response to therapy.
- High-resolution CT scanning is becoming an increasingly important tool in making the initial diagnosis and subsequent assessments of disease progression and/or responses to therapy.
Inpatient & Outpatient Medications
- Immunosuppressive and antifibrotic medications and supplemental oxygen may be indicated for some patients.
- Prompt treatment is necessary for complicating pulmonary disease such as cor pulmonale (oxygen, diuretics), pulmonary embolism (anticoagulants), and infection (antibiotics).
Transfer
- Most patients with DPLD can be treated in community settings.
- Transfer to a tertiary care center is indicated when the diagnosis is in doubt or when treatment is ineffective.
Deterrence/Prevention
- Prevention is predicated upon the specific diagnosis.
Complications
- Progressive respiratory failure
- Cor pulmonale
- Pulmonary embolism
- Pneumothorax
- Pneumonia
- Bronchogenic carcinoma
Prognosis
- The prognosis is variable and depends on the specific diagnosis and clinical, physiologic, and pathologic severity.
Patient Education
- Educate patients about the nature of the specific diagnosis and about potential toxicities of prescribed medications.
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