Eosinophilic pneumonia includes a group of disorders characterized by an accumulation of eosinophilic infiltrates in the pulmonary parenchyma with/without peripheral blood eosinophilia. These include a broad range of lung conditions that occur due to infectious or non-infectious causes. The two common pulmonary eosinophilic syndromes are :
Abnormally increased eosinophils in lung parenchyma occurs due to infectious and non-infectious causes.
Non-infectious causes include:
Idiopathic acute eosinophilic pneumonia can occur at any age but is more common in males of age 20-40 years. Associations for the condition also exist with chronic myelogenous leukemia (CML), HIV infection, and smoking.
The most common cohort for chronic eosinophilic pneumonia is white women with a peak incidence between 30-40 years. Asthma is present in 50 percent of these patients.
Eosinophils are granulocytic white blood cells (WBCs), which are primarily tissue-dwelling cells. The main functions of eosinophils include host defense, inflammation modulation, and tissue destruction. Eosinophils play an important role in killing parasites, tumor cells, and respiratory epithelial cells.
The normal absolute eosinophil count in the peripheral blood is 0 to 500 cells/microL. Eosinophilia is predominantly due to polyclonal expansion (reactive expansion) as compared to hematopoietic clonal stem cell expansion, which is rare. A count of over 1500 increases the risk of tissue damage. However, it can also occur at low eosinophil count. In eosinophilic lung diseases, eosinophils commonly affect parenchyma and airways. Based on the increase in eosinophils, eosinophilia can be:
Eosinophilic pneumonia occurs secondary to lung tissue damage by the activated eosinophils. The substances and chemical mediators released by these activated macrophages damage the tissues and contribute to the disease pathology. These include: 
In acute eosinophilic pneumonia, there is a marked infiltration of eosinophils in the alveolar spaces, bronchial walls, and, to a lesser extent, in the interstitium. Acute and/or organizing diffuse alveolar damage is present. However, granulomas or hemorrhage are absent.
In chronic eosinophilic pneumonia, leukocytic infiltrates in alveolar air spaces and interstitium. The infiltrates are predominantly eosinophilic with macrophages, lymphocytes, and occasional plasma cells.
Common symptoms include a cough, fever, dyspnea, night sweats.
Acute eosinophilic pneumonia follows a rapid course with symptoms developing within two weeks. Myalgias and pleuritic chest pain with dyspnea may also be present, which can progress to respiratory failure. These patients can present with apparent acute lung injury or acute respiratory distress syndrome (ARDS) without any antecedent illness. However, extrapulmonary failure and shock are absent, which differentiates it from ARDS. On auscultation, diffuse crackles are present.
Chronic eosinophilic pneumonia follows a progressive course. The presentation is subacute with symptoms present for months before diagnosis. These patients present with moderate weight loss besides the common symptoms. Over time, dyspnea progresses and presents with wheezing, especially in those with adult-onset asthma.
Idiopathic Acute eosinophilic pneumonia- is usually a diagnosis of exclusion.
Chronic eosinophilic pneumonia - the diagnosis is based on clinical, radiographic, and BAL findings and on the inability to document pulmonary or systemic infection.
Supportive care with supplemental oxygen and glucocorticoids are the initial management in acute cases. While waiting for the culture results, starting mechanical ventilation and empiric antibiotics are valid therapeutic measures.
Systemic glucocorticoid therapy (intravenous or oral) is recommended for all and started as soon as possible for rapid improvement within 12-48 hours. However, the dose depends on the severity. Without glucocorticoid therapy, there is a risk of progressive respiratory failure in acute eosinophilic pneumonia patients. Once the respiratory failure resolves, oral prednisone continued for 2-4 weeks with a subsequent slow taper over the next few weeks.
There is a dramatic response to corticosteroids with rapid resolution of symptoms within an hour and complete resolution of infiltrates within a month.
For chronic eosinophilic pneumonia, prednisone (40-60 mg) until two weeks after the resolution of symptoms and x-ray abnormalities. Treatment is maintained for at least three months and optimally for 6 to 9 months. Some patients may require longer maintenance. Later, inhaled corticosteroids can be started allowing discontinuation of oral steroids.
Once the diagnosis of acute eosinophilic pneumonia is established, and corticosteroid treatment started, the prognosis is excellent with a dramatic response to therapy.
Sometimes prolonged glucocorticoid therapy may be required when there is a risk of recurrence; the prognosis is generally good for patients with chronic eosinophilic pneumonia.
Eosinophilic pneumonia affects the lung and is predominantly idiopathic. It requires interprofessional care and the involvement of more than one subspecialty. This patient-centered approach involving a primary care provider with a team of other health professionals, including a pulmonologist, physiotherapists, respiratory therapists, nurses, pharmacists, and support groups working together for the patient, plays a vital role in improving the quality of care in pneumonia patients. Critical care nurses monitor patients, administer treatment, and are crucial to team communication. Pharmacists counsel patients about the importance of compliance with glucocorticoids and educate them about the side effects. The timely diagnosis and treatment are crucial, especially in patients with an acute presentation, as left untreated, it can progress to respiratory failure. [Level 5]
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