Evaluation Of Persistent Pulmonary Infiltrate - BMJ Best Practice

Evaluation of persistent pulmonary infiltrateView PDF Menu Closepadlock-lockedLog in or subscribe to access all of BMJ Best PracticeLast reviewed: 20 Nov 2025Last updated: 15 Aug 2025

Summary

Persistent pulmonary infiltrate results when a substance denser than air (e.g., pus, edema, blood, surfactant, protein, or cells) lingers within the lung parenchyma. Nonresolving and slowly resolving pneumonias are the most common broad categories of persistent pulmonary infiltrate.[1][2][3] Persistence is attributed to defects in host immune defense mechanisms, presence of unusual or resistant organisms, or diseases that mimic pneumonia.​[4][5]

Classification

The classification of these disorders may become quite complex, as some clinicians focus primarily on radiologic abnormalities, while others emphasize accompanying clinical features. Nonresolving or slowly resolving pneumonia is loosely defined as pneumonia that does not improve clinically, or even worsens, despite a minimum of 10 days of adequate antibiotic therapy or as radiographic infiltrate that does not resolve within 12 weeks.[6][7]​​ Slowly resolving pneumonia is usually defined as the persistence of radiographic infiltrate in a clinically improved patient for >4 weeks (<50% resolution in 1 month).[8][9][10][11]

A waiting period of 12 to 14 weeks is suggested for slowly resolving pneumonia to be considered nonresolving (or chronic) in older patients with nontuberculous bacterial pneumonia.[6] Nonresponding pneumonia is characterized by inadequate clinical response despite antibiotic treatment. It is an independent risk factor for death and delayed resolution of pulmonary infiltrate.[12][13]​ Noninfectious causes are responsible for about 20% of cases of nonresolving pneumonia.[12]

Therapeutic response

A good clinical response to pulmonary infiltrate is defined as a 50% clearing of chest radiographic findings at 4 weeks of therapy.[6] Clinical improvement and resolution of leukocytosis support the conclusion that the patient has responded to antibiotic therapy, even when chest radiographic abnormalities persist.[2] Most patients have a normal temperature and decreased cough within 3 to 5 days after beginning treatment. When clinical improvement has not occurred and chest radiographic findings are unchanged or worse, or if at least partial radiographic resolution is lacking by 4 weeks, further evaluation is essential, even in asymptomatic patients.[2][10][14]​ This is the case for pneumonia, but persistent pulmonary infiltrates may result from other reasons (e.g., pulmonary edema).

Variant response

Resolution of nonresolving pneumonia varies and depends on the causal agent, the severity of disease, and host factors.[4][6] Several risk factors may hinder the rate of radiographic clearing of the condition:[2][15]

  • Age over 60 years: radiographic clearance of pneumonic infiltrate on completion of antibiotic therapy decreases by 20% per decade after the age of 20 years​

  • Malnutrition

  • Comorbid conditions (COPD, cardiac failure, diabetes, renal failure, immunodeficiency, alcohol intake, smoking, occupational exposure, cancer, cancer treatment, systemic illness): patients with hematologic malignancies; immunosuppressive disorders; or exposure to silica, aluminum, or titanium dust are prone to persistent pulmonary infiltrate

  • Causal microorganism

  • Initial severity of the infection

  • Delay in initiation of therapy.

Differentials

Common

  • Community-acquired pneumonia (nonresolving)
  • Atypical pneumonia (nonresolving)
  • Hospital-acquired pneumonia (nonresolving)
  • Empyema
  • Lung abscess
  • Lung cancer (metastatic)
  • Small cell lung cancer
  • Non-small cell lung cancer
  • Tuberculosis
  • Aspiration pneumonia
  • HIV infection
  • Pneumocystis jiroveci pneumonia (nonresolving)
  • Pulmonary embolism
  • Cardiogenic pulmonary edema
Full details

Uncommon

  • Foreign body aspiration
  • Sarcoidosis
  • Interstitial lung disease
  • Organizing pneumonia
  • Systemic lupus erythematosus
  • Rheumatoid arthritis
  • Scleroderma
  • Dermatomyositis
  • Polymyositis
  • Sjogren syndrome
  • Asbestosis
  • Silicosis
  • Lymphoma and acute leukemia
  • Kaposi sarcoma
  • Diffuse alveolar hemorrhage
  • Systemic vasculitis
  • Granulomatosis with polyangiitis (formerly known as Wegener granulomatosis)
  • Churg-Strauss syndrome
  • Allergic bronchopneumonic aspergillosis
  • Loeffler syndrome
  • Hypersensitivity pneumonia (extrinsic allergic alveolitis)
  • Acute idiopathic eosinophilic pneumonia
  • Idiopathic chronic eosinophilic pneumonia
  • Drug-induced infiltrate
  • Cocaine use disorder
  • Radiation pneumonitis
  • Amyloidosis
  • Langerhans cell histiocytosis
  • Lymphangioleiomyomatosis
  • Lipoid pneumonia
  • Pulmonary alveolar proteinosis
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Contributors

Authors

VIEW ALLAuthors
Athanasia Pataka, MD

Respiratory Physician

Aristotle University

Thessaloniki

Greece

Disclosures

AP declares that she has no competing interests.

Acknowledgements

Dr Athanasia Pataka would like to gratefully acknowledge Dr Paraskevi Argyropoulou-Pataka, a previous contributor to this topic.

Disclosures

PAP declares that she has no competing interests.

Peer reviewers

VIEW ALLPeer reviewers
Cristine Radojicic, MD

Staff Physician

Cleveland Clinic

Cleveland

OH

Disclosures

CR declares that she has no competing interests.

Mathina Darmalingam, MBChB, FCP

Clinical Lead in Respiratory Medicine

Whipps Cross University Hospital

NHS Trust

London

UK

Disclosures

MD declares that she has no competing interests.

Ioannis P. Kioumis, MD, PhD

Assistant Professor

Pulmonary Medicine and Infectious Diseases

Pulmonary Medicine Clinic

Aristotle University

Thessaloniki

Greece

Disclosures

IPK declares that he has no competing interests.

Peer reviewer acknowledgements

BMJ Best Practice topics are updated on a rolling basis in line with developments in evidence and guidance. The peer reviewers listed here have reviewed the content at least once during the history of the topic.

Disclosures

Peer reviewer affiliations and disclosures pertain to the time of the review.

References

Our in-house evidence and editorial teams collaborate with international expert contributors and peer reviewers to ensure that we provide access to the most clinically relevant information possible.

Key articles

Woodhead M, Blasi F, Ewig S, Garau J, et al. Guidelines for the management of adult lower respiratory tract infections - full version. Clin Microbiol Infect. 2011 Nov;17 (Suppl 6):E1-59.Full text Abstract

Metlay JP, Waterer GW, Long AC, et al. Diagnosis and treatment of adults with community-acquired pneumonia. An official clinical practice guideline of the American Thoracic Society and Infectious Diseases Society of America. Am J Respir Crit Care Med. 2019 Oct 1;200(7):e45-67.Full text Abstract

Reference articles

A full list of sources referenced in this topic is available to users with access to all of BMJ Best Practice.
  • Evaluation of persistent pulmonary infiltrate images
  • Patient information

    Lung cancer (non-small-cell)

    Pneumonia

    More Patient information
  • Calculators

    PERC Rule for the Assessment of Possible Pulmonary Embolism

    Pulmonary Embolism Wells Score

    More Calculators
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