Monitoring and management of fibrosing interstitial lung diseases: a narrative review for practicing clinicians.

Ther Adv Respir Dis

Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Published: February 2022

AI Article Synopsis

  • Close monitoring of patients with fibrosing interstitial lung diseases (ILDs) is crucial for early detection and treatment of disease progression.
  • Regular assessments should include pulmonary function tests, symptom evaluations, and, if necessary, high-resolution CT scans.
  • A multidisciplinary and personalized management plan is vital, taking into account disease severity, progression indicators, patient risk factors, existing health issues, and individual patient preferences.

Article Abstract

Close monitoring of patients with fibrosing interstitial lung diseases (ILDs) is important to enable prompt identification and management of progressive disease. Monitoring should involve regular assessment of physiology (including pulmonary function tests), symptoms, and, when appropriate, high-resolution computed tomography. The management of patients with fibrosing ILDs requires a multidisciplinary approach and should be individualized based on factors such as disease severity, evidence of progression, risk factors for progression, comorbidities, and the preferences of the patient. In this narrative review, we discuss how patients with fibrosing ILDs can be effectively monitored and managed in clinical practice.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422822PMC
http://dx.doi.org/10.1177/17534666211039771DOI Listing

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