Respiratory Medicine
Volume 101, Issue 1 , Pages 93-97, January 2007

Pulmonary infections diagnosed by BAL: A 12-year experience in 1066 immunocompromised patients

  • Ladina Joos

      Affiliations

    • Department of Pulmonary Medicine and Pulmonary Cell Research, University Hospital Basel, Petersgraben 4, CH-4031 Basel, Switzerland
    • Corresponding Author InformationCorresponding author. Tel.: +41612655184; fax: +41612654587.
  • ,
  • Prashant N. Chhajed

      Affiliations

    • Department of Pulmonary Medicine and Pulmonary Cell Research, University Hospital Basel, Petersgraben 4, CH-4031 Basel, Switzerland
  • ,
  • Julia Wallner

      Affiliations

    • Department of Pulmonary Medicine and Pulmonary Cell Research, University Hospital Basel, Petersgraben 4, CH-4031 Basel, Switzerland
  • ,
  • Manuel Battegay

      Affiliations

    • Department of Infectiology, University Hospital, Basel, Switzerland
  • ,
  • Juerg Steiger

      Affiliations

    • Department of Nephrology, University Hospital, Basel, Switzerland
  • ,
  • Alois Gratwohl

      Affiliations

    • Department of Haematology, University Hospital, Basel, Switzerland
  • ,
  • Michael Tamm

      Affiliations

    • Department of Pulmonary Medicine and Pulmonary Cell Research, University Hospital Basel, Petersgraben 4, CH-4031 Basel, Switzerland

Received 2 January 2006; accepted 15 April 2006. published online 01 June 2006.

Summary 

Bronchoalveolar lavage (BAL) is a useful tool in the diagnosis of pulmonary infections in immunocompromised patients. We aimed to compare the spectrum of infectious pulmonary complications diagnosed using BAL in a large consecutive cohort of immunocompromised patients.

The diagnostic yield of 1066 BAL specimens was analyzed in 4 different groups of immunocompromised patients (HIV; solid organ transplants; high-dose chemotherapy and/or stem cell transplants; other immunosuppressive therapy) suffering from fever, respiratory symptoms and/or infiltrates on chest X-ray. Specimens were analyzed for bacteria, mycobacteria, fungi, Pneumocystis jiroveci, cytomegalovirus (CMV) and other viruses. Two time periods were compared (1992–1996; 1997–2003).

The overall diagnostic yield of BAL was 34% for bacteria, 22% for CMV, 15% for P. jiroveci, 6% for other viruses, 6% for mycobacteria and 2% for aspergillus. There were significant changes in the pattern of opportunistic infections between the 2 time periods. Mycobacterial infections decreased considerably in the HIV group (17.9 vs. 8.5%, ), while the incidence of P. jiroveci decreased mainly in the transplant group (32.6 vs. 7.9%, ).

This study demonstrates a changed pattern of pulmonary infections in immunocompromised patients diagnosed by BAL. The overall diagnostic yield of BAL remains high in immunocompromised patients with respiratory symptoms.

Keywords: Bronchoalveolar lavage, Bronchoscopy, Immunosuppression, Mycobacteria, Opportunistic infections, Pneumocystis jiroveci

Abbreviations: BAL, Bronchoalveolar lavage, CMV, Cytomegalovirus, HAART, Highly active antiretroviral therapy, MMF, Mycofenolate mofetil, HIV, Human immunodeficiency virus, HHV-8, Human herpesvirus 8, PCP, Pneumcoystis jiroveci pneumonia

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0954-6111(06)00216-2

doi:10.1016/j.rmed.2006.04.006

Respiratory Medicine
Volume 101, Issue 1 , Pages 93-97, January 2007