Accuracy of Pneumocystis jirovecii Plasma Cell-Free DNA PCR for Noninvasive Diagnosis of Pneumocystis Pneumonia.


Journal

Journal of clinical microbiology
ISSN: 1098-660X
Titre abrégé: J Clin Microbiol
Pays: United States
ID NLM: 7505564

Informations de publication

Date de publication:
18 05 2022
Historique:
pubmed: 8 4 2022
medline: 21 5 2022
entrez: 7 4 2022
Statut: ppublish

Résumé

Pneumocystis pneumonia (PCP) caused by Pneumocystis jirovecii is a serious infection in immunocompromised hosts which requires prompt diagnosis and treatment. The recommended specimen for diagnosis of PCP is bronchoalveolar lavage (BAL) fluid, which is invasive and may not be possible in unstable patients. The aim of this study was to evaluate the accuracy of noninvasive P. jirovecii plasma cell-free DNA (cfDNA) PCR using recently optimized preanalytical and analytical methods. Adult patients undergoing clinical testing for PCP with direct fluorescent antibody stain (DFA), respiratory PCR, and/or β-d-glucan were included in this study. Sensitivity and specificity P. jirovecii plasma cfDNA PCR was determined in PCP suspects categorized as proven and probable. A total of 149 patients were included in this study, of which 10 had proven and 27 had probable PCP. Most patients (95.9%, 143/149) were immunocompromised, including hematological malignancies (30.1%), bone marrow transplant (11.2%), solid organ transplantation (47.6%), and HIV/AIDS (4.2%). P. jirovecii plasma cfDNA PCR showed sensitivity and specificity of 100% (10/10; 95% confidence interval [CI], 69.2 to 100) and 93.4% (127/136; 95% CI, 87.8 to 96.9), and 48.6% (18/37; 95% CI, 31.9 to 65.6) and 99.1% (108/109; 95% CI, 94.9 to 100) in proven and proven/probable cases, respectively. P. jirovecii cell-free DNA PCR was similar in sensitivity but with substantially improved specificity over β-d-glucan (sensitivity, 60.0% [18/30; 95% CI, 40.6 to 77.3]); specificity, 66.7% [22/33; 95% CI, 48.2 to 82.0]) in patients with proven/probable PCP. Plasma cfDNA PCR offers a noninvasive testing option for early and accurate diagnosis of PCP, particularly in patients who cannot tolerate bronchoscopy.

Identifiants

pubmed: 35387472
doi: 10.1128/jcm.00101-22
pmc: PMC9116171
doi:

Substances chimiques

Cell-Free Nucleic Acids 0
Glucans 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0010122

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Auteurs

Angel Moreno (A)

Department of Pathology, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.

David Epstein (D)

Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford, California, USA.

Indre Budvytiene (I)

Clinical Microbiology Laboratory, Stanford Health Care, Palo Alto, California, USA.

Niaz Banaei (N)

Department of Pathology, Stanford University School of Medicinegrid.471392.a, Stanford, California, USA.
Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford, California, USA.
Clinical Microbiology Laboratory, Stanford Health Care, Palo Alto, California, USA.

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Classifications MeSH