Pneumocystis jirovecii Pneumonia Diagnosis with Oropharyngeal Wash PCR in Immunocompromised Patients-A Systematic

Vasco Salgado Costa1,2, José Pedro Cidade1,2, Inês Medeiros1

  • 1Department of Critical Care Medicine, Hospital de São Francisco Xavier, Unidade Local de Saúde Lisboa Ocidental (ULSLO), Estrada Forte do Alto Duque, 1449-005 Lisbon, Portugal.

Journal of Clinical Medicine
|September 27, 2025
PubMed

Insights

Oropharyngeal wash (OW) polymerase chain reaction (PCR) provides a safe and effective non-invasive method for diagnosing Pneumocystis jirovecii pneumonia (PJP). This diagnostic approach offers high specificity, making it a valuable tool when invasive testing is not feasible.

Area of Science:

  • Infectious Diseases
  • Diagnostic Microbiology
  • Pulmonology

Background:

  • Pneumocystis jirovecii pneumonia (PJP) is a significant cause of illness and death in immunocompromised individuals.
  • Bronchoalveolar lavage (BAL) is the standard diagnostic method but is invasive and challenging for critically ill patients.

Purpose of the Study:

  • To systematically review the diagnostic accuracy and clinical utility of oropharyngeal wash (OW) polymerase chain reaction (PCR) for PJP detection.
  • To evaluate OW-PCR as a non-invasive alternative to traditional diagnostic methods.

Main Methods:

  • Systematic review of 12 studies involving PCR-based PJP detection in OW samples from immunocompromised adults.
  • Bronchoalveolar lavage (BAL) or induced sputum served as reference standards.
  • Bivariate random-effects modeling was used to estimate pooled sensitivity and specificity.

Main Results:

  • Pooled sensitivity for OW-PCR was 68.3% (95% CI: 59.2-75.9) and pooled specificity was 91.8% (95% CI: 85.9-95.3).
  • The area under the receiver operating characteristic curve (AUC) was 0.887, indicating good diagnostic performance.
  • Diagnostic yield was improved by cough induction, prolonged gargling, early sampling, and higher fungal loads.

Conclusions:

  • OW-PCR is a highly specific and moderately sensitive diagnostic tool for PJP, suitable for immunocompromised patients.
  • This non-invasive method offers a safe, scalable, and patient-friendly alternative when invasive diagnostics are not practical.
  • Optimizing collection protocols and broadening evaluation to non-HIV populations could enhance its utility as an early screening tool.

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