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Pneumocystis jirovecii pneumonia in intensive care units: a multicenter study by ESGCIP and EFISG
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Abstract
Background
Pneumocystis jirovecii pneumonia (PJP) is an opportunistic, life-threatening disease commonly affecting immunocompromised patients. The distribution of predisposing diseases or conditions in critically ill patients admitted to intensive care unit (ICU) and subjected to diagnostic work-up for PJP has seldom been explored.
Materials and methods
The primary objective of the study was to describe the characteristics of ICU patients subjected to diagnostic workup for PJP. The secondary objectives were: (i) to assess demographic and clinical variables associated with PJP; (ii) to assess the performance of Pneumocystis PCR on respiratory specimens and serum BDG for the diagnosis of PJP; (iii) to describe 30-day and 90-day mortality in the study population.
Results
Overall, 600 patients were included in the study, of whom 115 had presumptive/proven PJP (19.2%). Only 8.8% of ICU patients subjected to diagnostic workup for PJP had HIV infection, whereas hematological malignancy, solid tumor, inflammatory diseases, and solid organ transplants were present in 23.2%, 16.2%, 15.5%, and 10.0% of tested patients, respectively. In multivariable analysis, AIDS (odds ratio [OR] 3.31; 95% confidence interval [CI] 1.13–9.64, p = 0.029), non-Hodgkin lymphoma (OR 3.71; 95% CI 1.23–11.18, p = 0.020), vasculitis (OR 5.95; 95% CI 1.07–33.22, p = 0.042), metastatic solid tumor (OR 4.31; 95% CI 1.76–10.53, p = 0.001), and bilateral ground glass on CT scan (OR 2.19; 95% CI 1.01–4.78, p = 0.048) were associated with PJP, whereas an inverse association was observed for increasing lymphocyte cell count (OR 0.64; 95% CI 0.42–1.00, p = 0.049). For the diagnosis of PJP, higher positive predictive value (PPV) was observed when both respiratory Pneumocystis PCR and serum BDG were positive compared to individual assay positivity (72% for the combination vs. 63% for PCR and 39% for BDG). Cumulative 30-day mortality and 90-day mortality in patients with presumptive/proven PJP were 52% and 67%, respectively.
Conclusion
PJP in critically ill patients admitted to ICU is nowadays most encountered in non-HIV patients. Serum BDG when used in combination with respiratory Pneumocystis PCR could help improve the certainty of PJP diagnosis.
Springer Science and Business Media LLC
Daniele Roberto Giacobbe
Silvia Dettori
Vincenzo Di Pilato
Erika Asperges
Lorenzo Ball
Enora Berti
Ola Blennow
Bianca Bruzzone
Laure Calvet
Federico Capra Marzani
Antonio Casabella
Sofia Choudaly
Anais Dartevel
Gennaro De Pascale
Gabriele Di Meco
Melissa Fallon
Louis-Marie Galerneau
Miguel Gallego
Mauro Giacomini
Adolfo González Sáez
Luise Hänsel
Giancarlo Icardi
Philipp Koehler
Katrien Lagrou
Tobias Lahmer
P. Lewis White
Laura Magnasco
Anna Marchese
Cristina Marelli
Mercedes Marín-Arriaza
Ignacio Martin-Loeches
Armand Mekontso-Dessap
Malgorzata Mikulska
Alessandra Mularoni
Anna Nordlander
Julien Poissy
Giovanna Russelli
Alessio Signori
Carlo Tascini
Louis-Maxime Vaconsin
Joel Vargas
Antonio Vena
Joost Wauters
Paolo Pelosi
Jean-Francois Timsit
Matteo Bassetti
Matteo Cerchiaro
Mario Zaccarelli
Chiara Robba
Denise Battaglini
Iole Brunetti
Filippo Del Puente
Sara Mora
Sofía de la Villa
Maricela Valerio
Patricia Muñoz
Gianmarco Lombardi
Melania Cesarano
Veronica Gennenzi
Philippe Meersseman
Greet Hermans
Alexander Wilmer
Keyvan Razazi
Guillaume Carteaux
Nicolas de Prost
Oliver A. Cornely
Danila Seidel
Ana Alastruey-Izquierdo
Jorge Garcia Borrega
Christine Bonnal
Etienne de Montmollin
Julien Dessajan
Mariaelena Ceresini
Francesco Mojoli
Ambra Vola
Cécile Garnaud
Emili Díaz
Oriol Gasch
Elena Prina
Sebastian Rasch
Miriam Dibos
Stefanie Haschka
Title: Pneumocystis jirovecii pneumonia in intensive care units: a multicenter study by ESGCIP and EFISG
Description:
Abstract
Background
Pneumocystis jirovecii pneumonia (PJP) is an opportunistic, life-threatening disease commonly affecting immunocompromised patients.
The distribution of predisposing diseases or conditions in critically ill patients admitted to intensive care unit (ICU) and subjected to diagnostic work-up for PJP has seldom been explored.
Materials and methods
The primary objective of the study was to describe the characteristics of ICU patients subjected to diagnostic workup for PJP.
The secondary objectives were: (i) to assess demographic and clinical variables associated with PJP; (ii) to assess the performance of Pneumocystis PCR on respiratory specimens and serum BDG for the diagnosis of PJP; (iii) to describe 30-day and 90-day mortality in the study population.
Results
Overall, 600 patients were included in the study, of whom 115 had presumptive/proven PJP (19.
2%).
Only 8.
8% of ICU patients subjected to diagnostic workup for PJP had HIV infection, whereas hematological malignancy, solid tumor, inflammatory diseases, and solid organ transplants were present in 23.
2%, 16.
2%, 15.
5%, and 10.
0% of tested patients, respectively.
In multivariable analysis, AIDS (odds ratio [OR] 3.
31; 95% confidence interval [CI] 1.
13–9.
64, p = 0.
029), non-Hodgkin lymphoma (OR 3.
71; 95% CI 1.
23–11.
18, p = 0.
020), vasculitis (OR 5.
95; 95% CI 1.
07–33.
22, p = 0.
042), metastatic solid tumor (OR 4.
31; 95% CI 1.
76–10.
53, p = 0.
001), and bilateral ground glass on CT scan (OR 2.
19; 95% CI 1.
01–4.
78, p = 0.
048) were associated with PJP, whereas an inverse association was observed for increasing lymphocyte cell count (OR 0.
64; 95% CI 0.
42–1.
00, p = 0.
049).
For the diagnosis of PJP, higher positive predictive value (PPV) was observed when both respiratory Pneumocystis PCR and serum BDG were positive compared to individual assay positivity (72% for the combination vs.
63% for PCR and 39% for BDG).
Cumulative 30-day mortality and 90-day mortality in patients with presumptive/proven PJP were 52% and 67%, respectively.
Conclusion
PJP in critically ill patients admitted to ICU is nowadays most encountered in non-HIV patients.
Serum BDG when used in combination with respiratory Pneumocystis PCR could help improve the certainty of PJP diagnosis.
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