P-2280. Community-Acquired Pneumonia in Immunosuppressed Patients Admitted to the ICU

Abstract Background Severe community-acquired pneumonia (sCAP) remains a crucial infectious cause of global mortality, accounting for a significant proportion of ICU admissions. Immunosuppressed patients frequently develop sCAP; however, the clinical characteristics and clinical outcomes of patients admitted to the ICU due to sCAP are not clear. Here, we attempted to bridge this gap in the literature. Figure 1 Isolated microorganisms in respiratory samples. A. General cohort; B. No immunosuppression risk factors group; C. Immunosuppression risk factors group Methods This secondary analysis of the prospective MIMIC-IV database included adults admitted to the ICU with CAP diagnosis. Patients were stratified based on the presence or absence of immunosuppression. Bivariate, multivariate, and survival analyses were conducted to identify factors associated with mortality within the immunosuppressed and their impact on hospital mortality. Figure 2 Kaplan-Meier survival curve of 1-year after discharge survival probability stratified by immunosuppression status. Patients with and without immunosuppression are represented, the first group with 1 (blue) and the last with 0 (red). Results A total of 4742 patients were included, with 1502/4742 (32%) being immunocompromised. The mean age (SD) was 66 ±16.1years, with 2627/4742 (55.4%) males. A total of 1384 respiratory isolations were obtained with Staphylococcus aureus (43.2% vs. 40.6%; p= 0.45) and Pseudomonas aeruginosa (10.20 % vs 11.69 %; p= 0.39) as the most representative in both groups (Figure 1). Immunosuppressed patients presented both higher Charlson comorbidity index (7.12, SD 3.14 vs. 4.97, SD 2.59; p < 0.01) and infection severity by the SAPS II score (39, [31-49] vs 37, [ 29-46]; p < 0.01). Immunosuppression was associated with increased mortality rates (IH: OR 1.99 [95% CI: 1.63-2.43]; 6 M: OR 1.79 [95% CI 1.52-2.12]; 12 M: OR 1.93 [95% CI 1.64-2.28]; p < 0.01) and both solid malignancy and infection severity were positively correlated with mortality (Table 1). Immunosuppressed patients had a lower survival rate even after adjusting for disease severity (Figure 2). Table 1 Univariate and multivariate analysis of risk factors associated with in-hospital, 6-month, and 12-month deaths in the immunosuppressed population. Conclusion Immunosuppression was independently associated with mortality and lower survival in sCAP patients. An individualized patient risk approach is necessary as immunosuppression affects mortality differently than immunocompetent patients. Disclosures All Authors: No reported disclosures

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Journal
Open Forum Infectious Diseases
Published
2025-01-29
DOI
https://doi.org/10.1093/ofid/ofae631.2433
Primary Topic
Pneumocystis jirovecii pneumonia detection and treatment
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article

P-2280. Community-Acquired Pneumonia in Immunosuppressed Patients Admitted to the ICU

Luis Felipe Reyes, Esteban García-Gallo, Sara Duque, Gabriela Guerrón-Gomez et al.
Open Forum Infectious Diseases
Pneumocystis jirovecii pneumonia detection and treatment
article

P-2280. Community-Acquired Pneumonia in Immunosuppressed Patients Admitted to the ICU

Luis Felipe Reyes, Esteban García-Gallo, Sara Duque, Gabriela Guerrón-Gomez, André Emilio Viñán Garcés, Natalia Sanabria-Herrera
article en

Abstract

Abstract Background Severe community-acquired pneumonia (sCAP) remains a crucial infectious cause of global mortality, accounting for a significant proportion of ICU admissions. Immunosuppressed patients frequently develop sCAP; however, the clinical characteristics and clinical outcomes of patients admitted to the ICU due to sCAP are not clear. Here, we attempted to bridge this gap in the literature. Figure 1 Isolated microorganisms in respiratory samples. A. General cohort; B. No immunosuppression risk factors group; C. Immunosuppression risk factors group Methods This secondary analysis of the prospective MIMIC-IV database included adults admitted to the ICU with CAP diagnosis. Patients were stratified based on the presence or absence of immunosuppression. Bivariate, multivariate, and survival analyses were conducted to identify factors associated with mortality within the immunosuppressed and their impact on hospital mortality. Figure 2 Kaplan-Meier survival curve of 1-year after discharge survival probability stratified by immunosuppression status. Patients with and without immunosuppression are represented, the first group with 1 (blue) and the last with 0 (red). Results A total of 4742 patients were included, with 1502/4742 (32%) being immunocompromised. The mean age (SD) was 66 ±16.1years, with 2627/4742 (55.4%) males. A total of 1384 respiratory isolations were obtained with Staphylococcus aureus (43.2% vs. 40.6%; p= 0.45) and Pseudomonas aeruginosa (10.20 % vs 11.69 %; p= 0.39) as the most representative in both groups (Figure 1). Immunosuppressed patients presented both higher Charlson comorbidity index (7.12, SD 3.14 vs. 4.97, SD 2.59; p < 0.01) and infection severity by the SAPS II score (39, [31-49] vs 37, [ 29-46]; p < 0.01). Immunosuppression was associated with increased mortality rates (IH: OR 1.99 [95% CI: 1.63-2.43]; 6 M: OR 1.79 [95% CI 1.52-2.12]; 12 M: OR 1.93 [95% CI 1.64-2.28]; p < 0.01) and both solid malignancy and infection severity were positively correlated with mortality (Table 1). Immunosuppressed patients had a lower survival rate even after adjusting for disease severity (Figure 2). Table 1 Univariate and multivariate analysis of risk factors associated with in-hospital, 6-month, and 12-month deaths in the immunosuppressed population. Conclusion Immunosuppression was independently associated with mortality and lower survival in sCAP patients. An individualized patient risk approach is necessary as immunosuppression affects mortality differently than immunocompetent patients. Disclosures All Authors: No reported disclosures

Open Forum Infectious DiseasesVol. 12(Supplement_1)
Universidad de La Sabana (CO), University of Oxford (GB)
Openalex Percentile: Top 98%
Pneumocystis jirovecii pneumonia detection and treatment
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