Abstract

The pneumonia severity index (PSI) accounts for many comorbidities, but not immunosuppression. To document the utility of the PSI to predict mortality in immunocompromised patients (IP) with community-acquired pneumonia (CAP). Charts of 284 patients with immunosuppression and CAP were reviewed, and these patients were compared with a contemporary sample of non-IP with CAP. The ability of the PSI to predict mortality was assessed by using multiple logistic regression. Discrimination of the PSI was studied by using the concordance index. Thirty-nine of 284 IP died. Mortality varied according to the etiology of the immunosuppression. Patients with HIV, solid organ transplantation or treatment with immunosuppressive drugs (n=118) had a low in-hospital mortality (4.3%) and were classified as low risk. IP with hematological malignancies, chemotherapy, chest radiation or marrow transplantation (n=166) had a high mortality (20%) and were classified as high risk. Compared with non-IP, low-risk IP had similar PSI-controlled mortality (OR=0.9, P=0.80), whereas high-risk IP had significantly greater mortality (OR=2.8, P<0.0001). The concordance index revealed similar discrimination for the PSI in low-risk IP (0.77) and in non-IP (0.7), but inferior discrimination in high-risk patients (0.6). Patients with CAP and immunosuppression can be divided into low-risk and high-risk groups. The low-risk IP have mortality similar to non-IP and can be risk stratified by using the PSI.

Highlights

  • The pneumonia severity index (PSI) accounts for many comorbidities, but not immunosuppression

  • We speculated that additional factors, especially those reflecting the nature of immune suppression, are important in predicting mortality in immunocompromised patients (IP) admitted to hospital with communityacquired pneumonia (CAP)

  • We note that IP could be divided into two groups based on the etiology of their immunosuppression

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Summary

Introduction

The pneumonia severity index (PSI) accounts for many comorbidities, but not immunosuppression. OBJECTIVES: To document the utility of the PSI to predict mortality in immunocompromised patients (IP) with communityacquired pneumonia (CAP). Patients with HIV, solid organ transplantation or treatment with immunosuppressive drugs (n=118) had a low in-hospital mortality (4.3%) and were classified as low risk. Compared with non-IP, lowrisk IP had similar PSI-controlled mortality (OR=0.9, P=0.80), whereas high-risk IP had significantly greater mortality (OR=2.8, P

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