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. 2014 Apr 21;9(4):e95865. doi: 10.1371/journal.pone.0095865

Table 1. Demographics, underlying disease/condition, and clinical characteristics of patients with severe hospital-acquired pneumonia.

HAP patients (n = 262)
Male, n (%) 191 (72.9)
Mean age (SD), y 64.5 (13.5)
Hospital stay prior to HAP, median (IQR), d 20 (10–42)
Underlying diseases or conditions, n (%)
Hematologic malignancy 76 (29.0)
Diabetes mellitus 76 (29.0)
Structural lung disease 60 (22.9)
 Chronic obstructive pulmonary disease 28 (10.7)
 Interstitial lung disease 19 (7.3)
 Tuberculous destroyed lung 17 (6. 5)
 Bronchiectasis 4 (1.5)
Solid cancer 59 (22.5)
Cerebrovascular attack 21 (8.0)
Heart failure 21 (8.0)
Bone marrow transplantation 20 (7.6)
Liver cirrhosis 12 (4.6)
Alcoholism 10 (3.8)
End-stage renal disease 10 (3.8)
Solid organ transplantation 10 (3.8)
Chronic renal failure 8 (3.1)
Immunocompromised statea 119 (45.4)
Receipt of immunosuppressive therapy 64 (24.4)
Receipt of recent chemotherapy (within 1 month) 57 (21.8)
Neutropoenia (absolute neutrophil count <500/mm3) 47 (17.9)
Recent surgery (within 1 month) 40 (15.3)
Active smoker 13 (5.0)
APACHE II score (SD) 25.4 (6.8)
SOFA score (SD) 10.0 (3.5)
Mechanical ventilation, n (%) 251 (95.8)
Septic shock at admission, n (%) 123 (46.9)

HAP = hospital-acquired pneumonia; APACHE = Acute Physiology and Chronic Health Evaluation; SOFA = Sequential Organ Failure Assessment.

a

The immunocompromised state was verified if the patients: (i) had daily administration of corticosteroids (at least 5 mg per day of prednisolone or an equivalent drug), (ii) were solid organ or hematopoietic stem cell transplant recipients, (iii) had received treatment with chemotherapy for an underlying malignancy during the 6 months prior to ICU admission, and (iv) had an underlying acquired immune deficiency disorder.