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Vol. 58. Issue 6.
Pages 520-522 (June 2022)
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Vol. 58. Issue 6.
Pages 520-522 (June 2022)
Scientific Letter
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Outcomes of Critically Ill Very Old Patients With Community-Acquired Pneumonia and Acute Respiratory Distress Syndrome
Catia Cillóniza,
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Corresponding author.
, Juan M. Pericàsb,c, Héctor Peronid, Enric Barbetaa, Albert Gabarrúsa, Antoni Torresa,
Corresponding author

Corresponding author.
a Department of Pneumology, Institut Clinic del Tòrax, Hospital Clinic of Barcelona, Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona (UB) – SGR 911 – Ciber de Enfermedades Respiratorias (Ciberes), Barcelona
b Department of Infectious Diseases, Hospital Clinic of Barcelona, Barcelona, Spain
c Vall d’Hebron Institute for Research (VHIR), Barcelona, Spain
d Internal Medicine Department, Respiratory Medicine Unit and Emergency Department, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina
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During the last decades the overall and relative number of patients with community-acquired pneumonia (CAP) requiring intensive care management has increased globally, especially among elderly people.1 The percentage of intensive care unit (ICU) admissions attributable to elderly patients ranges between 9 and 19% in European studies2,3 and 20–30% in American studies.4 Severe CAP is the most common cause of acute respiratory distress syndrome (ARDS), which occurs in approximately 7–10% ICU patients with CAP,5 although a recent study found 13% of ARDS among ICU patients with CAP, reaching 29% in those requiring mechanical ventilation.6 Interestingly, the number of quadrants on chest imaging seems to be associated with an increased risk of death in patients with acute hypoxaemic respiratory failure requiring mechanical ventilation.7 However, there is limited information on ARDS in very old patients (VOP ≥80 years old) with CAP. We aimed to assess the prevalence, clinical characteristics, outcomes and risk factors of ARDS in VOP with CAP.

Prospective observational cohort study of consecutive adult patients with CAP admitted to the ICU within 24h from hospital admission, between November 1996 and December 2019. Inclusion criteria were: (1) hospitalized patients ≥80 years old with diagnosis of CAP; (2) severe CAP (according to ATS/IDSA criteria)8; (3) ICU admission; and (4) either invasive (IMV) or non-invasive mechanical ventilation (NIMV) within 24h from admission. Patients were excluded if they had severe immunosuppression or active tuberculosis. ARDS diagnosis was based on Berlin definition.9 Chest-X-ray involvement was analyzed as follows: involvement of one quadrant was considered unilateral, while two quadrants could be unilateral or bilateral; involvement of three or four quadrants was considered bilateral.7

Descriptive statistics were used for basic features of study data and appropriate statistical tests were performed to compare groups. A propensity score for VOP with ARDS was developed by means of a logistic regression model. The score was entered as a continuous variable into four logistic regression analyses to assess association between ARDS and outcomes (i.e., in-hospital, ICU, 30-day, and 1-year mortality). A similar analysis was performed to assess association between lung imaging quadrants and outcomes.

For publication purposes, the study was approved by the Comité Ètic d’Investigació Clínica, register: 2009/5451. The need for written informed consent was waived due to the non-interventional study design.

Among 6547 CAP patients admitted during the study period, 4571 patients (69.8%) were<80 years old, 904 (24%) of them were admitted to the ICU; 448 (52%) were not ventilated, 123 (14%) received NIMV, and 297 (34%) received IMV; and 1976 (30%) were VOP, 197 (10%) of them were admitted to the ICU; 95 (48%) were not ventilated, 38 (19%) received NIMV, and 64 (32%) received IMV (Fig. 1, Panel A). Overtime, the proportion of VOP admitted to the ICU changed significantly between 14% and 45% (p<0.001) (Fig. 1, Panel B).

Fig. 1.

Flow chart of study population (Panel A) and rate of VOP admitted to the ICU per year (Panel B).


One hundred and fifteen (27%) patients<80 years old met the Berlin ARDS criteria, and 305 (73%) did not. Twenty-seven VOP (26%) met the Berlin ARDS criteria, and 75 cases (74%) did not.

In patients younger than 80 years, those with ARDS presented higher rates of comorbidities (79% vs. 65%, p=0.004) and higher median PSI score (120 vs. 108, p=0.012), than patients without ARDS, while there were not significant differences regarding in-hospital (23% vs.27%, p=0.443), 30-day (21% vs. 21%, p=0.974) and 1-year mortality (29% vs. 30%, p=0.809) between groups. Interestingly, when we compared ARDS patients <80 years old with ARDS VOP, we found that VOP with ARDS had a higher PSI score (108 vs. 140, p<0.001), higher in-hospital (27% vs. 52%, p=0.012), 30 days (21% vs. 56%, p<0.001) and 1-year mortality (30% vs. 68%, p<0.001) than patients<80 years old with ARDS.

Our study population therefore comprised 102 VOP patients (Fig. 1, Panel A). Amongst the 27 VOP with ARDS, 9 (35%), 13 (50%), and 5 (15%) patients had mild, moderate, and severe ARDS, respectively. Seventy-two (84%) non-ARDS VOP presented unilateral infiltrates (1 quadrant 84%; 2 quadrants 12%).

Compared to VOP without ARDS, VOP with ARDS had more frequently received previous antibiotic therapy, and had higher median C-reactive protein values (Table 1). An etiologic diagnosis was obtained in 52 VOP (51%). The most frequent pathogen in both groups was S. pneumoniae (22 out of 40 patients in the non-ARDS VOP group [55%] vs. 8 out 12 VOP in the ARDS group [67%], p=0.473). The most frequent antibiotic regimens were β-lactam plus either a respiratory fluoroquinolone (46%) or a macrolide (25%). There were not differences in the empiric treatment between ARDS and non-ARDS VOP.

Table 1.

Patients characteristic and outcomes according to the presence of ARDS.

Variable  ARDS
  No(n=75)  Yes(n=27)  p-Valuea 
Age, median (Q1; Q3), years  83 (81; 85)  83 (81; 86)  0.361 
Male sex, n (%)  52 (69)  15 (56)  0.196 
Previous antibiotic, n (%)  10 (15)  9 (38)  0.022 
Previous episode of pneumonia, n (%)  11 (16)  1 (4)  0.130 
Comorbidities, n (%)b  61 (81)  20 (74)  0.424 
Chronic respiratory disease  33 (45)  12 (48)  0.317 
Chronic cardiovascular disease  14 (19)  5 (19)  0.995 
Diabetes mellitus  29 (39)  8 (30)  0.402 
Neurological disease  14 (20)  4 (16)  0.661 
Chronic renal disease  12 (16)  4 (15)  0.864 
Chronic liver disease  2 (3)  2 (7)  0.276 
Nursing-home, n (%)  7 (10)  1 (4)  0.356 
C-reactive protein, median (Q1; Q3), mg/dL  15.0 (6.3; 22.4)  25.1 (13.2; 28.9)  0.015 
PSI score, median (Q1; Q3)  140 (121; 160)  141 (121; 179)  0.620 
Severe CAP, n (%)  61 (82)  23 (88)  0.552 
SOFA score, median (Q1; Q3)  5.5 (3; 7)  4.5 (3; 6)  0.525 
CXR quadrants involved, n (%)<0.001 
1 quadrant  63 (84)  0 (0)  <0.001 
2 quadrants  11 (15)  16 (59)  <0.001 
>2 quadrants  1 (1)  11 (41)  <0.001 
Unilateral/bilateral, n (%)<0.001 
Unilateral – 1 quadrant  63 (84)  0 (0)  <0.001 
Unilateral – 2 quadrants  9 (12)  0 (0)  <0.001 
Bilateral  3 (4)  27 (100)  <0.001 
Appropriate empiric treatment, n (%)  49 (82)  23 (96)  0.165 
Mechanical ventilation, n (%)c0.368 
Non-invasive  26 (35)  12 (44)   
Invasive  49 (65)  15 (56)   
Length of hospital stay, median (Q1; Q3), days  16 (11; 26)  17 (9; 23)  0.663 
In-hospital mortality, n (%)  24 (32)  14 (52)  0.067 
ICU mortality, n (%)  12 (16)  11 (41)  0.008 
30-day mortality, n (%)  24 (32)  15 (56)  0.031 
1-year mortality, n (%)  31 (42)  17 (68)  0.024 

Abbreviations: ARDS indicates acute respiratory distress syndrome; CAP, community acquired pneumonia; CXR, chest X-ray; ICU, intensive care unit; PSI, pneumonia severity index; Q1, first quartile; Q3, third quartile; SOFA, sequential organ failure assessment. We excluded patients with severe immunosuppression, active tuberculosis, CAP with sepsis that development septic shock, and unavailable data. Percentages calculated on non-missing data.


Categorical variables were compared with the Chi-square or the Fisher exact test when necessary; continuous variables were compared with the non-parametric Mann–Whitney test.


May have>1 comorbid condition.


Patients who received initially non-invasive ventilation but needed subsequently intubation were included in the invasive mechanical ventilation group.

ICU, 30-day and 1-year mortality were significantly higher in the ARDS VOP group (p=0.008, 0.031 and p=0.024, respectively). Main causes of death were respiratory failure (non-ARDS VOP: 56% vs. ARDS VOP: 55%) and refractory shock with multi-organ failure (non-ARDS VOP: 39% vs. ARDS VOP 36%). The propensity-adjusted analyses showed that ARDS patients had higher risk of in-hospital, ICU, 30-day and 1-year mortality compared to non-ARDS VOP (odds ratio [OR] 3.13 [95% confidence interval (CI) 1.02–9.61], OR 4.12 [95%CI 1.22–13.91], OR 3.32 [95%CI 1.09–10.13], and OR 4.80 [95%CI 1.40–16.43], respectively), and confirmed by internal validation using bootstrapping with 1000 bootstrap samples and bias-corrected.

VOP with bilateral infiltrates presented significantly higher ICU mortality rates than patients with unilateral/1-quadrant infiltrates (p<0.05). Propensity-adjusted analyses showed that VOP with bilateral infiltrates showed an increased risk of 1-year mortality compared to VOP with unilateral/1-quadrant infiltrates (OR 4.01 [95%CI 1.27–12.62]), confirmed by internal validation using bootstrapping with 1000 bootstrap samples and bias-corrected.

The main findings of our study are as follows. First, 10% of patients with CAP admitted to the ICU were VOP and there was an increase in the proportion of VOP admitted to the ICU overtime, which is in accordance with reports showing a progressive increase of critically ill VOP worldwide.1,2,10,11 Second, 52% of VOP admitted to ICU received MV, which is also consistent with prior studies. For instance, Storms et al.12 found that 42% of patients admitted to the ICU due to CAP received MV, whereas in a study including 930 with CAP admitted to the ICU, we observed that 46.5% received MV.6 Third, ARDS developed in 26% of very old CAP patients treated in ICU with either IMV or NIMV, which is similar to the overall percentage of ARDS found in studies also including non-VOP adults.6,13 Yet, some of these studies showed an age-dependent gradient in the incidence of ARDS in the general population, with a trend towards higher percentages of ARDS amongst older patients.13,14 Fourth, ARDS was associated with significantly higher risk of both short-term and long-term mortality, which provides insight for clinical decision-making, i.e., early implementation of measures to prevent ARDS development. Interestingly, in patients under 80 years old we did not observe differences in outcomes between ARDS and non-ARDS, which is consistent with prior findings of our group.6 Finally, patients with unilateral infiltrates had lower severity than patients with bilateral infiltrates while patients with bilateral infiltrates had higher ICU mortality than patients with unilateral infiltrates. Our results contrast with those of Pham et al.,7 who found that patients with unilateral-infiltrate had mortality rates comparable to that of patients with ARDS of similar severity.

Our study is limited by its small sample size, which precluded further relevant sub-analysis such as the impact of ARDS severity on mortality. However, to our knowledge ours is the first study providing information on ARDS due to CAP in VOP admitted to ICU.

In conclusion, ARDS in VOP with CAP admitted to ICU and ventilated is associated with higher risk of morbidity and mortality. Further research is required in order to enhance clinical decision-making in VOP with severe CAP.

Conflicts of interest

The authors declare that they have no conflicts of interest.

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