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Erschienen in: BMC Pulmonary Medicine 1/2018

Open Access 01.12.2018 | Research article

The mortality risk factor of community acquired pneumonia patients with chronic obstructive pulmonary disease: a retrospective cohort study

verfasst von: Ruo-Xuan Dai, Qing-Hua Kong, Bei Mao, Wen Xu, Ru-Jia Tao, Xiao-Ru Wang, Qing-Yao Kong, Jin-Fu Xu

Erschienen in: BMC Pulmonary Medicine | Ausgabe 1/2018

Abstract

Background

Chronic obstructive pulmonary disease (COPD) is one of the most common comorbidities in community acquired pneumonia (CAP) patients. We aimed to investigate the characteristics and mortality risk factors of COPD patients hospitalized with CAP.

Methods

A retrospective cohort study was conducted at Shanghai Pulmonary Hospital and Shanghai Dahua Hospital. Clinical and demographic data in patients diagnosed with CAP were collected between January 2015 and June 2016. Logistic regression analysis was performed to screen mortality risk factors of COPD patients hospitalized with CAP.

Results

Of the total 520 CAP patients, 230 (44.2%) patients had been diagnosed comorbid with COPD (COPD-CAP). CAP patients comorbid with COPD patients had higher rate of need for ICU admission (18.3% vs 13.1%) and need for NIMV (26.1% vs 1.4%) than without COPD (nCOPD-CAP). The PSI, CURB-65 and APACHE-II scores in COPD-CAP patients were higher than that in nCOPD-CAP patients (95 vs 79, P < 0.001; 1 vs 1, P < 0.001; 13 vs 8, P < 0.001, respectively). Logistic regression analysis indicated that aspiration, D-dimer > 2.0 μg/mL and CURB-65 ≥ 3 were risk factors associated with in-hospital mortality ((odd ratio) OR = 5.678, OR = 4.268, OR = 20.764, respectively) in COPD-CAP patients. The risk factors associated with 60-day mortality in COPD-CAP patients were comorbid with coronary heart disease, aspiration, need for NIMV (non-invasive mechanical ventilation) and CURB-65 ≥ 3 (OR = 5.206, OR = 7.921, OR = 3.974, OR = 18.002, respectively).

Conclusions

COPD patients hospitalized with CAP had higher rate of need for NIMV, need for ICU admission and severity scores than those without COPD. Aspiration, D-dimer > 2.0 μg/mL, comorbid with coronary heart disease, need for NIMV and CURB-65 ≥ 3 were mortality risk factors in CAP patients comorbid with COPD.
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Hinweise

Electronic supplementary material

The online version of this article (https://​doi.​org/​10.​1186/​s12890-018-0587-7) contains supplementary material, which is available to authorized users.
Abkürzungen
APACHE-II
Acute Physiology and Chronic Health Evaluation II
AUC
Area under the curve
BTS
British Thoracic Society
CAP
Community acquired pneumonia
CI
Confidence interval
COPD
Chronic obstructive pulmonary disease
COPD-CAP
CAP patients comorbid with COPD
CPAP
Continuous positive airway pressure
CRP
C-reactive protein
ICU
Intensive care unit
nCOPD-CAP
CAP patients comorbid without COPD
NIMV
Non-invasive mechanical ventilation
OR
Odds ratio
PaCO2
Partial pressure of arterial carbon dioxide
PaO2
Partial pressure of arterial oxygen
PSI
Pneumonia severity index
ROC curve
Receiver operating characteristic curve
Se
Sensitivity
Sp
Specificity
WBC
White blood cell

Background

Community acquired pneumonia (CAP) is a common disease associated with high morbidity, mortality and inpatients care costs [13]. The 2009–2014 British Thoracic Society (BTS) Audit Programme indicates that the overall 30-day inpatients mortality is 18.0% [4]. Chronic obstructive pulmonary disease (COPD) is a disease with persistent airflow limitation and chronic inflammatory response, which progresses slowly [5]. The number of COPD cases in China increases dramatically from 32.4 million in 1990 to 54.8 million in 2013, which poses a heavy economic burden in China [6, 7].
COPD is one of the most common comorbidities in CAP. In the U.S., from 2005 to 2007, the incidence of inpatients primary pneumonia among elders with COPD is 54.2/1000 person-years, which is nearly seven times higher than that in elders without COPD [8]. Fine M. J. et al. derived a prediction rule to evaluate 30-day mortality in patients with CAP, chronic pulmonary diseases were excluded as a risk factor [9]. Meanwhile, previous study demonstrated that COPD patients hospitalized with CAP had the same mortality rate and demographic features, except for age and gender, as patients without COPD [10]. On the contrary, Restrepo M. I. et al. studied CAP population and indicated that COPD patients hospitalized with CAP had higher 30- and 90-day mortality than patients without COPD [11]. Besides, Guertler C. et al. reported that COPD was one of the risk factors for long-term mortality in CAP patients during 18-month follow-up [12]. Since the influences of COPD on severity scoring and mortality in CAP are controversial, we want to make clear that whether COPD patients hospitalized with CAP have higher severity scores and higher mortality rate. Meanwhile the mortality risk factors for COPD patients hospitalized with CAP still need to be further studied.
The aim of the current study is to investigate the characteristics of CAP patients comorbid with and without COPD, and to find out the mortality risk factors in COPD patients hospitalized with CAP.

Methods

Study design and inclusion and exclusion criteria

To perform a retrospective cohort study, we recruited patients with the diagnosis of CAP who were admitted in hospital between January 2015 and June 2016.
Patients were included if they were: 1) age ≥ 18 years; 2) symptoms of an acute lower respiratory tract illness (cough and at least one other lower respiratory tract symptom); 3) new focal chest signs on examination; 4) at least one systemic feature (either a symptom complex of sweating, fevers, shivers, aches and pains and/or temperature of 38°C or more); 5) no other explanation for the illness, which is treated as CAP with antibiotics [3]. Patients were not eligible for inclusion if they had: 1) been diagnosed with asthma, bronchiectasis, interstitial lung disease or other pulmonary infectious diseases; 2) life-threatening diseases (i. e. advanced malignant tumor, severe cardiopulmonary dysfunction, renal or liver dysfunction, etc.) within the past year; 3) severe immunosuppressive such as HIV infection, using longtime high dose of immunosuppressive agents, chemotherapy or organ transplantation; 4) research-related data missing. We only used the first hospitalization information if patients were admitted more than once during our study period.

Definitions

Diagnosis of COPD was made in patients with clinical symptom (dyspnea, chronic cough or sputum production) and smoking history at least 10 years, and it was confirmed by spirometric evidence of airflow obstruction in stable stage (post-bronchodilator FEV1/FVC < 0.70) [5]. The classification of COPD severity was based on the Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria: GOLD stage I was defined as a forced expiratory volume in 1 s (FEV1) greater than 80% predicted, GOLD stage II as FEV1 between 50 and 80% pred., GOLD stage III as FEV1 between 30 and 50% pred. and GOLD stage IV less than FEV1 30% pred.. Aspiration pneumonia was applied to situations where a patient with risk factors including altered level of consciousness, neurological disorders such as stroke, presence of dysphagia, gastric disorders such as gastro-oesophageal reflux and setting up gastric tube [3]. Need for ICU admission was applied to situations when a patient met the criteria of severe pneumonia and admission to ICU was necessary [1]. Need for non-invasive mechanical ventilation (NIMV) was applied to situations when a patient met one of these criteria, diagnosed COPD with a respiratory acidosis pH 7.25–7.35 (H+ 45–56 nmol/l), hypercapnic respiratory failure secondary to chest wall deformity (scoliosis, thoracoplasty) or neuromuscular diseases, cardiogenic pulmonary edema unresponsive to continuous positive airway pressure (CPAP), weaning from tracheal intubation [13]. In-hospital mortality and 60-day mortality were categorized as primary outcomes and need for ICU admission and need for NIMV were categorized as secondary outcomes.

Severity scoring

Severity of CAP at admission was calculated according to the PSI, CURB-65 and APACHE-II scores. The PSI score is a 20-point scoring system which classifies patients into five risk categories [9]. The CURB-65 score consists of 5 points: confusion, blood urea nitrogen > 7 mmol/L, respiratory rate > 30 breaths/min, systolic blood pressure < 90 mmHg and/or diastolic blood pressure ≤ 60 mmHg, and age ≥ 65 yrs. [14]. The APACHE-II is a scoring system including initial age, previous health status and value of 12 routine physiologic measurements [15]. We categorized the severity of pneumonia into three classes. PSI score: mild, < 90; moderate, 90–130; severe, > 130. CURB-65 score: mild, 0–1; moderate, 2; severe, ≥3. APACHE-II score: mild, 0–9; moderate, 10–19; severe, ≥20.

Data collection

All data were independently collected by Dr. RXD and Dr. QHK retrospectively according to the inclusion criteria (1) age ≥ 18 years; 2) diagnosed with CAP on admission) with unified Excel table. The unified Excel table was designed by Dr. RXD and Dr. QHK, it included demographic data (gender, age, smoking status), comorbidities (diabetes, coronary heart disease, hypertension, cerebral infarction, asthma, bronchiectasis, interstitial lung diseases, pulmonary infectious diseases, tumor), physical examination (mental status, respiratory rate, pulse, blood pressure and body temperature), laboratory examination, lung function test and X-ray/chest radiographic reports. The severity scores were assessed using PSI, CURB-65 and APACHE-II scores by two researchers. The highest score within 72 h of admission was chosen and recorded. The in-hospital mortalities were assessed by medical records and 60-day mortalities were assessed by telephone survey.

Statistical analysis

Quantitative data, which were normally distributed, were analyzed with the Student’s t-test. Mann–Whitney U-test was used for calculating differences between data of two groups which were not normally distributed. For qualitative data, the χ2 test were used to assess differences. Covariates were recruited in the univariate analysis with in-hospital mortality and 60-day mortality as outcomes. Only when the covariates with a significant (P < 0.05) by univariate analysis were entered in the multivariate analysis. Multicollinearity was screened using Spearman rank correlation matrices when variables with |r| > 0.7. A backward stepwise approach in the multivariate analysis was considered to keep significant covariates with a cut-point of 0.05. The discriminatory values of PSI, CURB-65 and APACHE-II scores in relation to in-hospital mortality and 60-day mortality were analyzed by the receiver-operating characteristic (ROC) analysis. ROC curves were performed to obtain the area under the curves (AUCs), cut-off values, sensitivities, specificities. The diagnostic performance was referred as high (AUC > 0.9), moderate (AUC = 0.7–0.9), or low (AUC = 0.5–0.7). The optimal cut-off values were determined by the Youden index (maximum of sensitivity + specificity – 1) (Additional file 1: Figure S1). AUCs were compared among PSI, CURB-65 and APACHE-II using the method of DeLong et al. [16]. All the data were analyzed with SPSS Version 20.0 software (SPSS, Chicago, IL) and Medcalc Version 15.2.2 software (Mariakerke, Belgium).

Results

Patient characteristics

Among 605 CAP patients recruited in this study, 291 patients were diagnosed with COPD. 230 (44.2%) patients had been diagnosed comorbid with COPD (COPD-CAP), the recruiting procedure was described in Fig. 1. COPD patients hospitalized with CAP were significantly more likely to be older males and smokers (Table 1). Whereas CAP patients without COPD (nCOPD-CAP) showed higher rates of cough, fever and purulent expectoration. In addition, COPD-CAP patients were significantly more likely to be dyspnea and tachypnea. As for laboratory examinations, COPD-CAP patients presented more acidosis, hypoxemia and hypercapnia, and higher hemoglobin and hematocrit level than nCOPD-CAP. We also did arterial blood gas analysis of COPD-CAP patients during stable stage, and the records were collected in Additional file 2: Table S1. 24 (10.4%) COPD-CAP patients in stable stage had type 2 respiratory failure, less than on admission (52/22.6%). As a retrospective study, patients with post-bronchodilator FEV1/FVC ≥ 70% were recruited in nCOPD-CAP group. Therefore, nCOPD-CAP patients in this study had normal lung function. Whereas in COPD-CAP, most patients had severe airflow obstruction (mean pre FEV1% = 45.01, SD = 15.76). COPD-CAP patients had higher rate of need for NIMV, need for ICU admission and higher length of hospital stay than those without COPD. Although the mortality in COPD-CAP patients was higher than that in nCOPD-CAP patients, the difference in discriminate value between COPD-CAP and nCOPD-CAP was not significant.
Table 1
Baseline characteristics of CAP patients
Covariates
nCOPD-CAP
COPD-CAP
P Valuea
Subjects, n
290
230
 
Males
117(40.3)
170(73.9)
< 0.001
Age, years
79[67,86]
82[74,87]
0.003
Ex-smoker or current smoking
86(29.7)
162(70.4)
< 0.001
Comorbidities
 Diabetes
50(17.2)
47(20.4)
0.353
 Coronary heart disease
74(25.5)
93(40.4)
< 0.001
 Hypertension
145(50)
98(42.6)
0.093
 Cerebral infarction
50(17.2)
10(4.3)
< 0.001
Symptom
 Cough
288(99.3)
209(90.9)
< 0.001
 Fever ≥38 °C
154(53.1)
79(34.3)
< 0.001
 Dyspnea
52(17.9)
205(89.1)
< 0.001
 Expectoration
287(99)
226(98.3)
0.705
  Mucoid
66(22.8)
90(39.1)
< 0.001
  Purulent
211(73.5)
129(57.1)
 
  Haemoptysis
10(3.4)
7(3)
 
 Pleural pain
24(8.3)
13(5.7)
0.304
 Altered mental state
17(5.9)
9(3.9)
0.418
 Respiratory frequency > 30 breaths · min−1
11(3.8)
21(9.1)
0.016
Laboratory results
 Hemoglobin, g/L
120[108,130.25]
124[113.75,135]
0.001
 Hematocrit, %
36.15[32.78,39]
37.7[34.5,41]
< 0.001
 WBC count > 10 × 109 cell
84(29.0)
79(34.3)
0.189
 C-reactive protein, mg/L
24.25[5.08,70.57]
32.67[7.99,72.55]
0.267
 Arterial PH < 7.35
12(4.1)
58(25.2)
< 0.001
 PaO2 < 60 mmHg
44(15.2)
81(35.2)
< 0.001
 PaCO2 > 50 mmHg
16(5.5)
74(32.2)
< 0.001
 Albumin, g/L
34.35[31.2,37.35]
34.1[31.28,37.3]
0.728
 Pre-albumin, mg/L
146.779 ± 65.414
145.974 ± 65.850
0.889
 D-dimer > 2.0 μg/mL
62(21.4)
45(19.6)
0.611
Spirometry
 FEV1% predicted
≥70
45.01 ± 15.76
 
 GOLD 1b
 
9(3.9)
 
 GOLD 2
 
80(34.8)
 
 GOLD 3
 
88(38.3)
 
 GOLD 4
 
53(23)
 
Aspiration
53(18.3)
29(12.6)
0.078
Need for ICU admission
38(13.1)
42(18.3)
0.105
Need for NIMV
4(1.4)
60(26.1)
< 0.001
Outcome measures
 Length of hospital stay, d
14[12,19]
16[13.88,20.63]
< 0.001
 In-hospital mortality
19(6.6)
19(8.3)
0.457
 60-day mortality
26(9)
29(12.6)
0.180
Data given as n(%) or mean ± SD or median [interquartile range]
CAP community acquired pneumonia, COPD chronic obstructive pulmonary disease, nCOPD-CAP CAP patients without COPD, COPD-CAP CAP patients with COPD, ICU intensive care unit, NIMV non-invasive mechanical ventilation, WBC white blood cell, PaO 2 partial pressure of arterial oxygen, PaCO 2 partial pressure of arterial carbon dioxide, FEV 1 forced expiratory volume in one second
aValues in bold indicate P < 0.05
bGOLD I was defined as FEV1/FVC ratio < 70% and FEV1 > 80% predicted; GOLD II as FEV1/FVC ratio < 70% and FEV1 50%–80% predicted; GOLD III as FEV1/FVC ratio < 70% and FEV1 30%–50% predicted; GOLD IV as FEV1/FVC ratio < 70% and FEV1 < 30% predicted

Comparison of different primary outcomes of predictive rules

The COPD-CAP patients were more severe than nCOPD-CAP patients in PSI, CURB-65 and APACHE-II severity score systems (79 [64.75, 101.25] vs 95 [77,128.25], P < 0.001; 1 [1, 2] vs 1 [1, 2], P < 0.001; 8 [6, 12] vs 13 [9.75,17], P < 0.001) (Table 2). As for in-hospital mortality and 60-day mortality, only the constituent ratio (mild, moderate, severe) of APACHE-II score was statistically significant.
Table 2
Comparison of primary outcomes of predictive rules
Risk groups
No of patients (N = 520)
In-hospital mortality (N = 38)
60-day mortality (N = 55)
nCOPD-CAP
COPD-CAP
P valuea
nCOPD-CAP
COPD-CAP
P valuea
nCOPD-CAP
COPD-CAP
P value a
PSI
79[64.75,101.25]
95[77.128.25]
< 0.001
169.26 ± 31.52
170.37 ± 46.21
0.932
160.42 ± 32.1
164.93 ± 41.11
0.655
 Mild
184(63.4)
106(46.1)
< 0.001
0(0)
1(5.3)
0.171
0(0)
1(3.4)
0.907
 Moderate
77(26.6)
68(29.6)
 
2(10.5)
4(21)
 
5(19.2)
6(20.7)
 
 Severe
29(10)
56(24.3)
 
17(89.5)
14(73.7)
 
21(90.8)
22(75.9)
 
CURB-65
1[1,2]
1[1,2]
< 0.001
3.47 ± 0.84
3.37 ± 1.21
0.758
3.12 ± 0.99
3.10 ± 1.08
0.966
 Mild
214(73.8)
120(52.2)
< 0.001
0(0)
2(10.5)
0.2
1(3.8)
2(6.9)
0.929
 Moderate
53(18.3)
78(33.9)
 
1(5.3)
2(10.5)
 
5(19.2)
6(20.7)
 
 Severe
23(7.9)
32(13.9)
 
18(94.7)
15(79)
 
20(76.9)
21(72.4)
 
APACHE-II
8[6,12]
13[9.75,17]
< 0.001
28[26,32]
25[15,33]
0.253
26.62 ± 5.14
24.38 ± 8.12
0.234
 Mild
182(62.8)
57(24.8)
< 0.001
0(0)
0(0)
< 0.001
0(0)
0(0)
< 0.001
 Moderate
77(26.5)
134(58.2)
 
0(0)
6(31.6)
 
1(3.8)
9(31)
 
 Severe
31(10.7)
39(17)
 
19(100)
13(68.4)
 
25(96.2)
20(69)
 
Data given as n(%) or mean ± SD or median [interquartile range]
P valuea (Student’s t test and Mann–Whitney U test for PSI, CURB-65 or APACHE-II; χ2 test for mild, moderate and severe of PSI, CURB-65 or APACHE-II; Values in bold indicate P < 0.05)

Mortality risk factors

Thirteen covariates were recruited in the univariate analysis with in-hospital mortality and 60-day mortality as outcomes. Only 3 covariates had statistically significant difference (P < 0.05) in logistic regression of in-hospital mortality (Table 3). Aspiration (OR = 5.678, 95%CI = 1.590–20.277, P = 0.008), D-dimer > 2.0 μg/mL (OR = 4.268, 95%CI = 1.205–15.124, P = 0.025) and CURB-65 ≥ 3 (OR = 20.764, 95%CI = 5.632–76.559, P = < 0.001) were prognostic predictors of in-hospital mortality in CAP patients with COPD. Meanwhile, coronary heart disease (OR = 5.206, 95%CI = 1.531–17.703, P = 0.008), aspiration (OR = 7.921, 95%CI = 2.256–27.816, P = 0.011), need for NIMV (OR = 3.974, 95%CI = 1.245–12.688, P = 0.020) and CURB-65 ≥ 3 (OR = 18.002, 95%CI = 5.867–55.237, P < 0.001) were associated with 60-day mortality (Table 4). Additionally, we screened the risk factors for in-hospital mortality and 60-day mortality in nCOPD-CAP patients using logistic analysis (Additional file 3: Table S2 and Additional file 4: Table S3). Age ≥ 70, coronary heart disease, cerebral infarction, need for NIMV, albumin < 30 g/dl, D-dimer > 2.0 μg/mL, PSI > 130, CURB-65 ≥ 3, APACHE-II ≥ 20 were recruited in multivariate analysis. PSI > 130 (OR = 31.095, 95%CI = 1.443–670.154, P = 0.028), CURB-65 ≥ 3 (OR = 51.936, 95%CI = 3.130–861.725, P = 0.006) and APACHE-II ≥ 20 (OR = 43.210, 95%CI = 2.705–690.249, P = 0.008) were the risk factors for in-hospital mortality. Cerebral infarction (OR = 20.659, 95%CI = 2.001–213.26, P = 0.011), PSI > 130 (OR = 12.186, 95%CI = 1.744–85.153, P = 0.012) and CURB-65 ≥ 3 (OR =47.999, 95%CI = 2.619–879.551, P < 0.001) were the risk factors for 60-day mortality in nCOPD-CAP patients.
Table 3
Logistic regression analyses of the risk factors associated with in-hospital mortality in CAP patients with COPD
 
Univariate analysis
Multivariate analysis
OR (95%CI)
P valuea
OR (95%CI)
P valuea
Age ≥ 70
4.211(0.546,32.475)
0.168
  
Ex-smoker or current smoking
0.546(0.209,1.425)
0.216
  
Coronary heart disease
2.751(1.040,7.276)
0.041
  
Cerebral infarction
2.985(0.587,15.185)
0.188
  
Aspiration
19.563(6.806,56.228)
< 0.001
5.203(1.443,18.757)
0.012
Need for NIMV
1.140(0.359,3.620)
0.824
  
Albumin< 30 g/dl
4.855(1.833,12.859)
0.001
  
D-dimer> 2.0 μg/mL
9.247(3.390,25.222)
< 0.001
5.026(1.395,18.108)
0.014
Arterial PH < 7.35
3.634(1.396,9.461)
0.008
  
PaCO2 > 50 mmHg
2.552(0.990,6.580)
0.053
  
PSI > 130
11.267(3.843,33.030)
< 0.001
  
CURB-65 ≥ 3
42.794(12.771,143.399)
< 0.001
23.299(6.246,86.903)
< 0.001
APACHE-II ≥ 20
15.417(5.390,44.092)
< 0.001
  
OR odds ratio, CI confidence interval, NIMV non-invasive mechanical ventilation
aValues in bold indicate P < 0.05
Table 4
Logistic regression analyses of the risk factors associated with 60-day mortality in CAP patients with COPD
 
Univariate analysis
Multivariate analysis
OR (95%CI)
P valuea
OR (95%CI)
P valuea
Age ≥ 70
6.957(0.919,52.676)
0.060
  
Ex-smoker or current smoking
0.648(0.288,1.457)
0.294
  
Coronary heart disease
3.896(1.686,9.004)
< 0.001
5.206(1.531,17.703)
0.008
Cerebral infarction
1.787(0.360,8.860)
0.477
  
Aspiration
14.311(5.769,35.501)
< 0.001
7.921(2.256,27.816)
0.001
Need for NIMV
6.195(2.719,14.116)
< 0.001
3.974(1.245,12.688)
0.020
Albumin< 30 g/dl
4.024(1.746,9.270)
< 0.001
  
D-dimer> 2.0 μg/mL
5.118(2.248,11.654)
< 0.001
  
Arterial PH < 7.35
5.325(2.355,12.025)
< 0.001
  
PaCO2 > 50 mmHg
4.237(1.883,9.534)
< 0.001
  
PSI > 130
15.437(6.109,39.009)
< 0.001
  
CURB-65 ≥ 3
45.341(16.413,125.255)
< 0.001
18.002(5.867,55.237)
< 0.001
APACHE-II ≥ 20
21.287(8.503,53.292)
< 0.001
  
OR odds ratio, CI confidence interval, NIMV non-invasive mechanical ventilation
aValues in bold indicate P < 0.05

ROC curves

The discriminatory ability of PSI, CURB-65 and APACHE-II scores to predict in-hospital mortality and 60-day mortality of COPD-CAP patients were analyzed and compared using areas under receiver operating characteristic (ROCs) curves (Additional file 5: Figure S2). The PSI score had good discriminative ability for death than CURB-65 and APACHE-II scores (AUCin-hospital mortality = 0.896, Sein-hospital mortality = 73.7%, Spin-hospital mortality = 91.9%; AUC60-day mortality = 0.911, Se60-day mortality = 89.7%, Sp60-day mortality = 77.1%). Whereas, there was no significant difference among PSI, CURB-65 and APACHE-II scores in predicting in-hospital mortality (PSI vs CURB-65, Z statistic = 0.204, P = 0.839; PSI vs APACHE-II, Z statistic = 1.542, P = 0.123; CURB-65 vs APACHE-II, Z statistic = 0.536, P = 0.5920). The differences among PSI, CURB-65 and APACHE-II scores in predicting 60-day mortality were not significant (PSI vs CURB-65, Z statistic = 0.608, P = 0.5433; PSI vs APACHE-II, Z statistic = 0.609, P = 0.5428; CURB-65 vs APACHE-II, Z statistic = 0.296, P = 0.7673). Additionally, we compared secondary outcomes (need for ICU admission and need for NIMV) of predictive rules in Additional file 6: Figure S3. In predicting need for ICU admission, there was a trend toward significance between PSI and APACHE-II (Z statistic = 1.840, P = 0.0658), and there was no significance between PSI and CURB-65 (Z statistic = 1.355, P = 0.175), and between CURB-65 and APACHE-II (Z statistic = 0.0622, P = 0.9504). Moreover, there was a significance between PSI and CURB-65 (Z statistic = 3.411, P = 0.0006), and between CURB-65 and APACHE-II (Z statistic = 4.110, P < 0.0001) in predicting need for NIMV. There was no significance between PSI and APACHE-II (Z statistic = 0.679, P = 0.4969).

Discussion

In the present study, we showed that COPD patients hospitalized with CAP had higher rate of need for NIMV, need for ICU admission and severity scores than those without COPD. Aspiration, D-dimer > 2.0 μg/mL, comorbid with coronary heart disease, need for NIMV and CURB-65 ≥ 3 were mortality risk factors in CAP patients comorbid with COPD.
We found that COPD was a frequent comorbidity in CAP patients, less than half of the whole population (44.2%). These results were consistence with other researches in which the rates were between 16 and 45.4% [10, 11, 1720]. In the present study, COPD patients hospitalized with CAP were male, older age and smokers in predominance, and significantly more likely to be dyspnea and tachypnea. In addition, COPD-CAP patients presented more acidosis, hypoxemia and hypercapnia than nCOPD-CAP patients. COPD-CAP patients showed high rate of need for NIMV and need for ICU admission, meanwhile with higher PSI, CURB-65 and APACHE-II scores than nCOPD-CAP patients. We deemed that COPD-CAP patients presented more severe than nCOPD-CAP patients on admission. Therefore, chronic obstructive pulmonary disease should be taken into account as one of the comorbidities in assessment of severity of community acquired pneumonia.
The in-hospital mortality and 60-day mortality of COPD-CAP patients in our study was 8.3 and 12.6%. In a cohort of 262 sample size, the 30-day mortality of CAP patients with COPD was 8.4%, and there was no difference between CAP patient with and without COPD [10]. The same result was found in a cohort with 367 CAP patients [21]. Nevertheless, in the study of Restrepo M. I., COPD patients hospitalized with CAP, compared to patients without COPD, showed significantly higher 30- and 90-day mortality [11]. Three main reasons might account for the same mortality rate between COPD-CAP and nCOPD-CAP patients in our study. First, the CAP patients recruited in this study, no matter nCOPD-CAP or COPD-CAP, they were more likely to have higher mean age, more coexisting illnesses, different distribution of etiology and atypical clinical presentations. Meanwhile, the all-cause mortality, which was used in this study, was significantly related to individual conditions. Secondly, using systemic corticosteroid was found to be associated with decreased mortality of CAP-COPD patients admitted to ICU [22], which might account for same mortality between nCOPD-CAP and COPD-CAP patients. Thirdly, since CAP population was relatively small in this research and previous researches [10, 21], enlarge study population would be available to find the difference of mortality between nCOPD-CAP and COPD-CAP patients.
Few studies paid attention to the mortality risk factors of COPD patients hospitalized with COPD. We found that aspiration was associated with in-hospital mortality and 60-day mortality in COPD-CAP patients. Abnormal swallowing reflexes frequently occurred in COPD patients. Clayton N. A. et al. found that in COPD patients, reduced laryngopharyngeal sensitivity and impaired swallowing function might cause pharyngeal residue and subsequent inhalation of pharyngeal contents [23], which might cause bacterial colonization and recurrence of aspiration [24]. Patients at risk of aspiration pneumonia had poor short-term prognosis and the risk of recurrence of pneumonia [2527], which in accordance with COPD-CAP population in present study. D-dimer > 2.0 μg/mL were associated with in-hospital mortality in COPD-CAP patients. Coagulation abnormalities were common in CAP patients without organ dysfunction [28]. The endotoxins of pathogens might cause pro-inflammatory states and result in activation of the coagulation cascade and inhibition of fibrinolysis [29, 30], which impacted on the formation of D-dimer. Previous reports found that the level of D-dimer had predictive value for mechanical ventilation therapy and mortality risk (AUC = 0.75, AUC = 0.859) [31, 32]. But D-dimer > 2.0 μg/mL could not be a risk factor for long-term mortality. Incident cardiac complications were associated with increased risk of death at 30 days in CAP patients [33]. In the present study, comorbid with coronary heart disease was one of the risk factors of 60-day mortality in COPD-CAP patients. Previous study indicated that CAP promoted platelet activation and thrombosis, at the same time, created an imbalance between myocardial oxygen supply and demand, which might increase the cardiovascular events [34]. Whereas, in our present study, need for NIMV was associated with 60-day mortality in COPD-CAP patients. Non-invasive positive pressure ventilation was used when CAP patients in acute hypoxemic respiratory failure, which was well tolerated and was associated with a reduction of intubation rate and of stay in ICU [35]. The ICU mortality was 50% for COPD patients with CAP failed non-invasive ventilation [36]. CURB-65 ≥ 3 and PSI > 90 were found to be independent risk factors for case-fatality rate in CAP patients with COPD [20, 37]. In our analysis, CURB-65 ≥ 3, other than PSI > 130 or APACHE-II ≥ 20, was identified to be a high risk factor in relation to in-hospital mortality and 60-day mortality in COPD-CAP patients.
In ROC analysis, all scoring systems in COPD-CAP inpatients had good predictive values in mortality, whereas the predictive abilities among three severity scoring systems had no discrimination. In previous study, it was confirmed that PSI score was the best indicator in elder patients with CAP [38]. Richards G. et al. reported that PSI, CURB-65 and APACHE-II performed similarly in predicting in-hospital mortality and 28-day mortality in CAP population [39]. According to the results of ROC analysis, we thought PSI, CURB-65 and APACHE-II scores performed similarly in predicting in-hospital mortality and 60-day mortality in COPD-CAP inpatients.
There were some limitations that should be acknowledged in this study. Firstly, as a retrospective observational study, we still had a potential selection bias. To tackle these problems, we chose two researchers to collect and organize data independently; patients with indefinite diagnosis were not recruited in this study. Second, this study was performed in only two centers and the sample size was relatively small. Therefore, conducting multicenter study and enlarging sample size would be more available for further research.

Conclusions

In conclusion, our study demonstrated that COPD patients hospitalized with CAP were older, easier to present respiratory failure. COPD-CAP patients had higher rate of need for NIMV, need for ICU admission and severity scores than those without COPD. Nevertheless, CAP patients comorbid with COPD had the same mortality rate as patients without COPD. Aspiration, D-dimer > 2.0 μg/mL, comorbid with coronary heart disease, need for NIMV and CURB-65 ≥ 3 were mortality risk factors in CAP patients comorbid with COPD.

Acknowledgements

The authors appreciate the assistance of Qin-Yao Kong in preparing the manuscript and editorial support.
This study protocol was approved by both ethics committees of Shanghai Pulmonary Hospital and Shanghai Dahua Hospital. The approval number of the study is DHYY-201712. Requirement of written informed consent was waived due to the retrospective design of the study.

Funding

This work was supported by the National Science Foundation of China [NSFC81670006], Shanghai Leading Talent Program [2016036] and Shanghai Hospital Development Center Program [16CR3036A].

Availability of data and materials

Data relating to this study is available from corresponding author on reasonable request.
Not applicable.

Competing interests

The authors declare they have no competing interests.

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Additional files

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Metadaten
Titel
The mortality risk factor of community acquired pneumonia patients with chronic obstructive pulmonary disease: a retrospective cohort study
verfasst von
Ruo-Xuan Dai
Qing-Hua Kong
Bei Mao
Wen Xu
Ru-Jia Tao
Xiao-Ru Wang
Qing-Yao Kong
Jin-Fu Xu
Publikationsdatum
01.12.2018
Verlag
BioMed Central
Erschienen in
BMC Pulmonary Medicine / Ausgabe 1/2018
Elektronische ISSN: 1471-2466
DOI
https://doi.org/10.1186/s12890-018-0587-7

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