|Year : 2018 | Volume
| Issue : 1 | Page : 76-82
Combined pulmonary fibrosis and emphysema syndrome: clinical, functional, and radiological assessment
Maha K Ghanem, Hoda A Makhlouf, Ali A Hassan, Heba A Hamed
Department of Chest, Faculty of Medicine, Assiut University, Assuit, Egypt
|Date of Submission||09-Jun-2017|
|Date of Acceptance||10-Sep-2017|
|Date of Web Publication||12-Jan-2018|
Ali A Hassan
Department of Chest, Faculty of Medicine, Assiut University Hospital, Assiut University, Assuit 71111
Source of Support: None, Conflict of Interest: None
Background The coexistence of pulmonary fibrosis and emphysema is increasingly recognized.
Objective To assess the clinical, physiological and radiological characteristics of patients with combined pulmonary fibrosis and emphysema (CPFE) and compare it with patients with chronic obstructive pulmonary disease (COPD) and interstitial lung disease (ILD) alone.
Patients and methods One hundred-twenty patients were enrolled and divided into three groups; 40 had COPD based on poorly reversible airflow obstruction in spirometry; 40 had ILD based on high-resolution computed tomography (HRCT); and 40 had CPFE based on the presence of emphysematous changes in the upper lung zones and pulmonary fibrosis in lower zones in HRCT. Modified Medical Research Council dyspnea scale, arterial blood gas analysis, spirometry, diffusion capacity for carbon monoxide (DLCO), polythesmography, HRCT chest, and echocardiography were done.
Results More than 57% of patients with CPFE were men and the majority of them were smokers. There was no significant difference in dyspnea grade between CPFE group and other groups (P>0.05). The rate of exacerbation per year was significantly higher in the CPFE group (4.2±1.02) compared with either COPD group (3.33±1.56) or ILD group (3.15±1.05). CPFE patients had both emphysematous and fibrotic changes on radiological examination. Lung volumes were preserved but DLCO% was significantly lower and the mean pulmonary artery systolic pressure was significantly higher in the CPFE group compared with COPD and ILD.
Conclusion CPFE is a distinct syndrome that has characteristic radiological findings and lung function profile with a significant reduction of DLCO and a significant increase in pulmonary artery systolic pressure.
Keywords: diffusion capacity for carbon monoxide, high-resolution computed tomography, pulmonary hypertension
|How to cite this article:|
Ghanem MK, Makhlouf HA, Hassan AA, Hamed HA. Combined pulmonary fibrosis and emphysema syndrome: clinical, functional, and radiological assessment. Egypt J Bronchol 2018;12:76-82
|How to cite this URL:|
Ghanem MK, Makhlouf HA, Hassan AA, Hamed HA. Combined pulmonary fibrosis and emphysema syndrome: clinical, functional, and radiological assessment. Egypt J Bronchol [serial online] 2018 [cited 2018 Sep 22];12:76-82. Available from: http://www.ejbronchology.eg.net/text.asp?2018/12/1/76/223086
| Introduction|| |
Combined pulmonary fibrosis and emphysema (CPFE) syndrome is a recently defined clinical entity. However, the histopathologic coexistence of pulmonary fibrosis and emphysema was first described in the literature in the 1970s . Subsequently in the 1990s, the advent of computed tomography technology permitted enhanced clinical recognition of the coexistence of pulmonary fibrosis and emphysema in the same patients. Emphysema is usually encountered predominantly in the upper lobes followed by fibrosis of the lower lobe . The prevalence of CPFE is not known although a wide variation in different studies is present. It has been estimated to represent between 8 and 51% of cases of diffuse interstitial lung disease .
On the other hand, in patients with emphysema the proportion of pulmonary fibrosis was estimated to be about 4.4–8% by HRCT ,. Most patients are current or former smokers, predominantly men over 65 years of age, with severe dyspnea and exercise limitation .
High-resolution computed axial tomography (HRCT) of the chest is the mandatory tool to confirm the diagnosis in which centrilobular and/or paraseptal emphysemas in the upper lung zones coexist with pulmonary fibrosis in lower lobes in one individual. Pulmonary hypertension is highly prevalent in CPFE and is the main determinant of death. Tobacco smoking has been proposed as the leading factor in its etiology . It is not known whether CPFE represents a unique disease entity or a coincidence of two pulmonary diseases related to cigarette smoking. Moreover, the extent of emphysema and fibrosis needed to distinguish the patient with CPFE from patients with predominant emphysema or predominant fibrosis is still unclear . Usual interstitial pneumonia/idiopathic pulmonary fibrosis (IPF) appears to be the most common imaging or pathologic findings in CPFE; however, other fibrotic patterns have been reported in conjunction with emphysema . The aim of this study was to assess the clinical, physiological and radiological characteristics of patients with CPFE syndrome and to compare it with patients with chronic obstructive pulmonary disease (COPD) and disease interstitial lung disease (ILD) alone.
| Patients and methods|| |
This study was done in the Chest Department, Assiut University Hospital during the period from August 2015 to August 2016. The study was approved by the Ethical Committee of Faculty of Medicine, Assiut University. An informed consent was obtained from all patients. The confidentiality of patient’s information was maintained during all steps of the study.
In this analytic cross-sectional study 120 patients were enrolled and divided to three groups. The COPD group included 40 patients; 32 men and eight women. The ILD group included 40 patients; 16 men and 24 women and the CPFE group included 40 patients; 23 men and 17 women. The age range was from 38 to 70 years. COPD was diagnosed according to Global Initiative for Chronic Obstructive Lung Disease criteria by the presence of postbronchodilator fixed ratio of FEV1/FVC less than 0.70 . ILD was diagnosed using HRCT by the presence of reticular abnormality, ground glass abnormality, nodular or micronodular opacities, honeycombing with or without traction bronchiectasis . CPFE was diagnosed by the presence of emphysematous changes on HRCT, in the form of well-demarcated areas of decreased attenuation in comparison with the surrounding normal lung and marginated by a very thin (1 mm) or no wall, and/or multiple bullae (1 cm) with upper zone predominance combined with diffuse parenchymal lung disease with significant pulmonary fibrosis in the form of reticular opacities, and/or honeycombing, architectural distortion, traction bronchiectasis, bronchiolectasis and focal ground-glass opacities with peripheral and basal predominance . Patients with connective tissue disease, drug-induced interstitial lung disease, pneumoconiosis, hypersensitivity pneumonitis or sarcoidosis were not included in the CPFE group.
| Methods|| |
Patients were subjected to:
- Detailed medical history with an attention to demographic data, symptoms including dyspnea and its grade according to MRC scale  and the presence of comorbidities.
- Physical examinations: with special attention to the presence of cyanosis finger clubbing, signs of airflow obstruction, signs of cor-pulmonale, crackles and signs of hyperinflation.
- Plain chest radiography: posteroanterior and lateral views to search for emphysematous changes in COPD, fibrotic changes in ILD and both in CPFE.
- Arterial blood gases: Arterial blood samples were taken from all patients to check gases tension and acid base status using blood gases analyzers (Rapid lab 850; Chiron Diagnostics, Halstead, UK).
- High-resolution computed axial tomography (HRCT): HRCT examination (using Aquilion 64; Toshiba Medical Systems, Otawara, Japan) was performed by standard protocol scans were obtained at full inspiration from the apex to the lung base with the patients in the supine position.
- Echocardiogaraphy: (Philips xMATRIX Echo System; Philips, Eindhoven, The Netherlands) to measure pulmonary artery systolic pressure.
- Pulmonary function tests: Pulmonary function tests were done when the patient condition becomes stable. Standard spirometry and polythesmography were performed in all patients by means of a fully equipped computerized system (using Cosmed SrL, Quark PFTs ergo, P/N Co9035-12-99; Cosmed SrL, Rome, Italy, and D 97723, Zan 300; Zan, Oberthulba, Germany, respectively). Single-breath diffusing capacity for carbon monoxide (DLCO) was also measured using a single breath (using D 97723, Zan 300; Zan).
The data were tested for normality using the Anderson–Darling test and for homogeneity variances before further statistical analysis. Categorical variables were described by number and percent, where continuous variables were described by mean±SD. χ2-Test and Fisher’s exact test were used to compare between categorical variables where comparison between continuous variables by analysis of variance was followed least significant difference. A two-tailed P value less than 0.05 was considered statistically significant. All analyses were performed with the SPSS for windows version 16 (SPSS Inc., Chicago, IL, USA).
| Results|| |
As regards demographic data, the mean age of patients with CPFE (55.48±13.77 years) was significantly lower than that of COPD patients (62.05±8.1 years) and significantly higher than that of ILD patients (48.33±10.04 years) (P<0.01 for each). Men were the predominant sex in the COPD and the CPFE group (80 and 57%, respectively). Most patients with CPFE (87.5%) were exposed to tobacco smoke. There was no statistically significant difference regarding the residence or the presence of other comorbidities including hypertension or diabetes mellitus between the three groups (P>0.05 for each) as shown in [Table 1]. [Table 2] represented the clinical data of the studied patients. There was no statistical significant difference in Modified Medical Research Council (mMRC) dyspnea scale among the three groups (P>0.05). All patients with COPD had productive cough while most patients with CPFE and ILD had dry cough. Chest wheeze was significantly higher in COPD than either CPFE or ILD group. Finger clubbing was significantly higher in either CPFE group or ILD group compared with the COPD group (P<0.001, <0.01 respectively). Most patients with COPD and CPFE had hyperinflation. The presence of velcro crackles was significantly higher in either ILD group or CPFE group compared with COPD (P<0.001 for each). The rate of exacerbation per year was significantly higher in patients with CPFE than in COPD or ILD patients. In contrast to COPD who had hyperinflation and emphysematous changes and ILD who had reticulonodular and fibrotic changes, patients in the CPFE group had both hyperinflation and emphysematous changes combined with reticular, nodular, ground glass opacity, honeycombing and fibrotic changes on radiological examination ([Table 3] and [Table 4], and [Figure 1]).
|Table 1 Demographic data of patients with combined pulmonary fibrosis and emphysema syndrome compared with chronic obstructive pulmonary disease and interstitial lung disease patients|
Click here to view
|Table 2 Clinical data of patients with combined pulmonary fibrosis and emphysema syndrome compared with chronic obstructive pulmonary disease and interstitial lung disease patients|
Click here to view
|Table 3 Chest radiography findings among patients with combined pulmonary fibrosis and emphysema syndrome compared to chronic obstructive pulmonary disease and interstitial lung disease patients|
Click here to view
|Table 4 High-resolution computed tomography findings of patients with combined pulmonary fibrosis and emphysema syndrome compared to chronic obstructive pulmonary disease and interstitial lung disease patients|
Click here to view
|Figure 1 Upper lobe centrilobular and paraseptal emphysema (a) and lower lobe fibrosis (b).|
Click here to view
[Table 5] showed that the mean PaO2 and SaO2 and DLCO% were significantly lower in the CPFE group compared with the COPD group or ILD group and the mean pulmonary artery systolic pressure was significantly higher in the CPFE group in comparison to either COPD group or ILD group (P<0.001 for each). The mean FVC% was significantly lower in the ILD group in comparison to either COPD or CPFE groups (P<0.001, <0.05, respectively) and significantly lower in the CPFE group than the COPD group (P<0.001). The mean total lung capacity (TLC)%, mean residual volume (RV)%, mean RV/TLC%, and mean percentage function residual capacity were significantly higher in the COPD group when compared with either CPFE group or ILD group, and were significantly higher in the CPFE group in comparison with the ILD group (P<0.01 for each).
|Table 5 Arterial blood gas, pulmonary artery systolic pressure, and PFT among patients with combined pulmonary fibrosis and emphysema syndrome compared to chronic obstructive pulmonary disease and interstitial lung disease patients|
Click here to view
| Discussion|| |
In the past few years there is an increasing recognition of clinical, radiological, and pathological coexistence of variable degrees of emphysema and pulmonary fibrosis in the same patient, resulting in a clinical syndrome known as CPFE. That syndrome is characterized by shortness of breath and great abnormalities of gas exchange, frequently complicated by pulmonary hypertension and had significant mortality . We conducted this study to describe the characteristic of this syndrome in comparison to emphysema and pulmonary fibrosis alone.
In the current study, the mean age of patients with CPFE was 55.48±13.77 years which was significantly lower than that of COPD patients (62.05±8.1 years) and higher than that of ILD patients (48.33±10.04 years). This was in agreement with previous studies which found that the mean age of COPD was higher in comparison to CPFE . However, in the study of Akagi et al.  and Sugino et al.  the mean age of ILD patients was higher than CPFE patients (66.5±9.2 and 73.7±6.3, respectively).The cause beyond the difference from the results of this study may be due to the nature of patients as they studied only patients with IPF, which is predominant in elderly while this study also included patients with other ILD which had relatively younger age than IPF patients.
As regards sex distribution, this study was in concordance with previous studies regarding male sex predominance in CPFE syndrome. The male preponderance of cases of CPFE could be explained by greater exposure to smoking and other CPFE risk factors as dust and minerals in men than women . As in the case of emphysema, IPF is also more common in men than in women, especially in older age groups . Most patients with CPFE syndrome (87.5%) have been exposed to cigarette smoking. This is compatible with recent studies of CPFE which have shown a strong association with cigarette smoking . The relationship between CPFE and smoking may be explained by the associations between smoking and both COPD/emphysema and IPF, where a unique group of patients exposed to cigarette smoke is vulnerable to develop extensive CPFE disease. In the present study, there was no statistically significant difference in the grade of dyspnea based on mMRC dyspnea scale among the study groups. This result was in agreement with Tomioka et al. , who conducted a retrospective observational study on 17 CPFE patients and 49 COPD patients and found that mMRC dyspnea grade were comparable between the two groups. However, other authors reported that CPFE patients had more dyspnea at rest and following effort than COPD patients as those patients had extensive pathology than patients with either disease alone .
In this study patients with CPFE had a significantly higher rate of exacerbation per year than patients with COPD and ILD. This may be attributed to the great functional impairment of those patients. Although a consensus definition of CPFE syndrome does not currently exist, the diagnosis can be established using HRCT imaging. Characteristic radiologic findings in the CPFE syndrome include upper-lobe emphysema and lower-lobe interstitial fibrotic changes. The emphysema in CPFE includes bullous, paraseptal, and centrilobular changes and is typically distributed in the upper lobes ,,. In the current study centrilobular, paraceptal and panlobular emphysema were significantly higher in CPFE than in COPD patients. This was in agreement with that of Kitaguchi et al.  who have found that paraseptal emphysema was more common in the CPFE population than in the control group of patients with COPD (33.3 vs. 8.5%, respectively). Honeycombing, reticular abnormalities and ground glass attenuation are frequent in our study and comparable to that of ILD. Cottin et al.  support this finding.
In the present study, there is significant hypoxemia and significant decrease in DLCO in the CPFE group when compared with either COPD group or ILD group. The severe impairment of gas exchange in CPFE is likely due to reduced vascular surface area and pulmonary capillary blood volume plus alveolar membrane thickening resulting from the two coexistent diseases . Pulmonary hypertension is a well-known complication of CPFE syndrome. It appears to be more frequent and more severe in the CPFE population than in patients with emphysema or ILD alone . In one study most CPFE patients have moderate to severe PAH whereas that in COPD or ILD alone it is usually mild to moderate . The current study coincides with this and demonstrated that the mean pulmonary artery systolic pressure in CPFE patients was significantly higher than in COPD or ILD patients. This may be attributed to the presence of additional or synergistic effect of pulmonary vasoconstriction caused by hypoxemia and reduced capillary beds caused by the combination of emphysema and pulmonary fibrosis in CPFE .
In this study, we have found that in patients with CPFE despite extensive radiological changes, lung volumes are nearly preserved where TLC, RV, and function residual capacity were around normal values, while they are increased in COPD patients and decreased in ILD patients. The relatively normal lung volumes in CPFE usually are attributed to the counterbalancing effects of the restrictive defect of pulmonary fibrosis and the propensity to hyperinflation seen in emphysema . Gas exchange is markedly impaired in CPFE. This is manifested by a marked reduction in DLCO, PaO2, and SaO2. This may be due to the overlapping negative effects of both emphysema and pulmonary fibrosis on the gas exchange ,.
| Conclusion|| |
This study proved that CPFE is a distinct clinical syndrome with a characteristic presentation. HRCT is the main tool to confirm the diagnosis. Patients with CPFE syndrome had a characteristic functional profile, with preserved lung volumes and strongly impaired DLCO. Cigarette smoking and male sex were two major clinical characteristics linked to this syndrome. All patients with CPFE should be screened for possible complicating pulmonary hypertension as it was found in the majority of patients screened in this study.
Maha K. Ghanem, Hoda A. Makhlouf, and Ali A. Hassan were responsible for the conception and design. Haba A. Hamed collected the cases. Hoda A. Maklouf, Ali A. Hasan, and Heba A. Hamed were responsible for the analysis and interpretation of data. Hoda A. Makhlouf and Ali A. Hassan were responsible for drafting the article, revisingitcritically for important intellectual content, and final approval of the version to be published.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Auerbach O, Garfinkel L, Hammond EC. Relation of smoking and age to findings in lung parenchyma: a microscopic study. Chest
Cottin V, Nunes H, Brillet PY, Delaval P, Delaval P, Devouassoux G et al.
Combined pulmonary fibrosis and emphysema: a distinct underrecognised entity. Eur Respir J
Ryerson CJ, Hartman T, Elicker BM, Ley B, Lee JS, Abbritti M et al.
Clinical features and outcomes in combined pulmonary fibrosis and emphysema in idiopathic pulmonary fibrosis. Chest
Sakai F, Tominaga J, Kaga A, Usui Y, Kanazawa M, Ogura T et al.
Imaging diagnosisof interstitial pneumonia with emphysema (combinedpulmonary fibrosis and emphysema). Pulm Med
Fujimoto K, Kitaguchi Y, Kubo K, Honda T. Clinical analysis of chronic obstructive pulmonary disease phenotypes classified using high-resolution computed tomography. Respirology
Cottin V, Nunes H, Mouthon L, Gamondes D, Lazor R, Hachulla E. Combined pulmonary fibrosis and emphysema syndrome in connective tissue disease. Arthritis Rheum
Jankowich DM, Rounds SI. Combined pulmonary fibrosis and emphysema syndrome: a review. Chest
Jankowich MD, Polsky M, Klein M, Rounds S. Heterogeneity in combined pulmonary fibrosis and emphysema. Respiration
|9.| Global Initiative for Chronic Obstructive Lung Disease (GOLD): Global Strategy for the Diagnosis, Management, and Prevention of COPD
. 2017 Global Initiative for Chronic Obstructive Lung Disease, Inc.; GOLD Website, www.goldcopd.org
Raghu G, Collard HR, Egan JJ, Martinez FJ, Behr J, Brown KK et al.
ATS/ERS/JRS/ALAT committee on idiopathic pulmonary fibrosis. An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med
Bestall JC, Paul EA, Garrod R, Garnham R, Jones PW, Wedzicha JA. Usefulness of the Medical Research Council (MRC) dyspnoea scale as a measure of disability in patients with chronic obstructive pulmonary disease. Thorax
Weiner P, Novitzky T, Weiner D, Beckerman M. Chronic obstructive pulmonary disorder (COPD) patients with the syndrome of combined pulmonary fibrosis and emphysema, compared to patients with emphysema alone. Harefuah
:294–298 307, 308
Akagi T, Matsumoto T, Harada T, Tanaka M, Kuraki T, Fujita M et al.
Coexistent emphysema delays the decrease of vital capacity in idiopathic pulmonary fibrosis. Respir Med
Sugino K, Ishida F, Kikuchi N, Hirota N, Sano G, Sato K et al.
Comparison of clinical characteristics and prognostic factors of combined pulmonary fibrosis and emphysema versus idiopathic pulmonary fibrosis alone. Respirology
Raghu G, Weycker D, Edelsberg J, Bradford WZ, Oster G. Incidence and prevalence of idiopathic pulmonary fibrosis. Am J RespirCrit Care Med
Tomioka H, Mamesaya N, Yamashita S, Kida Y, Kaneko M, Sakai H. Combined pulmonary fibrosis and emphysema: effect of pulmonary rehabilitation in comparison with chronic obstructive pulmonary disease. BMJ Open Respir Res
Jankowich MD, Rounds S. Combined pulmonary fibrosisand emphysema alters physiology but has similar mortality topulmonary fibrosis without emphysema. Lung
Kitaguchi Y, Fujimoto K, Hanaoka M, Kawakami S, Honda T, Kubo K. Clinical characteristics of combined pulmonary fibrosis and emphysema. Respirology
Mejia M, Carrillo G, Rojas-Serrano J, Estrada A, Suarez T, Alonso D et al.
Idiopathic pulmonary fibrosis and emphysema: decreased survival associatedwith severe pulmonary arterial hypertension. Chest
Caminati A, Cassandro R, Harari S. Pulmonaryhypertension in chronic interstitial lung diseases. Eur Respir Rev
Cottin V, Le Pavec J, Prévot G, Mal H, Humbert M, Simonneau G et al.
Pulmonary hypertension in patients with combined pulmonary fibrosisand emphysema syndrome. Eur Respir J
Washko GR, Hunninghake GM, Fernandez IE, Nishino M, Okajima Y, Yamashiro T et al.
Lung volumes and emphysema in smokers with interstitial lung abnormalities. N Engl J Med
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5]