Background: Pleural effusion is an excess fluid that accumulates between two pleural layers.There are two types of effusions including Transudative and Exudative effusion.Common causes of exudative effusion include tuberculosis, parapneumonic effusion, viral infections, and malignancy. Pleural fluid analysis and cytology are the mainstays for diagnosing various pulmonary diseases. Aim of the study: A clinicopathological study of pleural effusion in a tertiary care hospital. Material and Methods: Prospective study was conducted in the department of General medicine at TRR medical college for duration of 1 year i.e. from March 2021 to Feb 2022. Results: In the present study Tuberculosis was commonly reported accounting 38.4%(25/65) , Pneumonia 30.7% (20/65), Empyema, Pancreatitis, Liver cirrhosis and Malignancy 7.6%(5/65). Purulent 76.8%(50/65), Hemorrhagic 15.3%(10/65) and Straw colored 7.6% (5/65) . Conclusion: Aetiological evaluation of pleural effusion is very important for management of the disease. This is important because management is different for different cases. Pleural fluid analysis can be considered as gold standard in evaluation of pleural effusion
Pleural effusion (PE) is an abnormal collection of fluid in the pleural space. The etiological spectrum of pleural effusion depends on the geographical region and the local incidence of different diseases that cause pleural effusions. In the developed countries, the common causes of pleural effusion in adult are cardiac failure, malignancy and pneumonia .1 Whereas, in developing countries tuberculosis and par pneumonic effusions are more. 2,3
Pleural effusion is a common finding among patients presenting with cardiopulmonary symptoms. A systemic approach to the investigations is needed due to the extensive differential diagnosis. Pleural effusions can be transudative or exudative.4 In cases with transudative pleural effusion, the diagnosis is usually made without much difficulties, but exudative pleural effusion requires careful differential diagnosis that includes parapneumonic effusion, tuberculosis (TB), and
metastatic cancers which are found to be the cases in large number of patients.
If metastatic cancer leads to hypoalbuminemia (e.g., due to liver metastasis causing liver failure or nephrotic syndrome), it may cause transudative effusion due to decreased oncotic pressure.
Light's criteria are frequently used to distinguish between exudative effusion and transudative effusion, the two types of pleural effusions.1 If any one of the following conditions is met, the pleural fluid is exudative: pleural fluid protein/serum protein ratio >0.5; pleural fluid lactate dehydrogenase/serum LDH ratio >0.6; or pleural fluid LDH level >2/3 the upper limit.
Prospective study was conducted in the department of General medicine at TRR medical college for duration of 1 year i.e. from March 2021 to Feb 2022. Ethical permission was taken from Institutional ethical committee. Written consent was obtained from all the study participants
Sample size: 65
Inclusion criteria
Exclusion criteria
Methodology
The demographic data collected included age, sex, and address. A detailed history was obtained inlcuding chief complaints, history of presenting illness, and significant history including the drug history. A through physical examination was done. Investigations such as complete hemogram, random blood sugar, renal function tests, serum albumin, chest-X-ray, and pleural fluid analysis and cytology were carried out in all the cases.
Pleural fluid analysis on neubar chamber: Total Leucocyte Count
LIGHT et al.’s criteria were used to distinguish exudative from transudative effusions. Predominant pleural fluid cell types were defined based on British Thoracic Society guidelines.
Pleural fluid cytology
The International System (TIS) for reporting serous fluid cytopathology was proposed by the International Academy of Cytology and the American Society of Cytopathology.6,
Table 1:Diagnostic categories of TIS for reporting serous effusion cytopathology8
Diagnostic categories and definitions |
I. Nondiagnostic (ND) |
Specimens with insufficient cellular elements for a cytologic interpretation |
II. Negative for malignancy (NFM) |
Specimens with cellular changes completely lacking evidence of mesothelial or nonmesothelial malignancy |
III. Atypia of undetermined significance (AUS) |
Specimens showing limited cellular (nuclear) and/or architectural atypia (e.g., papillary clusters or pseudoglandular formations) |
IV. Suspicious for malignancy (SFM) |
Specimens showing features suspicious but not definitively diagnostic for malignancy |
V. Malignant (MAL) |
Specimens include those with definitive findings and/or supportive studies indicating mesothelial or nonmesothelial malignancies |
Table 1: Age distribution
Age distribution |
No. of cases |
Percentage |
10-20 |
02 |
3.07 |
21-30 |
10 |
15.3 |
31-40 |
15 |
23.0 |
41-50 |
28 |
43.0 |
51-60 |
10 |
15.3 |
Total |
65 |
99.9% |
Gender distribution |
|
|
Females |
45 |
69.2% |
males |
20 |
30.7% |
Symptom |
|
|
Fever |
60 |
92.3% |
cough |
50 |
76.9% |
Breathlessness |
45 |
69.2% |
chest pain |
40 |
61.5% |
Side of distribution |
|
|
Right side |
50 |
76.9% |
left side |
15 |
23% |
Comorbidities |
|
|
Hypertension |
22 |
33.8% |
Coronary artery disease |
21 |
32.3% |
Diabetes mellitus |
11 |
16.9% |
Rheumatoid arthritis |
6 |
9.2% |
Pancreatitis |
6 |
9.2% |
In the present study age distribution varied from 10 - 60 years . Majority noted among 41-50 years constituting 43% (28/65) and 23% (15/65) among 31-40 years , 15.3%(10/65) among 21-30 years and 51-60 years .3.0% (2/65).
Females were predominant constituting 69.2% (45/65) and Males accounting 30.7%(20/65).
Fever was predominant symptom constituting 92.3% (60/65) ,followed by cough 76.9% (50/65), Breathlessness 69.2% (45/65), and chest pain 61.5%(40/65).
Right side 76.9%(50/65) was more common compared to Left side 23.0%(15/65)
Hypertension and Coronary artery disease constituting 33.8%(22/65) and 32.3%(21/65). Diabetes mellitus 16.9%(11/65),Rheumatoid arthritis 9.2% (6/65) and Pancreatitis 9.2% (6/65).
Table-2: Distribution of Nature of effusion
Nature of effusion
|
No. of cases |
Percentage |
Exudative |
40 |
61.5 |
Transudative |
25 |
38.4 |
Total |
65 |
99.9% |
Type Plueral fluid |
|
|
Purulent |
50 |
76.8% |
Hemorrhagic |
10 |
15.3% |
Straw colored |
5 |
7.6% |
In the present study Exudative 61.5%(40/65) and Transudative 38.4%(25/65). Purulent 76.8%( 50/65) , Hemorrhagic 15.3%(10/65) and Straw colored 7.6%(5/65) .
Table-3: Distribution of Clinical diagnosis
Clinical diagnosis
|
No. of cases |
Percentage |
Tuberculosis |
25 |
38.4 |
Empyema |
05 |
7.6 |
Malignancy |
05 |
7.6 |
Acute Pancreatitis |
05 |
7.6 |
Pneumonia |
20 |
30.7 |
Liver cirrhosis |
05 |
7.6 |
Total |
65 |
99.9% |
In the present study Tb was commonly reported accounting 38.4%(25/65) , Pneumonia 30.7% ( 20/65), Empyema , Pancreatitis ,Liver cirrhosis and Malignancy 7.6%(5/65)
Figure-1: Bar diagram showing Distribution of Clinical diagnosis
Table-4: DLC on Nuebar chamber
DLC |
Mean +SD |
Lymphocytes |
42.9+10.3 |
Nuetrophils |
58.3+20.9 |
In our study lymphocytes mean was 42.9+10.3 and Nuetrophils58.3+20.9
Table-5: Distribution of Cytological diagnosis
Cytological diagnosis |
No. of cases |
Percentage |
I.Nondiagnostic (ND) |
- |
- |
II.Negative for malignancy (NFM) |
60 |
92.4 |
III. Atypia of undetermined significance (AUS) |
- |
- |
IV. Suspicious for malignancy (SFM) |
05 |
7.6 |
V. Malignant (MAL) |
|
|
Total |
65 |
99.9% |
In our study No malignant cells noted in 92.4% cases and Malignant cells seen. In 7.6% cases.
In the present study age distribution varied from 10 - 60 years . Majority noted among 41-50 years constituting 43% (28/65) and 23% (15/65) among 31-40 years , 15.3%(10/65) among 21-30 years and 51-60 years .3.0% (2/65).In Shashikanth et al9 study mean age was 38.10 years. In Saurabh et al10 study mean age was 53.32 ± 9.15 years.
In the present study Females were predominant constituting 69.2% (45/65) and Males accounting 30.7%(20/65).Where as in Saurabh et al 10, Arif et al11 and Shashikanth et al study9 with Male gender were more common with (67.86%) , (66.9%) and 70 (70%).
In the present study Right side 76.9%(50/65) was more common compared to Left side 23.0%(15/65)/.Similar findings were noted with Arif et al 11.Saurabh al10 and Shashikanth et al9 study 46.9% ,58.93% and 41.07%.
In the present study Chest pain was predominant symptom Fever constituting 92.3% (60/65) ,followed by cough 76.9% (50/65), Breathlessness 69.2% (45/65), Fever 61.5%(40/65). In Arif et al11 study majority of pleural patients presented with chest pain (78.5%) followed by cough (50.7%), fever (46.1%) and breathlessness (32.2%).In Shashikanth et al9 study fever (53%) and breathlessness (45%) were most common symptoms, followed by, cough, chest pain, and abdominal pain .In Ranganathan et al12 study fever and cough are the most common seen 64 and 76 percentage respectively, followed by chest pain (44) and breathlessness (42%).In Saurabh et al 11 study cough (78.57%), chest pain (67.86%), decreased appetite (64.29%), fever (62.50%), breathlessness (58.93%), weight loss (21.43%) and joint pain (16.07%).
In the present study Tb was commonly reported accounting 38.4%(25/65) , Pneumonia 30.7% ( 20/65), Empyema , Pancreatitis ,Liver cirrhosis and Malignancy 7.6%(5/65). In Souruabh et al10 study Tuberculosis (58.93%) was most common cause of exudative pleural effusion followed by empyema (8.93%), malignant (5.36%), pancreatitis (5.36%), rheumatic arthritis (3.57%) and para pneumonic (1.79%). Undiagnosed cases were 16.07%.In Arif et al11 study tuberculosis (64.6%) was the most common followed by Para pneumonic (14.6% and malignancy (11.5%)
In the present study Exudative 61.5%(40/65) and Transudative 38.4%(25/65). .Similar findings were noted with Arif et al 11 and Shashikanth et al 9 study with 90.8% and 66% .
In the present study Purulent 76.8%( 50/65) , Hemorrhagic 15.3%(10/65) and Straw colored 7.6%(5/65). In Souraubh et al10 study pleural fluid Appearance was Straw colored (55.36 %) in majority cases and purulent in 5 cases .only (8.93 %). In Ranganathan et al12 study majority of the patients with tuberculous pleural had yellowish and turbid fluid, while malignant pleural effusion had hemorrhagic fluid.
In our study Predominant Neutrophilia seen in 46.1% cases where as in Ranganathan et al12, Souraubh et al10 study and Kaushal et al study113 shows predominant lymphocytosis .
Etiological evaluation of pleural effusion is very important for management of the disease. Among patients of exudative pleural effusion male gender, right sided effusion, tuberculosis, straw coloured pleural fluid, raised TLC were common findings. Knowledge of the etiological pattern of exudative pleural effusion helps
physicians to plan diagnostic tests, and to provide appropriate treatment to reduce mortality and morbidity rates resulting from Plueral effusion complication .