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Archives of Respiratory Research

Insights from 100 Broncho-alveolar Lavages: Exploring Lower Respiratory Tract Infections

Introduction

Lower respiratory tract infections (LRTIs) are a group of infections that affect the lower respiratory tract, including the trachea, bronchi, and lungs. LRTIs are a common cause of death in both children and adults worldwide [1]. It has significant burden on healthcare resources. These infections can be caused by a variety of microorganisms, including bacteria, viruses, fungi and parasites. Common LRTIs include pneumonia, bronchitis, and tuberculosis, among others. The symptoms of LRTIs can range from mild to severe and can include cough, fever, shortness of breath, chest pain, and fatigue [2].
The diagnosis of LRTIs can be challenging, as the symptoms can be nonspecific and the underlying cause can be multifactorial. Therefore, various diagnostic tools and methods have been developed to aid in the diagnosis and treatment of LRTIs. And a prompt and accurate identification of the causative organism is essential for effective treatment [3,4].
Bronchoscopy is a diagnostic procedure that involves the insertion of a flexible or rigid tube through the mouth or nose and into the airways. The procedure allows the identification and management of LRTIs by allowing for the collection of lower respiratory tract specimens for microbiological evaluation. Bronchoscopy can provide valuable information about the diagnosis and management of LRTIs, as it can provide valuable information about the underlying pathology and the causative organism. Bronchoscopy can also aid in the identification of malignancies and other non-infectious causes of respiratory symptoms [2,4,5].
BAL fluid analysis is a common diagnostic tool used in bronchoscopy [6]. BAL involves the instillation and subsequent aspiration of sterile saline solution into the lower respiratory tract, with the goal of collecting fluid and cellular material from the airways. BAL fluid can be evaluated for the presence of microorganisms, inflammatory cells, and other markers of respiratory pathology. AFB smear and gram stain culture sensitivity are commonly used microbiological tests that can be performed on BAL fluid to aid in the identification of the causative organism in LRTIs [3,7].
The aim of this study is to investigate Broncho-alveolar lavages in LRTI patients, with a focus on Broncho-alveolar lavage Acid Fast Bacilli smear and gram stain culture sensitivity.

Methods

Methods: The study was conducted at a tertiary care hospital and included patients with suspected LRTIs who underwent bronchoscopy between January 2019 and December 2020. This study retrospectively analysed microbiological profile of 100 patients with suspected LRTIs, who do not show clinical improvement after one weeks of antibiotics according to regional/institutional guideline and who underwent bronchoscopy at our institution. Radiological evaluation was done and shows radiological abnormalities. The study population included both male and female patients of various ages. Bronchoscopy was performed using a flexible bronchoscope, depending on the clinical indication. The bronchoscopy findings, including the presence of tumours and foreign bodies were noted and excluded from study. BAL fluid was collected from each patient and evaluated for the presence of microorganisms using AFB smear and gram stain culture sensitivity. Biopsy specimens were also collected in some patients, and the histopathological findings were analysed.

Results: The results of this study showed that bronchoscopy was a valuable diagnostic tool for the evaluation of LRTIs. The male-female ratio of patients was 56:44 and the Average Age of patients was 45.38 years. Out of the 100 patients included in the study, 59 underwent AFB smear evaluation for mycobacterium tuberculosis. Out of 59 patients, 40 patients tested negative for tuberculosis, while 19 patients were positive. This is an important finding, as it suggests that tuberculosis may be a significant cause of pneumonia in this patient population. Additionally, the fact that some patients were only mildly positive (1+ or 2+) while others were strongly positive (3+ or 4+) suggests that there may be varying degrees of tuberculosis infection severity in this population [Table 1].

Table 1: BAL fluid for AFB Smear results.

BAL FLUID AFB (59) Count of BAL FLUID AFB
Negative 40
Positive (+) 11
Positive (++) 2
Positive (+++) 3
Positive (++++) 3
Grand total 59

59 patients were evaluated for mycobacterium tuberculosis, out of 59 patients 40 came negative for tuberculosis and 19 patients were mycobacterium tuberculosis positive.11 patients were 1+ positive, 2 patients were 2+ positive and 3-3 patient were 3+ and 4+ positive respectively.

Out of 100 patients, 39 had no organisms grow in their BAL fluid culture, indicating that their pneumonia may have been caused by non-infectious factors such as aspiration or other non-infectious causes. However, 43 patients had positive cultures, with Klebsiella and pseudomonas being the most common bacterial species identified [Table 2]. This suggests that these bacteria may be particularly virulent or common causes of pneumonia in this patient population. Fungal culture evaluation was performed in 17 patients, and only one patient was positive for aspergillus. Biopsy specimens were collected in 16 patients, with squamous cell carcinoma being the most common finding. This suggests that some cases of pneumonia may be caused by underlying malignancies, which may have been missed by other diagnostic methods [Table 3].

Table 2: BAL fluid assessment for bacterial culture.

 

BAL fluid bacterial Culture and sensitivity (81) Frequency of Organism grow
No bacteria 39
Klebsiella species 10
Pseudomonas aeruginosa 17
E.coli 4
Staphylococcus aureus (MSSA) 2
Staphylococcus aureus (MRSA) 2
Pseudomonas species, klebsiella species 1
Enterobacter species 1

 

Out of 100 patients, no organism grow in 39 patients and came positive in 43 patients, Klebsiella was found in 10 patients, pseudomonas was found in 18 patients, E.coli in 4 patients, S. Aureus(MSSA) in 2 patients and 2 patients has MRSA and 1 patient came positive for Enterobacter and 1 patient came positive for both Pseudomonas and Klebsiella.

 

Table 3: Biopsy assessment for histopathological examination.

BIOPSY (16) Frequency
Squamous cell 8
Adenocarcinoma 2
Round cell tumor 1
Non-small cell carcinoma 1
Granulomatous lesion- tubercular 3
Fungal infection 1

 

Biopsy was done in 16 patients, 8 patients have squamous cell carcinoma, 1 patient found round cell tumours, 3 patients found granulomatous lesions, 1 patient found non-cell carcinoma and 1 patient found positive for fungal infections.

Five patients with pneumonia also have pleural effusions. Two out of the five patients who underwent pleural fluid evaluation were found to have adenocarcinoma.

Discussion: The demographic characteristics of the patients were recorded, including age and gender. These findings suggest that patients who likely had severe or complicated pneumonia that required further investigation beyond typical diagnostic methods such as chest X-rays or blood tests.

The results of this study showed that the average age of the patients was 45.38 years. The male-female ratio of patients was 56:44, indicating that pneumonia does not appear to have a significant gender bias. However, this sample size is relatively small, and further studies would be required to draw more conclusive gender-related findings.

In this study Samples of BAL fluid were collected and analysed for AFB smear and bacterial culture sensitivity, as well as for fungal culture sensitivity in a subset of patients. Biopsies were also performed on some patients to obtain tissue samples for pathological analysis. In terms of microbiological analysis, 59 patients underwent a BAL AFB smear, with 19 patients testing positive for mycobacterium tuberculosis. Of these, 11 patients were only mildly positive (1+ or 2+), while 8 patients were strongly positive (3+ or 4+) [Table 1]. Bacterial culture sensitivity was performed on BAL fluid samples from 100 patients, with no organism growth in 39 patients and positive growth in 43 patients. The most common bacterial species identified were Klebsiella 23.3% and Pseudomonas 41.9% [Table 2]. Fungal culture sensitivity was performed on BAL fluid samples from 17 patients, with only one patient testing positive for Aspergillus.

Previous research has suggested that mycobacterium tuberculosis can be an important cause of pneumonia, particularly in areas with high rates of tuberculosis infection [8,9]. The importance of bronchoscopy in sputum smear-negative tuberculosis patients was evaluated by Kalawar et al. BAL samples were positive in 82.2% of sputum smear-negative samples. The culture positivity of BAL samples was 90.9% as compared to sputum culture positivity which was 26.4%. Overall diagnosis could be established in 86.6% of patients with the help of fibre optic bronchoscopy [10]. The finding that 19 out of 59 patients tested positive for mycobacterium tuberculosis in this study is consistent with this previous research. Similarly, previous research has identified Klebsiella and pseudomonas as common causes of pneumonia, particularly in patients with risk factors such as chronic obstructive pulmonary disease (COPD) and immunosuppression [11]. The finding that these bacterial species were the most commonly identified in the BAL fluid samples of this study’s patient population aligns with this previous research. Finally, previous research has also suggested that fungal infections are relatively uncommon in patients with pneumonia, particularly in those who are not immunocompromised. The finding that only one patient tested positive for Aspergillus in the fungal culture sensitivity analysis of this study is consistent with this previous research.

The findings of this study highlight the complexity and multifactorial nature of LRTIs. While endobronchial tumours were the most common finding on bronchoscopy, the majority of patients had normal bronchoscopy findings. Microbiological analysis showed that mycobacterium tuberculosis and bacterial infections, particularly Klebsiella and pseudomonas, were significant causes of LRTIs in this patient population. Fungal infections appeared to be fewer common causes of LRTIs.

Previous research has suggested that endobronchial tumours are a common finding in patients undergoing bronchoscopy. The finding that endobronchial tumours were the most common bronchoscopy finding in this study’s patient population aligns with this previous research [12].

The majority of patients in this study had normal bronchoscopy findings. This is not surprising, as bronchoscopy is typically only performed when other diagnostic methods have failed to provide a diagnosis or when there is a suspicion of a specific condition that can be visualized by bronchoscopy.

The finding that squamous cell carcinoma was the most common biopsy finding in this study is consistent with previous research suggesting that lung cancer, particularly squamous cell carcinoma, is a common cause of respiratory symptoms [Table 3].

The finding that only one patient tested positive for fungal infection in this study is consistent with previous research suggesting that fungal infections are relatively uncommon in patients undergoing bronchoscopy.

The most common bronchoscopy finding was inflamed mucosa, endobronchial tumour and endobronchial lesion [13]. The majority of patients had normal bronchoscopy findings. Biopsies were performed on 16 patients, with squamous cell carcinoma being the most common finding (50%). Other findings included granulomatous lesions (12.5%), chronic inflammatory lesions (6.25%), and non-cell carcinoma (6.25%). One patient tested positive for fungal infection (6.25%).

The results of this study highlight the importance of bronchoscopy in the diagnosis and management of LRTIs. The identification of mycobacterium tuberculosis in a significant proportion of patients underscores the importance of considering tuberculosis in the differential diagnosis of LRTIs. The high prevalence of gram-negative bacterial infections, particularly Klebsiella and pseudomonas, suggests that these organisms may be particularly virulent or common in this patient population However, it is important to note that this is only an average, and the age range of the patients could vary significantly.

There are several limitations to this study that should be considered. Firstly, the sample size is relatively small, with only 100 patients included in the study. This may limit the generalizability of the findings to larger populations. Secondly, the study only included patients who underwent bronchoscopy, which may have introduced selection bias. Patients who were too ill to undergo the procedure or who had contraindications may have been excluded, which could affect the representativeness of the sample. Thirdly, the study did not include a control group, which makes it difficult to compare the findings with a group of patients who did not undergo bronchoscopy. Fourthly, the study was conducted at a single centre, which may limit the generalizability of the findings to other settings. Lastly, the study did not explore the cost-effectiveness of bronchoscopy as a diagnostic tool compared to other available methods, which could be an important consideration for healthcare providers and policymakers.

Conclusion

In conclusion, the results of this study indicate that bronchoscopy is a valuable diagnostic tool for evaluating lower respiratory tract infections. The study also highlights the prevalence of tuberculosis and bacterial species such as Klebsiella and pseudomonas as potential causes of pneumonia in this patient population. Furthermore, the study suggests that some cases of pneumonia may be caused by non-infectious factors such as aspiration, as well as underlying malignancies such as squamous cell carcinoma and adenocarcinoma. These findings highlight the importance of a comprehensive diagnostic approach to identify the underlying cause of pneumonia and guide appropriate treatment. Further research may be needed to confirm these results and investigate the potential implications for clinical practice.

Conflict of interest

There is no conflict of interest.

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*Corresponding author: Ankit Kumar, Department of Respiratory Medicine, King George Medical University, Uttar Pradesh, India, Email: ankyar007@gmail.com

Citation: Ankit Kumar (2023) Insights from 100 Broncho-alveolar Lavages: Exploring Lower Respiratory Tract Infections.Arch Resp Res 2: 002

Received: July 27, 2023; Accepted: August 25, 2023; Published: August 30, 2023

Copyright: © 2023 Ankit Kumar. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits un-restricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Ankit Kumar 1*, Laxmi Devi2, Shubham Chandra2, Shivanki Agarwal 2, Parul Sharma2 and
Yogendra Narayan Verma3
1Department of Respiratory Medicine, King George Medical University, Uttar Pradesh, India
2Department of Respiratory Medicine, Ganesh Shankar Vidyarthi Memorial Medical College, Uttar Pradesh, India
3Department of Pathology, Ganesh Shankar Vidyarthi Memorial Medical College, Uttar Pradesh, India