Bacteriological Profile of Acute Exacerbation of Nonspecific Interstitial Pneumonia (NSIP)
Article Information
Sourabh Pandey1, Harshit Jain2, Gaurav Verma3, Dinesh Singh Mahor* 4
1Senior resident, Department of Respiratory medicine, Shyam Shah medical College Rewa 2Senior resident, Department of Respiratory medicine, NSCB Medical College Jabalpur 3Assistant Professor, Department of Microbiology, RD Gardi Medical College Ujjain
4Senior resident, Department of Medicine, GRMC Gwalior
*Corresponding author: Dinesh Singh Mahor, Senior resident, Department of Medicine, GRMC Gwalior, India.
Received: January 29, 2025; Accepted: January 05, 2025; Published: February 18, 2025
Citation: Sourabh Pandey, Harshit Jain, Gaurav Verma, Dinesh Singh Mahor. Bacteriological Profile of Acute Exacerbation of Nonspecific Interstitial Pneumonia (NSIP). Fortune Journal of Health Sciences, 8 (2025): 107-110
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Introduction: Nonspecific interstitial pneumonia (NSIP) is a life-threatening disease of unknown etiology, characterized by distinct radiographic and pathological patterns. Patients with NSIP often experience a progressive decline in respiratory function, or a more acute deterioration referred to as acute exacerbation (AE-NSIP). Among infectious agents, bacterial involvement and its impact on alveolar healing remain underexplored. Recent studies suggest that impaired host defence mechanisms may predispose NSIP patients to infections, thereby influencing disease progression.
Aim: This study investigates bacterial isolates from sputum samples in patients with AE-NSIP and evaluates their clinical significance.
Materials and Methods: Sputum samples from 120 AE-NSIP patients admitted to a tertiary hospital between January 2021 and January 2022 were analysed. Patients unable to produce sputum or those pre-treated with antibiotics were excluded. Gram staining and culture tests were conducted on high-quality sputum samples. Chi-square tests were used to determine the statistical significance of bacterial isolates.
Results: Out of 120 patients, bacterial isolates were identified in 78.3% (n=94), while 21.7% (n=26) showed no isolates. Streptococcus pneumoniae (n=26) and Escherichia coli (n=24) were statistically significant (p<0.05). Other isolates such as Haemophilus influenzae (n=16), Klebsiella pneumoniae (n=8), Enterococcus (n=4), and Moraxella catarrhalis (n=6) were statistically insignificant.
Conclusion: Preservation of lung function in NSIP remains critical. The potential role of bacterial infections in worsening NSIP and the use of prophylactic antibiotics warrant larger, geographically diverse studies.
Keywords
NSIP, Lung function, Prophylactic antibiotics, Sputum, Tuberculosis, Bacterial infection
Article Details
Introduction
Nonspecific interstitial pneumonia (NSIP) is a severe disease with idiopathic origins, characterized by specific radiographic and pathological findings (1,2). Patients with NSIP may experience progressive respiratory decline or acute exacerbations (AE-NSIP) marked by rapid worsening of dyspnea, new radiographic opacities, and exclusion of alternative causes such as congestive heart failure or pulmonary embolism [2,3,4]. AE-NSIP carries a high mortality rate (>50%) (1,4).
Evidence suggests infections may play a role in AE-NSIP:
- Seasonal patterns with increased exacerbations during
- Similar mortality risks between respiratory infections and AE-NSIP.
- Diffuse alveolar damage observed in post-mortem examinations of infected patients.
- Immunosuppression-related vulnerability to exacerbations [5,9].
Bacterial involvement in NSIP remains under-investigated [6,7,8]. Kligerman et al. highlighted impaired host defences and susceptibility to infection as potential contributors to NSIP progression [1]. This study examines the bacterial profile in AE-NSIP patients to explore its clinical significance.
Material and Methods
This retrospective observational study analysed sputum samples from 120 AE-NSIP patients admitted to Gandhi Medical College, Bhopal, between January 2021 and January 2022.
Inclusion criteria: Clinico-radiologically diagnosed AE-NSIP.
Exclusion criteria: Inability to produce sputum. Prior antibiotic use for the current exacerbation.
Sample Analysis
Expectorated sputum samples were collected in sterile containers. Quality assessment was performed through macroscopic and microscopic examination. Samples underwent Gram staining, aerobic, and anaerobic cultures. Statistical analysis was conducted using Chi-square tests (p<0.05 considered significant).
Statistical Analysis
Chi-Square tests were used to find the significant association (p-value <0.05) between the bacterial isolates in the sputum samples.
Results
In the study 120 patients were analyzed. Among them there were isolates in 78.3% (n=94) and no isolates in 21.7% (n=26) of the subjects. Among the isolates Streptococcus pneumoniae was isolated in 24 patients and Escherichia coli (E. Coli) in 26 patients. Upon analysis using Chi-square to test the significance of these two isolates, the p value was found to be 0.042 (p<0.05) and 0.032 (p<0.05) for these two isolates respectively, revealing a statistically significant association [Table-1,2].
Table 1: Association of E. Coli between isolates and no isolates.
E. coli |
Group |
p-value |
||
No isolates (n=26) |
Isolates (n=94) |
Total |
||
Absent |
26 (100.0) |
68 (72.3) |
94 (78.3) |
0.032* |
Present |
0 (0.0) |
26 (27.7) |
26 (21.7) |
|
Total |
26 (100.0) |
94 (100.0) |
120 (100.0) |
Table- 2: Association of S. Pneumoniae between isolates and no isolates.
S. Pneumoniae |
Group |
p-value |
||
No isolates (n=26) |
Isolates (n=94) |
Total |
||
Absent |
26 (100.0) |
70 (74.5) |
96 (80.0) |
0.042* |
Present |
0 (0.0) |
24 (25.5) |
24 (20.0) |
|
Total |
26 (100.0) |
94 (100.0) |
120 (100.0) |
In contrast the other isolates were Haemophilus influenza in 18 patients (p value=0.087), klebsiella pneumonia in 16 patients (p value =0.110), Enterococcus in 4 patients (p value=0.449) and Moraxella catarrhalis in 6 patients (p value=0.350). all these were found to be statistically insignificant [Table- 3-6].
Table- 3: Association of Klebsiella between isolates and no isolates.
Klebsiella pneumonia |
Group |
p-value |
||
No isolates (n=26) |
Isolates (n=47) |
Total |
||
Absent |
26 (100.0) |
78 (82.9) |
104 (86.7) |
0.110 (N.S) |
Present |
0 (0.0) |
16 (17.1) |
16 (13.3) |
|
Total |
26 (100.0) |
94 (100.0) |
120 (100.0) |
Table- 4: Association of H. Influenza between isolates and no isolates. Chi-Square: 2.553; N.S: Not significant
H. Influenza |
Group |
p-value |
||
No isolates (n=26) |
Isolates (n=47) |
Total |
||
Absent |
26(100.0) |
78 (82.9) |
104 (86.7) |
0.110 (N.S) |
Present |
0 (0.0) |
16 (17.1) |
16 (13.3) |
|
Total |
26(100.0) |
94 (100.0) |
120 (100.0) |
Table- 5: Association of Enterococcus between isolates and no isolates. Chi-Square: 2.553; N.S: Not significant
Enterococcus |
Group |
p-value |
||
No isolates (n=26) |
Isolates (n=94) |
Total |
||
Absent |
26 (100.0) |
90 (95.7) |
116 (96.7) |
0.449 (N.S) |
Present |
0 (0.0) |
4 (4.3) |
4 (3.3) |
|
Total |
26 (100.0) |
94 (100.0) |
120 (100.0) |
Table- 6: Association of M. catarrhalis between isolates and no isolates.
M. catarrhalis |
Group |
p-value |
||
No isolates (n=26) |
Isolates (n=94) |
Total |
||
Absent |
26 (100.0) |
88 (93.6) |
114 (95.0) |
0.350 (N.S) |
Present |
0 (0.0) |
6 (6.4) |
6 (5.0) |
|
Total |
26 (100.0) |
94 (100.0) |
120 (100.0) |
Discussion
The study identified E. coli and S. pneumoniae as the most common and statistically significant bacterial isolates in AE-NSIP patients. These findings align with prior studies such as Seth J. Kligerman et al [1], which documented similar pathogens in NSIP patients using culture-independent methods. Other reports, like those by Hochhegger B et al [2], have also demonstrated positive cultures in NSIP patients, supporting the potential role of bacteria in disease progression. Unlike other pulmonary diseases where exacerbations are truly acute events, the onset of an acute exacerbation in NSIP is generally insidious [6]. Recently, molecular culture independent techniques have identified complex microbial species in the lower airways with distinct alterations in the microbiome occurring in many of respiratory diseases [7, 8]. In a Sambataro G et al [5], where they analyzed the microbial flora in the BAL of 20 patients with interstitial lung diseases including idiopathic pulmonary fibrosis, non-specific interstitial pneumonia and acute interstitial pneumonia using bacterial culture & gel electrophoresis. Both classic respiratory pathogens (e.g., Haemophilus influenza) and a variety of previously unrecognized or under-recognized organisms were identified.
Limitation
- Long-term follow-up was not conducted to evaluate recurrent isolates or colonization patterns.
- Viral and fungal co-infections were not
Conclusion
Infectious agents may contribute to NSIP progression, but their exact role remains unclear. Larger, multi-centre studies are needed to explore the impact of bacterial infections on disease outcomes and the potential benefits of prophylactic antibiotics in reducing mortality and morbidity in NSIP patients.
Transparency
Declaration of funding- The authors confirm that there are no funders to report. This study did not receive any third- party funding or sponsorship.
Declaration of financial other relationship- The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony,
grants or patents received or pending, or royalties. Peer reviewers on this manuscript have no relevant financial or other relationships to disclose.
Authors contributions- All authors participated in the conception and design of the work or the collection, interpretation or analysis of the study data, and in the drafting, critical revision, and approval of the final version of the manuscript.
Acknowledgements
We are thankful to all authors for their effort and thanks to department for helping.
References
- Seth Kligerman, Steve Groshong, Kevin K Brown, et al. Nonspecific Interstitial Pneumonia: Radiologic, Clinical, and Pathologic Considerations Radio Graphics 29 (2009): 73-87.
- Hochhegger B, Marchiori E, Zanon M, Rubin AS, Fragomeni R, Altmayer S, et al. Imaging in idiopathic pulmonary fibrosis: diagnosis and mimics. Clinics (Sao Paulo) 74 (2019): e225.
- Abdelghani R, Thakore S, Kaphle U, Lasky JA, Kheir F. Radial Endobronchial Ultrasound-guided Transbronchial Cryobiopsy. J Bronchology Interv Pulmonol (2019): 245-
- Wu EK, Ambrosini RD, Kottmann RM, Ritchlin CT, Schwarz EM, Rahimi H. Reinterpreting Evidence of Rheumatoid Arthritis-Associated Interstitial Lung Disease to Understand Etiology. Curr Rheumatol Rev 15 (2019): 277-289.
- Sambataro G, Sambataro D, Pignataro F, Torrisi SE, Vancheri A, et al. Interstitial Lung Disease in patients with Polymyalgia Rheumatica: A case Respir Med Case Rep 26 (2019): 126-130.
- Cottin V, Hirani NA, Hotchkin DL, Nambiar AM, Ogura T, et al. Presentation, diagnosis and clinical course of the spectrum of progressive-fibrosing interstitial lung diseases. Eur Respir Rev 27 (2018).
- Richeldi L, Varone F, Bergna M, de Andrade J, Falk J, Hallowell R, et al. Pharmacological management of progressive-fibrosing interstitial lung diseases: a review of the current evidence. Eur Respir Rev 27 (2018).
- Jain A, Shannon VR, Sheshadri A. Immune-Related Adverse Events: Pneumonitis. Adv Exp Med Biol 995 (2018): 131-149.
- Jakubczyc A, Neurohr C. [Diagnosis and Treatment of Interstitial Lung Diseases]. Dtsch Med Wochenschr 143 (2018): 1774-1777.
- Greenberger PA. Hypersensitivity pneumonitis: A fibrosing alveolitis produced by inhalation of diverse antigens. J Allergy Clin Immunol 143 (2019): 1295-1301.