STUDY OF BACTERIAL PATHOGENS AND THEIR ANTIBIOGRAM IN PULMONARY SAMPLES AT A RESPIRATORY CARE CENTRE IN HYDERABAD, INDIA
Ethel Vilangunuo Solo, P. Alekhya, P. Sunitha, V Sudha Rani- General Medicine
- Microbiology (medical)
- Immunology
- Immunology and Allergy
- General Agricultural and Biological Sciences
- General Earth and Planetary Sciences
- General Environmental Science
- Automotive Engineering
- Industrial and Manufacturing Engineering
- General Medicine
- General Medicine
- General Medicine
- General Medicine
Introduction: Lower respiratory tract infections are among the most common infectious diseases of humans worldwide and also a great challenge to the clinicians due to the increasing antimicrobial resistance. Aim: To identify the pathogens and their antibiotic sensitivity pattern from pulmonary samples of patients suspected to have LRTI. Materials And Methods: A retrospective study was conducted from August 2022 to January 2023 at a respiratory care centre. A total of 1977 samples were included. These samples were inoculated on Blood Agar and MacConkey agar. Identication of bacterial isolates was done by colony characteristics and biochemical tests. Antibiotic sensitivity was done by Kirby Bauer disc diffusion method on Mueller-Hinton agar using the appropriate antibiotic discs.Results: Out of 1977 samples, 68 were found to be culture positive out of which 48(70%) were from sputum sample, 8(11.7%) from bronchial wash, 11(16%) from pleural uid and 1 (1.4%) from ETT secretion. Male patients 51(75%) were more than female patients 17(25%). In-patients 66(97%) more than outpatients 2(2.9%). Out of 66 inpatients, 60 (88.2%) were ward patients and 8(11.7%) were ICU patients. Pseudomonas aeruginosa 32(47%) was the most common organism isolated followed by Klebsiella pneumoniae 23(33.8%), Acinetobacter 8(11.7%), and Staphylococcus aureus 5(7.3%). Out of the 5 Staphylococcus aureus, 1 was found to be Methicillin Resistant Staphylococcus aureus. 2 Conclusion: Bacterial isolates showed resistance to common antibiotics. Therefore, proper diagnosis and identication of the pathogenic microorganisms by culture and sensitivity test is vital for appropriate management of LRTIs.