Drug Resistance Patterns of Bacterial Pathogens in Adult Pneumonia Patients in a Tertiary Care Hospital
Keywords:
Antimicrobial Resistance, Multidrug-resistant Bacteria, Extensively Drug-resistant Bacteria, PneumoniaAbstract
BackgroundPneumonia remains one of the leading causes of morbidity and mortality around the world, with a disproportionate burden in low- and middle-income countries such as Pakistan. Antimicrobial resistance (AMR), especially multidrug-resistant (MDR) and extensively drug-resistant (XDR) bacteria, is becoming more common. This presents a serious obstacle to efficient therapeutic therapy and worsens patient consequences. ObjectiveTo determine the bacteriological profile, antimicrobial resistance patterns, and distribution of MDR and XDR pathogens among adult pneumonia patients, as well as to evaluate their clinical characteristics. MethodologyIn the present cross-sectional study, 385 respiratory specimens were collected from adult patients with pneumonia. Pathogens were isolated and identified using gram staining and culture by using different media such as MacConkey, blood agar, and chocolate agar. Biochemical tests were performed such catalase and coagulase for Staphylococcus spp, Oxidase test for P. aeruginosa and Indole, citrate Urease and TSI. ResultsIn the present study, 146 (37.9%) pneumonia patients needed intensive care management. The most affected age group was old age people (> 60) accounted for 169 (43.9%). Klebsiella pneumoniae 126 (32.7%) being the most commonly isolated pathogen, followed by Pseudomonas aeruginosa 104 (27%) and Acinetobacter baumannii 61 (15%). Biofilm formation was observed in 182 (47.3%) of the 385 bacterial isolates that were isolated from pneumonia patients. Conclusion Present study show that the most common etiological agents were Gram-negative organisms, specifically Klebsiella pneumoniae, Pseudomonas aeruginosa, and Acinetobacter baumannii. These organisms also showed alarmingly high resistance rates to commonly prescribed antibiotics, such as ?-lactams, tetracyclines, fluoroquinolones, and third-generation cephalosporins.References
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