{"id":120594,"date":"2025-11-07T13:59:07","date_gmt":"2025-11-07T13:59:07","guid":{"rendered":"https:\/\/www.newsbeep.com\/il\/120594\/"},"modified":"2025-11-07T13:59:07","modified_gmt":"2025-11-07T13:59:07","slug":"antimicrobial-resistance-in-bacterial-pathogens-from-postoperative-surgical-site-infections-in-a-tertiary-care-centre-in-india-bmc-microbiology","status":"publish","type":"post","link":"https:\/\/www.newsbeep.com\/il\/120594\/","title":{"rendered":"Antimicrobial resistance in bacterial pathogens from postoperative surgical site infections in a tertiary care centre in India | BMC Microbiology"},"content":{"rendered":"<p>Despite advancements in preventive measures, (SSIs) remain a significant healthcare challenge due to their high rates of morbidity and mortality. In this study, 104 samples were collected, of which 92.31% showed significant bacterial growth while 7.69% showed no growth, indicating a high incidence of SSIs. This reflects a considerable bacterial load in surgical wounds and highlights a serious concern for postoperative care. Similar finding was reported [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 27\" title=\"Chaudhary R, Thapa SK, Rana JC, Shah PK. Surgical site infection and antimicrobial resistance pattern. J Nepal Health Res Counc. 2017;15(36):120\u20133.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR27\" id=\"ref-link-section-d168785508e2568\" rel=\"nofollow noopener\" target=\"_blank\">27<\/a>], in Kathmandu, Nepal, although the bacterial growth rate observed here was higher than those reported [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 28\" title=\"Acharya J, Mishra SK, Katel HP, Rijal P, Pokherel BM. Bacteriology of wound infection among patients attending Tribhuvan University, teaching hospital, Kathmandu Nepal. J Nepal Assoc Med Lab Sci. 2008;9(1):76\u201380.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR28\" id=\"ref-link-section-d168785508e2571\" rel=\"nofollow noopener\" target=\"_blank\">28<\/a>, <a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 29\" title=\"Amatya J, Rijal M, Baidya R. Bacteriological study of the post operative wound sample and antibiotic susceptibility pattern of isolates in B &amp; B hospital. JSM Microbiol. 2015;3(1):10\u20139.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR29\" id=\"ref-link-section-d168785508e2574\" rel=\"nofollow noopener\" target=\"_blank\">29<\/a>]. These differences may be attributed to variations in hospital hygiene, environmental conditions, and infection control practices. According to [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 30\" title=\"Chipaga D, Majigo M, Malima B, Joachim A. Prevalence of multi-drug resistant bacteria causing surgical site infection at tertiary hospitals in Dar Es Salaam, Tanzania: a call for strengthening infection prevention and preoperative prophylaxis. Alexandria J Med. 2025;61(1):1\u20137.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR30\" id=\"ref-link-section-d168785508e2577\" rel=\"nofollow noopener\" target=\"_blank\">30<\/a>] reported 77.4% of isolates as MDR, while in our investigation, the proportion was comparable, reflecting the ongoing challenge of antimicrobial resistance in tertiary care settings.<\/p>\n<p>S. aureus was most frequently isolated from patients aged 31\u201350 years, while P. aeruginosa appeared more often in those aged 10\u201350 years. Overall, male patients showed higher infection rates than females, a trend also noted [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 31\" title=\"Kumara S, Ajai Veer SN, Sandeep KA. To evaluate the prevalence of P. aeruginosa and its antimicrobial sensitivity profile among postoperative wound infections. Int J Acad Med Pharm. 2020;2(3):334\u20138. &#010;                  https:\/\/doi.org\/10.29228\/Jamp.44922&#010;                  &#010;                .\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR31\" id=\"ref-link-section-d168785508e2594\" rel=\"nofollow noopener\" target=\"_blank\">31<\/a>], who suggested that occupational exposure and lifestyle differences may contribute to this gender disparity.<\/p>\n<p>S. aureus and P. aeruginosa were identified as the two predominant pathogens in surgical site at wound infections. The emergence of antibiotic-resistant strains has made the treatment of these infections increasingly difficult in both hospital and community settings [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 32\" title=\"Bertrand XM, Thouverez C, Patry P, Balvay TD. Pseudomonas aeruginosa: antibiotic susceptibility and genotypic characterization of strains isolated in the intensive care unit. Clin Microbiol Infect. 2002;7:706\u20138.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR32\" id=\"ref-link-section-d168785508e2611\" rel=\"nofollow noopener\" target=\"_blank\">32<\/a>]. SSIs are among the most common healthcare-associated infection, with reported prevalence rates ranging from 2.5 to 41.9% depending on the hospital and healthcare systems [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 33\" title=\"Jatoliya H, Pipal RK, Pipal DK, Biswas P, Pipal VR, Yadav S, Verma B, Vardhan V. Surgical site infections in elective and emergency abdominal surgeries: A prospective observational study about Incidence, risk Factors, Pathogens, and antibiotic sensitivity at a government tertiary care teaching hospital in India. Cureus. 2023;15(10). &#010;                  https:\/\/doi.org\/10.7759\/cureus.48071&#010;                  &#010;                .\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR33\" id=\"ref-link-section-d168785508e2614\" rel=\"nofollow noopener\" target=\"_blank\">33<\/a>].<\/p>\n<p>Gram-staining in this study revealed 28.98% Gram-positive and 71.02% were Gram-negative bacteria, which is consistent with findings [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 34\" title=\"Khatiwada S. Antibiotics sensitivity pattern of Post-Operative wound infections in a tertiary care hospital. Western Nepal, 2020; 1\u201316.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR34\" id=\"ref-link-section-d168785508e2620\" rel=\"nofollow noopener\" target=\"_blank\">34<\/a>], who reported higher prevalence of Gram-negative bacteria (65.7%) compared to Gram-positive bacteria (34.3%). The rate of infection varies from different country, healthcare settings and even different areas. In our study, S. aureus was 13.10% and P. aeruginosa accounted for 17.40% of infections, findings that were comparable to those reported [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 35\" title=\"Pateriya A, Agrawal M, Sharma R. Microbiological profile in post surgical wound infections and pattern of antimicrobial susceptibility at a tertiary care teaching hospital. Int J Pharm Clin Res. 2024;16(3):701\u20137. e-ISSN: 0975\u20131556, p-ISSN:2820\u2009\u2013\u20092643.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR35\" id=\"ref-link-section-d168785508e2632\" rel=\"nofollow noopener\" target=\"_blank\">35<\/a>]. Multiple bacterial isolates were observed in 48.08% of the samples, while 44.23% showed single isolates, and 7.69% showed no growth. In contrast [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 36\" title=\"Pradeep MSS, Vishnu Vardhana Rao K. A study on surgical site infections, their bacteriological profile and antimicrobial susceptibility pattern. IP International Journal of Medical Microbiology and Tropical Diseases. 2019;5(1):9\u201313.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR36\" id=\"ref-link-section-d168785508e2636\" rel=\"nofollow noopener\" target=\"_blank\">36<\/a>], reported multiple isolates in only 12.14% of cases. These variations may reflect differences in patient populations, sample sources, and infection control standards. Comparable prevalence of P. aeruginosa (13%) was reported in human pus samples in Egypt, highlighting the consistent global relevance of this opportunistic pathogen in postoperative infections. Variations in prevalence across studies may reflect differences in hospital hygiene, environmental conditions, patient populations, and infection control practices [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 37\" title=\"Hana MM, Abdeen EE. Phenotypic and molecular characterization of Pseudomonas aeruginosa isolated from human specimens. Alexandria J Vet Sci. 2024;81:19\u201326. &#010;                  https:\/\/doi.org\/10.5455\/ajvs.193630&#010;                  &#010;                .\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR37\" id=\"ref-link-section-d168785508e2645\" rel=\"nofollow noopener\" target=\"_blank\">37<\/a>].<\/p>\n<p>Biochemical characterization confirmed that all isolates of S. aureus and P. aeruginosa were catalase-positive, citrate-positive, and indole-negative. The catalase positive reaction observed in both organisms aligns with their well-known capacity to produce the catalase enzyme, which essential for protecting against oxidative stress by converting hydrogen peroxide into oxygen and water [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 18\" title=\"Cheesbrough M. District laboratory practice in tropical countries. 3rd ed. Cambridge University Press; 2022.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR18\" id=\"ref-link-section-d168785508e2661\" rel=\"nofollow noopener\" target=\"_blank\">18<\/a>]. Their capacity to use citrate as their only carbon source, further highlights their metabolic flexibility, particularly under nutrient limited conditions, a feature that is especially notable in opportunistic pathogens like P. aeruginosa [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 21\" title=\"Forbes BA, Sahm DF, Weissfeld AS. Bailey &amp; scott\u2019s diagnostic microbiology. 15th ed. Elsevier; 2023.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR21\" id=\"ref-link-section-d168785508e2668\" rel=\"nofollow noopener\" target=\"_blank\">21<\/a>]. Mannitol fermentation, a classical trait of S. aureus. The negative results for the indole test across all isolates reaffirm the established biochemical profiles of these organisms, as neither S. aureus nor P. aeruginosa generally possess the enzyme tryptophanase required for indole production [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 38\" title=\"MacFaddin JF. Biochemical Tests for Identification of Medical Bacteria, 2000; 3rd Edition, Lippincott Williams &amp; Wilkins, Philadelphia.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR38\" id=\"ref-link-section-d168785508e2687\" rel=\"nofollow noopener\" target=\"_blank\">38<\/a>].<\/p>\n<p>The antibiotic sensitivity profile of S. aureus isolates revealed complete susceptibility to Linezolid (100%), establishing it as the most effective antibiotic. Moderate susceptibility was observed with Tetracycline, Levofloxacin, Ampicillin\/Sulbactam, and Gentamicin, while Ciprofloxacin showed markedly poor activity (11.11%). Among the strains, IIMT-SA17 exhibited the highest sensitivity, as reflected by a large zone of inhibition on the antibiogram. The consistent sensitivity to Linezolid is encouraging and aligns with previous findings [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 39\" title=\"Parate A. Bacterial characteristics and antibiotic susceptibility pattern of surgical site infection. J Cardiovasc Disease Res. 2022;13(3):0975\u20133583.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR39\" id=\"ref-link-section-d168785508e2699\" rel=\"nofollow noopener\" target=\"_blank\">39<\/a>, <a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 40\" title=\"Hashemian SM, Farhadi T, Ganjparvar M, Linezolid. A review of its properties and use in critical care. Drug Des Devel Ther. 2018;12:1759\u201367.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR40\" id=\"ref-link-section-d168785508e2702\" rel=\"nofollow noopener\" target=\"_blank\">40<\/a>]. Tetracycline also showed promising activity against the isolates, suggesting that tetracycline resistance genes like tetK and tetM may not be widely prevalent in this region. This is consistent with reports indicating that tetracycline resistance varies significantly depending on local antibiotic usage patterns [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 41\" title=\"Chopra I, Roberts M. Tetracycline antibiotics: mode of action and resistance. Microbiol Mol Biol Rev. 2001;65(2):232\u201360.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR41\" id=\"ref-link-section-d168785508e2712\" rel=\"nofollow noopener\" target=\"_blank\">41<\/a>]. Fluoroquinolones such as Levofloxacin showed intermediate sensitivity, while Ciprofloxacin showed the highest resistance rate among all tested antibiotics. This high degree of resistance to Ciprofloxacin most likely reflects mutations in DNA gyrase and topoisomerase IV genes (gyrA, parC), or the operation of efflux pumps, which actively remove the antibiotic from bacterial cells [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 42\" title=\"Hooper DC. Fluoroquinolone resistance among Gram-positive cocci. Lancet Infect Dis. 2002;2(9):530\u20138.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR42\" id=\"ref-link-section-d168785508e2721\" rel=\"nofollow noopener\" target=\"_blank\">42<\/a>]. Ampicillin\/Sulbactam showed 50% effectiveness, possibly due to beta-lactamase inhibition by Sulbactam, although resistance suggests the presence of alternative mechanisms such as modified penicillin-binding proteins [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 43\" title=\"Boru K, Aliyo A, Daka D, Gamachu T, Husen O, Solomon Z. Bacterial surgical site infections: prevalence, antimicrobial susceptibility patterns, and associated risk factors among patients at Bule Hora University Teaching Hospital, Southern Ethiopia, IJID Regions, 2025; 14, 100565. &#010;                  https:\/\/doi.org\/10.1016\/j.ijregi.2024.100565&#010;                  &#010;                \" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR43\" id=\"ref-link-section-d168785508e2724\" rel=\"nofollow noopener\" target=\"_blank\">43<\/a>]. Gentamicin was likely due to aminoglycoside-modifying enzymes, commonly reported in nosocomial strains [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 44\" title=\"Vakulenko SB, Mobashery S. Versatility of aminoglycosides and prospects for their future. Clin Microbiol Rev. 2003;16(3):430\u201350.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR44\" id=\"ref-link-section-d168785508e2728\" rel=\"nofollow noopener\" target=\"_blank\">44<\/a>]. Multidrug resistance was particularly notable in isolates such as IIMT-SA11, SA06, SA07, and SA04, corroborating earlier reports of S. aureus as a major MDR pathogen in SSIs [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 45\" title=\"Munawar S, Sami A, Rafiq K, Ahmed Z, Shafique A, Ali H, Ahsan S. Analyzing the prevalence and patterns of Antibiotic-Resistant pathogens causing surgical site infections. Pakistan J Health Sci. 2024;268\u201376. &#010;                  https:\/\/doi.org\/10.54393\/pjhs.v5i08.1758&#010;                  &#010;                .\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR45\" id=\"ref-link-section-d168785508e2737\" rel=\"nofollow noopener\" target=\"_blank\">45<\/a>].<\/p>\n<p>Among P. aeruginosa isolates, the highest susceptibility was to Ofloxacin (75%), followed by Piperacillin, Amikacin, Gentamicin, Ampicillin\/Sulbactam, and Ciprofloxacin, respectively. Ofloxacin, a fluoroquinolone, appeared to be the most effective, likely due to fewer resistance-conferring mutations in the local population [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 42\" title=\"Hooper DC. Fluoroquinolone resistance among Gram-positive cocci. Lancet Infect Dis. 2002;2(9):530\u20138.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR42\" id=\"ref-link-section-d168785508e2749\" rel=\"nofollow noopener\" target=\"_blank\">42<\/a>, <a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 43\" title=\"Boru K, Aliyo A, Daka D, Gamachu T, Husen O, Solomon Z. Bacterial surgical site infections: prevalence, antimicrobial susceptibility patterns, and associated risk factors among patients at Bule Hora University Teaching Hospital, Southern Ethiopia, IJID Regions, 2025; 14, 100565. &#010;                  https:\/\/doi.org\/10.1016\/j.ijregi.2024.100565&#010;                  &#010;                \" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR43\" id=\"ref-link-section-d168785508e2752\" rel=\"nofollow noopener\" target=\"_blank\">43<\/a>]. Piperacillin and Amikacin also showed good activity, consistent with previous reports indicating that \u03b2-lactam antibiotics and aminoglycosides remain partially effective against Gram-negative isolates in this region [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 35\" title=\"Pateriya A, Agrawal M, Sharma R. Microbiological profile in post surgical wound infections and pattern of antimicrobial susceptibility at a tertiary care teaching hospital. Int J Pharm Clin Res. 2024;16(3):701\u20137. e-ISSN: 0975\u20131556, p-ISSN:2820\u2009\u2013\u20092643.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR35\" id=\"ref-link-section-d168785508e2755\" rel=\"nofollow noopener\" target=\"_blank\">35<\/a>].<\/p>\n<p>However, a high level of Ciprofloxacin resistance (87.50%) was observed, which aligns with global reports of P. aeruginosa resistance mediated by gyrA\/parC mutations, efflux pump overexpression (e.g., MexAB-OprM), and reduced outer membrane permeability [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 46\" title=\"Poole K. Multidrug efflux pumps and antimicrobial resistance in Pseudomonas aeruginosa. Antimicrob Agents Chemother. 2001;45(3):529\u201335.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR46\" id=\"ref-link-section-d168785508e2767\" rel=\"nofollow noopener\" target=\"_blank\">46<\/a>, <a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 47\" title=\"Breidenstein EBM, de la Fuente-N\u00fa\u00f1ez C, Hancock REW. Pseudomonas aeruginosa: all roads lead to resistance. Trends Microbiol. 2011;19(8):419\u201326.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR47\" id=\"ref-link-section-d168785508e2770\" rel=\"nofollow noopener\" target=\"_blank\">47<\/a>]. The most resistant strains (IIMT-PA12, PA13, PA11, and PA07) exhibited resistance to more than three antibiotics, reflecting extensive MDR likely associated with prolonged empirical therapy in clinical settings. These findings are consistent with [<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 36\" title=\"Pradeep MSS, Vishnu Vardhana Rao K. A study on surgical site infections, their bacteriological profile and antimicrobial susceptibility pattern. IP International Journal of Medical Microbiology and Tropical Diseases. 2019;5(1):9\u201313.\" href=\"http:\/\/bmcmicrobiol.biomedcentral.com\/articles\/10.1186\/s12866-025-04480-9#ref-CR36\" id=\"ref-link-section-d168785508e2773\" rel=\"nofollow noopener\" target=\"_blank\">36<\/a>], who reported complete resistance of P. aeruginosa to Erythromycin, Amoxicillin, Colistin, and Cephradine, with retained sensitivity to Imipenem (100%), Apramycin (92.31%), and Amikacin (84.61%).<\/p>\n<p>The high incidence of SSIs and MDR pathogens in this study also points to critical issues in hospital practices and infection control. Lapses in perioperative asepsis, sterilization protocols, and hand hygiene compliance may contribute to elevated infection rates. In addition, widespread empirical use of broad-spectrum antibiotics in tertiary care hospitals likely exerts selective pressure, accelerating resistance development. These findings underscore the urgent need for robust antibiotic stewardship programs, guided by routine antibiogram surveillance and strict adherence to institutional antibiotic policies. Restricting overuse of critical drugs, reinforcing staff training in aseptic techniques, and strengthening postoperative wound care protocols could help mitigate the SSI burden.<\/p>\n<p>Limitations of the current study<\/p>\n<p>There are a few limitations on the current study. It was carried out in a single tertiary care facility with a small sample size, which might limit how broadly the results can be applied. The lack of facilities prevented the molecular characterization of resistance genes, which limited our understanding of the genetic basis of antibiotic resistance. Furthermore, a wider variety of antibiotics and patient-related variables were excluded from the analysis. Notwithstanding these drawbacks, the study offers important new information about the patterns of antibiotic resistance in bacterial pathogens linked to surgical site infections following surgery. However, we are interested in conducting this analysis in the future if appropriate funding support becomes available.<\/p>\n","protected":false},"excerpt":{"rendered":"Despite advancements in preventive measures, (SSIs) remain a significant healthcare challenge due to their high rates of morbidity&hellip;\n","protected":false},"author":2,"featured_media":120595,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[10],"tags":[76698,4680,3181,163,85,46,3183,3488,76699,33251,47556,76700,18493,31093,76701],"class_list":{"0":"post-120594","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-health","8":"tag-antibiotic-sensitivity-test","9":"tag-biological-microscopy","10":"tag-general","11":"tag-health","12":"tag-il","13":"tag-israel","14":"tag-life-sciences","15":"tag-microbiology","16":"tag-multidrug-resistant","17":"tag-mycology","18":"tag-n-pseudomonas-aeruginosan","19":"tag-n-staphylococcus-aureusn","20":"tag-parasitology","21":"tag-virology","22":"tag-wound-infection"},"_links":{"self":[{"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/posts\/120594","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/comments?post=120594"}],"version-history":[{"count":0,"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/posts\/120594\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/media\/120595"}],"wp:attachment":[{"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/media?parent=120594"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/categories?post=120594"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.newsbeep.com\/il\/wp-json\/wp\/v2\/tags?post=120594"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}