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    <Identifier>dgkh000559</Identifier>
    <IdentifierDoi>10.3205/dgkh000559</IdentifierDoi>
    <IdentifierUrn>urn:nbn:de:0183-dgkh0005598</IdentifierUrn>
    <ArticleType>Research Article</ArticleType>
    <TitleGroup>
      <Title language="en">From access to reserve: antimicrobial resistance among etiological agents of central line-associated  bloodstream infections in the view of WHO&#8217;s AWaRe antimicrobial spectrum</Title>
      <TitleTranslated language="de">Vom Zugang zur Reserve: Antibiotikaresistenz unter den Erregern zentralven&#246;ser Katheterinfektionen im Hinblick auf das antimikrobielle Spektrum gem&#228;&#223; der AWaRe Klassifizierung der WHO</TitleTranslated>
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      <Creator>
        <PersonNames>
          <Lastname>Anand</Lastname>
          <LastnameHeading>Anand</LastnameHeading>
          <Firstname>Gargee</Firstname>
          <Initials>G</Initials>
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        <Address>
          <Affiliation>All India Institute of Medical Sciences, Patna, Bihar, India</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
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      <Creator>
        <PersonNames>
          <Lastname>Lahariya</Lastname>
          <LastnameHeading>Lahariya</LastnameHeading>
          <Firstname>Rijhul</Firstname>
          <Initials>R</Initials>
        </PersonNames>
        <Address>
          <Affiliation>All India Institute of Medical Sciences, Patna, Bihar, India</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
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      <Creator>
        <PersonNames>
          <Lastname>Priyadarshi</Lastname>
          <LastnameHeading>Priyadarshi</LastnameHeading>
          <Firstname>Ketan</Firstname>
          <Initials>K</Initials>
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        <Address>
          <Affiliation>All India Institute of Medical Sciences, Patna, Bihar, India</Affiliation>
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        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
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      <Creator>
        <PersonNames>
          <Lastname>Sarfraz</Lastname>
          <LastnameHeading>Sarfraz</LastnameHeading>
          <Firstname>Asim</Firstname>
          <Initials>A</Initials>
          <AcademicTitle>Dr.</AcademicTitle>
        </PersonNames>
        <Address>All India Institute of Medical Sciences, Phulwari Sharif, Patna, Bihar, 801507, India; phone: &#43;91 9955360903<Affiliation>All India Institute of Medical Sciences, Patna, Bihar, India</Affiliation></Address>
        <Email>drasims&#64;aiimspatna.org</Email>
        <Creatorrole corresponding="yes" presenting="no">author</Creatorrole>
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    <PublisherList>
      <Publisher>
        <Corporation>
          <Corporatename>German Medical Science GMS Publishing House</Corporatename>
        </Corporation>
        <Address>D&#252;sseldorf</Address>
      </Publisher>
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    <SubjectGroup>
      <SubjectheadingDDB>610</SubjectheadingDDB>
      <Keyword language="en">central line-associated bloodstream infections</Keyword>
      <Keyword language="en">CLABSI</Keyword>
      <Keyword language="en">antimicrobial resistance</Keyword>
      <Keyword language="en">WHO AWaRe</Keyword>
      <Keyword language="en">intensive care units</Keyword>
      <Keyword language="en">antimicrobial stewardship</Keyword>
      <Keyword language="en">infection control</Keyword>
      <Keyword language="en">pathogen-directed therapy</Keyword>
      <Keyword language="en">healthcare associated infection</Keyword>
      <Keyword language="de">ZVK-assoziierte Blutstrominfektion</Keyword>
      <Keyword language="de">CLABSI</Keyword>
      <Keyword language="de">Antibiotikaresistenz</Keyword>
      <Keyword language="de">WHO AWaRe</Keyword>
      <Keyword language="de">Intensivtherapiestation</Keyword>
      <Keyword language="de">Antibiotika Stewardship</Keyword>
      <Keyword language="de">Infektionskontrolle</Keyword>
      <Keyword language="de">Erreger angepasste Therapie</Keyword>
      <Keyword language="de">Healthcare-assoziierte Infektionen</Keyword>
    </SubjectGroup>
    <DatePublishedList>
      <DatePublished>20250617</DatePublished>
    </DatePublishedList>
    <Language>engl</Language>
    <License license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
      <AltText language="en">This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License.</AltText>
      <AltText language="de">Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung).</AltText>
    </License>
    <SourceGroup>
      <Journal>
        <ISSN>2196-5226</ISSN>
        <Volume>20</Volume>
        <JournalTitle>GMS Hygiene and Infection Control</JournalTitle>
        <JournalTitleAbbr>GMS Hyg Infect Control</JournalTitleAbbr>
      </Journal>
    </SourceGroup>
    <ArticleNo>30</ArticleNo>
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    <Abstract language="de" linked="yes"><Pgraph><Mark1>Zielsetzung:</Mark1> ZVK assoziierte Blutstrominfektionen (CLABSI) sind nach wie vor eine der Hauptursachen f&#252;r Morbidit&#228;t und Mortalit&#228;t bei schwerkranken Patienten. Die zunehmende antimikrobielle Resistenz (AMR) versch&#228;rft die Herausforderungen bei der Behandlung, weshalb die Untersuchung von Resistenzmustern der Erreger von entscheidender Bedeutung ist. In der Studie wird die Empfindlichkeit von CLABSI-assoziierten Erregern gegen&#252;ber Antibiotika anhand der AWaRe Klassifizierung der WHO analysiert, um Erkenntnisse f&#252;r eine gezielte Behandlung zu gewinnen und Strategien zur Infektionskontrolle zu st&#228;rken.</Pgraph><Pgraph><Mark1>Methode:</Mark1> In der Beobachtungsstudie (2021&#8211;2024) wurden Daten von Intensivstationen f&#252;r Erwachsene und Kinder ausgewertet, um die H&#228;ufigkeit von CLABSI, die mikrobielle &#196;tiologie und die Entwicklung der Empfindlichkeit gegen&#252;ber Antibiotika zu untersuchen. Wir kategorisierten die antimikrobiellen Substanzen auf der Grundlage des AWaRe-Klassifizierungssystems der WHO und analysierten ihre Empfindlichkeit gegen&#252;ber Access-, Watch- und Reserve-Antibiotika. Die statistische Analyse wurde mit SPSS Version 22 durchgef&#252;hrt.</Pgraph><Pgraph><Mark1>Ergebnisse:</Mark1> Unter 5.398 Patientenakten wurden 101 F&#228;lle von CLABSI best&#228;tigt. Die vorherrschenden Erreger waren <Mark2>Klebsiella (K.) pneumoniae</Mark2> (27,7&#37;), <Mark2>Acinetobacter</Mark2> spp. (19,8&#37;) und <Mark2>Candida</Mark2> spp. (17,8&#37;). Bei den wichtigsten Erregern wurde ein besorgniserregender R&#252;ckgang der Empfindlichkeit gegen&#252;ber antimikrobiellen Mitteln der Kategorien Access und Watch festgestellt. <Mark2>K. pneumoniae</Mark2> wies einen starken R&#252;ckgang der Empfindlichkeit gegen&#252;ber Mitteln der Kategorie &#8222;Access&#8220; auf, von 27,8&#37; im Jahr 2021 auf 16,7&#37; im Jahr 2023. Umgekehrt behielten die antimikrobiellen Mittel der Reservekategorie ihre 100&#37;ige Wirksamkeit &#252;ber den gesamten Studienzeitraum. <Mark2>Acinetobacter</Mark2> spp. wiesen bis 2024 eine Resistenz sowohl gegen antimikrobielle Mittel der Access- als auch der Watch-Kategorie auf. <Mark2>Pseudomonas aeruginosa</Mark2> zeigte einen drastischen R&#252;ckgang der Empfindlichkeit f&#252;r die Kategorie Watch von 44,5&#37; im Jahr 2021 auf 0&#37; im Jahr 2023, w&#228;hrend die Mittel der Kategorie Reserve wirksam blieben. Die Ergebnisse unterstreichen die zunehmende Abh&#228;ngigkeit von antimikrobiellen Mitteln der Reserve und die abnehmende Wirksamkeit der First line Mittel. Dar&#252;ber hinaus beobachteten wir eine Fluktuation der CLABSI-Raten, wobei die Infektionsraten im Jahr 2024 nach der Einf&#252;hrung verbesserter Infektionskontrollverfahren deutlich zur&#252;ckgingen.</Pgraph><Pgraph><Mark1>Schlussfolgerung:</Mark1> Die Studie verdeutlicht die eskalierenden Resistenzmuster von CLABSI-Erregern mit einem besorgniserregenden R&#252;ckgang der antimikrobiellen Wirksamkeit der Kategorien Access und Watch. Der AWaRe-Rahmen erweist sich als wertvoll f&#252;r die Identifizierung kritischer Resistenztrends und zeigt die Notwendigkeit eines gezielten antimikrobiellen Stewardships. Die Priorisierung von Access-Antibiotika als Erstlinientherapien, die sich an lokalen Resistenzdaten orientiert, kann die Wirksamkeit von Reserve-Wirkstoffen erhalten. Ein strategischer Fokus auf die AWaRe-Klassifizierung in Verbindung mit rigorosen Infektionskontroll- und Stewardship-Programmen ist unerl&#228;sslich, um die steigende AMR-Bedrohung zu bek&#228;mpfen und die Therapieergebnisse in der Intensivpflege zu optimieren.</Pgraph></Abstract>
    <Abstract language="en" linked="yes"><Pgraph><Mark1>Aim:</Mark1> Central line-associated bloodstream infections (CLABSI) remain a major contributor to morbidity and mortality in critically ill patients. The rise of antimicrobial resistance (AMR) exacerbates treatment challenges, making it crucial to examine pathogen resistance patterns. This study analyses CLABSI-associated pathogens&#8217; antimicrobial susceptibility using the WHO&#8217;s AWaRe antimicrobial framework, providing insights to guide targeted treatment and strengthen infection control strategies.</Pgraph><Pgraph><Mark1>Methods:</Mark1> This observational study (2021&#8211;2024) assessed data from adult and pediatric ICUs to evaluate CLABSI incidence, microbial etiology, and antimicrobial susceptibility trends. We categorized antimicrobials based on the WHO&#8217;s AWaRe classification system, analysing their susceptibility to Access, Watch, and Reserve antimicrobials. Statistical analysis was performed using SPSS version 22.</Pgraph><Pgraph><Mark1>Results:</Mark1> Among 5,398 patient records, 101 cases of CLABSI were confirmed. The predominant pathogens were <Mark2>Klebsiella (K.) pneumoniae</Mark2> (27.7&#37;), <Mark2>Acinetobacter</Mark2> spp. (19.8&#37;), and <Mark2>Candida</Mark2> spp. (17.8&#37;). A worrying decline in susceptibility to Access- and Watch-category antimicrobials was observed in key pathogens. <Mark2>K. pneumoniae</Mark2> demonstrated a steep decline in susceptibility to Access-category agents, from 27.8&#37; in 2021 to 16.7&#37; in 2023. Conversely, Reserve-category antimicrobials maintained 100&#37; efficacy across the study period. <Mark2>Acinetobacter</Mark2> spp. exhibited resistance to both Access- and Watch-category antimicrobials by 2024. <Mark2>Pseudomonas aeruginosa</Mark2> showed a drastic drop in Watch-category susceptibility, from 44.5&#37; in 2021 to 0&#37; in 2023, while Reserve-agents remained effective. These results underline the growing reliance on Reserve antimicrobials and the diminishing effectiveness of first-line agents. Furthermore, a fluctuation in CLABSI rates was also observed, with a significant reduction in infection rates in 2024 after the implementation of enhanced infection control practices.</Pgraph><Pgraph><Mark1>Conclusion:</Mark1> This study highlights the escalating resistance patterns of CLABSI pathogens, with a consternating decline in Access- and Watch-category antimicrobial efficacy. The AWaRe framework proves invaluable in identifying critical resistance trends, demonstrating the need for targeted antimicrobial stewardship. Prioritizing Access antimicrobials as first-line therapies, guided by local resistance data, can preserve the effectiveness of Reserve agents. A strategic focus on the AWaRe classification, coupled with rigorous infection control and stewardship programs, is essential to combat the rising AMR threat and optimize patient outcomes in critical care settings.</Pgraph></Abstract>
    <TextBlock name="Introduction" linked="yes">
      <MainHeadline>Introduction</MainHeadline><Pgraph>Global prevalence data from the World Health Organization (WHO) indicates that the risk of healthcare-associated infections (HAI) is particularly elevated in intensive care units (ICUs), affecting approximately 30&#37; of ICU patients and resulting in significant morbidity and mortality <TextLink reference="1"></TextLink>. The prevalence of HAIs differs markedly between developed and developing nations, with incidence rates of 7&#37; and 10&#37; respectively among hospitalized patients <TextLink reference="1"></TextLink>. Among all HAIs, CLABSIs represent a substantial economic burden, with an estimated per-case cost of USD 46,000 <TextLink reference="2"></TextLink>. A literature review indicates that CLABSIs significantly extend ICU length of stay, with reported excess hospitalization periods ranging from 2.7 to 48.5 days compared to non-infected patients <TextLink reference="3"></TextLink>. CLABSIs not only carry substantial risks of illness and death but also demand more intensive and costly treatments compared to other HAIs, resulting in an exceptionally high burden on both patient care and hospital resources. The collective burden of CLABSIs has been estimated as equivalent to the eigth leading cause of death in the United States <TextLink reference="4"></TextLink>. The emergence of antimicrobial resistance (AMR) coupled with biofilm formation on medical devices, particularly vascular catheters, presents significant therapeutic challenges <TextLink reference="4"></TextLink>. The WHO developed the AWaRe (Access, Watch, Reserve) classification framework to address escalating AMR concerns while preserving therapeutic efficacy of critical antimicrobials <TextLink reference="5"></TextLink>. This classification system strategically categorizes antimicrobial agents into three groups based on their therapeutic importance and resistance potential, and aims to mitigate the global health threat posed by AMR through enhanced surveillance, stewardship, and reduction of inappropriate antimicrobial consumption, strategically categorizing antimicrobials to optimize their use in healthcare settings <TextLink reference="5"></TextLink>, <TextLink reference="6"></TextLink>. The present study presents an in-depth analysis of antimicrobial susceptibility profiles in CLABSI-associated pathogens, leveraging the WHO&#8217;s AWaRe classification system to offer novel insights into resistance patterns and inform targeted treatment strategies. Hence, the present study examined three key aspects of CLABSIs: incidence rates, microbial etiology, and antimicrobial susceptibility patterns, analyzed through the WHO&#8217;s AWaRe framework, to strengthen the synergy between infection prevention and antimicrobial stewardship programs.</Pgraph></TextBlock>
    <TextBlock name="Methods" linked="yes">
      <MainHeadline>Methods</MainHeadline><SubHeadline>Study design </SubHeadline><Pgraph>This observational cross-sectional study encompassed patients from both adult and pediatric ICUs between 2021 and 2024. Inclusion criteria specified central line placement for more than 2 calendar days. Blood cultures were obtained for microbiological evaluation from patients presenting with clinical signs of bloodstream infection&#47;sepsis. Cases of secondary bloodstream infections were excluded from the analysis. Standardized surveillance definitions of CLABSIs as per Centers for Disease Control and Prevention, National Healthcare Safety Network (CDC, NHSN) were followed <TextLink reference="7"></TextLink>. An isolate was classified as multidrug-resistant (MDR) when it was non-susceptible to at least one antimicrobial agent in three or more antimicrobial classes <TextLink reference="8"></TextLink>. The CLABSI rate was calculated as: (number of CLABSI&#47;total central line days) &#215;1,000, expressed as CLABSI per 1,000 central line days <TextLink reference="7"></TextLink>. Interpretive breakpoints for antimicrobial susceptibility testing established by CLSI (Clinical and Laboratory Standards Institute), M 100 guidelines for bacterial isolates were used <TextLink reference="9"></TextLink>. Relevant data were collected and antimicrobial susceptibility patterns were analyzed using the WHO&#8217;s AWaRe classification <TextLink reference="5"></TextLink>.</Pgraph><SubHeadline>Data collection </SubHeadline><Pgraph>Patient data were retrospectively extracted from two institutional databases: the Hospital Information System (HIS) and HAI surveillance records. The HIS provided microbiological data, including blood culture results and antimicrobial susceptibility profile. HAI surveillance forms were used for gathering demographic information, clinical diagnosis, central line insertion sites, ICU length of stay, mortality&#47;patient outcomes, and daily clinical assessments for catheter-related infection manifestations.</Pgraph><SubHeadline>Patient and public involvement </SubHeadline><Pgraph>In this study, there was no patient or public involvement, as the data were solely collected from the records department.</Pgraph><SubHeadline>Statistical analysis </SubHeadline><Pgraph>All relevant data were entered in a Microsoft Excel 2019 spreadsheet. Normality distribution for all continuous variables was tested using Q-Q plots, histograms, and the Shapiro-wilk test. Continuous variables were expressed using mean (&#177;SD)&#47; median (IQR) according to their normality, while categorical variables were expressed as percentages&#47;proportions. as appropriate. Bivariate comparison of categorical variables was performed using the Chi-squared test and Fisher&#8217;s exact test. Graphs depicting antimicrobial susceptibility trend as per WHO&#8217;s AWaRe classification were made using Microsoft Excel 2019. Statistical analysis was conducted using Statistical Package for Social Sciences (SPSS) version 22. A p-value of &#60;0.05 was designated as statistically significant. </Pgraph></TextBlock>
    <TextBlock name="Results" linked="yes">
      <MainHeadline>Results</MainHeadline><Pgraph>Over the four-year (2021&#8211;2024) study period, records of 5398 patient who met the predefined inclusion criteria were assessed, of whom 101 patients developed CLABSI with Laboratory Confirmed Bloodstream Infection 1 (LCBI 1) criteria as per the CDC, NHSN surveillance criteria. The annual incidence of CLABSI is shown in Table 1 <ImgLink imgNo="1" imgType="table" />, and overall incidence of CLABSI is depicted in Table 2 <ImgLink imgNo="2" imgType="table" /> by type of ICU.</Pgraph><Pgraph>CLABSI more commonly occurred in patients having femoral access (22 CLABIS&#47;150 femoral line). Analysis revealed a statistically significant predilection for CLABSIs among patients with femoral venous catheterization (p&#61;0.001&#42;). </Pgraph><Pgraph>Microbiological analysis of CLABSIs revealed a predominance of Gram-negative organisms (76&#47;101; 75.3&#37;), with <Mark2>Candida</Mark2> spp. (18&#47;101; 17.8&#37;) and Gram-positive organisms (7&#47;101; 6.9&#37;) comprising the remaining isolates (Table 3 <ImgLink imgNo="3" imgType="table" />).</Pgraph><Pgraph>Analysis of antimicrobial susceptibility patterns across the WHO AWaRe categories revealed distinct temporal trends among isolated pathogens. <Mark2>K. pneumoniae</Mark2> exhibited a declining trend in Access-category susceptibility from 27.8&#37; (2021) to 16.7&#37; (2023), with a slight increase to 25.9&#37; in 2024. Watch-category susceptibility showed a marked decrease from 37.5&#37; (2021) to 2.5&#37; (2022), followed by gradual increase to 15.3&#37; (2024). Reserve-category antimicrobials maintained 100&#37; efficacy throughout the study period. <Mark2>Acinetobacter</Mark2> spp. demonstrated fluctuating Access-category susceptibility: 22.2&#37; (2022), increasing to 27.8&#37; (2023), before declining to 0&#37; (2024). Watch-category susceptibility showed consistently low rates, peaking at 9.52&#37; (2023). Reserve antimicrobials maintained 100&#37; efficacy from 2022&#8211;2024. <Mark2>E. coli</Mark2> susceptibility to Access-category antimicrobials decreased from 25&#37; (2023) to 0&#37; (2024), with a parallel decline in Watch-category susceptibility from 8.9&#37; to 0&#37;. However, Reserve-category antimicrobials maintained 100&#37; efficacy. <Mark2>Burkholderia</Mark2> spp. maintained consistent Access-category susceptibility (100&#37;) when isolated, while Watch-category susceptibility declined from 83.3&#37; (2021) to 50&#37; (2024). <Mark2>P. aeruginosa</Mark2> showed variable Watch-category susceptibility, decreasing from 44.5&#37; (2021) to 0&#37; (2023), with Reserve-category susceptibility declining from 66.7&#37; (2021&#8211;2022) to 50&#37; (2023).</Pgraph><Pgraph>Among Gram-positive organisms, <Mark2>Enterococcus</Mark2> spp. showed decreasing Access-category susceptibility from 50&#37; (2021) to 0&#37; (2023&#8211;2024), with Watch-category susceptibility declining from 50&#37; (2021) to 33.3&#37; (2023&#8211;2024). Reserve-category efficacy varied from 100&#37; to 0&#37;. <Mark2>S. aureus</Mark2> maintained relatively high Access-category susceptibility (60&#8211;80&#37;), with Watch-category susceptibility increasing from 33.3&#37; to 66.7&#37;, and consistent Reserve-category efficacy at 100&#37;. Overall susceptibility of access, Watch- and Reserve-category antimicrobials for various isolated microorganisms among CLABSI patients are shown in Figure 1 <ImgLink imgNo="1" imgType="figure" />. Annual susceptibility trend (2021&#8211;2024) for various antimicrobials among isolated organisms is depicted in Table 4 <ImgLink imgNo="4" imgType="table" />.</Pgraph></TextBlock>
    <TextBlock name="Discussion" linked="yes">
      <MainHeadline>Discussion</MainHeadline><Pgraph>This groundbreaking study is the first to analyse CLABSI pathogens&#8217; AMR using the WHO&#8217;s AWaRe framework, offering critical insights for targeted treatment strategies. Analysis of CLABSI incidence over the four-year surveillance period (2021&#8211;2024) revealed notable variations. The baseline CLABSI rate in 2021 was 6.18 per 1,000 central line days, which demonstrated a substantial decline to 1.69 per 1,000 central line days in 2022, representing a 72.7&#37; reduction. However, 2023 witnessed an increase to 3.75 per 1,000 central line days, followed by a subsequent decrease to 2.45 per 1,000 central line days in 2024.</Pgraph><Pgraph>This fluctuation in CLABSI rates warrants careful interpretation. The initial high rate in 2021 can be attributed to the lesser number of ICUs under surveillance and it might reflect the baseline period before implementation of enhanced prevention protocols. Following the elevated CLABSI rates in 2023 (3.75 per 1,000 central line days), implementation of enhanced insertion and maintenance-bundle practices led to a significant reduction in infection rates to 2.45 per 1,000 central line days in 2024, representing a 34.7&#37; decrease. Notably, the central line utilization showed a progressive increase from 2,911 days in 2021 to 10,583 days in 2024, suggesting expanded critical care services or increased patient complexity. This increased device utilization might have contributed to the observed variations in infection rates. </Pgraph><Pgraph>These findings align with the published literature reporting CLABSI rates of 5 per 1,000 catheter days, while other Indian studies reported CLABSI rates ranging from 0.48 to 27 per 1,000 catheter days in various healthcare settings <TextLink reference="10"></TextLink>, <TextLink reference="11"></TextLink>. The observed temporal variations underscore the dynamic nature of HAIs and emphasize the need for sustained vigilance in prevention strategies. </Pgraph><Pgraph>Statistical analysis showed a significantly greater predilection for CLABSI occurrence in the presence of femoral catheterization (p-value &#60;0.001&#42;) <TextLink reference="12"></TextLink>, <TextLink reference="13"></TextLink>. The differential risk of CLABSIs across insertion sites can be attributed to anatomical variations, local microbiological colonization patterns, and site-specific mechanical factors. </Pgraph><Pgraph>The etiological spectrum of CLABSI revealed a predominance of Gram-negative organisms, constituting 75.2&#37; of CLABSIs. Among these, <Mark2>K. pneumoniae</Mark2> emerged as the primary pathogen (27.7&#37;), followed by <Mark2>Acinetobacter</Mark2> spp. (19.8&#37;). This microbial distribution pattern corresponds with the literature, which documents the predominance of Gram-negative organisms in device-associated bloodstream infections <TextLink reference="14"></TextLink>.</Pgraph><Pgraph>Antimicrobial susceptibility testing of all CLABSI isolates revealed substantial AMR to first-line agents, a finding that aligns with a previous study <TextLink reference="15"></TextLink>.</Pgraph><Pgraph>The analysis of antimicrobial susceptibility patterns reveals concerning trends in pathogen resistance profiles across the WHO AWaRe classification framework. Analysis revealed worrying AMR patterns among predominant pathogens, with <Mark2>K. pneumoniae</Mark2> showing a progressive decline in Access-category susceptibility (27.8&#37; to 16.7&#37;) and <Mark2>Acinetobacter</Mark2> spp. demonstrating complete resistance to both Access- and Watch-categories by 2024. Notably, <Mark2>P. aeruginosa</Mark2> exhibited significant resistance development, with Watch-category susceptibility declining from 44.5&#37; to 0&#37; and Reserve-category efficacy decreasing from 66.7&#37; to 50&#37;. Despite these alarming trends, Access-category antimicrobials maintained better susceptibility profiles compared to Watch-category agents for most isolates. The sustained efficacy of Reserve-category antimicrobials (100&#37; susceptibility) among major Gram-negative pathogens, while therapeutically promising, raises concerns about increasing reliance on last-resort antimicrobials. This pattern of escalating resistance to first-line agents, necessitating increased usage of Reserve antimicrobials, underscores the critical need for robust antimicrobial stewardship programs to preserve therapeutic options across all AWaRe categories, hence cascade reporting of antimicrobial susceptibility test (AST) results is of utmost importance.</Pgraph><Pgraph>Among Gram-positive organisms, the decreasing susceptibility of <Mark2>Enterococcus</Mark2> spp. to Access- and Watch-category antimicrobials, coupled with variable Reserve-category efficacy, suggests emerging resistance patterns requiring careful monitoring. Conversely, <Mark2>S. aureus</Mark2> maintained relatively favourable susceptibility profiles, particularly to Access-category agents, potentially reflecting effective infection control measures.</Pgraph><Pgraph>A paradigm shift is necessary in prescribing practices within ICUs, emphasizing pathogen-directed therapy guided by local susceptibility data rather than defaulting to broad-spectrum Watch- and Reserve-group antimicrobials. Prioritizing Access antimicrobials as first-line therapies, wherever appropriate, will help preserve efficacy of Watch and Reserve agents <TextLink reference="16"></TextLink>. The most urgent step needed now is to implement targeted bundle care practices, antimicrobial stewardship strategies aligned with the WHO&#8217;s AWaRe classification, even in critical care settings <TextLink reference="17"></TextLink>, <TextLink reference="18"></TextLink>.</Pgraph></TextBlock>
    <TextBlock name="Conclusions" linked="yes">
      <MainHeadline>Conclusions</MainHeadline><Pgraph>The study highlights a precarious situation where the efficacy of Access&#47;Watch antimicrobials is compromised and thus increased reliance is placed on Reserve antimicrobials. This complicates patient management and poses a global health threat by AMR. Thus, prioritizing Access antimicrobials as first-line, where appropriate, will preserve the efficacy of Watch and Reserve agents, mitigating the emergence of extensively drug-resistant strains. This strategy, coupled with </Pgraph><Pgraph><UnorderedList><ListItem level="1">implementation of pathogen-directed therapy based on local resistance data rather than empiric broad-spectrum antimicrobial use,</ListItem><ListItem level="1">development of targeted antimicrobial stewardship programs aligned with the WHO AWaRe framework, specifically adapted for critical care settingsrigorous infection, and </ListItem><ListItem level="1">control measures and continuous surveillance</ListItem></UnorderedList></Pgraph><Pgraph>offers a promising path to combat AMR in HAIs while adhering to the WHO&#8217;s AWaRe even in critical care settings.</Pgraph></TextBlock>
    <TextBlock name="Notes" linked="yes">
      <MainHeadline>Notes</MainHeadline><SubHeadline>Competing interests</SubHeadline><Pgraph>The authors declare that they have no competing interests.</Pgraph><SubHeadline>Funding sources</SubHeadline><Pgraph>The authors hereby declare that no financial support was received for this study.</Pgraph><SubHeadline>Authors&#8217; ORCIDs</SubHeadline><Pgraph><UnorderedList><ListItem level="1">Anand G: <Hyperlink href="https:&#47;&#47;orcid.org&#47;0009-0008-0473-389X">https:&#47;&#47;orcid.org&#47;0009-0008-0473-389X</Hyperlink></ListItem><ListItem level="1">Lahariya R: <Hyperlink href="https:&#47;&#47;orcid.org&#47;0009-0003-5769-4509">https:&#47;&#47;orcid.org&#47;0009-0003-5769-4509</Hyperlink></ListItem><ListItem level="1">Priyadarshi K: <Hyperlink href="https:&#47;&#47;orcid.org&#47;0000-0003-4623-3523">https:&#47;&#47;orcid.org&#47;0000-0003-4623-3523</Hyperlink></ListItem><ListItem level="1">Sarfraz A: <Hyperlink href="https:&#47;&#47;orcid.org&#47;0000-0002-6256-7649">https:&#47;&#47;orcid.org&#47;0000-0002-6256-7649</Hyperlink></ListItem></UnorderedList></Pgraph></TextBlock>
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    <Media>
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          <MediaNo>1</MediaNo>
          <MediaID>1</MediaID>
          <Caption><Pgraph><Mark1>Table 1: Annual incidence of CLABSI (2021&#8211;2024) </Mark1></Pgraph></Caption>
        </Table>
        <Table format="png">
          <MediaNo>2</MediaNo>
          <MediaID>2</MediaID>
          <Caption><Pgraph><Mark1>Table 2: ICU-specific incidence of CLABSI</Mark1></Pgraph></Caption>
        </Table>
        <Table format="png">
          <MediaNo>3</MediaNo>
          <MediaID>3</MediaID>
          <Caption><Pgraph>Table 3: <Mark1>Microorganisms isolated from CLABSI cases (n&#61;101)</Mark1></Pgraph></Caption>
        </Table>
        <Table format="png">
          <MediaNo>4</MediaNo>
          <MediaID>4</MediaID>
          <Caption><Pgraph><Mark1>Table 4: Annual susceptibility trend (2021&#8211;2024) of various antibiotics against various CLABSI isolates (CLABSI cases 101)</Mark1></Pgraph></Caption>
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          <Caption><Pgraph><Mark1>Figure 1: Susceptibility of Access, Watch and Reserve antibiotics among CLABSI isolates by year</Mark1></Pgraph></Caption>
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