Pub Date : 2026-01-09eCollection Date: 2026-02-01DOI: 10.1093/jacamr/dlaf258
Rachel Berry, Tanya Miah, Maria Nasim, Diane Ashiru-Oredope
Background: An Antimicrobial Prescribing and Stewardship (APS) Competency Framework is an important resource for enhancing the practice of prescribers, in-line with national and global priorities for tackling antimicrobial resistance. Knowledge mobilization of such a framework is essential to maximize its utilization and impact.
Objectives: To utilize a Knowledge to Action (KTA) Framework approach to mobilize knowledge of the national APS Competency Framework, assess current integration and collect feedback from course-leaders of non-medical prescribing (NMP) programs at Higher Education Institutions (HEIs) in the UK.
Methods: UK HEIs accredited to provide NMP training to experienced nurses, pharmacists, and allied health professionals were identified through review of professional regulatory websites. A Microsoft Forms® survey with consent was developed and piloted; the final link and additional information were emailed to NMP course leads. The results were analysed using Microsoft Excel® and NVivo15®.
Results: Of 84 HEIs surveyed, 38 responded (45%). Over half (55%) already integrate the national APS framework in courses, with others signposting to it. Most (63%) found it helpful, though its length and detail posed challenges and some felt it lacked relevance for all students. Participation in the survey increased awareness of the APS framework and other resources for antimicrobial stewardship teaching.
Conclusions: This knowledge mobilization and evaluation demonstrated a high level of utilization of the framework within NMP programmes; feedback from users should be considered in future updates. It highlights the need for ongoing engagement with HEIs to embed AMS principles in all prescriber education to optimize antimicrobial use and reduce resistance.
{"title":"Knowledge mobilization and assessment of implementation of an updated national antimicrobial prescribing and stewardship competency framework.","authors":"Rachel Berry, Tanya Miah, Maria Nasim, Diane Ashiru-Oredope","doi":"10.1093/jacamr/dlaf258","DOIUrl":"10.1093/jacamr/dlaf258","url":null,"abstract":"<p><strong>Background: </strong>An Antimicrobial Prescribing and Stewardship (APS) Competency Framework is an important resource for enhancing the practice of prescribers, in-line with national and global priorities for tackling antimicrobial resistance. Knowledge mobilization of such a framework is essential to maximize its utilization and impact.</p><p><strong>Objectives: </strong>To utilize a Knowledge to Action (KTA) Framework approach to mobilize knowledge of the national APS Competency Framework, assess current integration and collect feedback from course-leaders of non-medical prescribing (NMP) programs at Higher Education Institutions (HEIs) in the UK.</p><p><strong>Methods: </strong>UK HEIs accredited to provide NMP training to experienced nurses, pharmacists, and allied health professionals were identified through review of professional regulatory websites. A Microsoft Forms<sup>®</sup> survey with consent was developed and piloted; the final link and additional information were emailed to NMP course leads. The results were analysed using Microsoft Excel<sup>®</sup> and NVivo15<sup>®</sup>.</p><p><strong>Results: </strong>Of 84 HEIs surveyed, 38 responded (45%). Over half (55%) already integrate the national APS framework in courses, with others signposting to it. Most (63%) found it helpful, though its length and detail posed challenges and some felt it lacked relevance for all students. Participation in the survey increased awareness of the APS framework and other resources for antimicrobial stewardship teaching.</p><p><strong>Conclusions: </strong>This knowledge mobilization and evaluation demonstrated a high level of utilization of the framework within NMP programmes; feedback from users should be considered in future updates. It highlights the need for ongoing engagement with HEIs to embed AMS principles in all prescriber education to optimize antimicrobial use and reduce resistance.</p>","PeriodicalId":14594,"journal":{"name":"JAC-Antimicrobial Resistance","volume":"8 1","pages":"dlaf258"},"PeriodicalIF":3.3,"publicationDate":"2026-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12785880/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145951814","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-08eCollection Date: 2026-02-01DOI: 10.1093/jacamr/dlaf231
Therese Renaa, Louise Emilsson, Sigurd Høye, Marius Skow, Guro H Fossum
Background: Correct use of antibiotics ensures necessary treatment for patients while antibiotic resistance is reduced. Respiratory tract infections (RTIs) are common in preschool children. Young children receive a large proportion of the total amount of antibiotics, and also in low-prescribing countries such as Norway.
Objectives: Explore the contacts, rate of antibiotic prescriptions and choice of antibiotics in the treatment of RTIs in preschool children in general practice from 2012 to 2019. Methods Descriptive registry study on complete population data of antibiotic prescriptions administered to Norwegian pre-school children with RTIs, in the period 2012 - 2019, after consultations with a general practitioner.
Results: The total prescription rate was reduced from 28% in 2012 to 19% in 2019. There were small yearly variations in prescription rates. Most antibiotics were prescribed to 1- and 2-year-olds. Upper RTI was the most used diagnosis and accounted for 25% of the total amount of antibiotics prescribed.Total RTI episode rate was 941 episodes/1000 children in 2012, reduced by 17% to 2019 when there were 777 episodes/1000 children. The reduction in antibiotic prescription to children with otitis was associated with a decline in episode rate.More than 81% of prescribed antibiotics were penicillins, only 16% were macrolides and 3% were other antibiotics. The use of phenoxymethylpenicillin increased in the period from 50% in 2012 to 68% in 2019.
Conclusions: There is room for improvement in adherence to guidelines and antibiotic stewardship also in low-prescribing countries. Antibiotic prescribing is closely linked to prescription rates and health-seeking behaviours, offering valuable insights for targeted antibiotic stewardship campaigns.
{"title":"Antibiotic prescriptions to preschool children with respiratory tract infections in primary healthcare.","authors":"Therese Renaa, Louise Emilsson, Sigurd Høye, Marius Skow, Guro H Fossum","doi":"10.1093/jacamr/dlaf231","DOIUrl":"10.1093/jacamr/dlaf231","url":null,"abstract":"<p><strong>Background: </strong>Correct use of antibiotics ensures necessary treatment for patients while antibiotic resistance is reduced. Respiratory tract infections (RTIs) are common in preschool children. Young children receive a large proportion of the total amount of antibiotics, and also in low-prescribing countries such as Norway.</p><p><strong>Objectives: </strong>Explore the contacts, rate of antibiotic prescriptions and choice of antibiotics in the treatment of RTIs in preschool children in general practice from 2012 to 2019. Methods Descriptive registry study on complete population data of antibiotic prescriptions administered to Norwegian pre-school children with RTIs, in the period 2012 - 2019, after consultations with a general practitioner.</p><p><strong>Results: </strong>The total prescription rate was reduced from 28% in 2012 to 19% in 2019. There were small yearly variations in prescription rates. Most antibiotics were prescribed to 1- and 2-year-olds. Upper RTI was the most used diagnosis and accounted for 25% of the total amount of antibiotics prescribed.Total RTI episode rate was 941 episodes/1000 children in 2012, reduced by 17% to 2019 when there were 777 episodes/1000 children. The reduction in antibiotic prescription to children with otitis was associated with a decline in episode rate.More than 81% of prescribed antibiotics were penicillins, only 16% were macrolides and 3% were other antibiotics. The use of phenoxymethylpenicillin increased in the period from 50% in 2012 to 68% in 2019.</p><p><strong>Conclusions: </strong>There is room for improvement in adherence to guidelines and antibiotic stewardship also in low-prescribing countries. Antibiotic prescribing is closely linked to prescription rates and health-seeking behaviours, offering valuable insights for targeted antibiotic stewardship campaigns.</p>","PeriodicalId":14594,"journal":{"name":"JAC-Antimicrobial Resistance","volume":"8 1","pages":"dlaf231"},"PeriodicalIF":3.3,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12780767/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145952008","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-07eCollection Date: 2026-02-01DOI: 10.1093/jacamr/dlaf240
Catherine E Porter, Caity Roleston, Claire Bethune, Jenny Boards, Colin S Brown, Ian Clarke, Joanne Fielding, Philip Howard, Conor Jamieson, Siraj A Misbah, Andrew C Moss, Sue H Pavitt, Neil Powell, Louise Savic, Sinisa Savic, Mamidipudi Thirumala Krishna, Sarah Tonkin-Crine, Iestyn Williams, Jonathan A T Sandoe
Globally, there is increasing evidence that incorrect penicillin allergy labels negatively affect patient outcomes, antibiotic prescribing and antimicrobial resistance, leading to growing concern about this patient safety issue and how to resolve it. While many millions of patients worldwide have incorrect penicillin allergy labels, there are too few specialist allergists and a lack of 'point-of-care' tests to address this problem. Numerous research studies now provide evidence of the feasibility and importance of widening access to penicillin allergy assessment. Researchers from two UK-based studies (SPACE and ALABAMA), in collaboration with key stakeholders including patient representatives, gave their views to shape a high-level implementation plan to facilitate widening access to penicillin allergy assessment in the UK. This Viewpoint describes the basis of the implementation plan and summarizes the key actions required for successful delivery. While the plan is intended for the UK, we hope to promote international shared learning and collaboration to address this global problem informed by the UK context.
{"title":"Widening access to penicillin allergy assessment in the United Kingdom-a proposed implementation plan for the National Health Service (NHS).","authors":"Catherine E Porter, Caity Roleston, Claire Bethune, Jenny Boards, Colin S Brown, Ian Clarke, Joanne Fielding, Philip Howard, Conor Jamieson, Siraj A Misbah, Andrew C Moss, Sue H Pavitt, Neil Powell, Louise Savic, Sinisa Savic, Mamidipudi Thirumala Krishna, Sarah Tonkin-Crine, Iestyn Williams, Jonathan A T Sandoe","doi":"10.1093/jacamr/dlaf240","DOIUrl":"10.1093/jacamr/dlaf240","url":null,"abstract":"<p><p>Globally, there is increasing evidence that incorrect penicillin allergy labels negatively affect patient outcomes, antibiotic prescribing and antimicrobial resistance, leading to growing concern about this patient safety issue and how to resolve it. While many millions of patients worldwide have incorrect penicillin allergy labels, there are too few specialist allergists and a lack of 'point-of-care' tests to address this problem. Numerous research studies now provide evidence of the feasibility and importance of widening access to penicillin allergy assessment. Researchers from two UK-based studies (SPACE and ALABAMA), in collaboration with key stakeholders including patient representatives, gave their views to shape a high-level implementation plan to facilitate widening access to penicillin allergy assessment in the UK. This Viewpoint describes the basis of the implementation plan and summarizes the key actions required for successful delivery. While the plan is intended for the UK, we hope to promote international shared learning and collaboration to address this global problem informed by the UK context.</p>","PeriodicalId":14594,"journal":{"name":"JAC-Antimicrobial Resistance","volume":"8 1","pages":"dlaf240"},"PeriodicalIF":3.3,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12776011/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145933292","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-07eCollection Date: 2026-02-01DOI: 10.1093/jacamr/dlaf251
Angela Klingmüller, Sylvia Zuber, Ada M Hoffmann, Niklas Köhler, Isabelle Suárez, Tim Preßel, Stefan Niemann, Viola Dreyer, Laurent A Decosterd, Eva Choong, Beatrice Schütz, Inna Friesen, Jan Rybniker
{"title":"Therapeutic drug monitoring-guided treatment of XDR TB with an RpoB I491F mutation-a case report.","authors":"Angela Klingmüller, Sylvia Zuber, Ada M Hoffmann, Niklas Köhler, Isabelle Suárez, Tim Preßel, Stefan Niemann, Viola Dreyer, Laurent A Decosterd, Eva Choong, Beatrice Schütz, Inna Friesen, Jan Rybniker","doi":"10.1093/jacamr/dlaf251","DOIUrl":"10.1093/jacamr/dlaf251","url":null,"abstract":"","PeriodicalId":14594,"journal":{"name":"JAC-Antimicrobial Resistance","volume":"8 1","pages":"dlaf251"},"PeriodicalIF":3.3,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12776349/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145933266","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-07eCollection Date: 2026-02-01DOI: 10.1093/jacamr/dlaf257
Thomas D Nguyen, Jacob T Sanborn, Brian M Ho, Tiffany Luong, Troy D Wood, Liang Chen, Dwayne R Roach, Nicholas M Smith
Background: There is a resurgence of interest in bacteriophage (phage) therapy as antimicrobials, resulting from growing antimicrobial resistance to small-molecule antibiotics. Phages are bacterial viruses long studied, but there is a need for high resolution and systematic assessment of clinical dosing strategies for phages to better inform therapy.
Methods: We hypothesized that empirical in vitro assessment of clinically relevant phages facilitates pharmacodynamic-driven individualization. Three clinically relevant phage strains (LUZ19, PYO2 and E215) were evaluated as mono- or dual-phage therapy against a clinical Pseudomonas aeruginosa in 24 h static time kills and in 7-day hollow fibre infection model.
Results: PYO2 single-bolus administration achieved a bacterial log reduction of 6.82 log10 cfu/mL, with eradication at 4 h. Dual-phage therapy (LUZ19 + PYO2) achieved a bacterial log reduction of 6.81 log10 cfu/mL, with delayed eradication at 12 h.
Conclusions: This highlights the potential of reverse translational pharmacokinetic/pharmacodynamic-driven approaches to guide rational phage selection strategies against individual clinical isolates while identifying potential antagonistic phage-phage interactions.
{"title":"Pharmacodynamic individualization of phage therapy against a KPC-5-producing <i>Pseudomonas aeruginosa</i>.","authors":"Thomas D Nguyen, Jacob T Sanborn, Brian M Ho, Tiffany Luong, Troy D Wood, Liang Chen, Dwayne R Roach, Nicholas M Smith","doi":"10.1093/jacamr/dlaf257","DOIUrl":"10.1093/jacamr/dlaf257","url":null,"abstract":"<p><strong>Background: </strong>There is a resurgence of interest in bacteriophage (phage) therapy as antimicrobials, resulting from growing antimicrobial resistance to small-molecule antibiotics. Phages are bacterial viruses long studied, but there is a need for high resolution and systematic assessment of clinical dosing strategies for phages to better inform therapy.</p><p><strong>Methods: </strong>We hypothesized that empirical <i>in vitro</i> assessment of clinically relevant phages facilitates pharmacodynamic-driven individualization. Three clinically relevant phage strains (LUZ19, PYO2 and E215) were evaluated as mono- or dual-phage therapy against a clinical <i>Pseudomonas aeruginosa</i> in 24 h static time kills and in 7-day hollow fibre infection model.</p><p><strong>Results: </strong>PYO2 single-bolus administration achieved a bacterial log reduction of 6.82 log<sub>10</sub> cfu/mL, with eradication at 4 h. Dual-phage therapy (LUZ19 + PYO2) achieved a bacterial log reduction of 6.81 log<sub>10</sub> cfu/mL, with delayed eradication at 12 h.</p><p><strong>Conclusions: </strong>This highlights the potential of reverse translational pharmacokinetic/pharmacodynamic-driven approaches to guide rational phage selection strategies against individual clinical isolates while identifying potential antagonistic phage-phage interactions.</p>","PeriodicalId":14594,"journal":{"name":"JAC-Antimicrobial Resistance","volume":"8 1","pages":"dlaf257"},"PeriodicalIF":3.3,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12776353/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145933331","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-07eCollection Date: 2026-02-01DOI: 10.1093/jacamr/dlaf254
Suhanya Prasad, Barbora Dratvova, Anezka Gryndlerova, Marie Brajerova, Petra Kabelikova, Jan Tkadlec, Pavel Drevinek, Marcela Krutova
Background: Increasing resistance to broad-spectrum beta-lactams and carbapenems is a significant concern in healthcare settings. This study aimed to determine the prevalence of intestinal carriage of extended-spectrum β-lactamase (ESBL)-producing and carbapenem-resistant Enterobacterales (CRE) in a tertiary care hospital and to evaluate the utility of long-read sequencing for carbapenem resistance surveillance.
Methods: In 2021, stool samples (n = 538) and rectal swabs (n = 256) from hospitalized patients were cultured after enrichment on selective chromogenic medium to detect ESBL and CRE carriage. CRE isolates were characterized by antimicrobial susceptibility testing and whole-genome sequencing.
Results: Among 794 patient samples, 239 (30%) Enterobacterales isolates grew on ESBL media. On CRE agar, 28 Enterobacterales were cultured, 27 confirmed carbapenem-resistant and identified as Klebsiella pneumoniae (n = 25), Escherichia coli (n = 1), and Enterobacter cloacae (n = 1). In CRE, 29.6% (8/27) were carbapenemase-producing Enterobacterales (CPE), carrying the blaOXA-48 (n = 7) or blaNDM-1 (n = 1) genes. The remaining 70.4% (19/27) were non-carbapenemase-producing CRE isolates (non-CP-CRE). The blaOXA-48 gene was localized on identical IncL plasmids with an inverted Tn1999.2 transposon in non-clonally related isolates. CPE isolates exhibited distinct resistance patterns to carbapenems, β-lactam/β-lactamase inhibitor combinations, with 87.5% resistant to cefiderocol. All non-CP-CRE isolates remained susceptible to imipenem; two were resistant to meropenem and carried either five or six copies of the blaCTX-M-15 gene along with mutations in porin genes.
Conclusions: A 30% prevalence of intestinal carriage of ESBL-producing Enterobacterales and a 3.4% carriage prevalence of CRE were found. Long-read sequencing revealed IncL plasmid-mediated dissemination of OXA-48 β-lactamase and blaCTX-M-15 gene amplification, demonstrating its added value for antimicrobial resistance monitoring.
{"title":"IncL plasmid-mediated dissemination of OXA-48 β-lactamase and <i>bla</i> <sub>CTX-M-15</sub> gene amplification identified <i>via</i> long-read sequencing in carbapenem-resistant Enterobacterales.","authors":"Suhanya Prasad, Barbora Dratvova, Anezka Gryndlerova, Marie Brajerova, Petra Kabelikova, Jan Tkadlec, Pavel Drevinek, Marcela Krutova","doi":"10.1093/jacamr/dlaf254","DOIUrl":"10.1093/jacamr/dlaf254","url":null,"abstract":"<p><strong>Background: </strong>Increasing resistance to broad-spectrum beta-lactams and carbapenems is a significant concern in healthcare settings. This study aimed to determine the prevalence of intestinal carriage of extended-spectrum β-lactamase (ESBL)-producing and carbapenem-resistant Enterobacterales (CRE) in a tertiary care hospital and to evaluate the utility of long-read sequencing for carbapenem resistance surveillance.</p><p><strong>Methods: </strong>In 2021, stool samples (<i>n</i> = 538) and rectal swabs (<i>n</i> = 256) from hospitalized patients were cultured after enrichment on selective chromogenic medium to detect ESBL and CRE carriage. CRE isolates were characterized by antimicrobial susceptibility testing and whole-genome sequencing.</p><p><strong>Results: </strong>Among 794 patient samples, 239 (30%) Enterobacterales isolates grew on ESBL media. On CRE agar, 28 Enterobacterales were cultured, 27 confirmed carbapenem-resistant and identified as <i>Klebsiella pneumoniae</i> (<i>n</i> = 25), <i>Escherichia coli</i> (<i>n</i> = 1), and <i>Enterobacter cloacae</i> (<i>n</i> = 1). In CRE, 29.6% (8/27) were carbapenemase-producing Enterobacterales (CPE), carrying the <i>bla</i> <sub>OXA-48</sub> (<i>n</i> = 7) or <i>bla</i> <sub>NDM-1</sub> (<i>n</i> = 1) genes. The remaining 70.4% (19/27) were non-carbapenemase-producing CRE isolates (non-CP-CRE). The <i>bla</i> <sub>OXA-48</sub> gene was localized on identical IncL plasmids with an inverted Tn<i>1999.2</i> transposon in non-clonally related isolates. CPE isolates exhibited distinct resistance patterns to carbapenems, β-lactam/β-lactamase inhibitor combinations, with 87.5% resistant to cefiderocol. All non-CP-CRE isolates remained susceptible to imipenem; two were resistant to meropenem and carried either five or six copies of the <i>bla</i> <sub>CTX-M-15</sub> gene along with mutations in porin genes.</p><p><strong>Conclusions: </strong>A 30% prevalence of intestinal carriage of ESBL-producing Enterobacterales and a 3.4% carriage prevalence of CRE were found. Long-read sequencing revealed IncL plasmid-mediated dissemination of OXA-48 β-lactamase and <i>bla</i> <sub>CTX-M-15</sub> gene amplification, demonstrating its added value for antimicrobial resistance monitoring.</p>","PeriodicalId":14594,"journal":{"name":"JAC-Antimicrobial Resistance","volume":"8 1","pages":"dlaf254"},"PeriodicalIF":3.3,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12776359/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145933351","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-07eCollection Date: 2026-02-01DOI: 10.1093/jacamr/dlaf228
C Roleston, M Wanat, F Mowbray, J Underhill, M Wilcock, S Jacklin, J Amos, K B Bamford, S Hughes, N Marsh, S Tonkin-Crine, N Powell
Background: Shared decision making (SDM) is a collaborative process between patients and prescribers and identified as a strategy to support antimicrobial stewardship. SDM can improve patient and clinician satisfaction and reduce antibiotic prescribing. However, little is known about how to implement antibiotic SDM in secondary care.
Objectives: Identify opportunities for antibiotic SDM between patients and clinicians in secondary care.
Methods: Semi-structured interviews were conducted with senior decision makers (registrar or consultant grade) and adult patients who had received antibiotics during their medical or surgical admission, recruited from three secondary care Trusts in England. Interviews explored participants' views on opportunities for SDM when prescribing antibiotics in secondary care, guided by the 'Start Smart, Then Focus' framework. Interviews were audio recorded, transcribed verbatim and analysed thematically.
Results: 18 clinicians and 20 patients were interviewed. Two themes were identified. In 'Pushing back against SDM', participants challenged the amenability and prioritization of SDM for antibiotics in inpatient settings, related to clinicians being seen as main decision makers, with patients not seeking further involvement. This was reinforced by the perceived urgency of treatment, the fast-paced hospital environment, and the view that antibiotic decisions were either too complex or too straightforward to invite shared input. In 'If not SDM, then what?', participants endorsed bi-directional communication and information provision as alternative priorities, highlighting its value.
Conclusions: SDM was not well understood or endorsed for antibiotic prescribing decision making in secondary care. Further work is warranted to educate and upskill clinicians in SDM as a concept within secondary care.
{"title":"Patient and clinician views on inpatient antibiotic shared decision-making: a qualitative study.","authors":"C Roleston, M Wanat, F Mowbray, J Underhill, M Wilcock, S Jacklin, J Amos, K B Bamford, S Hughes, N Marsh, S Tonkin-Crine, N Powell","doi":"10.1093/jacamr/dlaf228","DOIUrl":"10.1093/jacamr/dlaf228","url":null,"abstract":"<p><strong>Background: </strong>Shared decision making (SDM) is a collaborative process between patients and prescribers and identified as a strategy to support antimicrobial stewardship. SDM can improve patient and clinician satisfaction and reduce antibiotic prescribing. However, little is known about how to implement antibiotic SDM in secondary care.</p><p><strong>Objectives: </strong>Identify opportunities for antibiotic SDM between patients and clinicians in secondary care.</p><p><strong>Methods: </strong>Semi-structured interviews were conducted with senior decision makers (registrar or consultant grade) and adult patients who had received antibiotics during their medical or surgical admission, recruited from three secondary care Trusts in England. Interviews explored participants' views on opportunities for SDM when prescribing antibiotics in secondary care, guided by the 'Start Smart, Then Focus' framework. Interviews were audio recorded, transcribed verbatim and analysed thematically.</p><p><strong>Results: </strong>18 clinicians and 20 patients were interviewed. Two themes were identified. In 'Pushing back against SDM', participants challenged the amenability and prioritization of SDM for antibiotics in inpatient settings, related to clinicians being seen as main decision makers, with patients not seeking further involvement. This was reinforced by the perceived urgency of treatment, the fast-paced hospital environment, and the view that antibiotic decisions were either too complex or too straightforward to invite shared input. In 'If not SDM, then what?', participants endorsed bi-directional communication and information provision as alternative priorities, highlighting its value.</p><p><strong>Conclusions: </strong>SDM was not well understood or endorsed for antibiotic prescribing decision making in secondary care. Further work is warranted to educate and upskill clinicians in SDM as a concept within secondary care.</p>","PeriodicalId":14594,"journal":{"name":"JAC-Antimicrobial Resistance","volume":"8 1","pages":"dlaf228"},"PeriodicalIF":3.3,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12775835/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145933348","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-07eCollection Date: 2026-02-01DOI: 10.1093/jacamr/dlaf250
Emilien Lecomte, Martin Arys, Antoine Christiaens, Louise Doyen, Jean-Christophe Marot, Valérie Verbelen, Grégoire Wieërs
Background: Acute bacterial prostatitis (ABP) is a complicated urinary tract infection (UTI) requiring timely and appropriate antibiotic therapy. Because of growing concern over fluoroquinolone resistance, second-generation cephalosporins such as cefuroxime may offer a viable alternative.
Objectives: This study evaluates the use of cefuroxime as an empirical first-line intravenous treatment in hospitalized patients with ABP and compares outcomes following various oral antibiotic step-down regimens.
Methods: We conducted a single-centre retrospective cohort study at Clinique Saint-Pierre Ottignies, Belgium, including male patients ≥18 years diagnosed with ABP and treated empirically with intravenous cefuroxime between January 2019 and December 2023. Patients were grouped based on their oral antibiotic step-down therapy (cefuroxime, ciprofloxacin, trimethoprim-sulfamethoxazole or amoxicillin). The primary outcomes were bacterial failure and clinical recurrence within 6 months.
Results: Of 148 patients screened, 88 met inclusion criteria. No relapses were reported. Escherichia coli was the predominant pathogen (49/88); 100% were cefuroxime-susceptible, while four were fluoroquinolone-resistant. Among non-E. coli isolates, resistance to cefuroxime was significantly higher (OR 8.5, P = 0.003).
Conclusions: Empirical intravenous cefuroxime followed by oral step-down appears safe and effective for ABP, especially in the absence of known risk factors for resistant pathogens. These findings support fluoroquinolone-sparing approaches in empiric UTI management, tailored to local microbiological profiles and individual comorbidities.
背景:急性细菌性前列腺炎(ABP)是一种复杂的尿路感染(UTI),需要及时、适当的抗生素治疗。由于对氟喹诺酮类药物耐药性的关注日益增加,第二代头孢菌素如头孢呋辛可能提供一种可行的替代方案。目的:本研究评估头孢呋辛作为ABP住院患者的一线静脉治疗经验,并比较各种口服抗生素降压方案的结果。方法:我们在比利时Saint-Pierre Ottignies诊所进行了一项单中心回顾性队列研究,纳入了2019年1月至2023年12月期间诊断为ABP并经验性静脉注射头孢呋辛的男性患者,年龄≥18岁。患者根据口服抗生素降压治疗(头孢呋辛、环丙沙星、甲氧苄氨嘧啶-磺胺甲恶唑或阿莫西林)进行分组。主要结果为细菌治疗失败和6个月内临床复发。结果:148例患者中,88例符合纳入标准。无复发报告。大肠杆菌为优势致病菌(49/88);100%头孢呋辛敏感,4例氟喹诺酮耐药。non-E之一。大肠杆菌分离株对头孢呋辛的耐药性显著高于其他菌株(OR 8.5, P = 0.003)。结论:经验性静脉注射头孢呋辛后口服降压治疗ABP安全有效,特别是在缺乏已知耐药病原体危险因素的情况下。这些发现支持在经验性尿路感染管理中使用氟喹诺酮类药物,根据当地微生物情况和个体合并症量身定制。
{"title":"Prioritizing cefuroxime as empirical treatment in acute bacterial prostatitis: patient characteristics and outcome.","authors":"Emilien Lecomte, Martin Arys, Antoine Christiaens, Louise Doyen, Jean-Christophe Marot, Valérie Verbelen, Grégoire Wieërs","doi":"10.1093/jacamr/dlaf250","DOIUrl":"10.1093/jacamr/dlaf250","url":null,"abstract":"<p><strong>Background: </strong>Acute bacterial prostatitis (ABP) is a complicated urinary tract infection (UTI) requiring timely and appropriate antibiotic therapy. Because of growing concern over fluoroquinolone resistance, second-generation cephalosporins such as cefuroxime may offer a viable alternative.</p><p><strong>Objectives: </strong>This study evaluates the use of cefuroxime as an empirical first-line intravenous treatment in hospitalized patients with ABP and compares outcomes following various oral antibiotic step-down regimens.</p><p><strong>Methods: </strong>We conducted a single-centre retrospective cohort study at Clinique Saint-Pierre Ottignies, Belgium, including male patients ≥18 years diagnosed with ABP and treated empirically with intravenous cefuroxime between January 2019 and December 2023. Patients were grouped based on their oral antibiotic step-down therapy (cefuroxime, ciprofloxacin, trimethoprim-sulfamethoxazole or amoxicillin). The primary outcomes were bacterial failure and clinical recurrence within 6 months.</p><p><strong>Results: </strong>Of 148 patients screened, 88 met inclusion criteria. No relapses were reported. <i>Escherichia coli</i> was the predominant pathogen (49/88); 100% were cefuroxime-susceptible, while four were fluoroquinolone-resistant. Among non-<i>E. coli</i> isolates, resistance to cefuroxime was significantly higher (OR 8.5, <i>P</i> = 0.003).</p><p><strong>Conclusions: </strong>Empirical intravenous cefuroxime followed by oral step-down appears safe and effective for ABP, especially in the absence of known risk factors for resistant pathogens. These findings support fluoroquinolone-sparing approaches in empiric UTI management, tailored to local microbiological profiles and individual comorbidities.</p>","PeriodicalId":14594,"journal":{"name":"JAC-Antimicrobial Resistance","volume":"8 1","pages":"dlaf250"},"PeriodicalIF":3.3,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12776341/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145933336","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-07eCollection Date: 2026-02-01DOI: 10.1093/jacamr/dlaf249
Justin A Ellem, Mitchell J Brown, Indy Sandaradura, Brian P McSharry, Thiru Vanniasinkam
Objectives: One of the biggest challenges for healthcare providers is the difficulty with screening for carbapenemase-producing, carbapenem-resistant Pseudomonas aeruginosa (CP-CRPa; P. aeruginosa), given the variety of mechanisms that can mediate carbapenem resistance in P. aeruginosa. We sought to develop an improved algorithm to screen for carbapenemase activity in P. aeruginosa using routine antimicrobial susceptibility testing readily available in most clinical microbiology laboratories.
Methods: Antibiograms of a reference set of P. aeruginosa (n = 100) with diverse phenotypic and genotypic profiles were compared to determine which antibiotics optimally screen for and differentiate CP-CRPa from CRPa and non-CRPa. The developed algorithm was then applied to 1482 clinical P. aeruginosa isolates. Carbapenemase PCR and the modified carbapenem inactivation method were performed on all meropenem-resistant P. aeruginosa isolates.
Results: The CP-CRPa screening algorithm developed here uses meropenem, ceftazidime and tobramycin. Carbapenem resistance was identified in 85 (5.7%) isolates, of which 26 (1.8%) were confirmed as CP-CRPa. blaGES (57.7%) was the predominant carbapenemase detected, whilst blaNDM, blaVIM, blaIMP and blaKPC carbapenemases were also detected. The CP-CRPa screening algorithm was 100% sensitive (CI95% 84.0%-100%) and 96.6% specific (CI95% 87.3%-99.4%).
Conclusions: We present an antimicrobial susceptibility testing-based screening algorithm that uses meropenem, ceftazidime, and tobramycin to screen for CP-CRPa. When appropriate screening criteria are utilized, confirmatory testing can be significantly reduced, resulting in substantial time and resource savings, without compromising sensitivity, particularly in settings with varying carbapenemase epidemiology.
目的:医疗保健提供者面临的最大挑战之一是难以筛选产生碳青霉烯酶、耐碳青霉烯的铜绿假单胞菌(CP-CRPa; P. aeruginosa),因为铜绿假单胞菌可以介导碳青霉烯耐药性的多种机制。我们试图开发一种改进的算法,以筛选碳青霉烯酶活性的铜绿假单胞菌使用常规的抗菌药敏试验容易在大多数临床微生物实验室。方法:比较不同表型和基因型的铜绿假单胞菌(P. aeruginosa, n = 100)的抗生素谱,以确定哪种抗生素最适合筛选和区分CP-CRPa与CRPa和非CRPa。将该算法应用于临床分离的1482株铜绿假单胞菌。采用碳青霉烯酶PCR和改良的碳青霉烯灭活方法对所有耐美罗培烯铜绿假单胞菌进行检测。结果:本文建立的CP-CRPa筛选算法使用美罗培南、头孢他啶和妥布霉素。85株(5.7%)对碳青霉烯类耐药,其中26株(1.8%)为CP-CRPa。检测到的碳青霉烯酶主要为bla GES(57.7%),同时检测到bla NDM、bla VIM、bla IMP和bla KPC碳青霉烯酶。CP-CRPa筛选算法的敏感性为100% (CI95% 84.0% ~ 100%),特异性为96.6% (CI95% 87.3% ~ 99.4%)。结论:我们提出了一种基于抗菌药敏试验的筛选算法,使用美罗培南、头孢他啶和妥布霉素筛选CP-CRPa。当使用适当的筛选标准时,确认性测试可以显著减少,从而节省大量时间和资源,而不影响敏感性,特别是在碳青霉烯酶流行病学不同的环境中。
{"title":"An improved algorithm to screen for carbapenemase production in <i>Pseudomonas aeruginosa</i>.","authors":"Justin A Ellem, Mitchell J Brown, Indy Sandaradura, Brian P McSharry, Thiru Vanniasinkam","doi":"10.1093/jacamr/dlaf249","DOIUrl":"10.1093/jacamr/dlaf249","url":null,"abstract":"<p><strong>Objectives: </strong>One of the biggest challenges for healthcare providers is the difficulty with screening for carbapenemase-producing, carbapenem-resistant <i>Pseudomonas aeruginosa</i> (CP-CRPa; <i>P. aeruginosa</i>), given the variety of mechanisms that can mediate carbapenem resistance in <i>P. aeruginosa</i>. We sought to develop an improved algorithm to screen for carbapenemase activity in <i>P. aeruginosa</i> using routine antimicrobial susceptibility testing readily available in most clinical microbiology laboratories.</p><p><strong>Methods: </strong>Antibiograms of a reference set of <i>P. aeruginosa</i> (<i>n</i> = 100) with diverse phenotypic and genotypic profiles were compared to determine which antibiotics optimally screen for and differentiate CP-CRPa from CRPa and non-CRPa. The developed algorithm was then applied to 1482 clinical <i>P. aeruginosa</i> isolates. Carbapenemase PCR and the modified carbapenem inactivation method were performed on all meropenem-resistant <i>P. aeruginosa</i> isolates.</p><p><strong>Results: </strong>The CP-CRPa screening algorithm developed here uses meropenem, ceftazidime and tobramycin. Carbapenem resistance was identified in 85 (5.7%) isolates, of which 26 (1.8%) were confirmed as CP-CRPa. <i>bla</i> <sub>GES</sub> (57.7%) was the predominant carbapenemase detected, whilst <i>bla</i> <sub>NDM</sub>, <i>bla</i> <sub>VIM</sub>, <i>bla</i> <sub>IMP</sub> and <i>bla</i> <sub>KPC</sub> carbapenemases were also detected. The CP-CRPa screening algorithm was 100% sensitive (CI<sub>95%</sub> 84.0%-100%) and 96.6% specific (CI<sub>95%</sub> 87.3%-99.4%).</p><p><strong>Conclusions: </strong>We present an antimicrobial susceptibility testing-based screening algorithm that uses meropenem, ceftazidime, and tobramycin to screen for CP-CRPa. When appropriate screening criteria are utilized, confirmatory testing can be significantly reduced, resulting in substantial time and resource savings, without compromising sensitivity, particularly in settings with varying carbapenemase epidemiology.</p>","PeriodicalId":14594,"journal":{"name":"JAC-Antimicrobial Resistance","volume":"8 1","pages":"dlaf249"},"PeriodicalIF":3.3,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12776346/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145933196","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-07eCollection Date: 2026-02-01DOI: 10.1093/jacamr/dlaf245
Simonne Weeks, Aaron Drovandi, Rebecca Turner, Frances Garraghan, Robert Shorten, Lucie Byrne-Davis, Jo Hart
Background and objective: Antimicrobial resistance (AMR) is a global health challenge driven by inappropriate prescribing. Antimicrobial stewardship (AMS) education during undergraduate training is important to prepare future healthcare professionals for responsible prescribing, yet provision remains inconsistent across disciplines. To systematically review AMS educational interventions for undergraduate medical, pharmacy, nursing, dental, veterinary and midwifery students, and evaluate the behavioural coverage using the COM-B framework.
Methods: A protocol was registered on PROSPERO (CRD420250655653). Six databases were searched on 4 February 2025. Eligible studies evaluated AMS educational interventions for undergraduate students. Data were independently extracted in duplicate, methodological quality appraised using Medical Education Research Study Quality Instrument (MERSQI) and findings were synthesized narratively using COM-B.
Results: Of 7771 records screened, 42 studies were included, involving 8567 students across six continents. Most were single-group pre-/post-designs, with two randomized controlled trials. All studies addressed psychological capability, mainly by increasing knowledge and reasoning, while reflective motivation was supported in 25/42. Physical opportunity (20/42) and social opportunity (18/42) were less frequent, typically via structured cases or teamwork. Physical capability (9/42) and automatic motivation (2/42) were least represented, usually through simulation, supervised practice or affective engagement. MERSQI scores indicated moderate methodological quality overall.
Conclusions: Undergraduate AMS education is widespread but uneven in its coverage, with emphasis on knowledge and limited attention to skills, opportunities and motivation. Applying COM-B highlights the need for curricula to combine knowledge with rehearsal, authentic resources, teamwork, identity development and positive engagement to prepare graduates for stewardship practice.
{"title":"A systematic review of antimicrobial stewardship education for undergraduate students in medicine, nursing, pharmacy, dentistry, veterinary science and midwifery using COM-B framework.","authors":"Simonne Weeks, Aaron Drovandi, Rebecca Turner, Frances Garraghan, Robert Shorten, Lucie Byrne-Davis, Jo Hart","doi":"10.1093/jacamr/dlaf245","DOIUrl":"10.1093/jacamr/dlaf245","url":null,"abstract":"<p><strong>Background and objective: </strong>Antimicrobial resistance (AMR) is a global health challenge driven by inappropriate prescribing. Antimicrobial stewardship (AMS) education during undergraduate training is important to prepare future healthcare professionals for responsible prescribing, yet provision remains inconsistent across disciplines. To systematically review AMS educational interventions for undergraduate medical, pharmacy, nursing, dental, veterinary and midwifery students, and evaluate the behavioural coverage using the COM-B framework.</p><p><strong>Methods: </strong>A protocol was registered on PROSPERO (CRD420250655653). Six databases were searched on 4 February 2025. Eligible studies evaluated AMS educational interventions for undergraduate students. Data were independently extracted in duplicate, methodological quality appraised using Medical Education Research Study Quality Instrument (MERSQI) and findings were synthesized narratively using COM-B.</p><p><strong>Results: </strong>Of 7771 records screened, 42 studies were included, involving 8567 students across six continents. Most were single-group pre-/post-designs, with two randomized controlled trials. All studies addressed psychological capability, mainly by increasing knowledge and reasoning, while reflective motivation was supported in 25/42. Physical opportunity (20/42) and social opportunity (18/42) were less frequent, typically via structured cases or teamwork. Physical capability (9/42) and automatic motivation (2/42) were least represented, usually through simulation, supervised practice or affective engagement. MERSQI scores indicated moderate methodological quality overall.</p><p><strong>Conclusions: </strong>Undergraduate AMS education is widespread but uneven in its coverage, with emphasis on knowledge and limited attention to skills, opportunities and motivation. Applying COM-B highlights the need for curricula to combine knowledge with rehearsal, authentic resources, teamwork, identity development and positive engagement to prepare graduates for stewardship practice.</p>","PeriodicalId":14594,"journal":{"name":"JAC-Antimicrobial Resistance","volume":"8 1","pages":"dlaf245"},"PeriodicalIF":3.3,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12776017/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145933245","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}