Pub Date : 2025-12-13DOI: 10.1016/j.jhin.2025.12.002
O O Demir, S Icoz, K Aykac, S Kesici, Y Ozsurekci
{"title":"Nurse-led ventilator stewardship and bundle reliability to prevent paediatric VAP.","authors":"O O Demir, S Icoz, K Aykac, S Kesici, Y Ozsurekci","doi":"10.1016/j.jhin.2025.12.002","DOIUrl":"10.1016/j.jhin.2025.12.002","url":null,"abstract":"","PeriodicalId":54806,"journal":{"name":"Journal of Hospital Infection","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145764560","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-13DOI: 10.1016/j.jhin.2025.12.001
P A Jumaa, L Teare, P N Hoffman, S Smailes, V Edwards-Jones, C Thomas, L S P Moore, S Booth, M A Mugglestone, N S Moiemen
{"title":"Response to Marek et al.: is negative pressure for burns care the best approach?","authors":"P A Jumaa, L Teare, P N Hoffman, S Smailes, V Edwards-Jones, C Thomas, L S P Moore, S Booth, M A Mugglestone, N S Moiemen","doi":"10.1016/j.jhin.2025.12.001","DOIUrl":"10.1016/j.jhin.2025.12.001","url":null,"abstract":"","PeriodicalId":54806,"journal":{"name":"Journal of Hospital Infection","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145764595","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-12DOI: 10.1016/j.jhin.2025.09.025
C Elias, S Rasoanandrasana, A H Raherinandrasana, V Andriananja, P Razanakolona, M Randria, M Raberahona, L Raskine, P Vanhems, F-X Babin
Objectives: The overuse of antibiotics is a primary driver of resistance development, particularly in low-resource settings such as Madagascar where broad-spectrum antibiotic use is excessive. The objective was to identify factors that could influence changes to the initial antibiotic regimen upon receipt of the microbiological results in Malagasy hospitals.
Methods: This study was part of the TSARA antibiotic resistance surveillance system implemented in eight hospitals in Madagascar belonging to the RESAMAD (Réseau des Laboratoires à Madagascar) network. The outcome was the change in the spectrum or the discontinuation of the empiric antibiotic regimen upon receiving the laboratory results.
Results: Across the eight participating hospitals, 793 patients were included and the majority of the antibiotic regimens were broad-spectrum (78.8%) which were prescribed in 208 (99.1%) of 210 blood samples. Third-generation cephalosporins were most common (441, 32.1%), with ceftriaxone being the most frequently used antibiotic (421, 30.6%). Upon the receipt of the laboratory results, 21 (2.6%) patients had their empiric antibiotic therapy changed and 530 (66.8%) stopped. A total of 269 (33.9%) patients had positive cultures, with 105 (13.3%) infected by multi-drug-resistant bacteria - primarily third-generation cephalosporin-resistant Enterobacterales. The use of ≥3 empiric antibiotics mainly ceftriaxone, gentamicin, and metronidazole, increased the likelihood of discontinuation (adjusted odds ratio (aOR) = 2.85, P<0.001). Conversely, the availability of antibiotics susceptibility test results decreased the odds of antibiotic discontinuation (aOR = 0.37, P=0.004).
Conclusion: This study based in the TSARA surveillance system in Madagascar highlights the influence of clinical factors and microbiological data on antibiotic therapy adjustments. Broad-spectrum antibiotics were widely used as empiric treatment. Availability of the microbiological results decreased the odds of antibiotic discontinuation.
{"title":"Determinants of the change in empiric antibiotic therapy upon receipt of microbiological data: results from a nationwide antibiotic resistance and use surveillance programme in Madagascar, the TSARA project.","authors":"C Elias, S Rasoanandrasana, A H Raherinandrasana, V Andriananja, P Razanakolona, M Randria, M Raberahona, L Raskine, P Vanhems, F-X Babin","doi":"10.1016/j.jhin.2025.09.025","DOIUrl":"https://doi.org/10.1016/j.jhin.2025.09.025","url":null,"abstract":"<p><strong>Objectives: </strong>The overuse of antibiotics is a primary driver of resistance development, particularly in low-resource settings such as Madagascar where broad-spectrum antibiotic use is excessive. The objective was to identify factors that could influence changes to the initial antibiotic regimen upon receipt of the microbiological results in Malagasy hospitals.</p><p><strong>Methods: </strong>This study was part of the TSARA antibiotic resistance surveillance system implemented in eight hospitals in Madagascar belonging to the RESAMAD (Réseau des Laboratoires à Madagascar) network. The outcome was the change in the spectrum or the discontinuation of the empiric antibiotic regimen upon receiving the laboratory results.</p><p><strong>Results: </strong>Across the eight participating hospitals, 793 patients were included and the majority of the antibiotic regimens were broad-spectrum (78.8%) which were prescribed in 208 (99.1%) of 210 blood samples. Third-generation cephalosporins were most common (441, 32.1%), with ceftriaxone being the most frequently used antibiotic (421, 30.6%). Upon the receipt of the laboratory results, 21 (2.6%) patients had their empiric antibiotic therapy changed and 530 (66.8%) stopped. A total of 269 (33.9%) patients had positive cultures, with 105 (13.3%) infected by multi-drug-resistant bacteria - primarily third-generation cephalosporin-resistant Enterobacterales. The use of ≥3 empiric antibiotics mainly ceftriaxone, gentamicin, and metronidazole, increased the likelihood of discontinuation (adjusted odds ratio (aOR) = 2.85, P<0.001). Conversely, the availability of antibiotics susceptibility test results decreased the odds of antibiotic discontinuation (aOR = 0.37, P=0.004).</p><p><strong>Conclusion: </strong>This study based in the TSARA surveillance system in Madagascar highlights the influence of clinical factors and microbiological data on antibiotic therapy adjustments. Broad-spectrum antibiotics were widely used as empiric treatment. Availability of the microbiological results decreased the odds of antibiotic discontinuation.</p>","PeriodicalId":54806,"journal":{"name":"Journal of Hospital Infection","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2025-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145752396","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-09DOI: 10.1016/j.jhin.2025.11.043
X. Ji , P. Jin , Z. Zhang , M.O. Aung , S.J.M. Ong , H.X. Toh , L.C. Lee , K.Y. Tan , M.K.B. How , J.H. Seah , B.S. Ismail , I. Venkatachalam , D.C.M. Lai , M.L. Ling
Background
Whilst insertion and maintenance bundles serve as essential preventive measures for central line-associated bloodstream infections (CLABSIs), the efficacy of enhanced strategies such as chlorhexidine-impregnated dressings and alcohol-impregnated port protectors remains relatively unexplored on a hospital-wide scale. This study evaluates the impact of implementing 2% chlorhexidine gluconate-impregnated (CHG) dressings and 70% isopropyl alcohol-impregnated (IPA) port protectors in reducing CLABSI risks across a 1900-bed academic medical centre in Singapore.
Methods
Singapore General Hospital introduced CHG dressings in July 2020 and expanded their use hospital wide in January 2021. Additionally, IPA port protectors were implemented hospital wide in September 2021. The incidence rates of CLABSI per 1000 central line (CL)-days were monitored to evaluate outcomes.
Results
From November 2017 to January 2020 (baseline period), the CLABSI incidence rate was 0.81 per 1000 CL-days. For the period February 2021 to September 2021, prior to the implementation of IPA port protectors, the rate decreased to 0.53 per 1000 CL-days (incidence rate ratio (IRR) 0.61 (95% confidence interval (CI) 0.37–0.98); P=0.073). The rate further declined to 0.45 per 1000 CL-days from October 2021 to December 2024 (post-implementation of both strategies), representing a statistically significant reduction (IRR 0.53 (95% CI 0.40–0.71); P<0.001). The combined strategy of CHG dressings and IPA port protectors potentially reduced the risk of CLABSIs by 47%.
Conclusion
Our experience demonstrated a statistically significant reduction in CLABSI rates following the 3-year implementation of CHG dressings and IPA port protectors as part of routine hospital-wide preventive measures against CLABSI.
{"title":"Enhancing central-line-associated bloodstream infection prevention: evaluating enhanced strategies in an academic medical centre in Singapore","authors":"X. Ji , P. Jin , Z. Zhang , M.O. Aung , S.J.M. Ong , H.X. Toh , L.C. Lee , K.Y. Tan , M.K.B. How , J.H. Seah , B.S. Ismail , I. Venkatachalam , D.C.M. Lai , M.L. Ling","doi":"10.1016/j.jhin.2025.11.043","DOIUrl":"10.1016/j.jhin.2025.11.043","url":null,"abstract":"<div><h3>Background</h3><div>Whilst insertion and maintenance bundles serve as essential preventive measures for central line-associated bloodstream infections (CLABSIs), the efficacy of enhanced strategies such as chlorhexidine-impregnated dressings and alcohol-impregnated port protectors remains relatively unexplored on a hospital-wide scale. This study evaluates the impact of implementing 2% chlorhexidine gluconate-impregnated (CHG) dressings and 70% isopropyl alcohol-impregnated (IPA) port protectors in reducing CLABSI risks across a 1900-bed academic medical centre in Singapore.</div></div><div><h3>Methods</h3><div>Singapore General Hospital introduced CHG dressings in July 2020 and expanded their use hospital wide in January 2021. Additionally, IPA port protectors were implemented hospital wide in September 2021. The incidence rates of CLABSI per 1000 central line (CL)-days were monitored to evaluate outcomes.</div></div><div><h3>Results</h3><div>From November 2017 to January 2020 (baseline period), the CLABSI incidence rate was 0.81 per 1000 CL-days. For the period February 2021 to September 2021, prior to the implementation of IPA port protectors, the rate decreased to 0.53 per 1000 CL-days (incidence rate ratio (IRR) 0.61 (95% confidence interval (CI) 0.37–0.98); <em>P</em>=0.073). The rate further declined to 0.45 per 1000 CL-days from October 2021 to December 2024 (post-implementation of both strategies), representing a statistically significant reduction (IRR 0.53 (95% CI 0.40–0.71); <em>P</em><0.001). The combined strategy of CHG dressings and IPA port protectors potentially reduced the risk of CLABSIs by 47%.</div></div><div><h3>Conclusion</h3><div>Our experience demonstrated a statistically significant reduction in CLABSI rates following the 3-year implementation of CHG dressings and IPA port protectors as part of routine hospital-wide preventive measures against CLABSI.</div></div>","PeriodicalId":54806,"journal":{"name":"Journal of Hospital Infection","volume":"168 ","pages":"Pages 121-128"},"PeriodicalIF":3.1,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145745798","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-05DOI: 10.1016/j.jhin.2025.11.044
C. Dinh , A. Hennebique , M. Veloso , N. Gonnet , I. Pelloux , S. David-Tchouda , C. Landelle , S. Boisset
Background
The rapid detection of carriers of emerging extensively drug-resistant bacteria (eXDR), notably carbapenemase-producing organisms (CPOs) and vancomycin-resistant Enterococci, is crucial for controlling their spread and preventing infections.
Aim
To evaluate the impact of polymerase chain reaction (PCR) on turnaround time (TAT) for eXDR detection compared to culture methods under routine laboratory conditions, excluding night or weekend analyses.
Methods
A prospective before-and-after study was conducted at a French university hospital. Phase 1 (culture) occurred from February to September 2022, phase 2 (PCR) from September 2022 to March 2023. TAT was defined as the time from sample collection to result delivery to the infection control team and/or physician. Patients aged >18 years meeting specific screening criteria were included. Two PCR kits were utilized: the BD MAX Check-Points CPO kit and the VIASURE Vancomycin resistance Real Time PCR Detection Kit.
Findings
A total of 2049 and 1861 patients were included in phases 1 and 2, respectively. Sixteen patients tested eXDR positive for the first time in phase 1, and 25 in phase 2. The median TAT was significantly shorter in phase 2 (22.7 h; 16.0–41.3) compared to phase 1 (43.5 h; 31.9–69.7; P = 0.001). A significant decrease in the median number of contact patients was observed in phase 2 compared to phase 1. The number of total screening test secondary cases and the hospitalization costs were comparable regardless of the eXDR detection method.
Conclusion
Rapid rectal screening using PCR significantly reduces TAT for results in low-endemic contexts without increasing costs.
{"title":"Screening of carbapenemase-producing organisms and vancomycin-resistant enterococci by a molecular approach: impact and lessons learned","authors":"C. Dinh , A. Hennebique , M. Veloso , N. Gonnet , I. Pelloux , S. David-Tchouda , C. Landelle , S. Boisset","doi":"10.1016/j.jhin.2025.11.044","DOIUrl":"10.1016/j.jhin.2025.11.044","url":null,"abstract":"<div><h3>Background</h3><div>The rapid detection of carriers of emerging extensively drug-resistant bacteria (eXDR), notably carbapenemase-producing organisms (CPOs) and vancomycin-resistant Enterococci, is crucial for controlling their spread and preventing infections.</div></div><div><h3>Aim</h3><div>To evaluate the impact of polymerase chain reaction (PCR) on turnaround time (TAT) for eXDR detection compared to culture methods under routine laboratory conditions, excluding night or weekend analyses.</div></div><div><h3>Methods</h3><div>A prospective before-and-after study was conducted at a French university hospital. Phase 1 (culture) occurred from February to September 2022, phase 2 (PCR) from September 2022 to March 2023. TAT was defined as the time from sample collection to result delivery to the infection control team and/or physician. Patients aged >18 years meeting specific screening criteria were included. Two PCR kits were utilized: the BD MAX Check-Points CPO kit and the VIASURE Vancomycin resistance Real Time PCR Detection Kit.</div></div><div><h3>Findings</h3><div>A total of 2049 and 1861 patients were included in phases 1 and 2, respectively. Sixteen patients tested eXDR positive for the first time in phase 1, and 25 in phase 2. The median TAT was significantly shorter in phase 2 (22.7 h; 16.0–41.3) compared to phase 1 (43.5 h; 31.9–69.7; <em>P</em> = 0.001). A significant decrease in the median number of contact patients was observed in phase 2 compared to phase 1. The number of total screening test secondary cases and the hospitalization costs were comparable regardless of the eXDR detection method.</div></div><div><h3>Conclusion</h3><div>Rapid rectal screening using PCR significantly reduces TAT for results in low-endemic contexts without increasing costs.</div></div>","PeriodicalId":54806,"journal":{"name":"Journal of Hospital Infection","volume":"169 ","pages":"Pages 107-114"},"PeriodicalIF":3.1,"publicationDate":"2025-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145702846","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-05DOI: 10.1016/j.jhin.2025.11.042
I Beaugelin, C Radix, L Pineau
Background: Endoscopic procedures carry a risk of infection, often due to inadequate cleaning of internal channels. Manual cleaning is essential but prone to human error. Automated systems are emerging to standardize this step, yet no specific performance standard exists for these 'pre-cleaning' devices, making their evaluation challenging.
Aim: To propose a standardized evaluation approach for automated endoscope cleaning devices based on existing ISO benchmarks, and to assess the cleaning efficacy of the AquaTYPHOON device, a chemical-free and brushless system on the market.
Methods: The AquaTYPHOON was tested using protocols from ISO 15883-4:2018 and ISO 15883-5:2021. Cleaning efficacy was evaluated on: (i) surrogate devices with Pseudomonas aeruginosa biofilm; (ii) complex surrogate devices soiled with blood; and (iii) endoscopes contaminated with Austrian test soil. Residual protein and total organic carbon (TOC) levels were measured post-cleaning and compared with action levels (6.4 μg/cm2 for protein, 12 μg/cm2 for TOC).
Findings: Across all test conditions, the AquaTYPHOON achieved protein and TOC levels below the action levels, except for one surrogate position. The device showed significant reduction of soil levels, meeting the efficacy requirements for endoscope cleaning before disinfection.
Conclusion: This study supports the feasibility of using ISO-based methods to evaluate automated pre-cleaning devices, and confirms the effectiveness of the AquaTYPHOON. Establishing clear performance criteria for such systems is essential to improve patient safety, reduce human error, and standardize endoscope reprocessing practices in clinical settings.
{"title":"Standardizing manual cleaning of endoscopes: assessing the effectiveness of the AquaTYPHOON device.","authors":"I Beaugelin, C Radix, L Pineau","doi":"10.1016/j.jhin.2025.11.042","DOIUrl":"10.1016/j.jhin.2025.11.042","url":null,"abstract":"<p><strong>Background: </strong>Endoscopic procedures carry a risk of infection, often due to inadequate cleaning of internal channels. Manual cleaning is essential but prone to human error. Automated systems are emerging to standardize this step, yet no specific performance standard exists for these 'pre-cleaning' devices, making their evaluation challenging.</p><p><strong>Aim: </strong>To propose a standardized evaluation approach for automated endoscope cleaning devices based on existing ISO benchmarks, and to assess the cleaning efficacy of the AquaTYPHOON device, a chemical-free and brushless system on the market.</p><p><strong>Methods: </strong>The AquaTYPHOON was tested using protocols from ISO 15883-4:2018 and ISO 15883-5:2021. Cleaning efficacy was evaluated on: (i) surrogate devices with Pseudomonas aeruginosa biofilm; (ii) complex surrogate devices soiled with blood; and (iii) endoscopes contaminated with Austrian test soil. Residual protein and total organic carbon (TOC) levels were measured post-cleaning and compared with action levels (6.4 μg/cm<sup>2</sup> for protein, 12 μg/cm<sup>2</sup> for TOC).</p><p><strong>Findings: </strong>Across all test conditions, the AquaTYPHOON achieved protein and TOC levels below the action levels, except for one surrogate position. The device showed significant reduction of soil levels, meeting the efficacy requirements for endoscope cleaning before disinfection.</p><p><strong>Conclusion: </strong>This study supports the feasibility of using ISO-based methods to evaluate automated pre-cleaning devices, and confirms the effectiveness of the AquaTYPHOON. Establishing clear performance criteria for such systems is essential to improve patient safety, reduce human error, and standardize endoscope reprocessing practices in clinical settings.</p>","PeriodicalId":54806,"journal":{"name":"Journal of Hospital Infection","volume":" ","pages":"17-24"},"PeriodicalIF":3.1,"publicationDate":"2025-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145702865","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-04DOI: 10.1016/j.jhin.2025.11.040
L Gozdzielewska, K McAloney-Kocaman, S Lang, V Ness, G Lacey, J Reilly
Background: A six-step technique is recommended for applying alcohol-based hand rubs (ABHRs) in health care. However, evidence supporting the effectiveness of individual steps is limited and healthcare workers' (HCWs)' compliance is low, potentially due to low acceptability or feasibility or inadequate training. This study evaluated the effectiveness of the six-step hand rubbing technique for healthcare staff with consideration of microbiological efficacy, acceptability and feasibility.
Methods: A mixed-method design was used. Data were collected in two stages between 2017 and 2020. Stage 1 used a Latin square design with a modified EN 1500 procedure to compare the six-step technique with six variations omitting one step each, for bacterial load reduction and hand surface coverage (N = 35). Stage 2 was a cross-sectional online survey of the acceptability and feasibility of using the six-step hand rubbing technique in clinical practice (N = 78).
Results: Omitting step 4 (backs of fingers) resulted in significantly lower bacterial load reduction than with the full six-step technique (P = 0.001). Omitting step 1 (palms) or step 2 (dorsa) resulted in significantly lower hand coverage than with all other technique variations (P ≤ 0.001). Stage 2 participants perceived the six-step technique as acceptable and feasible, with step 1 as the most acceptable and feasible step.
Conclusion: Step 4 contributed most to bacterial load reduction, and steps 1 and 2 were key for hand coverage. HCWs should continue using the six-step technique, with efforts to improve compliance with individual steps. Future research should investigate the effects of altering step sequence and the contribution of individual steps during handwashing with soap and water.
{"title":"Deconstructing the six-step hand rubbing technique for healthcare staff: a mixed-methods investigation of efficacy, acceptability and feasibility.","authors":"L Gozdzielewska, K McAloney-Kocaman, S Lang, V Ness, G Lacey, J Reilly","doi":"10.1016/j.jhin.2025.11.040","DOIUrl":"10.1016/j.jhin.2025.11.040","url":null,"abstract":"<p><strong>Background: </strong>A six-step technique is recommended for applying alcohol-based hand rubs (ABHRs) in health care. However, evidence supporting the effectiveness of individual steps is limited and healthcare workers' (HCWs)' compliance is low, potentially due to low acceptability or feasibility or inadequate training. This study evaluated the effectiveness of the six-step hand rubbing technique for healthcare staff with consideration of microbiological efficacy, acceptability and feasibility.</p><p><strong>Methods: </strong>A mixed-method design was used. Data were collected in two stages between 2017 and 2020. Stage 1 used a Latin square design with a modified EN 1500 procedure to compare the six-step technique with six variations omitting one step each, for bacterial load reduction and hand surface coverage (N = 35). Stage 2 was a cross-sectional online survey of the acceptability and feasibility of using the six-step hand rubbing technique in clinical practice (N = 78).</p><p><strong>Results: </strong>Omitting step 4 (backs of fingers) resulted in significantly lower bacterial load reduction than with the full six-step technique (P = 0.001). Omitting step 1 (palms) or step 2 (dorsa) resulted in significantly lower hand coverage than with all other technique variations (P ≤ 0.001). Stage 2 participants perceived the six-step technique as acceptable and feasible, with step 1 as the most acceptable and feasible step.</p><p><strong>Conclusion: </strong>Step 4 contributed most to bacterial load reduction, and steps 1 and 2 were key for hand coverage. HCWs should continue using the six-step technique, with efforts to improve compliance with individual steps. Future research should investigate the effects of altering step sequence and the contribution of individual steps during handwashing with soap and water.</p>","PeriodicalId":54806,"journal":{"name":"Journal of Hospital Infection","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145696331","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-04DOI: 10.1016/j.jhin.2025.11.033
S. Bulot, L. Pineau
Background
Over the past 30 years, endoscope processing has improved significantly, guided by various standards and recommendations. None the less, contamination remains an issue, with 21.1% of endoscopes exceeding acceptable thresholds in 2021. Cleaning, including pre-treatment, is identified as critical for successful endoscope processing. ISO 15883–5 and AAMI guidelines provide frameworks for evaluating cleaning efficacy, with ANSI/AAMI ST91 recommending verification of cleanliness for high-risk and complex-design endoscopes after each cycle. This study assesses the EndoCheck protein detection kit (HEALTHMARK) as a rapid test for evaluating cleaning quality in endoscope channels.
Methods
The study was conducted in two phases: (1) performance testing (detection limit, extraction efficiency, and sensitivity), and (2) real-use testing (comparison with a standard flush sampling method).
Results
The EndoCheck kit consistently detected ≥5 μg of bovine serum albumin (BSA) in polytetrafluoroethylene (PTFE) tubes, equivalent to 0.4 μg/cm2, and recovered an average of 68 ± 11% of the initial soil. Under real-use conditions, it identified 51% of endoscopes as non-compliant, compared with 14% with the flush method. This discrepancy was more pronounced in bronchoscopes, likely due to the nature of the residual soil.
Conclusion
The EndoCheck kit is a highly sensitive, easy-to-use method for detecting residual protein in biopsy channels. Its greater stringency compared with current flush methods makes it a reliable tool for confirming cleanliness when results are negative. Positive results can serve as early indicators, prompting further investigation.
{"title":"Evaluation of a rapid quality control method for endoscope cleaning","authors":"S. Bulot, L. Pineau","doi":"10.1016/j.jhin.2025.11.033","DOIUrl":"10.1016/j.jhin.2025.11.033","url":null,"abstract":"<div><h3>Background</h3><div>Over the past 30 years, endoscope processing has improved significantly, guided by various standards and recommendations. None the less, contamination remains an issue, with 21.1% of endoscopes exceeding acceptable thresholds in 2021. Cleaning, including pre-treatment, is identified as critical for successful endoscope processing. ISO 15883–5 and AAMI guidelines provide frameworks for evaluating cleaning efficacy, with ANSI/AAMI ST91 recommending verification of cleanliness for high-risk and complex-design endoscopes after each cycle. This study assesses the EndoCheck protein detection kit (HEALTHMARK) as a rapid test for evaluating cleaning quality in endoscope channels.</div></div><div><h3>Methods</h3><div>The study was conducted in two phases: (1) performance testing (detection limit, extraction efficiency, and sensitivity), and (2) real-use testing (comparison with a standard flush sampling method).</div></div><div><h3>Results</h3><div>The EndoCheck kit consistently detected ≥5 μg of bovine serum albumin (BSA) in polytetrafluoroethylene (PTFE) tubes, equivalent to 0.4 μg/cm<sup>2</sup>, and recovered an average of 68 ± 11% of the initial soil. Under real-use conditions, it identified 51% of endoscopes as non-compliant, compared with 14% with the flush method. This discrepancy was more pronounced in bronchoscopes, likely due to the nature of the residual soil.</div></div><div><h3>Conclusion</h3><div>The EndoCheck kit is a highly sensitive, easy-to-use method for detecting residual protein in biopsy channels. Its greater stringency compared with current flush methods makes it a reliable tool for confirming cleanliness when results are negative. Positive results can serve as early indicators, prompting further investigation.</div></div>","PeriodicalId":54806,"journal":{"name":"Journal of Hospital Infection","volume":"168 ","pages":"Pages 129-133"},"PeriodicalIF":3.1,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145696327","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-03DOI: 10.1016/j.jhin.2025.11.029
B Aber, E Nyawere, F Owori, E Tartari, C Fankhauser, H M Villarreal, H Saito, D Pittet
{"title":"First Train-the-Trainers in Hand Hygiene in Uganda: a multilevel evaluation.","authors":"B Aber, E Nyawere, F Owori, E Tartari, C Fankhauser, H M Villarreal, H Saito, D Pittet","doi":"10.1016/j.jhin.2025.11.029","DOIUrl":"10.1016/j.jhin.2025.11.029","url":null,"abstract":"","PeriodicalId":54806,"journal":{"name":"Journal of Hospital Infection","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2025-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145688397","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}