المؤلفون: Mannala, GK, Rupp, M, Docheva, D, Alt, V

المصدر: Deutscher Kongress für Orthopädie und Unfallchirurgie (DKOU 2021); 20211026-20211029; Berlin; DOCAB63-1122 /20211026/

مصطلحات موضوعية: Bacteriophages, Staphylococcus aureus, Implant-associated bone infections, Biofilm and Osteoblasts, ddc: 610

العلاقة: http://dx.doi.org/10.3205/21dkou388Test; http://nbn-resolving.de/urn:nbn:de:0183-21dkou3886Test; http://www.egms.de/en/meetings/dkou2021/21dkou388.shtmlTest

الإتاحة: https://doi.org/10.3205/21dkou388Test
http://nbn-resolving.de/urn:nbn:de:0183-21dkou3886Test
http://www.egms.de/en/meetings/dkou2021/21dkou388.shtmlTest

المؤلفون: Alagboso, F, Mannala, GK, Steinmann, S, Docheva, D, Rupp, M, Brochhausen, C, Alt, V

المصدر: Deutscher Kongress für Orthopädie und Unfallchirurgie (DKOU 2021); 20211026-20211029; Berlin; DOCAB63-1006 /20211026/

مصطلحات موضوعية: Staphylococcus aureus, osteoblasts, rifampicin, osteogenesis, bone infection, ddc: 610

العلاقة: http://dx.doi.org/10.3205/21dkou391Test; http://nbn-resolving.de/urn:nbn:de:0183-21dkou3913Test; http://www.egms.de/en/meetings/dkou2021/21dkou391.shtmlTest

الإتاحة: https://doi.org/10.3205/21dkou391Test
http://nbn-resolving.de/urn:nbn:de:0183-21dkou3913Test
http://www.egms.de/en/meetings/dkou2021/21dkou391.shtmlTest

المؤلفون: Heudorf, U, Berres, M, Hofmann, S, Steul, K

المصدر: GMS Hygiene and Infection Control; VOL: 15; DOC15 /20200703/

مصطلحات موضوعية: multidrug-resistant organisms MDRO, methicillin-resistant Staphylococcus aureus MRSA, multidrug-resistant gram-negative pathogens MRGN, vancomycin-resistant enterococci VRE, rehabilitation, hygiene management, Multiresistente Erreger MRE, methicillinresistenter Staphylococcus aureus MRSA, multiresistente Gram-negative Erreger MRGN, vancomycinresistente Enterokokken VRE, Hygienemanagement, ddc: 610

العلاقة: Hessische Hygieneverordnung vom 1. Dezember 2011 (GVBl. I S. 745, 2012 S. 32), zuletzt geändert am 20. Dezember 2018; GvBL S 726ff); Hygienemaßnahmen bei Infektionen oder Besiedlung mit multiresistenten gramnegativen Stäbchen. Empfehlung der Kommission für Krankenhaushygiene und Infektionsprävention (KRINKO) beim Robert Koch-Institut (RKI) [Hygiene measures for infection or colonization with multidrug-resistant gram-negative bacilli. Commission recommendation for hospital hygiene and infection prevention (KRINKO) at the Robert Koch Institute (RKI)]. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2012 Oct;55(10):1311-54. DOI:10.1007/s00103-012-1549-5; Personelle und organisatorische Voraussetzungen zur Prävention nosokomialer Infektionen: Empfehlung der Kommission für Krankenhaushygiene und Infektionsprävention [Personnel and organizational requirements for the prevention of nosocomial infections: Recommendations from the Commission for Hospital Hygiene and Infection Prevention]. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2009 Sep;52(9):951-62. DOI:10.1007/s00103-009-0929-y; Empfehlung zum Kapazitätsumfang für die Betreuung von Krankenhäusern und anderen medizinischen Einrichtungen durch Krankenhaushygieniker/innen. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2016 09;59(9):1183-8. DOI:10.1007/s00103-016-2410-z; Hygienemaßnahmen zur Prävention der Infektion durch Enterokokken mit speziellen Antibiotikaresistenzen: Empfehlung der Kommission für Krankenhaushygiene und Infektionsprävention (KRINKO) beim Robert Koch-Institut. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2018 Oct;61(10):1310-61. DOI:10.1007/s00103-018-2811-2; Brandt C, Jahn-Mühl B, Parthé S, Pitten F, Merbs R, Heudorf U. MRSA/MRE in der Rehabilitation - Empfehlungen des MRE-Netz Rhein-Main [MRSA/MDRO in rehabilitation - recommendation of the MDRO-Network Rhein-Main]. Rehabilitation (Stuttg). 2012 Aug;51(4):254-8. DOI:10.1055/s-0032-1312661; Brolund A, Lagerqvist N, Byfors S, Struelens MJ, Monnet DL, Albiger B, Kohlenberg A; European Antimicrobial Resistance Genes Surveillance Network EURGen-Net Capacity Survey Group. Worsening epidemiological situation of carbapenemase-producing Enterobacteriaceae in Europe, assessment by national experts from 37 countries, July 2018. Euro Surveill. 2019 02;24(9):pii=1900123. DOI:10.2807/1560-7917.ES.2019.24.9.1900123; Doherty A, McNicholas S, Burger H, Boldrini P, Delargy M. European survey of management of patients with multidrug-resistant organisms in rehabilitation facilities. Eur J Phys Rehabil Med. 2019 Aug;55(4):418-423. DOI:10.23736/S1973-9087.19.05570-9; European Centre for Disease Prevention and Control. Surveillance of antimicrobial resistance in Europe 2018. Stockholm: ECDC; 2019 (last access 20 Apr 2020). https://www.ecdc.europa.eu/sites/default/files/documents/surveillance-antimicrobial-resistance-Europe-2018.pdfTest; Gastmeier P, Schröder C, Behnke M, Meyer E, Geffers C. Dramatic increase in vancomycin-resistant enterococci in Germany. J Antimicrob Chemother. 2014 Jun;69(6):1660-4. DOI:10.1093/jac/dku035; Gieffers J, Ahuja A, Giemulla R. Long term observation of MRSA prevalence in a German rehabilitation center: risk factors and variability of colonization rate. GMS Hyg Infect Control. 2016; Oct 5;11: Doc21. eCollection 2016.; Giufrè M, Ricchizzi E, Accogli M, Barbanti F, Monaco M, Pimentel de Araujo F, Farina C, Fazii P, Mattei R, Sarti M, Barozzi A, Buttazzi R, Cosentino M, Nardone M, Savini V, Spigaglia P, Pantosti A, Moro ML, Cerquetti M. Colonization by multidrug-resistant organisms in long-term care facilities in Italy: a point-prevalence study. Clin Microbiol Infect. 2017 Dec;23(12):961-967. DOI:10.1016/j.cmi.2017.04.006; Heudorf U, Färber D, Mischler D, Schade M, Zinn C, Nillius D, Herrmann M. Multiresistente Erreger in Rehabilitationseinrichtungen im Rhein-Main-Gebiet, Deutschland, 2014: II. Ärztliche Risikoanalyse und Hygienemaßnahmen [Multidrug-Resistant Organisms (MDRO) in Rehabilitation Clinics in the Rhine-Main District, Germany, 2014: Risk Analysis and Hygiene Procedures]. Rehabilitation (Stuttg). 2015 Dec;54(6):375-81. DOI:10.1055/s-0035-1564099; Heudorf U, Färber D, Mischler D, Schade M, Zinn C, Cuny C, Nillius D, Herrmann M. Multiresistente Erreger in Rehabilitationseinrichtungen im Rhein-Main-Gebiet, Deutschland, 2014: I. Prävalenz und Risikofaktoren [Multidrug-Resistant Organisms (MDRO) in Rehabilitation Clinics in the Rhine-Main-District, Germany, 2014: Prevalence and Risk Factors]. Rehabilitation (Stuttg). 2015 Oct;54(5):339-45. DOI:10.1055/s-0035-1559642; Heudorf U, Exner M. MRSA-Patienten in der Rehabilitation - eine ärztliche Risikoanalyse nach KRINKO. Hyg Med. 2014;39(12):512-6.; Heudorf U. Auftaktveranstaltung des MRE-Netzes Rhein-Main: Erfreulicher Anlass - mit ernstem Hintergrund. Hess Arztebl. 2010;70:493-5.; Heudorf U. Infektionsprävention und Rehabilitation. Vorab ärztliche Risikoanalyse. Dtsch Arztebl. 2014;111(47):A2063-6.; Hogardt M , Proba P , Mischler D , Cuny C , Kempf V A , Heudorf U . Current prevalence of multidrug-resistant organisms in long-term care facilities in the Rhine-Main district, Germany, 2013. Euro Surveill. 2015;20(26):pii=21171. DOI:10.2807/1560-7917.ES2015.20.26.21171; Kiefer T, Völler H, Nothroff J, Schikora M, von Podewils S, Sicher C, Bartels-Reinisch B, Heyne K, Haase H, Jünger M, Daeschlein G. Multiresistente Erreger in der onkologischen und kardiologischen Rehabilitation - Ergebnisse einer Surveillancestudie in Brandenburg [Multiresistant Pathogens in Oncological and Cardiological Rehabilitation - Results of a Surveillance Study in Brandenburg]. Rehabilitation (Stuttg). 2019 Apr;58(2):136-142. DOI:10.1055/a-0638-9226; Köck R, Winner K, Schaumburg F, Jurke A, Rossen JW, Friedrich AW. Admission prevalence and acquisition of nasal carriage of meticillin-resistant Staphylococcus aureus (MRSA) in German rehabilitation centres. J Hosp Infect. 2014 Jun;87(2):115-8. DOI:10.1016/j.jhin.2014.02.007; Kramer TS, Schröder C, Behnke M, Aghdassi SJ, Geffers C, Gastmeier P, Remschmidt C. Decrease of methicillin resistance in Staphylococcus aureus in nosocomial infections in Germany-a prospective analysis over 10 years. J Infect. 2019 03;78(3):215-219. DOI:10.1016/j.jinf.2018.12.005; Latour K, Huang TD, Jans B, Berhin C, Bogaerts P, Noel A, Nonhoff C, Dodémont M, Denis O, Ieven M, Loens K, Schoevaerdts D, Catry B, Glupczynski Y. Prevalence of multidrug-resistant organisms in nursing homes in Belgium in 2015. PLoS ONE. 2019;14(3):e0214327. DOI:10.1371/journal.pone.0214327; Ludden C, Cormican M, Vellinga A, Johnson JR, Austin B, Morris D. Colonisation with ESBL-producing and carbapenemase-producing Enterobacteriaceae, vancomycin-resistant enterococci, and meticillin-resistant Staphylococcus aureus in a long-term care facility over one year. BMC Infect Dis. 2015 Apr;15:168. DOI:10.1186/s12879-015-0880-5; Maechler F, Peña Diaz LA, Schröder C, Geffers C, Behnke M, Gastmeier P. Prevalence of carbapenem-resistant organisms and other Gram-negative MDRO in German ICUs: first results from the national nosocomial infection surveillance system (KISS). Infection. 2015 Apr;43(2):163-8. DOI:10.1007/s15010-014-0701-6; Pohl M, Bertram M, Bucka C, Hartwich M, Jöbges M, Ketter G, Leineweber B, Mertl-Rötzer M, Nowak DA, Platz T, Rollnik JD, Scheidtmann K, Thomas R, von Rosen F, Wallesch CW, Woldag H, Peschel P, Mehrholz J. Rehabilitationsverlauf von Patienten in der neurologisch-neurochirurgischen Frührehabilitation [Course of rehabilitation in early neurological/neurosurgical rehabilitation. Results of a 2014 multi-center evaluation in Germany]. Nervenarzt. 2016 Jun;87(6):634-44. DOI:10.1007/s00115-016-0093-1; Rollnik JD. Outcome of MRSA carriers in neurological early rehabilitation. BMC Neurol. 2014 Feb;14:34. DOI:10.1186/1471-2377-14-34; Rollnik JD. Outcome of Early Neurological Rehabilitation Patients Colonized with Extended- Spectrum Beta-Lactamase (ESBL) Producing Bacteria. Open J Ther Rehabil. 2015;3: 1-8. DOI:10.4236/ojtr.2015.31001; Ruscher C. Empfehlungen zur Prävention und Kontrolle von Methicillin-resistenten Staphylococcus aureus-Stämmen (MRSA) in medizinischen und pflegerischen Einrichtungen. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2014;57:695-732. DOI:10.1007/s00103-014-1980-x; Schweizer C, Hummel M, Klefisch FR, Stoliaroff A. Ablehnung der Behandlung von Patienten mit MDRO in geriatrischen Kliniken und Rehabilitationseinrichtungen: Einzelfälle oder gängige Praxis? Epid Bull. 2017;50:567-9.; Steul K, Jesche C, Berres M, Hofmann S, Klaus-Altschuck A, Hogardt M, Kempf V, Pohl M, Heudorf U. Multiresistente Erreger (MDRO) in der Rehabilitation: Prävalenz und Risikofaktoren für MRGN und VRE in Rehabilitationseinrichtungen im Bereich des MRE-Netz Rhein-Main, 2019. Rehabilitation. Forthcoming 2020.; van Dulm E, Tholen ATR, Pettersson A, van Rooijen MS, Willemsen I, Molenaar P, Damen M, Gruteke P, Oostvogel P, Kuijper EJ, Hertogh CMPM, Vandenbroucke-Grauls CMJE, Scholing M. High prevalence of multidrug resistant Enterobacteriaceae among residents of long term care facilities in Amsterdam, the Netherlands. PLoS ONE. 2019;14(9):e0222200. DOI:10.1371/journal.pone.0222200; van Loon K, Voor In 't Holt AF, Vos MC. A Systematic Review and Meta-analyses of the Clinical Epidemiology of Carbapenem-Resistant Enterobacteriaceae. Antimicrob Agents Chemother. 2018 01;62(1):e01730-17. DOI:10.1128/AAC.01730-17; http://dx.doi.org/10.3205/dgkh000350Test; http://nbn-resolving.de/urn:nbn:de:0183-dgkh0003509Test; http://www.egms.de/en/journals/dgkh/2020-15/dgkh000350.shtmlTest

الإتاحة: https://doi.org/10.3205/dgkh000350Test
https://doi.org/10.1007/s00103-012-1549-5Test
https://doi.org/10.1007/s00103-009-0929-yTest
https://doi.org/10.1007/s00103-016-2410-zTest
https://doi.org/10.1007/s00103-018-2811-2Test
https://doi.org/10.1055/s-0032-1312661Test
https://doi.org/10.2807/1560-7917.ES.2019.24.9.1900123Test
https://doi.org/10.23736/S1973-9087.19.05570-9Test
https://doi.org/10.1093/jac/dku035Test
https://doi.org/10.1016/j.cmi.2017.04.006Test

المؤلفون: Labus, D, Weinhold, L, Heller, J

المصدر: GMS Hygiene and Infection Control; VOL: 14; DOC18 /20191129/

مصطلحات موضوعية: methicillin-resistant Staphylococcus aureus, patient isolation, infection control, outcome and process assessment (health care), diagnostic techniques and procedures, patient safety, Methicillin-resistenter Staphylococcus aureus, Isolierungsmaßnahmen, Infektionsprävention, medizinischer Outcome, Versorgungsprozesse, apparative Diagnostik, Patientensicherheit, ddc: 610

العلاقة: (KRINKO) KfrKuI. Empfehlungen zur Prävention und Kontrolle von Methicillinresistenten Staphylococcus aureus-Stämmen (MRSA) in medizinischen und pflegerischen Einrichtungen - Empfehlung der Kommission für Krankenhaushygiene und Infektionsprävention (KRINKO) beim Robert Koch-Institut. Bundesgesundheitsblatt. 2014(57):696-732.; Catalano G, Houston SH, Catalano MC, Butera AS, Jennings SM, Hakala SM, Burrows SL, Hickey MG, Duss CV, Skelton DN, Laliotis GJ. Anxiety and depression in hospitalized patients in resistant organism isolation. South Med J. 2003 Feb;96(2):141-5. DOI:10.1097/01.SMJ.0000050683.36014.2E; Claus F, Sachse A, Ried W. Volkswirtschaftliche Kosten von MRSA in Deutschland [On the economic burden of MRSA in Germany]. Gesundheitswesen. 2014 Dec;76(12):800-6. DOI:10.1055/s-0034-1381987; Cosgrove SE, Qi Y, Kaye KS, Harbarth S, Karchmer AW, Carmeli Y. The impact of methicillin resistance in Staphylococcus aureus bacteremia on patient outcomes: mortality, length of stay, and hospital charges. Infect Control Hosp Epidemiol. 2005 Feb;26(2):166-74. DOI:10.1086/502522; Davies H, Rees J. Psychological effects of isolation nursing (1): Mood disturbance. Nurs Stand. 2000 Mar 29-Apr 4;14(28):35-8. DOI:10.7748/ns2000.03.14.28.35.c2799; de Kraker ME, Davey PG, Grundmann H; BURDEN study group. Mortality and hospital stay associated with resistant Staphylococcus aureus and Escherichia coli bacteremia: estimating the burden of antibiotic resistance in Europe. PLoS Med. 2011 Oct;8(10):e1001104. DOI:10.1371/journal.pmed.1001104; Gammon J. Analysis of the stressful effects of hospitalisation and source isolation on coping and psychological constructs. Int J Nurs Pract. 1998 Jun;4(2):84-96. DOI:10.1046/j.1440-172x.1998.00084.x; GmbH IfrdEiK. InEK Abschlussbericht Weiterentwicklung des G-DRG-Systems für das Jahr 2017. 2017.; Hahn JM. Checkliste Innere Medizin. 8. ed. Stuttgart: Thieme; 2018. Laborwerte - Normalbereiche; p. 815-20.; Hübner C, Hübner NO, Hopert K, Maletzki S, Flessa S. Analysis of MRSA-attributed costs of hospitalized patients in Germany. Eur J Clin Microbiol Infect Dis. 2014 Oct;33(10):1817-22. DOI:10.1007/s10096-014-2131-x; InEK. G-DRG German Diagnosis Related Groups, Version 2019, Definitionshandbuch Kompaktversion. Siegburg: Institut für das Entgeltsystem im Krankenhaus GmbH (InEK); 2018.; KDIGO Board. KDIGO Clinical Practice Guideline for Acute Kidney Injury. Kidney Int Suppl (2011). 2012 Mar;2(1).; Kennedy P, Hamilton LR. Psychological impact of the management of methicillin-resistant Staphylococcus aureus (MRSA) in patients with spinal cord injury. Spinal Cord. 1997 Sep;35(9):617-9.; Kiesel M, Holz H. Berechnung der Kosten für einen nosokomialen MRSA-Fall in einem Krankenhaus der Schwerpunktversorgung in Rheinland-Pfalz. aseptica. 2014;20(1):15-9.; Loveday HP, Pellowe CM, Jones SR, Pratt RJ. A systematic review of the evidence for interventions for the prevention and control of meticillin-resistant Staphylococcus aureus (1996-2004): report to the Joint MRSA Working Party (Subgroup A). J Hosp Infect. 2006 May;63 Suppl 1:S45-70. DOI:10.1016/j.jhin.2006.01.002; Moore C, Dhaliwal J, Tong A, Eden S, Wigston C, Willey B, McGeer A. Risk factors for methicillin-resistant Staphylococcus aureus (MRSA) acquisition in roommate contacts of patients colonized or infected with MRSA in an acute-care hospital. Infect Control Hosp Epidemiol. 2008 Jul;29(7):600-6. DOI:10.1086/588567; Morgan DJ, Diekema DJ, Sepkowitz K, Perencevich EN. Adverse outcomes associated with Contact Precautions: a review of the literature. Am J Infect Control. 2009 Mar;37(2):85-93. DOI:10.1016/j.ajic.2008.04.257; R Core Team. R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing; 2014. Available from: http://www.R-project.orgTest/; Saint S, Higgins LA, Nallamothu BK, Chenoweth C. Do physicians examine patients in contact isolation less frequently? A brief report. Am J Infect Control. 2003 Oct;31(6):354-6. DOI:10.1016/s0196-6553(02)48250-8; Spence MR, McQuaid M. The interrelationship of isolation precautions and adverse events in an acute care facility. Am J Infect Control. 2011 Mar;39(2):154-5. DOI:10.1016/j.ajic.2010.04.213; Stelfox HT, Bates DW, Redelmeier DA. Safety of patients isolated for infection control. JAMA. 2003 Oct;290(14):1899-905. DOI:10.1001/jama.290.14.1899; Tong SY, Davis JS, Eichenberger E, Holland TL, Fowler VG Jr. Staphylococcus aureus infections: epidemiology, pathophysiology, clinical manifestations, and management. Clin Microbiol Rev. 2015 Jul;28(3):603-61. DOI:10.1128/CMR.00134-14; Wernitz MH, Keck S, Swidsinski S, Schulz S, Veit SK. Cost analysis of a hospital-wide selective screening programme for methicillin-resistant Staphylococcus aureus (MRSA) carriers in the context of diagnosis related groups (DRG) payment. Clin Microbiol Infect. 2005 Jun;11(6):466-71. DOI:10.1111/j.1469-0691.2005.01153.x; Wilkins EG, Ellis ME, Dunbar EM, Gibbs A. Does isolation of patients with infections induce mental illness? J Infect. 1988 Jul;17(1):43-7. DOI:10.1016/s0163-4453(88)92308-0; http://dx.doi.org/10.3205/dgkh000333Test; http://nbn-resolving.de/urn:nbn:de:0183-dgkh0003335Test; http://www.egms.de/en/journals/dgkh/2019-14/dgkh000333.shtmlTest

الإتاحة: https://doi.org/10.3205/dgkh000333Test
https://doi.org/10.1097/01.SMJ.0000050683.36014.2ETest
https://doi.org/10.1055/s-0034-1381987Test
https://doi.org/10.1086/502522Test
https://doi.org/10.7748/ns2000.03.14.28.35.c2799Test
https://doi.org/10.1371/journal.pmed.1001104Test
https://doi.org/10.1046/j.1440-172x.1998.00084.xTest
https://doi.org/10.1007/s10096-014-2131-xTest
https://doi.org/10.1016/j.jhin.2006.01.002Test
https://doi.org/10.1086/588567Test

المؤلفون: Adeiza, SS, Onaolapo, JA, Olayinka, BO

المصدر: GMS Hygiene and Infection Control; VOL: 15; DOC25 /20201012/

مصطلحات موضوعية: Staphylococcus aureus, dendrogram, antimicrobial resistance, methicillin resistance, regression, Dendrogramm, antimikrobielle Resistenz, Methicillin-Resistenz, ddc: 610

العلاقة: Abiye JP, Moses A, Gospel NE, Udogadi AU. Prevalence of risk factors associated with MRSA nasal carriage among HIV-patients on HAART at a tertiary hospital in Niger Delta, Nigeria. Ann Med Health Sci Res. 2018;8:39-43.; Adesida SA, Abioye OA, Bamiro BS, Brai BI, Smith SI, Amisu KO, Ehichioya DU, Ogunsola FT, Coker AO. Associated risk factors and pulsed field gel electrophoresis of nasal isolates of Staphylococcus aureus from medical students in a tertiary hospital in Lagos, Nigeria. Braz J Infect Dis. 2007 Feb;11(1):63-9. DOI:10.1590/s1413-86702007000100016; Sokoto (State, Nigeria) - Population Statistics, Charts, Map and Location. 2019 [cited 2019 Nov 1]. Available from: https://citypopulation.de/php/nigeria-admin.php?adm1id=NGA034Test; Ansari S, Gautam R, Shrestha S, Ansari SR, Subedi SN, Chhetri MR. Risk factors assessment for nasal colonization of Staphylococcus aureus and its methicillin resistant strains among pre-clinical medical students of Nepal. BMC Res Notes. 2016 Apr;9:214. DOI:10.1186/s13104-016-2021-7; Anyanwu NCJ, John WC. Conventional and rapid methods for identification of Staphylococcus aureus from clinical specimens. Am J Biomed Life Sci. 2013;1(3):41-3. DOI:10.11648/j.ajbls.20130103.11; Asensio A, Guerrero A, Quereda C, Lizán M, Martinez-Ferrer M. Colonization and infection with methicillin-resistant Staphylococcus aureus: associated factors and eradication. Infect Control Hosp Epidemiol. 1996 Jan;17(1):20-8. DOI:10.1086/647184; Befus MB, Miko BA, Herzig CT, Keleekai N, Mukherjee DV, Larson E, Lowy FD. HIV and colonization with Staphylococcus aureus in two maximum-security prisons in New York State. J Infect. 2016 12;73(6):568-577. DOI:10.1016/j.jinf.2016.08.016; Burkey MD, Wilson LE, Moore RD, Lucas GM, Francis J, Gebo KA. The incidence of and risk factors for MRSA bacteraemia in an HIV-infected cohort in the HAART era. HIV Med. 2008 Nov;9(10):858-62. DOI:10.1111/j.1468-1293.2008.00629.x; Calfee DP, Durbin LJ, Germanson TP, Toney DM, Smith EB, Farr BM. Spread of methicillin-resistant Staphylococcus aureus (MRSA) among household contacts of individuals with nosocomially acquired MRSA. Infect Control Hosp Epidemiol. 2003 Jun;24(6):422-6. DOI:10.1086/502225; Chang HH, Cohen T, Grad YH, Hanage WP, O'Brien TF, Lipsitch M. Origin and proliferation of multiple-drug resistance in bacterial pathogens. Microbiol Mol Biol Rev. 2015 Mar;79(1):101-16. DOI:10.1128/MMBR.00039-14; Chen CC, Pass SE. Risk factors for and impact of methicillin-resistant Staphylococcus aureus nasal colonization in patients in a medical intensive care unit. Am J Infect Control. 2013 Nov;41(11):1100-1. DOI:10.1016/j.ajic.2013.01.035; CLSI. Performance Standards for Antimicrobial Susceptibility Testing. CLSI supplement M100. 29th ed. Wayne, PA: Clinical and Laboratory Standards Institute; 2019.; Conceição T, Coelho C, Santos-Silva I, de Lencastre H, Aires-de-Sousa M. Epidemiology of methicillin-resistant and -susceptible Staphylococcus aureus in Luanda, Angola: first description of the spread of the MRSA ST5-IVa clone in the African continent. Microb Drug Resist. 2014 Oct;20(5):441-9. DOI:10.1089/mdr.2014.0007; Cuny C, Layer F, Hansen S, Werner G, Witte W. Nasal Colonization of Humans with Occupational Exposure to Raw Meat and to Raw Meat Products with Methicillin-Susceptible and Methicillin-Resistant. Toxins (Basel). 2019 Mar;11(4):190. DOI:10.3390/toxins11040190; Daeschlein G, Assadian O, Rangous I, Kramer A. Risk factors for Staphylococcus aureus nasal carriage in residents of three nursing homes in Germany. J Hosp Infect. 2006 Jun;63(2):216-20. DOI:10.1016/j.jhin.2005.12.014; Donker T, Wallinga J, Slack R, Grundmann H. Hospital networks and the dispersal of hospital-acquired pathogens by patient transfer. PLoS ONE. 2012;7(4):e35002. DOI:10.1371/journal.pone.0035002; Dunyach-Remy C, Courtais-Coulon C, DeMattei C, Jourdan N, Schuldiner S, Sultan A, Carrière C, Alonso S, Sotto A, Lavigne JP. Link between nasal carriage of Staphylococcus aureus and infected diabetic foot ulcers. Diabetes Metab. 2017 Apr;43(2):167-171. DOI:10.1016/j.diabet.2016.09.003; Dupieux C, Trouillet-Assant S, Tasse J, Freydière AM, Raulin O, Roure-Sobas C, Salord H, Tigaud S, Laurent F. Evaluation of a commercial immunochromatographic assay for rapid routine identification of PBP2a-positive Staphylococcus aureus and coagulase-negative staphylococci. Diagn Microbiol Infect Dis. 2016 Nov;86(3):262-264. DOI:10.1016/j.diagmicrobio.2016.08.012; Eko KE, Forshey BM, Carrel M, Schweizer ML, Perencevich EN, Smith TC. Molecular characterization of methicillin-resistant Staphylococcus aureus (MRSA) nasal colonization and infection isolates in a Veterans Affairs hospital. Antimicrob Resist Infect Control. 2015;4:10. DOI:10.1186/s13756-015-0048-5; El Aila NA, Al Laham NA, Ayesh BM. Nasal carriage of methicillin resistant Staphylococcus aureus among health care workers at Al Shifa hospital in Gaza Strip. BMC Infect Dis. 2017 01;17(1):28. DOI:10.1186/s12879-016-2139-1; El-Mokhtar MA, Hetta HF. Ambulance vehicles as a source of multidrug-resistant infections: a multicenter study in Assiut City, Egypt. Infect Drug Resist. 2018;11:587-594. DOI:10.2147/IDR.S151783; Falagas ME, Karageorgopoulos DE, Leptidis J, Korbila IP. MRSA in Africa: filling the global map of antimicrobial resistance. PLoS ONE. 2013;8(7):e68024. DOI:10.1371/journal.pone.0068024; Gonsu KH, Kouemo SL, Toukam M, Ndze VN, Koulla SS. Nasal carriage of methicillin resistant Staphylococcus aureus and its antibiotic susceptibility pattern in adult hospitalized patients and medical staff in some hospitals in Cameroon. J Microbiol Antimicrob. 2013;5(3):29-33. DOI:10.5897/JMA2012.0232; Grecu AM, Dave DM, Saffer H. Mandatory Access Prescription Drug Monitoring Programs and Prescription Drug Abuse. J Policy Anal Manage. 2019;38(1):181-209.; Harkins CP, Pichon B, Doumith M, Parkhill J, Westh H, Tomasz A, de Lencastre H, Bentley SD, Kearns AM, Holden MTG. Methicillin-resistant Staphylococcus aureus emerged long before the introduction of methicillin into clinical practice. Genome Biol. 2017 07;18(1):130. DOI:10.1186/s13059-017-1252-9; Hasnain A, Nasim W, Mubarak H, Mirza N, Khan S, Su X, Ahmed S, Hashmi MZ. Antibiotics Resistance Genes. In: Hashmi M, Strezov V, Varma A, editors. Antibiotics and Antibiotics Resistance Genes in Soils. Soil Biology, vol 51. Basel: Springer; 2017. p. 19-37. DOI:10.1007/978-3-319-66260-2_2; Health Policy Plus (HP+). Nigeria Population and Development: Sokoto State Factsheet. 2017 Sep. Available from: http://www.healthpolicyplus.com/ns/pubs/7149-7285_SokotoRAPIDFactSheet.pdfTest; Jian J, Chen L, Xie Z, Zhang M. Dissemination of cfr-mediated linezolid resistance among Staphylococcus species isolated from a teaching hospital in Beijing, China. J Int Med Res. 2018 Sep;46(9):3884-9. DOI:10.1177/0300060518781636; Kildow BJ, Conradie JP, Robson RL. Nostrils of healthy volunteers are independent with regard to Staphylococcus aureus carriage. J Clin Microbiol. 2012 Nov;50(11):3744-6. DOI:10.1128/JCM.01488-12; Kwoji ID, Jauro S, Musa JA, Lekko YM, Salihu SI, Danchuwa HA. Phenotypic detection of methicillin-resistant aureus in village chickens from poultry markets in Maiduguri, Nigeria. J Adv Vet Anim Res. 2019 Jun;6(2):163-167. DOI:10.5455/javar.2019.f327; Liu SH, Chen KF, Chen CJ, Lin YH, Huang YC. Intermittent nasal carriage with Staphylococcus aureus within a menstrual cycle: Results from a prospective cohort of healthy carriers. Medicine (Baltimore). 2016 Jun;95(26):e4040. DOI:10.1097/MD.0000000000004040; Lucet JC, Chevret S, Durand-Zaleski I, Chastang C, Régnier B; Multicenter Study Group. Prevalence and risk factors for carriage of methicillin-resistant Staphylococcus aureus at admission to the intensive care unit: results of a multicenter study. Arch Intern Med. 2003 Jan;163(2):181-8. DOI:10.1001/archinte.163.2.181; Magiorakos AP, Srinivasan A, Carey RB, Carmeli Y, Falagas ME, Giske CG, Harbarth S, Hindler JF, Kahlmeter G, Olsson-Liljequist B, Paterson DL, Rice LB, Stelling J, Struelens MJ, Vatopoulos A, Weber JT, Monnet DL. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect. 2012 Mar;18(3):268-81. DOI:10.1111/j.1469-0691.2011.03570.x; Maina EK, Kiiyukia C, Wamae CN, Waiyaki PG, Kariuki S. Characterization of methicillin-resistant Staphylococcus aureus from skin and soft tissue infections in patients in Nairobi, Kenya. Int J Infect Dis. 2013 Feb;17(2):e115-9. DOI:10.1016/j.ijid.2012.09.006; Mao P, Peng P, Liu Z, Xue Z, Yao C. Risk Factors And Clinical Outcomes Of Hospital-Acquired MRSA Infections In Chongqing, China. Infect Drug Resist. 2019;12:3709-17. DOI:10.2147/IDR.S223536; Montanaro L, Ravaioli S, Ruppitsch W, Campoccia D, Pietrocola G, Visai L, Speziale P, Allerberger F, Arciola CR. Molecular Characterization of a Prevalent Ribocluster of Methicillin-Sensitive Staphylococcus aureus from Orthopedic Implant Infections. Correspondence with MLST CC30. Front Cell Infect Microbiol. 2016;6:8. DOI:10.3389/fcimb.2016.00008; Montoya A, Schildhouse R, Goyal A, Mann JD, Snyder A, Chopra V, Mody L. How often are health care personnel hands colonized with multidrug-resistant organisms? A systematic review and meta-analysis. Am J Infect Control. 2019 06;47(6):693-703. DOI:10.1016/j.ajic.2018.10.017; Natale A, Stelling J, Meledandri M, Messenger LA, D'Ancona F. Use of WHONET-SaTScan system for simulated real-time detection of antimicrobial resistance clusters in a hospital in Italy, 2012 to 2014. Euro Surveill. 2017 Mar;22(11):. DOI:10.2807/1560-7917.ES.2017.22.11.30484; Oche OM, Gana GJ, Yahaya M, Khalid I, Sambo MLA. Prevalence and effect of social media on sleep among students of higher institutions in Sokoto Metropolis, Sokoto State Nigeria. Ann Med Health Sci Res. 2019;9:729-35.; Opal SM, Mayer KH, Stenberg MJ, Blazek JE, Mikolich DJ, Dickensheets DL, Lyhte LW, Trudel RR, Musser JM. Frequent acquisition of multiple strains of methicillin-resistant Staphylococcus aureus by healthcare workers in an endemic hospital environment. Infect Control Hosp Epidemiol. 1990 Sep;11(9):479-85. DOI:10.1086/646215; Pendolino AL, Lund VJ, Nardello E, Ottaviano G. The nasal cycle: a comprehensive review. Rhinol Online. 2018;1:67-76. DOI:10.4193/RHINOL/18.021; Price JR, Cole K, Bexley A, Kostiou V, Eyre DW, Golubchik T, Wilson DJ, Crook DW, Walker AS, Peto TEA, Llewelyn MJ, Paul J; Modernising Medical Microbiology informatics group. Transmission of Staphylococcus aureus between health-care workers, the environment, and patients in an intensive care unit: a longitudinal cohort study based on whole-genome sequencing. Lancet Infect Dis. 2017 02;17(2):207-214. DOI:10.1016/S1473-3099(16)30413-3; Sabbagh P, Riahi SM, Gamble HR, Rostami A. The global and regional prevalence, burden, and risk factors for methicillin-resistant Staphylococcus aureus colonization in HIV-infected people: A systematic review and meta-analysis. Am J Infect Control. 2019 03;47(3):323-333. DOI:10.1016/j.ajic.2018.06.023; Samutela MT, Kalonda A, Mwansa J, Lukwesa-Musyani C, Mwaba J, Mumbula EM, Mwenya D, Simulundu E, Kwenda G. Molecular characterisation of methicillin-resistant Staphylococcus aureus (MRSA) isolated at a large referral hospital in Zambia. Pan Afr Med J. 2017;26:108. DOI:10.11604/pamj.2017.26.108.10982; Schaumburg F, Alabi AS, Peters G, Becker K. New epidemiology of Staphylococcus aureus infection in Africa. Clin Microbiol Infect. 2014 Jul;20(7):589-96. DOI:10.1111/1469-0691.12690; Schulte DM, Duster M, Warrack S, Valentine S, Jorenby D, Shirley D, Sosman J, Catz S, Safdar N. Feasibility and patient satisfaction with smoking cessation interventions for prevention of healthcare-associated infections in inpatients. Subst Abuse Treat Prev Policy. 2016 Apr;11:15. DOI:10.1186/s13011-016-0059-0; Shadyab AH, Crum-Cianflone NF. Methicillin-resistant Staphylococcus aureus (MRSA) infections among HIV-infected persons in the era of highly active antiretroviral therapy: a review of the literature. HIV Med. 2012 Jul;13(6):319-32. DOI:10.1111/j.1468-1293.2011.00978.x; Shet A, Mathema B, Mediavilla JR, Kishii K, Mehandru S, Jeane-Pierre P, Laroche M, Willey BM, Kreiswirth N, Markowitz M, Kreiswirth BN. Colonization and subsequent skin and soft tissue infection due to methicillin-resistant Staphylococcus aureus in a cohort of otherwise healthy adults infected with HIV type 1. J Infect Dis. 2009 Jul;200(1):88-93. DOI:10.1086/599315; Shibabaw A, Abebe T, Mihret A. Nasal carriage rate of methicillin resistant Staphylococcus aureus among Dessie Referral Hospital Health Care Workers; Dessie, Northeast Ethiopia. Antimicrob Resist Infect Control. 2013 Oct;2(1):25. DOI:10.1186/2047-2994-2-25; Solomon PO, Okpala HO, Oladeinde BH, Olley M, Okon KO. Prevalence of nasal staphylococcus aureus colonization amongst medical students of Igbinedion University Okada. Int J Trop Dis Health. 2018;34(2):1-5. DOI:10.9734/IJTDH/2018/46076; Thrusfield MV. Veterinary Epidemiology. 3. ed., reissued in paperback with updates. Oxford: Blackwell Science; 2007.; Tigabu A, Tiruneh M, Mekonnen F. Nasal Carriage Rate, Antimicrobial Susceptibility Pattern, and Associated Factors of with Special Emphasis on MRSA among Urban and Rural Elementary School Children in Gondar, Northwest Ethiopia: A Comparative Cross-Sectional Study. Adv Prev Med. 2018;2018:9364757. DOI:10.1155/2018/9364757; Tumbarello M, de Gaetano Donati K, Tacconelli E, Citton R, Spanu T, Leone F, Fadda G, Cauda R. Risk factors and predictors of mortality of methicillin-resistant Staphylococcus aureus (MRSA) bacteraemia in HIV-infected patients. J Antimicrob Chemother. 2002 Sep;50(3):375-82. DOI:10.1093/jac/dkf126; Uddin MJ, Ahn J. Associations between resistance phenotype and gene expression in response to serial exposure to oxacillin and ciprofloxacin in Staphylococcus aureus. Lett Appl Microbiol. 2017 Dec;65(6):462-8. DOI:10.1111/lam.12808; Utay NS, Roque A, Timmer JK, Morcock DR, DeLeage C, Somasunderam A, Weintrob AC, Agan BK, Estes JD, Crum-Cianflone NF, Douek DC. MRSA Infections in HIV-Infected People Are Associated with Decreased MRSA-Specific Th1 Immunity. PLoS Pathog. 2016 Apr;12(4):e1005580. DOI:10.1371/journal.ppat.1005580; Verhoeven PO, Grattard F, Carricajo A, Lucht F, Cazorla C, Garraud O, Pozzetto B, Berthelot P. An algorithm based on one or two nasal samples is accurate to identify persistent nasal carriers of Staphylococcus aureus. Clin Microbiol Infect. 2012 Jun;18(6):551-7. DOI:10.1111/j.1469-0691.2011.03611.x; van Belkum A, Melles DC, Nouwen J, van Leeuwen WB, van Wamel W, Vos MC, Wertheim HF, Verbrugh HA. Co-evolutionary aspects of human colonisation and infection by Staphylococcus aureus. Infect Genet Evol. 2009 Jan;9(1):32-47. DOI:10.1016/j.meegid.2008.09.012; van Bijnen EM, Paget J, de Lange-de Klerk ES, den Heijer CD, Versporten A, Stobberingh EE, Goossens H, Schellevis FG; collaboration with the APRES Study Team. Antibiotic Exposure and Other Risk Factors for Antimicrobial Resistance in Nasal Commensal Staphylococcus aureus: An Ecological Study in 8 European Countries. PLoS ONE. 2015;10(8):e0135094. DOI:10.1371/journal.pone.0135094; Wang JT, Liao CH, Fang CT, Chie WC, Lai MS, Lauderdale TL, Lee WS, Huang JH, Chang SC. Prevalence of and risk factors for colonization by methicillin-resistant Staphylococcus aureus among adults in community settings in Taiwan. J Clin Microbiol. 2009 Sep;47(9):2957-63. DOI:10.1128/JCM.00853-09; http://dx.doi.org/10.3205/dgkh000360Test; http://nbn-resolving.de/urn:nbn:de:0183-dgkh0003600Test; http://www.egms.de/en/journals/dgkh/2020-15/dgkh000360.shtmlTest

الإتاحة: https://doi.org/10.3205/dgkh000360Test
https://doi.org/10.1590/s1413-86702007000100016Test
https://doi.org/10.1186/s13104-016-2021-7Test
https://doi.org/10.11648/j.ajbls.20130103.11Test
https://doi.org/10.1086/647184Test
https://doi.org/10.1016/j.jinf.2016.08.016Test
https://doi.org/10.1111/j.1468-1293.2008.00629.xTest
https://doi.org/10.1086/502225Test
https://doi.org/10.1128/MMBR.00039-14Test
https://doi.org/10.1016/j.ajic.2013.01.035Test

المؤلفون: Bhooshan, S, Negi, V, Khatri, PK

المصدر: GMS Hygiene and Infection Control; VOL: 15; DOC32 /20201202/

مصطلحات موضوعية: Staphylococcus aureus, Staphylococcus pseudintermedius, zoonosis, Zoonose, ddc: 610

العلاقة: Bannoehr J, Brown JK, Shaw DJ, Fitzgerald RJ, van den Broek AH, Thoday KL. Staphylococccus pseudintermedius surface proteins SpsD and SpsO mediate adherence to ex vivo canine corneocytes. Vet Dermatol. 2012 Apr;23(2):119-24, e26. DOI:10.1111/j.1365-3164.2011.01021.x; Bannoehr J, Franco A, Iurescia M, Battisti A, Fitzgerald JR. Molecular diagnostic identification of Staphylococcus pseudintermedius. J Clin Microbiol. 2009 Feb;47(2):469-71. DOI:10.1128/JCM.01915-08; Bannoehr J, Ben Zakour NL, Waller AS, Guardabassi L, Thoday KL, van den Broek AH, Fitzgerald JR. Population genetic structure of the Staphylococcus intermedius group: insights into agr diversification and the emergence of methicillin-resistant strains. J Bacteriol. 2007 Dec;189(23):8685-92. DOI:10.1128/JB.01150-07; Bannoehr J, Ben Zakour NL, Reglinski M, Inglis NF, Prabhakaran S, Fossum E, Smith DG, Wilson GJ, Cartwright RA, Haas J, Hook M, van den Broek AH, Thoday KL, Fitzgerald JR. Genomic and surface proteomic analysis of the canine pathogen Staphylococcus pseudintermedius reveals proteins that mediate adherence to the extracellular matrix. Infect Immun. 2011 Aug;79(8):3074-86. DOI:10.1128/IAI.00137-11; Bannoehr J, Guardabassi L. Staphylococcus pseudintermedius in the dog: taxonomy, diagnostics, ecology, epidemiology and pathogenicity. Vet Dermatol. 2012 Aug;23(4):253-66, e51-2. DOI:10.1111/j.1365-3164.2012.01046.x; Bean DC, Wigmore SM. Carriage rate and antibiotic susceptibility of coagulase-positive staphylococci isolated from healthy dogs in Victoria, Australia. Aust Vet J. 2016 Dec;94(12):456-60. DOI:10.1111/avj.12528; Ben Zakour NL, Bannoehr J, van den Broek AH, Thoday KL, Fitzgerald JR. Complete genome sequence of the canine pathogen Staphylococcus pseudintermedius. J Bacteriol. 2011 May;193(9):2363-4. DOI:10.1128/JB.00137-11; Ben Zakour NL, Guinane CM, Fitzgerald JR. Pathogenomics of the staphylococci: insights into niche adaptation and the emergence of new virulent strains. FEMS Microbiol Lett. 2008 Dec;289(1):1-12. DOI:10.1111/j.1574-6968.2008.01384.x; Black CC, Solyman SM, Eberlein LC, Bemis DA, Woron AM, Kania SA. Identification of a predominant multilocus sequence type, pulsed-field gel electrophoresis cluster, and novel staphylococcal chromosomal cassette in clinical isolates of mecA-containing, methicillin-resistant Staphylococcus pseudintermedius. Vet Microbiol. 2009 Nov;139(3-4):333-8. DOI:10.1016/j.vetmic.2009.06.029; Börjesson S, Landén A, Bergström M, Andersson UG. Methicillin-resistant Staphylococcus pseudintermedius in Sweden. Microb Drug Resist. 2012 Dec;18(6):597-603. DOI:10.1089/mdr.2012.0069; Börjesson S, Gómez-Sanz E, Ekström K, Torres C, Grönlund U. Staphylococcus pseudintermedius can be misdiagnosed as Staphylococcus aureus in humans with dog bite wounds. Eur J Clin Microbiol Infect Dis. 2015 Apr;34(4):839-44. DOI:10.1007/s10096-014-2300-y; Chuang CY, Yang YL, Hsueh PR, Lee PI. Catheter-related bacteremia caused by Staphylococcus pseudintermedius refractory to antibiotic-lock therapy in a hemophilic child with dog exposure. J Clin Microbiol. 2010 Apr;48(4):1497-8. DOI:10.1128/JCM.02033-09; CLSI. Performance Standards for Antimicrobial Susceptibility Testing. 28th ed. CLSI supplement M100. Wayne, PA: Clinical and Laboratory Standards Institute; 2018.; Couto N, Belas A, Oliveira M, Almeida P, Clemente C, Pomba C. Comparative RNA-seq-Based Transcriptome Analysis of the Virulence Characteristics of Methicillin-Resistant and -Susceptible Staphylococcus pseudintermedius Strains Isolated from Small Animals. Antimicrob Agents Chemother. 2016 Feb;60(2):962-7. DOI:10.1128/AAC.01907-15; Cree RG, Noble WC. In vitro indices of tissue adherence in Staphylococcus intermedius. Lett Appl Microbiol. 1995 Mar;20(3):168-70. DOI:10.1111/j.1472-765x.1995.tb00418.x; De Martino L, Nocera FP, Mallardo K, Nizza S, Masturzo E, Fiorito F, Iovane G, Catalanotti P. An update on microbiological causes of canine otitis externa in Campania Region, Italy. Asian Pac J Trop Biomed. 2016;6(5):384-9. DOI:10.1016/j.apjtb.2015.11.012; Decristophoris P, Fasola A, Benagli C, Tonolla M, Petrini O. Identification of Staphylococcus intermedius Group by MALDI-TOF MS. Syst Appl Microbiol. 2011 Feb;34(1):45-51. DOI:10.1016/j.syapm.2010.11.004; Dufour P, Jarraud S, Vandenesch F, Greenland T, Novick RP, Bes M, Etienne J, Lina G. High genetic variability of the agr locus in Staphylococcus species. J Bacteriol. 2002 Feb;184(4):1180-6. DOI:10.1128/jb.184.4.1180-1186.2002; Duim B, Verstappen KMHW, Kalupahana RS, Ranathunga L, Fluit AC, Wagenaar JA. Methicillin-resistant Staphylococcus pseudintermedius among dogs in the description of novel SCCmec variants. Vet Microbiol. 2018 Jan;213:136-41. DOI:10.1016/j.vetmic.2017.11.022; Dziewanowska K, Edwards VM, Deringer JR, Bohach GA, Guerra DJ. Comparison of the beta-toxins from Staphylococcus aureus and Staphylococcus intermedius. Arch Biochem Biophys. 1996 Nov;335(1):102-8. DOI:10.1006/abbi.1996.0486; Edwards VM, Deringer JR, Callantine SD, Deobald CF, Berger PH, Kapur V, Stauffacher CV, Bohach GA. Characterization of the canine type C enterotoxin produced by Staphylococcus intermedius pyoderma isolates. Infect Immun. 1997 Jun;65(6):2346-52. DOI:10.1128/IAI.65.6.2346-2352.1997; European Medicines Agency; Committee for Medicinal Products for Veterinary Use. Advice on implementing measures under Article 37(4) of Regulation (EU) 2019/6 on veterinary medicinal products - Criteria for the designation of antimicrobials to be reserved for treatment of certain infections in humans. EMA/CVMP/158366/2019. 2019 Oct 31. Available from: https://www.ema.europa.eu/en/documents/regulatory-procedural-guideline/advice-implementing-measures-under-article-374-regulation-eu-2019/6-veterinary-medicinal-products-criteria-designation-antimicrobials-be-reserved-treatment-certain_en.pdfTest; Fazakerley J, Williams N, Carter S, McEwan N, Nuttall T. Heterogeneity of Staphylococcus pseudintermedius isolates from atopic and healthy dogs. Vet Dermatol. 2010 Dec;21(6):578-85. DOI:10.1111/j.1365-3164.2010.00894.x; Feng Y, Tian W, Lin D, Luo Q, Zhou Y, Yang T, Deng Y, Liu YH, Liu JH. Prevalence and characterization of methicillin-resistant Staphylococcus pseudintermedius in pets from South China. Vet Microbiol. 2012 Dec;160(3-4):517-24. DOI:10.1016/j.vetmic.2012.06.015; Forsythe PJ, Hill PB, Thoday KL, Brown J. Use of computerized image analysis to quantify staphylococcal adhesion to canine corneocytes: does breed and body site have any relevance to the pathogenesis of pyoderma? Vet Dermatol. 2002 Feb;13(1):29-36. DOI:10.1046/j.0959-4493.2001.00269.x; Foster TJ, Höök M. Surface protein adhesins of Staphylococcus aureus. Trends Microbiol. 1998 Dec;6(12):484-8. DOI:10.1016/s0966-842x(98)01400-0; Futagawa-Saito K, Sugiyama T, Karube S, Sakurai N, Ba-Thein W, Fukuyasu T. Prevalence and characterization of leukotoxin-producing Staphylococcus intermedius in Isolates from dogs and pigeons. J Clin Microbiol. 2004 Nov;42(11):5324-6. DOI:10.1128/JCM.42.11.5324-5326.2004; Futagawa-Saito K, Makino S, Sunaga F, Kato Y, Sakurai-Komada N, Ba-Thein W, Fukuyasu T. Identification of first exfoliative toxin in Staphylococcus pseudintermedius. FEMS Microbiol Lett. 2009 Dec;301(2):176-80. DOI:10.1111/j.1574-6968.2009.01823.x; Futagawa-Saito K, Ba-Thein W, Sakurai N, Fukuyasu T. Prevalence of virulence factors in Staphylococcus intermedius isolates from dogs and pigeons. BMC Vet Res. 2006 Jan;2:4. DOI:10.1186/1746-6148-2-4; Futagawa-Saito K, Suzuki M, Ohsawa M, Ohshima S, Sakurai N, Ba-Thein W, Fukuyasu T. Identification and prevalence of an enterotoxin-related gene, se-int, in Staphylococcus intermedius isolates from dogs and pigeons. J Appl Microbiol. 2004;96(6):1361-6. DOI:10.1111/j.1365-2672.2004.02264.x; Gangil R, Audarya S, Chhabra D, Sikrodia R, Sharda R. Multi Drug Resistant Staphylococcus pseudintermedius isolates from Canine Pyoderma. Ind J Anim Res. 2015;5(4):749-52. DOI:10.5958/2277-940X.2015.00124.2; Garbacz K, Zarnowska S, Piechowicz L, Haras K. Pathogenicity potential of Staphylococcus pseudintermedius strains isolated from canine carriers and from dogs with infection signs. Virulence. 2013 Apr;4(3):255-9. DOI:10.4161/viru.23526; Geoghegan JA, Smith EJ, Speziale P, Foster TJ. Staphylococcus pseudintermedius expresses surface proteins that closely resemble those from Staphylococcus aureus. Vet Microbiol. 2009 Sep;138(3-4):345-52. DOI:10.1016/j.vetmic.2009.03.030; Gharsa H, Ben Slama K, Gómez-Sanz E, Lozano C, Klibi N, Jouini A, Messadi L, Boudabous A, Torres C. Antimicrobial resistance, virulence genes, and genetic lineages of Staphylococcus pseudintermedius in healthy dogs in tunisia. Microb Ecol. 2013 Aug;66(2):363-8. DOI:10.1007/s00248-013-0243-y; Gold RM, Cohen ND, Lawhon SD. Amikacin resistance in Staphylococcus pseudintermedius isolated from dogs. J Clin Microbiol. 2014 Oct;52(10):3641-6. DOI:10.1128/JCM.01253-14; Grönthal T, Eklund M, Thomson K, Piiparinen H, Sironen T, Rantala M. Antimicrobial resistance in Staphylococcus pseudintermedius and the molecular epidemiology of methicillin-resistant S. pseudintermedius in small animals in Finland. J Antimicrob Chemother. 2017 07;72(7):2141. DOI:10.1093/jac/dkx086; Grönthal T, Moodley A, Nykäsenoja S, Junnila J, Guardabassi L, Thomson K, Rantala M. Large outbreak caused by methicillin resistant Staphylococcus pseudintermedius ST71 in a Finnish Veterinary Teaching Hospital-from outbreak control to outbreak prevention. PLoS ONE. 2014;9(10):e110084. DOI:10.1371/journal.pone.0110084; Grönthal T, Eklund M, Thomson K, Piiparinen H, Sironen T, Rantala M. Antimicrobial resistance in Staphylococcus pseudintermedius and the molecular epidemiology of methicillin-resistant S. pseudintermedius in small animals in Finland. J Antimicrob Chemother. 2017 04;72(4):1021-30. DOI:10.1093/jac/dkw559; Haenni M, de Moraes NA, Châtre P, Médaille C, Moodley A, Madec JY. Characterisation of clinical canine meticillin-resistant and meticillin-susceptible Staphylococcus pseudintermedius in France. J Glob Antimicrob Resist. 2014 Jun;2(2):119-23. DOI:10.1016/j.jgar.2014.02.002; Hajek V. Staphylococcus intermedius, a new species isolated from animals. Int J Syst Bacteriol. 1976;26:401-08. DOI:10.1099/00207713-26-4-401; Han JI, Rhim H, Yang CH, Park HM. Molecular characteristics of new clonal complexes of Staphylococcus pseudintermedius from clinically normal dogs. Vet Q. 2018 Dec;38(1):14-20. DOI:10.1080/01652176.2017.1400710; Hendricks A, Schuberth HJ, Schueler K, Lloyd DH. Frequency of superantigen-producing Staphylococcus intermedius isolates from canine pyoderma and proliferation-inducing potential of superantigens in dogs. Res Vet Sci. 2002 Dec;73(3):273-7. DOI:10.1016/s0034-5288(02)00107-8; Iyori K, Hisatsune J, Kawakami T, Shibata S, Murayama N, Ide K, Nagata M, Fukata T, Iwasaki T, Oshima K, Hattori M, Sugai M, Nishifuji K. Identification of a novel Staphylococcus pseudintermedius exfoliative toxin gene and its prevalence in isolates from canines with pyoderma and healthy dogs. FEMS Microbiol Lett. 2010 Nov;312(2):169-75. DOI:10.1111/j.1574-6968.2010.02113.x; Iyori K, Futagawa-Saito K, Hisatsune J, Yamamoto M, Sekiguchi M, Ide K, Son WG, Olivry T, Sugai M, Fukuyasu T, Iwasaki T, Nishifuji K. Staphylococcus pseudintermedius exfoliative toxin EXI selectively digests canine desmoglein 1 and causes subcorneal clefts in canine epidermis. Vet Dermatol. 2011 Aug;22(4):319-26. DOI:10.1111/j.1365-3164.2011.00952.x; Kang JH, Chung TH, Hwang CY. Clonal distribution of methicillin-resistant Staphylococcus pseudintermedius isolates from skin infection of dogs in Korea. Vet Microbiol. 2017 Oct;210:32-7. DOI:10.1016/j.vetmic.2017.08.017; Kang MH, Chae MJ, Yoon JW, Kim SG, Lee SY, Yoo JH, Park HM. Antibiotic resistance and molecular characterization of ophthalmic Staphylococcus pseudintermedius isolates from dogs. J Vet Sci. 2014;15(3):409-15. DOI:10.4142/jvs.2014.15.3.409; Kizerwetter-Swida M, Chrobak-Chmiel D, Rzewuska M, Binek M. Changes in the population structure of canine methicillin-resistant Staphylococcus pseudintermedius in Poland. Vet Microbiol. 2017 Sep;208:106-9. DOI:10.1016/j.vetmic.2017.07.025; Kjellman EE, Slettemeås JS, Small H, Sunde M. Methicillin-resistant Staphylococcus pseudintermedius (MRSP) from healthy dogs in Norway - occurrence, genotypes and comparison to clinical MRSP. Microbiologyopen. 2015 Dec;4(6):857-66. DOI:10.1002/mbo3.258; Kloos WE, Bannerman TL. Update on clinical significance of coagulase-negative staphylococci. Clin Microbiol Rev. 1994 Jan;7(1):117-40. DOI:10.1128/cmr.7.1.117; Kmieciak W, Szewczyk EM, Ciszewski M. Searching for Beta-Haemolysin hlb Gene in Staphylococcus pseudintermedius with Species-Specific Primers. Curr Microbiol. 2016 Jul;73(1):148-52. DOI:10.1007/s00284-016-1038-4; Lautz S, Kanbar T, Alber J, Lämmler C, Weiss R, Prenger-Berninghoff E, Zschöck M. Dissemination of the gene encoding exfoliative toxin of Staphylococcus intermedius among strains isolated from dogs during routine microbiological diagnostics. J Vet Med B Infect Dis Vet Public Health. 2006 Nov;53(9):434-8. DOI:10.1111/j.1439-0450.2006.00999.x; Lehner G, Linek M, Bond R, Lloyd DH, Prenger-Berninghoff E, Thom N, Straube I, Verheyen K, Loeffler A. Case-control risk factor study of methicillin-resistant Staphylococcus pseudintermedius (MRSP) infection in dogs and cats in Germany. Vet Microbiol. 2014 Jan;168(1):154-60. DOI:10.1016/j.vetmic.2013.10.023; Lu YF, McEwan NA. Staphylococcal and micrococcal adherence to canine and feline corneocytes: quantification using a simple adhesion assay. Vet Dermatol. 2007 Feb;18(1):29-35. DOI:10.1111/j.1365-3164.2007.00567.x; Maaland M, Guardabassi L. In vitro antimicrobial activity of nitrofurantoin against Escherichia coli and Staphylococcus pseudintermedius isolated from dogs and cats. Vet Microbiol. 2011 Aug;151(3-4):396-9. DOI:10.1016/j.vetmic.2011.03.009; McCarthy AJ, Harrison EM, Stanczak-Mrozek K, Leggett B, Waller A, Holmes MA, Lloyd DH, Lindsay JA, Loeffler A. Genomic insights into the rapid emergence and evolution of MDR in Staphylococcus pseudintermedius. J Antimicrob Chemother. 2015 Apr;70(4):997-1007. DOI:10.1093/jac/dku496; Meroni G, Soares Filipe JF, Drago L, Martino PA. Investigation on Antibiotic-Resistance, Biofilm Formation and Virulence Factors in Multi Drug Resistant and Non Multi Drug Resistant. Microorganisms. 2019 Dec;7(12). DOI:10.3390/microorganisms7120702; Moodley A, Stegger M, Ben Zakour NL, Fitzgerald JR, Guardabassi L. Tandem repeat sequence analysis of staphylococcal protein A (spa) gene in methicillin-resistant Staphylococcus pseudintermedius. Vet Microbiol. 2009 Mar;135(3-4):320-6. DOI:10.1016/j.vetmic.2008.09.070; Novick RP, Geisinger E. Quorum sensing in staphylococci. Annu Rev Genet. 2008;42:541-64. DOI:10.1146/annurev.genet.42.110807.091640; Perreten V, Kadlec K, Schwarz S, Grönlund Andersson U, Finn M, Greko C, Moodley A, Kania SA, Frank LA, Bemis DA, Franco A, Iurescia M, Battisti A, Duim B, Wagenaar JA, van Duijkeren E, Weese JS, Fitzgerald JR, Rossano A, Guardabassi L. Clonal spread of methicillin-resistant Staphylococcus pseudintermedius in Europe and North America: an international multicentre study. J Antimicrob Chemother. 2010 Jun;65(6):1145-54. DOI:10.1093/jac/dkq078; Phumthanakorn N, Fungwithaya P, Chanchaithong P, Prapasarakul N. Enterotoxin gene profile of methicillin-resistant Staphylococcus pseudintermedius isolates from dogs, humans and the environment. J Med Microbiol. 2018 Jun;67(6):866-73. DOI:10.1099/jmm.0.000748; Pietrocola G, Gianotti V, Richards A, Nobile G, Geoghegan JA, Rindi S, Monk IR, Bordt AS, Foster TJ, Fitzgerald JR, Speziale P. Fibronectin Binding Proteins SpsD and SpsL Both Support Invasion of Canine Epithelial Cells by Staphylococcus pseudintermedius. Infect Immun. 2015 Oct;83(10):4093-102. DOI:10.1128/IAI.00542-15; Pires Dos Santos T, Damborg P, Moodley A, Guardabassi L. Systematic Review on Global Epidemiology of Methicillin-Resistant: Inference of Population Structure from Multilocus Sequence Typing Data. Front Microbiol. 2016;7:1599. DOI:10.3389/fmicb.2016.01599; Pompilio A, De Nicola S, Crocetta V, Guarnieri S, Savini V, Carretto E, Di Bonaventura G. New insights in Staphylococcus pseudintermedius pathogenicity: antibiotic-resistant biofilm formation by a human wound-associated strain. BMC Microbiol. 2015 May;15:109. DOI:10.1186/s12866-015-0449-x; Ponnuraj K, Bowden MG, Davis S, Gurusiddappa S, Moore D, Choe D, Xu Y, Hook M, Narayana SV. A "dock, lock, and latch" structural model for a staphylococcal adhesin binding to fibrinogen. Cell. 2003 Oct;115(2):217-28. DOI:10.1016/s0092-8674(03)00809-2; Prevost G, Bouakham T, Piemont Y, Monteil H. Characterisation of a synergohymenotropic toxin produced by Staphylococcus intermedius. FEBS Lett. 1995 Dec;376(3):135-40. DOI:10.1016/0014-5793(95)01260-9; Riegel P, Jesel-Morel L, Laventie B, Boisset S, Vandenesch F, Prévost G. Coagulase-positive Staphylococcus pseudintermedius from animals causing human endocarditis. Int J Med Microbiol. 2011 Mar;301(3):237-9. DOI:10.1016/j.ijmm.2010.09.001; Rubin JE, Chirino-Trejo M. Prevalence, sites of colonization, and antimicrobial resistance among Staphylococcus pseudintermedius isolated from healthy dogs in Saskatoon, Canada. J Vet Diagn Invest. 2011 Mar;23(2):351-4. DOI:10.1177/104063871102300227; Ruscher C, Lübke-Becker A, Semmler T, Wleklinski CG, Paasch A, Soba A, Stamm I, Kopp P, Wieler LH, Walther B. Widespread rapid emergence of a distinct methicillin- and multidrug-resistant Staphylococcus pseudintermedius (MRSP) genetic lineage in Europe. Vet Microbiol. 2010 Aug;144(3-4):340-6. DOI:10.1016/j.vetmic.2010.01.008; Ruscher C, Lübke-Becker A, Wleklinski CG, Soba A, Wieler LH, Walther B. Prevalence of Methicillin-resistant Staphylococcus pseudintermedius isolated from clinical samples of companion animals and equidaes. Vet Microbiol. 2009 Apr;136(1-2):197-201. DOI:10.1016/j.vetmic.2008.10.023; Saijonmaa-Koulumies LE, Lloyd DH. Adherence of Staphylococcus intermedius to canine corneocytes in vitro. Vet Dermatol. 2002 Aug;13(4):169-76. DOI:10.1046/j.1365-3164.2002.00294.x; Sasaki T, Kikuchi K, Tanaka Y, Takahashi N, Kamata S, Hiramatsu K. Reclassification of phenotypically identified staphylococcus intermedius strains. J Clin Microbiol. 2007 Sep;45(9):2770-8. DOI:10.1128/JCM.00360-07; Sasaki T, Tsubakishita S, Tanaka Y, Sakusabe A, Ohtsuka M, Hirotaki S, Kawakami T, Fukata T, Hiramatsu K. Multiplex-PCR method for species identification of coagulase-positive staphylococci. J Clin Microbiol. 2010 Mar;48(3):765-9. DOI:10.1128/JCM.01232-09; Savini V, Barbarini D, Polakowska K, Gherardi G, Bialecka A, Kasprowicz A, Polilli E, Marrollo R, Di Bonaventura G, Fazii P, D'Antonio D, Miedzobrodzki J, Carretto E. Methicillin-resistant Staphylococcus pseudintermedius infection in a bone marrow transplant recipient. J Clin Microbiol. 2013 May;51(5):1636-8. DOI:10.1128/JCM.03310-12; Simou C, Hill PB, Forsythe PJ, Thoday KL. Species specificity in the adherence of staphylococci to canine and human corneocytes: a preliminary study. Vet Dermatol. 2005 Jun;16(3):156-61. DOI:10.1111/j.1365-3164.2005.00452.x; Soedarmanto I, Kanbar T, Ülbegi-Mohyla H, Hijazin M, Alber J, Lämmler C, Akineden Ö, Weiss R, Moritz A, Zschöck M. Genetic relatedness of methicillin-resistant Staphylococcus pseudintermedius (MRSP) isolated from a dog and the dog owner. Res Vet Sci. 2011 Dec;91(3):e25-7. DOI:10.1016/j.rvsc.2011.01.027; Solyman SM, Black CC, Duim B, van Duijkeren E, Wagenaar JA, Eblerlein LC, et al. Multilocus sequence typing (MLST) for characterization of methicillin-resistant and methicillin- susceptible clones of Staphylococcus pseudintermedius, in Speaker Abstract S2:5. In: American Society for Microbiology, editor. 2nd ASM-ESCMID Conference on Methicillin-resistant Staphylococci in Animals: Veterinary and Public Health Implications. Washington, 2011 Sep 8-11. Washington, DC: ASM;17-18. Available from: https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=web&cd=&ved=2ahUKEwiagrbM7bXrAhWMOcAKHR9mDxUQFjACegQIBBAB&url=https%3A%2F%2Fwww.escmid.org%2Fescmid_publications%2Fescmid_elibrary%2Fmaterial%2F%3Fmid%3D11144&usg=AOvVaw3Xqxu5h_zS2aduh5zADLyBTest; Somayaji R, Priyantha MA, Rubin JE, Church D. Human infections due to Staphylococcus pseudintermedius, an emerging zoonosis of canine origin: report of 24 cases. Diagn Microbiol Infect Dis. 2016 Aug;85(4):471-6. DOI:10.1016/j.diagmicrobio.2016.05.008; Stegmann R, Burnens A, Maranta CA, Perreten V. Human infection associated with methicillin-resistant Staphylococcus pseudintermedius ST71. J Antimicrob Chemother. 2010 Sep;65(9):2047-8. DOI:10.1093/jac/dkq241; Summers JF, Hendricks A, Brodbelt DC. Prescribing practices of primary-care veterinary practitioners in dogs diagnosed with bacterial pyoderma. BMC Vet Res. 2014 Oct;10:240. DOI:10.1186/s12917-014-0240-5; Talan DA, Staatz D, Staatz A, Overturf GD. Frequency of Staphylococcus intermedius as human nasopharyngeal flora. J Clin Microbiol. 1989 Oct;27(10):2393. DOI:10.1128/JCM.27.10.2393-.1989; Tanabe T, Toyoguchi M, Hirano F, Chiba M, Onuma K, Sato H. Prevalence of staphylococcal enterotoxins in Staphylococcus pseudintermedius isolates from dogs with pyoderma and healthy dogs. Microbiol Immunol. 2013 Sep;57(9):651-4. DOI:10.1111/1348-0421.12069; Terauchi R, Sato H, Hasegawa T, Yamaguchi T, Aizawa C, Maehara N. Isolation of exfoliative toxin from Staphylococcus intermedius and its local toxicity in dogs. Vet Microbiol. 2003 Jun;94(1):19-29. DOI:10.1016/s0378-1135(03)00048-8; Terauchi R, Sato H, Endo Y, Aizawa C, Maehara N. Cloning of the gene coding for Staphylococcus intermedius exfoliative toxin and its expression in Escherichia coli. Vet Microbiol. 2003 Jun;94(1):31-8. DOI:10.1016/s0378-1135(03)00047-6; Tse H, Tsoi HW, Leung SP, Urquhart IJ, Lau SK, Woo PC, Yuen KY. Complete genome sequence of the veterinary pathogen Staphylococcus pseudintermedius strain HKU10-03, isolated in a case of canine pyoderma. J Bacteriol. 2011 Apr;193(7):1783-4. DOI:10.1128/JB.00023-11; Van Hoovels L, Vankeerberghen A, Boel A, Van Vaerenbergh K, De Beenhouwer H. First case of Staphylococcus pseudintermedius infection in a human. J Clin Microbiol. 2006 Dec;44(12):4609-12. DOI:10.1128/JCM.01308-06; Ventrella G, Moodley A, Grandolfo E, Parisi A, Corrente M, Buonavoglia D, Guardabassi L. Frequency, antimicrobial susceptibility and clonal distribution of methicillin-resistant Staphylococcus pseudintermedius in canine clinical samples submitted to a veterinary diagnostic laboratory in Italy: A 3-year retrospective investigation. Vet Microbiol. 2017 Nov;211:103-6. DOI:10.1016/j.vetmic.2017.09.015; Verstappen KM, Huijbregts L, Spaninks M, Wagenaar JA, Fluit AC, Duim B. Development of a real-time PCR for detection of Staphylococcus pseudintermedius using a novel automated comparison of whole-genome sequences. PLoS ONE. 2017;12(8):e0183925. DOI:10.1371/journal.pone.0183925; Videla R, Solyman SM, Brahmbhatt A, Sadeghi L, Bemis DA, Kania SA. Clonal Complexes and Antimicrobial Susceptibility Profiles of Staphylococcus pseudintermedius Isolates from Dogs in the United States. Microb Drug Resist. 2018 Jan/Feb;24(1):83-8. DOI:10.1089/mdr.2016.0250; Vincze S, Paasch A, Walther B, Ruscher C, Lübke-Becker A, Wieler LH, Barbara K. Multidrug- and methicillin resistant Staphylococcus pseudintermedius as a cause of canine pyoderma: a case report. Berl Munch Tierarztl Wochenschr. 2010 Sep-Oct;123(9-10):353-8.; Weese JS, van Duijkeren E. Methicillin-resistant Staphylococcus aureus and Staphylococcus pseudintermedius in veterinary medicine. Vet Microbiol. 2010 Jan;140(3-4):418-29. DOI:10.1016/j.vetmic.2009.01.039; Wladyka B, Piejko M, Bzowska M, Pieta P, Krzysik M, Mazurek L, Guevara-Lora I, Bukowski M, Sabat AJ, Friedrich AW, Bonar E, Miedzobrodzki J, Dubin A, Mak P. A peptide factor secreted by Staphylococcus pseudintermedius exhibits properties of both bacteriocins and virulence factors. Sci Rep. 2015 Sep;5:14569. DOI:10.1038/srep14569; Woolley KL, Kelly RF, Fazakerley J, Williams NJ, Nuttall TJ, McEwan NA. Reduced in vitro adherence of Staphylococcus species to feline corneocytes compared to canine and human corneocytes. Vet Dermatol. 2008 Feb;19(1):1-6. DOI:10.1111/j.1365-3164.2007.00649.x; Worthing KA, Marcus A, Abraham S, Trott DJ, Norris JM. Qac genes and biocide tolerance in clinical veterinary methicillin-resistant and methicillin-susceptible Staphylococcus aureus and Staphylococcus pseudintermedius. Vet Microbiol. 2018 Mar;216:153-8. DOI:10.1016/j.vetmic.2018.02.004; Worthing KA, Abraham S, Coombs GW, Pang S, Saputra S, Jordan D, Trott DJ, Norris JM. Clonal diversity and geographic distribution of methicillin-resistant Staphylococcus pseudintermedius from Australian animals: Discovery of novel sequence types. Vet Microbiol. 2018 Jan;213:58-65. DOI:10.1016/j.vetmic.2017.11.018; Yoon JW, Lee KJ, Lee SY, Chae MJ, Park JK, Yoo JH, Park HM. Antibiotic resistance profiles of Staphylococcus pseudintermedius isolates from canine patients in Korea. J Microbiol Biotechnol. 2010 Dec;20(12):1764-8.; Yoon JW, Lee GJ, Lee SY, Park C, Yoo JH, Park HM. Prevalence of genes for enterotoxins, toxic shock syndrome toxin 1 and exfoliative toxin among clinical isolates of Staphylococcus pseudintermedius from canine origin. Vet Dermatol. 2010 Oct;21(5):484-9. DOI:10.1111/j.1365-3164.2009.00874.x; Youn JH, Park YH, Hang'ombe B, Sugimoto C. Prevalence and characterization of Staphylococcus aureus and Staphylococcus pseudintermedius isolated from companion animals and environment in the veterinary teaching hospital in Zambia, Africa. Comp Immunol Microbiol Infect Dis. 2014 Mar;37(2):123-30. DOI:10.1016/j.cimid.2014.01.003; http://dx.doi.org/10.3205/dgkh000367Test; http://nbn-resolving.de/urn:nbn:de:0183-dgkh0003679Test; http://www.egms.de/en/journals/dgkh/2020-15/dgkh000367.shtmlTest

الإتاحة: https://doi.org/10.3205/dgkh000367Test
https://doi.org/10.1111/j.1365-3164.2011.01021.xTest
https://doi.org/10.1128/JCM.01915-08Test
https://doi.org/10.1128/JB.01150-07Test
https://doi.org/10.1128/IAI.00137-11Test
https://doi.org/10.1111/j.1365-3164.2012.01046.xTest
https://doi.org/10.1111/avj.12528Test
https://doi.org/10.1128/JB.00137-11Test
https://doi.org/10.1111/j.1574-6968.2008.01384.xTest
https://doi.org/10.1016/j.vetmic.2009.06.029Test

المؤلفون: Barthel, J, Ketter, V, Spies-Naumann, A, Paletta, JRJ, Frink, M, Ruchholtz, S, Lechler, P

المصدر: Deutscher Kongress für Orthopädie und Unfallchirurgie (DKOU 2018); 20181023-20181026; Berlin; DOCPT13-740 /20181106/

مصطلحات موضوعية: periprothetische Infektion, Hüft-TEP-Infektionen, Knie-TEP-Infektionen, Erregerspektrum, Staphylococcus aureus, Staphylococcus epidermidis, Koagulase-negative Staphylokokken, ddc: 610

العلاقة: http://dx.doi.org/10.3205/18dkou606Test; http://nbn-resolving.de/urn:nbn:de:0183-18dkou6069Test; http://www.egms.de/en/meetings/dkou2018/18dkou606.shtmlTest

الإتاحة: https://doi.org/10.3205/18dkou606Test
http://nbn-resolving.de/urn:nbn:de:0183-18dkou6069Test
http://www.egms.de/en/meetings/dkou2018/18dkou606.shtmlTest

المؤلفون: Monecke, S, Ruppelt-Lorz, A, Müller, E, Reissig, A, Thürmer, A, Shore, AC, Coleman, DC, Ehricht, R, Jatzwauk, L

المصدر: GMS Hygiene and Infection Control; VOL: 12; DOC19 /20171120/

مصطلحات موضوعية: methicillin-resistant Staphylococcus aureus, MRSA, mupirocin, high-level mupirocin resistance, mupA, "Barnim Epidemic Strain", Methicillin-resistente Staphylococcus aureus, hochgradige Mupirocin-Resistenz, "Barnimer Epidemiestamm", ddc: 610

العلاقة: Al-Doori Z, Goroncy-Bermes P, Gemmell CG, Morrison D. Low-level exposure of MRSA to octenidine dihydrochloride does not select for resistance. J Antimicrob Chemother. 2007 Jun;59(6):1280-1. DOI:10.1093/jac/dkm092; Albrecht N, Jatzwauk L, Slickers P, Ehricht R, Monecke S. Clonal replacement of epidemic methicillin-resistant Staphylococcus aureus strains in a German university hospital over a period of eleven years. PLoS ONE. 2011;6(11):e28189. DOI:10.1371/journal.pone.0028189; Antonov NK, Garzon MC, Morel KD, Whittier S, Planet PJ, Lauren CT. High prevalence of mupirocin resistance in Staphylococcus aureus isolates from a pediatric population. Antimicrob Agents Chemother. 2015;59(6):3350-6. DOI:10.1128/AAC.00079-15; Coates T, Bax R, Coates A. Nasal decolonization of Staphylococcus aureus with mupirocin: strengths, weaknesses and future prospects. J Antimicrob Chemother. 2009 Jul;64(1):9-15. DOI:10.1093/jac/dkp159; Hodgson JE, Curnock SP, Dyke KG, Morris R, Sylvester DR, Gross MS. Molecular characterization of the gene encoding high-level mupirocin resistance in Staphylococcus aureus J2870. Antimicrob Agents Chemother. 1994 May;38(5):1205-8.; Monecke S, Coombs G, Shore AC, Coleman DC, Akpaka P, Borg M, Chow H, Ip M, Jatzwauk L, Jonas D, Kadlec K, Kearns A, Laurent F, O'Brien FG, Pearson J, Ruppelt A, Schwarz S, Scicluna E, Slickers P, Tan HL, Weber S, Ehricht R. A field guide to pandemic, epidemic and sporadic clones of methicillin-resistant Staphylococcus aureus. PLoS ONE. 2011 Apr;6(4):e17936. DOI:10.1371/journal.pone.0017936; Monecke S, Jatzwauk L, Müller E, Nitschke H, Pfohl K, Slickers P, Reissig A, Ruppelt-Lorz A, Ehricht R. Diversity of SCCmec Elements in Staphylococcus aureus as Observed in South-Eastern Germany. PLoS ONE. 2016;11(9):e0162654. DOI:10.1371/journal.pone.0162654; Monecke S, Nitschke H, Slickers P, Ehricht R, Swanston W, Manjunath M, Roberts R, Akpaka PE. Molecular epidemiology and characterisation of MRSA isolates from Trinidad and Tobago. Eur J Clin Microbiol Infect Dis. 2012 Jul;31(7):1497-500. DOI:10.1007/s10096-011-1469-6; Monecke S, Slickers P, Ehricht R. Assignment of Staphylococcus aureus isolates to clonal complexes based on microarray analysis and pattern recognition. FEMS Immunol Med Microbiol. 2008 Jul;53(2):237-51. DOI:10.1111/j.1574-695X.2008.00426.x; Morton TM, Johnston JL, Patterson J, Archer GL. Characterization of a conjugative staphylococcal mupirocin resistance plasmid. Antimicrob Agents Chemother. 1995 Jun;39(6):1272-80.; Orrett FA. The emergence of mupirocin resistance among clinical isolates of methicillin-resistant Staphylococcus aureus in Trinidad: a first report. Jpn J Infect Dis. 2008 Mar;61(2):107-10.; Rossney A, O'Connell S. Emerging high-level mupirocin resistance among MRSA isolates in Ireland. Euro Surveill. 2008 Apr 3;13(14). pii: 8084.; Shore AC, Rossney AS, Brennan OM, Kinnevey PM, Humphreys H, Sullivan DJ, Goering RV, Ehricht R, Monecke S, Coleman DC. Characterization of a novel arginine catabolic mobile element (ACME) and staphylococcal chromosomal cassette mec composite island with significant homology to Staphylococcus epidermidis ACME type II in methicillin-resistant Staphylococcus aureus genotype ST22-MRSA-IV. Antimicrob Agents Chemother. 2011 May;55(5):1896-905. DOI:10.1128/AAC.01756-10; Thomas CM, Hothersall J, Willis CL, Simpson TJ. Resistance to and synthesis of the antibiotic mupirocin. Nat Rev Microbiol. 2010 Apr;8(4):281-9. DOI:10.1038/nrmicro2278; Williamson DA, Monecke S, Heffernan H, Ritchie SR, Roberts SA, Upton A, Thomas MG, Fraser JD. High usage of topical fusidic acid and rapid clonal expansion of fusidic acid-resistant Staphylococcus aureus: a cautionary tale. Clin Infect Dis. 2014 Nov;59(10):1451-4. DOI:10.1093/cid/ciu658; Witte W, Enright M, Schmitz FJ, Cuny C, Braulke C, Heuck D. Characteristics of a new epidemic MRSA in Germany ancestral to United Kingdom EMRSA 15. Int J Med Microbiol. 2001 Mar;290(8):677-82. DOI:10.1016/S1438-4221(01)80006-0; http://dx.doi.org/10.3205/dgkh000304Test; http://nbn-resolving.de/urn:nbn:de:0183-dgkh0003048Test; http://www.egms.de/en/journals/dgkh/2017-12/dgkh000304.shtmlTest

الإتاحة: https://doi.org/10.3205/dgkh000304Test
https://doi.org/10.1093/jac/dkm092Test
https://doi.org/10.1371/journal.pone.0028189Test
https://doi.org/10.1128/AAC.00079-15Test
https://doi.org/10.1093/jac/dkp159Test
https://doi.org/10.1371/journal.pone.0017936Test
https://doi.org/10.1371/journal.pone.0162654Test
https://doi.org/10.1007/s10096-011-1469-6Test
https://doi.org/10.1111/j.1574-695X.2008.00426.xTest
https://doi.org/10.1128/AAC.01756-10Test

المؤلفون: Claus, F, Ried, W

المصدر: GMS Hygiene and Infection Control; VOL: 12; DOC21 /20171218/

مصطلحات موضوعية: health-related quality of life, preference-based measure of health, economic evaluation, multidrug-resistant organism, methicillin-resistant Staphylococcus aureus, gesundheitsbezogene Lebensqualität, präferenzbasierter Nutzwert, gesundheitsökonomische Evaluation, multiresistente Bakterien, Methicillin-resistenter Staphylococcus aureus, ddc: 610

العلاقة: Adler A, Gniadkowski M, Baraniak A, Izdebski R, Fiett J, Hryniewicz W, Malhotra-Kumar S, Goossens H, Lammens C, Lerman Y, Kazma M, Kotlovsky T, Carmeli Y; MOSAR WP5 and WP2 study groups. Transmission dynamics of ESBL-producing Escherichia coli clones in rehabilitation wards at a tertiary care centre. Clin Microbiol Infect. 2012 Dec;18(12):E497-505. DOI:10.1111/j.1469-0691.2012.03999.x; Empfehlungen zur Prävention und Kontrolle von Methicillinresistenten Staphylococcus aureus-Stämmen (MRSA) in medizinischen und pflegerischen Einrichtungen. Empfehlung der Kommission für Krankenhaushygiene und Infektionsprävention (KRINKO) beim Robert Koch-Institut (RKI) [Recommendations for prevention and control of methicillin-resistant staphylococcus aureus (MRSA) in medical and nursing facilities. Commission recommendation for hospital hygiene and infection prevention (KRINKO) at the Robert Koch Institute (RKI)]. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2014 Jun;57(6):696-732. DOI:10.1007/s00103-014-1980-x; Hygienemaßnahmen bei Infektionen oder Besiedlung mit multiresistenten gramnegativen Stäbchen. Empfehlung der Kommission für Krankenhaushygiene und Infektionsprävention (KRINKO) beim Robert Koch-Institut (RKI) [Hygiene measures for infection or colonization with multidrug-resistant gram-negative bacilli. Commission recommendation for hospital hygiene and infection prevention (KRINKO) at the Robert Koch Institute (RKI)]. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2012 Oct;55(10):1311-54. DOI:10.1007/s00103-012-1549-5; Bacher J. Statistisches Matching: Anwendungsmöglichkeiten, Verfahren und ihre praktische Umsetzung in SPSS. ZA-Information. 2002;51:38-66.; Brazier J, Roberts J, Deverill M. The estimation of a preference-based measure of health from the SF-36. J Health Econ. 2002 Mar;21(2):271-92. DOI:10.1016/S0167-6296(01)00130-8; Chaberny IF, Ziesing S, Mattner F, Bärwolff S, Brandt C, Eckmanns T, Rüden H, Sohr D, Weist K, Gastmeier P. The burden of MRSA in four German university hospitals. Int J Hyg Environ Health. 2005;208(6):447-53. DOI:10.1016/j.ijheh.2005.08.004; Drummond MF, Sculpher MJ, Torrance GW, O'Brien BJ, Stoddart GL. Methods for the economic evaluation of health care programmes. Oxford, New York: Oxford University Press; 2005.; Dulon M, Haamann F, Peters C, Schablon A, Nienhaus A. MRSA prevalence in European healthcare settings: a review. BMC Infect Dis. 2011 May;11:138. DOI:10.1186/1471-2334-11-138; Escaut L, Bouam S, Frank-Soltysiak M, Rudant E, Saliba F, Kassis N, Presiozi P, Vittecoq D. Eradication of an outbreak of vancomycin-resistant Enterococcus (VRE): the cost of a failure in the systematic screening. Antimicrob Resist Infect Control. 2013 Jun;2(1):18. DOI:10.1186/2047-2994-2-18; European Centre for Disease Prevention and Control. Annual epidemiological report: Antimicrobial resistance and healthcare-associated infections 2014. Stockholm: ECDC; 2015.; Gavaldà L, Masuet C, Beltran J, Garcia M, Garcia D, Sirvent JM, Ramon JM. Comparative cost of selective screening to prevent transmission of methicillin-resistant Staphylococcus aureus (MRSA), compared with the attributable costs of MRSA infection. Infect Control Hosp Epidemiol. 2006 Nov;27(11):1264-6. DOI:10.1086/507968; Gerlich MG, Piegsa J, Schäfer C, Hübner NO, Wilke F, Reuter S, Engel G, Ewert R, Claus F, Hübner C, Ried W, Flessa S, Kramer A, Hoffmann W. Improving hospital hygiene to reduce the impact of multidrug-resistant organisms in health care - a prospective controlled multicenter study. BMC Infect Dis. 2015 Oct;15:441. DOI:10.1186/s12879-015-1184-5; Goulenok T, Ferroni A, Bille E, Lécuyer H, Join-Lambert O, Descamps P, Nassif X, Zahar JR. Risk factors for developing ESBL E. coli: can clinicians predict infection in patients with prior colonization? J Hosp Infect. 2013 Aug;84(4):294-9. DOI:10.1016/j.jhin.2013.04.018; Greiner BF. Auswirkung der MRSA Infektion auf die postoperative Lebensqualität unfallchirurgischer Patienten [Dissertation]. München: Technische Universität München; 2007.; Gupta K, Martinello RA, Young M, Strymish J, Cho K, Lawler E. MRSA nasal carriage patterns and the subsequent risk of conversion between patterns, infection, and death. PLoS ONE. 2013;8(1):e53674. DOI:10.1371/journal.pone.0053674; HICARE Aktionsbündnis gegen multiresistente Bakterien. Gemeinsam gegen MRE - Gesundheitsregion Ostseeküste Greifswald. Projektlaufzeit 2011-2015, Abschlussdokumentation; 2015. Available from: http://www.hicare.de/fileadmin/hicare/user_upload/materialien/HICARE-Abschlussdokumentation.pdfTest; Hübner C, Hübner NO, Hopert K, Maletzki S, Flessa S. Analysis of MRSA-attributed costs of hospitalized patients in Germany. Eur J Clin Microbiol Infect Dis. 2014 Oct;33(10):1817-22. DOI:10.1007/s10096-014-2131-x; Ibert F, Eckstein M, Günther F, Mutters NT. The relationship between subjective perception and the psychological effects of patients in spatial isolation. GMS Hyg Infect Control. 2017;12:Doc11. DOI:10.3205/dgkh000296; Jakob J. MRSA-Befall und Lebensqualität am Beispiel herzchirurgischer Patienten [Dissertation]. Regensburg: Universität Regensburg; 2010.; Laudermilch DJ, Fedorka CJ, Heyl A, Rao N, McGough RL. Outcomes of revision total knee arthroplasty after methicillin-resistant Staphylococcus aureus infection. Clin Orthop Relat Res. 2010 Aug;468(8):2067-73. DOI:10.1007/s11999-010-1304-x; Lloyd-Smith P, Younger J, Lloyd-Smith E, Green H, Leung V, Romney MG. Economic analysis of vancomycin-resistant enterococci at a Canadian hospital: assessing attributable cost and length of stay. J Hosp Infect. 2013 Sep;85(1):54-9. DOI:10.1016/j.jhin.2013.06.016; Macedo-Viñas M, De Angelis G, Rohner P, Safran E, Stewardson A, Fankhauser C, Schrenzel J, Pittet D, Harbarth S. Burden of meticillin-resistant Staphylococcus aureus infections at a Swiss University hospital: excess length of stay and costs. J Hosp Infect. 2013 Jun;84(2):132-7. DOI:10.1016/j.jhin.2013.02.015; Magiorakos AP, Srinivasan A, Carey RB, Carmeli Y, Falagas ME, Giske CG, Harbarth S, Hindler JF, Kahlmeter G, Olsson-Liljequist B, Paterson DL, Rice LB, Stelling J, Struelens MJ, Vatopoulos A, Weber JT, Monnet DL. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect. 2012 Mar;18(3):268-81. DOI:10.1111/j.1469-0691.2011.03570.x; Mauldin PD, Salgado CD, Hansen IS, Durup DT, Bosso JA. Attributable hospital cost and length of stay associated with health care-associated infections caused by antibiotic-resistant Gram-negative bacteria. Antimicrob Agents Chemother. 2010 Jan;54(1):109-15. DOI:10.1128/AAC.01041-09; Morfeld M, Kirchberger I, Bullinger M. Fragebogen zum Gesundheitszustand: Deutsche Version des Short Form-36 Health Survey, Manual. Göttingen: Hogrefe; 2011.; Mutters NT, Brooke RJ, Frank U, Heeg K. Low risk of apparent transmission of vancomycin-resistant Enterococci from bacteraemic patients to hospitalized contacts. Am J Infect Control. 2013 Sep;41(9):778-81. DOI:10.1016/j.ajic.2012.11.019; Müller H, Franke A, Resch KL. Application of the German SF-36 in hospitals: overestimations in the psycho-social scales. Int J Public Health. 2007;52(1):60-1. DOI:10.1007/s00038-006-5091-9; Müller H, Franke A, Schuck P, Resch KL. Eine kliniktaugliche Version des deutschsprachigen SF-36 und ihr psychometrischer Vergleich mit dem Originalfragebogen [A hospital suited version of the German SF-36 and its psychometric comparison with the original questionnaire]. Soz Praventivmed. 2001;46(2):96-105. DOI:10.1007/BF01299726; Olivier CN, Blake RK, Steed LL, Salgado CD. Risk of vancomycin-resistant Enterococcus (VRE) bloodstream infection among patients colonized with VRE. Infect Control Hosp Epidemiol. 2008 May;29(5):404-9. DOI:10.1086/587647; Pada SK, Ding Y, Ling ML, Hsu LY, Earnest A, Lee TE, Yong HC, Jureen R, Fisher D. Economic and clinical impact of nosocomial meticillin-resistant Staphylococcus aureus infections in Singapore: a matched case-control study. J Hosp Infect. 2011 May;78(1):36-40. DOI:10.1016/j.jhin.2010.10.016; Resch A, Wilke M, Fink C. The cost of resistance: incremental cost of methicillin-resistant Staphylococcus aureus (MRSA) in German hospitals. Eur J Health Econ. 2009 Jul;10(3):287-97. DOI:10.1007/s10198-008-0132-3; Salgado CD. The risk of developing a vancomycin-resistant Enterococcus bloodstream infection for colonized patients. Am J Infect Control. 2008 Dec;36(10):S175.e5-8. DOI:10.1016/j.ajic.2008.10.010; Smith HL. Matching with multiple controls to estimate treatment effects in observational studies. Sociol Methodol. 1997;27(1):325-53. DOI:10.1111/1467-9531.271030; Statistisches Bundesamt. Grunddaten der Krankenhäuser 2015. Wiesbaden: Statistisches Bundesamt; 2016. (Fachserie 12 Reihe 6.1.1 - 2016). Available from: https://www.destatis.de/DE/Publikationen/Thematisch/Gesundheit/Krankenhaeuser/GrunddatenKrankenhaeuser2120611157004.pdf?__blob=publicationFileTest; Tacconelli E, Cataldo MA, Dancer SJ, De Angelis G, Falcone M, Frank U, Kahlmeter G, Pan A, Petrosillo N, Rodríguez-Baño J, Singh N, Venditti M, Yokoe DS, Cookson B; European Society of Clinical Microbiology. ESCMID guidelines for the management of the infection control measures to reduce transmission of multidrug-resistant Gram-negative bacteria in hospitalized patients. Clin Microbiol Infect. 2014 Jan;20 Suppl 1:1-55. DOI:10.1111/1469-0691.12427; The University of Sheffield. Non Commercial end user license application for health measures. Available from: https://www.sheffield.ac.uk/scharr/sections/heds/mvh/paediatric/noncommercialTest; Tübbicke A, Hübner C, Kramer A, Hübner NO, Fleßa S. Transmission rates, screening methods and costs of MRSA -- a systematic literature review related to the prevalence in Germany. Eur J Clin Microbiol Infect Dis. 2012 Oct;31(10):2497-511. DOI:10.1007/s10096-012-1632-8; Walters SJ. Quality of Life Outcomes in Clinical Trials and Health-Care Evaluation. Chichester, UK: John Wiley & Sons Ltd.; 2009. DOI:10.1002/9780470840481; Wernitz MH, Keck S, Swidsinski S, Schulz S, Veit SK. Cost analysis of a hospital-wide selective screening programme for methicillin-resistant Staphylococcus aureus (MRSA) carriers in the context of diagnosis related groups (DRG) payment. Clin Microbiol Infect. 2005 Jun;11(6):466-71. DOI:10.1111/j.1469-0691.2005.01153.x; Zwingmann C, Metzger D, Jäckel WH. Short Form-36 Health Survey (SF-36): Psychometrische Analysen der deutschen Version bei Rehabilitanden mit chronischen Rückenschmerzen. [Short Form-36 Health Survey (SF-36): Psychometric analyses of the German version with chronic low back pain rehabilitation patients]. Diagnostica. 1998;44(4):209-19.; http://dx.doi.org/10.3205/dgkh000306Test; http://nbn-resolving.de/urn:nbn:de:0183-dgkh0003063Test; http://www.egms.de/en/journals/dgkh/2017-12/dgkh000306.shtmlTest

الإتاحة: https://doi.org/10.3205/dgkh000306Test
https://doi.org/10.1111/j.1469-0691.2012.03999.xTest
https://doi.org/10.1007/s00103-014-1980-xTest
https://doi.org/10.1007/s00103-012-1549-5Test
https://doi.org/10.1016/S0167-6296Test(01)00130-8
https://doi.org/10.1016/j.ijheh.2005.08.004Test
https://doi.org/10.1186/1471-2334-11-138Test
https://doi.org/10.1186/2047-2994-2-18Test
https://doi.org/10.1086/507968Test
https://doi.org/10.1186/s12879-015-1184-5Test

المؤلفون: Kacmaz, B, Gul, S

المصدر: GMS Hygiene and Infection Control; VOL: 11; DOC06 /20160310/

مصطلحات موضوعية: environmental contamination, methicillin-resistant Staphylococcus aureus, MRSA, paper, Umgebungskontamination, Methicillin-resistenter Staphylococcus aureus, Papier, ddc: 610

العلاقة: Alsubaie S, Maither Ab, Alalmaei W, Al-Shammari AD, Tashkandi M, Somily AM, Alaska A, BinSaeed AA. Determinants of hand hygiene noncompliance in intensive care units. Am J Infect Control. 2013 Feb;41(2):131-5. DOI:10.1016/j.ajic.2012.02.035; Chemaly RF, Simmons S, Dale C Jr, Ghantoji SS, Rodriguez M, Gubb J, Stachowiak J, Stibich M. The role of the healthcare environment in the spread of multidrug-resistant organisms: update on current best practices for containment. Ther Adv Infect Dis. 2014 Jun;2(3-4):79-90. DOI:10.1177/2049936114543287; Chen KH, Chen LR, Wang YK. Contamination of medical charts: an important source of potential infection in hospitals. PLoS One. 2014 Feb 18;9(2):e78512. DOI:10.1371/journal.pone.0078512; Fafliora E, Bampalis VG, Lazarou N, Mantzouranis G, Anastassiou ED, Spiliopoulou I, Christofidou M. Bacterial contamination of medical devices in a Greek emergency department: impact of physicians' cleaning habits. Am J Infect Control. 2014 Jul;42(7):807-9. DOI:10.1016/j.ajic.2014.03.017; German Institute for Standardization (DIN). DIN 58940-2 Beiblatt 2:2002-10. Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 2: Active substance carriers for the agar diffusion test; Carrier loads and values required for drawing a standard curve. Berlin: Beuth; 2002.; Hayden MK, Blom DW, Lyle EA, Moore CG, Weinstein RA. Risk of hand or glove contamination after contact with patients colonized with vancomycin-resistant enterococcus or the colonized patients' environment. Infect Control Hosp Epidemiol. 2008 Feb;29(2):149-54. DOI:10.1086/524331; Hübner NO, Hübner C, Kramer A, Assadian O. Survival of bacterial pathogens on paper and bacterial retrieval from paper to hands: preliminary results. Am J Nurs. 2011 Dec;111(12):30-4; quiz 35-6. DOI:10.1097/01.NAJ.0000408181.37017.82; Kramer A, Schwebke I, Kampf G. How long do nosocomial pathogens persist on inanimate surfaces? A systematic review. BMC Infect Dis. 2006;6:130. DOI:10.1186/1471-2334-6-130; Lopez PJ, Ron O, Parthasarathy P, Soothill J, Spitz L. Bacterial counts from hospital doctors' ties are higher than those from shirts. Am J Infect Control. 2009 Feb;37(1):79-80. DOI:10.1016/j.ajic.2008.09.018; Munoz-Price LS, Arheart KL, Mills JP, Cleary T, Depascale D, Jimenez A, Fajardo-Aquino Y, Coro G, Birnbach DJ, Lubarsky DA. Associations between bacterial contamination of health care workers' hands and contamination of white coats and scrubs. Am J Infect Control. 2012 Nov;40(9):e245-8. DOI:10.1016/j.ajic.2012.03.032; Neely AN, Maley MP. Survival of enterococci and staphylococci on hospital fabrics and plastic. J Clin Microbiol. 2000 Feb;38(2):724-6.; Randle J, Arthur A, Vaughan N. Twenty-four-hour observational study of hospital hand hygiene compliance. J Hosp Infect. 2010 Nov;76(3):252-5. DOI:10.1016/j.jhin.2010.06.027; Selim HS, Abaza AF. Microbial contamination of mobile phones in a health care setting in Alexandria, Egypt. GMS Hyg Infect Control. 2015 Feb 2;10:Doc03. DOI:10.3205/dgkh000246; http://dx.doi.org/10.3205/dgkh000266Test; http://nbn-resolving.de/urn:nbn:de:0183-dgkh0002663Test; http://www.egms.de/en/journals/dgkh/2016-11/dgkh000266.shtmlTest

الإتاحة: https://doi.org/10.3205/dgkh000266Test
https://doi.org/10.1016/j.ajic.2012.02.035Test
https://doi.org/10.1177/2049936114543287Test
https://doi.org/10.1371/journal.pone.0078512Test
https://doi.org/10.1016/j.ajic.2014.03.017Test
https://doi.org/10.1086/524331Test
https://doi.org/10.1097/01.NAJ.0000408181.37017.82Test
https://doi.org/10.1016/j.ajic.2008.09.018Test
https://doi.org/10.1016/j.ajic.2012.03.032Test
https://doi.org/10.1016/j.jhin.2010.06.027Test