Prolonged suppressive antibiotic therapy for prosthetic joint infection in the elderly: a national multicentre cohort study

During prosthetic joint infection (PJI), optimal surgical management with exchange of the device is sometimes impossible, especially in the elderly population. Thus, prolonged suppressive antibiotic therapy (PSAT) is the only option to prevent acute sepsis, but little is known about this strategy. W...

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Veröffentlicht in:European journal of clinical microbiology & infectious diseases 2017-09, Vol.36 (9), p.1577-1585
Hauptverfasser: Prendki, V., Ferry, T., Sergent, P., Oziol, E., Forestier, E., Fraisse, T., Tounes, S., Ansart, S., Gaillat, J., Bayle, S., Ruyer, O., Borlot, F., Le Falher, G., Simorre, B., Dauchy, F.-A., Greffe, S., Bauer, T., Bell, E. N., Martha, B., Martinot, M., Froidure, M., Buisson, M., Waldner, A., Lemaire, X., Bosseray, A., Maillet, M., Charvet, V., Barrelet, A., Wyplosz, B., Noaillon, M., Denes, E., Beretti, E., Berlioz-Thibal, M., Meyssonnier, V., Fourniols, E., Tliba, L., Eden, A., Jean, M., Arvieux, C., Guignery-Kadri, K., Ronde-Oustau, C., Hansmann, Y., Belkacem, A., Bouchand, F., Gavazzi, G., Herrmann, F., Stirnemann, J., Dinh, A.
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container_title European journal of clinical microbiology & infectious diseases
container_volume 36
creator Prendki, V.
Ferry, T.
Sergent, P.
Oziol, E.
Forestier, E.
Fraisse, T.
Tounes, S.
Ansart, S.
Gaillat, J.
Bayle, S.
Ruyer, O.
Borlot, F.
Le Falher, G.
Simorre, B.
Dauchy, F.-A.
Greffe, S.
Bauer, T.
Bell, E. N.
Martha, B.
Martinot, M.
Froidure, M.
Buisson, M.
Waldner, A.
Lemaire, X.
Bosseray, A.
Maillet, M.
Charvet, V.
Barrelet, A.
Wyplosz, B.
Noaillon, M.
Denes, E.
Beretti, E.
Berlioz-Thibal, M.
Meyssonnier, V.
Fourniols, E.
Tliba, L.
Eden, A.
Jean, M.
Arvieux, C.
Guignery-Kadri, K.
Ronde-Oustau, C.
Hansmann, Y.
Belkacem, A.
Bouchand, F.
Gavazzi, G.
Herrmann, F.
Stirnemann, J.
Dinh, A.
description During prosthetic joint infection (PJI), optimal surgical management with exchange of the device is sometimes impossible, especially in the elderly population. Thus, prolonged suppressive antibiotic therapy (PSAT) is the only option to prevent acute sepsis, but little is known about this strategy. We aimed to describe the characteristics, outcome and tolerance of PSAT in elderly patients with PJI. We performed a national cross-sectional cohort study of patients >75 years old and treated with PSAT for PJI. We evaluated the occurrence of events, which were defined as: (i) local or systemic progression of the infection (failure), (ii) death and (iii) discontinuation or switch of PSAT. A total of 136 patients were included, with a median age of 83 years [interquartile range (IQR) 81–88]. The predominant pathogen involved was Staphylococcus (62.1%) ( Staphylococcus aureus in 41.7%). A single antimicrobial drug was prescribed in 96 cases (70.6%). There were 46 (33.8%) patients with an event: 25 (18%) with an adverse drug reaction leading to definitive discontinuation or switch of PSAT, 8 (5.9%) with progression of sepsis and 13 died (9.6%). Among patients under follow-up, the survival rate without an event at 2 years was 61% [95% confidence interval (CI): 51;74]. In the multivariate Cox analysis, patients with higher World Health Organization (WHO) score had an increased risk of an event [hazard ratio (HR) = 1.5, p  = 0.014], whereas patients treated with beta-lactams are associated with less risk of events occurring (HR = 0.5, p  = 0.048). In our cohort, PSAT could be an effective and safe option for PJI in the elderly.
doi_str_mv 10.1007/s10096-017-2971-2
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We evaluated the occurrence of events, which were defined as: (i) local or systemic progression of the infection (failure), (ii) death and (iii) discontinuation or switch of PSAT. A total of 136 patients were included, with a median age of 83 years [interquartile range (IQR) 81–88]. The predominant pathogen involved was Staphylococcus (62.1%) ( Staphylococcus aureus in 41.7%). A single antimicrobial drug was prescribed in 96 cases (70.6%). There were 46 (33.8%) patients with an event: 25 (18%) with an adverse drug reaction leading to definitive discontinuation or switch of PSAT, 8 (5.9%) with progression of sepsis and 13 died (9.6%). Among patients under follow-up, the survival rate without an event at 2 years was 61% [95% confidence interval (CI): 51;74]. In the multivariate Cox analysis, patients with higher World Health Organization (WHO) score had an increased risk of an event [hazard ratio (HR) = 1.5, p  = 0.014], whereas patients treated with beta-lactams are associated with less risk of events occurring (HR = 0.5, p  = 0.048). 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N.</creatorcontrib><creatorcontrib>Martha, B.</creatorcontrib><creatorcontrib>Martinot, M.</creatorcontrib><creatorcontrib>Froidure, M.</creatorcontrib><creatorcontrib>Buisson, M.</creatorcontrib><creatorcontrib>Waldner, A.</creatorcontrib><creatorcontrib>Lemaire, X.</creatorcontrib><creatorcontrib>Bosseray, A.</creatorcontrib><creatorcontrib>Maillet, M.</creatorcontrib><creatorcontrib>Charvet, V.</creatorcontrib><creatorcontrib>Barrelet, A.</creatorcontrib><creatorcontrib>Wyplosz, B.</creatorcontrib><creatorcontrib>Noaillon, M.</creatorcontrib><creatorcontrib>Denes, E.</creatorcontrib><creatorcontrib>Beretti, E.</creatorcontrib><creatorcontrib>Berlioz-Thibal, M.</creatorcontrib><creatorcontrib>Meyssonnier, V.</creatorcontrib><creatorcontrib>Fourniols, E.</creatorcontrib><creatorcontrib>Tliba, L.</creatorcontrib><creatorcontrib>Eden, A.</creatorcontrib><creatorcontrib>Jean, M.</creatorcontrib><creatorcontrib>Arvieux, C.</creatorcontrib><creatorcontrib>Guignery-Kadri, K.</creatorcontrib><creatorcontrib>Ronde-Oustau, C.</creatorcontrib><creatorcontrib>Hansmann, Y.</creatorcontrib><creatorcontrib>Belkacem, A.</creatorcontrib><creatorcontrib>Bouchand, F.</creatorcontrib><creatorcontrib>Gavazzi, G.</creatorcontrib><creatorcontrib>Herrmann, F.</creatorcontrib><creatorcontrib>Stirnemann, J.</creatorcontrib><creatorcontrib>Dinh, A.</creatorcontrib><title>Prolonged suppressive antibiotic therapy for prosthetic joint infection in the elderly: a national multicentre cohort study</title><title>European journal of clinical microbiology &amp; infectious diseases</title><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><description>During prosthetic joint infection (PJI), optimal surgical management with exchange of the device is sometimes impossible, especially in the elderly population. Thus, prolonged suppressive antibiotic therapy (PSAT) is the only option to prevent acute sepsis, but little is known about this strategy. We aimed to describe the characteristics, outcome and tolerance of PSAT in elderly patients with PJI. We performed a national cross-sectional cohort study of patients &gt;75 years old and treated with PSAT for PJI. We evaluated the occurrence of events, which were defined as: (i) local or systemic progression of the infection (failure), (ii) death and (iii) discontinuation or switch of PSAT. A total of 136 patients were included, with a median age of 83 years [interquartile range (IQR) 81–88]. The predominant pathogen involved was Staphylococcus (62.1%) ( Staphylococcus aureus in 41.7%). A single antimicrobial drug was prescribed in 96 cases (70.6%). There were 46 (33.8%) patients with an event: 25 (18%) with an adverse drug reaction leading to definitive discontinuation or switch of PSAT, 8 (5.9%) with progression of sepsis and 13 died (9.6%). Among patients under follow-up, the survival rate without an event at 2 years was 61% [95% confidence interval (CI): 51;74]. In the multivariate Cox analysis, patients with higher World Health Organization (WHO) score had an increased risk of an event [hazard ratio (HR) = 1.5, p  = 0.014], whereas patients treated with beta-lactams are associated with less risk of events occurring (HR = 0.5, p  = 0.048). In our cohort, PSAT could be an effective and safe option for PJI in the elderly.</description><subject>Age Factors</subject><subject>Aged, 80 and over</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Antibiotics</subject><subject>Antimicrobial agents</subject><subject>Arthritis, Infectious - drug therapy</subject><subject>Arthritis, Infectious - epidemiology</subject><subject>Arthritis, Infectious - microbiology</subject><subject>Arthritis, Infectious - mortality</subject><subject>Bacteriology</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cohort analysis</subject><subject>Confidence intervals</subject><subject>Female</subject><subject>Geriatrics</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Immunology</subject><subject>Infections</subject><subject>Internal Medicine</subject><subject>Joint diseases</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Medical Microbiology</subject><subject>Microbiology and Parasitology</subject><subject>Older people</subject><subject>Original Article</subject><subject>Pathogens</subject><subject>Patients</subject><subject>Prostheses</subject><subject>Prosthesis-Related Infections - drug therapy</subject><subject>Prosthesis-Related Infections - epidemiology</subject><subject>Prosthesis-Related Infections - microbiology</subject><subject>Prosthesis-Related Infections - mortality</subject><subject>Sepsis</subject><subject>Survival</subject><subject>Therapy</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Virology</subject><issn>0934-9723</issn><issn>1435-4373</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kU1v1DAQhi0EotvCD-CCLHGhh4A_a5tbVdEWaSU4wNlykgnrlTcOtlNp1T-Po5SqQurFHzPPOx7Pi9A7Sj5RQtTnXFdz0RCqGmYUbdgLtKGCy0ZwxV-iDTFcNEYxfoJOc96TqtFKvUYnTHOlmeAbdP8jxRDH39DjPE9Tgpz9HWA3Ft_6WHyHyw6Sm454iAlPKeZ6X8L76MeC_ThAV3wc62khMYQeUjh-wQ6Pbkm4gA9zqAoYSwLcxV1MBecy98c36NXgQoa3D_sZ-nX99efVbbP9fvPt6nLbdEKK0ojeOa4IUADojZRKt9pR1-tBUyI4HzpohTGac9nSVjKtXDuYQbteSucuBD9D52vdnQt2Sv7g0tFG5-3t5dYuMUINVXUkd7SyH1e2fvXPDLnYg88dhOBGiHO2VGshFBN6KfvhP3Qf51Q_XCnDlJGMS14pulJdnV1OMDx2QIldXLSri7UJZRcXLaua9w-V5_YA_aPin20VYCuQa6qal548_WzVv-kDqXY</recordid><startdate>20170901</startdate><enddate>20170901</enddate><creator>Prendki, V.</creator><creator>Ferry, T.</creator><creator>Sergent, P.</creator><creator>Oziol, E.</creator><creator>Forestier, E.</creator><creator>Fraisse, T.</creator><creator>Tounes, S.</creator><creator>Ansart, S.</creator><creator>Gaillat, J.</creator><creator>Bayle, S.</creator><creator>Ruyer, O.</creator><creator>Borlot, F.</creator><creator>Le Falher, G.</creator><creator>Simorre, B.</creator><creator>Dauchy, F.-A.</creator><creator>Greffe, S.</creator><creator>Bauer, T.</creator><creator>Bell, E. 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N. ; Martha, B. ; Martinot, M. ; Froidure, M. ; Buisson, M. ; Waldner, A. ; Lemaire, X. ; Bosseray, A. ; Maillet, M. ; Charvet, V. ; Barrelet, A. ; Wyplosz, B. ; Noaillon, M. ; Denes, E. ; Beretti, E. ; Berlioz-Thibal, M. ; Meyssonnier, V. ; Fourniols, E. ; Tliba, L. ; Eden, A. ; Jean, M. ; Arvieux, C. ; Guignery-Kadri, K. ; Ronde-Oustau, C. ; Hansmann, Y. ; Belkacem, A. ; Bouchand, F. ; Gavazzi, G. ; Herrmann, F. ; Stirnemann, J. ; Dinh, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c454t-4daa370e1eeed95578b8a1ad8f810433fceb4998335b1b5287abf9f8ad55aa643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Age Factors</topic><topic>Aged, 80 and over</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Antibiotics</topic><topic>Antimicrobial agents</topic><topic>Arthritis, Infectious - drug therapy</topic><topic>Arthritis, Infectious - epidemiology</topic><topic>Arthritis, Infectious - microbiology</topic><topic>Arthritis, Infectious - mortality</topic><topic>Bacteriology</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cohort analysis</topic><topic>Confidence intervals</topic><topic>Female</topic><topic>Geriatrics</topic><topic>Health risk assessment</topic><topic>Humans</topic><topic>Immunology</topic><topic>Infections</topic><topic>Internal Medicine</topic><topic>Joint diseases</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Medical Microbiology</topic><topic>Microbiology and Parasitology</topic><topic>Older people</topic><topic>Original Article</topic><topic>Pathogens</topic><topic>Patients</topic><topic>Prostheses</topic><topic>Prosthesis-Related Infections - drug therapy</topic><topic>Prosthesis-Related Infections - epidemiology</topic><topic>Prosthesis-Related Infections - microbiology</topic><topic>Prosthesis-Related Infections - mortality</topic><topic>Sepsis</topic><topic>Survival</topic><topic>Therapy</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Prendki, V.</creatorcontrib><creatorcontrib>Ferry, T.</creatorcontrib><creatorcontrib>Sergent, P.</creatorcontrib><creatorcontrib>Oziol, E.</creatorcontrib><creatorcontrib>Forestier, E.</creatorcontrib><creatorcontrib>Fraisse, T.</creatorcontrib><creatorcontrib>Tounes, S.</creatorcontrib><creatorcontrib>Ansart, S.</creatorcontrib><creatorcontrib>Gaillat, J.</creatorcontrib><creatorcontrib>Bayle, S.</creatorcontrib><creatorcontrib>Ruyer, O.</creatorcontrib><creatorcontrib>Borlot, F.</creatorcontrib><creatorcontrib>Le Falher, G.</creatorcontrib><creatorcontrib>Simorre, B.</creatorcontrib><creatorcontrib>Dauchy, F.-A.</creatorcontrib><creatorcontrib>Greffe, S.</creatorcontrib><creatorcontrib>Bauer, T.</creatorcontrib><creatorcontrib>Bell, E. 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N.</au><au>Martha, B.</au><au>Martinot, M.</au><au>Froidure, M.</au><au>Buisson, M.</au><au>Waldner, A.</au><au>Lemaire, X.</au><au>Bosseray, A.</au><au>Maillet, M.</au><au>Charvet, V.</au><au>Barrelet, A.</au><au>Wyplosz, B.</au><au>Noaillon, M.</au><au>Denes, E.</au><au>Beretti, E.</au><au>Berlioz-Thibal, M.</au><au>Meyssonnier, V.</au><au>Fourniols, E.</au><au>Tliba, L.</au><au>Eden, A.</au><au>Jean, M.</au><au>Arvieux, C.</au><au>Guignery-Kadri, K.</au><au>Ronde-Oustau, C.</au><au>Hansmann, Y.</au><au>Belkacem, A.</au><au>Bouchand, F.</au><au>Gavazzi, G.</au><au>Herrmann, F.</au><au>Stirnemann, J.</au><au>Dinh, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prolonged suppressive antibiotic therapy for prosthetic joint infection in the elderly: a national multicentre cohort study</atitle><jtitle>European journal of clinical microbiology &amp; infectious diseases</jtitle><stitle>Eur J Clin Microbiol Infect Dis</stitle><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><date>2017-09-01</date><risdate>2017</risdate><volume>36</volume><issue>9</issue><spage>1577</spage><epage>1585</epage><pages>1577-1585</pages><issn>0934-9723</issn><eissn>1435-4373</eissn><abstract>During prosthetic joint infection (PJI), optimal surgical management with exchange of the device is sometimes impossible, especially in the elderly population. Thus, prolonged suppressive antibiotic therapy (PSAT) is the only option to prevent acute sepsis, but little is known about this strategy. We aimed to describe the characteristics, outcome and tolerance of PSAT in elderly patients with PJI. We performed a national cross-sectional cohort study of patients &gt;75 years old and treated with PSAT for PJI. We evaluated the occurrence of events, which were defined as: (i) local or systemic progression of the infection (failure), (ii) death and (iii) discontinuation or switch of PSAT. A total of 136 patients were included, with a median age of 83 years [interquartile range (IQR) 81–88]. The predominant pathogen involved was Staphylococcus (62.1%) ( Staphylococcus aureus in 41.7%). A single antimicrobial drug was prescribed in 96 cases (70.6%). There were 46 (33.8%) patients with an event: 25 (18%) with an adverse drug reaction leading to definitive discontinuation or switch of PSAT, 8 (5.9%) with progression of sepsis and 13 died (9.6%). Among patients under follow-up, the survival rate without an event at 2 years was 61% [95% confidence interval (CI): 51;74]. In the multivariate Cox analysis, patients with higher World Health Organization (WHO) score had an increased risk of an event [hazard ratio (HR) = 1.5, p  = 0.014], whereas patients treated with beta-lactams are associated with less risk of events occurring (HR = 0.5, p  = 0.048). In our cohort, PSAT could be an effective and safe option for PJI in the elderly.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>28378243</pmid><doi>10.1007/s10096-017-2971-2</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-5843-4819</orcidid><orcidid>https://orcid.org/0000-0002-2388-1838</orcidid><orcidid>https://orcid.org/0000-0003-3082-7001</orcidid></addata></record>
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issn 0934-9723
1435-4373
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source MEDLINE; Springer Nature - Complete Springer Journals
subjects Age Factors
Aged, 80 and over
Anti-Bacterial Agents - therapeutic use
Antibiotics
Antimicrobial agents
Arthritis, Infectious - drug therapy
Arthritis, Infectious - epidemiology
Arthritis, Infectious - microbiology
Arthritis, Infectious - mortality
Bacteriology
Biomedical and Life Sciences
Biomedicine
Cohort analysis
Confidence intervals
Female
Geriatrics
Health risk assessment
Humans
Immunology
Infections
Internal Medicine
Joint diseases
Life Sciences
Male
Medical Microbiology
Microbiology and Parasitology
Older people
Original Article
Pathogens
Patients
Prostheses
Prosthesis-Related Infections - drug therapy
Prosthesis-Related Infections - epidemiology
Prosthesis-Related Infections - microbiology
Prosthesis-Related Infections - mortality
Sepsis
Survival
Therapy
Time Factors
Treatment Outcome
Virology
title Prolonged suppressive antibiotic therapy for prosthetic joint infection in the elderly: a national multicentre cohort study
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