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JOURNAL CLUB
- DR. MOTE SRIKANTH
BACKGROUND
• Patients with infective endocarditis on the left side of the heart are
typically treated with intarvenous antibiotic agents up to 6 weeks
,whether a shift from intravenous to oral antibiotics once the patient
is stable condition would result in efficacy and safety .
1. NAME OF THE JOURNAL: The NEW ENGLAND JOURNAL of
MEDICINE
2. IMPACT FACTOR: 79.258
• RANKING: First of 153 journals in the category ”General & Internal
Medicine”
1. TYPE OF ARTICLE: RANDOMISED CONTROLLED TRIAL
2. NAME OF THE AUTHORS: Kasper Iversen, M.D., D.M.Sc., Nikolaj Ihlemann, M.D., Ph.D.,
Sabine U. Gill, M.D., Ph.D., Trine Madsen, M.D., Ph.D., Hanne Elming, M.D., Ph.D., Kaare
T. Jensen, M.D., Ph.D., Niels E. Bruun, M.D., D.M.Sc.,
Dan E. Høfsten, M.D., Ph.D., Kurt Fursted, M.D., D.M.Sc.,
Jens J. Christensen, M.D., D.M.Sc., Martin Schultz, M.D., Christine F. Klein, M.D., Emil L.
Fosbøll, M.D., Ph.D., Flemming Rosenvinge, M.D.,
Henrik C. Schønheyder, M.D., D.M.Sc., Lars Køber, M.D., D.M.Sc., Christian
Torp‐Pedersen, M.D., D.M.Sc., Jannik Helweg‐Larsen, M.D., D.M.Sc., Niels Tønder, M.D.,
D.M.Sc., Claus Moser, M.D., Ph.D.,
and Henning Bundgaard, M.D., D.M.Sc
1. STUDY DESIGN: Open label Randomised Controlled Trial
interventional, non-inferiority. (POET – PARTIAL ORAL TREATMENT
OF ENDOCARDITIS)
2. STUDY CENTRE: Multicentre
3. PLACE OF STUDY: Denmark
4. TIME OF STUDY: 15 June 2011– 30 August 2017
5. TRIAL SPONSOR: Danish Heart Foundation, Capital Regions Research
Council, Hartmann’s Foundation, Svend Aage Andersens Foundation,
Novo Nordisk Foundation
AIM OF THE STUDY
• AIM: To study if treatment with oral antibiotics instead of
intravenous antibiotics safe in stable patients with infective
endocarditis.
RESEARCH QUESTION ?
• Is treatment with oral antibiotics instead of intravenous antibiotics safe in stable
patients with endocarditis?
MATERIALS & METHODS:
1. POET TRIAL : The POET study is a Danish multicenter, prospective,
randomized, open label study. The primary aim is to show non-inferiority of
partial oral treatment with antibiotics of endocarditis compared to full
parenteral treatment.
2. 400 participants
• Study variables: The following data are collected for the included patients:
• Demographics, vitals, clinical status and results of clinical, biochemical,
microbiological and imaging examinations.
• Personal Identification number (Danish Civil Registration number )
• Results of the routine blood tests at admission and at randomization. Routine
biomarkers: Hemoglobin, Leukocytes, thrombocytes, sodium, potassium, C-
reactive protein, e GFR, Creatinine, Albumin. Echocardiography
• Gender.
• Comorbidity.
• Finding of a primary focus.
• Result from the Echocardiography at admission and prior to randomization.
• Results from additional imaging studies.
• Results from blood cultures, including resistance for relevant antbiotics.
• Samples will be drawn at 0.5, 1, 2, 4 and 8 hours after the first dose of
antibiotics.
SAMPLE SIZE:
• SAMPLE SIZE – 400
• Patient receiving intravenous antibiotics :199
• Patient receiving oral antibiotics: 201
ANTIBIOTICS USED
• Intravenous : It was administered in accordance with guidelines of the European
Society of cardiology .
• POET : Amoxicillin, fusidic acid, Linezolid, rifampicin,
dicoxallin,Moxifloxacin,clindamycin
• Oral regimens recommended in the POET trial
Penicillin and methicillin sensitive Staphylococcus aureus and coagulase-negative
staphylococci:
• 1) Amoxicillin 1 g x 4 and fusidic acid 0.75 g x 2
• 2) Amoxicillin 1 g x 4 and rifampicin 0.6 g x 2
• 3) Linezolid 0.6 g x 2 and fusidic acid 0.75 g x 2
• 4) Linezolid 0.6 g x 2 and rifampicin 0.6 g x 2
• Methicillin sensitive Staphylococcus aureus and coagulase-negative staphylococci
• 1) Dicloxacillin 1 g x 4 and fusidic acid 0.75 g x 2
• 2) Dicloxacillin 1 g x 4 and rifampicin 0.6 g x 2
• 3) Linezolid 0.6 g x 2 and fucidic acid 0.75g x 2
• 4) Linezolid 0.6 g x 2 and rifampicin 0.6 g x 2
• Methicillin resistant coagulase-negative staphylococci
• 1) Linezolid 0.6 g x 2 and fusidic acid
• 2) Linezolid 0.6 g x 2 and rifampicin 0.6 g x2
• Enterococcus faecalis:
• 1) Amoxicillin 1 g x 4 and rifampicin 0.6 g x 2
• 2) Amoxicillin 1 g x 4 and moxifloxacin 0.4 g x 1
• 3) Linezolid 0.6 g x 2 and rifampicin 0.6 g x 2
• 4) Linezolid 0.6 g x 2 and moxifloxacin 0.4 g x 1
• Streptococci with a minimal inhibitory concentration for penicillin of <1 mg/L: 17
• 1) Amoxicillin 1 g x 4 and rifampicin 0.6 g x 2
• 2) Linezolid 0.6 g x 2 and rifampicin 0.6 g x 2
• 3) Linezolid 0.6 g x 2 and moxifloxacin 0.4 g x1
• Streptococci with a minimal inhibitory concentration for penicillin of ≥1 mg/L:
• 1)Linezolid 0,6 g x2 and rifampicin 0.6 g x 2
• 2)Moxifloxacin 0.4 g x 1 and rifampicin 0.6 g x 2
• 3)Moxifloxacin 0.4 g x 1 and clindamycin 0.6 g x3
RANDOMIZATION:
INCLUSION CRITERIA
• Left-sided endocarditis based on the Duke’ criteria
• Infected with one of the following microorganisms:
• Streptococci
• Enterococcus faecalis
• Staphylococcus aureus
• Coagulase-negative staphylococci
• ≥ 18 years
• ≥ 10 days of appropriate parenteral antibiotic treatment overall, and at least 1
week of appropriate parenteral treatment after valve surgery .
• T<38.0°C)>2days .
• C-reactive protein dropped to less than 25% of peak value or < 20 mg/L, and
white blood cell count < 15 x 109/L during antibiotic treatment .
• No sign of abscess formation revealed by echocardiography .
• Transthoracic and transesophageal echocardiography performed within 48 hours
of randomization .
EXCLUSION CRITERIA:
1. Body mass index > 40.
2. Concomitant infection requiring intravenous antibiotic therapy.
3. Inability to give informed consent to participation.
4. Suspicion of reduced absorption of oral treatment due to abdominal disorder.
5. Reduced compliance .
STATISTICAL METHODS
• Variables presented as means /standard deviation/median/interquartile ranges
• Mann-Whitney U test
• Chi-square test
• SPSS software
• Yates’s correction for continuity
PRIMARY OUTCOMES
RESULTS
LIMITATIONS
• Endocarditis on the left side of heart .
• Patient with endocarditis caused by certain bacterial species were eligible .
• Patient with simultaneous infection of cardiovascular implantable electronic
device or endocarditis on the right side side of the heart were not excluded .
• Discharge of patients who were receiving oral treatment to outpatient treatment
was not mandatory .
CONCLUSION
• The patients who have endocarditis on the lest side of the heart caused by
streptococcus ,E faecalis ,S.aureus, or Couglase-negative staphylococci and who
were in stable condition , a shift from intravenously administred to orally
administered antibiotic treatment was noninferior to continued itravenous
antibiotic treatment .
REFERENCES
• 1. Baddour LM, Wilson WR, Bayer AS, et al. Infective endocarditis in adults: diag- nosis, antimicrobial therapy, and man- agement of complications: a
scientific statement for healthcare professionals from the American Heart Association. Circulation 2015;132:1435-86.
• 2. Habib G, Lancellotti P, Antunes MJ, et al. 2015 ESC guidelines for the manage- ment of infective endocarditis: the Task Force for the Management
of Infective Endocarditis of the European Society of Cardiology (ESC). Endorsed by: European Association for Cardio-Thoracic Surgery (EACTS), the
European Association of Nuclear Medicine (EANM). Eur Heart J 2015;36:3075-128.
• 3. Delahaye F, Alla F, Béguinot I, et al. In-hospital mortality of infective endocar- ditis: prognostic factors and evolution over an 8-year period. Scand J
Infect Dis 2007;39:849-57.
• 4. Mistiaen WP. What are the main pre- dictors of in-hospital mortality in pa- tients with infective endocarditis: a re- view. Scand Cardiovasc J
2018;52:58-68. 5. Sy RW, Kritharides L. Health care ex- posure and age in infective endocarditis: results of a contemporary population- based profile
of 1536 patients in Austra- lia. Eur Heart J 2010;31:1890-7.
• 6. Dickerman SA, Abrutyn E, Barsic B, et al. The relationship between the initiation of antimicrobial therapy and the inci- dence of stroke in infective
endocarditis: an analysis from the ICE Prospective Co- hort Study (ICE-PCS). Am Heart J 2007; 154:1086-94.
• 7. Martín-Dávila P, Navas E, Fortún J, et al. Analysis of mortality and risk factors associated with native valve endocarditis in drug users: the
importance of vegeta- tion size. Am Heart J 2005;150:1099-106. 8. Murdoch DR, Corey GR, Hoen B, et al.
• 8. Murdoch DR, Corey GR, Hoen B, et al.
• n engl j med nejm.org
• Clinical presentation, etiology, and out- come of infective endocarditis in the 21st century: the International
Collaboration on Endocarditis-Prospective Cohort Study. Arch Intern Med 2009;169:463-73.
• 9. Kehlet H. Fast-track colorectal sur- gery. Lancet 2008;371:791-3.
10. Khoo CK, Vickery CJ, Forsyth N, Vinall NS, Eyre-Brook IA. A prospective random- ized controlled trial of
multimodal periop- erative management protocol in patients undergoing elective colorectal resection for cancer.
Ann Surg 2007;245:867-72.
• 11. Wind J, Polle SW, Fung Kon Jin PH, et al. Systematic review of enhanced recov- ery programmes in colonic
surgery. Br J Surg 2006;93:800-9.
• 12. Andrews MM, von Reyn CF. Patient selection criteria and management guide- lines for outpatient parenteral
antibiotic therapy for native valve infective endocar- ditis. Clin Infect Dis 2001;33:203-9.
• 13. Lacroix A, Revest M, Patrat-Delon S, et al. Outpatient parenteral antimicrobial therapy for infective endocarditis: a cost- effective strategy. Med Mal Infect
2014; 44:327-30.
• 14. Al-Omari A, Cameron DW, Lee C, Corrales-Medina VF. Oral antibiotic ther- apy for the treatment of infective endocar- ditis: a systematic review. BMC Infect
Dis 2014;14:140.
• 15. Heldman AW, Hartert TV, Ray SC, et al. Oral antibiotic treatment of right-sided staphylococcal endocarditis in injection drug users: prospective randomized
com- parison with parenteral therapy. Am J Med 1996;101:68-76.
• 16. Dworkin RJ, Lee BL, Sande MA, Chambers HF. Treatment of right-sided Staphylococcus aureus endocarditis in in- travenous drug users with ciprofloxacin and
rifampicin. Lancet 1989;2:1071-3.
• 17. Iversen K, Høst N, Bruun NE, et al. Partial oral treatment of endocarditis. Am Heart J 2013;165:116-22.
18. Mzabi A, Kernéis S, Richaud C, Podg- lajen I, Fernandez-Gerlinger MP, Mainar-
• di JL. Switch to oral antibiotics in the treatment of infective endocarditis is not associated with increased risk of mortal- ity in non-severely ill patients. Clin Micro-
biol Infect 2016;22:607-12.
• 19. Li JS, Sexton DJ, Mick N, et al. Pro- posed modifications to the Duke criteria for the diagnosis of infective endocardi- tis. Clin Infect Dis 2000;30:633-8.
• 20. Infectious endocarditis. Danish guide- lines. 2017. (In Danish) (http://www.nbv .cardio.dk/endocarditis).
21. The European Committee on Antimi- crobial Susceptibility Testing (EUCAST) home page. 2017 (http://eucast.org).
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Journal club 1

  • 1. JOURNAL CLUB - DR. MOTE SRIKANTH
  • 2.
  • 3. BACKGROUND • Patients with infective endocarditis on the left side of the heart are typically treated with intarvenous antibiotic agents up to 6 weeks ,whether a shift from intravenous to oral antibiotics once the patient is stable condition would result in efficacy and safety .
  • 4. 1. NAME OF THE JOURNAL: The NEW ENGLAND JOURNAL of MEDICINE 2. IMPACT FACTOR: 79.258 • RANKING: First of 153 journals in the category ”General & Internal Medicine”
  • 5. 1. TYPE OF ARTICLE: RANDOMISED CONTROLLED TRIAL 2. NAME OF THE AUTHORS: Kasper Iversen, M.D., D.M.Sc., Nikolaj Ihlemann, M.D., Ph.D., Sabine U. Gill, M.D., Ph.D., Trine Madsen, M.D., Ph.D., Hanne Elming, M.D., Ph.D., Kaare T. Jensen, M.D., Ph.D., Niels E. Bruun, M.D., D.M.Sc., Dan E. Høfsten, M.D., Ph.D., Kurt Fursted, M.D., D.M.Sc., Jens J. Christensen, M.D., D.M.Sc., Martin Schultz, M.D., Christine F. Klein, M.D., Emil L. Fosbøll, M.D., Ph.D., Flemming Rosenvinge, M.D., Henrik C. Schønheyder, M.D., D.M.Sc., Lars Køber, M.D., D.M.Sc., Christian Torp‐Pedersen, M.D., D.M.Sc., Jannik Helweg‐Larsen, M.D., D.M.Sc., Niels Tønder, M.D., D.M.Sc., Claus Moser, M.D., Ph.D., and Henning Bundgaard, M.D., D.M.Sc
  • 6. 1. STUDY DESIGN: Open label Randomised Controlled Trial interventional, non-inferiority. (POET – PARTIAL ORAL TREATMENT OF ENDOCARDITIS) 2. STUDY CENTRE: Multicentre 3. PLACE OF STUDY: Denmark 4. TIME OF STUDY: 15 June 2011– 30 August 2017 5. TRIAL SPONSOR: Danish Heart Foundation, Capital Regions Research Council, Hartmann’s Foundation, Svend Aage Andersens Foundation, Novo Nordisk Foundation
  • 7. AIM OF THE STUDY • AIM: To study if treatment with oral antibiotics instead of intravenous antibiotics safe in stable patients with infective endocarditis.
  • 8. RESEARCH QUESTION ? • Is treatment with oral antibiotics instead of intravenous antibiotics safe in stable patients with endocarditis?
  • 9. MATERIALS & METHODS: 1. POET TRIAL : The POET study is a Danish multicenter, prospective, randomized, open label study. The primary aim is to show non-inferiority of partial oral treatment with antibiotics of endocarditis compared to full parenteral treatment. 2. 400 participants
  • 10. • Study variables: The following data are collected for the included patients: • Demographics, vitals, clinical status and results of clinical, biochemical, microbiological and imaging examinations. • Personal Identification number (Danish Civil Registration number ) • Results of the routine blood tests at admission and at randomization. Routine biomarkers: Hemoglobin, Leukocytes, thrombocytes, sodium, potassium, C- reactive protein, e GFR, Creatinine, Albumin. Echocardiography
  • 11. • Gender. • Comorbidity. • Finding of a primary focus. • Result from the Echocardiography at admission and prior to randomization. • Results from additional imaging studies. • Results from blood cultures, including resistance for relevant antbiotics. • Samples will be drawn at 0.5, 1, 2, 4 and 8 hours after the first dose of antibiotics.
  • 12. SAMPLE SIZE: • SAMPLE SIZE – 400 • Patient receiving intravenous antibiotics :199 • Patient receiving oral antibiotics: 201
  • 13.
  • 14. ANTIBIOTICS USED • Intravenous : It was administered in accordance with guidelines of the European Society of cardiology . • POET : Amoxicillin, fusidic acid, Linezolid, rifampicin, dicoxallin,Moxifloxacin,clindamycin
  • 15. • Oral regimens recommended in the POET trial Penicillin and methicillin sensitive Staphylococcus aureus and coagulase-negative staphylococci: • 1) Amoxicillin 1 g x 4 and fusidic acid 0.75 g x 2 • 2) Amoxicillin 1 g x 4 and rifampicin 0.6 g x 2 • 3) Linezolid 0.6 g x 2 and fusidic acid 0.75 g x 2 • 4) Linezolid 0.6 g x 2 and rifampicin 0.6 g x 2
  • 16. • Methicillin sensitive Staphylococcus aureus and coagulase-negative staphylococci • 1) Dicloxacillin 1 g x 4 and fusidic acid 0.75 g x 2 • 2) Dicloxacillin 1 g x 4 and rifampicin 0.6 g x 2 • 3) Linezolid 0.6 g x 2 and fucidic acid 0.75g x 2 • 4) Linezolid 0.6 g x 2 and rifampicin 0.6 g x 2
  • 17. • Methicillin resistant coagulase-negative staphylococci • 1) Linezolid 0.6 g x 2 and fusidic acid • 2) Linezolid 0.6 g x 2 and rifampicin 0.6 g x2
  • 18. • Enterococcus faecalis: • 1) Amoxicillin 1 g x 4 and rifampicin 0.6 g x 2 • 2) Amoxicillin 1 g x 4 and moxifloxacin 0.4 g x 1 • 3) Linezolid 0.6 g x 2 and rifampicin 0.6 g x 2 • 4) Linezolid 0.6 g x 2 and moxifloxacin 0.4 g x 1
  • 19. • Streptococci with a minimal inhibitory concentration for penicillin of <1 mg/L: 17 • 1) Amoxicillin 1 g x 4 and rifampicin 0.6 g x 2 • 2) Linezolid 0.6 g x 2 and rifampicin 0.6 g x 2 • 3) Linezolid 0.6 g x 2 and moxifloxacin 0.4 g x1
  • 20. • Streptococci with a minimal inhibitory concentration for penicillin of ≥1 mg/L: • 1)Linezolid 0,6 g x2 and rifampicin 0.6 g x 2 • 2)Moxifloxacin 0.4 g x 1 and rifampicin 0.6 g x 2 • 3)Moxifloxacin 0.4 g x 1 and clindamycin 0.6 g x3
  • 21.
  • 22.
  • 24. INCLUSION CRITERIA • Left-sided endocarditis based on the Duke’ criteria • Infected with one of the following microorganisms: • Streptococci • Enterococcus faecalis • Staphylococcus aureus • Coagulase-negative staphylococci • ≥ 18 years
  • 25. • ≥ 10 days of appropriate parenteral antibiotic treatment overall, and at least 1 week of appropriate parenteral treatment after valve surgery . • T<38.0°C)>2days . • C-reactive protein dropped to less than 25% of peak value or < 20 mg/L, and white blood cell count < 15 x 109/L during antibiotic treatment . • No sign of abscess formation revealed by echocardiography . • Transthoracic and transesophageal echocardiography performed within 48 hours of randomization .
  • 26. EXCLUSION CRITERIA: 1. Body mass index > 40. 2. Concomitant infection requiring intravenous antibiotic therapy. 3. Inability to give informed consent to participation. 4. Suspicion of reduced absorption of oral treatment due to abdominal disorder. 5. Reduced compliance .
  • 27. STATISTICAL METHODS • Variables presented as means /standard deviation/median/interquartile ranges • Mann-Whitney U test • Chi-square test • SPSS software • Yates’s correction for continuity
  • 30.
  • 31.
  • 32.
  • 33.
  • 34.
  • 35.
  • 36.
  • 37.
  • 38. LIMITATIONS • Endocarditis on the left side of heart . • Patient with endocarditis caused by certain bacterial species were eligible . • Patient with simultaneous infection of cardiovascular implantable electronic device or endocarditis on the right side side of the heart were not excluded . • Discharge of patients who were receiving oral treatment to outpatient treatment was not mandatory .
  • 39. CONCLUSION • The patients who have endocarditis on the lest side of the heart caused by streptococcus ,E faecalis ,S.aureus, or Couglase-negative staphylococci and who were in stable condition , a shift from intravenously administred to orally administered antibiotic treatment was noninferior to continued itravenous antibiotic treatment .
  • 40. REFERENCES • 1. Baddour LM, Wilson WR, Bayer AS, et al. Infective endocarditis in adults: diag- nosis, antimicrobial therapy, and man- agement of complications: a scientific statement for healthcare professionals from the American Heart Association. Circulation 2015;132:1435-86. • 2. Habib G, Lancellotti P, Antunes MJ, et al. 2015 ESC guidelines for the manage- ment of infective endocarditis: the Task Force for the Management of Infective Endocarditis of the European Society of Cardiology (ESC). Endorsed by: European Association for Cardio-Thoracic Surgery (EACTS), the European Association of Nuclear Medicine (EANM). Eur Heart J 2015;36:3075-128. • 3. Delahaye F, Alla F, Béguinot I, et al. In-hospital mortality of infective endocar- ditis: prognostic factors and evolution over an 8-year period. Scand J Infect Dis 2007;39:849-57. • 4. Mistiaen WP. What are the main pre- dictors of in-hospital mortality in pa- tients with infective endocarditis: a re- view. Scand Cardiovasc J 2018;52:58-68. 5. Sy RW, Kritharides L. Health care ex- posure and age in infective endocarditis: results of a contemporary population- based profile of 1536 patients in Austra- lia. Eur Heart J 2010;31:1890-7. • 6. Dickerman SA, Abrutyn E, Barsic B, et al. The relationship between the initiation of antimicrobial therapy and the inci- dence of stroke in infective endocarditis: an analysis from the ICE Prospective Co- hort Study (ICE-PCS). Am Heart J 2007; 154:1086-94. • 7. Martín-Dávila P, Navas E, Fortún J, et al. Analysis of mortality and risk factors associated with native valve endocarditis in drug users: the importance of vegeta- tion size. Am Heart J 2005;150:1099-106. 8. Murdoch DR, Corey GR, Hoen B, et al.
  • 41. • 8. Murdoch DR, Corey GR, Hoen B, et al. • n engl j med nejm.org • Clinical presentation, etiology, and out- come of infective endocarditis in the 21st century: the International Collaboration on Endocarditis-Prospective Cohort Study. Arch Intern Med 2009;169:463-73. • 9. Kehlet H. Fast-track colorectal sur- gery. Lancet 2008;371:791-3. 10. Khoo CK, Vickery CJ, Forsyth N, Vinall NS, Eyre-Brook IA. A prospective random- ized controlled trial of multimodal periop- erative management protocol in patients undergoing elective colorectal resection for cancer. Ann Surg 2007;245:867-72. • 11. Wind J, Polle SW, Fung Kon Jin PH, et al. Systematic review of enhanced recov- ery programmes in colonic surgery. Br J Surg 2006;93:800-9. • 12. Andrews MM, von Reyn CF. Patient selection criteria and management guide- lines for outpatient parenteral antibiotic therapy for native valve infective endocar- ditis. Clin Infect Dis 2001;33:203-9.
  • 42. • 13. Lacroix A, Revest M, Patrat-Delon S, et al. Outpatient parenteral antimicrobial therapy for infective endocarditis: a cost- effective strategy. Med Mal Infect 2014; 44:327-30. • 14. Al-Omari A, Cameron DW, Lee C, Corrales-Medina VF. Oral antibiotic ther- apy for the treatment of infective endocar- ditis: a systematic review. BMC Infect Dis 2014;14:140. • 15. Heldman AW, Hartert TV, Ray SC, et al. Oral antibiotic treatment of right-sided staphylococcal endocarditis in injection drug users: prospective randomized com- parison with parenteral therapy. Am J Med 1996;101:68-76. • 16. Dworkin RJ, Lee BL, Sande MA, Chambers HF. Treatment of right-sided Staphylococcus aureus endocarditis in in- travenous drug users with ciprofloxacin and rifampicin. Lancet 1989;2:1071-3. • 17. Iversen K, Høst N, Bruun NE, et al. Partial oral treatment of endocarditis. Am Heart J 2013;165:116-22. 18. Mzabi A, Kernéis S, Richaud C, Podg- lajen I, Fernandez-Gerlinger MP, Mainar- • di JL. Switch to oral antibiotics in the treatment of infective endocarditis is not associated with increased risk of mortal- ity in non-severely ill patients. Clin Micro- biol Infect 2016;22:607-12. • 19. Li JS, Sexton DJ, Mick N, et al. Pro- posed modifications to the Duke criteria for the diagnosis of infective endocardi- tis. Clin Infect Dis 2000;30:633-8. • 20. Infectious endocarditis. Danish guide- lines. 2017. (In Danish) (http://www.nbv .cardio.dk/endocarditis). 21. The European Committee on Antimi- crobial Susceptibility Testing (EUCAST) home page. 2017 (http://eucast.org).