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Oral versus intravenous antibiotics for bone and joint infections: the OVIVA non-inferiority RCT.
Scarborough, Matthew; Li, Ho Kwong; Rombach, Ines; Zambellas, Rhea; Walker, A Sarah; McNally, Martin; Atkins, Bridget; Kümin, Michelle; Lipsky, Benjamin A; Hughes, Harriet; Bose, Deepa; Warren, Simon; Mack, Damien; Folb, Jonathan; Moore, Elinor; Jenkins, Neil; Hopkins, Susan; Seaton, R Andrew; Hemsley, Carolyn; Sandoe, Jonathan; Aggarwal, Ila; Ellis, Simon; Sutherland, Rebecca; Geue, Claudia; McMeekin, Nicola; Scarborough, Claire; Paul, John; Cooke, Graham; Bostock, Jennifer; Khatamzas, Elham; Wong, Nick; Brent, Andrew; Lomas, Jose; Matthews, Philippa; Wangrangsimakul, Tri; Gundle, Roger; Rogers, Mark; Taylor, Adrian; Thwaites, Guy E; Bejon, Philip.
Afiliação
  • Scarborough M; Nuffield Orthopaedic Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Li HK; Nuffield Orthopaedic Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Rombach I; Division of Infectious Diseases, Imperial College London, London, UK.
  • Zambellas R; Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Science, University of Oxford, Oxford, UK.
  • Walker AS; Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Science, University of Oxford, Oxford, UK.
  • McNally M; MRC Clinical Trials Unit, University College London, London, UK.
  • Atkins B; Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Kümin M; Nuffield Orthopaedic Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Lipsky BA; Nuffield Orthopaedic Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Hughes H; Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Bose D; Green Templeton College, University of Oxford, Oxford, UK.
  • Warren S; Department of Microbiology and Public Health, University Hospital of Wales, Public Health Wales, Cardiff, Wales.
  • Mack D; Department of Orthopaedic Surgery, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Folb J; Infectious Diseases and Microbiology, Royal National Orthopaedic Hospital NHS Trust, Stanmore, UK.
  • Moore E; Infectious Diseases and Microbiology, Royal Free London NHS Foundation Trust, London, UK.
  • Jenkins N; Infectious Diseases and Microbiology, Royal National Orthopaedic Hospital NHS Trust, Stanmore, UK.
  • Hopkins S; Infectious Diseases and Microbiology, Royal Free London NHS Foundation Trust, London, UK.
  • Seaton RA; Department of Microbiology, Royal Liverpool and Broadgreen University Hospitals NHS Trust, Liverpool, UK.
  • Hemsley C; Infectious Diseases and Microbiology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Sandoe J; Infectious Diseases, Heart of England NHS Foundation Trust, Birmingham, UK.
  • Aggarwal I; Infectious Diseases and Microbiology, Royal Free London NHS Foundation Trust, London, UK.
  • Ellis S; Infectious Diseases and Microbiology, Gartnaval General Hospital, NHS Greater Glasgow and Clyde, Glasgow, UK.
  • Sutherland R; Department of Microbiology and Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Geue C; Department of Microbiology, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • McMeekin N; Department of Microbiology and Infectious Diseases, Ninewells Hospital, NHS Tayside, Dundee, UK.
  • Scarborough C; Infectious Diseases, Northumbria Healthcare NHS Foundation Trust, Cramlington, UK.
  • Paul J; Infectious Diseases Unit, Regional Infectious Diseases Unit, Western General Hospital, NHS Lothian, Edinburgh, UK.
  • Cooke G; Health Economics and Health Technology Assessment, University of Glasgow, Glasgow, UK.
  • Bostock J; Health Economics and Health Technology Assessment, University of Glasgow, Glasgow, UK.
  • Khatamzas E; Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Wong N; National Infection Service, Public Health England, Horsham, UK.
  • Brent A; Division of Infectious Diseases, Imperial College London, London, UK.
  • Lomas J; Patient and Public Representative, Division of Health and Social Care Research, King's College London, , London, UK.
  • Matthews P; Nuffield Orthopaedic Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Wangrangsimakul T; Nuffield Orthopaedic Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Gundle R; Nuffield Orthopaedic Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Rogers M; Nuffield Orthopaedic Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Taylor A; Nuffield Orthopaedic Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Thwaites GE; Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Bejon P; Nuffield Orthopaedic Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Health Technol Assess ; 23(38): 1-92, 2019 08.
Article em En | MEDLINE | ID: mdl-31373271
Treatment of bone and joint infection usually requires a long course of antibiotics. Doctors usually give these by injection through a vein (intravenously) for the first 4­6 weeks, rather than by mouth (orally). Although intravenous (IV) administration is more expensive and less convenient for patients, most doctors believe that it is more effective. However, there is little evidence to support this. The OVIVA (Oral Versus IntraVenous Antibiotics) trial set out to challenge this assumption. A total of 1054 patients from 26 UK hospitals were randomly allocated to receive the first 6 weeks of antibiotic therapy either intravenously or orally. Irrespective of the route of administration, the choice of antibiotic was left to an infection specialist so as to ensure that the most appropriate antibiotics were given. Patients were followed up for 1 year. Thirty-nine participants were lost to follow-up. Among the remaining 1015 participants, treatment failure occurred in 14.6% of those treated intravenously and 13.2% of those treated with PO antibiotics. This difference could easily have occurred by chance. Even if it was not by chance, the difference does not suggest that PO therapy is associated with worse outcomes than IV therapy and is too small to conclude that PO therapy is better than IV therapy. Participants in the IV group stayed in hospital longer and 10% of them had complications related to the IV line used for administering the antibiotics. In addition, their treatment was, overall, more expensive. We conclude that PO antibiotic therapy has no disadvantages for the early management of bone and joint infection. It is also cheaper and associated with fewer complications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções Bacterianas / Doenças Ósseas Infecciosas / Esquema de Medicação / Artropatias / Antibacterianos Tipo de estudo: Clinical_trials / Guideline / Health_technology_assessment / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções Bacterianas / Doenças Ósseas Infecciosas / Esquema de Medicação / Artropatias / Antibacterianos Tipo de estudo: Clinical_trials / Guideline / Health_technology_assessment / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2019 Tipo de documento: Article