Evaluation of new anti-infective drugs for the treatment of osteomyelitis in adults. Infectious Diseases Society of America and the Food and Drug Administration
- PMID: 1477223
- DOI: 10.1093/clind/15.supplement_1.s155
Evaluation of new anti-infective drugs for the treatment of osteomyelitis in adults. Infectious Diseases Society of America and the Food and Drug Administration
Abstract
Cases of osteomyelitis can be divided into four categories: acute hematogenous, vertebral, secondary to a contiguous focus of infection without vascular disease, and secondary to a contiguous focus of infection with vascular disease. Each category may be further divided into acute and chronic forms. Clinical symptoms persisting for > or = 10 days correlate roughly with the development of necrotic bone and chronic osteomyelitis. Patients enrolled in clinical trials should generally be > or = 12 years of age. Prior antimicrobial treatment does not exclude patients if the culture of a bone sample obtained at the time of enrollment yields pathogenic bacteria. Randomized, double-blind, active-control comparative studies are encouraged. Clinical outcome should be assessed during therapy and within 5-9 days, 4-6 weeks, and 11-13 months after completion of therapy. In the final assessment, clinical appraisal is paramount.
Similar articles
-
Evaluation of new anti-infective drugs for the treatment of acute hematogenous osteomyelitis in children. Infectious Diseases Society of America and the Food and Drug Administration.Clin Infect Dis. 1992 Nov;15 Suppl 1:S162-6. doi: 10.1093/clind/15.supplement_1.s162. Clin Infect Dis. 1992. PMID: 1477224
-
Evaluation of new anti-infective drugs for the treatment of infectious arthritis in adults. Infectious Diseases Society of America and the Food and Drug Administration.Clin Infect Dis. 1992 Nov;15 Suppl 1:S167-71. doi: 10.1093/clind/15.supplement_1.s167. Clin Infect Dis. 1992. PMID: 1477225
-
Evaluation of new anti-infective drugs for the treatment of infections of prosthetic hip joints. Infectious Diseases Society of America and the Food and Drug Administration.Clin Infect Dis. 1992 Nov;15 Suppl 1:S177-81. doi: 10.1093/clind/15.supplement_1.s177. Clin Infect Dis. 1992. PMID: 1477227
-
Treatment of osteomyelitis.Clin Pharm. 1983 May-Jun;2(3):213-24. Clin Pharm. 1983. PMID: 6349907 Review.
-
Novel endpoints and design of early clinical trials.Ann Oncol. 2002;13 Suppl 4:139-43. doi: 10.1093/annonc/mdf651. Ann Oncol. 2002. PMID: 12401680 Review. No abstract available.
Cited by
-
Lack of microbiological concordance between bone and non-bone specimens in chronic osteomyelitis: an observational study.BMC Infect Dis. 2002 May 16;2:8. doi: 10.1186/1471-2334-2-8. BMC Infect Dis. 2002. PMID: 12015818 Free PMC article.
-
Use of quinolones in osteomyelitis and infected orthopaedic prosthesis.Drugs. 1999;58 Suppl 2:85-91. doi: 10.2165/00003495-199958002-00017. Drugs. 1999. PMID: 10553713 Review.
-
Distinct expression trend of signature antigens of Staphylococcus aureus osteomyelitis correlated with clinical outcomes.J Orthop Res. 2021 Feb;39(2):265-273. doi: 10.1002/jor.24961. Epub 2020 Dec 29. J Orthop Res. 2021. PMID: 33336817 Free PMC article.
-
Detecting Chronic Post-Traumatic Osteomyelitis of Mouse Tibia via an IL-13Rα2 Targeted Metallofullerene Magnetic Resonance Imaging Probe.Bioconjug Chem. 2017 Feb 15;28(2):649-658. doi: 10.1021/acs.bioconjchem.6b00708. Epub 2017 Feb 6. Bioconjug Chem. 2017. PMID: 28061526 Free PMC article.
-
Nanomaterials and synergistic low-intensity direct current (LIDC) stimulation technology for orthopedic implantable medical devices.Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2013 May-Jun;5(3):191-204. doi: 10.1002/wnan.1201. Epub 2013 Jan 17. Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2013. PMID: 23335493 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical