Disclaimer: The views expressed in this article are those of the authors and do not necessarily reflect those of the Centers for Disease Control and Prevention or the position or policy of the Department of Veterans Affairs.
Financial Support: Support for the Michigan Hospital Medicine Safety Consortium is provided by Blue Cross Blue Shield of Michigan (BCBSM) and Blue Care Network as part of the BCBSM Value Partnerships program.
Disclosures: Dr. Flanders reports personal fees for expert testimony, grants from Blue Cross Blue Shield of Michigan and the Agency for Healthcare Research and Quality, and personal fees from Wiley Publishing outside the submitted work. Dr. Chopra reports grants from Blue Cross Blue Shield of Michigan during the conduct of the study and royalties from Wolters Kluwer Publishing and Oxford University Press, personal fees from universities and medical centers for visiting professorships, and personal fees for serving as an expert witness outside the submitted work. Authors not named here have disclosed no conflicts of interest. Disclosures can also be viewed at
www.acponline.org/authors/icmje/ConflictOfInterestForms.do?msNum=M18-3640.
Editors' Disclosures: Christine Laine, MD, MPH, Editor in Chief, reports that her spouse has stock options/holdings with Targeted Diagnostics and Therapeutics. Darren B. Taichman, MD, PhD, Executive Editor, reports that he has no financial relationships or interests to disclose. Cynthia D. Mulrow, MD, MSc, Senior Deputy Editor, reports that she has no relationships or interests to disclose. Jaya K. Rao, MD, MHS, Deputy Editor, reports that she has stock holdings/options in Eli Lilly and Pfizer. Catharine B. Stack, PhD, MS, Deputy Editor, Statistics, reports that she has stock holdings in Pfizer, Johnson & Johnson, and Colgate-Palmolive. Christina C. Wee, MD, MPH, Deputy Editor, reports employment with Beth Israel Deaconess Medical Center. Sankey V. Williams, MD, Deputy Editor, reports that he has no financial relationships or interests to disclose. Yu-Xiao Yang, MD, MSCE, Deputy Editor, reports that he has no financial relationships or interest to disclose.
Reproducible Research Statement: Study protocol: Available from Dr. Vaughn (e-mail,
[email protected]).
Statistical code: Available from Ms. Snyder (e-mail,
[email protected]).
Data set: Not available.
Corresponding Author: Valerie M. Vaughn, MD, MSc, Assistant Professor of Medicine, Division of Hospital Medicine, Michigan Medicine, North Campus Research Complex, 2800 Plymouth Road, Building 16, Room 472C, Ann Arbor, MI 48109-2800; e-mail,
[email protected].
Current Author Addresses: Dr. Vaughn: Assistant Professor of Medicine, Division of Hospital Medicine, Michigan Medicine, North Campus Research Complex, 2800 Plymouth Road, Building 16, Room 472C, Ann Arbor, MI 48109-2800.
Dr. Flanders: Professor of Medicine, Chief Clinical Strategy Officer, University of Michigan, 2800 Plymouth Road, Ann Arbor, MI 48109.
Drs. Flanders, Conlon, Rogers, Chopra, and Gandhi; Ms. Snyder; Ms. McLaughlin; and Ms. Bloemers: Department of Internal Medicine, University of Michigan Medical School, 3110 Taubman Center, SPC 5368, 1500 East Medical Center Drive, Ann Arbor, MI 48109.
Dr. Malani: St. Joseph Mercy Health System, IHA Infectious Diseases Consultants, 5333 McAuley Drive, Suite 6109, Ypsilanti, MI 48197.
Dr. Srinivasan: Division of Healthcare Quality Promotion, Centers for Disease Control and Prevention, 1600 Clifton Road, MS H16-2, Atlanta, GA 30306.
Dr. Nagel: Michigan Medicine, 1111 East Catherine Street, Ann Arbor, MI 48109.
Dr. Kaatz: Henry Ford Hospital, OFP 413, 2799 West Grand Boulevard, Detroit, MI 48202.
Dr. Osterholzer: Hurley Medical Center, 2 Hurley Plaza, Suite 212, Flint, MI 48503.
Dr. Thyagarajan: Beaumont Infectious Disease – Dearborn, 18181 Oakwood Boulevard, Pharmacy Administration – Dearborn, Suite 101, Dearborn, MI 48124.
Dr. Hsaiky: Beaumont Infectious Disease – Dearborn, 18101 Oakwood Boulevard, Pharmacy Administration – Dearborn, Suite 101, Dearborn, MI 48124.
Author Contributions: Conception and design: V.M. Vaughn, S.A. Flanders, A.N. Malani, J. Nagel, L. Hsaiky, V. Chopra, T.N. Gandhi.
Analysis and interpretation of the data: V.M. Vaughn, A. Snyder, A. Conlon, A.N. Malani, J. Nagel, S. Kaatz, V. Chopra, T.N. Gandhi.
Drafting of the article: V.M. Vaughn, A.N. Malani, J. Nagel, V. Chopra.
Critical revision of the article for important intellectual content: V.M. Vaughn, S.A. Flanders, M.A.M. Rogers, A.N. Malani, A. Srinivasan, S. Kaatz, D. Osterholzer, R. Thyagarajan, L. Hsaiky, V. Chopra, T.N. Gandhi.
Final approval of the article: V.M. Vaughn, S.A. Flanders, A. Snyder, A. Conlon, M.A.M. Rogers, A.N. Malani, E. McLaughlin, S. Bloemers, A. Srinivasan, J. Nagel, S. Kaatz, D. Osterholzer, R. Thyagarajan, L. Hsaiky, V. Chopra, T.N. Gandhi.
Statistical expertise: V.M. Vaughn, A. Snyder, A. Conlon, M.A.M. Rogers.
Obtaining of funding: S.A. Flanders, V. Chopra.
Administrative, technical, or logistic support: E. McLaughlin, S. Bloemers, A. Srinivasan, J. Nagel.
Collection and assembly of data: V.M. Vaughn, A. Conlon, E. McLaughlin, V. Chopra, T.N. Gandhi.
This article was published at
Annals.org on 9 July 2019.
Comments on "Excess Antibiotic Treatment Duration and Adverse Events in Patients Hospitalized With Pneumonia."
In this study, the authors reported that a respiratory culture was associated with higher rates of excess treatment. The present study did not insist on a causal relationship owing to its retrospective design and the authors discussed that sputum testing may reflect greater concern regarding severe disease. Nevertheless, it should be explicitly stated that disease severity could be a critical confounding factor and the above-mentioned association does not deny the importance of sputum culture testing.
Previous studies have suggested the clinical usefulness of gram staining and sputum cultures for the identification of pathogens, thereby, may optimize diagnosis and treatment2). Despite its low sensitivity, sputum culture is clinically useful, particularly for infectious diseases caused by S.pneumoniae and H.influenzae3). De-escalation of broad-spectrum antibiotics based on culture results might reduce the risk of infection with drug-resistant organisms and drug-related adverse events including Clostridium difficile infection4).
We hope that further studies on adequate antibiotic treatment duration will be conducted considering the clinical usefulness of respiratory cultures.
1. Vaughn, V. M., Flanders, S. A., Snyder, A., et al. Excess Antibiotic Treatment Duration and Adverse Events in Patients Hospitalized With Pneumonia. Annals of Internal Medicine, 43. https://doi.org/10.7326/M18-3640
2. Strålin K. Usefulness of aetiological tests for guiding antibiotic therapy in community-acquired pneumonia. Int J Antimicrob Agents. 2008;31(1):3-11. doi:10.1016/j.ijantimicag.2007.06.037
3. Miyashita N, Shimizu H, Ouchi K, et al. Assessment of the usefulness of sputum Gram stain and culture for diagnosis of community-acquired pneumonia requiring hospitalization. Med Sci Monit. 2008;14(4):CR171-6. http://www.ncbi.nlm.nih.gov/pubmed/18376343.
4. Rac H, Haggard E, Mediwala KN, et al. Role of Early De-escalation of Antimicrobial Therapy on Risk of Clostridioides difficile Infection following Enterobacteriaceae Bloodstream Infections. Clinical Infectious Diseases, Volume 69, Issue 3, 1 August 2019, Pages 414-420, https://doi.org/10.1093/cid/ciy863
Disclosures: None declared.