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Limitations in Study on Benefits of Clindamycin

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1 5 J A N U A R Y

Correspondence

Limitations in Study on

Benefits of Clindamycin

TO THE EDITOR—With great interest we have read the study by Carapetis et al [1] about the benefit of clindamycin and

intravenous immunoglobulins, as well as the risk of disease in close contacts with patients with invasive group A strepto-coccal infections. The study indicates im-proved outcome even after adjustment of underlying diseases. However, several limitations of the study were not ade-quately addressed: (1) The observational approach limits an in-depth analysis of the comparison of standard treatment vs standard treatment plus clindamycin plus possibly immunoglobulins, as the authors did not have any influence of the choice of treatment. Most important, only data for antimicrobial therapy are shown. (2) As mentioned in the accom-panying editorial [2], early aggressive sur-gical intervention is critical in cases with necrotizing fasciitis, but no data about surgical debridement, which is the single most important therapy [3], are shown. Therefore, patients with more severe group A streptococcal infections might have benefited from (earlier) surgical de-bridement, explaining in part the im-proved outcome in younger patients [4]. (3) Data on underlying comorbidities are not provided in details, potentially leading to a bias that is not discussed in the paper. (4) Current data indicate that clindamycin should be given prior to the addition of aβ-lactam therapy. The article does not show any data regarding the sequence in which the antibiotics have been administered. In addition, data on the time to needle—an additional critical factor for survival—are lacking [5]. (5) The extrapolation of the risk of

close contacts to the patient population, namely, a risk >2000-fold that of the healthy population, lacks sufficient evi-dence to support routine treatment of close contacts, as the authors suggest in the abstract.

We believe that this study provides im-portant information, and given the rarity of the disease, a randomized clinical trial will unlikely be conducted in the close fu-ture. More observational studies support-ing the recommendations of the authors should be conducted before the recom-mended treatment strategy becomes the standard.

Note

Potential conflicts of interest. All authors: No potential conflicts of interest.

All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Florian Banderet-Uglioni,1Manuel Battegay,1 Maja Weisser,1Reno Frei,2and Andreas F. Widmer1 Divisions of1Infectious Diseases and Hospital Epidemiology, and2Clinical Microbiology, University Hospital Basel, Switzerland

References

1. Carapetis JR, Jacoby P, Carville K, Ang SJ, Curtis N, Andrews R. Effectiveness of clinda-mycin and intravenous immunoglobulin, and risk of disease in contacts, in invasive group A streptococcal infections. Clin Infect Dis2014; 59:358–65.

2. Tan LKK, Sriskandan S. Editorial commen-tary: step on the GAS: are we almost there for clindamycin and intravenous immuno-globulin? Clin Infect Dis2014; 59:366–8. 3. Ustin JS, Malangoni MA. Necrotizing

soft-tissue infections. Crit Care Med 2011; 39: 2156–62.

4. Lancerotto L, Tocco I, Salmaso R, Vindigni V, Bassetto F. Necrotizing fasciitis: classification,

diagnosis, and management. J Trauma Acute Care Surg2012; 72:560–6.

5. Gaieski DF, Mikkelsen ME, Band RA, et al. Impact of time to antibiotics on survival in patients with severe sepsis or septic shock in whom early goal-directed therapy was initiat-ed in the emergency department. Crit Care Med2010; 38:1045–53.

Correspondence: Andreas F. Widmer, MD, MS, FIDSA, FSHEA, Division of Infectious Diseases and Hospital Epidemiology, University Hospital Basel, Petersgraben 4, 4031 Basel, Switzerland (andreas.widmer@usb.ch).

Clinical Infectious Diseases®

2015;60(2):323 © The Author 2014. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals. permissions@oup.com.

DOI: 10.1093/cid/ciu825

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Division of Infectious Diseases and Hospital Epidemiology, University Hospital Basel, Petersgraben 4, 4031 Basel, SwitzerlandM. e-mail: