Letter to the Editor: Prevalence and Antibiotic Resistance of Neonatal Sepsis Pathogens

AUTHORS

Anirban Mandal 1 , * , Puneet Kaur Sahi 2

1 Department of Pediatrics, Sitaram Bhartia Institute of Science and Research, New Delhi, India

2 Department of Pediatrics, Kalawati Saran Children’s Hospital, New Delhi, India

How to Cite: Mandal A, Kaur Sahi P. Letter to the Editor: Prevalence and Antibiotic Resistance of Neonatal Sepsis Pathogens, Arch Pediatr Infect Dis. 2016 ; 4(4):e40578. doi: 10.5812/pedinfect.40578.

ARTICLE INFORMATION

Archives of Pediatric Infectious Diseases: 4 (4); e40578
Published Online: August 3, 2016
Article Type: Letter
Received: July 3, 2016
Accepted: July 5, 2016
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Keywords

Newborn Sepsis Antimicrobial Resistance

Copyright © 2016, Pediartric Infections Research Center. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.

Dear Editor,

We read with great interest the original article by Behmadi et al. (1) in the most recent issue of your journal. We would like to commend the authors for their endeavor but at the same time feel that few necessary clarifications and comments would benefit the general readers of the journal:

1) The abstract mentions that “the aim of this study was to determine the prevalence and evaluate the antimicrobial susceptibility patterns of bacterial infections at a neonatal unit,” but the main text states that the objective was “to determine the frequency and antibiotic resistance of pathogens at the neonatal intensive-care unit (NICU) and neonatal ward of our hospital.” The study, being “cross-sectional” in design, is able to give prevalence but not frequency or incidence (2). Furthermore, the pathogens associated with neonatal sepsis include viruses and parasites, in addition to bacteria (3).

2) The authors mention the total number of culture (blood, urine and cerebrospinal fluid (CSF)) samples and their positivity rates, but not the total number of newborns being assessed (sample size). Therefore, the percentage of newborns who ultimately have culture (blood, urine or CSF)-positive sepsis indicative of prevalence of bacterial infection, which is one of the study’s primary objectives, can never be ascertained.

3) The authors do not provide a definition for terms such as “late-onset sepsis” and “clinical findings suggesting urinary tract infection (UTI).” Different epidemiological studies have used cut-offs ranging from 3 to 7 days to define late-onset sepsis, depending on the gestational age and birth weight of the newborn (4). Also, there are no clinical findings that specifically suggest UTI in a newborn.

4) The methodology does not state how the urine sample for bacterial culture was collected. It should ideally be collected by suprapubic aspiration (5); other methods are associated with high chances of contamination.

5) The authors also do not mention whether hospital-acquired infections were included in the late-onset sepsis group. The causative organisms and the antibiotic sensitivity pattern are expected to vary considerably depending on whether the source of infection is the community or a heath care facility (5). Hospital-acquired pathogens could also explain the high prevalence of antibiotic resistance in the isolated organisms.

6) The finding that coagulase-negative staphylococcus (CONS) was the commonest organism in both early- and late-onset sepsis should be viewed with caution in light of the great controversy about the criteria for defining CONS sepsis in newborns (6). These criteria have often resulted in CONS being overrepresented as a true pathogen in neonatal sepsis (7). In an attempt to decrease false-positivity rates, various investigators have proposed different diagnostic algorithms based upon quantitative culture and colony count, presence of an indwelling central venous catheter (8) or time to positivity of blood culture (9).

Footnote

References

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