|
Indian Pediatr 2014;51: 752-753 |
 |
Antimicrobial Susceptibility Profile of
Isolates from Pediatric Blood Stream Infections
|
Winsley Rose, *Balaji Veeraraghavan, *Agila Kumari Pragasam and Valsan
Philip Verghese
From the Departments of Pediatrics and *Microbiology,
Christian Medical College, Vellore, India.
Email:
[email protected]
|
We describe the pathogens and their antimicrobial profile causing blood
stream infections in children over a 4-year period. The commonest
pathogens were: non-fermenting Gram negative bacilli other than
Pseudomonas, Salmonella species, Escherichia coli,
Staphylococcus aureus and Klebsiella species. High rates of
drug-resistance were observed.
Keywords: Antibiotic, Bacteremia, Resistance.
|
Blood stream infections are important causes of morbidity and mortality
in children [1]. Successful outcome of these infections relies on prompt
and timely empiric therapy with broad spectrum antibiotics [2].
Inadequate empiric therapy results in poor outcome with increased
mortality rate and emergence of antibiotic resistance [3]. Drug
resistant organisms such as extended spectrum beta-lactamase (ESBL)
producing organisms and Methicillin - resistant Staphylococcus aureus
(MRSA) concern health care providers, especially in the developing
countries [4]. Surveillance of prevalence and antimicrobial
susceptibility of pathogens is essential for empiric treatment choice in
pediatric blood stream infections. We present the distribution of
pathogens and their antibiotic susceptibility profile from blood
cultures in children who presented with clinical features of sepsis over
a 4-year period.
All children aged between 30 days and 15 years of
age, who presented to Christian Medical College, Vellore from January
2010 to December 2013 with clinical features of sepsis had their blood
samples drawn under aseptic condition. The specimens were inoculated and
processed by BacT/ALERT system followed by Gram staining and
sub-cultures on MacConckey agar and 5% sheep blood agar. Biochemical
identification of the pathogen was done using standard procedures, and
followed by antibiotic susceptibility testing as per standard Clinical
and Laboratory Standards Institute (CLSI) guidelines. Organisms such as
Coagulase negative Staphylococcus aureus (CONS), Diphtheroids and
Aerobic spore formers (ASF) were considered contaminants and excluded
from analysis.
A total of 41457 blood cultures were done during the
study period with positive cultures in 4.8% (n=2015); 3.6% (n=1507)
Gram negative bacilli (GNB) and 1.2% (n=508) Gram positive
cocci (GPC). Table I shows the predominant pathogens and
their antibiotic susceptibility profile. The other pathogens were alpha-hemolytic
Streptococci (n=46, 2.3%), beta-hemolytic Streptococci (n=40,
2%) and other Gram negative bacilli (n=29, 1.4%). Non-fermenting
Gram-negative bacteria other than Pseudomonas spp. (NFGNB) were
commonly isolated. Further characterization showed Acinetobacter spp
– 202, Burkholderia cepacia – 41, Sphingobacterium multi-vorum
– 6, Ralstonia spp – 4 and undifferentiated NFGNB - 269.
TABLE I Antibiotic Susceptibility Profile for the Predominant Bacteria Isolated from Blood Cultures
Pathogen |
Number (%) |
Antibiotic Susceptibility in Percentage |
|
|
PEN/AMP/OXA |
P/T |
GEN |
AK |
3rd gen. Ceph. |
CIP |
MER |
COL |
TIG |
VAN |
LIN |
NFGNB |
522 (25.9) |
|
75 |
|
60 |
70 |
|
73 |
90 |
|
|
|
Salmonella spp. |
349 (17.3) |
95 (AMP) |
|
|
|
100 |
5 |
|
|
|
|
|
E. coli |
221 (11) |
|
55 |
43 |
83 |
28 |
26 |
92 |
100 |
99 |
|
|
Klebsiella spp. |
200 (9.9) |
|
56 |
44 |
60 |
31 |
37 |
78 |
100 |
91 |
|
|
Pseudomonas spp. |
128 (6.4) |
|
91 |
|
90 |
90 |
|
88 |
|
|
|
|
Enterobacter spp. |
58 (2.9) |
|
74 |
43 |
76 |
33 |
64 |
86 |
98 |
98 |
|
|
S. aureus |
217 (10.8) |
60 (OXA) |
|
58 |
|
|
32 |
|
|
|
100 |
100 |
Enterococcus spp. |
111 (5.5) |
50 (AMP) |
|
50 (HLG) |
|
|
|
|
|
|
86 |
100 |
S. pneumoniae |
94 (4.7) |
97 (PEN) |
|
|
|
98 |
|
|
|
|
|
|
PEN-Penicillin; AMP-Ampicillin; OXA-Oxacillin; P/T-Piperacillin/tazobactam;
Gen-Gentamicin; AK-Amikacin; 3rd gen. Ceph.-3rd generation
cephalosporin; CIP-Ciprofoloxacin; MER-Meropenem; COL-Colistin;
TIG-Tigecycline; VAN-Vancomycin; LIN-Linezolid; HLG-high level
Gentamicin; NFGNB – Non-fermenting Gram negative bacilli other
than Pseudomonas. |
NFGNB are increasingly being recognized as a source
of healthcare associated infections [5]. The hospital- based nature of
our study may be a reason for high number of NFGNB in our study. Our
study also shows high rates of extended spectrum
b-lactamase
production (71%) among E. coli and Klebsiella spp.
Carbapenemase producing organisms were found in 22% of Klebsiella spp.
and 9% of E.coli. Among the Gram positive organisms, 40% of the
Staphylococcus aureus were methicillin-resistant. All of them
were susceptible to Vancomycin and Linezolid. Among Streptococcus
pneumoniae, 97% were susceptible to penicillin compared to 94.1%
reported by CDC in 2012 [6]. Fourteen per cent of enterococci in our
study were resistant to vencomycin.
To conclude, we documented a high level of drug
resistance in gram positive and gram negative bacterial isolates. Urgent
efforts are needed to combat increasing drug-resistance in our country.
Contributors: WR and BV: study design; AP:
data collection. All the authors were involved in data analysis and
manuscript preparation.
Funding: None; Competing interests: None
stated.
References
1. Schaffner J, Chochua S, Kourbatova EV, Barragan M,
Wang YF, Blumberg HM, et al. High mortality among patients with
positive blood cultures at a children’s hospital in Tbilisi, Georgia. J
Infect Dev Ctries. 2009;3:267-72.
2. Kollef MH. Inadequate antimicrobial treatment: An
important determinant of outcome for hospitalized patients. Clin Infect
Dis. 2000;31:S131-8.
3. Behrendt G, Schneider S, Brodt HR, Just-Nübling G,
Shah PM. Influence of antimicrobial treatment on mortality in septicemia.
J Chemother. 1999;11:179-86.
4. Bhattacharjee A, Sen MR, Prakash P, Gaur A,
Anupurba S. Increased prevalence of extended spectrum beta lactamase
producers in neonatal septicaemic cases at a tertiary referral hospital.
Indian J Med Microbiol. 2008;26:356-60.
5. Malini A, Deepa EK, Gokul BN, Prasad SR.
Nonfermenting gram-negative bacilli infections in a tertiary care
hospital in Kolar, Karnataka. J Lab Physicians. 2009;1:62-6.
6. Centers for Disease Control and Prevention. 2013.
Active Bacterial Core Surveillance Report, Emerging Infections Program
Network, Streptococcus pneumoniae, 2012.
|
|
 |
|