|
Indian Pediatr 2009;46: 617-620 |
|
Urinary Tract Infections: Bacteriology and
Antibiotic Resistance Patterns |
Rasoul Yousefi Mashouf*, Hooshang Babalhavaeji† and
Javad Yousef*
From the Departments of *Medical Microbiology and
Urology† and Faculty of Medicine, Hamadan University of Medical Sciences,
Hamadan, Iran.
Correspondence to: Dr Rasoul Yousefi Mashouf, Department
of Microbiology, Hamadan University of Medical Sciences, PO Box 518,
Hamadan, Iran.
Email: [email protected]
Manuscript received: May 19, 2008;
Initial review: July 10, 2008;
Accepted: September 5, 2008.
|
Abstract
The aim of this study was to identify the bacteria
causing community acquired urinary tract infections (UTI) and detection
of antibiotics resistance of isolates in 912 children below 18 years in
the west of Iran. Data were analyzed for 4 age groups: infants,
toddlers, preteens and teens. Fourteen antibiotics were tested by
gel-diffusion method. Of 912 patients, 34.2% had positive bacterial
cultures. The most common isolates were E. coli (57.4%), K.
pneumoniae (9.7%), S. aureus (5.8%) and A. baumannii
(2.2%). Most isolates showed high resistance against ampicillin,
cotrimoxazole, nalidixic acid, tobramycin and nitrofurantoin.
Klebsiella isolates showed more resistance against tested
antibiotics than E. coli isolates.
Keywords: Antibiotics, Iran, Resistance, Urinary tract
infection.
|
C ommunity acquired urinary tract
infections (UTI) cause significant illness in the first 2 years of life
and are considered as common disease in school and pre-school children,
particularly in our country(1-3). Etiologic agents of UTI are variable and
usually depend on time, geographical location and age of patients.
However, Enterobacteriacea species including Escherichia coli, Proteus
mirabilis, Enterobacter agglomerans, Citrobacter freundii and
Klebsiella pneumoniae account for over 70% cases(2-5).
Based on the microbial sensitivity test results, drugs
that are usually administered against uropathogens include cotrimoxazole,
amoxicillin, ampicillin, aminoglycosides, cephalosporins, nalidixic acid
and nitrofurantoin. However, many reports have indicated the presence of
multi-drug resistance in organisms causing UTI(6-9). Prior to this study,
the antibiotic susceptibility of isolates has not been previously
determined in this region. Therefore, the aim of this study was to
identify the most common bacteria causing UTI and detection of antibiotic
susceptibility of isolates in children.
Methods
A cross-sectional study was performed on 912 children
with UTI admitted to the pediatric department of hospital of Ekbatan in
Hamadan, in the west of Iran, between March 2004 and April 2006. Only
patients who had pyuria (>10 white blood cells/µL), acute voiding symptoms
and significant bacteriuria (>105 CFU/mL) were included in the
microbiological analysis. Data were analyzed separately for four age
groups: infants (0-4 weeks), toddlers (5 weeks-24 months), preteens (2-12
years) and teens (13-18 years). Urine collection, culture and
identification of organisms were performed as per methods outlined in
standard text(2,10).
Susceptibility testing was performed by VITEK (BioMérieux,
Inc.) automated system for Enterobacteriaceae. Disk diffusion test (Oxoid,
Basingstoke, Hampshire, UK) was used for Gram-positive bacteria and P.
aeruginosa. Fourteen antibiotics of different classes (Table
I) were tested against isolates. Interpretative criteria for
antimicrobials tested were those recommended by NCCLS guidelines(11).
E. coli ATCC 25922, S. aureus
ATCC 25923 and P. aeruginosa ATCC 27853 were used as quality
controls.
TABLE I
Antibiotics Resistance in Escherichia coli and Klebsiella Pneumoniae in Children with UTI
|
Escherichia coli (n=179) |
Klebsiella pneumoniae (n=30) |
Antibiotics |
Resistance (%) |
Intermediate (%) |
Susceptible (%) |
Resistance (%) |
Intermediate (%) |
Susceptible (%) |
Imipenem |
0.0 |
2.3 |
97.7 |
6.6 |
3.3 |
90.1 |
Netilmicin |
2.3 |
1.1 |
96.7 |
16.6 |
0.0 |
83.4 |
Aztreonam |
3.4 |
3.9 |
92.7 |
13.3 |
6.6 |
80.1 |
Cefepime |
4.5 |
2.3 |
93.2 |
9.9 |
3.3 |
86.8 |
Ciprofloxacin, |
5.5 |
1.1 |
93.4 |
23.3 |
0.0 |
72.7 |
Amikacin |
6.1 |
0.0 |
93.9 |
36.6 |
3.3 |
60.1 |
Ceftriaxone |
7.8 |
2.3 |
89.9 |
9.9 |
6.6 |
83.5 |
Coamoxiclav |
11.1 |
5.5 |
83.4 |
9.9 |
0.0 |
90.1 |
Gentamicin |
18.8 |
3.9 |
77.3 |
43.3 |
6.6 |
50.1 |
Tobramycin |
22.2 |
5.0 |
72.8 |
39.9 |
13.2 |
46.9 |
Nitrofurantoin |
42.1 |
6.1 |
51.8 |
47.3 |
6.6 |
46.1 |
Nalidixic acid |
43.6 |
0.0 |
56.3 |
46.6 |
9.9 |
43.5 |
Cotrimoxazole |
56.4 |
2.9 |
40.7 |
63.2 |
16.5 |
20.3 |
Ampicillin |
61.9 |
2.0 |
36.1 |
96.6 |
3.3 |
0.0 |
Results
Of 912 children, 34.2% had positive cultures. The most
common isolates were E. coli (57.4%), K. pneumoniae
(9.7%), E. aerogenes (7.0%), S. aureus (5.8%), C.
fruendii (5.1%), P. mirabilis (4.5%), P. aeruginosa
(3.2%), A. baumannii (2.2%), coagulase-negative Staphylococcus
(3.2%) and E. fecalis (1.9%). The most common age were teens
(49.6%), preteens (26.8%), toddlers (15.0%) and infants (8.6%),
respectively. Most gram-negative isolates were found in toddlers and
preteens patients, whereas most gram-positive cocci, particularly E.
faecalis isolates were found in teen patients. Acinetobacter
baumannii isolates were found mostly (85%) in preteen patients.
The antimicrobial potency of 14 selected antimicrobial
agents against the two most frequent uropathogens (E.coli and K.
pneumoniae) are summarized in Table I. Among
b-lactam
antibiotics, imipenem had the widest coverage against E. coli
isolates. E. coli resistance to ampicillin peaked in preteens
(76.4%) but was high in teens (65.7%), toddlers (53.4%), and infants
(47.6%). Resistance to cotrimoxazole peaked in teens (68.3%) but was high
in preteens (59.1%), infants (49.4%) and toddlers (47.6%).
Klebsiella isolates also showed high susceptibility against imipenem.
Antibiotic resistance patterns of other isolates are shown in Table
II. Among gram negative bacteria, P. aeruginosa was most
resistant isolates against tested antibiotics. Among gram positive cocci,
E. fecalis isolates showed highest resistance followed by
Staphylococcus isolates. Resistance to two or more antibiotics varied
across age groups; teens (36.1%), preteens (33.1%), infants (29.7%) and
toddlers (24.9%).
TABLE II
Antibiotic Susceptibility Patterns of Other Bacteria in Children With UTI
Isolate
|
Frequency of resistance of isolates to antibiotics (%) |
|
IMP |
NET |
AZN |
CEF |
CIP |
AMK |
CFX |
NIT |
AMC |
GEM |
TOB |
NAL |
COT |
AMP |
E. aerogenes |
9 |
0 |
4.5 |
9 |
18 |
4.5 |
9 |
18 |
0 |
9 |
27 |
22 |
36 |
54 |
S. aureus |
22 |
11 |
–** |
16 |
33 |
33 |
44 |
55 |
11 |
44 |
55 |
66 |
83 |
94 |
C. freundii |
0 |
12 |
0 |
6 |
0 |
12 |
6 |
18 |
24 |
12 |
6 |
0 |
12 |
18 |
P. mirabilis |
0 |
0 |
14 |
0 |
14 |
7 |
7 |
21 |
21 |
0 |
14 |
28 |
42 |
35 |
P. aeruginosa |
30 |
10 |
50 |
30 |
70 |
20 |
80 |
100 |
80 |
60 |
60 |
70 |
90 |
100 |
CONS |
40 |
10 |
– |
10 |
60 |
80 |
60 |
80 |
40 |
70 |
40 |
60 |
70 |
80 |
A. baumannii |
14 |
14 |
28 |
|
57 |
28 |
21 |
28 |
0 |
14 |
21 |
71 |
14 |
71 |
E. fecalis |
50 |
33 |
– |
16 |
33 |
50 |
66 |
50 |
66 |
50 |
16 |
66 |
83 |
100 |
Imipenem (IMP), netilmicin (NET), aztreonam (AZN),
cefepime (CEF), ciprofloxacin (CIP), amikacin (AMK), ceftriaxone
(CFT), nitrofurantoin (NIT), coamoxiclav (AMC), gentamicin (GEM),
tobramycin (TOB), nalidixic acid (NAL), cotrimoxazole (COT),
ampicillin (AMP). **Not tested for gram-posirive
cocci; CONS: Cogulase negative staphylococci. |
Discussion
This is the first study to evaluate the bacteriology
and susceptibility patterns of bacteria
isolated from children with UTI in west of Iran. The present study showed
that the rate of UTI (34.2%) among children was more than that reported
previously(1,2,4-6, 12). Entrobactericae isolates were the dominant
bacterial agents, in agreement with previous works(4-6,12, 13). E. coli
was the commonest isolate, particularly among the toddlers and preteens
patients. K. pneumoniae was the second most common uropathogen and
was dominant in teens. Gram-positive cocci had low contribution in causing
UTI.
This study provides valuable laboratory
data on antibiotics susceptibilities of uropathogens and allows comparison
of the situation in our area with that in other countries. A limitation of
this study was that some antibiotics such as fluoroquinolones and
cephalosporins were not available at the time of sensitivity testing. On
the basis of reports by Antimicrobial Surveillance Program, isolates from
Canada, USA and Latin American countries show the lowest susceptibility
rates to most antimicrobial agents followed by Asian-Pacific isolates and
European strains(8,9,13,14). Of 14 tested antibiotics in this study, the
most active antibiotics against all gram-negative isolates were imipenem,
netilmicin, aztreonam, cefepime and ciprofloxacin. Most of these isolates
showed high resistance against ampicillin, cotrimoxazole, nalidixic acid,
tobramycin and nitrofurantoin. The inadequate dosage of these antibiotics
used during self-medication in our community is likely to be a factor
contributing to the development of resistant strains. These findings are
similar to studies from Africa, South-Asia and some Middle East
countries(6,7,12,13,15).
Klebsiella isolates in this study showed
more resistance than E. coli isolates. The major difference was
observed for gentamicin and amikacin; E. coli isolates showed low
resistance to amikacin and gentamicin, while Klebsiella
isolates showed high resistance to these agents despite being
sensitive for many years(2,8,14).
Contributors: RYM was responsible for the study
design interpretation of data and drafting the article. HB, JY
collected data, conducted the laboratory tests and analyzed them. All
authors approved the final manuscript.
Funding: This study was funded by Internal funds of
the Deputy of Research Center of Hamadan University of Medical Sciences,
Iran, Islamic Republic.
Competing interests: None stated.
What This Study Adds?
• In children with culture positive UTI in
Hamadan, Iran, E. coli and K. pneumoniae were
the predominant uropathogens, sensitive to imipenem, netilmicin,
cefepime and ciprofloxacin.
|
References
1. Schlager T. Urinary tract infections in infants and
children. Infect Dis Clin North Am. 2003; 17: 353-365.
2. Wald ER. Cystitis and pyelonephritis. In: Feigin RD,
Chery JD, Demmier GJ, Kapian SL, eds. Textbook of Pediatric Infectious
Diseases, 5th edn,
Philadelphia: Saunders 2004; p 541-53.
3. Fallahzadeh MH, Alamdarlu HM. Prevalence of
urinary tract infection in pre-school febrile children. Iranian J of Med
Sci 1999; 24: 35-39.
4. Ma JF, Shortliffe LM. Urinary tract infection in
children: etiology and epidemiology. Urol Clin North Am 2004; 3: 517-526.
5. Adjei O, Opoku C Urinary tract infections in African
infants. Int J Antimicrob Agents 2004; 24 Suppl 1: S32-34.
6. Yüksel S, Oztürk B, Kavaz A, Ozçakar ZB, Acar B,
Güriz H, et al. Antibiotic resistance of urinary tract pathogens
and evaluation of empirical treatment in Turkish children with urinary
tract infections. Int J Antimicrob Agents 2006; 28: 413-416.
7. Yildiz B, Kural N, Durmaz G, Yarar C, Ak I, Akcar N.
Antibiotic resistance in children with complicated urinary tract
infection. Saudi Med J 2007; 28: 1850-1854.
8. Mathai D, Jones RN, Pfaller MA. SENTRY Participant
Group North America. Epidemiology and frequency of resistance among
pathogens causing urinary tract infections in 1,510 hospitalized patients:
a report from the SENTRY Antimicrobial Surveillance Program (North
America). Diagn Microbiol Infect Dis 2001; 40: 129-136.
9. Kahlmeter G. Prevalence and antimicrobial
susceptibility of pathogens in uncomplicated cystitis. The ECO SENS study.
Int J Antimicrob Agents 2003; 22: 49-52.
10. Forbes BA, Sahm DF, Weissfeld AS. Bailey & Scott’s
Diagnostic Microbiology, 11th edn. Philadelphia: Mosby 2002: pp.133-148
and 907-912.
11. Clinical and Laboratory Standard Institute.
Performance standards for antimicrobial disk susceptibility tests. NCCLS
documents M 100 S15. Wayne, PA, USA: Clinical and Laboratory Standard
Institute; 2005.
12. Tessema B, Kassu A, Mulu A, Yismaw GP. Predominant
isolates of urinary tract pathogens and their antimicrobial susceptiblity
patterns in Gondar University Teaching Hospital, northwest Ethiopia.
Ethiop Med J 2007; 45: 61-67.
13. Akram M, Shahid M, Khan AU. Etiology and antibiotic
resistance patterns of community-acquired urinary tract infections in JNMC
Hospital Aligarh, India. Ann Clin Microbiol Antimicrob 2007; 6: 4.
14. Kiffer CR, Mendes C, Oplustil CP, Sampaio JL.
Antibiotic resistance and trend of urinary pathogens in general
outpatients from a major urban city. Int Braz J Urol 2007; 33: 267-269.
15. Randrianirina F, Soares JL, Carod JF, Ratsima E,
Thonnier V, Combe P, et al. Antimicrobial resistance among
uropathogens that cause community-acquired urinary tract infections in
Antananarivo, Madagascar. J Antimicrobial Chem 2007; 59: 309-312.
|
|
|
|