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Journal of Clinical Microbiology, September 1999, p. 3051-3052, Vol. 37, No. 9
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Evaluation of the Leukocyte Esterase and Nitrite
Urine Dipstick Screening Tests for Detection of Bacteriuria in
Women with Suspected Uncomplicated Urinary Tract Infections
Heather
Semeniuk1 and
Deirdre
Church1,2,*
Departments of Pathology and Laboratory
Medicine and Medicine, University of Calgary,2
and Calgary Laboratory Services (CLS),1 Calgary,
Alberta, Canada
Received 1 February 1999/Returned for modification 20 March
1999/Accepted 9 June 1999
 |
ABSTRACT |
A positive dipstick urinalysis (i.e., leukocyte esterase test
and/or nitrite test) did not reliably detect significant bacteriuria in
479 ambulatory women with suspected uncomplicated urinary tract infection; 18.9% of the urine samples that demonstrated significant bacteriuria would have been rejected by the laboratory based on a
negative urinalysis screen.
 |
TEXT |
Physicians in our region frequently
order a dipstick urinalysis to screen for the presence of pyuria and
significant bacteriuria in women with suspected uncomplicated urinary
tract infection, and a culture is requested only when the urinalysis is
positive. The Chemstrip-10 dipsticks (Roche Diagnostics,
Montreal, Quebec, Canada) detect leukocyte esterase (LE) activity
as an indicator of pyuria and urinary nitrite (NIT) production as an
indicator of bacteriuria. Although use of both the NIT and LE tests has been shown to improve detection of significant bacteriuria (i.e., colony count
105 CFU/ml) (1-3, 5, 7, 8,
11), it was of interest to focus our study on women with
uncomplicated urinary tract infection, whose urine colony counts may be
as low as 103 CFU/ml (4, 9, 10).
Each of 479 ambulatory women aged 15 to 65 years submitted a fresh,
morning first-void mid-stream urine sample in a sterile container. A
fresh, random mid-stream urine sample was also accepted. A Chemstrip-10
(Boehringer Mannheim) urinalysis (2-min procedure) to detect LE and NIT
was immediately performed according to the manufacturer's
instructions. A positive urinalysis result occurred when either the LE
test or NIT test or both were positive. A positive NIT test indicates
that nitrite has been produced from the reduction of nitrate by enteric
bacteria, most commonly by genera of the Enterobacteriaceae
family (practical sensitivity limit, 0.05 mg/dl or 11 mmol/liter). The
LE test is an indirect measure of pyuria since it detects the
production of this enzyme by the host's polymorphonuclear cells.
A calibrated 0.001-ml bacteriologic loop was used to inoculate urine
onto 5% Columbia blood agar (P1350) and MacConkey agar plates within
30 min of collection (P1800) (PML, Seattle, Wash.). The inoculated
plates were incubated overnight aerobically at 37°C for up to 24 h (a minimum of 18 h). Uropathogens included genera of the
Enterobacteriaceae family, group D enterococci, Staphylococcus saprophyticus, group B streptococci, and
staphylococci other than S. saprophyticus when the patient
was symptomatic. Urine colony counts were recorded as follows: (i) no
growth, (ii) no significant growth (<103 CFU/ml), and
(iii) significant bacteriuria (
103 CFU/ml). Urines that
grew contaminants (i.e., coagulase-negative staphylococci,
lactobacilli, diphtheroids, and Streptococcus spp. other
than group D spp.) were reported as demonstrating normal periurethral
flora. Mixed growth was recorded for urines that grew multiple
organisms (two or more). Significant urine bacterial isolates were
identified by conventional biochemical procedures (6).
Urinalysis results were correlated to results of urine cultures. Urine
cultures demonstrating significant bacteriuria (i.e., one or two
uropathogens) were separated by the following colony count breakpoints
for the performance analyses: (i)
103 to 104
CFU/ml, (ii)
104 to 105 CFU/ml, and (iii)
105 CFU/ml. Performance of urinalysis tests was evaluated
by calculating, using standard methods, sensitivity, specificity, and
positive and negative predictive values.
The average age of the 479 women was 36.6 years (range, 15 to 65 years). Most of the women were young, were not pregnant, and had a
urine culture requested because they had symptoms suggestive of a
urinary tract infection. All of the urine samples were mid-stream collections, but only 5% were first-void specimens. Only 90 (18.8%) urine cultures had a pure growth of one or two potential uropathogens, while 203 (42.4%) showed either no growth (60 cultures [12.5%]) or
no significant growth (143 cultures [29.9%]). The rest of the urine
cultures either grew contaminants or showed mixed growth.
Table 1 outlines the performance of the
urinalysis tests for detection of significant bacteriuria at varying
colony counts. Urinalysis had the highest sensitivity for urine colony
counts that were greater than 105 CFU/ml. At this colony
count, the detection of both pyuria and bacteriuria (positive results
for both LE and NIT) or pyuria alone (positive result for LE) had much
better sensitivity than the detection of bacteriuria alone (positive
result for NIT). The positive predictive value of a positive urinalysis
result was poor at the lower colony counts and improved only when both
pyuria and bacteruria (positive results for both LE and NIT) were
detected by urinalysis. Detection of bacteriuria (positive result for
NIT) and pyuria (positive result for LE) had excellent specificity and
negative predictive value for all colony counts. Overall, a positive
urinalysis had a sensitivity of 81.1%, a specificity of 59.4%,
positive and negative predictive values of 31.6% and 93.2%,
respectively, and an overall agreement of 63.5% for detection of
significant bacteriuria at any colony count greater than
103 CFU/ml.
Most infections were due to Escherichia coli or members of
other genera in the Enterobacteriaceae family (74 infections
[82.2%]), and a smaller number were due to S. saprophyticus and other gram-positive organisms (16 infections
[17.8%]). Group B streptococci were the only potential uropathogen
isolated in nine patients, and all of these women had positive
urinalysis results (i.e., they had positive result for LE). Urinalysis
tests detected significantly more gram-negative infections (63 of 74 infections [85.1%]) than those due to gram-positive bacteria (10 of
16 infections [62.5%]) because the NIT test did not detect the
presence of gram-positive pathogens.
The results of this study confirm and expand the previous findings, of
Stamm et al. (9, 10), that many women with urinary tract
symptoms have bacterial counts in their urine of less than 105 CFU/ml. Furthermore, the report by Kunin et al.
(4) suggests that women with bacteriuria with very low count
(>102 to 104 CFU/ml) may be in the early phase
of urinary tract infection that is possibly localized to the urethra.
If this is the case, then pyuria may not be present in the urine until
the bacterial count in the bladder reaches very high counts
(>105 CFU/ml). In this study, the combination of positive
LE and NIT tests gives better overall performance than either test
alone in detecting bacteriuria at higher colony counts
(
105 CFU/ml). Although the presence of bacteriuria alone
is not diagnostic of a urinary tract infection, all of the women had
urine cultures done because they had symptoms suggestive of acute
cystitis. However, the decreased sensitivity of urine dipstick tests in
detecting lower colony counts limits the utility of this method in
diagnosing uncomplicated urinary tract infections in women. If the
laboratory cultured only urine samples with a positive urinalysis
result this policy would eliminate 51.8% of all urine cultures.
Although this approach would save the laboratory considerable time and expense, approximately one of every five women with symptoms of a
urinary tract infection and positive urine cultures would be missed.
Alternatively, negative urinalysis results (for both LE and NIT), due
to the high specificity and negative predictive value of these tests,
could be used to screen for urines that do not need to be cultured.
This approach would have missed 17 (18.9%) samples from symptomatic
women who had significant bacteriuria due to gram-positive organisms
other than S. saprophyticus. Group B streptococci have been
previously shown to cause bacteriuria, and detection is particularly
important in pregnant women (12). Use of a positive dipstick
urinalysis result as the only screening method for urinary tract
infection and performance of a urine culture in this population are not recommended.
 |
FOOTNOTES |
*
Corresponding author. Mailing address: Calgary
Laboratory Services (CLS), 1638 10th Ave., S.W., Calgary, Alberta T3C
0J5 Canada. Phone: (403) 209-5281. Fax: (403) 209-5347. E-mail:
dchurch{at}cml.ab.ca.
 |
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Journal of Clinical Microbiology, September 1999, p. 3051-3052, Vol. 37, No. 9
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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