- Research article
- Open Access
- Open Peer Review
Urine sampling techniques in symptomatic primary-care patients: a diagnostic accuracy review
© The Author(s). 2016
- Received: 19 October 2015
- Accepted: 23 May 2016
- Published: 8 June 2016
Choice of urine sampling technique in urinary tract infection may impact diagnostic accuracy and thus lead to possible over- or undertreatment. Currently no evidencebased consensus exists regarding correct sampling technique of urine from women with symptoms of urinary tract infection in primary care. The aim of this study was to determine the accuracy of urine culture from different sampling-techniques in symptomatic non-pregnant women in primary care.
A systematic review was conducted by searching Medline and Embase for clinical studies conducted in primary care using a randomized or paired design to compare the result of urine culture obtained with two or more collection techniques in adult, female, non-pregnant patients with symptoms of urinary tract infection. We evaluated quality of the studies and compared accuracy based on dichotomized outcomes.
We included seven studies investigating urine sampling technique in 1062 symptomatic patients in primary care. Mid-stream-clean-catch had a positive predictive value of 0.79 to 0.95 and a negative predictive value close to 1 compared to sterile techniques. Two randomized controlled trials found no difference in infection rate between mid-stream-clean-catch, mid-stream-urine and random samples.
At present, no evidence suggests that sampling technique affects the accuracy of the microbiological diagnosis in non-pregnant women with symptoms of urinary tract infection in primary care. However, the evidence presented is in-direct and the difference between mid-stream-clean-catch, mid-stream-urine and random samples remains to be investigated in a paired design to verify the present findings.
- “Urinary tract infections” [Mesh]
- “Urine” [Mesh], “Specimen handling” [Mesh]
- “Urine specimen collection” [Mesh]
- “Primary health care” [Mesh]
- “General practice” [Mesh]
Symptomatic urinary tract infection (UTI) in women is a common condition in general practice, and every day general practitioners or their staff instruct women in delivering urine samples for examination . The main concern when sampling urine is that inadequate handling may increase the risk of contamination in turn leading to overdiagnosis and overtreatment of UTI. Sterile collection of urine samples can be performed using suprapubic puncture or urethral catheterization and use of these collection techniques could possibly reduce contamination and thereby overdiagnosis and overtreatment. However, in a primary care setting these methods are considered obsolete today due to the associated discomfort for the patient and a minor risk of iatrogenic infection and other complications. Current methods include i) mid-stream-clean-catch technique (MSCC) where the patient is instructed to clean the labia before voiding using tap water, soap or disinfectants, ii) mid-stream urine (MSU) without prior cleaning, iii) random samples delivered without instruction or iv) home-voided samples with or without standardized transport media. These sampling techniques are mostly based on tradition or expert opinion and ease-of-use for patient and doctor rather than stringent evidence. A study from 2000 conducted in primary care found no evidence that sampling technique affected contamination rate or infection rate in urine samples , but new evidence within this area is often questioned and debated [3–5]. Since sampling techniques (MSCC, MSU, random samples and home voiding) differ extensively in preparation time and discomfort, ease-of-use for doctors as well as their patients, it is relevant to review their diagnostic yield. The aim of this study was to conduct a systematic review to determine the accuracy of urine culture from different sampling techniques in symptomatic patients in primary care.
We searched Medline and Embase for clinical studies conducted in primary care published before May 2015 in English, Swedish, Danish or Norwegian. Combinations of the words “urinary tract infection”, cystitis, bacteriuria, urine, specimen, handling, urinalysis, collection, midstream and” clean catch” were used. To identify more studies from before 1970, a slightly different search-string was used for the older studies in Medline. The literature search and inclusion of studies was performed by AH. The full search strings can be seen in Appendix A.
Clinical studies randomizing or using a paired design to compare the result of urine culture obtained with two or more collection techniques in adult, self-helped, non-pregnant (and not post-partum) women with symptoms of UTI in primary care (general practice, outpatients clinics or comparable settings). We did not discriminate between complicated and uncomplicated cases of UTI.
Studies investigating mainly patients who were not self-helped, were asymptomatic, pregnant, children or men (wrong group)
Studies conducted in the secondary sector (wrong setting)
Studies using other modalities than culture as reference (wrong gold standard)
Studies where data for the selected outcome was not available (missing data)
Studies using a different design than described in the inclusion criteria (wrong design)
The references of included studies were screened and experts in the field were contacted to provide additional literature.
Data from included studies were entered into a data-form with information on setting, number of patients, age, inclusion- and exclusion-criteria for the study, reference and index text, the assigned cut off for infection vs. contamination, the bacteria identified and study design. Data on absolute numbers of infected urine samples, true and false positives and negatives or predictive values of one sampling method versus another were likewise extracted from the included studies. If these measures were not directly provided in the article, we calculated them if possible. Selected outcomes were dichotomized for the planned analyses as negative/positive culture. Culture results presented as equivocal and contaminated were grouped with the negative results. Data from the relevant patients were extracted when studies also included patients covered by the exclusion criteria. Data extraction was done by both authors and discrepancies were discussed and corrected. When data was not available or incomplete we referred from contacting authors, as most studies were more than 10 years old.
Definition of reference standard
Assuming an increasing contamination rate in the order of: 1) Suprapubic puncture, 2) urethral catheterization samples, 3) MSCC, 4) MSU, 5) Random samples, 6) Home-voided urine, the least contaminated was used as reference and the most contaminated as index test. For example, if a study investigated both MSCC and random urine sampling in a paired design, MSCC was used as reference standard and random samples as index test.
This review included both paired studies and randomized controlled trials (RCT). RCTs were analysed separately.
The included studies were evaluated using QUADAS-2 for assessment of diagnostic accuracy studies . No study was excluded based on low quality according to this tool. Both studies using paired samples and randomized controlled trials were assessed with QUADAS-2.
The specified dichotomized outcomes were used to calculate predictive values, sensitivity and specificity in paired studies. The generated sensitivity and specificity values were used to create forest plots on the diagnostic accuracy. Diagnostic accuracy plots were performed using Review Manager (RevMan) Version 5.3. Copenhagen: The Nordic Cochrane Centre, the Cochrane Collaboration, 2014.
Characteristics of included studies
MSCC vs. Cat
Random vs. MSCCc
≥ 102 cfu/ml
≥ 102 cfu/ml
Home vs. MSCC
≥ 104 cfu/ml
≥ 104 cfu/ml
MSCC vs. Cat
≥ 105 cfu/ml
≥ 105 cfu/ml
MSU vs. MSCC
> 105 cfu/ml
> 105 cfu/ml
Outpatient clinic/student clinic
MSCC vs. Cat/Sup
Reporting absolute counts
MSCC vs. Sup
Reporting absolute counts
Reporting absolute numbers
Quality of included studies according to Quadas-2
Data from included studies
Paired design studies
The studies by Stamm and Mabeck reported absolute counts of colony-forming units in the voided urine samples and this allowed us to investigate the current cut-off for primary uropathogens of 103 cfu/ml in voided urine samples against 10 cfu/ml in suprapubic puncture . Using these current cut-offs we calculated the sensitivity of MSCC to be 0.81 (0.71-0.88) in the study by Stamm and 0.96 (0.85-0.99) in the study by Mabeck. Corresponding specificities were 0.90 (0.82-0.95) in the study by Stamm and 0.59 (0.43-0.73) in the study by Mabeck.
Randomized controlled trials
Randomized controlled trials and infection rates
Index infected (95 % CI)
Reference infected (95 % CI)
MSU vs. MSCC
Random vs. MSCC
This diagnostic accuracy review is the first to assess the available evidence from different urine sampling techniques on symptomatic patients with suspected UTI in primary care. Overall, we did not find consistent evidence to suggest important differences in diagnostic accuracy among the included urine sampling techniques (MSCC, MSU or random voiding). The slightly lower specificity of voided samples compared to invasive sampling techniques (suprapubic puncture and catheter) will cause 5–10 % of healthy patients to be overdiagnosed. This does not, in our opinion, outweigh the discomfort and risk of complications associated with sterile techniques. The quality of the studies was moderate and substantial heterogeneity was present between study designs and applied diagnostic cut-offs. With the available evidence, each general practitioner can choose freely the sampling technique most appropriate for his or her practice and patients.
The current review included two studies from general practice and 5 from outpatient clinics or student clinics. Participants were symptomatic patients under investigation for urinary tract infection. We have no reason to suspect the included patients differ from the average UTI patient in primary care. Thus we believe the results can be considered applicable to most primary care settings including general practice.
The included methods of urine sampling included, the different cut-offs for infection applied and the time span between studies of up to 50 years does however suggest that the overall results regarding their diagnostic accuracy should be considered with caution.
The current consensus regarding a cut-off for infection (eg. 103 cfu/ml for primary uropathogens) was not directly assessed in any of the studies, but we calculated the sensitivity and specificity based on the two studies by Mabeck and Stamm. While the sensitivity was above 0.80 in both studies, the specificity differed between studies and was low (0.59) in the study by Mabeck. However, this could be a chance finding and caution should be excised when interpreting these results as they are based on few older studies and we do not know if this result would still apply today with current microbiological procedures. Furthermore, current cut-offs are based on microbiological assessments and have, to our knowledge, never been validated in relation to patient-relevant outcomes like cure-rate or impact on daily activities. The development of such patient-centred outcomes may be more applicable to a general practice setting.
The European urine analysis guideline recommends a MSCC without detergents . However, this guideline is based on studies including pregnant, asymptomatic as well as hospitalized patients and their conclusions do not necessarily apply to the average patient in general practice. Studies based in secondary care have found varying accuracy of voided urine samples depending on their patient group, design and gold standard [14–18]. However, studies investigating symptomatic, otherwise healthy women seem to essentially reproduce our findings [19, 20].
The present review does not present evidence to suggest one urine sampling technique over another according to diagnostic performance; rather this should at present depend on ease of use and convenience for patients and practices. This lack of evidence is in part due to few available studies and further testing on current diagnostic cut-offs as well as new patient-centred outcomes is warranted.
FN, false negatives; FP, false positives; MSCC, mid-stream-clean-catch technique; MSU, mid-stream urine; NPV, negative predictive value; PPV, positive predictive value; RCT, randomized controlled trials; SEN, sensitivity; SPE, specificity; TN, true negatives; TP, true positives; UTI, urinary tract infection.
We would like to thank Niels Frimodt-Møller and Chris Del Mar for their suggestions for supplementary literature and the UC CARE cooperation for setting higher standards in the fight against antibiotic resistance.
This study was funded by UC CARE, University of Copenhagen.
Availability of data and materials
Complete list of excluded studies and full quality evaluation can be found in appendices. For additional data, please contact the corresponding author.
The literature search and inclusion of studies was performed by AH. Both authors performed the data extraction and quality assessment. Both authors have critically revised the manuscript and approved the final version.
Anne Holm: Medical Doctor and PhD-fellow at The Research Unit for General Practice and Section of General Practice, Department of Public Health, University of Copenhagen, Denmark.
Rune Aabenhus: General Practitioner and PhD-fellow at The Research Unit for General Practice and Section of General Practice, Department of Public Health, University of Copenhagen, Denmark.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
The authors declare, they have followed the PRISMA Guidelines in conducting this study.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Forskningsenheden for Almen Praksis Aarhus Universitet, Afdeling for Almen Medicin Aarhus Universitet: Kontakt- Og Sygdomsmønsterundersøgelse KOS 2008. 2008.Google Scholar
- Lifshitz E, Kramer L. Outpatient urine culture: does collection technique matter? Arch Intern Med. 2000;160:2537–40.View ArticlePubMedGoogle Scholar
- Jaffe JS. Collection of urine for culture. N Engl J Med. 1994;331:617–8.PubMedGoogle Scholar
- Payton S. Infection: Utility of midstream urine cultures questioned. Nat Rev Urol. 2013;11:3–3.View ArticlePubMedGoogle Scholar
- Smith G. Diagnosis of coliform infection in acutely dysuric women. N Engl J Med. 1983;309:1393–4.PubMedGoogle Scholar
- Whiting PF, Rutjes AWS, Westwood ME, Mallet S, Deeks JJ, Reitsma JB, Leeflang MMG, Sterne JAC, Bossuyt PMM. QUADAS-2: a revised tool for the quality assessment of diagnostic accuracy studies. Ann Intern Med. 2011;155:529–36.View ArticlePubMedGoogle Scholar
- Hooton TM, Roberts PL, Cox ME, Stapleton AE. Voided midstream urine culture and acute cystitis in premenopausal women. N Engl J Med. 2013;369:1883–91.View ArticlePubMedPubMed CentralGoogle Scholar
- Stamm W, Counts G. Diagnosis of coliform infection in acutely dysuric women. N Engl J Med. 1982;307:463–8.View ArticlePubMedGoogle Scholar
- Walter F, Knopp R. Urine sampling in ambulatory women: midstream clean-catch versus catheterization. Ann Emerg Med. 1989;18:166–72.View ArticlePubMedGoogle Scholar
- Mabeck C. Studies in urinary tract infections. The diagnosis of bacteriuria in women. Acta Med Scand. 1969;186:35–8.View ArticlePubMedGoogle Scholar
- Baerheim A, Laerum E. Home-voided urine specimens in women. Diagnostic agreement with clean-catch midstream specimens. Scand J Prim Health Care. 1990;8:207–11.View ArticlePubMedGoogle Scholar
- Aspevall O, Hallander H, Gant V, Kouri T. European guidelines for urinalysis: a collaborative document produced by European clinical microbiologists and clinical chemists under ECLM in collaboration with ESCMID. Scand J Clin Lab Invest. 2000;60:1–96.View ArticleGoogle Scholar
- Bradbury SM. Collection of urine specimens in general practice: to clean or not to clean? J R Coll Gen Pract. 1988;38:363–5.PubMedPubMed CentralGoogle Scholar
- Dawborn JK, Plunkett PJ. The collection and assessment of midstream urine samples in the diagnosis of urinary tract infection in women. Med J Aust. 1963;50:540–3.PubMedGoogle Scholar
- Barnes WF, Albers DD. Comparison of paired midstream voided and catheterized urine samples from female patients in a general hospital. J Okla State Med Assoc. 1978;71:82–4.PubMedGoogle Scholar
- Craig I. The collection of urine for bacteriological investigation. Br J Clin Pract. 1965;19:557–63.PubMedGoogle Scholar
- Prandoni D, Boone MH, Larson E, Blane CG, Fitzpatrick H. Assessment of urine collection technique for microbial culture. Am J Infect Control. 1996;24:219–21.View ArticlePubMedGoogle Scholar
- Merritt A, Sanford J, Durham N. Sterile-voided urine culture; an evaluation in 100 consecutive hospitalized women. J Lab Clin Med. 1958;52:463–70.PubMedGoogle Scholar
- Lemieux G, St-Martin M. Reliability of clean-voided mid-stream urine specimens for the diagnosis of significant bacteriuria in the female patient. Can Med Assoc J. 1968;98:241–5.PubMedPubMed CentralGoogle Scholar
- Shrestha R, Gyawali N, Gurung R, Amatya R, Bhattacharya SK. Effect of urogenital cleaning with paper soap on bacterial contamination rate while collecting midstream urine specimens. J Lab Physicians. 2013;5:17–20.View ArticlePubMedPubMed CentralGoogle Scholar