BMJ 2007;334:572 (17 March), doi:10.1136/bmj.39119.595081.55 (published 20 February 2007)
Ghulam Nabi, clinical lecturer1, J Cook, Statistician2, J N'Dow, professor of urology1, S McClinton, consultant urological surgeon1
1 Academic Urology Unit, Institute of Applied Health Sciences, College of Life Sciences and Medicine, University of Aberdeen, Health Sciences Building, Aberdeen AB25 2ZD, 2 Health Services Research Unit, Institute of Applied Health Sciences, College of Life Sciences and Medicine, University of Aberdeen
Correspondence to: G Nabi g.nabi@abdn.ac.uk
Design Systematic review and meta-analysis of randomised controlled trials.
Data sources Cochrane controlled trials register (2006 issue 2), Embase, and Medline (1966 to 31 March 2006), without language restrictions.
Review methods We included all randomised controlled trials that reported various outcomes with or without stenting after ureteroscopy. Two reviewers independently extracted data and assessed quality. Meta-analyses used both fixed and random effects models with dichotomous data reported as relative risk and continuous data as a weighted mean difference with 95% confidence intervals.
Results Nine randomised controlled trials (reporting 831 participants) were identified. The incidence of lower urinary tract symptoms was significantly higher in participants who had a stent inserted (relative risk 2.25, 95% confidence interval 1.14 to 4.43, for dysuria; 2.00, 1.11 to 3.62, for frequency or urgency) after ureteroscopy. There was no significant difference in postoperative requirement for analgesia, urinary tract infections, stone free rate, and ureteric strictures in the two groups. Because of marked heterogeneity, formal pooling of data was not possible for some outcomes such as flank pain. A pooled analysis showed a reduced likelihood of unplanned medical visits or admission to hospital in the group with stents (0.53, 0.17 to 1.60), although this difference was not significant. None of the trials reported on health related quality of life. Cost reported in three randomised controlled trials favoured the group without stents. The overall quality of trials was poor and reporting of outcomes inconsistent.
Conclusions Patients with stents after ureteroscopy have significantly higher morbidity in the form of irritative lower urinary symptoms with no influence on stone free rate, rate of urinary tract infection, requirement for analgesia, or long term ureteric stricture formation. Because of the marked heterogeneity and poor quality of reporting of the included trials, the place of stenting in the management of patients after uncomplicated ureteroscopy remains unclear.
Ureteroscopy is now performed with small calibre endoscopes and better intracorporeal lithotripsy devices such as holmium laser so that most patients can be treated without ureteric dilation. As a result, the need for a postprocedural stent remains questionable.
We determined the evidence that outcome with routine ureteric stent placement after uncomplicated ureteroscopy is inferior to that without stent placement.
To be included randomised controlled trials had to compare stenting with no stenting after uncomplicated ureteroscopy in adults with a clinical diagnosis of ureteric stone who required intervention or who were undergoing diagnostic or therapeutic ureteroscopy for upper tract transitional cell carcinoma and had at least one of the predetermined outcomes of interest.
Outcome measures
Outcomes of interest were pain rated by patients on a validated
scale, need for analgesia, lower urinary tract symptoms, unplanned
medical visits or admission to hospital, complications related to the
stent (such as migration, encrustation, fragmentation, ureteric
erosion, and fistulas), return to normal physical activities,
participants' satisfaction, health economics and health related
quality of life. Trials reporting on pain were classified into two
groups: those that reported pain score within or at three days or
those that reported pain at or after day seven after the procedure.
Quality assessment and data
abstraction
Two reviewers (GN, SMcC)
independently assessed study quality using the checklist developed
for the Cochrane renal group.6 Discrepancies were resolved by
discussion and arbitration by a third party if necessary. They
assessed concealment of allocation, intention to treat analysis,
completeness of follow-up, and blinding of investigators,
participants, and outcome assessors.
They screened identified titles and abstracts independently. Potentially relevant trials were retained and the full text examined. The reviewers independently extracted data. When important data were not reported, we tried to contact the authors.
Study characteristics and
quantitative data synthesis
Whenever possible,
we classified the studies by size and site of stones and type of
ureteroscope and intracorporeal lithotripsy device used. When two or
more studies reported on the same outcome we quantitatively combined
results. We calculated relative risks for dichotomous data and
weighted mean differences, with 95% confidence intervals, for
continuous data. A fixed effects model (Mantel-Haenszel) was used
unless there was evidence of substantial statistical heterogeneity,
in which case we used the DerSimonian and Laird random effects model.
Statistical heterogeneity of treatment effects between studies was
formally tested with Cochran's test for heterogeneity (P<0.1). The
I2
statistic was also examined.7 We explored possible sources
of heterogeneity (participants, treatments, study quality). When we
could not combine data quantitatively they were assessed
qualitatively. All meta-analyses were performed using RevMan software
(version 4.2.8).
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Seven studies included participants irrespective of the site of stones in the ureterw1 w2 w4-w8 and a few selectively recruited participants with stones in the lower ureter.w3 w9 There was no significant difference in stone size between the groups that did or did not receive a stent. Participants with intraoperative ureteric perforation or any other complications that otherwise would have required postprocedural placement of a ureteric stent were specifically excluded from the trials. One trial included participants after diagnostic or therapeutic ureteroscopy for transitional cell carcinoma of ureter or pelvicalyceal system.w4
One trial mentioned the material of the ureteric stents used.w2 Size of stents used varied from 6 French gaugew2 w3 w4 w6 w9 to 7 French gauge,w5 w7 but two studies did not specify size.w1 w8 All trials except two used semirigid or rigid ureteroscopes ranging in size from 6.0 to 9.5 French gauge. One trial routinely used a 7.4 French gauge flexible ureteroscope for upper ureteric stonesw1 while another did so occasionally.w4 Two studies carried out ureteral dilatation in both groups before the introduction of the ureteroscope.w3 w9 One study excluded participants who required dilatation.w4 In three trials ureteral dilatation to facilitate ureteroscopy was not required.w5 w6 w8 Different sources of intracorporeal lithotripsy were used for fragmentation of large calculi, including holmium:YAG (yttrium-aluminium-garnet) laser,w1 w3 w4 w6 electromechanical,w7 w9 electrohydraulic,w5 and ultrasonic lithotrite.w8
Most of the included trials failed to
meet our quality criteria
because of lack of information rather than explicit reporting
of methods that did not conform to the criteria. The trial designs
were heterogeneous with regard to ureteroscope sizes, intracorporeal
lithotripsy devices, postoperative analgesia, and outcome assessment
and reporting. Only one trial reported on blinding (table 2)
.
Patients' outcomes
Patients' pain scores?Five trials measured pain scores at
variable intervals after the procedure: at day one,w9 days
one and three,w6
only at day three,w5 at days three, seven, and 15,w2
and at one, six, and 12 weeks.w1 They all used a 10 cm
visual analogue scale with 0 representing no pain and 10
representing severe pain. Experimental studies in minipigs have
reported persistent mechanical ureteric oedema and urinary tract
obstruction up to 96 hours after dilatation,9 suggesting that
the cause of flank pain in the first three days after ureteroscopy is
multifactorial and not caused by stents alone. Two trials reported no
significant difference in pain scores within three days of the
procedure between the groups,w5 w9
whereas one trial favoured those without stents within three days of
the procedure.w2 There was evidence of substantial heterogeneity
between studies for pain scores between both immediate (within or at
three days) and delayed (seven days) postoperative periods. Because
of the large degree of heterogeneity we could not pool data. One
trial reported a significantly higher pain score at four weeks in
those with stents,w3 whereas two trials reported no significant
difference at two and 12 weeks after the procedure.w1 w2 In
two studies the reported data were not suitable for inclusion in the
meta-analysis,w3 w4 with both trials reporting a higher
pain score in participants with stents. In one other trial the method
of pain measurement was not clear,w7 though it reported no
significant difference in pain perception between groups.
Requirement of analgesia?Four trials reported on the requirement for analgesia after ureteroscopic removal of ureteric stones.w1 w6-w8 None of these studies found any significant difference in the proportion of participants who required analgesia after ureteroscopy with or without stents. Only two trials gave data suitable for meta-analysis.w4 w7 There was no difference in use of analgesics between the two groups (relative risk 1.03, 95% confidence interval 0.73 to 1.47).
Lower urinary tract symptoms?Eight
trials reported on lower urinary tract symptoms at various lengths of
follow-up.w1-w7
w9 Combined analysis of four of these studies that reported
urinary frequency or urgency showed a higher rate in participants
with stents (2.00, 1.11 to 3.62; fig 2)
. There was also a higher rate of haematuria (2.18,
0.72 to 6.61) and dysuria (2.25, 1.14 to 4.43) in those with stents.
Data from three trials, which could not be used for meta-analysis,
also showed higher rates of lower urinary tract symptoms in those
with stents.w1 w3 w4
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Efficacy outcomes
Ureteric strictures/stone free rate?Of the nine trials, six
reported on the rate of ureteric stricture formation.w1-w3 w6 w8
w9 There was no difference in the proportion of participants
developing strictures with or without stents. Similarly, none of the
trials reported significant differences in the stone free rates
between participants with or without a stent.
Health related quality of life
None of the trials reported on the quality of life of participants.
One of the trials assessed participants' preference by asking those
who received a stent whether they would prefer to undergo
ureteroscopy without placement of a stent if they needed one in the
future.w9
Around two thirds of participants in the stented group said they
would prefer not to have stents after any future ureteroscopy.
Health economics
Three studies reported on the cost per patient with or without a
stent.w4 w8 w9 Though costs were higher for the group with
stents in all the three trials, the methods used to estimate costs
were not well described and it is unclear how appropriate any of the
costs estimates were and whether any were transferable to other
settings. In one trial, the reported costs per patient were based on
hospital charges but had been incorrectly calculated.w8 The operation
time (minutes), a key cost driver, was consistently longer in the
group with stents (weighted mean difference 5.37, 95% confidence
interval 2.37 to 8.36,
I2=0, fig 5).
w1-w6 w9
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We found no significant difference between the groups with and without stents in the need for postprocedural analgesia, urinary tract infection, stone clearance rates, and ureteric stricture development. These outcomes, however, were not reported consistently across the studies. None of the trials reported on health related quality of life. No trials investigated the impact of stent design and material on outcome, especially as related to quality of life. In a randomised study Joshi et al showed no difference in the impact on patients' quality of life between ureteric stents composed of firm or soft polymer.11 This trial, however, did not have a control group of participants without stents. In a non-randomised study, up to 80% of participants experienced urinary symptoms and pain associated with indwelling ureteric stents, which interfere with daily activities and result in a reduced quality of life.3 Chen et al reported return to normal physical activity in 80% of participants on the day after the procedures in both groups.w5
A few trials reported on cost implications. Not surprisingly, there was a higher cost associated with use of ureteric stents, but none of the trials reported on the cost effectiveness of this intervention.
Limitations
Lack of definition of uncomplicated ureteroscopy?Because of a
lack of standardisation of the definition of "uncomplicated
ureteroscopy," the decision not to insert a stent can be difficult.
This was evident from the included trials. This decision is often
affected by the technique, technology used, and experience of the
operating surgeon. Denstedt et al defined uncomplicated ureteroscopy
as no evidence of perforation or lack of clinically important oedema.w1
They did not, however, propose any objective criteria to assess the
clinical importance of any oedema after the procedure but suggested
that free flow of contrast into the bladder on retrograde pyelography
should rule it out. Other studies used an endoscopic, non-validated
grading of ureteric trauma and oedema on a scale of 0 (mild) to 2
(severe).2w6
Performance and reporting of studies?There was a lack of standardisation of outcome measures, length of trial, and duration of stenting. The use of preprocedural antibiotics, trial design, stent material, patient population, assessment of health related quality of life, and cost-effectiveness data were all inconsistent. Studies reported pain scores as means with variance, although it is well recognised that data from visual analogue scales are often skewed and therefore may be more accurately analysed as medians. We were unable to access data from individual patients to assess whether comparison of medians rather than means may have altered our findings. Some trials allowed withdrawal after randomisation because of intraoperative complications,w2 w3 leading to potential reporting bias. The longest follow-up was only six months.w2
Quality of reporting?The
general quality of trials was poor (table 2).
Some participants were excluded from the analysis
in a few trials because of intraoperative complications, making
it difficult to assess the true effect of intervention. Most of
the trials had small sample sizes.
Implications for practice
As stent placement after ureteroscopy seems to cause undesirable
lower urinary tract symptoms maybe it should not be a standard
practice. There are, however, many unanswered questions, and any
recommendations would be potentially flawed because of a lack of
standardisation of outcome measures, marked clinical heterogeneity,
withdrawal after randomisation, imprecision in measurement of
outcomes (large confidence intervals), and poor reporting of
published clinical trials.
Implications for research
Research efforts should now be concentrated on higher quality, more
rigorous randomised trials. As a minimum, these should use predefined
ideally standardised measures of outcome and be multicentred to
ensure that the studies give sufficiently precise estimate of the
various outcomes. Trials should be protocol driven and a detailed
protocol of how the project is to be conducted should be agreed
before the start. The protocol should state the research objectives,
reasons for the study, issues related to recruitment (inclusion and
exclusion criteria), information to be collected at entry to the
study, and interventions of interest, and there should be an agreed
follow-up protocol.
Outcome measures must include outcomes assessed by patients and
ideally health economic outcome measures. The impact of variations in
stent design, size, and material, and the effect of different types
of intracorporeal lithotripsy sources on the requirement for stents
need to be examined.
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Contributors: GN, SMcC, and JN'D contributed to the idea and designed the review protocol. GN and SMcC undertook screening of articles, data extraction, and quality assessment. JN'D contributed to the drafting and critical revision of the report. JC performed the statistical analyses. All authors contributed to drafting the manuscript and approved the final version. GN is guarantor.
Funding: None.
Competing interests: None declared.
Ethical approval: Not required.