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National Clinical Guideline Centre (UK). Urinary Incontinence in Neurological Disease: Management of Lower Urinary Tract Dysfunction in Neurological Disease. London: Royal College of Physicians (UK); 2012 Aug. (NICE Clinical Guidelines, No. 148.)

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Urinary Incontinence in Neurological Disease: Management of Lower Urinary Tract Dysfunction in Neurological Disease.

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14Monitoring and surveillance protocols

Patients with neurogenic lower urinary tract dysfunction (NLUTD) are known to be at high risk of suffering from urinary tract symptoms and complications. For some conditions, such as spina bifida and spinal cord injury, there is a risk of silent renal deterioration due to the development of hydronephrosis or the formation or renal stones. Furthermore, some patients with NLUTD will have progressive neurological conditions which will be expected to have an increasing adverse impact on LUT function. The effect of ageing on a damaged LUT will often be greater than its effect on the normally innervated LUT.

For all these reasons, there is an argument to be made for offering patients with NLUTD long-term monitoring of their urinary tract. However, as with any surveillance programme, there has to be a balance struck between benefits accrued and the risks, costs and inconvenience that are attached to surveillance. There are inherent difficulties in measuring benefit because it can be multi-faceted; for example, regular follow up has the potential to protect renal function, reduce the frequency and severity of urinary tract infections, reduce troublesome symptoms by providing regular advice and provide psychological support. On the other hand, offering long-term follow up to large groups of patients is expensive in terms of clinical, patient and carer time and investigation costs. Investigations may also have risks from radiation exposure or, in the case of invasive tests, discomfort and infection; some patients will also find follow up processes psychologically stressful.

Life-long renal surveillance is currently in use in some groups of patients with neurological disease such as spinal cord injury and spinal dysraphisms (including spina bifida). There is a need to define whether all such patients will benefit from follow up and whether patients with other neurological conditions might also gain from long-term monitoring.

14.1. Monitoring and surveillance protocols

14.1.1. Does monitoring or do surveillance protocols improve patient outcomes?

Clinical Methodological Introduction
Population:
Intervention:Monitoring and surveillance protocols
  • Ultrasound
  • Renography
  • intravenous urograms
  • abdominal x-rays
  • urodynamics
  • blood tests
  • blood pressure
Comparison:na
Outcomes:
  • Kidney function
  • Renal impairment (hydronephrosis, urinary tract stones, urinary tract infection, malignancy (bladder cancer)
  • Unplanned hospital admissions

14.1.1.1. Clinical evidence review

We searched for observational studies reporting on monitoring and surveillance protocols for the management of incontinence in patients with spinal cord injury, multiple sclerosis, spina bifida or anorectal malformations.

17 observational studies 214; 215; 216; 217; 218; 219; 220; 221; 222; 223; 224; 225; 226; 227; 228; 229; 230 were identified that reported on monitoring on surveillance protocols for the management incontinence in patients with spinal cord injury, multiple sclerosis, spina bifida or anorectal malformations. – Evidence was found for creatinine, ultrasound, cystoscopy and renal scintigraphic scan. All of the studies were in adults except for the study in patients with anorectal malformations 224. Table 1 summarises the population, intervention, comparison and length of follow up for each of the studies.

Table 1. Summary of studies included in the clinical evidence review.

Table 1

Summary of studies included in the clinical evidence review.

Quality of evidence

The majority of studies were retrospective observational studies, predominantly with a before and after design, and without a control group. The studies were therefore graded low by default (see Chapter 4). Further downgrading was due to increased the risk of confounding by uncontrolled factors such as time effects. In addition, a number of the studies reported on interventions that were performed once only and therefore did not form part of an ongoing monitoring and surveillance programme.

MONITORING AND SURVEILLANCE PROTOCOLS
Creatinine
Spinal cord injury

One study (n=36) assessed the sensitivity of serum creatinine levels in detecting clinically important and early deterioration of renal function in patients with spinal cord injury 219.

Of the 36 patients 11 (31%) had a measured creatinine clearance of <100 mL/min (mean 84.8) and a corresponding normal serum creatinine level. Creatinine clearance calculated by the Cockcroft-Gault formula did not correlate well with that measured by the 24 hr endogenous clearance (r=0.426) and 99mTc-DTPA clearance (r=0.366), overestimating creatinine clearance in all but three patients. The mean (SD) difference between the creatinine clearance measured by the 24 hr and DTPA clearance technique was 17.7 (16.5%) and the correlation between these techniques was good (r=0.71) 219.

One study (N=70) reported on patients with spinal cord injury who had annual inpatient evaluations for 5 separate years 222.

For individual patients, the results of 24 hr Ccr were highly variable from one evaluation to the next; the within-subject standard deviation (SD) for Ccr was 25.9 mL/min. The within-subject SD for serum creatinine was 0.12 mg/dL. For all comparisons variability and reliability, serum creatinine was superior to Ccr. No medical management decisions were made based on the result of the 24 hr creatinine clearance 222.

58/70 patients had bilateral normal kidneys on 5 consecutive annual evaluation ultrasounds. Four had kidney stones on 1 or more ultrasound studies and 5 patients had at least one renal ultrasound that showed hydronephrosis. For the 3 patients who had normal renal ultrasounds at time one, but developed abnormalities over subsequent studies (hydronephrosis for 2, cortical scarring for 1), the largest change in Ccr was 19.7% which is less than the mean variability between serial Ccr measurements. The remaining two patients who developed new renal ultrasound abnormalities had changes in Ccr of less than 1% 222.

ULTRASOUND
Spinal cord injury

One study (n=86) investigated the effectiveness of office ultrasonography of the bladder and kidneys to provide routine urological follow-up in the outpatient spinal cord injury clinic 214.

106 scans were performed on 86 asymptomatic spinal cord injury patients. Of the patients, 68 had a blinded excretory urography for comparison, including 20 who underwent additional studies (computerised tomography scans of the abdomen and pelvis, and/or radiologist-performed ultrasound examination of the kidneys and bladder). Office ultrasound detected 5 of 6 kidney stones, 6 of 6 hydronephrotic kidneys, 5 of 7 renal masses (4 of 6 cysts and 1 of 1 renal tumour), 3 of 3 bladder stones and 3 of 3 bladder diverticula. Subtle changes of chronic renal infection noted on excretory urography in 4 patients were not detected on corresponding ultrasound scans but voiding cystourethrograms revealed no reflux, and comparison to prior studies confirmed that these renal units were stable 214.

One study (n=54) compared ultrasound findings with those obtained from excretory urogram (IVP) and/or voiding cystourethrogram in spinal cord injury patients 215. Kidneys: For 15/54 there were concerns regarding renal abnormalities based on the excretory urogram (IVP). Of these 15 patients ultrasound confirmed the radiographic findings in five (two with renal calculi, one with chronic pyelonephritis, one with peripelvic cyst and one with focal pyelonephrtitis), ruled out questionable radiographic findings in six and revealed abnormalities not present radiographically in four (one with renal cyst, one with hydronephrosis, one with cortical atrophy and one with renal calculi). Ureters: Of the 15 patients in whom the ureters were examined nine had different degrees of vescioureteric reflux on voiding cystourethrography, which was confirmed by ultrasound in five (56%) and not demonstrated in four. The remaining 6 patients had ureterctasis on an IVP, which was confirmed by ultrasound in two (33%) and not noted successfully in 4. In two patients with a known allergy to the contrast medium ultrasound demonstrated vesicoureteral reflux in one, and hydroureter and hydronephrosis in one. Bladder: The bladder was examined in 32 patients during ultrasound voiding cystourethrography but was imaged adequately in only 30. Ultrasound confirmed the positive radiographic findings in 23 (six with bladder calculi, three with trabeculated bladders and 12 with normal bladders), ruled out questionable radiographic findings in three and yielded additional information in four (one with bladder calculi, two with lithogenic bladder sediment and one with calcific crust on the Foley catheter balloon) 215.

One study (n=162) reported on the results of a comparison between renal ultrasound (RUS) and renal nuclear scans (RNS) as part of upper tract surveillance in spinal cord injury patients 216.

Only the results of the renal ultrasound scan are reported here. A RUS scan was judged to be positive if it demonstrated any degree of caliectasis or pyelocaliectasis; parenchymal disease; or the presence of complex cysts, calculi, solid masses, or other renal and/or peri-renal processes. Simple renal cysts were not considered an abnormality because they did not dictate any change in patient management. RUS abnormalities were found in 57/162 patients (35.2%). Of the 75 positive ultrasound studies, 39 were positive for hydronephrosis, 39 revealed parenchymal disease, 22 revealed renal stones, and 8 revealed solid renal mass (renal malignancy found in 2 of these 8 patients). Many ultrasounds had more than one pathologic finding 216.

One study (n=109) reported on the diagnostic accuracy of ultrasound and radioisotope renography compared to intravenous urography to detect hydronephrosis in patients with spinal cord injury 226.

Of 235 kidneys studied, 43 kidneys in 23 patients showed hydronephrosis on the final findings. The estimated prevalence was 21% (23/109) in the study. The diagnostic accuracy of sonography and renal ultrasound are summarised in table 2.

Table 2. Diagnostic accuracy of ultrasound and radioisotope renography compared to intravenous urography.

Table 2

Diagnostic accuracy of ultrasound and radioisotope renography compared to intravenous urography.

One study (n=100) reported on the findings from routine radiological surveillance in patients with spinal cord injury 217. In paraplegics, 26/47 patients had abnormalities (upper tract changes, calculi, bladder abnormalities, persistent post-voidal residual urine > 100 ml) detected on routine radiological screening. 24/26 abnormalities were detected 0 to 10 years after the injury compared with only 2/26 after 10 yrs of injury. For tetraplegics, 35/50 abnormalities were detected. All of these were detected within 10 yrs after the injury 217.

One study (n=75) reported on patients with spinal paralysis who had undergone intravenous urography (IVU) and renal ultrasonography as part of routine assessment of the upper urinary tract 220.

The results are presented in table 111, table 112 and table 5 below.

Table 111. Normal IVU and abnormal ultrasound.

Table 111

Normal IVU and abnormal ultrasound.

Table 112. Abnormal IVU and normal ultrasound.

Table 112

Abnormal IVU and normal ultrasound.

Table 5. Abnormalities demonstrated by IVU and also indicated or shown by ultrasound.

Table 5

Abnormalities demonstrated by IVU and also indicated or shown by ultrasound.

One study compared Kidney, Ureter, Bladder (KUB) radiography with ultrasound in 100 consecutive patients with spinal cord injury 225. A total of 199 kidneys and 99 urinary bladders were examined. On average, less than 50% of the renal area and about 70–75% of the urinary bladders were visualised. Five patients had renal stones identified on KUB radiograph, and of these two were seen on ultrasound. There were no stones seen on ultrasound only. Ultrasound identified renal abnormalities in a further 14 patients. There were seven patients with renal scarring in eight kidneys. There were five patients with hydonephrosis in six kidneys; all cases were mild to moderate. There were two patients with a small kidney with thinned cortex. The KUB identified none of these patients. Ultrasound identified a number of other abnormalities. There was one patient with a duplex renal collecting system, one case of nephrectony, one case of adrenal myolipoma, one situs inversus, one case of abnormally high echogenicity of the liver and two cases of gallstones. In one of these an additional gallbladder polyp was seen. One of the cases of gallstones was also identified on the KUB; all other abnormalities were not seen on the radiographs. Abnormalities of the urinary bladder were seen in 20 cases. A total of 19 cases showed evidence of bladder wall hypertrophy, and one case of incomplete bladder emptying. There was one case of previous cystectomy and a neobladder. KUB did not identify any of the abnormalities. Therefore, apart from the renal stones and one patients with gallstones, KUB did not identify any of the other abnormalities seen on ultrasound 225.

One study (n=108) reported on patients who underwent ultrasound who had no urinary symptoms compared with patients who had urinary symptoms 227.

In the asymptomatic group no abnormalities were reported in 63 patients. The following findings were reported in 24 patients (Table 113).

Table 113. Ultrasound findings in asymptomatic patients.

Table 113

Ultrasound findings in asymptomatic patients.

There were 21 spinal cord injury patients who exhibited urinary symptoms (passing purulent urine, temperature, rigors, passing blood in urine, severe kidney/bladder pain, recurrent urine infections) when they underwent ultrasound examination of the urinary tract. Abnormalities such as hydronephrosis, pyonephrosis, bladder calculi, or bladder polyp were detected in 20 of 21 patients and, subsequently, all 20 patients required therapeutic intervention on the basis of ultrasound findings 227.

MULTIPLE SCLEROSIS

One study (n=66) reported on the incidence of upper tract abnormalities using renal ultrasound in patients with multiple sclerosis referred to the neurourology clinic for evaluation of lower urinary tract symptoms 218.

One study (n=48) reported on ultrasound findings in patients with multiple sclerosis with symptoms of neurogenic bladder dysfunction (exacerbation-free for 6 months) 223

Renal ultrasound examination showed significant MS-related upper urinary tract abnormalities in 10 patients (21%) . These abnormalities included renal stones in five patients, grade one hydronephrosis in two patients, cortical atrophy in two patients, and a reflecting pattern in the renal pelvis of one patient representing an early stone or vascular calcifications. In addition, 14 ultrasounds identified bladder trabeculation (29%), which was considered a non-significant MS-related change. Only five of these were associated with abnormal upper tract findings. Eight patients had incidental findings 223.

Table 114. Radiologic findings in patients with abnormal renal ultrasound findings.

Table 114

Radiologic findings in patients with abnormal renal ultrasound findings.

Spina bifida

One study (n=25) reported ultrasound on children with myelodysplasia with normal urodynamics at birth 224. The mean follow up was 9.1 yrs (range 1 to 18.6 yrs). No child had hydronephrosis or reflux 224.

One study (n=40) reported on ultrasound and serum creatinine in adults with spina bifida who were using clean intermittent catheterisation 221. In patients with normal ultrasound and normal serum creatinine (1.5 mg/dl), there were no individuals (0/20) whose average catheterised volume corresponded to a bladder pressure of >40 cm H2O on cystometry. However, in patients with hydronephrosis and/or elevated creatinine, 30% (6/20) had average catheterised volumes corresponding to a bladder pressure of >40 cm H2O 221.

CYSTOSCOPY
Spinal cord injury

One study (N=59) reported on the results of an annual health maintenance evaluation to include cystoscopy on patients with spinal cord injury who were continuously catheterised for 10 more years, or were smokers and catheterised for 5 or more years 229 Ninety three bladder biopsies and 18 urine cytologies were obtained, none of which demonstrated malignant changes. No bladder cancers were diagnosed through screening. During the same six year period four spinal cord injury patients were diagnosed at the hospital with bladder cancer, all outside of the surveillance protocol 229.

One study 230 reviewed all 14 SCI patients diagnosed with squamous cell bladder cancer during a 16 year period and divided them into those who had 1) been given annual cytoscopy for at least 10 years and were asymptomatic when diagnosed with cytoscopy (n=5), and 2) those who had not been routinely screened and were symptomatic at presentation (n=14). Those receiving annual screening had a higher cancer-specific survival (100% compared to 50% in the symptomatic group). In addition, the stage of disease was less advanced at presentation in the screened group. In the non-screened group pathological stage was more advanced at diagnosis, with 7 patients at stage pT3a or pT3b, 1 with pT1N0M0, and 1 at stage pT2N0M0. By contrast in the screened group 3 patients were at pT1n0M0, 1 was at pT3aN0M0 and 1 had pT3bN0M0 disease. However these differences were not statistically significant.

RENAL SCINTIGRAPHIC SCAN
Spinal cord injury

One study (n=160) reported that there were no significant differences between patients with spinal cord injury who had missed two or more consecutive annual examinations compared with patients who were compliant with their annual examinations on mean-adjusted Effective Renal Plasma Flow (ERPF) (left kidney 311 vs 308 mL/min, right 301 vs 276; ns) 228.

14.1.1.2. Economic Evidence

No relevant economic evaluations comparing monitoring strategies or surveillance protocols were identified.

We conducted an original economic analysis to assess the costs related to different guideline management programmes for the monitoring of patients with incontinence from neurological disease.

Model overview

Our model compared follow-up strategies for renal surveillance and monitoring of incontinence as defined in different guidelines. The population considered was patients with neurological conditions with or at risk of incontinence.

The base case time horizon was 10 years but this was varied between 1 and 20 years in a sensitivity analysis. We adopted a NHS and Personal Social Services perspective and used a 3.5% discount rate.

Deviations from NICE reference case

Our model considered a 10 year time horizon (altered in a sensitivity analysis); in fact, a lifetime analysis was unfeasible due to the fact that no average age of the population could be obtained from any of the sources.

No outcome or quality of life data were used due to the unavailability of this data. A threshold analysis was conducted to determine the number of QALYs that would be required by each strategy to make it cost effective at a willingness-to-pay of £20,000/QALY and £30,000/QALY.

Approach to modelling

There is no data available comparing the effectiveness or outcomes of different intensity of monitoring and surveillance strategies for patients with bladder dysfunction of neurological origin. However, the GDG considered this question a high priority for economic analysis due to the likelihood of a high cost impact. This impact is likely to be dependent on the cost and intensity of the resources used in each strategy. Therefore an analysis on the cost of monitoring strategies recommended by national and international guidelines on neurological incontinence was undertaken.

Identification of strategies

We carried out a systematic review of guidelines that included key neurological conditions and neurological incontinence. The search identified guidelines, studies that evaluated guidelines and discussions of guidelines and various other types of recommendations. Only the actual guidelines or papers that made recommendations on assessment or monitoring were included for further analysis. Each of the guidelines was then studied to identify the recommendations made on monitoring and renal surveillance. Those that made no specific recommendations were immediately excluded from further analysis. Many guidelines which made recommendations on assessment but not monitoring or surveillance were excluded after discussion with the GDG. The papers that were excluded can be found in Table 115

Table 115. Excluded Guidelines.

Table 115

Excluded Guidelines.

Of the four guidelines included (Table 116), one made recommendations for neurological patients generally, two for specific diseases (spinal injury and multiple sclerosis) and one for children. The strategies that each guideline outlined were extracted and broken up into their constituent parts, which are described in Table 116.

Table 116. Included Guidelines.

Table 116

Included Guidelines.

Definition of Risk

2 studies divided patients up into high and low risk. The guidelines define the risk as the following:

  • Strategy from guideline 3231 (MS):
    • High Risk – at least one definite risk factor or more than two probable risk factors (see Table 117: Definition of Risk factors in Strategy 3)
    • Low Risk – no definite risk factor and no more than two probable risk factors
  • Strategy from guideline232 4 (RPB):
    • Move from low risk to high risk in the case of:

      New onset hydronephrosis

      Febrile urinary tract infection

      Evidence of urinary retention

Table 117. Definition of Risk factors in Strategy 3.

Table 117

Definition of Risk factors in Strategy 3.

Model structure

The Model is a cost analysis constructed in Windows Excel. It is worked out so that the costs were calculated for each strategy in one year cycles (no movement between heath states). Each monitoring or surveillance strategy (strategy 1–4, outlined in Table 116) was modelled over a ten year time horizon with the costs discounted at the NICE reference case discount rate of 3.5% per year. The costs were applied to interventions/tests according to the frequency indicated in the guidelines. If an intervention/test was less frequent than 12 months, it was assumed that it happened in the first year and then at the specified interval after that. Where the frequency was expressed as a range, the midpoint was taken for the base case and an extreme scenario sensitivity analysis was carried out on the maximum and minimum frequencies. If data was unavailable on frequency or populations that require the intervention, the GDG made appropriate assumptions. For the frequency of urodynamics in strategy 2, we assumed that everyone would have it in the first year and then every five years subsequently, with one in six people requiring it in the second year. In the case of cystoscopy in strategy 2, we assumed that 50% of the monitored population would fall into the indications described in the strategy.

Uncertainty

In order to take into account the uncertainty around the costs in the model we carried out various sensitivity analyses. Where the frequency of a test was expressed as a range an extreme scenario sensitivity analysis was carried out on the maximum and minimum frequencies. The various strategies were also analysed over different time periods: 1 year, 5 years and 20 years.

The parameters in the model were made probabilistic by defining a probability distribution for each model input parameter. When the model was run, a value for each input was randomly selected from its respective probability distribution simultaneously and mean costs of each strategy calculated using these values. The model was run repeatedly – in this case 1000 times – and results are summarised. This averaging of results can provide a more accurate measure of the average cost. It also provides an estimate of the uncertainty brought about by random variation, in the form of confidence intervals. Probability distributions in the analysis were based on error estimates from data sources, for example confidence intervals.

Where the NHS Reference costs were used, the uncertainty around each cost was available in the form of an upper and lower quartile range. A gamma distribution was assumed for the costs in the model as this prevents ‘negative costs’ from occurring. For the costs obtained from the Personal Social Services Research Unit (PSSRU) and the NHS Supply Chain Catalogue this uncertainty was not available so these costs were not made probabilistic.

Resource use and cost

With the identification and breakdown of each of these strategies it was possible to cost them. The costs for the constituent parts of each comparator strategies were identified (Table 118) using national data sources. In order to take into account the uncertainty around the costs in the model, the data was made probabilistic.

Table 118. Resource Costs.

Table 118

Resource Costs.

Certain assumptions were made that enabled the costs to be applied. Uroflowmetry and postvoid residual measures were assumed to take 30 minutes of specialist nurse time. A three day voiding chart and counselling were both assumed to be equivalent to the cost of a consultation with a specialist nurse.

Results
Base case results

The base-case analysis, using probabilistic data (Table 119) showed that over a ten year period the least costly monitoring strategy was the strategy that monitored low risk patients in the MS population (strategy 3a). This strategy however is only monitoring low risk patients; the high risk patient population was considerably more expensive, almost double the cost. The lowest cost strategy that considered a mixed population was strategy 2, in spinal cord injury patients. If we consider strategy 4 separate due to it being in a paediatric population, the most costly strategy is strategy 1 for general neurogenic lower urinary tract disorders. The probabilistic analysis enables us to fit confidence intervals around both the costs and the difference in costs. It shows when each of the strategies are compared to strategy 1 - as it is the most commonly followed guideline - the average differences are significant at the p=0.05 level in all strategies apart from 4b. For the low risk strategies strategy 3a remains the lowest cost and for the mixed and high risk strategies, strategy 2 is the least costly.

Table 119. Base-case results (Probabilistic).

Table 119

Base-case results (Probabilistic).

As most of these strategies are for quite heterogeneous populations considering them together carries heavy limitations. Therefore considering the absolute costs is more informative. Threshold Analysis

In order to account for the lack of data on outcomes, a threshold analysis was carried out that calculated the incremental QALYs that each strategy would have to generate in order for them to be cost effective compared to “do nothing.” The incremental QALYs per patient that would be required to make a strategy cost effective are calculated at two thresholds, £20,000/QALY and £30,000/QALY. It is possible to see from the results in Table 120 that the more expensive strategies would have to generate more additional QALYs compared to ‘do nothing’ in order to account for the increased cost.

Table 120. Threshold Analysis on number of incremental QALYs needed for a strategy to be cost effective compared to ‘do nothing’.

Table 120

Threshold Analysis on number of incremental QALYs needed for a strategy to be cost effective compared to ‘do nothing’.

Sensitivity analysis

Where the frequency of a test was expressed as a range, an extreme scenario sensitivity analysis was carried out on the maximum and minimum frequencies. Table 121 and Figure 9 show that there was no change in the order of the least and most costly strategies compared to the base case analysis. The lowest cost strategies remain 3a for low risk and strategy 2 for combined and high risk populations. Strategy 3b shows the biggest difference between minimum and maximum frequency with a difference of around £1000. This means that it is probably the strategy most open to interpretation in terms of its frequency.

Table 121. Sensitivity Analysis of high versus low frequency strategies.

Table 121

Sensitivity Analysis of high versus low frequency strategies.

Figure 9. Sensitivity analysis of the high versus low frequency strategies.

Figure 9

Sensitivity analysis of the high versus low frequency strategies.

The results from varying the time horizon using probabilistic cost results can be found in Table 122. This variation shows that strategy 1 is relatively low cost in the first year but quickly becomes the most costly as the time horizon increases.

Table 122. Sensitivity analysis varying the time horizon.

Table 122

Sensitivity analysis varying the time horizon.

Figure 10 shows that strategy 2 increases in cost at a much slower rate over the same period. Between years ten and twenty there is very little change in the relative costs of each strategy, apart from 3b and 4a. But as these two are in different populations this is not a direct comparison. After an initial sharp increase in cost, it is possible to see the costs plateau out from around the five year mark. Despite this flattening out, strategy 1 continues to increase in cost at a faster rate than the other costs. The only point at which Strategy 1 is not highest cost of the non-paediatric strategies is at year 1.

Figure 10. Monitoring costs over 20 years.

Figure 10

Monitoring costs over 20 years. Note Strategy 1: Neurogenic lower urinary tract symptoms (European Association of Urology), strategy 2: Spinal Cord Injury (VHA Handbook), Strategy 3: Multiple Sclerosis (Sèze et al.), Strategy 4: Paediatric bladder (more...)

Discussion
Summary of results

The probabilistic base-case results show that among non-paediatric strategies, strategy 1 is the highest cost strategy at every horizon period, apart from year 1. When comparing strategies in the low risk population, strategy 3a emerges as the least costly, while in high risk populations, strategy 2 is the least costly.

Limitations and interpretation

The results obtained in this analysis give an indication of the cost of monitoring strategies over a given time period (10 years as base case). The absolute cost of monitoring strategies over 10 years ranges between £800 and £3000 per patient depending on risk, age and condition. The cost of paediatric monitoring is considerably high, particularly in the high risk population. Even in the low risk group, paediatric monitoring has a similar cost to the strategy for high risk patients with Multiple Sclerosis (MS). The GDG believed that the strategy in the paediatric population overstated the importance of imaging and monitoring.

Strategy 1 was the most costly strategy when considering a mixed population with mixed risk levels. This strategy was also the most costly at different time horizons, different frequencies of monitoring and different risk profiles. It was the opinion of the GDG that the regular urodynamics and physical examination in a specialist urological centre determined the high cost of this strategy. This was considered to be an over-use of specialist, invasive testing.

The least costly strategy when considering a mixed population with mixed risk levels was strategy2, while in a low risk population the least costly was strategy 3, which was the lowest cost strategy overall. The GDG noted that this shows that the risk profile is important when defining the monitoring strategy for a patient. A clear definition of high and low risk is crucial and it has been described elsewhere in the guideline (See Introduction).

No clinical outcome associated with any of the monitoring strategies was available, so it is not possible to conclude which is the most cost effective strategy. Another limitation of our analysis is that it does not consider the inevitable extra or unnecessary treatment associated with the monitoring strategies. As in any screening programme, the more often tests are done the more likely it is that false positives results will be picked up requiring an unnecessary treatment. This adds to the cost and impacts treatment effectiveness and patient quality of life. A further limitation is that the strategies are themselves based on guideline recommendations that are largely consensus driven.

In cases where the guidelines were unclear on the testing frequency, assumptions were made by the GDG. These assumptions were, however, tested extensively in probabilistic and deterministic sensitivity analyses. A further point to make is that all the populations for which the strategies are recommended are different. This limits the validity of comparisons between the strategies but not the validity of the absolute costs.

Generalisability to other populations/settings

The analysis was conducted from a UK perspective using: one international, one European, one US and one Scottish guideline. The strategies also made recommendations in different populations: general neurogenic incontinence patients, MS patients, Spinal cord injury patients and paediatric patients.

14.1.1.3. Evidence Statements

Clinical evidence statements

Two observational studies of 106 patients reported on the use of creatinine testing in patients with spinal cord injury. Neither study supported the use of creatinine for the early detection of renal impairment (5.57 yrs) (low quality)

Eight observational studies of 894 patients reported on ultrasound in patients with spinal cord injury. Overall, the studies supported the routine use of ultrasound for the detection of conditions such as hydronephrosis in patients with spinal cord injury (2 months to 23.9 yrs) (low quality)

Two observational studies of 114 patients reported on ultrasound in patients with multiple sclerosis. One study supported the routine use, and one study did not support the routine use, of ultrasound in patients with multiple sclerosis (not reported) (low quality)

Two observational studies of 65 patients reported on ultrasound in patients with spina bifida, one on adults and one on children. The study on children with normal urodynamics at birth detected no case of hydronephrosis or reflux. The study on adults supported the routine use of ultrasound (9.1 yrs) (low quality)

Two observational studies of 73 patients reported on the use of cystoscopy in patients with spinal cord injury. One study did not support its use and another was inconclusive(6–8.2 years) (low quality)

One observational study of 160 patients reported on the use of a renal scintigraphic scan in patients with spinal cord injury. The study did not support the long term, routine use of this test (not reported) (low quality)

Economic evidence statement

The absolute costs per patient of the strategies are not considered by the GDG to be extreme. However, the cost could be brought down still further as the frequency of some, but not all, of the proposed investigations is still considered to be too high in most strategies. A more realistic recommendation could be made on monitoring strategies that would better reflect best practice.

14.1.2. Recommendations and links to evidence

Recommendations:MONITORING AND SURVEILLANCE PROTOCOLS
56.

Do not rely on serum creatinine and estimated glomerular filtration rate in isolation for monitoring renal functionp in people with neurogenic lower urinary tract dysfunction.

57.

Consider using isotopic glomerular filtration rate when an accurate measurement of glomerular filtration rate is required (for example, if imaging of the kidneys suggests that renal function might be compromised)p.

58.

Offer lifelong ultrasound surveillance of the kidneys to people who are judged to be at high risk of renal complications (for example, consider surveillance ultrasound scanning at annual or 2 yearly intervals). Those at high risk include people with spinal cord injury or spina bifida and those with adverse features on urodynamic investigations such as impaired bladder compliance, detrusor-sphincter dyssynergia or vesicoureteric reflux.

59.

Do not use plain abdominal radiography for routine surveillance in people with neurogenic lower urinary tract dysfunction.

60.

Consider urodynamic investigations as part of a surveillance regimen for people at high risk of urinary tract complications (for example, people with spina bifida, spinal cord injury or anorectal abnormalities).

61.

Do not use cystoscopy for routine surveillance in people with neurogenic lower urinary tract dysfunction.

62.

Do not use renal scintigraphy for routine surveillance in people with neurogenic lower urinary tract dysfunction.

Relative value placed on the outcomes consideredThe outcomes included in the review were: kidney function and renal disease, quality of life and hospital admissions. The GDG considered that detecting silent disease to be an important outcome as early intervention may prevent more progressive renal damage.
Quality of evidenceSeventeen observational studies evaluating creatinine, ultrasound, cystoscopy and renal scintigraphic scanning were found. The majority of studies were retrospective observational studies without a control group. The overall quality of the evidence was low. A number of the studies reported on interventions that were performed only once and therefore did not form part of an ongoing monitoring and surveillance programme.
The GDG made recommendations on the basis of a very limited evidence base and no studies demonstrated outcomes from routine surveillance/monitoring that matched requirements for the adoption of screening programmes. The recommendations were made by consensus based on existing practice and deductions from the studies that have been examined.
Eight studies on the use of ultrasound for spinal cord injury patients and two for spina bifida patients supported its routine use. The GDG noted that the studies all produced reasonable results (between 15–30%) in finding abnormalities
The GDG agreed that the use of Serum Creatinine in isolation has been shown to be unreliable because of a number of factors (most importantly – muscle mass).
One study on cystoscopy did not support its use and one study on renal scintigraphic scans did not support routine long term use. One study on cystoscopy suggested that it may be possible to improve outcomes for patients with spinal cord injury who develop bladder cancer through surveillance cystoscopy, but the study was inconclusive, and the GDG agreed that this study should not be considered
Trade-off between clinical benefits and harmsThe GDG noted the surveillance being advocated minimises exposure to ionising radiation. The GDG agreed that abdominal X-ray should not be recommended because of the associated risks but noted that some centres continue to use abdominal radiography in this context.
The GDG considered that lifelong ultrasound was appropriate for those people who were at high risk of renal complications such as the development of hydronephrosis or the formation or renal stones and this was current practice for particular groups such as those with spinal cord injury or spina bifida.
The question of using cystoscopy as a screening tool for bladder cancer was considered. It was noted that while the incidence of bladder cancer is probably raised in some populations with neurogenic lower urinary tract dysfunction, it remains a relatively rare condition. Therefore the morbidity of routine cystoscopy and resource implications suggests that it is unlikely that cystoscopy would meet the requirements for use as a screening test. The GDG emphasized the importance of early referral of patients with red flag symptoms.
Economic considerationsAn extensive cost analysis was done on the various monitoring programmes recommended by different published guidelines. This analysis showed that over ten years of monitoring, None of the strategies compared are associated with considerable costs. The most expensive strategy was under £3,000 for a ten year period. No effectiveness data or quality of life data could be found that matched the interventions; therefore a full economic evaluation could not be carried out. We conducted a threshold sensitivity analysis on the number of incremental QALYs that each strategy would have to generate compared to ‘do nothing’ in order to be cost-effective at a threshold of £20,000/QALY. Over ten years the QALYs gain would have to be 0.13 for the most costly strategy or less than this for the other strategies. The GDG considered this number to be low for a ten year period; therefore the monitoring strategies compared in the cost analysis are likely to be cost-effective. However, our analysis does not consider the unnecessary treatment associated with the ‘false positive’ cases resulting from the monitoring strategies. These would lead to unnecessary treatments and further investigation, making the monitoring strategy less cost effective.
Strategies assessed here included regular eGFR measurements, ultrasound and cystoscopy as well as other techniques involved in renal surveillance. All of these strategies were judged to be low cost therefore lifelong renal surveillance and the individual components that make this up could be recommended.
Other considerationsThe GDG agreed that isotopic techniques are widely regarded as being the most accurate of the available techniques for measuring the glomerular filtration rate.
The GDG acknowledged that the interval between monitoring visits was, in general, arbitrarily set at one year. However, it was felt that it was important to tailor surveillance to the individual patient’s circumstances. Some patients with adverse factors, such as concerning urodynamic findings or a history of frequent stone formation, might need to be seen more often than once a year. On the other hand, some patients who were in low risk groups, such as female MS patients, might not require regular surveillance investigations at all.
p

For more information on the measurement of kidney function, see ‘Chronic kidney disease’ (NICE clinical guideline 73).

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