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Article

Cost-Effectiveness of Treating Upper Limb Spasticity Due to Stroke with Botulinum Toxin Type A: Results from the Botulinum Toxin for the Upper Limb after Stroke (BoTULS) Trial

1
School of Health and Related Research, University of Sheffield, Regent Court, 30 Regent Street, Sheffield S1 4DA, UK
2
Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne NE4 5PL, UK
3
Institute for Applied Health Research, School of Health and Life Sciences, Glasgow Caledonian University, Cowcaddens Road, Glasgow G4 0BA, UK
4
International Centre for Neurorehabilitation, Walkergate Park, Benfield Road, Newcastle upon Tyne NE6 4QD, UK
5
Institute of Health and Society, Newcastle University, Newcastle upon Tyne NE2 4AA, UK
*
Author to whom correspondence should be addressed.
Submission received: 30 August 2012 / Revised: 12 November 2012 / Accepted: 21 November 2012 / Published: 27 November 2012
(This article belongs to the Special Issue Clinical Use of Botulinum Toxins)

Abstract

:
Stroke imposes significant burdens on health services and society, and as such there is a growing need to assess the cost-effectiveness of stroke treatment to ensure maximum benefit is derived from limited resources. This study compared the cost-effectiveness of treating post-stroke upper limb spasticity with botulinum toxin type A plus an upper limb therapy programme against the therapy programme alone. Data on resource use and health outcomes were prospectively collected for 333 patients with post-stroke upper limb spasticity taking part in a randomized trial and combined to estimate the incremental cost per quality adjusted life year (QALY) gained of botulinum toxin type A plus therapy relative to therapy alone. The base case incremental cost-effectiveness ratio (ICER) of botulinum toxin type A plus therapy was £93,500 per QALY gained. The probability of botulinum toxin type A plus therapy being cost-effective at the England and Wales cost-effectiveness threshold value of £20,000 per QALY was 0.36. The point estimates of the ICER remained above £20,000 per QALY for a range of sensitivity analyses, and the probability of botulinum toxin type A plus therapy being cost-effective at the threshold value did not exceed 0.39, regardless of the assumptions made.

1. Introduction

Stroke is a major cause of mortality and morbidity and imposes a significant burden on both health services and society [1,2,3]. In the United Kingdom (UK) it is estimated that the annual direct costs of stroke are approximately £4 billion, which constitutes around 5.5% of the total UK expenditure on health care [3]. If the costs of lost productivity and informal care are taken into account, the total annual societal costs of stroke are estimated to be around £9 billion [3]. In England, over 900,000 people are living with the consequences of stroke, 300,000 of whom are moderately or severely disabled [4]. As the proportion of older people in society increases, so the burden of stroke is likely to grow.
Upper limb spasticity after stroke is an important clinical problem and its identification and treatment are key components of stroke rehabilitation [5]. Upper limb spasticity may cause deformity, reduced function and pain [6]. Botulinum toxin type A, which when given by intramuscular injection causes temporary local muscle paresis by blocking neuromuscular transmission [7], has become an established treatment for spasticity due to stroke. Randomised controlled trials have shown that botulinum toxin reduces muscle tone [8] and improves the performance of basic upper limb functional tasks such as hand opening for cleaning and ease of dressing [9,10,11]. However, the impact on active upper limb function (e.g., reaching and grasping) and the efficacy of repeated treatment is less clear.
The BoTULS trial was a pragmatic multi-centre randomised controlled trial to evaluate the clinical and cost-effectiveness of botulinum toxin type A plus an upper limb therapy programme in the treatment of post stroke upper limb spasticity. The clinical results indicated that botulinum toxin type A did not improve active upper limb function (as measured by the Action Research Arm Test (ARAT)), but that there may be benefits in terms of decreased muscle tone, improved upper limb strength, improved ease of performance of basic upper limb functional activities and reduction in pain [12]. This article describes the results of the cost-effectiveness analysis.

2. Methods

In this multi-centre trial, 333 adults with spasticity and reduced upper limb function due to stroke greater than one month previously were randomised to receive botulinum toxin type A (Dysport®) plus a four week upper limb therapy programme comprising of one hour of therapy twice weekly (n = 170), or the upper limb therapy programme alone (n = 163). Repeat botulinum toxin type A and/or therapy was available at three, six and nine months. Patients were assessed at baseline and at one, three, and 12 months. Study methods have been reported in detail elsewhere [12]. The trial received ethical and NHS approvals, and the study participants provided informed consent.
The economic evaluation follows the technology appraisal guidelines used by the National Institute for Health and Clinical Excellence (NICE) and as such adopts the perspective of the UK National Health Service and Social Services [13]. The time horizon for the analysis was three months from randomisation, with all costs reported in 2007 prices.
Table 1. Breakdown of resource use and corresponding unit cost data.
Table 1. Breakdown of resource use and corresponding unit cost data.
ResourceUnit cost (2007 prices)Source of unit cost data
Upper limb therapy and botulinum toxin type A
therapist£40 per session aReference14
botulinum toxin type A£153.21 per 500 unit vialReference 15
Other antispasticity medication
gabapentin£96.73 per monthReference 15
baclofen£9.13 per monthReference 15
tizanidine£74.83 per monthReference 15
dantrolene33.76 per monthReference 15
methocarbamol7.60 per monthReference 15
Other health care & social services
day hospital£83 per place per dayReference 14
home care services£19 per contact bReference 14
private home help£11.33 per contact bReference 14
day centre£147 per attendanceReference 14
meals on wheels£3.63 per mealReference 14
laundry service£3 per washAssumption c
GP£36 per consultationReference 14
practice nurse£9 per consultationReference 14
district nurse£24 per home visitReference 14
health visitor£36 per home visitReference 14
physiotherapist£40 per contact bReference 14
occupational therapist£40 per contact bReference 14
speech and language therapist£40 per contact bReference 14
dietician£32 per contact bReference 14
chiropodist£18 per contact bReference 14
social worker£34 per contact bReference 14
clinical psychologist£67 per contact bReference 14
continence advisor£24 per home visitReference 14
bath attendant£11.33 per contact bAssumption d
orthotist£40.00 per contact bAssumption e
a Assumes therapist administers injection; bAssumes one hour per contact; c Based on local council fees of £3 per wash; d Assumed same rate as private home help; e Assumed Agenda for Change Band 5.
Participants’ use of resources was categorised under five general headings: (1) botulinum toxin type A; (2) upper limb therapy sessions provided by chartered physiotherapists; (3) other antispasticity medication; (4) management of adverse events attributable to botulinum toxin type A and/or upper limb therapy requiring a hospital contact; and (5) other health care and social services resource use. Patients’ use of these resources was recorded throughout the trial using a combination of case record forms, adverse event monitoring forms and participant responses to specific resource use questions in the participant assessment questionnaires. Where data were missing, resource use was inferred. Unit cost data were obtained from national sources [14,15]. All unit costs are reported in Table 1 and are in pounds sterling.
Participant health related quality of life was assessed using the EuroQol (EQ-5D) [16] which was included in the participant assessment questionnaires. Participant responses to the EQ-5D questionnaire were converted to health state utility values using the UK tariff values [17].These values were then multiplied by duration in each health state to estimate quality adjusted life years (QALYs). QALYs were estimated using an area under the curve (AUC) approach [18] using participant responses at baseline and three months to map out the curve.
In order to assess the relative cost-effectiveness of botulinum toxin type A plus upper limb therapy relative to upper limb therapy alone, data on cost and outcome were brought together to estimate an incremental cost-effectiveness ratio (ICER), specifically, the incremental cost per QALY gained. Uncertainty surrounding the point estimate of the ICER was taken into account through the approach of non-parametric bootstrapping and the construction of a cost-effectiveness acceptability curve (CEAC), which summarises the evidence in support of botulinum toxin type A plus therapy being cost-effective for a range of threshold values of societal willingness to pay for a QALY [19].
In addition to addressing the uncertainty surrounding the point estimate of the ICER, sensitivity analysis was undertaken to investigate the impact on the results of making different assumptions and varying key parameters. As part of the sensitivity analysis, in order to take into account missing data, an additional set of analyses were carried out using the technique of multiple imputation in which missing data were imputed using the NORM package [20]. Five datasets were imputed using age, sex, place of residence, Barthel ADL score and time between stroke and randomisation as explanatory variables. A point estimate of the ICER and accompanying CEAC for botulinum toxin type A plus therapy were estimated.

3. Results

The base case analysis used data from 283/333 (85%) participants who provided EQ-5D responses at baseline and three months, of whom 150 were in the botulinum toxin type A plus therapy group and 133 were in the therapy alone group. The randomisation groups were well matched at baseline with regard to demography, stroke characteristics, comorbidity, upper limb problems, and quality of life (including EQ-5D scores).

3.1. Resource Use and Costs

There was no significant difference in the mean number of upper limb therapy sessions received by participants in the botulinum toxin type A plus therapy and therapy alone groups (7.64 versus 7.56 respectively; 95% CI of the difference = −0.281 to 0.127). The numbers of participants taking other antispasticity drugs were 38 in the botulinum toxin type A plus therapy group and 31 in the therapy alone group, with the difference between the groups not being significant (odds ratio (OR) = 1.116; 95% CI = 0.647 to 1.925). While there were cases of participants encountering hospital services as a consequence of their initial stroke, clinical review showed that none of the hospital contacts were attributable to either therapy or botulinum toxin type A. As a result, hospital resource use due to adverse events does not feature in the cost-effectiveness analysis.
A breakdown of other health care and social services resource use among participants is presented in Table 2. With respect to the proportion of participants in each group reporting a contact, there were significantly more practice nurse contacts (OR = 1.878; 95% CI = 1.083 to 3.255) and social worker contacts (OR = 1.917; 95% CI = 1.051 to 3.497) in the botulinum toxin type A plus therapy group.
The only significant difference in the average number of contacts among participants reporting a contact was with respect to day hospital contacts, with participants in the therapy alone group having significantly more contacts on average (9.4 versus 3.1 respectively; 95% CI of the difference = 2.42 to 10.18).
Table 2. Breakdown of other health care and social services resource use.
Table 2. Breakdown of other health care and social services resource use.
Item of resource useMean (SD) number of contacts among patients reporting a contact (n)Mean difference in number of contacts (95% CI of difference)
Therapy aloneTherapy plus botulinum toxin
Mean (SD)nMean (SD)n
day hospital9.4 (9.0)253.1 (2.7)216.3 (2.4 to 10.2)
home care services87.5 (75.7)45114.6 (76.5)56−27.1 (−57.3 to 3.2)
private home help32.7 (53.5)1738.9 (60.1)16−6.2 (−46.6 to 34.1)
day centre16.3 (8.3)2514.1 (10.3)242.2 (−3.1 to 7.6)
meals on wheels6.0156.0 (38.6)3−50.0 (−241.7 to 141.7)
laundry service14.7 (18.5)318.0 (11.1)3−3.3 (−38.0 to 31.3)
GP2.8 (1.4)602.8 (1.9)860.0 (−0.6 to 0.6)
practice nurse2.6 (1.8)242.9 (2.9)44−0.3 (−1.6 to 1.0)
district nurse8.3 (14.6)274.0 (5.0)304.3 (−1.8 to 10.2)
health visitor *-11.01-
physiotherapist13.3 (12.7)7412.0 (10.5)871.3 (−2.46 to 4.8)
occupational therapist8.2 (8.8)268.5 (9.1)38−0.3 (−4.9 to 4.2)
speech and language therapist4.6 (5.3)288.9 (9.7)20−4.3 (−9.2 to 0.6)
dietician2.2 (1.2)613.0 (15.6)2−10.8 (−149.5 to 127.8)
chiropodist2.0 (1.2)242.3 (1.1)40−0.3 (−0.9 to 0.3)
social worker2.8 (1.7)172.5 (2.0)350.3 (−0.8 to 1.5)
clinical psychologist3.1 (2.5)82.5 (1.3)40.6 (−2.4 to 3.7)
continence advisor1.8 (1.0)41.010.8 (−2.7 to 4.2)
bath attendant19.5 (18.9)1318.2 (11.4)131.3 (−11.3 to 14.0)
orthotist1.0012.7 (1.2)3−1.7 (−7.4 to 4.1)
* The one patient in the therapy alone group who reported a health visitor contact did not indicate the number of contacts.
Table 3 shows the contribution of botulinum toxin type A costs, upper limb therapy costs, other antispasticity medication costs, and other health care and social services costs to the overall mean cost per participant. The overall mean cost per participant was higher in the botulinum toxin type A plus therapy group, although the difference was not significant. There were also no significant differences between the groups with respect to upper limb therapy costs, antispasticity medication costs and other health care and social services costs. The biggest contributor to total costs for both groups was the cost of other health care and social services contacts, accounting for 81% in the therapy alone group and 77% in the botulinum toxin type A plus therapy group. The mean difference in costs indicates that even if the cost of botulinum toxin type A were zero, there would still a positive net cost associated with the botulinum toxin type A group. This is largely attributable to the botulinum toxin type A group having higher other health care and social services costs.
Table 3. The contribution of botulinum toxin type A costs, upper limb therapy costs, other antispasticity medication costs, and other health care and social services costs to overall mean cost per participant.
Table 3. The contribution of botulinum toxin type A costs, upper limb therapy costs, other antispasticity medication costs, and other health care and social services costs to overall mean cost per participant.
Breakdown of overall mean cost per participantMean (SD) cost per participant (£)Mean difference in costs (£) (95% CI of difference)
Therapy aloneTherapy plus botulinum toxin
Overall1796 (1944)2170 (2007)−374 (−837 to 90)
Botulinum toxin3 a (23)154 (28)−151 (−157 to −145)
Upper limb therapy300 (45)303 (41)−3 (−13 to 7)
Antispasticity medication37 (93)38 (90)−1 (−22 to 21)
Other b1456 (1923)1675 (2001)−219 (−679 to 242)
a EQ-5D data were complete for 3 of 4 participants in the control group who received botulinum toxin; b Other health care and social services costs.
Table 4. Summary of cost-effectiveness results for botulinum toxin type A plus therapy for alternative scenarios.
Table 4. Summary of cost-effectiveness results for botulinum toxin type A plus therapy for alternative scenarios.
Cost-effectiveness analysis scenarioIC (£)IQ (QALYs)ICER (£)Probability botulinum toxin type A plus therapy is cost-effective at threshold ratio
£10 k£20 k£50 k£100 k
Base case data a3740.00493,5000.290.360.410.42
Complete EQ-5D data b4820.00768,8570.290.340.400.43
Base case data and zero cost for botulinum toxin2230.00455,7500.310.390.420.43
Base case data and best-worst QALY assumptions3740.00662,3330.290.350.430.45
Missing data imputed using multiple imputation4300.00586,0000.340.390.420.46
IC = Incremental cost; IQ = Incremental QALYs; ICER = Incremental cost-effectiveness ratio; a EQ-5D responses at baseline and 3 months; b EQ-5D responses at baseline, 1 month and 3 months.

3.2. Base Case Cost-Effectiveness Analysis

The results of the base case cost-effectiveness analysis are summarised in the first row of Table 4. Compared to therapy alone, botulinum toxin type A plus therapy was associated with an incremental cost of £374 and an incremental QALY gain of 0.004. When combined, these data gave an ICER for botulinum toxin type A plus therapy of £93,500 per QALY gained. Bootstrapping this point estimate enabled the derivation of the CEAC for botulinum toxin type A plus therapy relative to therapy alone shown in Figure 1. The probabilities of botulinum toxin type A plus therapy being cost-effective at threshold ratios of £10,000, £20,000, £50,000 and £100,000 per QALY were 0.29, 0.36, 0.41 and 0.42 respectively.
Figure 1. CEAC for botulinum toxin type A plus therapy relative to therapy alone.
Figure 1. CEAC for botulinum toxin type A plus therapy relative to therapy alone.
Toxins 04 01415 g001

3.3. Sensitivity Analysis

The impact on the results of the following sensitivity analyses were explored: re-running the analysis using data from participants with complete EQ-5D data at baseline and at one and three months; allowing the cost of botulinum toxin type A to fall to zero; a best-worst QALY analysis investigating the impact of alternative assumptions regarding the timing of health state changes; and re-running the analysis following multiple imputation of missing data. All the results are summarised in Table 4.
Re-running the analysis to include only those participants for whom complete EQ-5D data were available (248 respondents, of whom 116 were in the botulinum type plus therapy group and 132 were in the therapy alone group) had little impact on the results. The ICER for botulinum toxin type A plus therapy relative to therapy alone was £68,857 and the probabilities of its being cost-effective at threshold ratios of £10,000, £20,000, £50,000 and £100,000 per QALY were 0.29, 0.34, 0.40 and 0.43 respectively.
Re-running the base case analysis assuming a zero cost for botulinum toxin type A resulted in an ICER for botulinum toxin type A plus therapy of £55,750. The probabilities of its being cost-effective at threshold ratios of £10,000, £20,000, £50,000 and £100,000 per QALY were 0.31, 0.39, 0.42 and 0.43 respectively.
The AUC approach to estimating QALYs described above assumes that the rate of change in health status between any two points (in this case, EQ-5D tariff values) is linear. For example, if the baseline value is 0.5 and the three months value is 0.8, then it is assumed that after one month, the health state value is 0.6, and after two months it is 0.7. This is the method most commonly employed in AUC analyses in the literature [18]. However, many other assumptions could be made, each of which may have an impact on the results. In light of the relatively high ICERs associated with botulinum toxin type A plus therapy, it was decided to investigate the impact on the results of the timing of the health state changes favouring the use of botulinum toxin type A. Specifically, it was assumed in the botulinum toxin type A plus therapy group that participants moved into the health state value reported at three months almost immediately (approximately three days or 0.1 of a month) after baseline. This can be regarded as the best case outcome scenario for botulinum toxin type A. On the flip side, a worst case outcome scenario for the therapy alone group was defined whereby it was assumed that participants in this group remained in their baseline reported health state for 2.9 months, at which point they moved into the health state value reported at three months. The results of these assumptions were that botulinum toxin type A plus therapy had an ICER of £62,333 and the probabilities of its being cost-effective at threshold ratios of £10,000, £20,000, £50,000 and £100,000 per QALY were 0.29, 0.35, 0.43 and 0.45, respectively.
Imputing missing data using multiple imputation resulted in botulinum toxin type A plus therapy having an ICER of £86,000. Figure 2 shows the CEAC for botulinum toxin type A plus therapy relative to therapy alone when missing data have been imputed. The probabilities of botulinum toxin type A plus therapy being cost-effective at threshold ratios of £10,000, £20,000, £50,000 and £100,000 per QALY were 0.34, 0.39, 0.42 and 0.46, respectively.
Figure 2. Cost-effectiveness acceptability curve (CEAC) for botulinum toxin type A plus therapy relative to therapy alone following multiple imputation of missing data.
Figure 2. Cost-effectiveness acceptability curve (CEAC) for botulinum toxin type A plus therapy relative to therapy alone following multiple imputation of missing data.
Toxins 04 01415 g002

4. Discussion

The base case incremental cost-effectiveness ratio (ICER) for botulinum toxin type A plus therapy was £93,500, which is well in excess of the £20,000 threshold value used by NICE [21]. Estimation of the CEAC for botulinum toxin type A plus therapy indicated that there was only a 0.36 probability of its being cost-effective at a threshold ratio of £20,000 per QALY.
Sensitivity analysis using participants with complete EQ-5D data at three months produced an improved point estimate for the ICER of £68,857, but this was still over three times the NICE threshold value. The CEAC for these participants suggests that the probability of botulinum toxin type A plus therapy being cost-effective at £20,000 per QALY was actually lower than in the base case (0.34 versus 0.36 respectively).
Sensitivity analysis on the cost of botulinum toxin type A revealed that even if the cost of the drug were zero, the point estimate of the ICER still exceeded the NICE threshold value (£55,750 versus £20,000, respectively), and the probability of botulinum toxin type A plus therapy being cost-effective at £20,000 was little changed from the base case (0.39 versus 0.36 respectively).
Altering the assumptions regarding the timing of the health state changes following treatment so that they favoured botulinum toxin type A plus therapy (best-worst QALY analysis) resulted in a lower ICER than in the base case analysis (£62,333 versus £93,500, respectively). However, the probability that botulinum toxin plus therapy was cost-effective at £20,000 per QALY was actually lower than in the base case analysis (0.35 versus 0.36, respectively).
Imputing missing data had little impact on the results, with the use of multiple imputation resulting in an ICER of £86,000 for botulinum toxin plus therapy and a probability of 0.39 of its being cost-effective at £20,000 per QALY.
The study does have limitations. Arguably the main limitation was the relatively short time horizon over which the cost-effectiveness analysis was conducted. The rationale for adopting a three month time horizon rather than 12 months was the loss of participant responses due to a curtailment of 12 month follow up. The proportion of participants providing EQ-5D data at 12 months was 52.4%. This is considerably lower than the corresponding figures for baseline, one month and three months which were 100%, 83.7% and 85.2%, respectively.
One option would have been to impute the missing 12 month data, but this would have meant that even if the estimation of QALYs was restricted to the baseline and 12 month EQ-5D values only, data would have to be imputed for almost half the sample. If the intermediate EQ-5D values were also used in the QALY estimation, then data for more than half the sample would need to be imputed. Thus, a decision was made to conduct the analysis over three months where levels of missing data were much lower. This is not to say that there would not be benefits in extrapolating costs and outcomes over a longer time period. This could be done using economic modelling which would incorporate data from the trial and other relevant sources to estimate cost-effectiveness beyond the time horizon of the trial. While such an exercise was beyond the scope of the study reported here, it would be a potentially worthwhile piece of future research.
Another limitation was the need to infer resource use on occasions when data were not readily available. For example, for a number of patients it was necessary to make assumptions regarding length of time on specific antispasticity medications and the dosages taken. Assumptions also had to be made regarding the use of other health care and social services resources during the second month of the three month analysis period. This was due to resource use questions in the participant assessment questionnaires asking about resource use over the previous month only.
Another potential limitation arises from the possibility that the EQ-5D may not be sensitive enough to pick up all aspects of improvement associated with the interventions, such as botulinum toxin type A recipients having decreased muscle tone, improved upper limb strength, improved ease of performance of basic upper limb functional activities and reduction in pain. Use of a more sensitive condition-specific outcome measure in the economic analysis may have produced results more favourable to botulinum toxin type A. However, the use of condition-specific measures to make cross programme comparisons is controversial, and NICE currently recommends that health states are described using a standardised and validated generic instrument, with the EQ-5D being its measure of choice.
With respect to how our results compare with other cost-effectiveness analyses of botulinum toxin type A in this treatment context, to our knowledge only one other published study exists [22]. This study adopted a decision analytic approach to compare the cost-effectiveness of botulinum toxin type A injections with oral therapy in the treatment of post-stroke spasticity. It concluded that botulinum toxin type A is a cost-effective treatment for post-stroke spasticity, which is contrary to our findings. However, we believe that our study is methodologically superior for a number of reasons. Chief among these is the source of data on resource use and outcomes. Our study collected these data from actual patients as part of a prospective randomized trial using carefully designed and validated measures whereas the earlier study [22] relied exclusively on expert opinion. In addition, the measure of outcome used in the earlier study [22] was cost per successfully treated month which does not explicitly encompass quality of life impacts and is a much more limited measure of outcome than cost per QALY gained.

5. Conclusions

In conclusion, the results of this study indicated that even the lowest point estimate of the ICER for botulinum toxin type A plus therapy was over two and a half times the NICE cost-effectiveness threshold value (£55,750 versus £20,000, respectively), and the probability of its being cost-effective at the threshold value did not exceed 0.39, regardless of the assumptions made. Therefore, according to current criteria for cost-effectiveness in England and Wales [21], the economic analysis provides no evidence to suggest that botulinum toxin type A plus therapy is a cost-effective alternative to therapy alone in this patient group.

Acknowledgments

The BoTULS trial was funded by the UK National Institute for Health Research, Health Technology Assessment Programme. The views and opinions expressed here are those of the authors and do not necessarily reflect those of the UK Department of Health. Ipsen Ltd provided the botulinum toxin type A (Dysport®) free of charge. The study was adopted by the NIHR Stroke Research Network.
We thank the following for their contribution: the patients who participated in the trial; participating centres and principal investigators; study therapists; co-ordinating centre staff; outpatient staff at the International Centre for Neurorehabilitation, Newcastle upon Tyne; the Data Monitoring and Ethics committee; the Trial Steering Committee and Tony Field (deceased), who was involved in designing and planning the study.

Conflict of interest

Ipsen Ltd provided the botulinum toxin type A used by the study free of charge. They also provided sponsorship for launch meetings at study sites. The design, analysis and reporting of the study was undertaken independently of Ipsen Ltd.
P.S., L.S., C.P., F.W., G.F., N.S. and H.R. have no competing interests.
M.B. and L.G. use botulinum toxin regularly in clinical practice. They have received sponsorship from Ipsen Ltd to attend and teach at conferences and meetings.

References

  1. Youman, P.; Wilson, K.; Harraf, F.; Kalra, L. The economic burden of stroke in the United Kingdom. Pharmacoeconomics 2003, 21, 43–50. [Google Scholar]
  2. Evers, S.M.A.A.; Struijs, J.N.; Ament, A.J.H.A.; van Genugten, M.L.L.; Jager, J.H.C.; van den Bos, G.A.M. International comparison of stroke cost studies. Stroke 2004, 35, 1209–1215. [Google Scholar] [CrossRef]
  3. Saka, O.; McGuire, A.; Wolfe, C. Cost of stroke in the United Kingdom. Age Ageing 2009, 38, 27–32. [Google Scholar]
  4. Reducing Brain Damage: Faster Access to Better Stroke Care; National Audit Office: London, UK, 2005.
  5. Intercollegiate Stroke Working Party, National Clinical Guideline for Stroke, 3rd ed; Royal College of Physicians: London, UK, 2008.
  6. Spasticity in Adults: Management Using Botulinum Toxin: National Guidelines; Royal College of Physicians: London, UK, 2009.
  7. Dolly, J.O.; Aoki, K.R. The structure and mode of action of different botulinum toxins. Eur. J. Neurol. 2006, 13, 1–9. [Google Scholar] [CrossRef]
  8. Garces, K.; McCormick, A.; McGahan, L.; Skidmore, B. Botulinum Toxin A for Upper and Lower Limb Spasticity: A Systematic Review; (Technology report no 51) Canadian Coordinating Office for Health Technology Assessment: Ottawa, Canada, 2005. [Google Scholar]
  9. Hesse, S.; Reiter, F.; Konrad, M.; Jahnke, M.T. Botulinum toxin type A and short-term electrical stimulation in the treatment of upper limb flexor spasticity after stroke: A randomized, double-blind, placebo-controlled trial. Clin. Rehabil. 1998, 12, 381–388. [Google Scholar] [CrossRef]
  10. Bhakta, B.B.; Cozens, J.A.; Chamberlain, M.A.; Bamford, J.M. Impact of botulinum toxin type A on disability and carer burden due to arm spasticity after stroke: A randomised double blind placebo controlled trial. J. Neurol. Neurosurg. Psychiatry 2000, 69, 217–221. [Google Scholar] [CrossRef]
  11. Brashear, A.; Gordon, M.F.; Elovic, E.; Kassicieh, V.D.; Marciniak, C.; Do, M.; Lee, C.H.; Jenkins, S.; Turkel, C. Botox post-stroke spasticity study group. Intramuscular injection of botulinum toxin for the treatment of wrist and finger spasticity after a stroke. N. Engl. J. Med. 2002, 347, 395–400. [Google Scholar] [CrossRef]
  12. Shaw, L.; Price, C.; van Wijck, F.; Shackley, P.; Steen, N.; Barnes, M.; Ford, G.; Graham, L.; Rodgers, H. Botulinum toxin for the upper limb after stroke (BoTULS) trial: Effect upon impairment, activity limitation and pain. Stroke 2011, 42, 1371–1379. [Google Scholar]
  13. Guide to the Methods of Technology Appraisal; National Institute for Clinical Excellence: London, UK, 2004.
  14. Curtis, L. Unit Costs of Health and Social Care; PSSRU,University of Kent: Canterbury,UK, 2007. [Google Scholar]
  15. British Medical Association and Royal Pharmaceutical Society of Great Britain, British National Formulary 53; BMJ Publishing Group Ltd and RPS Publishing: London, UK, 2007.
  16. Brooks, R. EuroQol: The current state of play. Health Policy 1996, 37, 53–72. [Google Scholar] [CrossRef]
  17. Dolan, P. Modeling valuations for EuroQol health states. Med. Care 1997, 35, 1095–108. [Google Scholar] [CrossRef]
  18. Richardson, G.; Manca, A. Calculation of quality adjusted life years in the published literature: A review of methodology and transparency. Health Econ. 2004, 13, 1203–1210. [Google Scholar] [CrossRef]
  19. O’Brien, B.; Briggs, A.H. Analysis of uncertainty in health care cost-effectiveness studies: An introduction to statistical issues and methods. Stat. Methods Med. Res. 2002, 11, 455–468. [Google Scholar]
  20. Schafer, J.L. Analysis of Incomplete Multivariate Data; Chapman and Hall: London, UK, 1997. [Google Scholar]
  21. Rawlins, M.D.; Culyer, A.J. National institute for clinical excellence and its value judgments. BMJ 2004, 329, 224–227. [Google Scholar] [CrossRef]
  22. Ward, A.; Roberts, G.; Warner, J.; Gillard, S. Cost-effectiveness of botulinum toxin type a in the treatment of post-stroke spasticity. J. Rehabil. Med. 2005, 37, 252–257. [Google Scholar]

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MDPI and ACS Style

Shackley, P.; Shaw, L.; Price, C.; Wijck, F.V.; Barnes, M.; Graham, L.; Ford, G.A.; Steen, N.; Rodgers, H. Cost-Effectiveness of Treating Upper Limb Spasticity Due to Stroke with Botulinum Toxin Type A: Results from the Botulinum Toxin for the Upper Limb after Stroke (BoTULS) Trial. Toxins 2012, 4, 1415-1426. https://0-doi-org.brum.beds.ac.uk/10.3390/toxins4121415

AMA Style

Shackley P, Shaw L, Price C, Wijck FV, Barnes M, Graham L, Ford GA, Steen N, Rodgers H. Cost-Effectiveness of Treating Upper Limb Spasticity Due to Stroke with Botulinum Toxin Type A: Results from the Botulinum Toxin for the Upper Limb after Stroke (BoTULS) Trial. Toxins. 2012; 4(12):1415-1426. https://0-doi-org.brum.beds.ac.uk/10.3390/toxins4121415

Chicago/Turabian Style

Shackley, Phil, Lisa Shaw, Christopher Price, Frederike Van Wijck, Michael Barnes, Laura Graham, Gary A. Ford, Nick Steen, and Helen Rodgers. 2012. "Cost-Effectiveness of Treating Upper Limb Spasticity Due to Stroke with Botulinum Toxin Type A: Results from the Botulinum Toxin for the Upper Limb after Stroke (BoTULS) Trial" Toxins 4, no. 12: 1415-1426. https://0-doi-org.brum.beds.ac.uk/10.3390/toxins4121415

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