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Economic evaluation of a tailored therapist-guided internet-based cognitive behavioural treatment for patients with psoriasis: a randomized controlled trial

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Article details

Beugen S. van, Ferwerda M., Middendorp H. van, Smit J.V., Zeeuwen-Franssen M.E.J., Kroft E.B.M., Jong E.M.G.J. de, Kerkhof P.C.M. van de, Kievit W. & & Evers A.W.M. (2019), Economic evaluation of a tailored therapist-guided internet-based cognitive behavioural treatment for patients with psoriasis: a randomized controlled trial, British Journal of Dermatology 181(3): 614-616.

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Economic evaluation of a tailored

therapist-guided internet-based cognitive

behavioural treatment for patients with

psoriasis: a randomized controlled trial

DOI: 10.1111/bjd.17848

DEAR EDITOR, The high prevalence and physical, psychological

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decreased disease impact in patients with psoriasis.4The current study examines the cost-effectiveness of this intervention.

This economic evaluation from a societal perspective was conducted alongside an open-label parallel-group RCT com-paring the effects of care as usual (CAU; regular dermato-logical care) with additional ICBT aimed at reducing the impact of psoriasis on daily life (ICBT+CAU) in 131 patients with psoriasis. Methodological details are described elsewhere.4 The ICBT focused on itch, pain, fatigue, nega-tive mood and social relationships. Costs (self-reported health care and medication use, patient travel costs, loss of productivity costs in paid labour and ICBT costs4) and effects [quality-adjusted life years (QALYs)4] were assessed at baseline, post-treatment and 6-month follow-up. Baseline between-group cost differences were analysed with indepen-dent-samples t-tests. An incremental cost–utility ratio (ICUR) was calculated by dividing between-group cost differences by the QALY differences for the 12-month study period. Uncertainty surrounding the ICUR was based on boot-strapped samples (1000 replications).

No baseline between-group differences in sociodemographic and disease-related characteristics, and outcomes were found (P-values ≥ 010), except for a higher clinician-rated disease severity in the ICBT+CAU group (P = 003). The primary cost– utility analysis showed no between-group differences in effects (average QALY ICBT+CAU vs. CAU 079 vs. 078; mean QALY

difference –0014; 25–975 percentile –0062 to 0038) or costs (average costs ICBT+CAU vs. CAU €6641 vs. €5346; mean difference €1295; 25–975 percentile –€1502 to €4176) at post-treatment and 6-months follow-up (P≥ 045). The north-west quadrant of the cost-effectiveness plane (Fig. 1a) con-tained the majority of ICURs (58%), suggesting larger societal costs and QALY losses after ICBT+CAU than CAU alone. Greater QALY improvements in the ICBT+CAU group, but at higher societal costs (northeast quadrant), had a 24% probability.

Although the intervention was aimed at patients with moder-ate-to-high disease burden, the sample had relatively low disease burden.4 To examine the impact of disease burden, four post hoc subgroup analyses were performed on patients with high vs. low (median split) baseline scores on (i) self-assessed disease severity; (ii) clinician-assessed disease severity; (iii) psychologi-cal distress; and (iv) self-perceived disease impact. For patients with high self-reported disease severity and high self-reported disease impact, ICBT+CAU was generally associated with greater effects at lower societal costs than CAU (i.e. 60% and 78% ICURs in the southeast quadrant, respectively, compared with 0% and 0% in low-scoring patients; Fig. 1b–e). The probability that ICBT is cost-effective for patients with high self-reported disease severity and impact at a willingness to pay of€20 000 per QALY gained5is 78% (mean ICUR–55978; mean cost reduction –€ 593; mean QALY increase 005) and 95% (mean ICUR –94371; mean cost reduction –€2562; mean QALY increase 003),

-€ 4,000 -€ 3,000 -€ 2,000 -€ 1,000 € 0 € 1,000 € 2,000 € 3,000 € 4,000 € 5,000 € 6,000 -0.06 -0.04 -0.02 - 0.02 0.04 0.06 Additional costs Additional effects -€ 8,000 -€ 6,000 -€ 4,000 -€ 2,000 € 0 € 2,000 € 4,000 € 6,000 -0.06 -0.04 -0.02 - 0.02 0.04 0.06 Addit ional costs Additional effects -€ 1,000 € 0 € 1,000 € 2,000 € 3,000 € 4,000 € 5,000 -0.06 -0.04 -0.02 - 0.02 0.04 0.06 Addit ional cost s Additional effects -€ 10,000 -€ 8,000 -€ 6,000 -€ 4,000 -€ 2,000 € 0 € 2,000 € 4,000 -0.06 -0.04 -0.02 - 0.02 0.04 0.06 Additional co st s Additional effects -€ 1,000 € 0 € 1,000 € 2,000 € 3,000 € 4,000 € 5,000 -0.06 -0.04 -0.02 - 0.02 0.04 0.06 Additional co st s Additional effects (a) (b) (c) (d) (e) € 20.000 WTP threshold

Fig 1. Cost-effectiveness planes for main cost-effectiveness analysis (a), and subgroups of high (b) vs. low (c) self-assessed disease severity, and high (d) vs. low (e) self-assessed disease impact. WTP, willingness to pay.

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respectively. In contrast, for patients with high clinician-assessed disease severity and high psychological distress, ICBT+CAU was generally associated with lower effects at higher costs than CAU (86% and 78% of ICURs in the northwest quadrant, respectively, compared with 31% and 4% in low-scoring patients).

That ICBT+CAU was not cost-effective compared with CAU in the total group may be explained by between-group imbalance [i.e. higher disease severity and descriptively higher baseline costs, systemic medication use and greater labour market partici-pation (more possible productivity losses) in the ICBT+CAU group]. Moreover, the generic effect measure (EQ-5D) may not be specific enough to detect health-related quality of life (HRQoL) aspects in dermatological samples,6 combined with limited responsiveness and ceiling effects across conditions.7,8

The finding that ICBT+CAU was cost-effective for patients with high self-reported disease severity and impact clearly sug-gests the target audience of this intervention. As societal costs were lower in the ICBT+CAU than CAU group at 6-month fol-low-up, the intervention may be cost-effective even when soci-ety is not willing to pay anything for it. However, follow-up trials including patients with higher disease burden are needed to corroborate these findings. Strengths of this study include the RCT design, outpatient sample and analysis of direct and indirect costs. Including a sensitive-to-change dermatology-spe-cific HRQoL measure might aid the assessment of clinically rele-vant improvement in future cost-effectiveness studies.

In conclusion, although ICBT was not considered cost-effec-tive in comparison with CAU in the overall sample, subgroup analyses suggested cost-effectiveness for patients who experience high self-assessed disease severity and impact. Screening for these characteristics, and offering ICBT specifically to patients with ele-vated levels, may be cost-effective and clinically relevant.

S . V A N BE U G E N1,2 M . FE R W E R D A1 , 2 iD H . V A NMI D D E N D O R P1 , 2 iD J . V . SM I T3 M . E . J . ZE E U W E N- FR A N S S E N4 E . B . M . KR O F T5 E . M . G . J . D EJO N G6 , 7 P . C . M . V A N D E KE R K H O F6 iD W . KI E V I T8 A . W . M . EV E R S1 , 2 iD 1

Institute of Psychology, Health, Medical and Neuropsychology Unit, Leiden University, Leiden, the Netherlands

2

Department of Medical Psychology,

6

Department of Dermatology, Radboud University Medical Center, Nijmegen, the Netherlands

3

Department of Dermatology, Rijnstate Hospital, Velp, the Netherlands

4

Department of Dermatology, Canisius-Wilhelmina Hospital, Nijmegen, the Netherlands

5

Department of Dermatology, Ziekenhuisgroep Twente, Almelo, the Netherlands

7

Radboud University, Nijmegen, the Netherlands

8

Department for Health Evidence, Radboud University Medical Center, Nijmegen, the Netherlands

E-mail: s.van.beugen@fsw.leidenuniv.nl

M.F. and H.v.M. contributed equally to this work.

References

1 Hay RJ, Johns NE, Williams HC et al. The global burden of skin dis-ease in 2010: an analysis of the prevalence and impact of skin con-ditions. J Invest Dermatol 2014;134:1527–34.

2 Lavda A, Webb T, Thompson A. A meta-analysis of the effectiveness of psychological interventions for adults with skin conditions. Br J Dermatol 2012; 167:970–9.

3 van Beugen S, Ferwerda M, Hoeve D et al. Internet-based cognitive behavioral therapy for patients with chronic somatic conditions: a meta-analytic review. J Med Internet Res 2014;16:e88.

4 van Beugen S, Ferwerda M, Spillekom-van Koulil S et al. Tailored thera-pist-guided internet-based cognitive behavioral treatment for psoriasis: a randomized controlled trial. Psychother Psychosom 2016;85:297–307. 5 Zwaap J, Knies S, van der Meijden C et al. [Cost-effectiveness in

Prac-tice.] Diemen: Zorginstituut Nederland, 2015 (in Dutch).

6 Pereira F, Basra MK, Finlay AY, Salek M. The role of the EQ-5D in the economic evaluation of dermatological conditions and therapies. Dermatol 2012; 225:45–53.

7 Bharmal M, Thomas J. Comparing the EQ-5D and the SF-6D descriptive systems to assess their ceiling effects in the US general population. Value Health 2006;9:262–71.

8 Brazier J, Roberts J, Tsuchiya A, Busschbach J. A comparison of the EQ-5D and SF-6D across seven patient groups. Health Econ 2004; 13:873–84.

Funding sources: this study was supported by grants from Pfizer (WS682746; www.pfizer.nl) and The Netherlands Organisation for Health Research and Development (ZonMw; 170992803;

www.zonmw.nl). The funders had no role in study design, data collec-tion and analysis, decision to publish or preparacollec-tion of the manuscript.

Conflicts of interest: none to declare.

© 2019 British Association of Dermatologists British Journal of Dermatology (2019)181, pp593–636

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