Cost-effectiveness of treating vascular leg ulcers with UrgoStart(®) and UrgoCell(®) Contact

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Cost-effectiveness of treating vascular leg ulcers with UrgoStart(®) and UrgoCell(®) Contact. / Augustin, Matthias; Herberger, Katharina; Kroeger, Knut; Muenter, Karl C; Goepel, Lisa; Rychlik, Reinhard.

In: INT WOUND J, Vol. 13, No. 1, 2016, p. 82-87.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

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@article{0e82be80639b45c0b92571193424d265,
title = "Cost-effectiveness of treating vascular leg ulcers with UrgoStart({\textregistered}) and UrgoCell({\textregistered}) Contact",
abstract = "Although chronic wounds have a high socio-economic impact, data on comparative effectiveness of treatments are rare. UrgoStart({\textregistered}) is a hydroactive dressing containing a nano-oligosaccharide factor (NOSF). This study aimed at evaluating the cost-effectiveness of this NOSF-containing wound dressing in vascular leg ulcers compared with a similar neutral foam dressing (UrgoCell({\textregistered}) Contact) without NOSF. Cost-effectiveness analysis from the perspective of the German statutory health care system was performed using a decision tree model for a period of 8 weeks. Cost and outcome data were derived from the clinical study 'Challenge' suggesting a response rate (≥40% wound size reduction) of UrgoStart({\textregistered}) of 65·6% versus 39·4% for the comparator. In the treatment model, effect-adjusted costs of €849·86 were generated after 8 weeks for treatment with UrgoStart({\textregistered}) versus €1335·51 for the comparator resulting in an effect-adjusted cost advantage of €485·64 for UrgoStart({\textregistered}) . In linear sensitivity analyses, the outcomes were stable for varying assumptions on prices and response rates. In an 8-week period of treatment for vascular leg ulcers, UrgoStart({\textregistered}) shows superior cost-effectiveness when compared with the similar neutral foam dressing without any active component (NOSF). As demonstrated within a randomised, double-blind clinical trial, UrgoStart({\textregistered}) is also more effective in wound area reduction than the neutral foam dressing. Wound healing was not addressed in this clinical trial. Follow-up data of 12 months to allow for reulceration assessment were not generated.",
author = "Matthias Augustin and Katharina Herberger and Knut Kroeger and Muenter, {Karl C} and Lisa Goepel and Reinhard Rychlik",
note = "{\textcopyright} 2014 The Authors. International Wound Journal {\textcopyright} 2014 Medicalhelplines.com Inc and John Wiley & Sons Ltd.",
year = "2016",
doi = "10.1111/iwj.12238",
language = "English",
volume = "13",
pages = "82--87",
journal = "INT WOUND J",
issn = "1742-4801",
publisher = "Wiley-Blackwell",
number = "1",

}

RIS

TY - JOUR

T1 - Cost-effectiveness of treating vascular leg ulcers with UrgoStart(®) and UrgoCell(®) Contact

AU - Augustin, Matthias

AU - Herberger, Katharina

AU - Kroeger, Knut

AU - Muenter, Karl C

AU - Goepel, Lisa

AU - Rychlik, Reinhard

N1 - © 2014 The Authors. International Wound Journal © 2014 Medicalhelplines.com Inc and John Wiley & Sons Ltd.

PY - 2016

Y1 - 2016

N2 - Although chronic wounds have a high socio-economic impact, data on comparative effectiveness of treatments are rare. UrgoStart(®) is a hydroactive dressing containing a nano-oligosaccharide factor (NOSF). This study aimed at evaluating the cost-effectiveness of this NOSF-containing wound dressing in vascular leg ulcers compared with a similar neutral foam dressing (UrgoCell(®) Contact) without NOSF. Cost-effectiveness analysis from the perspective of the German statutory health care system was performed using a decision tree model for a period of 8 weeks. Cost and outcome data were derived from the clinical study 'Challenge' suggesting a response rate (≥40% wound size reduction) of UrgoStart(®) of 65·6% versus 39·4% for the comparator. In the treatment model, effect-adjusted costs of €849·86 were generated after 8 weeks for treatment with UrgoStart(®) versus €1335·51 for the comparator resulting in an effect-adjusted cost advantage of €485·64 for UrgoStart(®) . In linear sensitivity analyses, the outcomes were stable for varying assumptions on prices and response rates. In an 8-week period of treatment for vascular leg ulcers, UrgoStart(®) shows superior cost-effectiveness when compared with the similar neutral foam dressing without any active component (NOSF). As demonstrated within a randomised, double-blind clinical trial, UrgoStart(®) is also more effective in wound area reduction than the neutral foam dressing. Wound healing was not addressed in this clinical trial. Follow-up data of 12 months to allow for reulceration assessment were not generated.

AB - Although chronic wounds have a high socio-economic impact, data on comparative effectiveness of treatments are rare. UrgoStart(®) is a hydroactive dressing containing a nano-oligosaccharide factor (NOSF). This study aimed at evaluating the cost-effectiveness of this NOSF-containing wound dressing in vascular leg ulcers compared with a similar neutral foam dressing (UrgoCell(®) Contact) without NOSF. Cost-effectiveness analysis from the perspective of the German statutory health care system was performed using a decision tree model for a period of 8 weeks. Cost and outcome data were derived from the clinical study 'Challenge' suggesting a response rate (≥40% wound size reduction) of UrgoStart(®) of 65·6% versus 39·4% for the comparator. In the treatment model, effect-adjusted costs of €849·86 were generated after 8 weeks for treatment with UrgoStart(®) versus €1335·51 for the comparator resulting in an effect-adjusted cost advantage of €485·64 for UrgoStart(®) . In linear sensitivity analyses, the outcomes were stable for varying assumptions on prices and response rates. In an 8-week period of treatment for vascular leg ulcers, UrgoStart(®) shows superior cost-effectiveness when compared with the similar neutral foam dressing without any active component (NOSF). As demonstrated within a randomised, double-blind clinical trial, UrgoStart(®) is also more effective in wound area reduction than the neutral foam dressing. Wound healing was not addressed in this clinical trial. Follow-up data of 12 months to allow for reulceration assessment were not generated.

U2 - 10.1111/iwj.12238

DO - 10.1111/iwj.12238

M3 - SCORING: Journal article

C2 - 24618370

VL - 13

SP - 82

EP - 87

JO - INT WOUND J

JF - INT WOUND J

SN - 1742-4801

IS - 1

ER -