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  • von Felten, Stefanie  (2)
  • 2015-2019  (2)
  • 1
    In: Cardiovascular Therapeutics, Wiley, Vol. 35, No. 1 ( 2017-02), p. 19-25
    Abstract: The British National Institute of Clinical Excellence ( NICE ) guidelines recommend to use drug‐eluting stents ( DES ) instead of bare‐metal stents ( BMS ) only in lesions 〉 15 mm in length or in vessels 〈 3 mm in diameter. We analyzed the impact of stent length and stent diameter on in‐stent restenosis ( ISR ) in the BASKET ‐ PROVE study population and evaluated the cost‐effectiveness of DES compared to BMS . Methods/Results The BASKET ‐ PROVE trial compared DES vs BMS in large coronary arteries (≥3 mm). We calculated incremental cost‐effectiveness ratios ( ICER s) and cost‐effectiveness acceptability curves with regard to quality‐adjusted life years ( QALY s) gained and target lesion revascularizations ( TLR s) avoided. A total of 2278 patients were included in the analysis. A total of 74 ISR in 63 patients were observed. In‐stent restenosis was significantly more frequent in segments treated with a BMS compared to segments treated with a DES (5.4% vs 0.76%; P 〈 .001). The benefit of a DES compared to a BMS regarding ISR was consistent among the subgroups of stent length 〉 15 mm and ≤15 mm, respectively. With the use of DES in short lesions, there was only a minimal gain of 0.005 in QALY s. At a threshold of 10 000 CHF per TLR avoided, DES had a high probability of being cost‐effective. Conclusion In the BASKET ‐ PROVE study population, the strongest predictor of ISR is the use of a BMS , even in patients in need of stents ≥3.0 mm and ≤15 mm lesion length and DES were cost‐effective. This should prompt the NICE to reevaluate its recommendation to use DES instead of BMS only in vessels 〈 3.0 mm and lesions 〉 15 mm length.
    Type of Medium: Online Resource
    ISSN: 1755-5914 , 1755-5922
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2017
    detail.hit.zdb_id: 2417088-4
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  • 2
    In: Dermatology, S. Karger AG, Vol. 232, No. 6 ( 2016), p. 655-663
    Abstract: 〈 b 〉 〈 i 〉 Background: 〈 /i 〉 〈 /b 〉 Randomized controlled trials have shown the efficacy of systemic treatments in moderate-to-severe psoriasis. Clinical outcomes in psoriasis patients under real-world conditions are less well understood. 〈 b 〉 〈 i 〉 Objective: 〈 /i 〉 〈 /b 〉 This study compared Psoriasis Area and Severity Index (PASI) and Dermatological Life Quality Index (DLQI) improvement in all psoriasis patients registered in the Swiss Dermatology Network for Targeted Therapies. We asked whether outcomes differed between 4 treatment strategies, namely biologic monotherapy versus conventional systemic monotherapy, versus combined biologic and conventional systemic drugs, and versus therapy adaptation (switching from one type to another). 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 PASI and DLQI within 1 year after onset of systemic treatment, measured at 3, 6, and 12 months, were compared among the 4 groups using generalized linear mixed-effects models. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 Between March 2011 and December 2014, 334 patients were included; 151 received conventional systemic therapeutics, 145 biologics, 13 combined treatment, and 25 had a therapy adaptation. With regard to the absolute PASI, neither the biologic cohort nor the combined treatment cohort significantly differed from the conventional systemic therapeutics cohort. The odds of reaching PASI90 was significantly increased with combined therapy compared to conventional systemic therapeutics ( 〈 i 〉 p 〈 /i 〉 = 0.043) and decreased with a higher body mass index ( 〈 i 〉 p 〈 /i 〉 = 0.041). At visits 3 and 4, the PASI was generally lower than at visit 2 (visit 3 vs. visit 2, 〈 i 〉 p 〈 /i 〉 = 0.0019; visit 4 vs. visit 2, 〈 i 〉 p 〈 /i 〉 〈 0.001). After 12 months, patients with biologic treatment had a significantly lower DLQI than those with conventional systemic therapeutics ( 〈 i 〉 p 〈 /i 〉 = 0.001). 〈 b 〉 〈 i 〉 Conclusion: 〈 /i 〉 〈 /b 〉 This study suggests that after 1 year of treatment, biologics are superior in improving the subjective disease burden compared to conventional systemic drugs.
    Type of Medium: Online Resource
    ISSN: 1018-8665 , 1421-9832
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2016
    detail.hit.zdb_id: 1482189-8
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