Wilsmann-Theis Dagmar, Jacobi Arnd, Frambach Yvonne, Philipp Sandra, Weyergraf Ansgar, Schill Tillmann, Steinz Kirsten, Gerdes Sascha, Mössner Rotraut
Department of Dermatology and Allergology, University Bonn, Germany.
Dermatol Online J. 2017 Apr 15;23(4):13030/qt0h15613d.
Palmoplantar pustulosis (PPP) is a recalcitrant chronic inflammatory skin disease. Data relevant for the medical care of patients with PPP are scarce. Thus, the aim of this work was to investigate the disease burden, clinical characteristics, and comorbidity of PPP patients in Germany.
PPP patients were examined in a crosssectional study at seven specialized psoriasis centers in Germany.
Of the 172 included patients with PPP, 79.1% were female and 69.8% were smokers.In addition, 25.0% suffered from psoriasis vulgaris, 28.2% had documented psoriatic arthritis, and 30.2% had a family history of psoriasis. In 77 patients the mean Dermatology Life Quality Index (DLQI) was 12.2 ± 7.7 (mean ± SD). The mean Psoriasis Palmoplantar Pustulosis Area and Severity Index (PPPASI) was 12.6 ± 8.6. Mean body mass index was above average at 27.1 ± 5.5. The PPP patients had previously received an average of 2.6 ± 2.1 different anti-psoriatic systemic drugs or UV-therapies. The systemic drugs that had been used most frequently were corticosteroids in 40.1% of patients, followed by acitretin (37.8%), and methotrexate (27.9%). The PPPASI was 13.4 ± 8.9 in patients without current systemic therapy and 10.4 ± 7.9 in patients with systemic therapy.
Many PPP patients had a concomitant diagnosis of psoriasis vulgaris and/or psoriatic arthritis or had a family history of psoriasis. Despite the fact that many of the patients were using anti-psoriatic therapies, there was still a high burden of disease within this PPP cohort. This insufficient control of symptoms demonstrates the urgent need for new PPP treatments.
掌跖脓疱病(PPP)是一种顽固的慢性炎症性皮肤病。有关PPP患者医疗护理的相关数据稀缺。因此,本研究旨在调查德国PPP患者的疾病负担、临床特征和合并症。
在德国七个专门的银屑病中心对PPP患者进行了一项横断面研究。
纳入的172例PPP患者中,79.1%为女性,69.8%为吸烟者。此外,25.0%患有寻常型银屑病,28.2%有银屑病关节炎记录,30.2%有银屑病家族史。77例患者的皮肤病生活质量指数(DLQI)平均为12.2±7.7(平均值±标准差)。掌跖脓疱病面积和严重程度指数(PPPASI)平均为12.6±8.6。平均体重指数高于平均水平,为27.1±5.5。PPP患者此前平均接受过2.6±2.1种不同的抗银屑病全身药物或紫外线治疗。最常使用的全身药物是皮质类固醇,占患者的40.1%,其次是阿维A(37.8%)和甲氨蝶呤(27.9%)。未接受当前全身治疗的患者PPPASI为13.4±8.9,接受全身治疗的患者为10.4±7.9。
许多PPP患者同时诊断为寻常型银屑病和/或银屑病关节炎,或有银屑病家族史。尽管许多患者正在使用抗银屑病疗法,但该PPP队列中的疾病负担仍然很高。症状控制不足表明迫切需要新的PPP治疗方法。