期刊
ARCHIVES OF DERMATOLOGICAL RESEARCH
卷 314, 期 7, 页码 633-641出版社
SPRINGER
DOI: 10.1007/s00403-021-02272-5
关键词
Plaque psoriasis; Calcipotriol betamethasone compounding agent; Clinical efficacy; Clinical safety; Meta-analysis
类别
资金
- Tianjin municipal health and Health Committee [ZC20114]
This study evaluated the clinical efficacy and safety of using calcipotriol-betamethasone compounding agent for psoriasis treatment through a systematic review and meta-analysis, suggesting that the sequential therapy may be more effective than using only calcipotriol in short-term treatment, with no significant difference in adverse reaction rate between the two groups. Further research may be needed for a more detailed evaluation.
The main objective is to evaluate clinical efficacy and safety of using calcipotriol-betamethasone compounding agent for psoriasis treatment through a systematic review and meta-analysis. We searched MEDLINE, Embase, The Cochrane Library, China National Knowledge Infrastructure (CNKI), China Biomedical Literature Database (CBM), and WanFang Data from inception till July 31, 2020. Efficacy was evaluated based on primary outcome indicators including skin lesion improvement and overall adverse reaction rate. Secondary outcome indicators included degree of life quality improvement, clinical effectiveness rate, and specific adverse reaction rates. RevMan5.3 was used to perform the meta-analysis. 22 studies finally met our inclusion criteria for the meta-analysis. The results indicated that for short-term treatment, a sequential therapy that uses calcipotriol betamethasone compounding agent and calcipotriol improves PASI score (MD = -0.94, 95% CI - 1.38 similar to - 0.49, P < 0.0001, I-2 = 49%), comparing with using only calcipotriol. From a drug safety perspective, the difference in overall adverse reaction rate is not significant between the calcipotriol group and the sequential treatment group (RR = 0.50, 95% CI 0.22 similar to 1.14, P = 0.10, I-2 = 33%). Calcipotriol betamethasone compounding agent may be more effective in plaque psoriasis treatment compared to use only calcipotriol, with no significant difference in adverse reaction rate between the two groups. Although the data were collected from 13 comparison groups, each group may not have sufficient data for a thorough and comprehensive analysis. Further research may be necessary for a more detailed evaluation of effectiveness of using calcipotriol betamethasone compounding agent for plaque psoriasis treatment.
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