crisaborole 软膏对小儿特应性皮炎的疗效和安全性:为期四周的开放标签研究

Abhishek De, Disha Chakraborty, B. N. Grisilda, Sirshendu Chaudhuri, K. Godse, Sandipan Dhar
{"title":"crisaborole 软膏对小儿特应性皮炎的疗效和安全性:为期四周的开放标签研究","authors":"Abhishek De, Disha Chakraborty, B. N. Grisilda, Sirshendu Chaudhuri, K. Godse, Sandipan Dhar","doi":"10.25259/ijsa_45_2023","DOIUrl":null,"url":null,"abstract":"\n\nManaging mild-to-moderate atopic dermatitis (AD) often necessitates topical therapies, and one such recently introduced option is crisaborole ointment. This study sets out to assess the efficacy and safety of crisaborole ointment in pediatric cases of AD over four weeks.\n\n\n\nNineteen children between 2 and 16 years old with mild-to-moderate AD were enrolled and treated with crisaborole ointment twice daily in affected areas for 30 days. The primary objective was to appraise the shift in the investigator’s static global assessment (ISGA) scores (0–4) every week for the four-week follow-up. The severity of pruritus score (SPS) was another secondary objective. Furthermore, individual indicators of clinical signs that included erythema, exudation, excoriation, induration/papulation, and lichenification, were examined with subjective scores (0–3). Children’s dermatology quality of life index (CDLQI) was employed to study the quality of life.\n\n\n\nFollowing four weeks of crisaborole ointment treatment, the average ISGA score declined from 2.58 ± 0.61 to 0.95 ± 0.78, signifying a substantial reduction in AD severity (P < 0.001). The SPS score also decreased from a mean of 2.32 ± 0.478 to 0.84 ± 0.60 (P < 0.001), underscoring a significant reduction in itching. Moreover, individual markers for clinical signs of AD, including erythema, exudation, excoriation, induration/papulation, and lichenification, all exhibited statistically significant improvement. Crisaborole ointment was well tolerated. Only 6 of the 19 patients reported a localized burning sensation, which was manageable. No patient needed to be withdrawn during the study period. The CDLQI showed a substantial drop in scores, decreasing from an average of 13.79 ± 3.57 at the commencement to 6.74 ± 1.97 (P < 0.001). Furthermore, 14 out of 19 patients met the study’s primary goal, achieving at least a 2-point reduction in ISGA along with the attainment of clear or nearly clear skin (ISGA 0–1).\n\n\n\nOur study found crisaborole ointment significantly improved pediatric AD symptoms and was well-tolerated. The only adverse event was localized burning in a few patients. Further, research is needed for validation.\n","PeriodicalId":340475,"journal":{"name":"Indian Journal of Skin Allergy","volume":"13 7","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Efficacy and safety of crisaborole ointment in pediatric atopic dermatitis: A 4-week open-label study\",\"authors\":\"Abhishek De, Disha Chakraborty, B. N. Grisilda, Sirshendu Chaudhuri, K. Godse, Sandipan Dhar\",\"doi\":\"10.25259/ijsa_45_2023\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\nManaging mild-to-moderate atopic dermatitis (AD) often necessitates topical therapies, and one such recently introduced option is crisaborole ointment. This study sets out to assess the efficacy and safety of crisaborole ointment in pediatric cases of AD over four weeks.\\n\\n\\n\\nNineteen children between 2 and 16 years old with mild-to-moderate AD were enrolled and treated with crisaborole ointment twice daily in affected areas for 30 days. The primary objective was to appraise the shift in the investigator’s static global assessment (ISGA) scores (0–4) every week for the four-week follow-up. The severity of pruritus score (SPS) was another secondary objective. Furthermore, individual indicators of clinical signs that included erythema, exudation, excoriation, induration/papulation, and lichenification, were examined with subjective scores (0–3). Children’s dermatology quality of life index (CDLQI) was employed to study the quality of life.\\n\\n\\n\\nFollowing four weeks of crisaborole ointment treatment, the average ISGA score declined from 2.58 ± 0.61 to 0.95 ± 0.78, signifying a substantial reduction in AD severity (P < 0.001). The SPS score also decreased from a mean of 2.32 ± 0.478 to 0.84 ± 0.60 (P < 0.001), underscoring a significant reduction in itching. Moreover, individual markers for clinical signs of AD, including erythema, exudation, excoriation, induration/papulation, and lichenification, all exhibited statistically significant improvement. Crisaborole ointment was well tolerated. Only 6 of the 19 patients reported a localized burning sensation, which was manageable. No patient needed to be withdrawn during the study period. The CDLQI showed a substantial drop in scores, decreasing from an average of 13.79 ± 3.57 at the commencement to 6.74 ± 1.97 (P < 0.001). Furthermore, 14 out of 19 patients met the study’s primary goal, achieving at least a 2-point reduction in ISGA along with the attainment of clear or nearly clear skin (ISGA 0–1).\\n\\n\\n\\nOur study found crisaborole ointment significantly improved pediatric AD symptoms and was well-tolerated. The only adverse event was localized burning in a few patients. Further, research is needed for validation.\\n\",\"PeriodicalId\":340475,\"journal\":{\"name\":\"Indian Journal of Skin Allergy\",\"volume\":\"13 7\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-02-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Indian Journal of Skin Allergy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.25259/ijsa_45_2023\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Skin Allergy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25259/ijsa_45_2023","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

轻度至中度特应性皮炎(AD)的治疗通常需要外用疗法,而最近推出的一种外用疗法就是crisaborole软膏。这项研究旨在评估 crisaborole 软膏对儿童过敏性皮炎的疗效和安全性,为期四周。19 名患有轻度至中度过敏性皮炎、年龄在 2 岁至 16 岁之间的儿童参加了这项研究,他们在 30 天内每天两次在患处涂抹 crisaborole 软膏。主要目的是评估研究者静态总体评估(ISGA)评分(0-4分)在四周随访期间每周的变化情况。瘙痒严重程度评分(SPS)是另一个次要目标。此外,还对包括红斑、渗出、剥脱、压痕/丘疹和苔藓化在内的临床症状的单项指标进行了主观评分(0-3 分)。采用儿童皮肤病生活质量指数(CDLQI)对生活质量进行了研究。经过四周的清热解毒软膏治疗后,ISGA的平均得分从2.58±0.61分降至0.95±0.78分,表明AD的严重程度大幅降低(P<0.001)。SPS 评分也从平均值 2.32 ± 0.478 降至 0.84 ± 0.60(P < 0.001),表明瘙痒症状显著减轻。此外,AD 临床症状的各项指标,包括红斑、渗出、剥脱、压痕/丘疹和苔藓化,均有统计学意义的显著改善。患者对 Crisaborole 软膏的耐受性良好。19 位患者中只有 6 位出现了局部烧灼感,但这种感觉是可以控制的。在研究期间,没有患者需要停药。CDLQI 分数大幅下降,从开始时的平均值(13.79 ± 3.57)降至(6.74 ± 1.97)(P < 0.001)。此外,19 名患者中有 14 名达到了研究的主要目标,即 ISGA 至少下降 2 分,皮肤透明或接近透明(ISGA 0-1)。唯一的不良反应是少数患者出现局部烧灼感。还需要进一步的研究来验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy and safety of crisaborole ointment in pediatric atopic dermatitis: A 4-week open-label study
Managing mild-to-moderate atopic dermatitis (AD) often necessitates topical therapies, and one such recently introduced option is crisaborole ointment. This study sets out to assess the efficacy and safety of crisaborole ointment in pediatric cases of AD over four weeks. Nineteen children between 2 and 16 years old with mild-to-moderate AD were enrolled and treated with crisaborole ointment twice daily in affected areas for 30 days. The primary objective was to appraise the shift in the investigator’s static global assessment (ISGA) scores (0–4) every week for the four-week follow-up. The severity of pruritus score (SPS) was another secondary objective. Furthermore, individual indicators of clinical signs that included erythema, exudation, excoriation, induration/papulation, and lichenification, were examined with subjective scores (0–3). Children’s dermatology quality of life index (CDLQI) was employed to study the quality of life. Following four weeks of crisaborole ointment treatment, the average ISGA score declined from 2.58 ± 0.61 to 0.95 ± 0.78, signifying a substantial reduction in AD severity (P < 0.001). The SPS score also decreased from a mean of 2.32 ± 0.478 to 0.84 ± 0.60 (P < 0.001), underscoring a significant reduction in itching. Moreover, individual markers for clinical signs of AD, including erythema, exudation, excoriation, induration/papulation, and lichenification, all exhibited statistically significant improvement. Crisaborole ointment was well tolerated. Only 6 of the 19 patients reported a localized burning sensation, which was manageable. No patient needed to be withdrawn during the study period. The CDLQI showed a substantial drop in scores, decreasing from an average of 13.79 ± 3.57 at the commencement to 6.74 ± 1.97 (P < 0.001). Furthermore, 14 out of 19 patients met the study’s primary goal, achieving at least a 2-point reduction in ISGA along with the attainment of clear or nearly clear skin (ISGA 0–1). Our study found crisaborole ointment significantly improved pediatric AD symptoms and was well-tolerated. The only adverse event was localized burning in a few patients. Further, research is needed for validation.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信