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      重組貽貝粘蛋白水凝膠敷料聯(lián)合他克莫司軟膏治療面部皮炎的臨床效果

      2023-01-23 12:01:50陳明充
      醫(yī)學(xué)美學(xué)美容 2022年24期

      陳明充

      【摘 要】目的 觀(guān)察重組貽貝粘蛋白水凝膠敷料聯(lián)合他克莫司軟膏治療面部皮炎的臨床效果。方法 選取昆明市東川區(qū)人民醫(yī)院皮膚科2020年4月-2022年4月收治的87例面部皮炎患者為研究對(duì)象,按照隨機(jī)數(shù)字表法分為對(duì)照組43例和治療組44例。對(duì)照組予以他克莫司軟膏+0.9%生理鹽水噴劑,治療組予以他克莫司軟膏+重組貽貝粘蛋白水凝膠敷料,比較兩組瘙癢改善程度(瘙癢評(píng)分、止癢起效時(shí)間、止癢持續(xù)時(shí)間)、皮膚屏障功能(經(jīng)表皮失水量、角質(zhì)層含水量、油脂含量)、臨床療效、不良反應(yīng)發(fā)生情況及復(fù)發(fā)率。結(jié)果 治療組治療后VAS評(píng)分低于對(duì)照組,止癢起效時(shí)間早于對(duì)照組,止癢持續(xù)時(shí)間長(zhǎng)于對(duì)照組,差異有統(tǒng)計(jì)學(xué)意義(P<0.05);治療組治療后角質(zhì)層含水量和皮脂含量均高于對(duì)照組,經(jīng)表皮失水量低于對(duì)照組,差異有統(tǒng)計(jì)學(xué)意義(P<0.05);治療組治療總有效率為90.91%,高于對(duì)照組的62.79%,差異有統(tǒng)計(jì)學(xué)意義(P<0.05);治療組不良反應(yīng)總發(fā)生率為4.55%,低于對(duì)照組的27.91%,差異有統(tǒng)計(jì)學(xué)意義(P<0.05);治療組復(fù)發(fā)率為4.55%,低于對(duì)照組的34.88%,差異有統(tǒng)計(jì)學(xué)意義(P<0.05)。結(jié)論 重組貽貝粘蛋白水凝膠敷料輔助他克莫司軟膏聯(lián)合治療面部皮炎的效果確切,可有效改善患者瘙癢程度,促進(jìn)皮膚屏障功能恢復(fù),且耐受性及安全性高,復(fù)發(fā)幾率較低,值得臨床應(yīng)用。

      【關(guān)鍵詞】面部皮炎;瘙癢;重組貽貝粘蛋白;皮膚屏障功能

      中圖分類(lèi)號(hào):R751.05 文獻(xiàn)標(biāo)識(shí)碼:A 文章編號(hào):1004-4949(2022)24-0046-04

      Clinical Effect of Recombinant Mussel Adhesive Protein Hydrogel Dressing Combined with Tacrolimus Ointment in the Treatment of Facial Dermatitis

      CHEN Ming-chong

      (Department of Dermatology, Dongchuan District Peoples Hospital, Kunming 654100, Yunnan, China)

      【Abstract】Objective To observe the clinical effect of recombinant mussel adhesive protein hydrogel dressing combined with tacrolimus ointment in the treatment of facial dermatitis. Methods A total of 87 patients with facial dermatitis in Department of Dermatology, Dongchuan District Peoples Hospital of Kunming from April 2020 to April 2022 were randomly divided into control group (43 cases) and treatment group (44 cases). The control group was treated with tacrolimus ointment+0.9% normal saline spray, and the treatment group was treated with tacrolimus ointment+recombinant mussel adhesive protein hydrogel dressing. The degree of pruritus improvement (pruritus score, itching onset time, itching duration ), skin barrier function (transepidermal water loss, stratum corneum water content, oil content), clinical efficacy, adverse reactions and recurrence rate were compared between the two groups. Results After treatment, the VAS score of the treatment group was lower than that of the control group, the onset time of itching was earlier than that of the control group, and the duration of itching was longer than that of the control group, the differences were statistically significant (P<0.05). After treatment, the water content and sebum content of stratum corneum in the treatment group were higher than those in the control group, and the transepidermal water loss was lower than that in the control group, the differences were statistically significant (P<0.05). The total effective rate of treatment in the treatment group was 90.91%, which was higher than 62.79% of the control group, and the differences were statistically significant (P<0.05). The total incidence of adverse reactions in the treatment group was 4.55%, which was lower than 27.91% in the control group, and the differences were statistically significant (P<0.05). The recurrence rate of the treatment group was 4.55%, which was lower than 34.88% of the control group, and the differences were statistically significant (P<0.05). Conclusion Recombinant mussel adhesive protein hydrogel dressing combined with tacrolimus ointment is effective in the treatment of facial dermatitis, which can effectively improve the degree of pruritus and promote the recovery of skin barrier function, with high tolerance and safety, and low recurrence rate. It is worthy of clinical application.

      【Key words】Facial dermatitis; Itching; Recombinant mussel adhesive protein; Skin barrier function

      面部皮炎(facial dermatitis)為主要發(fā)生在面部的非傳染性皮膚炎癥,常以瘙癢性、反復(fù)性和遷延性?xún)A向?yàn)橹饕R床特征,以濕疹類(lèi)型疾病為主。根據(jù)病因及癥狀分類(lèi)將其分為特應(yīng)性皮炎、脂溢性皮炎、接觸性皮炎等,臨床表現(xiàn)為丘疹、紅斑等客觀(guān)癥狀,主觀(guān)癥狀包括顯著性自覺(jué)瘙癢,部分患者伴有灼熱等癥狀[1]。循證治療中推薦使用他克莫司等鈣調(diào)磷酸抑制劑類(lèi)藥物治療該疾病[2],但局部用藥對(duì)皮膚刺激反應(yīng)較大,常引起皮膚過(guò)敏、紅斑、皰疹等不良反應(yīng)[3]。臨床治療中常聯(lián)合保濕劑,增加療效同時(shí)可減輕他克莫司帶來(lái)的不良反應(yīng)[4]。貽貝粘蛋白具有良好的促愈、抗炎、止癢等療效,對(duì)面部皮炎患者具有正向輔助意義[5]?;诖耍狙芯恐荚谟^(guān)察重組貽貝粘蛋白水凝膠敷料聯(lián)合他克莫司軟膏治療面部皮炎的臨床效果,現(xiàn)報(bào)道如下。

      1 資料與方法

      1.1 一般資料 選取昆明市東川區(qū)人民醫(yī)院皮膚科2020年4月-2022年9月收治的87例面部皮炎患者為研究對(duì)象,按照隨機(jī)數(shù)字表法分為對(duì)照組43例和治療組44例。對(duì)照組男8例,女35例;年齡18~42歲,平均年齡(23.66±7.25)歲;病程3~36個(gè)月,平均病程(11.57±2.82)個(gè)月;疾病類(lèi)型:特應(yīng)性皮炎15例,脂溢性皮炎6例,接觸性皮炎22例。治療組男6例,女38例;年齡18~47歲,平均年齡(24.73±6.01)歲;病程3~36個(gè)月,平均病程(12.93±4.41)個(gè)月;疾病類(lèi)型:特應(yīng)性皮炎13例,脂溢性皮炎8例,接觸性皮炎23例。兩組性別、年齡及疾病類(lèi)型比較,差異無(wú)統(tǒng)計(jì)學(xué)意義(P>0.05),具有可比性。本研究所有患者均知情同意,并簽署知情同意書(shū)。

      1.2 納入及排除標(biāo)準(zhǔn) 納入標(biāo)準(zhǔn)[6]:表現(xiàn)為面頸部大小不等的瘙癢性片狀紅斑、脫屑,確診特應(yīng)性皮炎者;表現(xiàn)為接觸外源性物質(zhì)后引起多樣且不典型性反應(yīng),確診接觸性皮炎者;表現(xiàn)為面部油脂分泌旺盛區(qū)域有暗紅色斑片上蓋脂溢性鱗屑,確診脂溢性皮炎者。排除標(biāo)準(zhǔn):合并濕疹類(lèi)疾病者;合并痤瘡、蕁麻疹、皰疹、系統(tǒng)性紅斑狼瘡等其他疾病引起的面部炎癥性疾病者;近期使用糖皮質(zhì)激素藥物、抗組胺藥物、免疫抑制藥物者;妊娠期或哺乳期女性。

      1.3 方法 對(duì)照組予以他克莫司軟膏+0.9%生理鹽水噴劑:患者清潔皮膚后使用0.9%生理鹽水的安慰噴劑噴涂面部,5 min后在患處皮膚均勻薄涂他克莫司軟膏(Astellas Pharma Manufacturing, Inc.,國(guó)藥準(zhǔn)字J20060030,規(guī)格:0.03%),首次使用在臨床負(fù)責(zé)專(zhuān)屬醫(yī)師指導(dǎo)下操作,后續(xù)家居使用每日早晚各使用1次,連續(xù)使用14 d,治療結(jié)束后4周隨訪(fǎng)。治療組予以他克莫司軟膏+重組貽貝粘蛋白水凝膠敷料:將對(duì)照組中0.9%生理鹽水的安慰噴劑改為重組貽貝粘蛋白水凝膠敷料(湖南科妍創(chuàng)美醫(yī)療科技有限公司,湘械注準(zhǔn)20222142096),其余操作同對(duì)照組一致。

      1.4 觀(guān)察指標(biāo) 比較兩組瘙癢改善程度(瘙癢評(píng)分、止癢起效時(shí)間、止癢持續(xù)時(shí)間)、皮膚屏障功能、臨床療效、不良反應(yīng)發(fā)生情況及復(fù)發(fā)率。①瘙癢評(píng)分:于治療前及首次治療24 h后使用采用瘙癢視覺(jué)模擬評(píng)分(VAS)[7]評(píng)價(jià),總分0~10分,0分為無(wú)癥狀、1~3分為輕度瘙癢、4~7分為中度瘙癢、8~10分為重度瘙癢;②止癢起效時(shí)間:首次治療24 h內(nèi)瘙癢癥狀消失或中度或重度瘙癢緩解為輕度瘙癢的緩解時(shí)間;③止癢持續(xù)時(shí)間:止癢起效時(shí)間開(kāi)始到瘙癢再次加重的時(shí)間;④皮膚屏障功能:室溫環(huán)境下于治療前及治療14 d后采用皮膚檢測(cè)儀器(德國(guó)Courage & Khazaka公司,型號(hào):Corneometer CM 760)檢測(cè)皮膚角質(zhì)層含水量、皮脂含量和經(jīng)表皮失水量;⑤臨床療效:治療前及治療14 d后評(píng)估瘙癢、疼痛、灼熱、干燥/緊繃4項(xiàng)主觀(guān)癥狀及紅斑丘疹、鱗屑、膿皰、毛細(xì)血管擴(kuò)張4項(xiàng)客觀(guān)癥狀,總分均為0~4分,分?jǐn)?shù)越高癥狀越重;療效評(píng)估為治療前后的療效改善百分率,痊愈為≥90%,好轉(zhuǎn)為60%~89%,有效為30%~59%,無(wú)效為<30%;總有效率=痊愈率+好轉(zhuǎn)率;⑥不良反應(yīng)發(fā)生情況及復(fù)發(fā)率:不良反應(yīng)情況包括皮膚過(guò)敏、紅斑、皰疹;治療結(jié)束后2周后進(jìn)行隨訪(fǎng)記錄復(fù)發(fā)情況。1.5 統(tǒng)計(jì)學(xué)方法 采用SPSS 25.0統(tǒng)計(jì)學(xué)軟件處理本研究數(shù)據(jù),計(jì)量資料以(x-±s)表示,行t檢驗(yàn);計(jì)數(shù)資料以[n(%)]表示,行χ2檢驗(yàn);以P<0.05為差異有統(tǒng)計(jì)學(xué)意義。

      2 結(jié)果

      2.1 兩組瘙癢改善程度比較 治療組治療后VAS評(píng)分低于對(duì)照組,止癢起效時(shí)間早于對(duì)照組,止癢持續(xù)時(shí)間長(zhǎng)于對(duì)照組,差異有統(tǒng)計(jì)學(xué)意義(P<0.05),見(jiàn)表1。

      2.2 兩組皮膚屏障功能比較 治療組治療后角質(zhì)層含水量和皮脂含量均高于對(duì)照組,經(jīng)表皮失水量低于對(duì)照組,差異有統(tǒng)計(jì)學(xué)意義(P<0.05),見(jiàn)表2。

      2.3 兩組臨床療效比較 治療組治療總有效率高于對(duì)照組,差異有統(tǒng)計(jì)學(xué)意義(P<0.05),見(jiàn)表3。

      2.4 兩組不良反應(yīng)發(fā)生情況及復(fù)發(fā)率比較 治療組不良反應(yīng)總發(fā)生率低于對(duì)照組,差異有統(tǒng)計(jì)學(xué)意義(P<0.05),見(jiàn)表4;治療組復(fù)發(fā)率為4.55%(2/44),低于對(duì)照組的34.88%(15/43),差異有統(tǒng)計(jì)學(xué)意義(χ2=12.731,P=0.000)。

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