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外用莫米松。其药理特性及治疗皮肤疾病的应用综述。

Topical mometasone. A review of its pharmacological properties and therapeutic use in the treatment of dermatological disorders.

作者信息

Prakash A, Benfield P

机构信息

Adis International Limited, Auckland, New Zealand.

出版信息

Drugs. 1998 Jan;55(1):145-63. doi: 10.2165/00003495-199855010-00009.

Abstract

Mometasone, a synthetic 16 alpha-methyl analogue of beclomethasone, is classified as a 'potent' glucocorticoid for dermatological use. It is available as 0.1% cream, ointment and lotion formulations for the treatment of patients with inflammatory glucocorticoid-responsive dermatoses. In patients with atopic dermatitis, the effect of mometasone 0.1% applied once daily over 2 to 3 weeks were similar to those of other glucocorticoids of similar potency, such as betamethasone dipropionate 0.05% twice daily and methylprednisolone aceponate 0.1% once daily. Mometasone 0.1% was significantly superior to twice-daily application of less potent glucocorticoids such as clobetasone 0.05%, hydrocortisone 1.0%, hydrocortisone butyrate and hydrocortisone valerate 0.2%. In patients with seborrhoeic dermatitis, mometasone 0.1% was more effective than ketoconazole 2.0% and hydrocortisone 1.0% in trials lasting 4 or 6 weeks. In the management of scalp psoriasis and psoriasis vulgaris, mometasone 0.1% applied once daily for 2 to 8 weeks was generally more effective than other glucocorticoids of similar or weaker potency such as betamethasone valerate 0.1%, fluocinolone acetonide 0.025%, fluticasone propionate 0.005%, triamcinolone acetonide 0.1% and hydrocortisone 1.0% and as effective as diflucortolone valerate 0.1%. Alternate day application of mometasone 0.1% for 2 weeks was as effective as once-daily application in maintaining symptom control in a small number of patients with psoriasis vulgaris. Although mometasone demonstrates greater anti-inflammatory activity and a longer duration of action than betamethasone, it has low potential to cause adverse systemic effects such as suppression of the hypothalamic-pituitary-adrenal (HPA) axis. Moreover, its atrophogenic potential is low and no greater than that of other glucocorticoids in its class, such as betamethasone valerate. Transient, mild to moderate, local adverse effects such as burning, stinging, folliculitis, dryness, acneiform eruptions and signs of skin atrophy have been reported with mometasone. Mometasone has shown a low risk of primary sensitisation and cross-reactions in preliminary patch test studies. Mometasone is a well tolerated topical glucocorticoid effective in the management of patients with atopic dermatitis, seborrhoeic dermatitis, scalp psoriasis and psoriasis vulgaris. In addition to its low potential for causing primary sensitisation and cross-reactions with other topical glucocorticoids, mometasone offers the convenience of once-daily administration.

摘要

莫米松是倍氯米松的一种合成16α-甲基类似物,在皮肤科被归类为“强效”糖皮质激素。它有0.1%的乳膏、软膏和洗剂制剂,用于治疗对糖皮质激素有反应的炎症性皮肤病患者。在特应性皮炎患者中,每天使用一次0.1%的莫米松,持续2至3周,其效果与其他同等效力的糖皮质激素相似,如每天两次使用0.05%的二丙酸倍他米松和每天一次使用0.1%的醋丙甲泼尼龙。0.1%的莫米松明显优于每天两次使用效力较弱的糖皮质激素,如0.05%的氯倍他索、1.0%的氢化可的松、丁酸氢化可的松和0.2%的戊酸氢化可的松。在脂溢性皮炎患者中,在持续4周或6周的试验中,0.1%的莫米松比2.0%的酮康唑和1.0%的氢化可的松更有效。在头皮银屑病和寻常型银屑病的治疗中,每天使用一次0.1%的莫米松,持续2至8周,通常比其他同等或效力较弱的糖皮质激素更有效,如0.1%的戊酸倍他米松、0.025%的醋酸氟轻松、0.005%的丙酸氟替卡松、0.1%的曲安奈德和1.0%的氢化可的松,且与0.1%的双氟可龙戊酸酯效果相当。在少数寻常型银屑病患者中,隔天使用一次0.1%的莫米松,持续2周,在维持症状控制方面与每天使用一次效果相同。尽管莫米松比倍他米松表现出更强的抗炎活性和更长的作用持续时间,但它引起下丘脑-垂体-肾上腺(HPA)轴抑制等全身性不良反应的可能性较低。此外,其导致皮肤萎缩的可能性较低,且不高于同类中的其他糖皮质激素,如戊酸倍他米松。使用莫米松后曾报告有短暂、轻度至中度的局部不良反应,如烧灼感、刺痛感、毛囊炎、皮肤干燥、痤疮样皮疹和皮肤萎缩迹象。在初步的斑贴试验研究中,莫米松显示出较低的原发性致敏风险和交叉反应风险。莫米松是一种耐受性良好的外用糖皮质激素,对特应性皮炎、脂溢性皮炎、头皮银屑病和寻常型银屑病患者的治疗有效。除了引起原发性致敏和与其他外用糖皮质激素交叉反应的可能性较低外,莫米松还具有每天一次给药的便利性。

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