Abelson M B, Lanier R Q
Ophthalmic Research Associates, North Andover, MA 01845, USA.
Acta Ophthalmol Scand Suppl. 1999(228):53-6. doi: 10.1111/j.1600-0420.1999.tb01175.x.
Allergic conjunctivitis very often occurs simultaneously with rhinitis in seasonal allergy sufferers. While systemic anti-allergic and antihistaminic agents are effective against many signs and symptoms of allergy, they may not adequately control ocular signs and symptoms in patients with multiple target organ hypersensitivity. Patanol (olopatadine hydrochloride 0.1% ophthalmic solution, Alcon Laboratories, Inc., Fort Worth, TX), a new effective anti-allergic mast cell stabilizer with antihistaminic properties, is approved for the prevention of ocular itching due to allergic conjunctivitis.
To determine whether Patanol in combination with the systemic antihistamine Claritin (loratadine, Schering, Kenilworth, NJ) reduces the ocular itching associated with allergic conjunctivitis more effectively than Claritin alone. A topical ocular antigen challenge induced the allergic conjunctivitis in 15 subjects.
This was a randomized, double-masked study in which the contralateral eye served as the control. On Visit 1, an allergen dose which elicited response scores > 2 for ocular itching was identified. Itching was graded by the subject using a 0 to 4 point scale. At Visit 2, the threshold allergen concentration was confirmed. At Visit 3, the onset of action challenge, in addition to Claritin (10 mg tablet), each subject received Patanol in one eye and placebo in the fellow eye in a randomized, double-masked fashion. Allergen was instilled one hour after dosing, and ocular itching was graded at 3, 7, 10 and 20 minutes after challenge. At Visit 4, the duration of action challenge, the same drug regimen was followed as in Visit 3. However, allergen challenge was performed eight hours after dosing, and itching graded after 3, 7, 10 and 20 minutes.
Patient eyes treated with Patanol were significantly less itchy than those treated with systemic Claritin alone at critical time points 3, 7, and 10 minutes after the onset of action challenge (p < 0.05), and at 3 and 7 minutes after the duration of action challenge (p < 0.05).
The addition of topical Patanol to systemic Claritin therapy significantly reduced ocular itching associated with allergic conjunctivitis compared to treatment with Claritin alone. These findings prove the added benefit of local Patanol therapy in the treatment of ocular allergic symptoms in patients receiving systemic antihistamines for concomitant systemic allergies.
在季节性过敏患者中,过敏性结膜炎常常与鼻炎同时发生。虽然全身性抗过敏和抗组胺药物对许多过敏症状有效,但对于多靶器官过敏的患者,它们可能无法充分控制眼部症状。帕坦洛(0.1%盐酸奥洛他定滴眼液,爱尔康实验室公司,得克萨斯州沃思堡)是一种新型有效的具有抗组胺特性的抗过敏肥大细胞稳定剂,已被批准用于预防过敏性结膜炎引起的眼部瘙痒。
确定帕坦洛与全身性抗组胺药开瑞坦(氯雷他定,先灵葆雅公司,新泽西州肯尼沃思)联合使用是否比单独使用开瑞坦更有效地减轻与过敏性结膜炎相关的眼部瘙痒。通过局部眼部抗原激发在15名受试者中诱发过敏性结膜炎。
这是一项随机、双盲研究,对侧眼作为对照。在第1次就诊时,确定能引起眼部瘙痒反应评分>2的变应原剂量。受试者使用0至4分的量表对瘙痒进行分级。在第2次就诊时,确认阈值变应原浓度。在第3次就诊时,即起效挑战时,除了开瑞坦(10毫克片剂)外,每位受试者一只眼接受帕坦洛,另一只眼接受安慰剂,采用随机、双盲方式。给药1小时后滴入变应原,并在激发后3、7、10和20分钟对眼部瘙痒进行分级。在第4次就诊时,即作用持续时间挑战时,采用与第3次就诊相同的给药方案。然而,在给药8小时后进行变应原激发,并在3、7、10和20分钟后对瘙痒进行分级。
在起效挑战后3、7和10分钟的关键时间点(p<0.05)以及作用持续时间挑战后3和7分钟(p<0.05),用帕坦洛治疗的患者眼睛瘙痒明显少于单独用全身性开瑞坦治疗的眼睛。
与单独使用开瑞坦治疗相比,在全身性开瑞坦治疗中添加局部用帕坦洛可显著减轻与过敏性结膜炎相关的眼部瘙痒。这些发现证明了在接受全身性抗组胺药治疗全身性过敏的患者中,局部用帕坦洛治疗眼部过敏症状的额外益处。