Clarke P S
Royal Hobart Hospital, Tasmania, Australia.
Ann Allergy. 1988 Jan;60(1):57-60.
A simple and safe method of nasal provocation for out-patients that requires no special equipment is described. A total of 2,645 cases were tested by nasal provocation tests. Of the total, 1,175 were tested with Dermatophagoides pteronyssinus, 825 with mixed grass pollens, 352 with plantain (Plantago lanceolata), and 125 for cats and correlating nasal tests with skin tests yielded 80%, 90%, and 85%, respectively. Immunotherapy for allergic rhinitis was only considered justifiable when the nasal provocation test was positive. The nasal provocation test was repeated at the end of the normal course of injections recommended by the manufacturer. If the nasal provocation test was still positive, further injections were given until the test became negative. This method of improving diagnostic accuracy and monitoring results of immunotherapy was used with both aqueous extracts which were used for skin testing (Australian Government Commonwealth Serum Laboratories) and with Allpyral pyridine-extracted alum-precipitated extracts (Dome Laboratories, England). The number of injections of allergen required to convert a positive nasal provocation test to negative varied from 26 to 69 for mite aqueous injections with only 12 to 19 for mite suspension and 47 to 98 for grass aqueous injections compared with 12 to 36 for grass suspension. Direct provocation tests of the nose should give a more accurate diagnosis than RAST or skin tests and are required for monitoring therapy because considerable individual variations in sensitivity and response to treatment were demonstrated. Standard dosage schedules are not suitable for individual patients, who should have their immunotherapy personalized.
本文描述了一种简单、安全的门诊患者鼻腔激发试验方法,该方法无需特殊设备。共有2645例患者接受了鼻腔激发试验。其中,1175例用尘螨进行测试,825例用混合草花粉进行测试,352例用窄叶车前草进行测试,125例用猫毛进行测试,鼻腔试验与皮肤试验的相关性分别为80%、90%和85%。只有当鼻腔激发试验呈阳性时,才认为过敏性鼻炎的免疫疗法是合理的。在制造商推荐的正常注射疗程结束时重复进行鼻腔激发试验。如果鼻腔激发试验仍为阳性,则继续注射直至试验变为阴性。这种提高诊断准确性和监测免疫治疗结果的方法,既适用于用于皮肤试验的水性提取物(澳大利亚政府联邦血清实验室),也适用于Allpyral吡啶提取的明矾沉淀提取物(英国多姆实验室)。将阳性鼻腔激发试验转为阴性所需的变应原注射次数,螨水性注射为26至69次,螨悬液为12至19次,草水性注射为47至98次,而草悬液为12至36次。鼻腔直接激发试验应比放射性变应原吸附试验(RAST)或皮肤试验给出更准确的诊断,并且由于已证明个体在敏感性和对治疗的反应方面存在相当大的差异,因此监测治疗需要进行该试验。标准剂量方案不适用于个体患者,患者的免疫治疗应个性化。