Boznański A, Domanasiewicz M, Rudzka D, Pirogowicz I
III Katedry i Kliniki Pediatrii i Alergologii Akademii Medycznej we Wrocławiu.
Pneumonol Alergol Pol. 1994;62(1-2):80-3.
Preparations, in which composition disodium cromoglycate goes into, have been for many years the admitted way of bronchial asthma treatment. The introduction, to the therapy, of preparation that contains reproterol as well makes possible the early remission of disease symptoms. The aim of the study was the estimation of the effectiveness of DNCG-comp. preparation. Twenty one children, aged 7-17 years, with recognized bronchial asthma were examined. The atopic basis of the disease was found on the ground of results of skin prick tests, and elevated concentration of serum IgE and positive atopic family interview. We resigned the hitherto treatment for 3 days, carried out the spirometric measurements (PEF, FEV1, FEV1%VC, MEF25,50,75). DNCG-comp. was given 4-times per twenty-four hours in 2 inhalations at each time, for three weeks. Every day, the PEF value and the score of disease symptoms were established. After the study, side effects were not observed and final results of spirometric estimation evidence the possibility of wide application of DNCG-comp. preparation in the treatment of bronchial asthma in childhood.
多年来,色甘酸二钠作为成分的制剂一直是公认的支气管哮喘治疗方法。含有瑞普特罗的制剂引入该疗法也使得疾病症状的早期缓解成为可能。本研究的目的是评估色甘酸二钠复合制剂的有效性。对21名年龄在7至17岁、确诊为支气管哮喘的儿童进行了检查。根据皮肤点刺试验结果、血清IgE浓度升高以及特应性家族访谈阳性,确定了该疾病的特应性基础。我们停用了之前的治疗3天,进行了肺功能测量(呼气峰值流速、第1秒用力呼气容积、第1秒用力呼气容积占肺活量百分比、最大呼气中期流速25%、50%、75%)。色甘酸二钠复合制剂每24小时给药4次,每次2吸,持续3周。每天记录呼气峰值流速值和疾病症状评分。研究结束后,未观察到副作用,肺功能评估的最终结果证明色甘酸二钠复合制剂在儿童支气管哮喘治疗中广泛应用的可能性。