Moss J
Ann Fr Anesth Reanim. 1985;4(2):221-4. doi: 10.1016/S0750-7658(85)80204-5.
The American experience concerning the epidemiology of anaphylactic reactions following chemonucleolysis with chymopapain (Chymodiactin) were presented. The first study involved 1,585 patients of whom 17% were premedicated with some drug with either an H1 or H2 antagonist or both. The rate of anaphylaxis was 0.82%. Following its clinical introduction, a postmarketing surveillance study was undertaken. During the first 30,000 cases of which 93% were premedicated with combined H1 and H2 antagonists, the frequency of anaphylactic reactions was 0.78%. Subsequently, following the introduction of an immunologic test to screen for circulating IgE, the reaction rate fell to 0.44% in 45,000 cases of which 92% were premedicated with combined H1 and H2 antagonists. Females were far more likely to experience an anaphylactic event. Overall mortality from anaphylaxis decreased from one in 800 to one in 25,000 administrations. The decreased number and severity of these reactions correspond to the development of an immunologic screening test and utilization of prophylactic antihistamines.
介绍了美国关于木瓜凝乳蛋白酶(Chymodiactin)化学溶核术后过敏反应流行病学的经验。第一项研究涉及1585名患者,其中17%的患者预先使用了某种H1或H2拮抗剂或两者兼用的药物。过敏反应发生率为0.82%。在其临床应用后,开展了一项上市后监测研究。在前30000例病例中,93%的患者预先使用了H1和H₂拮抗剂联合用药,过敏反应发生率为0.78%。随后,在引入一种用于筛查循环IgE的免疫检测方法后,在45000例病例中反应率降至0.44%,其中92%的患者预先使用了H1和H₂拮抗剂联合用药。女性发生过敏事件的可能性要大得多。过敏反应导致的总体死亡率从每800次给药中有1例死亡降至每25000次给药中有1例死亡。这些反应数量和严重程度的降低与免疫筛查试验的开展以及预防性抗组胺药的使用有关。