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使用口服β-内酰胺类抗生素对青霉素过敏患者进行脱敏治疗。

Desensitization of patients allergic to penicillin using orally administered beta-lactam antibiotics.

作者信息

Sullivan T J, Yecies L D, Shatz G S, Parker C W, Wedner H J

出版信息

J Allergy Clin Immunol. 1982 Mar;69(3):275-82. doi: 10.1016/s0091-6749(82)80004-3.

Abstract

When patients allergic to penicillin develop life-endangering infections that require treatment with beta-lactam antibiotics, they face a fatal infection or the possibility of a fatal allergic reaction. We have approached this situation by using an oral desensitization procedure before full-dose antibiotic therapy. Thirty consecutive patients with histories of allergic reactions to penicillin, positive immediate wheal and flare skin-test reactions to penicillin determinants, and life-threatening infections were studied. Bacterial endocarditis requiring penicillin G therapy led to desensitization of 19 patients, Pseudomonas sepsis of pneumonia requiring treatment led to desensitization of nine subjects, and staphylococcal infections requiring therapy with a penicillinase-resistant penicillin led to desensitization of two patients. Penicillin G or carbenicillin were administered orally, beginning with 100 U or 60 microgram, respectively. At 15-min intervals, progressively doubled doses were given during continuous monitoring for the appearance of allergic reactions. Within 5 hr, full therapeutic doses were administered intravenously. Skin-test reactions disappeared or diminished in all 23 subjects who were retested after desensitization. Full courses of antibiotic therapy and cure of the infections were accomplished in 30 of 30 patients. No deaths, anaphylaxis, or severe acute allergic reactions occurred. Pruritic cutaneous eruptions appeared in nine patients (30%) 6 to 48 hr after the onset of therapy. One patient developed reversible nephritis 3 wk into therapy with penicillin G. The results of this study suggest that oral desensitization is an effective, relatively safe approach to administering beta-lactam antibiotics to penicillin-allergic patients with life-threatening infections.

摘要

当对青霉素过敏的患者发生危及生命的感染且需要使用β-内酰胺类抗生素进行治疗时,他们面临着致命感染或致命过敏反应的可能性。我们通过在全剂量抗生素治疗前采用口服脱敏程序来应对这种情况。对30例有青霉素过敏史、对青霉素决定簇即刻皮肤风团和潮红试验反应呈阳性且患有危及生命感染的患者进行了研究。需要青霉素G治疗的细菌性心内膜炎使19例患者脱敏,需要治疗的铜绿假单胞菌败血症性肺炎使9例患者脱敏,需要用耐青霉素酶青霉素治疗的葡萄球菌感染使2例患者脱敏。分别从100单位或60微克开始口服给予青霉素G或羧苄青霉素。每隔15分钟,在持续监测过敏反应出现的情况下逐渐加倍剂量给药。在5小时内静脉给予全治疗剂量。在脱敏后重新进行检测的所有23例受试者中,皮肤试验反应消失或减弱。30例患者中有30例完成了抗生素全疗程治疗且感染治愈。未发生死亡、过敏反应或严重急性过敏反应。9例患者(30%)在治疗开始后6至48小时出现瘙痒性皮肤疹。1例患者在青霉素G治疗3周后发生可逆性肾炎。本研究结果表明,口服脱敏是一种为患有危及生命感染的青霉素过敏患者施用β-内酰胺类抗生素的有效且相对安全的方法。

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