Haeberle Helene A, Lupic Daniela, Midoro-Horiuti Terumi, Kiefer Ralph T, Schroeder Torsten H, Unertl Klaus, Dieterich Hans Juergen
Department of Anesthesiology, Clinical University Tübingen, Hoppe-Seyler-Str. 3, 72076, Tübingen, Germany.
J Clin Anesth. 2003 Nov;15(7):495-504. doi: 10.1016/s0952-8180(03)00112-0.
To determine the applicability and reliability of a screening questionnaire to detect patients at high-risk of latex allergy; to assess the importance of other allergies such as profilin allergies (pollinosis) for presence of latex sensitization; and to determine the clinical effectiveness of preemptive avoidance of latex exposure in high-risk patients.
Prospective, clinical trial.
Operative theater of a university hospital.
95 adult patients.
Patients were preoperatively screened and classified for present latex allergy (high-risk and low-risk group) according to a specially designed screening questionnaire. Anesthesia and surgery in the high-risk group were performed strictly avoiding latex-containing materials. The low-risk group (other allergies including pollinosis) received routine treatment, without latex-avoidance. Effects of latex avoidance or exposure were evaluated by measuring specific IgE titers perioperatively.
According to the questionnaire, 45 patients at high risk were defined. Validity of classification of high-risk patients is supported by significantly higher total IgE and latex and grass profilin specific IgE compared to the low-risk group. There were no significant differences in other profilin-specific IgEs. In one case of severe anaphylactic reaction a drop of latex-specific IgE during surgery could be observed.
The questionnaire allowed the identification of most patients at high risk for latex allergy. In isolated pollinosis no changes in any specific IgE levels were detectable. Strict avoidance of perioperative latex exposure in high-risk patients increases safety during anesthesia and surgery.
确定一份筛查问卷在检测乳胶过敏高危患者方面的适用性和可靠性;评估其他过敏(如肌动蛋白过敏,花粉症)对乳胶致敏的影响;并确定在高危患者中预先避免接触乳胶的临床效果。
前瞻性临床试验。
大学医院手术室。
95名成年患者。
根据一份专门设计的筛查问卷,对患者进行术前筛查,并分类为现患乳胶过敏(高危组和低危组)。高危组的麻醉和手术严格避免使用含乳胶材料。低危组(包括花粉症在内的其他过敏)接受常规治疗,不避免接触乳胶。通过围手术期测量特异性IgE滴度评估避免或接触乳胶的效果。
根据问卷,确定了45名高危患者。与低危组相比,高危患者分类的有效性得到总IgE、乳胶和草肌动蛋白特异性IgE显著更高的支持。其他肌动蛋白特异性IgE无显著差异。在1例严重过敏反应中,可观察到手术期间乳胶特异性IgE下降。
该问卷能够识别出大多数乳胶过敏高危患者。单纯花粉症患者任何特异性IgE水平均无变化。高危患者围手术期严格避免接触乳胶可提高麻醉和手术期间的安全性。