Division of Allergy and Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Division of Immunology, University of Cincinnati, Cincinnati, Ohio.
Ann Allergy Asthma Immunol. 2014 Aug;113(2):198-203. doi: 10.1016/j.anai.2014.05.009. Epub 2014 Jun 11.
Current guidelines recommend short-term prophylaxis (STP) before invasive procedures to prevent hereditary angioedema (HAE) attacks; however, adherence to these guidelines may be variable because this indication lacks Food and Drug Administration approval in the United States.
To ascertain the STP experiences of patients with HAE and HAE-treating physicians.
Online questionnaires focusing on STP experiences were distributed by the US Hereditary Angioedema Association to the first 250 patients with HAE and to registered HAE-treating physicians. SAS 9.3 was used to perform descriptive statistics and to test the difference between patients who underwent procedures and those who did not using Pearson χ(2) test, Fisher exact test, and 2-sample t test.
For the patient survey, 219 respondents met the criteria for HAE type 1 and 2; 37 (17%) underwent 66 invasive procedures, and all reported receiving STP. Eight patients (22%) reported failed STP, but only 3 required on-demand therapy. For STP, anabolic steroids and plasma-derived C1 inhibitor were the most and second-most commonly used, respectively. For the physician survey, 37 physicians reported caring for 433 patients with HAE. Depending on the procedure, 19% to 54% of physicians used STP and 30% to 86% prescribed on-demand therapy; 69% and 78% of physicians prescribed plasma-derived C1 inhibitor as STP for minimally invasive and invasive procedures, respectively. Physicians reported excellent efficacy for the STP treatments used.
Physicians reported excellent outcomes using primarily newer STP therapies, namely plasma-derived C1 inhibitor, which was discordant to patient-reported outcomes using older STP therapies, namely anabolic steroids. Well-controlled STP studies are needed to clarify use for patients with HAE in the United States.
目前的指南建议在侵袭性操作前进行短期预防(STP)以预防遗传性血管性水肿(HAE)发作;然而,由于美国食品和药物管理局(FDA)尚未批准该适应证,因此对这些指南的遵循可能存在差异。
明确 HAE 患者和 HAE 治疗医生的 STP 经验。
美国遗传性血管水肿协会(USHereditary Angioedema Association)通过在线问卷,向 250 名 HAE 患者和注册的 HAE 治疗医生调查 STP 经验。使用 SAS 9.3 进行描述性统计,使用 Pearson χ(2)检验、Fisher 确切检验和 2 样本 t 检验,比较行侵袭性操作和未行侵袭性操作的患者之间的差异。
在患者调查中,219 名应答者符合 HAE 1 型和 2 型的标准;37 名(17%)患者行 66 次侵袭性操作,均接受 STP。8 名(22%)患者报告 STP 失败,但仅 3 名患者需要按需治疗。对于 STP,合成代谢类固醇和血浆衍生 C1 抑制剂分别是最常和第二常使用的药物。在医生调查中,37 名医生报告治疗了 433 名 HAE 患者。根据操作的不同,19%54%的医生使用 STP,30%86%的医生开具按需治疗;69%和 78%的医生分别将血浆衍生 C1 抑制剂作为微创和侵袭性操作的 STP 治疗药物。医生报告使用的 STP 治疗具有良好的疗效。
医生报告使用主要是较新的 STP 治疗药物(即血浆衍生 C1 抑制剂)取得了极好的疗效,这与患者报告使用较旧的 STP 治疗药物(即合成代谢类固醇)的结果不一致。需要进行良好对照的 STP 研究,以阐明美国 HAE 患者的使用情况。