Lang D M, Alpern M B, Visintainer P F, Smith S T
Department of Medicine, Hahnemann University, Philadelphia, Pa.
Arch Intern Med. 1993 Sep 13;153(17):2033-40.
A case-control study, with both retrospective and concurrent subject selection, was performed (1) to determine whether greater risk for anaphylactoid reaction from contrast media associated with beta-blocker exposure reflects presence, or is independent of underlying cardiovascular disorder; and (2) to characterize further the risk of anaphylactoid reaction from contrast media in patients with cardiovascular disorders and patients with asthma.
Adverse reactions from intravenous contrast media were recorded in accordance with quality assurance guidelines. Anaphylactoid reactions were classified as mild to moderate (urticaria/angioedema), severe (stridor, bronchospasm, or hypotension), or major and life-threatening (hypotension with or without the need for subsequent hospitalization). Medical records from reactors were compared with those from matched (gender, age, date, and type of contrast study) controls who received conventional contrast media without adverse reaction.
Of 34,371 intravenous contrast media procedures performed, 122 anaphylactoid reactions were recorded. The risk of anaphylactoid reaction was significantly associated with asthma (odds ratio [OR], 8.74; 95% confidence interval [CI], 2.36 to 32.35; P = .0012). The risk of bronchospasm was associated with beta-blocker exposure (OR, 3.73; 95% CI, 1.18 to 11.75; P = .025) and with asthma (OR, 16.39; 95% CI, 4.30 to 62.46; P = .0001). The risk of major and life-threatening reaction was associated with the presence of cardiovascular disorder (OR, 7.71; 95% CI, 1.04 to 57.23; P = .046). Among patients with severe reactions, the risk of hospitalization was elevated by the presence of cardiovascular disorder (P = .001), exposure to beta-blockers (OR, 7.67; 95% CI, 1.79 to 32.85; P = .029), or asthma (OR, 20.7; 95% CI, 1.21 to 355.55; P = .065). Although beta-blocker exposure and the presence of cardiovascular disorder were highly associated (chi 2 = 49, P < .001), a greater risk of bronchospasm with severe reaction was observed in nonasthmatic patients with cardiovascular disorders receiving beta-blockers (OR, 15.75; P = .023). Among reactors with asthma, receiving beta-blockers, or with a cardiovascular disorder, 60.8% (31/51) experienced severe anaphylactoid reactions, compared with 35.2% (25/71) of patients without these risk factors (OR, 3.62; P = .005).
beta-Blocker exposure and cardiovascular disorder are both statistically significant risk factors for severe anaphylactoid reaction from contrast media. Thus, patients receiving beta-adrenergic blockers and patients with asthma, on the basis of greater risk for bronchospasm, and patients with cardiovascular disorders, on the basis of elevated risk of major and life-threatening reaction, are appropriate target populations for risk reduction measures before receiving intravenous infusion of contrast media.
进行了一项病例对照研究,采用回顾性和同期受试者选择方法,目的如下:(1)确定与β受体阻滞剂暴露相关的造影剂类过敏反应风险增加是否反映潜在心血管疾病的存在,或与之无关;(2)进一步明确心血管疾病患者和哮喘患者中造影剂类过敏反应的风险。
根据质量保证指南记录静脉注射造影剂的不良反应。类过敏反应分为轻至中度(荨麻疹/血管性水肿)、重度(喘鸣、支气管痉挛或低血压)或严重且危及生命(伴有或不伴有后续住院需求的低血压)。将发生反应者的病历与接受常规造影剂且未出现不良反应的匹配(性别、年龄、日期和造影检查类型)对照者的病历进行比较。
在34371例静脉注射造影剂操作中,记录到122例类过敏反应。类过敏反应风险与哮喘显著相关(优势比[OR],8.74;95%置信区间[CI],2.36至32.35;P = 0.0012)。支气管痉挛风险与β受体阻滞剂暴露(OR,3.73;95%CI,1.18至11.75;P = 0.025)以及哮喘(OR,16.39;95%CI,4.30至62.46;P = 0.0001)相关。严重且危及生命反应的风险与心血管疾病的存在相关(OR,7.71;95%CI,1.04至57.23;P = 0.046)。在严重反应患者中,心血管疾病的存在、β受体阻滞剂暴露(OR,7.67;95%CI,1.79至32.85;P = 0.029)或哮喘(OR,20.7;95%CI,1.21至355.55;P = 0.065)会增加住院风险。尽管β受体阻滞剂暴露与心血管疾病的存在高度相关(χ² = 49,P < 0.001),但在接受β受体阻滞剂的非哮喘心血管疾病患者中,观察到严重反应时支气管痉挛风险更高(OR,15.75;P = 0.023)。在患有哮喘、接受β受体阻滞剂治疗或患有心血管疾病的反应者中,60.8%(31/51)发生了严重类过敏反应,而无这些危险因素的患者中这一比例为35.2%(25/71)(OR,3.62;P = 0.005)。
β受体阻滞剂暴露和心血管疾病均是造影剂严重类过敏反应的统计学显著危险因素。因此,基于支气管痉挛风险增加,接受β肾上腺素能阻滞剂的患者和哮喘患者,以及基于严重且危及生命反应风险升高,患有心血管疾病的患者,是在接受静脉注射造影剂前采取风险降低措施的合适目标人群。