Angiotensin converting enzyme inhibitor induced angio-oedema: a review of the pathophysiology and risk factors

被引:97
作者
Hoover, T. [1 ]
Lippmann, M. [2 ]
Grouzmann, E. [3 ]
Marceau, F. [4 ]
Herscu, P. [5 ]
机构
[1] Div Clin Res, Herscu Lab, Amherst, MA 01002 USA
[2] Albert Einstein Med Ctr, Thomas Jefferson Sch Med, Philadelphia, PA 19141 USA
[3] CHU Vaudois, Div Pharmacol & Toxicol Clin, CH-1011 Lausanne, Switzerland
[4] Univ Laval, Ctr Rech Rhumatol & Immunol, Quebec City, PQ G1K 7P4, Canada
[5] Personalized Pharmaceut Syst, Div Res & Dev, Amherst, MA USA
关键词
DIPEPTIDYL PEPTIDASE-IV; BRADYKININ-MEDIATED ANGIOEDEMA; FRESH-FROZEN PLASMA; C-REACTIVE PROTEIN; ACE-INHIBITORS; HEREDITARY ANGIOEDEMA; CLINICAL-EXPERIENCE; ANGIONEUROTIC-EDEMA; GENE POLYMORPHISM; AMINOPEPTIDASE-P;
D O I
10.1111/j.1365-2222.2009.03323.x
中图分类号
R392 [医学免疫学];
学科分类号
100108 [医学免疫学];
摘要
P>Angio-oedema (AE) is a known adverse effect of angiotensin converting enzyme inhibitor (ACE-I) therapy. Over the past several decades, evidence of failure to diagnose this important and potentially fatal reaction is commonly found in the literature. Because this reaction is often seen first in the primary care setting, a review was undertaken to analyse and document the keys to both diagnostic criteria as well as to investigate potential risk factors for ACE-I AE occurrence. A general review of published literature was conducted through Medline, EMBASE, and the Cochrane Database, targeting ACE-I-related AE pathomechanism, diagnosis, epidemiology, risk factors, and clinical decision making and treatment. The incidence and severity of AE appears to be on the rise and there is evidence of considerable delay in diagnosis contributing to significant morbidity and mortality for patients. The mechanism of AE due to ACE-I drugs is not fully understood, but some genomic and metabolomic information has been correlated. Additional epidemiologic data and clinical treatment outcome predictors have been evaluated, creating a basis for future work on the development of clinical prediction tools to aid in risk identification and diagnostic differentiation. Accurate recognition of AE by the primary care provider is essential to limit the rising morbidity associated with ACE-I treatment-related AE. Research findings on the phenotypic indicators relevant to this group of patients as well as basic research into the pathomechanism of AE are available, and should be used in the construction of better risk analysis and clinical diagnostic tools for ACE-I AE. Cite this as: T. Hoover, M. Lippmann, E. Grouzmann, F. Marceau and P. Herscu, Clinical & Experimental Allergy, 2010 (40) 50-61.
引用
收藏
页码:50 / 61
页数:12
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