TY - JOUR
T1 - Hereditary Angioedema
T2 - Implications of Management
AU - Pathria, Mohini
AU - Krishnaswamy, Guha
AU - Guarderas, Juan C.
PY - 2017/2/1
Y1 - 2017/2/1
N2 - Hereditary angioedema (HAE) is a genetic condition that is characterized by frequent episodes of localized angioedema. It is a rare disorder that a primary care provider, otolaryngologist, dermatologist, or rheumatologist may encounter only occasionally. This disease is being reviewed because of the significant advances in further understanding the genetics, biology, and therapeutic management surrounding the condition. Histamine-mediated angioedema responds to steroids, antihistamines, and epinephrine, whereas bradykinin-mediated angioedema is resistant to those interventions and requires specialized therapy. Previously used medications have significant adverse effects. Approved medications for HAE have been effective in decreasing morbidity and mortality in patients with this condition. We review the presentation, diagnosis, and available pharmaceutical options for HAE and explore the limitations of implementing recommended therapy.
AB - Hereditary angioedema (HAE) is a genetic condition that is characterized by frequent episodes of localized angioedema. It is a rare disorder that a primary care provider, otolaryngologist, dermatologist, or rheumatologist may encounter only occasionally. This disease is being reviewed because of the significant advances in further understanding the genetics, biology, and therapeutic management surrounding the condition. Histamine-mediated angioedema responds to steroids, antihistamines, and epinephrine, whereas bradykinin-mediated angioedema is resistant to those interventions and requires specialized therapy. Previously used medications have significant adverse effects. Approved medications for HAE have been effective in decreasing morbidity and mortality in patients with this condition. We review the presentation, diagnosis, and available pharmaceutical options for HAE and explore the limitations of implementing recommended therapy.
KW - C1 esterase inhibitor
KW - C1 esterase inhibitor deficiency
KW - C1 inhibitor deficiency
KW - hereditary angioedema
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U2 - 10.14423/SMJ.0000000000000604
DO - 10.14423/SMJ.0000000000000604
M3 - Review article
C2 - 28158879
AN - SCOPUS:85011702204
SN - 0038-4348
VL - 110
SP - 101
EP - 106
JO - Southern Medical Journal
JF - Southern Medical Journal
IS - 2
ER -