Angioedema Hereditario Guía de la Sociedad Mundial Alergia WAO

Tenemos el gusto de  anunciar el titulo del  próximo seminario  25 de  enero  2014.
Hora :  730  am ;  Sede :  Clínica  de  Asma  y Alergia, Managua  Nicaragua.
Llámenos :227891169, 22703359, 89465022C, 84316459 C, 88825513M.

WAO Guideline for the Management of Hereditary Angioedema

Timothy Craig¹, Emel Aygören Pürsün², Konrad Bork³, Tom Bowen⁴, Henrik Boysen⁵,Henriette Farkas⁶, Anete Grumach⁷, Constance H Katelaris⁸, Richard Lockey⁹, Hilary Longhurst¹⁰, William Lumry¹¹, Markus Magerl¹², Immaculada Martinez-Saguer²,Bruce Ritchie¹³, Alexander Nast¹², Ruby Pawankar¹⁴, Bruce Zuraw¹⁵ and Marcus Maurer^12*

Abstract         Full text html        . pdf

Hereditary Angioedema (HAE) is a rare disease and for this reason proper diagnosis and appropriate therapy are often unknown or not available for physicians and other health care providers. For this reason we convened a group of specialists that focus upon HAE from around the world to develop not only a consensus on diagnosis and management of HAE, but to also provide evidence based grades, strength of evidence and classification for the consensus. Since both consensus and evidence grading were adhered to the document meets criteria as a guideline. The outcome of the guideline is to improve diagnosis and management of patients with HAE throughout the world and to help initiate uniform care and availability of therapies to all with the diagnosis no matter where the residence of the individual with HAE exists.

Keywords: 

Hereditary Angioedema; Guidelines; HAE; therapy; management; diagnosis; medications; international