نتایج جستجو برای: angioedema

تعداد نتایج: 6905  

Journal: :The New England journal of medicine 1980
M Phillips

BACKGROUND Hereditary angioedema due to C1 inhibitor deficiency is characterized by recurrent acute attacks of swelling that can be painful and sometimes life-threatening. METHODS We conducted two randomized trials to evaluate nanofiltered C1 inhibitor concentrate in the management of hereditary angioedema. The first study compared nanofiltered C1 inhibitor concentrate with placebo for treatm...

2012
Josef Yayan

Alteplase (recombinant tissue plasminogen activator) has been used in the treatment of acute ischemic stroke for 10 years. The application of this drug is considered safe and effective. However, alteplase is also associated with side effects. The author is reporting on an unusual side effect of angioedema that is triggered by alteplase. Angioedema occurs through alteplase according to this stud...

Journal: :Postgraduate medical journal 2002
N P Kumar G Wild K A Ramasamy J Snape

Angioedema is a recognised side effect of rofecoxib, a cyclo-oxygenase-2 (COX-2) inhibitor. But death resulting from a haemorrhagic pulmonary oedema after its ingestion has not been recorded. The case of a 60 year old man who died from haemorrhagic pulmonary oedema in the presence of angioedema after the ingestion of two doses of 12.5 mg of rofecoxib is reported.

Journal: :The New England journal of medicine 2017
Aleena Banerji Paula Busse Mustafa Shennak William Lumry Mark Davis-Lorton Henry J Wedner Joshua Jacobs James Baker Jonathan A Bernstein Richard Lockey H Henry Li Timothy Craig Marco Cicardi Marc Riedl Ahmad Al-Ghazawi Carolyn Soo Ryan Iarrobino Daniel J Sexton Christopher TenHoor Jon A Kenniston Ryan Faucette J Gordon Still Harvey Kushner Robert Mensah Chris Stevens Joseph C Biedenkapp Yung Chyung Burt Adelman

BACKGROUND Hereditary angioedema with C1 inhibitor deficiency is characterized by recurrent, unpredictable swelling episodes caused by uncontrolled plasma kallikrein generation and excessive bradykinin release resulting from cleavage of high-molecular-weight kininogen. Lanadelumab (DX-2930) is a new kallikrein inhibitor with the potential for prophylactic treatment of hereditary angioedema with...

2018
P Staubach M Metz N Chapman-Rothe C Sieder M Bräutigam M Maurer K Weller

BACKGROUND The X-ACT study aimed to examine the effect of omalizumab treatment on quality of life (QoL) in chronic spontaneous urticaria (CSU) patients with angioedema refractory to high doses of H1 -antihistamines. METHODS In X-ACT, a phase III, double-blind, placebo-controlled study, CSU patients (18-75 years) with ≥4 angioedema episodes during the 6 months before inclusion were randomized ...

2010
Renata C Alencar Roberta A Cobas Marília B Gomes

BACKGROUND Angiotensin-converting enzyme (ACE) inhibitors are widely prescribed for patients with diabetes as a nephroprotector drug or to treat hypertension. Generally they are safe for clinical practice, but the relationship between these drugs and angioedema is known. The exact mechanism for ACE inhibitors-induced angioedema is not clear and it is still a matter of discussion. CASE REPORT ...

Journal: :Asploro Journal of Biomedical and clinical Case Reports 2022

ACE-inhibitor induced angioedema is a rare, potentially life-threatening phenomenon with unpredictable symptoms. With advanced angioedema, orotracheal intubation may not be possible necessitating nasotracheal or cricothyroidotomy. This case describes 76-year-old male history of hypertension controlled lisinopril-hydrochlorothiazide who developed sudden-onset angioedema. Additionally, this was c...

2015
Samuel Michael Lipski Georges Casimir Martine Vanlommel Mathieu Jeanmaire Pierre Dolhen

C1 esterase inhibitor (Berinert®) is generally used to treat severe attack of hereditary angioedema. We describe here the case of a patient who presented with a severe angioedema induced by angiotensin-converting enzyme inhibitors (ACEIs) endangering her life. It could be successfully treated with that medicine.

2017
Brendan N. Wong Peter Vadas

RATIONALE Angioedema without co-existent urticaria is due to a limited number of causes, including hereditary and acquired C1 esterase inhibitor deficiency, drug-induced angioedema or idiopathic histaminergic or non-histaminergic angioedema. We describe a cohort of patients with recurrent angioedema whose clinical features and response to medications are distinct from the causes above. METHOD...

2017
Da Woon Sim Kyung Hee Park Jae-Hyun Lee Jung-Won Park

Hereditary angioedema is a disease of congenital deficiency or functional defect in the C1 esterase inhibitor (C1-INH) consequent to mutation in the SERPING1 gene, which encodes C1-INH. This disease manifests as recurrent, non-pitting, non-pruritic subcutaneous, or submucosal edema as well as an erythematous rash in some cases. These symptoms result from the uncontrolled localized production of...

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