Angioedema associated with thrombolysis for ischemic stroke: analysis of a case-control study.


Journal

Journal of internal medicine
ISSN: 1365-2796
Titre abrégé: J Intern Med
Pays: England
ID NLM: 8904841

Informations de publication

Date de publication:
12 2019
Historique:
pubmed: 19 7 2019
medline: 26 5 2020
entrez: 19 7 2019
Statut: ppublish

Résumé

Bradykinin-mediated angioedema (AE) is a complication associated with thrombolysis for acute ischemic stroke. Risk factors are unknown and management is discussed. To clarify risk factors associated with bradykinin-mediated AE after thrombolysis for acute ischemic stroke. In a case-control study conducted at a French reference centre for bradykinin angiœdema, patients with thrombolysis for acute ischemic stroke and a diagnosis of bradykinin-mediated angiœdema, were compared to controls treated with thrombolysis treatment without angiœdema. Fifty-three thrombolysis-related AE were matched to 106 control subjects. The sites of attacks following thrombolysis for ischemic stroke mainly included tongue (34/53, 64%) and lips (26/53, 49%). The upper airways were involved in 37 (70%) cases. Three patients required mechanical ventilation. Patients with bradykinin-mediated angiœdema were more frequently women [33 (62%) vs. 44 (42%); P = 0.01], had higher frequency of prior ischemic stroke [12 (23%) vs. 9 (8%); P = 0.01], hypertension [46 (87%) vs. 70 (66%); P = 0.005], were more frequently treated with angiotensin-converting enzyme inhibitor [37 (70%) vs. 28 (26%); P < 0.001] and were more frequently hospitalized in intensive care medicine [ICU; 11 (21%) vs. 5 (5%); P = 0.004]. In multivariate analysis, factors associated with thrombolysis-related AE were female sex [odds ratio (OR), 3.04; 95% confident interval (CI), 1.32-7.01; P = 0.009] and treatment with angiotensin-converting enzyme inhibitors [(OR), 6.08; 95% (CI), 2.17-17.07; P < 0.001]. This case-control study points out angiotensin-converting enzyme inhibitors and female sex as risk factors of bradykinin AE associated with thrombolysis for ischemic stroke.

Sections du résumé

BACKGROUND
Bradykinin-mediated angioedema (AE) is a complication associated with thrombolysis for acute ischemic stroke. Risk factors are unknown and management is discussed.
OBJECTIVES
To clarify risk factors associated with bradykinin-mediated AE after thrombolysis for acute ischemic stroke.
METHODS
In a case-control study conducted at a French reference centre for bradykinin angiœdema, patients with thrombolysis for acute ischemic stroke and a diagnosis of bradykinin-mediated angiœdema, were compared to controls treated with thrombolysis treatment without angiœdema.
RESULTS
Fifty-three thrombolysis-related AE were matched to 106 control subjects. The sites of attacks following thrombolysis for ischemic stroke mainly included tongue (34/53, 64%) and lips (26/53, 49%). The upper airways were involved in 37 (70%) cases. Three patients required mechanical ventilation. Patients with bradykinin-mediated angiœdema were more frequently women [33 (62%) vs. 44 (42%); P = 0.01], had higher frequency of prior ischemic stroke [12 (23%) vs. 9 (8%); P = 0.01], hypertension [46 (87%) vs. 70 (66%); P = 0.005], were more frequently treated with angiotensin-converting enzyme inhibitor [37 (70%) vs. 28 (26%); P < 0.001] and were more frequently hospitalized in intensive care medicine [ICU; 11 (21%) vs. 5 (5%); P = 0.004]. In multivariate analysis, factors associated with thrombolysis-related AE were female sex [odds ratio (OR), 3.04; 95% confident interval (CI), 1.32-7.01; P = 0.009] and treatment with angiotensin-converting enzyme inhibitors [(OR), 6.08; 95% (CI), 2.17-17.07; P < 0.001].
CONCLUSIONS
This case-control study points out angiotensin-converting enzyme inhibitors and female sex as risk factors of bradykinin AE associated with thrombolysis for ischemic stroke.

Identifiants

pubmed: 31319000
doi: 10.1111/joim.12962
doi:

Substances chimiques

Angiotensin-Converting Enzyme Inhibitors 0
Bradykinin S8TIM42R2W

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

702-710

Informations de copyright

© 2019 The Association for the Publication of the Journal of Internal Medicine.

Références

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Auteurs

C Vigneron (C)

From the, AP-HP, Médecine Interne, DHUi2B, Centre de Référence Associé sur les Angiœdèmes à Kinines (CRéAk), Hôpital Saint-Antoine, Université Paris 6, Paris, France.

A Lécluse (A)

Neurologie, CHU Angers, Angers, France.

T Ronzière (T)

Neurologie, CHU Pontchaillou, Rennes, France.

L Bouillet (L)

Médecine Interne, Centre de Référence sur les Angiœdèmes à Kinines (CRéAk), CHU de Grenoble, Grenoble, France.

I Boccon-Gibod (I)

Médecine Interne, Centre de Référence sur les Angiœdèmes à Kinines (CRéAk), CHU de Grenoble, Grenoble, France.

S Gayet (S)

AP-HM, Médecine Interne, Centre de Compétence Angioedèmes non Histaminiques, Hôpital la Timone, Marseille, France.

E Doche (E)

AP-HM, Neurologie, Hôpital la Timone, Marseille, France.

D Smadja (D)

Neurologie, CH Sud Francilien, Corbeil-Essonnes, France.

S Di Legge (S)

Neurologie, CH du Pays d'Aix-CH Intercommunal Aix-Pertuis, Aix-en-Provence, France.

F Dumont (F)

Neurologie, CH Tourcoing, Tourcoing, France.

M Gaudron (M)

Neurologie, CHU Tours, Tours, France.

I Ion (I)

Neurologie, CHU Nîmes, Nîmes, France.

S Marcel (S)

Neurologie, CH Métropole Savoie, Chambéry, France.

M Sévin (M)

Neurologie Institut du Thorax et du Système Nerveux, CHU Nantes, Nantes, France.

M B Vlaicu (MB)

AP-HP, Service de Neurochirurgie, Hôpital Pitié Salpétrière, INSERM U955, Hôpital Orsay, Paris, France.

D Launay (D)

U995-LIRIC-Lille Inflammation Research International Center, INSERM, U995, Département de Médecine Interne et Immunologie Clinique, Centre de Référence sur les Angiœdèmes à Kinines (CRéAk), Université de Lille, CHU de Lille, Lille, France.

I Arnaud (I)

Neurologie, CHU Pointe-à-Pitre, Pointe-à-Pitre, France.

P Girard-Madoux (P)

Neurologie, L'hôpital Nord-Ouest, Gleize, France.

C Héroum (C)

Neurologie, GH Portes-de-Provence, Montélimar, France.

S Lefèvre (S)

Institut d'allergologie, CHR Metz-Thionville, Metz, France.

G Marc (G)

Neurologie, CH Saint-Nazaire, Saint-Nazaire, France.

M Obadia (M)

Neurologie, Fondation Ophtalmologique Rothschild, Paris, France.

D Sablot (D)

Neurologie, CH Perpignan, Perpignan, France.

I Sibon (I)

Neurologie, CHU Bordeaux, Université de Bordeaux, Bordeaux, France.

L Suissa (L)

Neurologie, CHU Nice, Nice, France.

D Gobert (D)

From the, AP-HP, Médecine Interne, DHUi2B, Centre de Référence Associé sur les Angiœdèmes à Kinines (CRéAk), Hôpital Saint-Antoine, Université Paris 6, Paris, France.

O Detante (O)

Neurologie, CHU de Grenoble, Grenoble, France.

S Alamowitch (S)

AP-HP, Service de Neurologie, Hôpital Saint-Antoine, Sorbonne Universités, UPMC Univ Paris 06, UMRS 938, Paris, France.

O Fain (O)

From the, AP-HP, Médecine Interne, DHUi2B, Centre de Référence Associé sur les Angiœdèmes à Kinines (CRéAk), Hôpital Saint-Antoine, Université Paris 6, Paris, France.

N Javaud (N)

AP-HP, Urgences, CréAk, Hôpital Louis Mourier, Université Paris 7, Colombes, France.

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