CATASTROPHIC ANTIPHOSPHOLIPID SYNDROME AND POSTERIOR OCULAR INVOLVEMENT: Case Series of 11 Patients and Literature Review
To describe the posterior ophthalmic manifestations of catastrophic antiphospholipid syndrome. Retrospective case series of patients presenting with catastrophic antiphospholipid syndrome and posterior segment ocular manifestations. The main outcomes were the type of posterior segment manifestations...
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Published in | Retina (Philadelphia, Pa.) Vol. 41; no. 11; p. 2332 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
01.11.2021
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Abstract | To describe the posterior ophthalmic manifestations of catastrophic antiphospholipid syndrome.
Retrospective case series of patients presenting with catastrophic antiphospholipid syndrome and posterior segment ocular manifestations. The main outcomes were the type of posterior segment manifestations at catastrophic antiphospholipid syndrome diagnosis, specifically retinal vascular occlusion, vasculitis, or choroidopathy, and the final best-corrected visual acuity.
This study included 23 patients (11 cases treated by the authors and 12 published case reports); 21 (91%) of them female. Their median age at diagnosis was 28 years (range, 16-79 years). Ophthalmologic manifestations were usually bilateral (n = 19, 83%) and involved vascular occlusive retinopathy (n = 17, 74%), choroidopathy (n = 11, 48%), or retinal vasculitis (n = 1, 4%). Final best-corrected visual acuity was not significantly worse than the best-corrected visual acuity at diagnosis (P = 0.16). Retinal vascular occlusions were associated with poorer final visual acuity than choroidopathy (P = 0.002). After a median follow-up of 14 months (range, 2-132 months), nearly half the patients (n = 11, 48%) had permanent vision loss including best-corrected visual acuity of <20/400 for 4 patients.
Posterior ophthalmic manifestations of catastrophic antiphospholipid syndrome were mainly bilateral retinal vascular occlusion, which had the worst visual prognosis, followed by choroidopathy and retinal vasculitis. Permanent visual loss was common. |
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AbstractList | To describe the posterior ophthalmic manifestations of catastrophic antiphospholipid syndrome.
Retrospective case series of patients presenting with catastrophic antiphospholipid syndrome and posterior segment ocular manifestations. The main outcomes were the type of posterior segment manifestations at catastrophic antiphospholipid syndrome diagnosis, specifically retinal vascular occlusion, vasculitis, or choroidopathy, and the final best-corrected visual acuity.
This study included 23 patients (11 cases treated by the authors and 12 published case reports); 21 (91%) of them female. Their median age at diagnosis was 28 years (range, 16-79 years). Ophthalmologic manifestations were usually bilateral (n = 19, 83%) and involved vascular occlusive retinopathy (n = 17, 74%), choroidopathy (n = 11, 48%), or retinal vasculitis (n = 1, 4%). Final best-corrected visual acuity was not significantly worse than the best-corrected visual acuity at diagnosis (P = 0.16). Retinal vascular occlusions were associated with poorer final visual acuity than choroidopathy (P = 0.002). After a median follow-up of 14 months (range, 2-132 months), nearly half the patients (n = 11, 48%) had permanent vision loss including best-corrected visual acuity of <20/400 for 4 patients.
Posterior ophthalmic manifestations of catastrophic antiphospholipid syndrome were mainly bilateral retinal vascular occlusion, which had the worst visual prognosis, followed by choroidopathy and retinal vasculitis. Permanent visual loss was common. |
Author | Piette, Jean-Charles Haroche, Julien Pérard, Laurent Mehawej, Hanane Maillard, Nicolas Roumier, Mathilde Godeau, Bertrand Morel, Nathalie Brezin, Antoine Benhamou, Ygal Bodaghi, Bahram Le Guern, Véronique Costedoat-Chalumeau, Nathalie Bonnet, Clémence Yelnik, Cécile M Lambert, Marc |
Author_xml | – sequence: 1 givenname: Nathalie surname: Morel fullname: Morel, Nathalie organization: AP-HP, Cochin Hospital, Internal Medicine Department, Centre de Référence Maladies Auto-immunes et Systémiques Rares de l'Ile de France, AP-HP, Cochin Hospital, Paris, France – sequence: 2 givenname: Clémence surname: Bonnet fullname: Bonnet, Clémence organization: Ophthalmology Department, AP-HP, Cochin Hospital, Paris, France – sequence: 3 givenname: Hanane surname: Mehawej fullname: Mehawej, Hanane organization: AP-HP, Cochin Hospital, Internal Medicine Department, Centre de Référence Maladies Auto-immunes et Systémiques Rares de l'Ile de France, AP-HP, Cochin Hospital, Paris, France – sequence: 4 givenname: Véronique surname: Le Guern fullname: Le Guern, Véronique organization: AP-HP, Cochin Hospital, Internal Medicine Department, Centre de Référence Maladies Auto-immunes et Systémiques Rares de l'Ile de France, AP-HP, Cochin Hospital, Paris, France – sequence: 5 givenname: Laurent surname: Pérard fullname: Pérard, Laurent organization: Centre Hospitalier Saint Joseph Saint Luc, Internal Medicine Department, Centre Hospitalier Saint Joseph Saint Luc, Lyon, France – sequence: 6 givenname: Mathilde surname: Roumier fullname: Roumier, Mathilde organization: Internal Medicine Department, Foch Hospital, Suresnes, France – sequence: 7 givenname: Antoine surname: Brezin fullname: Brezin, Antoine organization: Ophthalmology Department, AP-HP, Cochin Hospital, Paris, France – sequence: 8 givenname: Bertrand surname: Godeau fullname: Godeau, Bertrand organization: Internal Medicine Department, AP-HP, Henri Mondor Hospital, Creteil, France – sequence: 9 givenname: Julien surname: Haroche fullname: Haroche, Julien organization: Internal Medicine Department, Centre de Référence Maladies Auto-immunes et Systémiques Rares de l'Ile de France, AP-HP, Louisiana Pitié-Salpêtrière Hospital, Paris, France – sequence: 10 givenname: Ygal surname: Benhamou fullname: Benhamou, Ygal organization: Department of Internal Medicine, Vascular and Thrombosis Unit, Normandie Université, UNIROUEN, Rouen University Hospital, Rouen, France – sequence: 11 givenname: Marc surname: Lambert fullname: Lambert, Marc organization: Internal Medicine Department, Centre National de Référence Maladies Systémiques et Auto-Immunes Rares, European Reference Network on Rare Connective Tissue and Musculoskeletal Diseases (ReCONNECT), University Lille, INSERM U1167, CHU Lille, Lille, France – sequence: 12 givenname: Cécile M surname: Yelnik fullname: Yelnik, Cécile M organization: Internal Medicine Department, Centre National de Référence Maladies Systémiques et Auto-Immunes Rares, European Reference Network on Rare Connective Tissue and Musculoskeletal Diseases (ReCONNECT), University Lille, INSERM U1167, CHU Lille, Lille, France – sequence: 13 givenname: Nicolas surname: Maillard fullname: Maillard, Nicolas organization: Department of Internal Medicine, CHU, de Saint-Etienne, France; and – sequence: 14 givenname: Bahram surname: Bodaghi fullname: Bodaghi, Bahram organization: Internal Medicine Department, Centre de Référence Maladies Auto-immunes et Systémiques Rares de l'Ile de France, AP-HP, Louisiana Pitié-Salpêtrière Hospital, Paris, France – sequence: 15 givenname: Jean-Charles surname: Piette fullname: Piette, Jean-Charles organization: Internal Medicine Department, Centre de Référence Maladies Auto-immunes et Systémiques Rares de l'Ile de France, AP-HP, Louisiana Pitié-Salpêtrière Hospital, Paris, France – sequence: 16 givenname: Nathalie surname: Costedoat-Chalumeau fullname: Costedoat-Chalumeau, Nathalie organization: AP-HP, Cochin Hospital, Internal Medicine department, Centre de référence maladies auto-immunes et systémiques rares de l'Ile de France, INSERM U 1153, Center for Epidemiology and Statistics, Sorbonne Paris Cité (CRESS), Université Paris Descartes-Sorbonne Paris Cité, Paris, France |
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SubjectTerms | Adolescent Adult Aged Antiphospholipid Syndrome - complications Female Fluorescein Angiography - methods Fundus Oculi Humans Male Middle Aged Retrospective Studies Severity of Illness Index Tomography, Optical Coherence - methods Vision Disorders - diagnosis Vision Disorders - etiology Visual Acuity Young Adult |
Title | CATASTROPHIC ANTIPHOSPHOLIPID SYNDROME AND POSTERIOR OCULAR INVOLVEMENT: Case Series of 11 Patients and Literature Review |
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