Purpose: To describe the clinical features of persons who developed central retinal vein occlusion (CVO) while being treated with Coumadin for chronic anticoagulation.
Methods: In a retrospective, comparative, noninterventional case series of patients diagnosed with CVO while being treated with Coumadin as a systemic anticoagulant, visual and anatomical outcomes were compared with those for a cohort of patients diagnosed with CVO who were not treated with any systemic anticoagulation.
Results: Fourteen eyes of 14 patients treated with Coumadin were identified. At presentation, the median international normalization ratio (INR) was 2.20 (range, 1.3-5.0). Eight patients (57%) had a therapeutic INR at the time of CVO. Their visual acuity and perfusion status were similar to those of patients with subtherapeutic INR. At the last follow-up (median, 16 months), visual acuity and perfusion status of the group of 14 eyes were similar to baseline findings (P = 0.62). Clinical features and outcomes were similar to those for a cohort of patients with CVO who were not being treated with systemic anticoagulation.
Conclusion: CVO can occur in patients being treated with Coumadin for systemic anticoagulation. Final visual acuity and perfusion status were similar to those in a cohort of patients with CVO who were not treated with Coumadin. Although visual acuity is unaffected, ensuring that the INR for these patients remains in the therapeutic range may be important to help prevent secondary systemic thrombotic and embolic disease.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1097/00006982-200603000-00006 | DOI Listing |
J Vasc Surg Venous Lymphat Disord
November 2024
CHU Sud Reunion, Site Alfred Isautier, Chirurgie Vasculaire, Saint-Pierre, France.
Objective: Central vein occlusion (CVO) is a significant complication in patients undergoing chronic hemodialysis, often leading to dialysis inefficacy, disabling symptoms, and, most critically, major risk of access failure. Although stenting has been proposed as a technique to maintain vascular access patency following the recanalization of occluded central veins, the data supporting its long-term efficacy remains limited. This study aims to evaluate the long-term effectiveness of stenting occluded superior vena cava (SVC) and/or brachiocephalic veins to preserve vascular access patency, ensure continued dialysis efficacy, and relieve SVC syndrome.
View Article and Find Full Text PDFBMC Pulm Med
October 2024
Boehringer Ingelheim Pharmaceuticals, Inc, Ridgefield, CT, USA.
Background: The Myositis Interstitial Lung Disease Nintedanib Trial (MINT) is a hybrid trial, which is enrolling patients both at local sites and remotely via a decentralised site. The trial will investigate the efficacy and safety of nintedanib in patients with progressive myositis-associated interstitial lung disease (MA-ILD).
Methods/design: MINT is an exploratory, prospective randomised placebo-controlled trial.
Int J Gen Med
October 2024
Department of Emergency, The First People's Hospital of Changde City, Changde, Hunan Province, People's Republic of China.
Eur J Vasc Endovasc Surg
October 2024
St Joseph Heart & Vascular Centre, Orange, CA, USA.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!