TY - JOUR
T1 - Characteristics and long-term outcome of patients with noninfectious retinal vasculitis
AU - Shulman, Shiri
AU - Kramer, Michal
AU - Amer, Radgonde
AU - Sorkin, Nir
AU - Schaap-Fogler, Michal
AU - Rosenblatt, Amir
AU - Habot-Wilner, Zohar
PY - 2015
Y1 - 2015
N2 - Purpose: To investigate the characteristics and long-term outcome of patients with noninfectious retinal vasculitis. Methods: This was a retrospective multicenter study. Main outcome measures included patients' characteristics, ocular findings, treatment modalities, and best-corrected visual acuity. All patients had at least 12-month follow-up time. Results: Eighty-two eyes (45 patients) were included. Median follow-up was 46 months (range, 12-210 months). At presentation, 12 of the 45 patients (26.6%) had a known associated systemic or ocular disease. A diagnosis of a new systemic disease was found in additional 14 of 33 patients (42.5%) and birdshot chorioretinopathy in 3 of 33 patients (9.1%). The most common systemic disease was Behcet disease (17/24 patients; 70.8%). Laboratory tests had a low diagnostic value. The most common clinical findings were vitritis (58.5%) and perivascular sheathing (50.5%). Most patients were treated with immunosuppressive medications. Mean best-corrected visual acuity improved significantly during follow-up, patients with Behcet disease and worse visual acuity at baseline were more likely to have visual acuity improvement (P , 0.001). Conclusion: A new systemic or ocular disease associated with retinal vasculitis was found in more than half of the patients. Behcet disease was the most common newly diagnosed disease. Specific diagnosis leading to proper management is important to maintain favorable long-term visual outcome.
AB - Purpose: To investigate the characteristics and long-term outcome of patients with noninfectious retinal vasculitis. Methods: This was a retrospective multicenter study. Main outcome measures included patients' characteristics, ocular findings, treatment modalities, and best-corrected visual acuity. All patients had at least 12-month follow-up time. Results: Eighty-two eyes (45 patients) were included. Median follow-up was 46 months (range, 12-210 months). At presentation, 12 of the 45 patients (26.6%) had a known associated systemic or ocular disease. A diagnosis of a new systemic disease was found in additional 14 of 33 patients (42.5%) and birdshot chorioretinopathy in 3 of 33 patients (9.1%). The most common systemic disease was Behcet disease (17/24 patients; 70.8%). Laboratory tests had a low diagnostic value. The most common clinical findings were vitritis (58.5%) and perivascular sheathing (50.5%). Most patients were treated with immunosuppressive medications. Mean best-corrected visual acuity improved significantly during follow-up, patients with Behcet disease and worse visual acuity at baseline were more likely to have visual acuity improvement (P , 0.001). Conclusion: A new systemic or ocular disease associated with retinal vasculitis was found in more than half of the patients. Behcet disease was the most common newly diagnosed disease. Specific diagnosis leading to proper management is important to maintain favorable long-term visual outcome.
KW - Behcet disease
KW - Immunosuppressive treatment
KW - Noninfectious retinal vasculitis
KW - Posterior uveitis
KW - Retinal vasculitis
UR - http://www.scopus.com/inward/record.url?scp=84948455455&partnerID=8YFLogxK
U2 - 10.1097/IAE.0000000000000623
DO - 10.1097/IAE.0000000000000623
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C2 - 26035402
AN - SCOPUS:84948455455
SN - 0275-004X
VL - 35
SP - 2633
EP - 2640
JO - Retina
JF - Retina
IS - 12
ER -