Abstract

BackgroundTo report the outcomes of vitreous hemorrhage (VH) associated with hemorrhagic polypoidal choroidal vasculopathy (PCV).MethodsA retrospective study of 28 eyes of 27 consecutive patients of hemorrhagic PCV with VH, which were managed surgically between January 2003 and December 2011, was performed. All patients underwent pars plana vitrectomy for VH associated with PCV. The main outcome measure was best-corrected visual acuity (BCVA) at baseline, at 1, 3 and 6 months post operatively and at last follow up.ResultsThe visual acuity measured on early treatment diabetic retinopathy study (ETDRS) chart improved in 16 eyes (57.1 %) by two or more lines, remained unchanged in nine eyes (32.1 %) and decreased in three (10.7 %) after surgery when compared to baseline VA. The mean baseline VA was 2.69 ± 0.57 logMAR units (<20/2000) which improved to 1.65 ± 0.93 logMAR units (20/800) at 1 month post operative visit and was sustained at 1.72 ± 1.12 (20/800) with an improvement of 0.96 logMAR units (p < 0.001, 95 % CI 0.54–1.37). The average postoperative follow up was for 14.2 months (range 1–84). The complications noted in postoperative follow up were cataract (n = 10), macular scaring (n = 9), organised dehemoglobinised blood (n = 7), retinal tear or detachment (n = 5), recurrent VH (n = 3) and choroidal detachment (n = 1).ConclusionMajority of patients with loss of vision due to VH secondary to hemorrhagic PCV have sustained improvement in visual acuity following surgery.

Highlights

  • To report the outcomes of vitreous hemorrhage (VH) associated with hemorrhagic polypoidal choroidal vasculopathy (PCV)

  • In the current study we report the incidence, clinical characteristics, management and surgical outcome in haemorrhagic PCV presenting with vitreous haemorrhage

  • Medical records of all cases having a diagnosis ICD coding of PCV and vitreous haemorrhage who underwent pars plana vitrectomy (PPV) were identified and studied

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Summary

Introduction

To report the outcomes of vitreous hemorrhage (VH) associated with hemorrhagic polypoidal choroidal vasculopathy (PCV). Polypoidal choroidal vasculopathy (PCV) is a persistent and chronic disease with a variable course [1]. Leakage in the vessel wall at dilatations leads to serous pigment epithelial detachments (PED) and lipid deposition in the exudative form. Narayanan et al Int J Retin Vitr (2015) 1:25 of PCV while recurrent serosanguinous detachments of the retinal pigment epithelium and neurosensory retina are the predominant manifestation of hemorrhagic PCV. Massive hemorrhages may develop from rupture of venules and occasionally arteries. Sequelae of this is a sudden onset severe visual loss due to break through vitreous hemorrhage (VH) [1, 6,7,8,9,10]

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