Figs. 1 & 2. Relevant posterior segment findings.

Discussion
Additional studies included examination B scan ultrasonography.

The diagnosis in this issue is blood staining of the posterior lens capsule secondary to vitreous hemorrhage secondary to retinal vein occlusion.

Branch retinal vein occlusion (BRVO) is a commonly encountered intraretinal vascular event.^1-3 Reports on retinal vasculopathy recognize its prevalence second only to diabetic retinopathy.^2,3 Patients who are symptomatic, typically present with a chief complaint of painless blurry vision in one eye, although vein occlusion can occur bilaterally.^1-4 Since the disease itself is often the result of the systemic and local genetic factors that induced the event, there is no gender predilection, there is no racial preference and there are no concrete epidemiologic data as that information is subcategorized to the specific diseases that increase its risk.^3,5  

Retinal vein occlusions are categorized as nonischemic BRVO, which permit vascular perfusion, and ischemic BRVO, which produce vascular stasis, limiting blood circulation. Patients who present with large, ischemic BRVO may present with an afferent papillary defect. Patients with ischemic BRVO where the macula is involved may have significantly reduced visual acuity with a poorer prognosis than their nonischemic counterparts.⁶ In contradistinction, patients presenting with nonischemic BRVO may have minimal to no functional interruptions. In general, BRVO has a good prognosis.^1-6 

The retinal observations seen in BRVO include dilated, tortuous retinal veins, sectoral, flame-shaped intraretinal hemorrhages, variable local patches of retinal ischemia (cotton wool infarcts), intraretinal exudates, and variable retinal or macular edema or both.^3,6 The site of the occlusion can typically be observed at or just adjacent to the site of an arteriovenous crossing where retinal arteries and veins share a common adventitial sheath.¹ Here, an increased (broadened) retinal arteriolar reflex can be seen connoting ongoing general vascular arteriolar and atheromatous vascular decompensation along with venous nicking, representing the mechanical forces applied by the overlying vessel.^3,7 Complications which can be observed following a BRVO include variable retinal edema, macular edema, capillary nonperfusion, retinal neovascularization, vitreous hemorrhage and tractional retinal detachment.^7,8

Fig. 3. The patient’s ultrasound. Do these images hint at a diagnosis?

Upwards of 50% to 60% of eyes recover a final visual acuity of 20/40 or better without treatment.⁸ The entity rarely occurs idiopathically, rather it is frequently associated with systemic coagulopathy, hyperviscosity, infection, inflammation, hypertension, diabetes mellitus, dyslipidemia, antiphospholipid antibody syndromes, cardiac and carotid etiologies.^1-9 Since most branch retinal vein occlusions resolve without sequellae, requiring no treatment, the most important initial step in formulating a management plan is to commit to discovering the underlying cause.^1-9 

The provoking mechanism of BRVO is classically related to disorders of the blood tissue (blood dyscrasias) which incite platelet aggregation through coagulopathy syndromes or hyperviscosity syndromes or by mechanical mechanisms (venous compression secondary to an overlying artery’s expansion and hardening via atheromatous formation) which extinguishes forward venous blood flow.^3,7 This causes the venous wall to be overcome by the forces of an abnormal volume with in its lumen. As the walls of the vessel decompensate, deoxygenated venous blood gains access to the retina via the nerve fiber layer, where the large caliber retinal veins reside.^3,7 This produces an inflammatory and immunological reaction in the affected tissue.^1,6 The discontinuation of venous blood flow also interrupts the arterial blood flow; blocked venous egress leaves no direct pathway for the venous blood or arterial blood to proceed.^3-7 The overall flow in both systems becomes sluggish as the blood is forced through other anastamoses around the formed thrombus.^1-11 The deoxygenated blood introduced into retinal tissues, along with other chemokines, cytokines and cellular players initiates tissue demolition in preparation for repair.^1,5,6-9 These active substances as well as the setting of an ischemic environment can provoke the release of a vasoproliferative messengers known as vascular endothelial growth factors (VEGF).^12,13 This category of substances stimulates new vessel growth by inducing neovascular “budding” off of existing arterial tissues. These new vessels lack normal architecture, become “scaffolded” to the vitreous body and have the potential to cause pre-retinal or vitreous hemorrhage and tractional retinal detachment.¹⁴

Since the pathophysiology of the event itself is painless, the symptomatology in these cases is directly related to interrupted function. In the initial stages, this is the direct effect of the light being blocked from reaching the photoreceptors. In cases where chronic, inner-retinal ischemia develops, capillary occlusion can result secondary to failed vascular “push.” Here increased hydrostatic (back) pressure in the vessels becomes transmitted to the capillary bed causing effected areas of the retina to become malnourished and hypoxic.  This creates an environment conducive to retinal cellular death and persistent edema, both deleterious to function.⁷ 

All vein occlusion patients should be assessed both ocularly and systemically.³ While intraretinal neovascular formation is uncommon in cases involving branch retinal venous occlusion, ischemic processes are plausible, requiring the tissue to be observed through complete resolution.^1,3 Systemic laboratory testing should include: blood pressure evaluation, complete blood count (CBC), Westergren sedimentation rate (ESR), fasting treponemal antibody absorption test (FTA-Abs), reactive plasma regain (RPR), lipid profile and fasting blood sugar (FBS), homosystein, protein S and protein C, lupus anticoagulant, electocardiogram (EKG) and in appropriate cases carotid doppler testing.^3,11 Infectious and inflammatory diseases have also been reported as sources for branch vein occlusion. Testing for sarcoidosis, tuberculosis, rheumatoid arthritris and lyme infection should be considered when vascular risks are small or laboratory work returns negative.^15-17 

While rare and dependent on the extent and location of the induced retinal ischemia, clinicians should monitor the IOP and iris for signs of rubeosis irides (iris/angle neovascularization).¹⁸ In the rare event a secondary glaucoma develops cycloplegics, topical steriods and oral/topical ocular hypotensives are required along with laser therapy.

The retinal treatment for all forms of vein occlusion is aimed at minimizing the loss of acuity from macular edema and preventing neovascularization.^19-23 Clincal management for BRVO is guided by the classic works of The National Institutes of Health, National Eye Institute.  These include the Branch Retinal vein Occlusion Study (BRVOS) and The Standard Care versus Corticosteriod Treatment for Branch Vein Occlusion (SCORE) studies.^21-23

Results from the 8-year BRVOS determined that prophylactic scatter argon laser photocoagulation (panretinal photocoagulation–PRP) would not prevent the development of neovascularization or vitreous hemorrhage in cases of BRVO and that macular argon laser photocoagulation (grid or focal photocoagulation) could improve visual acuity in eyes with persistent macular edema following branch retinal vein occlusion where vision was 20/40 or worse following the resolution of the event.^21,22 Importantly, pan retinal laser photogogulation was found to be of benefit once neovasculaization was observed, significantly reducing the likelihood of vitreous hemorrhage by 30%.²¹ This modality of treatment remains the standard of care.

The SCORE study was designed to compare the effectiveness and safety of between the standard care of BRVO (grid and focal laser photocoagulation) and intravitreal injection of triamcinolone for treating macular edema associated with both branch and central retinal vein occlusion (CRVO).²³ The results of the trial found that there was no benefit for improving visual acuity for the steroid group compared to the standard care group in cases of BRVO.²²  Interestingly, rates of adverse events (particularly elevated intraocular pressure and cataract) were increased in the steroid group receiving the 4mg injection.²² The study concluded that grid or focal photocoagulation should remain the standard of care for the  treatment of macular edema secondary to BRVO compared against intravitreal steroids alone.²³ New studies have demonstrated renewed support for the use of intrivitreal steroid preparations in combination with VEGF ibnhibitors.^24-26 

New treatment possibilities are being explored consistent with the VEGF inhibitor revolution for all kinds of retinal vascular diseases.^11,27-31 A recently published report investigated 12-month follow-up results of intravitreal bevacizumab therapy for macular edema secondary to branch retinal vein occlusion.^24-27 With a mean number of injections at two, ranging from one to four, the study demonstrated a benefit for all patients with younger patients having the best visual acuity improvement during and after the 12 month follow up period.²⁴ Better pretreatment visual acuity was associated with better visual acuity at 12 months, but with less improvement of the visual acuity.^11,27 The researchers have opened the door for considering all VEGF inhibitors alone or in combination with other accepted treatments as a long-term effective treatment for macular edema secondary to BRVO.^11,27-31

In summary:

1. Optical coherence tomography (OCT) is an excellent adjunct to observation for diagnosing intraretinal tissue abnormalities,
2. While neovascularization of the iris (rubeosis) and retina are rare, branch retinal vein occlusions should be monitored every four to six weeks for the first four months to rule out related complications.³ 

While elevated intraocular pressure (IOP), especially in patients with undiagnosed or poorly controlled glaucoma is reportedly  a significant risk factor for developing central and hemiretinal venous occlusion, it seems less of a risk factor in the development of BRVO.⁴

Lowering IOP provides little benefit in involved eyes whose IOP is already normal (10mm Hg to 22mm Hg). Laboratory testing for inflammatory and infectious disorders might include an angiotensin converting enzyme study (ACE) and gallium scan for sarcoidosis, a chest X-ray (CXR) for tuberculosis and sarcoidosis, a lyme titre for lyme disease, antinuclear antibody testing for lupus and rheumatoid factor for arthritic disease.³