intravitreal bevacizumab for symptomatic retinal arterial macroaneurysm

1
CORRESPONDENCE Intravitreal Bevacizumab for Symptomatic Retinal Arterial Macroaneurysm EDITOR: I OFFER THE FOLLOWING OBSERVATIONS REGARDING THE recent study by Cho and associates. 1 Intravitreal bevacizumab for exudative complications of retinal artery macroaneurysm was first reported in 2009. 2 Since then, there have been several reports indicating benefit from intravitreal bavacizu- mab for both hemorrhagic and exudative complications of retinal artery macroaneurysm. 1,3 However, there seems to be little benefit or rationale for such therapy for subfoveal hemorrhage from ruptured retinal artery macroaneurysm. Hemorrhage from retinal artery macroaneurysm, unlike exudation, which is a continuous process that can be demonstrated by leakage on fluorescein angiography, is generally a one-time event that commonly leads to fibrosis and occlusion of retinal artery macroaneurysm. Visual loss usually results from atrophy of retinal pigment epithelium owing to well-established toxicity of subfoveal blood. 4 Both patients in the present study (Patients 10 and 12) who presented with subfoveal bleed suffered further loss of vision > _0.3 logMAR because of retinal pigment epithelial atrophy. Bevacizumab-induced clearing of blood in 4 weeks, as opposed to 8 weeks natural history as reported by the authors, might still be too slow to prevent irreversible damage to pho- toreceptors. 4 Thus, early evacuation of subfoveal blood offers the best chance for improvement in vision in such eyes. Since the initial report of tissue plasminogen activator–assisted evacuation of submacular blood from ruptured retinal artery macroaneurysm, 5 excellent visual outcomes have been reported with this approach by others. Each of the 9 eyes achieved significant improvement in vision with tissue plasminogen-assisted removal of blood without any laser treatment to the retinal artery macroaneurysm. 6 KAMAL KISHORE Peoria, Illinois CONFLICT OF INTEREST DISCLOSURES: THE AUTHOR HAS completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest and none were reported. REFERENCES 1. Cho HJ, Rhee TK, Kim HS, et al. Intravitreal bevacizumab for symptomatic retinal arterial macroaneurysm. Am J Ophthalmol 2013;155(5):898–904. 2. Chanana B, Azad RV. Intravitreal bevacizumab for macular edema secondary to retinal macroaneurysm. Eye (Lond) 2009;23(2):493–494. 3. Javey G, Moshfeghi AN, Moshfeghi AA. Management of ruptured retinal arterial macroaneurysm with intravitreal bevacizumab. Ophthalmic Surg Lasers Imaging 2010;41(4):1–5. 4. Glatt H, Machemer R. Experimental subretinal hemorrhage in rabbits. Am J Ophthalmol 1982;94(6):762–773. 5. Peyman GA, Nelson NC Jr, Alturki W, et al. Tissue plasmin- ogen activating factor assisted removal of subretinal hemor- rhage. Ophthalmic Surg 1991;22(10):575–582. 6. Humayun M, Lewis H, Flynn HW Jr, Sternberg P Jr, Blumenkranz MS. Management of submacular hemorrhage associated with retinal arterial macroaneurysms. Am J Ophthal- mol 1998;126(3):358–361. REPLY WE APPRECIATE DR KISHORE’S INTEREST IN OUR RECENTLY published manuscript. 1 He questioned the use of bevacizu- mab (1.25 mg/0.05 mL; Avastin; Genentech Inc, San Francisco, California, USA) for the treatment of subfoveal hemorrhage secondary to retinal arterial macroaneurysm and stated that it has limited benefits. We agree that beva- cizumab monotherapy could be insufficient for submacular hemorrhage treatment. He noted that in our study, 2 (Patients 10 and 12) out of 4 patients with submacular hemorrhage showed poor visual outcomes after bevaci- zuamb injections. However, there were also patients with good visual outcomes in spite of submacular hemorrhage after treatment. In our study, in 2 patients (Patients 14 and 19) with submacular hemorrhage, the visual acuity increased by more than 0.3 logarithm of the minimal angle of resolution (logMAR) after treatment. 1 To date, the pre- cise treatment effects or anti–vascular endothelial growth factor mechanisms for submacular hemorrhage have not yet been clearly elucidated. Various factors, including symptom duration, submacular hemorrhage size, or subfo- veal hemorrhage thickness, could be associated with the efficacy of bevacizumab injection for the submacular hem- orrhage. The factors associated with a good visual outcome after bevacizumab injection for patients with submacular hemorrhage require further investigation. Dr Kishore mentioned that recombinant tissue plasmin- ogen activator (rTPA) may be effective in retinal arterial macroaneurysm treatment. However, the minimum safe concentration and retinal toxicity of rTPA is still contro- versial. 2 Moreover, some reports suggest that cases with submacular hemorrhage secondary to retinal arterial macro- aneurysm have an increased risk of dense vitreous hemor- rhage after intravitreal rTPA injection. 3 Furthermore, if 260 0002-9394/$36.00 http://dx.doi.org/10.1016/j.ajo.2013.08.021 Ó 2014 BY ELSEVIER INC.ALL RIGHTS RESERVED.

Upload: kamal

Post on 30-Dec-2016

212 views

Category:

Documents


0 download

TRANSCRIPT

CORRESPONDENCE

Intravitreal Bevacizumab forSymptomatic Retinal ArterialMacroaneurysm

EDITOR:

I OFFER THE FOLLOWING OBSERVATIONS REGARDING THE

recent study by Cho and associates.1 Intravitreal bevacizumabfor exudative complications of retinal artery macroaneurysmwas first reported in 2009.2 Since then, there have beenseveral reports indicating benefit from intravitreal bavacizu-mab for both hemorrhagic and exudative complications ofretinal artery macroaneurysm.1,3 However, there seems tobe little benefit or rationale for such therapy for subfovealhemorrhage from ruptured retinal artery macroaneurysm.Hemorrhage from retinal artery macroaneurysm, unlikeexudation, which is a continuous process that can bedemonstrated by leakage on fluorescein angiography, isgenerally a one-time event that commonly leads to fibrosisand occlusion of retinal artery macroaneurysm. Visual lossusually results from atrophy of retinal pigment epitheliumowing to well-established toxicity of subfoveal blood.4 Bothpatients in the present study (Patients 10 and 12) whopresented with subfoveal bleed suffered further loss of vision>_0.3 logMAR because of retinal pigment epithelial atrophy.Bevacizumab-induced clearing of blood in 4 weeks, asopposed to 8 weeks natural history as reported by the authors,might still be too slow to prevent irreversible damage to pho-toreceptors.4 Thus, early evacuation of subfoveal blood offersthe best chance for improvement in vision in such eyes. Sincethe initial report of tissue plasminogen activator–assistedevacuation of submacular blood from ruptured retinal arterymacroaneurysm,5 excellent visual outcomes have beenreported with this approach by others. Each of the 9 eyesachieved significant improvement in vision with tissueplasminogen-assisted removal of blood without any lasertreatment to the retinal artery macroaneurysm.6

KAMAL KISHORE

Peoria, Illinois

CONFLICT OF INTEREST DISCLOSURES: THE AUTHOR HAScompleted and submitted the ICMJE Form for Disclosure of PotentialConflicts of Interest and none were reported.

REFERENCES

1. Cho HJ, Rhee TK, Kim HS, et al. Intravitreal bevacizumab forsymptomatic retinal arterial macroaneurysm. Am J Ophthalmol2013;155(5):898–904.

260 � 2014 BY ELSEVIER INC.

2. Chanana B, Azad RV. Intravitreal bevacizumab for macularedema secondary to retinal macroaneurysm. Eye (Lond)2009;23(2):493–494.

3. Javey G, Moshfeghi AN, Moshfeghi AA. Management ofruptured retinal arterial macroaneurysm with intravitrealbevacizumab. Ophthalmic Surg Lasers Imaging 2010;41(4):1–5.

4. Glatt H, Machemer R. Experimental subretinal hemorrhage inrabbits. Am J Ophthalmol 1982;94(6):762–773.

5. Peyman GA, Nelson NC Jr, Alturki W, et al. Tissue plasmin-ogen activating factor assisted removal of subretinal hemor-rhage. Ophthalmic Surg 1991;22(10):575–582.

6. Humayun M, Lewis H, Flynn HW Jr, Sternberg P Jr,Blumenkranz MS. Management of submacular hemorrhageassociated with retinal arterial macroaneurysms.Am J Ophthal-mol 1998;126(3):358–361.

REPLY

WE APPRECIATE DR KISHORE’S INTEREST IN OUR RECENTLY

published manuscript.1 He questioned the use of bevacizu-mab (1.25 mg/0.05 mL; Avastin; Genentech Inc, SanFrancisco, California, USA) for the treatment of subfovealhemorrhage secondary to retinal arterial macroaneurysmand stated that it has limited benefits. We agree that beva-cizumab monotherapy could be insufficient for submacularhemorrhage treatment. He noted that in our study, 2(Patients 10 and 12) out of 4 patients with submacularhemorrhage showed poor visual outcomes after bevaci-zuamb injections. However, there were also patients withgood visual outcomes in spite of submacular hemorrhageafter treatment. In our study, in 2 patients (Patients 14and 19) with submacular hemorrhage, the visual acuityincreased by more than 0.3 logarithm of the minimal angleof resolution (logMAR) after treatment.1 To date, the pre-cise treatment effects or anti–vascular endothelial growthfactor mechanisms for submacular hemorrhage have notyet been clearly elucidated. Various factors, includingsymptom duration, submacular hemorrhage size, or subfo-veal hemorrhage thickness, could be associated with theefficacy of bevacizumab injection for the submacular hem-orrhage. The factors associated with a good visual outcomeafter bevacizumab injection for patients with submacularhemorrhage require further investigation.Dr Kishore mentioned that recombinant tissue plasmin-

ogen activator (rTPA) may be effective in retinal arterialmacroaneurysm treatment. However, the minimum safeconcentration and retinal toxicity of rTPA is still contro-versial.2 Moreover, some reports suggest that cases withsubmacular hemorrhage secondary to retinal arterial macro-aneurysm have an increased risk of dense vitreous hemor-rhage after intravitreal rTPA injection.3 Furthermore, if

0002-9394/$36.00http://dx.doi.org/10.1016/j.ajo.2013.08.021

ALL RIGHTS RESERVED.