|Year : 2017 | Volume
| Issue : 6 | Page : 482-487
Tissue plasminogen activator-assisted vitrectomy for submacular hemorrhage due to age-related macular degeneration
Mustafa Gok1, V Levent Karabaş2, Mehmet S Aslan3, Özgür Kara4, Süleyman Karaman5, Fatih Yenihayat2
1 Department of Ophthalmology, Ministry of Health, Ordu University Research and Training Hospital, Ordu, Turkey
2 Department of Ophthalmology, Medical School, Kocaeli University, Kocaeli, Turkey
3 Department of Ophthalmology, Arnavutköy Government Hospital, İstanbul, Turkey
4 Department of Ophthalmology, Fatsa Government Hospital, Ordu, Turkey
5 Department of Ophthalmology, Ağrı State Hospital, Ağrı, Turkey
|Date of Submission||22-Apr-2016|
|Date of Acceptance||22-May-2017|
|Date of Web Publication||23-Jun-2017|
Department of Ophthalmology, Ministry of Health, Ordu University Training and Research Hospital, 52200 Ordu
Source of Support: None, Conflict of Interest: None
Purpose: The purpose of this study was to evaluate the treatment efficacy of vitrectomy combined with subretinal recombinant tissue plasminogen activator (r-tPA) and factors affecting visual improvement in patients with submacular hemorrhage (SMH) due to neovascular age-related macular degeneration (nAMD). Materials and Methods: Medical records of 17 consecutive patients diagnosed with SMH secondary to nAMD were retrospectively reviewed. The initial surgical procedure involved a 23-gauge transconjunctival vitrectomy, subretinal r-tPA application through a self-sealing inferior retinotomy, and sulfur hexafluoride gas for tamponade in all patients. The duration, size, and thickness of the hemorrhage and the pre- and post-operative visual acuity (VA) using a Snellen chart were recorded. VA was converted to logMAR for statistical analysis. Results: The average duration and size of the SMH were 12.8 ± 18.2 days and 8.6 ± 5.3 disc areas, respectively. The mean follow-up time was 16.9 ± 4.7 months. A statistically significant visual improvement was found when comparing initial VA with postoperative best-corrected VA (BCVA) and final BCVA (Wilcoxon rank test, P ≤ 0.01). There was no significant correlation between the size of the hemorrhage and postoperative BCVA and final BCVA (Spearman's rho test). There was no statistically significant correlation between the initial VA and postoperative BCVA and final BCVA (Spearman's rho test). There was no significant correlation between the duration of hemorrhage and postoperative BCVA and final BCVA (Spearman's rho test). The preoperative thickness of hemorrhage (747.5 ± 30 μm) was not correlated with postoperative BCVA or final BCVA (Pearson's test). Conclusions: Vitrectomy combined with subretinal r-tPA injection and gas tamponade is an effective surgical intervention to preserve VA in selected patients with apparent SMH.
Keywords: Expansile gas, recombinant tissue plasminogen activator, subretinal hemorrhage, vitrectomy
|How to cite this article:|
Gok M, Karabaş V L, Aslan MS, Kara &, Karaman S, Yenihayat F. Tissue plasminogen activator-assisted vitrectomy for submacular hemorrhage due to age-related macular degeneration. Indian J Ophthalmol 2017;65:482-7
|How to cite this URL:|
Gok M, Karabaş V L, Aslan MS, Kara &, Karaman S, Yenihayat F. Tissue plasminogen activator-assisted vitrectomy for submacular hemorrhage due to age-related macular degeneration. Indian J Ophthalmol [serial online] 2017 [cited 2020 Apr 7];65:482-7. Available from: http://www.ijo.in/text.asp?2017/65/6/482/208872
The prognosis of untreated submacular hemorrhage (SMH) due to neovascular age-related macular degeneration (nAMD) and other causes is poor., Iron released from the hemorrhage as a result of the fibrinolytic process has a toxic effect on the photoreceptor cells and constitutes a mechanical barrier that prevents normal metabolism of the retina.
The use of recombinant tissue plasminogen activator (r-tPA) with various treatment approaches has been used for the treatment of SMH. In part of the submacular surgery trials (SSTs), direct subretinal surgery was performed for the evacuation of SMH with the use of r-tPA that involved a 45-min intraoperative waiting period for clot liquefaction. Retinal pigment epithelium (RPE) and photoreceptor injury as well as postoperative high retinal detachment rates were the disadvantages of this technique. In addition, there was no significant difference in visual improvement when comparing surgery and the long-term observation in the SST Group B.
Heriot described a less invasive technique “expansile gas technique” of intravitreal r-tPA injection for clot liquefaction following perfluoropropane gas for displacement of the SMH (Heriot WJ. Intravitreal gas and t-PA: An outpatient procedure for SMH. AAO Annual Vitreoretinal Update, 1996; Chicago, IL, USA). Subsequently, several studies have evaluated the anatomical and functional results of this approach.,,,,,,,
We treated our patients with a vitrectomy technique previously described by Haupert et al. Our surgical intervention involved vitrectomy, direct subretinal injection of r-tPA with a 41-gauge cannula through an inferior self-sealing retinotomy for clot liquefaction, and sulfur hexafluoride (SF6) gas for tamponade. In the following study, we evaluated the effects of both the surgical method and other prognostic parameters on the anatomical and functional results in the treatment of SMH caused by nAMD.
| Materials and Methods|| |
This study was approved by the local Ethics Committee and adhered to the tenets of the Declaration of Helsinki. In this retrospective, nonrandomized, consecutive case series, medical records of 17 patients presenting with SMH due to nAMD were reviewed. Informed consent forms were signed by all patients before the surgery. A complete ophthalmic examination was performed before the treatment, 1–7 days after surgery, and at 4–6-week intervals during follow-up. Biomicroscopy showed thick subretinal hemorrhage involving the foveal zone, causing an obvious elevation of the retina with obscuration of the RPE in all patients.
Baseline data such as age, sex, initial visual acuity (VA), and duration and dimension of the hemorrhage were recorded. Pre- and post-operative optical coherence tomography (OCT) images (including measurement of the central subfoveal thickness of the SMH) and color fundus photographs of the patients were taken. In addition, fundus fluorescein angiography (Heidelberg Spectralis HRA + OCT; Heidelberg Engineering, Heidelberg, Germany) was performed at the surgeon's discretion for certain visits. The central subfoveal thickness of the SMH was obtained by measuring the distance between the upper surface of the SMH and the inner surface of the RPE [Figure 1].
|Figure 1: (a) Preoperative color fundus photograph of a 67-year-old female patient presented with a thick submacular hemorrhage. (c) Preoperative optical coherence tomography image of the same patient. The subfoveal central height of submacular hemorrhage measured through manually considering most detectable foveal depression and a presumed retinal pigment epithelium line that connecting the evident retinal pigment epithelium at the both edge of the hemorrhage. (b) Postoperative color fundus photograph; total displacement of submacular hemorrhage have been achieved. (d) Postoperative optical coherence tomography image|
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All patients were treated by the same experienced vitreoretinal surgeon (VLK). After a 23-gauge three-port transconjunctival pars plana vitrectomy (Alcon Accurus ®; Alcon Laboratories, Fort Worth, TX, USA), a posterior vitreous detachment was created if not already present. Subretinal r-tPA (Actilyse; Boehringer, Ingelheim, Germany) was injected to the subretinal space through an inferior self-sealing retinotomy using a 41-gauge cannula at a concentration of 12.5 μg in 0.1 mL (injected volumes ranged from 0.05 to 0.15 mL) until sufficient retinal detachment was created in the posterior pole. After clot liquefaction, a complete fluid-air exchange was performed. SF6 gas (18% or 20%) was used for the tamponade. After surgery, patients remained in the prone position for a minimum of 3 days.
Eleven of the 17 eyes in the study were phakic, and 6 eyes were pseudophakic. During the follow-up, 5 (45%) patients were scheduled for phacoemulsification surgery because of cataract development. Patients with massive SMH extending to the equator, with vitreous hemorrhage, or with old khaki-colored hemorrhages were excluded from the study. Patients who could not tolerate the postoperative prone position were also excluded from the study.
VA was converted to logMAR for statistical analyses. At the discretion of the treating physician, postoperative photodynamic therapy and antivascular endothelial growth factor (anti-VEGF) agents were used to treat some patients because of reactivation of the lesions. Second surgeries were performed in two patients because of recurrence of SMH and rhegmatogenous retinal detachment (RRD) [Table 1].
The Shapiro–Wilk test was used to determine whether variables were distributed normally. The Wilcoxon signed-rank test was used to compare initial and final VA and OCT data. Pearson's test was used for the correlation analyses of normally distributed variables, and Spearman's rho test was used for the correlation analyses of nonnormally distributed variables. All values were expressed as means ± standard deviations, and values of P ≤ 0.05 were considered statistically significant.
| Results|| |
Of the 17 patients included in the study, 6 were male and 11 were female with a mean age of 70.8 ± 11.2 years (range, 49–90 years). The average duration of SMH was 12.8 ± 18.2 days. The size of the SMH ranged from 5 to 25 macular photocoagulation study disc areas, and the average size was 8.6 ± 5.3 disc areas. The mean follow-up time of patients was 16.9 ± 4.7 months. The demographic and pre- and post-operative baseline data of the patients are presented in [Table 2].
There was a statistically significant difference between the initial VA (mean logMAR, 1.8 ± 0.3) and the postoperative best-corrected VA (BCVA) (mean logMAR, 1.0 ± 0.5) and the final BCVA (mean logMAR, 0.97 ± 0.52) (Wilcoxon rank test, P ≤ 0.01). However, there was no statistically significant correlation between the initial VA and the postoperative BCVA (Spearman's rho test, r = 0.417, P = 0.096) or the final BCVA (Spearman's rho test, r = 0.227, P = 0.381). The VA improved by ≥2 lines in 8 (47%) patients, improved by 1 line in 4 (23.5%) patients, improved from CF ≤1 M to level of 1–5 M range in three patients (17.6%), remained unchanged in 1 (5.8%) patients (underlying old large scar), and worsened in 1 (5.8%) patient due to postoperative RRD. There was a significant difference in the comparison of pre- (mean, 747.5 ± 309.6 μm) and post-operative (mean, 314.2 ± 80.8 μm) thicknesses of the hemorrhages obtained from OCT images (Wilcoxon rank test, P ≤ 0.01). There was no significant correlation between the size of the hemorrhages and postoperative BCVA (Spearman's rho test, r = 0.078, P = 0.765) or the final BCVA (Spearman's rho test, r = 0.015, P = 0.955).
Total subfoveal blood displacement was achieved in 14 eyes (82.0%) [Figure 1] and [Figure 2] with subtotal displacement in 1 (5.8%) eye. During the follow-up, recurrence of SMH (1 month after the initial surgery) developed in one patient and RRD in another patient. These patients were scheduled for secondary surgeries. Besides these two patients, fundus fluorescein angiography images were obtained from the other 15 patients. Because of activated lesions and leakage, three patients underwent intravitreal ranibizumab and one patient underwent photodynamic therapy at scheduled recurring intervals. There was no significant correlation between the initial thickness of the SMH (747.5 ± 30 μm) and the postoperative BCVA (Pearson's test, r = 0.259, P = 0.315) or the final BCVA (Pearson test, r = −0.153, P = 0.559). There was also no significant correlation between the duration of hemorrhage and the postoperative BCVA (Spearman's rho test, r = −0.109, P = 0.678) or the final BCVA (Spearman's rho test, r = 0.274, P = 0.287).
|Figure 2: Postoperative fundus fluorescein angiography images of the same patient; there was no leakage from the underlying choroidal neovascular membrane. (a) Autofluorescence image of the lesion, (b) Early phase of the FFA, (c) Mid phase of the FFA (d) Late phase of the FFA|
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| Discussion|| |
SMH is a serious condition that can develop during nAMD. An increase in the incidence of SMH has been reported for certain nAMD subtypes treated with anti-VEGF agents. Goverdhan and Lochhead  reported that 40% of patients with nAMD treated with bevacizumab (BZB) developed SMH during the follow-up. SMH has been considered an exclusion criterion in large-scale studies evaluating anti-VEGF effectiveness in patients with nAMD,, so there is currently inadequate data with which to establish a standard treatment protocol for SMH.
A number of parameters such as initial VA, the duration and size of hemorrhages, the status of nAMD causing SMH, and patient tolerability to the treatment must be taken into consideration when deciding on a treatment for SMH. Thus, numerous treatment modalities have been used to treat this disorder.
Direct surgical subretinal removal of the SMH caused photoreceptor and RPE damage, and a high incidence of postoperative RRD has been observed in SST reports. Furthermore, any significant superiority considering visual improvements has been determined in comparison to observation and surgery in SST Group-B.,
Shienbaum et al. achieved significant visual improvement with anti-VEGF monotherapy for small SMHs in a 12-month follow-up. Kim et al. also reported significant visual improvement with the use of anti-VEGF agents, but only in patients who had a better initial VA and a small SMH size, while more invasive surgical interventions were proposed for larger, older, and thicker lesions in this study.
The “expansile gas technique” first described by Heriot is better for the treatment of relatively new, elevated, and large lesions. Although several subsequent studies reported different results using this technique,,,,,,,, this less invasive procedure has advantages because it avoids vitrectomy and its complications.
Anti-VEGF agents were added to this treatment modality to improve treatment efficacy. Meyer et al. reported that significant visual recovery was achieved in 19 consecutive patients treated with intravitreal BZB + r-tPA + gas. The mean duration of symptoms was 9.3 days (range, 4–12 days), and the initial size of the subfoveal hemorrhages were 1–3 disc diameters. Guthoff et al. reported statistically significant visual improvement in a group treated with intravitreal gas + r-tPA + BZB compared with a group treated with intravitreal gas + r-tPA alone.
However, some studies have suggested that intravitreally injected r-tPA cannot diffuse the subretinal space sufficiently., Vitrectomy combined with subretinal r-tPA with old and large SMHs should therefore be performed in selected cases to preserve peripheral vision.
We performed vitrectomy with the assistance of subretinal r-tPA as previously described by Haupert et al. The average size of the SMH was 8.6 ± 5.3 disc areas, and the mean duration of symptoms was 12.8 ± 18.2 days in our study. We found no significant correlation among the size, duration of hemorrhage, and postoperative and final BCVAs.
However, some previous studies have reported different results. Hattenbach et al. observed a significant correlation between the size of the hemorrhage and postoperative VA, and a better postoperative visual improvement was detected in a subgroup of 21 eyes with a hemorrhage duration ≤14 days. Sobolewska et al. reported that the minimum time for improved VA was 4 days for the treatment of SMH. Moisseiev et al. found a significant correlation between the size and duration of SMH and the final VA. Dewilde et al. reported a correlation between delayed surgery and poor visual outcomes in a series of 74 patients treated with vitrectomy + r-tPA + gas. Sandhu et al. reported that SMHs with ≤5.5 disc diameters and a mean duration ≤12.5 days had better visual outcomes, but their results were not statistically significant. Another study reported by Gopalakrishan et al. longer than 30-day duration of SMH has been used as exclusion criteria.
In a large-scale study by Chang et al. using vitrectomy, the average duration of SMHs was 16 days (range, 1–60 days). Statistically significant visual improvement was reported after surgery in this study. However, there was no significant correlation between postoperative BCVA and the duration of the hemorrhage in this study. In the postoperative follow-up, a group of patients treated with anti-VEGF because of the progression of nAMD showed better visual improvement than did other patients. Retinal detachment, vitreous hemorrhage, and recurrence of SMH were the major postoperative complications in that study. In another recent study using vitrectomy, Rishi et al. reported a significant correlation among the size of the hemorrhage, duration of the hemorrhage, and postoperative BCVA.
In our study, RRD developed in one patient and recurrence of SMH in another patient. These two patients were successfully treated with secondary surgeries. Overall, we achieved complete anatomical success (total hemodisplacement of the SMH) in 82% of the patients. This result compares favorably with those of previous studies.,,,,,,
The localization of the hemorrhage rather than its size may be the most important determinant of postoperative VA. A small hemorrhage located very close to the fovea may be associated with a worse VA compared to lesions away from the fovea. Histological localization of the hemorrhage can also be a predictor of functional success. Subretinal lesions had better visual prognosis than sub-RPE lesions for both the vitrectomy technique and the expansile gas technique.
Hassan et al. and Hesse et al. reported that preoperative VA was a predictive parameter for postoperative visual improvement. In our study, we observed a weak positive correlation between the initial and postoperative VAs, but this correlation was not statistically significant. The results may depend on the nature of the previous underlying lesion and/or the degree of photoreceptor loss. OCT may therefore assist in determining the location (subretinal versus sub-RPE) of the SMH as well as predicting the postoperative visual recovery.
There was a significant difference between the pre- and post-operative central subfoveal thicknesses of the SMHs. Although it was not statistically significant, we observed a reverse correlation between the preoperative central subfoveal thickness of the SMH and the postoperative final BCVA. Hirashima et al. recently reported that there was a significant relationship between a better postoperative BCVA and SMH height <400 milimicron. This report is the only one to evaluate vertical height and OCT findings of SMHs.
There are advantages of vitrectomy technique over the expansile gas technique. The r-tPA administered to the subretinal space in different doses provides a more effective hemorrhage dissolution and less shearing stress on the photoreceptors than does intravitreal administration.,
The disadvantages of vitrectomy include a reduced duration and more rapid clearance of intravitreal anti-VEGF agents after surgery. Although several studies have reported the relationship between vitreomacular traction and nAMD, an another advantage of the vitrectomy technique is the elimination of this relationship. In addition, increased macular oxygenation after vitrectomy has a positive effect on retinal functions.
Various complications such as recurrent SMH, retinal detachment, vitreous hemorrhage, and cataract may occur after vitreoretinal surgery.,,,,,, Postoperative recurrence of SMH may not be associated with vitrectomy combined with r-tPA because 40% of patients with AMD treated and followed after anti-VEGF therapy developed SMH in the natural course of the disease. We observed recurrence of SMH in 1 patient after surgery. Besides, 10 of our patients were previously treated and followed under anti-VEGF therapy presented with SMH for the first time. During the follow-up, we diagnosed cataracts in 5 of the 11 phakic (45%) patients. These patients were scheduled for phaco surgery. r-tPA toxicity has been reported in several studies after surgery. We did not observe any r-tPA toxicity in our study.
There were limitations of our study. The number of patients who were treated with additional anti-VEGF agents and photodynamic therapy after surgery because of nAMD activation was not enough to compare statistically with others for the visual improvement. Moreover, this work was noncontrolled and nonrandomized study and could not reveal a comparative result of different surgical techniques.
| Conclusions|| |
Vitrectomy combined with r-tPA + gas tamponade is an effective treatment to preserve and maintain vision in selected patients with thick and wide SMHs due to nAMD. Compared with expansile gas and other treatment modalities, vitrectomy has many advantages in the treatment of thick, wide, and sub-RPE SMHs. Our results compare favorably with previously reported studies that used expansile gas displacement and vitrectomy technique with the assistance of r-tPA. Large-scale, randomized, controlled clinical studies are therefore needed to provide a standard treatment algorithm for the patients presenting with SMH due to nAMD.
We gratefully acknowledge Professor V. Levent Karabaş for his valuable contributions.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Avery RL, Fekrat S, Hawkins BS, Bressler NM. Natural history of subfoveal subretinal hemorrhage in age-related macular degeneration. Retina 1996;16:183-9.
Scupola A, Coscas G, Soubrane G, Balestrazzi E. Natural history of macular subretinal hemorrhage in age-related macular degeneration. Ophthalmologica 1999;213:97-102.
Shultz RW, Bakri SJ. Treatment for submacular hemorrhage associated with neovascular age-related macular degeneration. Semin Ophthalmol 2011;26:361-71.
Bressler NM, Bressler SB, Hawkins BS, Marsh MJ, SternbergP Jr., Thomas MA; Submacular Surgery Trials Pilot Study Investigators. Submacular surgery trials randomized pilot trial of laser photocoagulation versus surgery for recurrent choroidal neovascularization secondary to age-related macular degeneration: I. Ophthalmic outcomes submacular surgery trials pilot study report number 1. Am J Ophthalmol 2000;130:387-407.
Bressler NM, Bressler SB, Childs AL, Haller JA, Hawkins BS, Lewis H, et al.
Surgery for hemorrhagic choroidal neovascular lesions of age-related macular degeneration: Ophthalmic findings: SST report no 13. Ophthalmology 2004;111:1993-2006.
Hassan AS, Johnson MW, Schneiderman TE, Regillo CD, Tornambe PE, Poliner LS, et al.
Management of submacular hemorrhage with intravitreous tissue plasminogen activator injection and pneumatic displacement. Ophthalmology 1999;106:1900-6.
Hesse L, Schroeder B, Heller G, Kroll P. Quantitative effect of intravitreally injected tissue plasminogen activator and gas on subretinal hemorrhage. Retina 2000;20:500-5.
Hattenbach LO, Klais C, Koch FH, Gümbel HO. Intravitreous injection of tissue plasminogen activator and gas in the treatment of submacular hemorrhage under various conditions. Ophthalmology 2001;108:1485-92.
Schulze SD, Hesse L. Tissue plasminogen activator plus gas injection in patients with subretinal hemorrhage caused by age-related macular degeneration: Predictive variables for visual outcome. Graefes Arch Clin Exp Ophthalmol 2002;240:717-20.
Olivier S, Chow DR, Packo KH, MacCumber MW, Awh CC. Subretinal recombinant tissue plasminogen activator injection and pneumatic displacement of thick submacular hemorrhage in age-related macular degeneration. Ophthalmology 2004;111:1201-8.
Mizutani T, Yasukawa T, Ito Y, Takase A, Hirano Y, Yoshida M, et al.
Pneumatic displacement of submacular hemorrhage with or without tissue plasminogen activator. Graefes Arch Clin Exp Ophthalmol 2011;249:1153-7.
Ratra D, Basia A. Intravitreous tissue plasminogen activator with pneumatic displacement in submacular hemorrhage. Arch Ophthalmol 2012;130:795-6.
Fujikawa M, Sawada O, Miyake T, Kakinoki M, Sawada T, Kawamura H, et al.
Comparison of pneumatic displacement for submacular hemorrhages with gas alone and gas plus tissue plasminogen activator. Retina 2013;33:1908-14.
Haupert CL, McCuen BW 2nd
, Jaffe GJ, Steuer ER, Cox TA, Toth CA, et al.
Pars plana vitrectomy, subretinal injection of tissue plasminogen activator, and fluid-gas exchange for displacement of thick submacular hemorrhage in age-related macular degeneration. Am J Ophthalmol 2001;131:208-15.
Kauffmann Y, Isaico R, Lefebvre A, Bron AM, Creuzot-Garcher C. Relationship between intravitreal anti-VEGF therapy and subretinal hemorrhage in patients with exudative age-related macular degeneration. J Fr Ophtalmol 2014;37:195-201.
Goverdhan SV, Lochhead J. Submacular haemorrhages after intravitreal bevacizumab for large occult choroidal neovascularisation in age-related macular degeneration. Br J Ophthalmol 2008;92:210-2.
Brown DM, Michels M, Kaiser PK, Heier JS, Sy JP, Ianchulev T; ANCHOR Study Group. Ranibizumab versus verteporfin photodynamic therapy for neovascular age-related macular degeneration: Two-year results of the ANCHOR study. Ophthalmology 2009;116:57-65.e5.
Rofagha S, Bhisitkul RB, Boyer DS, Sadda SR, Zhang K; SEVEN-UP Study Group. Seven-year outcomes in ranibizumab-treated patients in ANCHOR, MARINA, and HORIZON: A multicenter cohort study (SEVEN-UP). Ophthalmology 2013;120:2292-9.
Shienbaum G, Garcia Filho CA, Flynn HW Jr., Nunes RP, Smiddy WE, Rosenfeld PJ. Management of submacular hemorrhage secondary to neovascular age-related macular degeneration with anti-vascular endothelial growth factor monotherapy. Am J Ophthalmol 2013;155:1009-13.
Kim JH, Chang YS, Kim JW, Kim CG, Yoo SJ, Cho HJ. Intravitreal anti-vascular endothelial growth factor for submacular hemorrhage from choroidal neovascularization. Ophthalmology 2014;121:926-35.
Meyer CH, Scholl HP, Eter N, Helb HM, Holz FG. Combined treatment of acute subretinal haemorrhages with intravitreal recombined tissue plasminogen activator, expansile gas and bevacizumab: A retrospective pilot study. Acta Ophthalmol 2008;86:490-4.
Guthoff R, Guthoff T, Meigen T, Goebel W. Intravitreous injection of bevacizumab, tissue plasminogen activator, and gas in the treatment of submacular hemorrhage in age-related macular degeneration. Retina 2011;31:36-40.
Kamei M, Misono K, Lewis H. A study of the ability of tissue plasminogen activator to diffuse into the subretinal space after intravitreal injection in rabbits. Am J Ophthalmol 1999;128:739-46.
Hillenkamp J, Surguch V, Framme C, Gabel VP, Sachs HG. Management of submacular hemorrhage with intravitreal versus subretinal injection of recombinant tissue plasminogen activator. Graefes Arch Clin Exp Ophthalmol 2010;248:5-11.
Yiu G, Mahmoud TH. Subretinal hemorrhage. Dev Ophthalmol 2014;54:213-22.
Sobolewska B, Utebey E, Bartz-Schmidt KU, Tatar O. Long-term visual outcome and its predictive factors following treatment of acute submacular hemorrhage with intravitreous injection of tissue plasminogen factor and gas. J Ocul Pharmacol Ther 2014;30:567-72.
Moisseiev E, Ben Ami T, Barak A. Vitrectomy and subretinal injection of tissue plasminogen activator for large submacular hemorrhage secondary to AMD. Eur J Ophthalmol 2014;24:925-31.
Dewilde E, Delaere L, Vaninbroukx I, Van Calster J, Stalmans P. Subretinal tissue plasminogen activator injection to treat submacular haemorrhage during age-related macular degeneration. Acta Ophthalmol 2014;92:e497-8.
Sandhu SS, Manvikar S, Steel DH. Displacement of submacular hemorrhage associated with age-related macular degeneration using vitrectomy and submacular tPA injection followed by intravitreal ranibizumab. Clin Ophthalmol 2010;4:637-42.
Gopalakrishan M, Giridhar A, Bhat S, Saikumar SJ, Elias A, Sandhya N. Pneumatic displacement of submacular hemorrhage: Safety, efficacy, and patient selection. Retina 2007;27:329-34.
Chang W, Garg SJ, Maturi R, Hsu J, Sivalingam A, Gupta SA, et al.
Management of thick submacular hemorrhage with subretinal tissue plasminogen activator and pneumatic displacement for age-related macular degeneration. Am J Ophthalmol 2014;157:1250-7.
Rishi E, Gopal L, Rishi P, Sengupta S, Sharma T. Submacular hemorrhage: A study amongst Indian eyes. Indian J Ophthalmol 2012;60:521-5.
] [Full text]
Hirashima T, Moriya T, Bun T, Utsumi T, Hirose M, Oh H. Optıcal coherence tomography fındıngs and surgıcal outcomes of tıssue plasmınogen actıvator-assısted vıtrectomy for submacular hemorrhage secondary to age-related macular degeneratıon. Retina 2015;35:1969-78.
Lee SS, Ghosn C, Yu Z, Zacharias LC, Kao H, Lanni C, et al.
Vitreous VEGF clearance is increased after vitrectomy. Invest Ophthalmol Vis Sci 2010;51:2135-8.
Green-Simms AE, Bakri SJ. Vitreomacular traction and age-related macular degeneration. Semin Ophthalmol 2011;26:137-8.
Williamson TH, Grewal J, Gupta B, Mokete B, Lim M, Fry CH. Measurement of PO2
during vitrectomy for central retinal vein occlusion, a pilot study. Graefes Arch Clin Exp Ophthalmol 2009;247:1019-23.
Chen SN, Yang TC, Ho CL, Kuo YH, Yip Y, Chao AN. Retinal toxicity of intravitreal tissue plasminogen activator: Case report and literature review. Ophthalmology 2003;110:704-8.
[Figure 1], [Figure 2]
[Table 1], [Table 2]