Treatment of recurrent myopic macular hole using membrane of plasma rich in growth factors.

PURPOSE: To describe the case of a patient with a recurrent large myopic macular hole (MH), who was successfully treated with a plasma rich in growth factors (PRGF) membrane. CASE REPORT: A 71-year-old patient presented a myopic MH in his right eye. One month later, pars plana vitrectomy with internal limiting membrane (ILM) peeling was performed, achieving closure of the MH. Three months later a recurrence was observed (700 µm) without visual acuity (VA) improvement. A new surgery was carried out placing an autologous PRGF-membrane into the MH, and performing a fluid-gas exchange at the end of the surgery. After two months of follow-up, the MH was completely closed, obtaining the anatomic recovery of the foveal depression, and improving the VA to 0.1. No adverse reactions were associated with the use of PRGF and there were no new recurrences of the MH in a follow-up period of six months.
CONCLUSION: The use of PRGF-membrane can be used as adjunctive therapy in the surgical repair of recurrent large myopic MHs, thus improving anatomic and visual outcomes.

Introduction

Macular hole (MH) is a common clinical finding, in patients with high myopia. The pathophysiology of myopic MHs is not fully understood; however, it is postulated that the myopic maculopathy traction may be the cause of this disease;1 the participation of epiretinal membranes, the rigidity of the internal limiting membrane (ILM) and the rigid retinal vessels are situations that promote the development of MH in myopic patients.2 Pars plana vitrectomy (PPV) is the most commonly used treatment for MH being associated with ILM peeling, acting on the inner retina to release the tensile forces.3 In the treatment of recurrent myopic MH, new surgical techniques are used (inverted ILM flap technique and the autologous transplantation of ILM), which seems to improve the final postoperative outcome.4 However, patients have recurrences of the MH despite these surgical techniques.

Plasma rich in growth factors (PRGF) is a novel autologous ophthalmic therapy that contains a large number of biologically active agents, including EGF (epidermal growth factor), PDGF (platelet-derived growth factor), insulin-like growth factor 1, fibronectin and vitamin A,5 that promote tissue regeneration, healing modulation and anti-inflammatory properties, among others.5 PRGF-Endoret technology can be used to obtain different formulations, like eye drops and membranes, for the treatment of several ophthalmic diseases.6 The PRGF membrane has similar mechanical and biological properties to the amniotic membrane7 and it has been used in ocular and corneal surface surgery with good clinical results.8

The efficacy and safety of PRGF therapy have been widely demonstrated, particularly in dry eye syndrome, persistent epithelial defects, and corneal ulcers.9 Other authors have reported the efficacy of platelet derived (liquid use as supernatant)1 for the treatment of myopic MHs; however, to our knowledge this is the first report that uses the PRGF-membrane technology for the treatment of myopic MH closure.

Case report

A 71-year-old male patient with history of cataract surgery (previous refraction: −12.5 sphere, −1.00 to 0º cylinder), with diffractive lens implant and high myopia (axial length of 30.19 mm) in the right eye, developed a MH 15 days after the cataract surgery, associated with metamorphopsia and decreased visual acuity (VA, count fingers). One month later, PPV with ILM peeling was performed achieving the closure of the MH. Three months later, the visual symptoms returned (metamorphopsia), the VA had not improved (count fingers), and a MH recurrence was observed (700 µm), associated with subretinal fluid, intraretinal hemorrhages, and pigment dispersion (Figure 1).

Figure 1

Retinography and optical coherence tomography (OCT) of recurrent myopic macular hole. (A) Retinography of the right eye showing the macular hole. (B) OCT of recurrent myopic macular hole in the right eye.

A new surgery was carried out in order to achieve the MH closure. The PRGF-membrane was prepared according to Endoret® technology (BTI Biotechnology Institute, S.L., Miñano, Álava, Spain).7 The surgical procedure consisted in enlarging the peeling of the ILM, close to the optic nerve and the vascular arcade and tap the edges of the MH (to increase the probability of closing the MH, technique proposed by the retina surgeon: AFVS). Then, the PRGF membrane was introduced through the trocar and placed inside the MH (the thickness of the membrane was 100 µm), without pressure and without forcing the adhesion (PRGF fibrin membrane have adhesion properties when it comes into contact with the cell surface) trying to avoid the potential damage to the retinal pigment epithelium; subsequently three drops of liquid PRGF were placed in the MH, and a fluid-gas (C3F8) exchange was performed at the end of the surgery (Figure 2).

Figure 2

Surgery in the recurrent myopic macular hole (PPV + extended Internal Limiting Membran (ILM) peeling + PRGF-membrane). (A) Macular hole staining. (B) Extended ILM peeling. (C) Tap the edges of the macular hole. (D) PRGF-membrane introduction into vitreous cavity. (E) PRGF-membrane position into the macular hole. (F) fluid-air-gas exchange.

Abbreviations: PRGF, plasma rich in growth factors; PPV, pars plana vitrectomy.

To obtain the PRGF-membrane, 81 mL of the patient’s blood was extracted in 9 mL tubes with 3.8% sodium citrate as an anticoagulant. The blood was centrifuged at 580 g at room temperature for 8 mins (Endoret system®). The fraction 2 (F2) was defined as 2 mL of plasma just above the buffy coat and fraction 1 (F1) was defined as the remaining plasma above F2. To make each PRGF membrane, 5 mL of F2 was activated with 10% calcium chloride and then incubated in 35 mm diameter wells at 37°C for 30 mins. Once the fibrin clots were formed, they were placed in a shaping vessel and pressed for 30 s, yielding 100 µm thick PRGF-membrane. The F1 (liquid) was placed after the PRGF membrane was introduced into the MH. This preparation does not contain cells.

After two months of follow-up, the MH was completely closed. Anatomic recovery of the foveal depression (assessed by SD-OCT) was observed and the mild intraretinal hemorrhages and subretinal fluid disappear, improving the VA to 0.1. An alteration was observed in the outer layers of the retina in the foveal area, but no adverse reactions were associated with the PRGF. We did not have any new recurrences of the MH in a follow-up period of six months, and VA remained stable during this period (Figure 3).

Figure 3

Post-surgical follow-up. (A) Three months after treatment with PPV + PRGF membrane. (B) Retinography of the right eye: Image of closed macular hole, macular pigmentary changes.

Abbreviations: PPV, pars plana vitrectomy; PRGF, plasma rich in growth factor.

Discussion

The MH is a common finding in patients with high myopia, it is thought that its formation can be caused by the combination of tractional forces, at the macular level.1 The usual treatment for this pathology is PPV associated with procedures on ILM to decrease the tractional forces in the macula,1 such as the inverted ILM flap, the ILM peeling alone or with autologous PRPs (platelet-rich plasma) injection over the hole, autologous transplantation of ILM membrane, lens capsular flap, or neurosensory retina.10 In the inverted ILM flap technique, as well as in the autologous transplantation, the ILM acts as a scaffold for reactive gliosis and proliferation of glial cells, and therefore the anatomic closure of the MH is more easily produced.11 Likewise, the ILM could act as a barrier that prevents the penetration of fluids from the vitreous cavity to the macular orifice, preserving the function of the retinal pigment epithelium. However, the closure of the myopic MH is unpredictable, and a second surgery may be required.12

PRPs are platelet products suspended in plasma, which contain growth factors [such as PDGF, transforming growth factor-β, basic fibroblast growth factor (b-FGF), EGF, among others] and other molecules, which are involved in tissue regeneration and inflammatory modulation.6 There are different preparation protocols for PRPs; however, their clinical effectiveness is given by the platelet concentration, presence or absence of the leukocytes, the activation process, the production method (closed, open), and the storage process and dispensing.13 PRGF is a special type of PRP that uses Endoret® technology for its elaboration, with closed method, moderate concentration of platelets, absence of leukocytes, platelet activation, and storage up to three months, preserving the concentration of growth factors.6

The eye drops PRGF has shown in different in vitro, in vivo, and clinical studies to have a higher concentration of growth factors, proliferation capacity, migration and tissue regeneration in the ocular surface and cornea.14 The PRGF fibrin membrane has mechanical properties and resistance that allow its use in surgical procedures, it has been shown that inside of it contains a wide range of growth factors, which are released progressively over time.15,16 It has also been shown that the PRGF membrane serves as scaffolding for cell expansion in advanced therapy studies.7

In our case report, we describe a patient with myopic MH, who had not responded to PPV surgery with ILM peeling; a second surgery was carried out with an extension of the ILM peeling margins, and with a PRGF membrane placement into the MH. The anatomic closure and vision recovery were observed. There are some publications using liquid PRPs in myopic MH,1 however our case report would be the first one which uses an autologous fibrin membrane (PRGF) as adjuvant therapy to retinal surgery. The mechanism involved in the closure of the MH could be due to the trophic action of the growth factors (PDGF, b-FGF, EGF), which enhance the activation of Müller cells,1 and it also works as a scaffold for the cell growth. The use of PRGF-membrane can increase the anatomic and visual results in the surgical repair of recurrent MHs; no complications were observed after its use. PRGF-membrane can be used as adjunctive therapy for the treatment of recurrent large myopic MHs.

In conclusion, the placement of PRGF-membrane inside the hole can improve anatomic and visual results in the surgical repair of recurrent MHs, helping to restore the anatomy of the macular area. The present clinical case could open the door to new investigations in the retina, aimed at the process of tissue regeneration.