Introduction
The choroidal neovascularisation is a manifestation of the diseases affecting choroid, Bruch's membrane and retinal pigment epithelium (RPE).1 CNVM may occur as an idiopathic entity or in association with number of pathological conditions like age-related macular degeneration (ARMD),2 pathologic myopia, trauma, ocular hisptoplasmosis (POHS),3 angiod streaks, choroidal tears and in certain inflammatory diseases of choroid and retina. It can cause severe visual loss due to leakage, haemorrhage and scar tissue formation damaging the photoreceptors and the RPE.4
Initialy the treatment approaches are laser photocoagulation, then approach change to photodynamic therapy with verteporfin, trans-pupillary thermotherapy, sub-macular surgery. Laser photocoagulation is only useful in a small percentage of patients that have well-defined areas of classic CNV. Moreover, recurrences after laser photocoagulation are common and occur in approximately 50% of patients5
Now currently the treatment of choice for CNVM is intravitreal anti-VEGF therapy, anti-VEGF agent have revolutionized the treatment of CNVM.
Ranibizumab is a recombinantly produced, humanized antibody fragment that binds VEGF. It binds to and inhibits all active forms of VEGF-A and their active degradation products. The usual dose is 0.5mg in 0.05ML.6
Bevacizumab is a full-length humanized monoclonal antibody against human VEGF. Treatment with BCZ result in lower economic burden to healthcare system as compared to RBZ.
Aflibercept is recombinant solution VEGF receptor protein in which the binding domains of VEGF receptor 1 and 2 are combined with the Fc portion of immunoglobulin G.7
The present study is being done to evaluate the clinical profile and types of CNVM and the effectivity and outcome of anti VEGF therapy.
Material and Methods
The present study was carried out as facility based cross sectional study in Department of Ophthalmology, Gandhi Medical College and associated Hamidia Hospital, Bhopal M.P. All the patients attending eye OPD and detected as choroidal neovascularization (CNVM) based on regular fundus examination. Study was undertaken from 1st March 2017 to 31st August 2018 that is for a period of eighteen months.
The inclusion criteria was all cases of CNVM diagnosed in eye OPD of Hamidia Hospital and giving consent for the study; patients referred from other departments having CNVM and patients referred from other special ophthalmic clinics with diagnosis of CNVM. The exclusion criteria was patients with other systemic diseases affecting retina; other retinal/ macular pathologies and previously treated macular disorders. All the patients diagnosed as CNVM, fulfilling inclusion criteria were selected using purposive sampling. After obtaining informed consent, all participants included in the study were interviewed and information was recorded on a predesigned, pre-tested and semi-structured questionnaire. The questionnaire included socio-demographic variables and details regarding relevant history and thorough ocular examination.
Patients were explained regarding the seriousness of disease, nature of treatment that they would be offered, the potential risks, benefits, adverse effects, alternative treatment options and possible treatment outcomes. Once they consented for treatment, affected eye was dilated using topical mydriatic drug and then shifted to operation theatre. After taking all aseptic precautions, injection Ranibizumab 0.5 mg was given intravitreally at 4.0 mm from the limbus in phakic eye and 3.5 mm in pseudophakic eye under topical anesthesia. The patients were then instructed to take an antibiotic eye drop for a week. A repeat injection was given to all the patients after one month of first injection using aseptic precautions under topical anesthesia, followed by a course of topical antibiotic for a weak. All the participants were followed up next day to look for site discomfort, transient elevation of intraocular pressure, inflammation, redness or any other discomfort to the patient and then after 7 days, 1 month and on PRN basis to look for response to treatment which mainly focussed on visual acuity. PRN is reference to dosage of prescribed medication that is not scheduled. The PRN regimen showed good visual result but requires monthly monitoring.
Change in BCVA by more than or less than 2 lines on Snellen chart was considered as improvement or worsening, respectively. Patients with change in visual acuity of less than 2 Snellen lines were considered to be stable.
Observation and Results
Table 1
Sociodemographic variables | Frequency | Percent | |
Age group (years) | 21-40 | 4 | 13.3% |
41-60 | 7 | 23.3% | |
>60 | 19 | 63.3% | |
Gender | Male | 18 | 60% |
Female | 12 | 40% |
Mean age of study participants is 62.2±15.9. Majority (63.3%) of the patients were more than 60 years of age. Only 13.3% were less than 40 years of age. Out of 30 cases, 60% were male & 40% were female.
Table 2
Etiological factors | No. (30) | Mean age | SD |
Pathological Myopia | 7 | 48.57 | 10.289 |
ARMD | 20 | 68.00 | 10.137 |
Trauma | 1 | 57.00 | |
Idiopathic CNVM | 2 | 32.00 | 4.243 |
It was observed that the mean age in the ARMD group at Presentation was 68±10.13, pathological myopia was 48.57±10.28, Trauma was 57.00 and idiopathic CNVM was 32±4.23. This shows that ARMD predominantly affects older 68±10.13 people whereas like pathological myopia, Idiopathic CNVM are seen in younger age groups.
Table 3
Most common presenting complaints was gradual diminution of vision in all etiological groups followed by metamorphopsia. In participants with pathological myopia, 72% participants complained of gradual diminution of vision and metamorphopsia. Amongst participants with ARMD, 95% participants complained of gradual diminution of vision followed by metamorphopsia in 75% participants. Mode of presentation in patient with trauma was metamorphopsia and in idiopathic CNVM, it was gradual diminution of vision in 100% and metamorphopsia in 50% participants.
Table 4
As the difference in visual acuity at pre and post treatment is p<0.01 it is highly significant (t=5.65,p -value =0.01). Pre treatment mean was 1.29±0.488 and post treatment mean was 1.04±0471 with std. deviation 0.26±0.28 at CI 0.16-0.35, test of significance was found to be highly significant (p=0.01).
Table 5
Improvement in visual acuity was seen in eyes of pathological myopia (p=0.001) and ARMD (p=0.001).
There was only one eye with trauma thus statistical test could not be applied. While the Idiopathic CNVM cases showed improvement which was statistically significant (p=0.02).
Table 6
As the difference in OCT at pre and post treatment is p<0.01 it is highly significant (t=7.66, p-value =0.01). Pre treatment mean was 455.9 and post treatment mean was 335.13. Paired t test was applied to compare the means of pre treatment and post treatment mean was 120.82 (88.69-152.94 CI), test of significance was found to be highly significant (p=0.01).
Discussion
In present study, 30 patients of CNVM were included in the age range of 20 to 85 years. Mean age of study participants was 62.2±15.9 years. It was observed that the mean age in the ARMD group at presentation was 68±10.13 years, whereas the mean age in patients with pathological myopia, trauma and idiopathic CNVM was 48.57±10.28 years, 57.00 years and 32±4.23 years respectively. This shows that ARMD predominantly affects older 68±10.13 people where as other etiologies like pathological myopia, Idiopathic CNVM are seen in younger age groups.
It was estimated that 8 million people will be affected with AMD worldwide by the year 2020. Robinal , et al (2004) reported the prevalence of early and late AMD at 2.7% (95% CI, 2.2 – 3.2) and 0.6% (95% CI, 0.4 – 0.8), respectively from a population-based study from rural India.8
Majority (60%) of patients were male in the present study. With reference to etiological groups female patients were more than male in pathological myopia whereas in CNVM due to ARMD, Trauma and Idiopathic CNVM male patients were more than female. Vongphanit J et al (2002) estimated that the prevalence of CNVM among high myopic patients was 4%-11% and there was a 2-fold higher risk among women.9
The high proportion of CNVM due to pathological myopia in females can be explained on the basis of study by Kobayashi K et al (2002), which suggested that predominance of myopic CNV in females may be due to oestrogen receptor expression in CNV and the external influence of oestrogen. The male preponderance could be due to behavioural and social aspects in our society causing less reporting of cases of female as compare to male.
In present study 89.7% cases presented with gradual diminution of vision whereas sudden diminution of vision was seen only in 10.2% patients. Metamorphopsia was present in 61%, central scotoma in 53% and paracentral scotoma in 2.5% patients.
Aditya shudhalkar et al (2015) in their study stated that the most common complaint was decreased vision (94.5%), followed by inability to recognize faces (80.42%) and reading disability (78.4%). One-hundred seven patients (26.22%) had metamorphopsia. Only 17 patients (4%) of these were asymptomatic.10
In present study, the mean of log-MAR visual acuity at presentation and at final follow up of 6 month with a mean number of visit 6.9±1.15 was calculated and the test of significance (paired t test) showed highly statistical significant difference between the pre-treatment and post-treatment visual acuity (p<0.01). Mean number of injection in present study was 2.97±0.59.
Similar to log-MAR, the mean of central retinal thickness at presentation and at final follow up was calculated. The difference in central retinal thickness at pre and post treatment was found to be highly significant statistically (p<0.01).
Pathological myopia
The mean log-MAR in patients with pathological myopia at baseline and at final follow up with a mean of 6.4 visits in the 6-month period was 1.5±0.5 and 1.12±0.45 respectively. The observed difference between the baseline and final visual acuity was found to be highly significant (p<0.01). Similarly, the difference between mean of Central retinal thickness at baseline and final follow up was found to be significant (p<0.01) in present study.
Sindhu S et al (2017) in their study found mean BCVA at baseline was 0.64 log MAR and 0.48 log MAR at 1 year follow up. This difference was found to be statistically significant (P = 0.04).11
ARMD
The mean log-MAR in patients with ARMD at baseline and at final follow up with 7.3 mean number of visit in the 6 month period, was 1.3±0.5 and 1.08±0.5 respectively. The observed difference between the baseline and final visual acuity was found to be highly significant (p<0.01). The difference between mean of Central retinal thickness at baseline and final follow up was found to be significant (p<0.01) in this group in present study. The PrONTO (2009) (prospective optical coherence tomography imaging of patients with neovascular AMD treated with intraocular ranibizumab) trial also showed improvement in visual acuity following Ranibizumab injections (p=0.001). The mean number of injections was 9.9. The difference in pre-treatment and post-treatment OCT was also significant (p<0.01) in PrONTO study.12
Conclusion
ARMD and pathological myopia were the most commonly associated factors of CNVM in present study.
In present study, it was observed that the mean age at presentation of CNVM in patients of pathological myopia was lower as compared to ARMD group.
Gradual diminution of vision was the most common presenting complaint followed by metamorphopsia and o ccult CNVM was the most common type of CNVM in the present study.
Following Ranibizumab injections, the improvement in visual acuity at 6 month follow-up as elicited by log-MAR value was found to be statistically significant.
No serious drug related ocular or systemic adverse events were identified.