|Year : 2020 | Volume
| Issue : 1 | Page : 2
Quality of life results after vitreolysis in patients with symptomatic vitreous floaters
Renzo Canote, Daniela Rodríguez, Luis Izquierdo, Roger Moncada, Carmen Maldonado, Alejandra Henriquez Maria
Research Department, Oftalmosalud Eye Institute, Lima, Peru
|Date of Submission||21-Nov-2019|
|Date of Acceptance||16-Dec-2019|
|Date of Web Publication||23-Jan-2020|
Dr. Daniela Rodríguez
Oftalmosalud Institute of eyes, Av. Javier Prado Este 1142, San Isidro, Lima 27
Source of Support: None, Conflict of Interest: None
Purpose: The purpose of the study was to evaluate the quality of life and visual results after yttrium aluminum garnet (YAG) vitreolysis in symptomatic vitreous floaters.
Methods: This was a prospective case series study including patients with symptomatic floaters attending the Oftalmosalud Institute of eyes and underwent YAG laser vitreolysis. All patients completed the National Eye Institute Visual Functioning Questionnaire 25 for the quality of life assessment and the presence of floaters as well as the measure of the visual acuity reported preprocedure and after 3-month follow-up. Statistical analysis was done using score 0–100 for each question, and a sign test for paired samples was used.
Results: Twenty eyes of 20 patients were evaluated. The comparisons for the questionnaire show an improvement in the general vision (P = 0.008), near vision (P = 0.001), and distance vision (P = 0.012). Furthermore, the dependency of glasses (P = 0.012), the score of mental health (P = 0.007), and the best visual acuity (P = 0.004) were improved. Patients who referred improvement in the quality of life were 75% pseudophakic patients and 25% phakic patients. The complications were high intraocular pressure and subcapsular cataract.
Conclusions: Our study revealed a moderate improvement in floater symptoms and in quality of life and visual outcomes.
Keywords: National Eye Institute Visual Functioning Questionnaire-25, quality of life, vitreous floaters, yttrium aluminum garnet vitreolysis
|How to cite this article:|
Canote R, Rodríguez D, Izquierdo L, Moncada R, Maldonado C, Maria AH. Quality of life results after vitreolysis in patients with symptomatic vitreous floaters. Pan Am J Ophthalmol 2020;2:2
|How to cite this URL:|
Canote R, Rodríguez D, Izquierdo L, Moncada R, Maldonado C, Maria AH. Quality of life results after vitreolysis in patients with symptomatic vitreous floaters. Pan Am J Ophthalmol [serial online] 2020 [cited 2021 Jan 19];2:2. Available from: https://www.thepajo.org/text.asp?2020/2/1/2/276597
| Introduction|| |
The vitreous is a hydrated extracellular matrix comprised primarily with water, collagens, and hyaluronan, organized into a homogeneously transparent gel that helps to maintain the shape of the eye and achieve a uniform surface of the retina.,
During the first year of life, the vitreous gel is transparent, which allows an excellent refraction of the light, but with aging, molecular alterations take place as the dissociation of the collagen and the hyaluronic acid produces a liquefaction of the gel and the organization of collagen fibrils that leads to symptomatic floaters causing light scattering and entoptic phenomena to the patient, ultimately resulting in posterior vitreous detachment (PVD) which is present in the 60% of the population older than 60 years.
The treatments for this pathology are observation, vitrectomy, and yttrium aluminum garnet (YAG) vitreolysis; from this option, the vitrectomy presents complications such as secondary cataract, hypertension, and retinal breaks; on the other hand, the YAG vitreolysis has a revolutionary prism lighting system which is a split prism tower that produces semi-coaxial illumination, which illuminates deeper inside the vitreous and does not obstruct the laser beam allowing the clinician to see better and treat floats and opacities, making the treatment more controllable, accurate, and convenient.
Most of the patients tolerate their symptoms without problems; however, some patients find the floaters very problematic because it can reduce sensitivity to contrast and to quality of life  and also generate discomfort in daily activities. The visual quality and quality of life are measured with the National Eye Institute Visual Function Questionnaire (NEI VFQ) originally developed for patients with age-related macular degeneration, cataracts, diabetic neuropathy, and glaucoma and used in other ocular pathologies.
The aim of this study was to evaluate the quality of life after YAG vitreolysis in patients with symptomatic vitreous floaters.
| Methods|| |
This was a prospective and descriptive case series study performed between June 2017 and November 2017 and included 20 eyes of 20 patients, at Oftalmosalud Instituto de Ojos, Lima, Peru. The study complied with the Declaration of Helsinki; the ethics committee of Oftalmosalud approved the study and written informed consent was obtained from all the participants.
The inclusion criteria were as follows: all patients who attended the clinic due to flashes of color, to a perception of floating flies or persistent mobile hairs secondary to PVD, and to the persistence of floating symptoms of at least 1 month, documented in the clinical examination. The diagnosis of PVD was confirmed by the retina specialist through a fundus examination and by B-ultrasound; it confirmed the presence of vitreous condensations, vitreous posterior detachment, and the presence of Weiss ring. Only one eye per participant was included in the study.
Patients with vitreous floaters secondary to vitreous hemorrhages, to vitreous retina surgeries, to asteroid hyalosis, to scintillating sinquisis, to inflammatory processes, other severe ocular diseases, and to postoperative retinal detachment by vitrectomy were excluded from the study.
All patients were examined by indirect ophthalmoscopy done by a retinal specialist who projected a light into the eye, using Keeler's Vantage plus indirect ophthalmoscope and Volk 2.2 pan retinal magnifying glass to visualize the fundus; also, patients underwent ultrasound test to confirm the diagnosis.
The best-corrected visual acuity and intraoperative and postoperative complications were recorded.
National Eye Institute Visual Function Questionnaire-25
The NEI VFQ-25 (https://www.nei.nih.gov/faqs/resources-visual-function-questionnaire-25-vfq-25) was completed by each patient before the opesration and 3 months after the procedure. This questionnaire is an instrument that allows assessing the quality of life related to vision. It consists of 1 general health item and 25 items grouped into 11 subscales [Table 1]: general vision (1 question), ocular pain (2 questions), near activities (3 questions), distance activities (3 questions), social functioning (2 questions), mental health (4 questions), role limitations (2 questions), dependency (3 questions), driving (3 questions), color vision (1 question), and peripheral vision (1 question). This questionnaire helped us to evaluate the subjective satisfaction that patients felt before and after the procedure (3 months postsurgery) in multiple aspects of everyday life. Furthermore, we added the following question to evaluate the reduction of visual discomfort after the treatment: Did the visual discomfort improved after the treatment? with a yes or no answer. A total of 26 questions were answered.
|Table 1: National Eye Institute Visual Functioning Questionnaire-25 Questions according to the 11 scales|
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All the answers in every question were scored between 0 and 100 points, where 0 is the lowest and 100 is the best possible score, and the questions were separated in the 11 scales and the vision-related subscale scores were averaged without the general health question.,
The patient's pupil was dilated with tetracaine hydrochloride (5.0 mg), 1 drop every 5 min for 15 min; it was recommended for patients to keep their eyes closed, after confirming the eyes dilatation. One drop of anesthetic (tropicamide) was applied, and one drop of gel carbomer was instilled into the lens that was used to perform the process (Ocular Peyman 18 mm Vit. Lens, Karickhoff 21 mm Vitreous Eyepiece, and Karickhoff Eyepiece 25 mm Vit. Off Axis). The patient was asked to fix the gaze at a fixed point.
YAG vitreolysis was performed with LIGHTLas YAG/selective laser trabeculoplasty Deux (Lightmed, San Clemente, California, United States). A maximum energy per pulse of 7 mJ was used, as described by Tsai et al.,, The energy was initially shown at 2.5 mJ. It is recommended to start the treatment with a simple pulse per shot. The energy was set to the minimum level required to create the interruption in the vitreous cavity (usually 2.5 mJ). Most treatments can be performed using energy between 2.5 mJ and 4–5 mJ. It is possible to increase to two pulses (double) or three pulses (triple) per shot before increasing the energy per shot. It is recommended to limit the number of shots to a maximum of 450–500 per vitreolysis session. If more sessions are required, it can be done with a period of 1 month with a maximum of 500 shots per se ssion. Additional sessions were considered if the patient reported that the perception of the flies did not disappear completely and had no complications.
The sessions were repeated until the patients reported that the improvement was complete and consent for a new procedure; the maximum session per patient was 4.
After treatment with YAG laser, no topical therapy was given postoperatively. All the patients were checked a week after to evaluate the perception of the vitreous floaters and for the follow-up of the intraocular pressure. If the patients reported total improvement, they were checked a month after the procedure. If the patients improved partially or no improvement, it was scheduled more visits with a space of 15 days apart until the vitreous floaters disappeared.
Statistical analysis was performed usingthe R program version 3.6.0 from the R fundation, Vienna, Austria. (https://www.r-project.org/). The 25 questions (without the question of general health) were scored 0–100 for each question (according to the number of options for each question, it was given a score 0–100). The questions on each scale were averaged.
The data collected were summarized using the statistics: mean, standard deviation (SD), and range (minimum and maximum values). The sign test for paired samples was performed to compare the measurements before and after the ophthalmologic intervention. For all statistical tests, a type I error equal to 0.05 was considered.
| Results|| |
Of twenty patients, 20 eyes were treated for symptomatic acute floaters; all were followed-up for 3 months. The mean ± SD age of participants was 59.4 ± 7.6 years. The mean best-corrected visual acuity before and after the procedure was 0.11 ± 0.12 and 0.3 ± 0.6, respectively, with a significant improvement (P = 0.002) [Figure 1]. [Table 2] shows the characteristics pre procedure and the complications post follow-up.
Most of the patients received only laser treatment (60%, 12/20) with a mean total power of 3.33 ± 0.82 mJ and 333.92 ± 90.07 shots. About 15% (3/20) of the patients received two sessions with a mean total power of 3.33 ± 0.58 mJ with a mean of shots of 280 ± 103.92 in the first session and a mean total power of 3.33 ± 0.058 mJ with a mean of shots of 306 ± 38.11 in the second session. Furthermore, 15% (3/20) of the patients received three sessions with a mean total power and a mean shot in the first session of 3.3 ± 0.75 mJ and 413.33 ± 99.48 shots, in the second session, they were 3 ± 0.26 mJ and 320 ± 36.38 shots, and in the third session, they were 3.66 ± 1.15 mJ and 452.33 ± 91.36 shots. Only 10% (2/20) of the patients received four sessions with a mean total power and a mean of shots of 4.05 ± 1.48 mJ and 500 ± 0 shots in the first session, 3.5 ± 0.71 mJ and 500 ± 0 shots in the second session, 4 ± 0 mJ and 244 ± 69.29 shots in the third session, and 4 ± 0 mJ and 250 ± 0 shots in the fourth session. All the patients who underwent second, third, or four session reported a partial or no improvement. For the question 26, in general, 60% of the patients reported an improvement in the visual discomfort at the first session and 40% none or partial improvement. From the 60% (12/20 patients) of the patients, 4 did not receive additional sessions due to a complication. From the 40% (8/20) of the patients received an additional session, 25% (5/20) reported partial improvement and 10% (3/20) did not improve despite having four laser sessions in total; this fourthsession was the last one. The visual acuity improves from pretreatment to posttreatment (P = 0.004) [Figure 1].
The quality of life was evaluated with the NEI VFQ-25, in which the questions were grouped into 11 scales and scored from 0 to 100; all questions in each scale were averaged and compared pre- and posttreatment values.
[Figure 2] shows the results of the visual scales, where the general vision scale has an improvement (P = 0.008), where the score was greater at the follow-up, and the near vision and distance vision have a higher score in the post procedure with a significant P value, P = 0.001 and P = 0.012, respectively. The peripheral vision continues the same in the follow-up.
|Figure 2: Results of visual scales from National Eye Institute Visual Functioning Questionnaire-25. All scales were scored (0-100) and compare. The general vision, near vision, peripheral vision and distance vision had an improvement in the score after 3 months of follow up|
Click here to view
For the other scales [Figure 3], it was a significant improvement in the dependency scale (P = 0.012) and in the mental health (0.007).
|Figure 3: Results from quality of life scale from National Eye Institute Visual Functioning Questionnaire-25. The scales were scored (0-100) and compare after 3 months of follow up. The dependency of glasses (P=0.012) and mental health (P=0.007) had the best improvement in the score after the procedure|
Click here to view
During the vitreolysis procedure, 1 patient, with only one session with 300 shots and 3 mJ of power, had a rupture of the posterior capsule of the crystalline lens; after 3 days, it had a localized opacity of the crystalline lens, which led to a subcapsular cataract; due to this, a phacoemulsification surgery with an intraocular lens implant was performed.
Transient ocular hypertension was present on 3 patients a week after the first session: two of them received 420 shots with 3 mJ and the third patient received 329 shots with 5 mJ. Hypertension was managed with antihypertensive drops, 1 drop twice a day (beta-blocker timolol). The intraocular pressure was monitored weekly if the patient presented a low pressure in the 2nd week the medication was withdrawn, and all patients were controlled for 4 more weeks.
The patients who did present hypertension had a mean laser shot of 389 ± 52.54 (3/20) in the unique session, comparing with the first session of patients with no hypertension 287.3 ± 125.62 (17/20), there was no significant difference (P = 0.27).
| Discussion|| |
Vitreous floaters are a visual phenomenon caused by vitreous opacities which leads to produce linear gray shadows with focal dark spots or nodules. These visual phenomena affect not only the vision of the patient but also the quality of life.
The use of neodymium (Nd)-YAG laser for the treatment of floaters was already described since 1987,, in some studies; only a third part of the patients refers improvement in the symptoms after the procedure, but these vary from one study to other. Furthermore, this treatment is noninvasive and considered by several authors as effective, safe, and innocuous , for the patients and could improve the quality of life.
In the present study, we evaluated the quality of life after using YAG vitreolysis in patients with symptomatic vitreous floaters.
The visual acuity of these patients improves after 3 months' postsurgery; also, there were 60% (12/20) of the patients with an improvement after the first session, and these results can be study in a larger sample, due to in some studies, the improvement varies from 0% to 100%. These results could have this variation according to the type of floaters and the location.
These findings appear to show similar efficacy than those reported in an analysis of 39 patients treated for PVD-related floaters by Delaney et al. where they used a maximum pulse energy of 1.2 mJ with a mean power of 310.4 mJ per se ssion and reported that 38% found Nd:YAG vitreolysis moderately improved their symptoms, while 61.5% found no improvement.
The NEI VFQ-25 is a questionnaire that assesses the influence of visual impairment in the daily activities, comfort, and mental health among other scales; it measures the patient perception to all these different scales and let us to assess the impact of different conditions and treatments in the patient's life. Using this questionnaire, the questions were grouped into 11 scales and were scored from 0 to 100(included all 25 questions). In this study, we can observe an improvement in almost all scales related to the vision of the patient such as general vision, near vision, and distance vision. This confirms the results obtained in the visual acuity that let us know the patients had a better vision with the correction and less discomfort for the remain floaters.
Other important result in the assessment is the dependency on others due to vision and mental health symptoms due to vision scale where also it was improvement, reflecting the state of minds of the patients. Wagle AM et al. reported the utility value of floaters, as expressed by patients. This indicates that floaters have a significant negative impact on the quality of life as compared to ocular as well as systemic diseases; they reported that these patients were willing to take an 11% risk of death and a 7% risk of blindness to get rid of symptoms related to floaters. This indicates the importance to treat symptomatic vitreous floaters.
The surgical complication was caused by the operator's learning curve when performing the treatment. All complications were managed clinically.
It had been reported due to the use of the Nd-YAG laser in the posterior segment between the endothelium corneal damage, cataract, hemovitreous, and retinal breaks or retinal detachment.,,, In our series cases, complications included local opacification of the crystalline lens in 1 eye, and 3 patients had transitory intraocular hypertension after YAG vitreolysis treatment. There was no retinal tear or retinal detachment, which was checked by indirect ophthalmoscopy and ultrasonography.
To avoid the cataract complications, it is described as a safe distance between the target tissue and the neighboring tissues of 2–5 mm. Due to their location, most often in the anterior vitreous or mid-vitreous, vitreous floaters can be treated with the Nd-YAG laser while keeping a safe distance from the lens and from the retina. Although the new YAG laser is safer to perform procedures, it depends on the operator, and due to that, it could occur complications such as those presented in the current study.
Transient hypertension can be attributed to the inflammation in relation to the number of shots administered in each session at higher doses, and this is associated with the size of the floater, small floaters will need fewer sessions, fewer numbers of shots to dissolve them, and larger floaters will need more sessions and more shots, as described by Chirag.
The current study has several limitations, including its small sample size and short follow-up period. Longer follow-up is required to determine the long-term stability of results and the degree of adverse events associated with the procedure.
| Conclusions|| |
The current study suggests that YAG vitreolysis improves the quality of life and visual outcomes in patients presenting visual disturbance secondary to clinically confirmed vitreous floaters, both subjectively symptoms, with a few adverse events in this series.
The authors would like to thank Jose Chauca for the statistical support.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2], [Figure 3]
[Table 1], [Table 2]