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1.
J Cataract Refract Surg ; 46(2): 287-292, 2020 02.
Article in English | MEDLINE | ID: mdl-32126043

ABSTRACT

PURPOSE: To analyze the incidence, risk factors, and outcomes of cataract surgery complicated by a dropped nucleus. SETTING: Patients who have received cataract surgery in 18 European countries. DESIGN: Retrospective cross-sectional register-based study. METHODS: Data from the European Registry of Quality Outcomes for Cataract and Refractive Surgery (EUREQUO) were analyzed. The EUREQUO contains preoperative baseline, intraoperative, and follow-up data. Intraoperative data include dropped nucleus as a complication. Baseline data such as demographic data, ocular comorbidities, surgical difficulties, and visual and refractive outcomes were tested for association with a dropped nucleus for the study period from January 1, 2008, to December 31, 2018. RESULTS: The number of reported patients with complete data was 1 715 348. Dropped nucleus was reported in 1221 eyes (0.071%) during the study period. White cataract, previous vitrectomy, poor preoperative visual acuity, small pupil, pseudoexfoliation, diabetic retinopathy, and male sex were significantly related to dropped nucleus. Year of surgery showed a significant trend of decreasing occurrence of dropped nucleus over time. Eyes with the complication of a dropped nucleus also had a poorer visual and refractive outcome compared with eyes with existing risk factors but no such complication. CONCLUSIONS: Many risk factors for dropped nucleus complications were identified. A significant trend of decreasing occurrence of dropped nucleus was found for the study period. The visual and refractive outcome was poorer for eyes with a dropped nucleus.


Subject(s)
Intraoperative Complications/epidemiology , Lens Nucleus, Crystalline/pathology , Outcome Assessment, Health Care/standards , Phacoemulsification/standards , Aged , Cross-Sectional Studies , Europe/epidemiology , Female , Humans , Incidence , Intraoperative Complications/pathology , Male , Refraction, Ocular/physiology , Registries , Retrospective Studies , Risk Factors , Visual Acuity/physiology , Vitrectomy
3.
Graefes Arch Clin Exp Ophthalmol ; 257(12): 2671-2676, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31641883

ABSTRACT

PURPOSE: To evaluate the safety of phacoemulsification of cataract in patients taking new oral anticoagulants (NOACs). METHODS: In a prospective case series, consecutive patients on NOACs (dabigatran, rivaroxaban, or apixaban) who were referred for uncomplicated cataract surgery to the eye institute underwent a thorough ophthalmological and hematological evaluation. Rivaroxaban and apixaban anti-factor Xa tests, and diluted thrombin time for dabigatran, were used for monitoring anticoagulation levels in blood. Blood was drawn for these tests just prior to surgery and at a peak level of the drug at about 4 h post-surgery (2 h after the drug was given). All surgeries were videotaped and patients were examined at 1 and 7 days after the operation. The main outcome measures included assessment of intra-operative, postoperative ocular bleeding, and other related complications. RESULTS: Thirty-five eyes of 25 unrelated patients ranging in age from 63 to 92 years (mean 77.6 years) underwent phacoemulsification. Intra-operative bleeding was observed in 5 eyes from the conjunctiva or limbus at the main incision site. No intraocular bleeding occurred. No hemorrhagic complications were observed during the 1-week follow-up. According to anti-factor Xa levels prior to surgery and following surgery, 85% of the patients were on therapeutic levels of NOACs. CONCLUSIONS: Clear corneal incision phacoemulsification performed under topical anesthesia can be safely performed in simple cases of cataract without discontinuing NOAC treatment.


Subject(s)
Blood Loss, Surgical/statistics & numerical data , Dabigatran/administration & dosage , Eye Hemorrhage/chemically induced , Phacoemulsification/standards , Postoperative Hemorrhage/chemically induced , Pyrazoles/administration & dosage , Pyridones/administration & dosage , Rivaroxaban/administration & dosage , Administration, Oral , Aged , Aged, 80 and over , Antithrombins/administration & dosage , Antithrombins/adverse effects , Dabigatran/adverse effects , Eye Hemorrhage/epidemiology , Factor Xa Inhibitors/administration & dosage , Factor Xa Inhibitors/adverse effects , Female , Follow-Up Studies , Humans , Incidence , Israel/epidemiology , Male , Middle Aged , Postoperative Hemorrhage/epidemiology , Prospective Studies , Pyrazoles/adverse effects , Pyridones/adverse effects , Rivaroxaban/adverse effects , Thromboembolism/prevention & control
5.
J Pak Med Assoc ; 68(1): 81-84, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29371724

ABSTRACT

OBJECTIVE: To evaluate the accuracy of biometry in the post-op phase of cataract surgery. METHODS: This study was conducted at Liaquat National Hospital, Karachi, from June 2015 to July 2016, and comprised the audit of patients who underwent cataract surgery during the period. Keratometry was done on Haag-Strait manual keratometer and A-scan was done by applanation contact method on SonoMed machine. Theoretic-T formula was used to calculate desired intraocular lens power for all kinds of axial lengths. A single surgeon operated upon the same Alcon Constellation phacoemulsification machine. Postoperative follow-up was done by monitoring auto refraction and visual acuity on days 1, 7, 30 and 90. SPSS 21 was used for data analysis.. RESULTS: Of 244 patients, 121(49.60%) were males and 123(50.40%) were females. There were 123(50.40%) right eyes and 121(49.60%) left eyes. Overall, 132(54.10%) achieved postoperative refraction within ±0.5 D of target and 193(79.10%) within ±1 D of target. Age, gender and laterality had no significant effect on outcomes (p>0.05 each). CONCLUSIONS: Postoperative refraction corresponded quite closely with global recommendations.


Subject(s)
Lens Implantation, Intraocular/standards , Lenses, Intraocular , Phacoemulsification/standards , Adult , Aged , Biometry , Female , Humans , Lenses, Intraocular/standards , Lenses, Intraocular/statistics & numerical data , Male , Medical Audit , Middle Aged , Pakistan , Tertiary Care Centers , Visual Acuity/physiology
6.
J Fr Ophtalmol ; 40(8): 636-641, 2017 Oct.
Article in French | MEDLINE | ID: mdl-28882391

ABSTRACT

INTRODUCTION: Since 2013, at the French society of ophthalmology (FSO) meetings, two simulators for intraocular surgeries have been available. The goal of this study was to assess the satisfaction of the participants in these organized training sessions. MATERIALS AND METHODS: A questionnaire was mailed to participants in the FSO sessions as well as those carried out during the annual congress. This questionnaire collected data on the participants and the practical modalities of the sessions, and assessed participants' feelings and satisfaction with these sessions. RESULTS: The participants in the SFO sessions were young members of the SFO (31.8±12.3 years). 53.8 % were in training, looking to improve a problematic surgical step (capsulorhexis in 51.5 %). They spent nearly 5hours on simulators (4.8hours) and were alone on a simulator 50 % of the time. The sessions held during the annual congress were used by older physicians (41.9±26.4 years) already in practice (66.6 %). The goal of such training was curiosity in a third of the cases (to try the simulators). The majority spent less than an hour on the devices and were at least two participants per machine. Despite these differences, participants cited a role for their surgical learning curve and recommended such training to their colleagues. CONCLUSIONS: The participants' enthusiasm for this new training technique is highlighted by the results of this study.


Subject(s)
Education, Medical, Continuing , Internship and Residency , Ophthalmologic Surgical Procedures/education , Ophthalmology/education , Simulation Training , Adult , Clinical Competence , Computer Simulation , Education, Medical, Continuing/methods , Education, Medical, Continuing/standards , France , Humans , Internship and Residency/methods , Internship and Residency/standards , Job Satisfaction , Middle Aged , Ophthalmology/organization & administration , Phacoemulsification/education , Phacoemulsification/methods , Phacoemulsification/standards , Simulation Training/methods , Simulation Training/standards , Societies, Medical/organization & administration , Vitrectomy/education , Vitrectomy/methods , Vitrectomy/standards , Young Adult
7.
J Cataract Refract Surg ; 42(3): 385-91, 2016 Mar.
Article in English | MEDLINE | ID: mdl-27063518

ABSTRACT

PURPOSE: To identify the clinical and operative factors predicting reoperation within 30 days of resident-performed cataract surgery and correlate them with 1-year visual outcomes. SETTING: Michael E. DeBakey Veterans Affairs Medical Center, Houston, Texas, USA. DESIGN: Retrospective cohort study. METHODS: The study assessed patients who had resident-performed cataract surgery between 2005 and 2013 and required return to the operating room for a second surgery on the same eye within 30 days. Preoperative and intraoperative risk factors were assessed. Outcome measures included corrected distance visual acuity (CDVA) at 1 year. RESULTS: A review of 6644 resident-performed cataract surgeries showed that 54 eyes (0.85%) of 54 patients required a return to the operating room within 30 days. The reoperation rate was higher in the first half of the academic year (1.18%) than in the second half (0.55%) (P = .004). The mean CDVA 1 year postoperatively was 20/40, with a loss of lines of vision in 4 eyes. The mean operative time was 59.23 minutes ± 35.05 (SD). A longer intraoperative time was predictive of a worse visual outcome (P < .01). CONCLUSIONS: Despite the need for reoperation within 30 days, most patients achieved improved visual acuity. The reoperation rate was significantly lower in the second half of the academic year. Increased operation times correlated with worse visual acuity independent of other variables.


Subject(s)
Internship and Residency/standards , Intraoperative Complications , Ophthalmology/education , Phacoemulsification/standards , Postoperative Complications , Reoperation/statistics & numerical data , Cohort Studies , Female , Humans , Lens Implantation, Intraocular , Male , Operating Rooms/statistics & numerical data , Operative Time , Patient Outcome Assessment , Retrospective Studies , Visual Acuity/physiology
8.
J Cataract Refract Surg ; 42(3): 370-84, 2016 Mar.
Article in English | MEDLINE | ID: mdl-27063517

ABSTRACT

PURPOSE: To explore visual outcomes, functional visual improvement, and events in resident-operated cataract surgery cases. SETTING: Veterans Affairs Ophthalmic Surgery Outcomes Database Project across 5 Veterans Affairs Medical Centers. DESIGN: Retrospective data analysis of deidentified data. METHODS: Cataract surgery cases with residents as primary surgeons were analyzed for logMAR corrected distance visual acuity (CDVA) and vision-related quality of life (VRQL) measured by the modified National Eye Institute Vision Function Questionnaire and 30 intraoperative and postoperative events. In some analyses, cases without events (Group A) were compared with cases with events (Group B). RESULTS: The study included 4221 cataract surgery cases. Preoperative to postoperative CDVA improved significantly in both groups (P < .0001), although the level of improvement was less in Group B (P = .03). A CDVA of 20/40 or better was achieved in 96.64% in Group A and 88.25% in Group B (P < .0001); however, Group B had a higher prevalence of preoperative ocular comorbidities (P < .0001). Cases with 1 or more events were associated with a higher likelihood of a postoperative CDVA worse than 20/40 (odds ratio, 3.82; 95% confidence interval, 2.92-5.05; P < .0001) than those who did not experience an event. Both groups had a significant increase in VRQL from preoperative levels (both P < .0001); however, the level of preoperative to postoperative VRQL improvement was significantly less in Group B (P < .0001). CONCLUSION: Resident-operated cases with and without events had an overall significant improvement in visual acuity and visual function compared with preoperatively, although this improvement was less marked in those that had an event. FINANCIAL DISCLOSURE: None of the authors has a financial or proprietary interest in any material or method mentioned.


Subject(s)
Internship and Residency , Ophthalmologists/education , Phacoemulsification/standards , Quality of Health Care/standards , Quality of Life/psychology , Veterans Health , Visual Acuity/physiology , Clinical Competence , Humans , Intraoperative Complications , Outcome Assessment, Health Care , Postoperative Complications , Retrospective Studies , Sickness Impact Profile , Surveys and Questionnaires , United States , United States Department of Veterans Affairs
9.
Ophthalmology ; 123(4): 723-8, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26804760

ABSTRACT

PURPOSE: To identify safety and effectiveness outcomes of office-based cataract surgery. Each year, approximately 3.7 million cataract surgeries in the United States are performed in Ambulatory Surgery Center (ASC) and Hospital Outpatient Department (HOPD) locations. Medicare in July 2015 published a solicitation for expert opinion on reimbursing office-based cataract surgery. DESIGN: Large-scale, retrospective, consecutive case series of cataract surgeries performed in Minor Procedure Rooms (MPRs) of a large US integrated healthcare center. PARTICIPANTS: More than 13 500 patients undergoing elective office-based cataract surgery. METHODS: Phacoemulsification cataract surgery performed in MPRs of Kaiser Permanente Colorado from 2011 to 2014. MAIN OUTCOME MEASURES: Postoperative visual acuity and intraoperative and postoperative adverse events (AEs). RESULTS: Office-based cataract surgery was completed in 21 501 eyes (13 507 patients, age 72.6±9.6 years). Phacoemulsification was performed in 99.9% of cases, and manual extracapsular extraction was performed in 0.1% of cases. Systemic comorbidities included hypertension (53.5%), diabetes (22.3%), and chronic obstructive pulmonary disease (9.4%). Postoperative mean best-corrected visual acuity measured 0.14±0.26 logarithm of the minimum angle of resolution units. Intraoperative ocular AEs included 119 (0.55%) cases of capsular tear and 73 (0.34%) cases of vitreous loss. Postoperative AEs included iritis (n = 330, 1.53%), corneal edema (n = 110, 0.53%), and retinal tear or detachment (n = 30, 0.14%). No endophthalmitis was reported. Second surgeries were performed in 0.70% of treated eyes within 6 months. There were no life- or vision-threatening intraoperative or perioperative AEs. CONCLUSIONS: This is the largest US study to investigate the safety and effectiveness of office-based cataract surgery performed in MPRs. Office-based efficacy outcomes were consistently excellent, with a safety profile expected of minimally invasive cataract procedures performed in ASCs and HOPDs.


Subject(s)
Ambulatory Surgical Procedures/standards , Intraoperative Complications , Lens Implantation, Intraocular , Phacoemulsification/standards , Postoperative Complications , Visual Acuity/physiology , Aged , Aged, 80 and over , Ambulatory Care Facilities/standards , Ambulatory Surgical Procedures/adverse effects , Databases, Factual , Female , Humans , Male , Middle Aged , Outcome and Process Assessment, Health Care , Phacoemulsification/adverse effects , Retrospective Studies , Treatment Outcome , United States
12.
Clin Exp Ophthalmol ; 43(6): 514-22, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25644026

ABSTRACT

BACKGROUND: To provide local data on visual acuity and surgical outcomes for cataract surgery performed in an Australian teaching hospital. DESIGN: Continuous audit over 7 years in a public teaching hospital. PARTICIPANTS: A total of 3740 eyes had cataract surgery performed at The Queen Elizabeth Hospital, South Australia, from May 2006 to September 2013. METHODS: Visual acuity and complication rates were recorded for cataract surgery cases operated on between May 2006 and September 2013 on a digital database with data entry contemporaneous with final follow-up. MAIN OUTCOME MEASURES: Visual acuity and surgical complications. RESULTS: Of the patients, 91.4% achieved postoperative best-measured vision better than preoperative best-measured vision. The rate of posterior capsular tear was 2.59%, endophthalmitis was 0.11% and the overall complication rate was 11.7%. CONCLUSIONS: This audit is the first to document modern cataract surgery, overwhelmingly dominated by phacoemulsification in an Australian population and can be used to benchmark cataract surgery outcome in an urban Australian population.


Subject(s)
Hospitals, Teaching/statistics & numerical data , Hospitals, Urban/statistics & numerical data , Intraoperative Complications , Medical Audit , Phacoemulsification/standards , Postoperative Complications , Visual Acuity/physiology , Anesthesia/methods , Anesthetics/administration & dosage , Humans , Phacoemulsification/statistics & numerical data , Prognosis , Quality Assurance, Health Care/standards , Refraction, Ocular/physiology , South Australia/epidemiology
13.
Ophthalmology ; 122(2): 281-7, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25444350

ABSTRACT

OBJECTIVE: To evaluate whether an ophthalmologist-led, non-anesthesia-supported, limited monitoring pathway for phacoemulsification/intraocular lens cataract surgery, can be performed safely with only a medical emergency team providing support. DESIGN: Retrospective, observational, cohort study. PARTICIPANTS: All patients who underwent elective phacoemulsification/intraocular lens surgery under topical anesthesia in the ophthalmology outpatient unit between January 1, 2011, and December 31, 2012. METHODS: Cataract surgery was performed by phacoemulsification under topical anesthesia. The intake process mainly embraced ophthalmic evaluation, obtaining a medical history, and proposing the procedure. A staff ophthalmologist performed the procedure assisted by 2 registered nurses in an independent outpatient clinic operating room within the hospital. The clinical pathway was without dedicated presence of or access to anesthesia service. Perioperative monitoring was limited to blood pressure and plethysmography preoperatively and intraoperatively. Patients were offered supportive care and instructed to avoid fasting and continue all their chronic medication. MAIN OUTCOME MEASURES: The primary outcome measure was the incidence of adverse events requiring medical emergency team (MET) interventions throughout the pathway. Secondary outcome measures were surgical ocular complication rates, use of oral sedatives, and reported reasons to perform the surgery in the classical operation room complex. RESULTS: Within the cataract pathway, 6961 cases (4347 patients) were eligible for analysis. Three MET interventions related to the phacoemulsification/intraocular lens pathway occurred in the 2-year study period, resulting in an intervention rate of 0.04%. None of the interventions was intraoperative. All 3 patients were diagnosed as vasovagal collapse and recuperated uneventfully. No hospital admittance was required. Eight other incidents occurred within the general ophthalmology outpatient unit population during the study period. CONCLUSIONS: Cataract surgery can be safely performed in an outpatient clinic, in the absence of the anesthesia service and with limited workup and monitoring. Basic first aid and basic life support skills seem to be sufficient in case of an adverse event. An MET provides a generous failsafe for this low-risk procedure.


Subject(s)
Ambulatory Surgical Procedures/standards , Lens Implantation, Intraocular , Ophthalmology/standards , Phacoemulsification/standards , Practice Guidelines as Topic/standards , Aged , Aged, 80 and over , Anesthesia, Local/methods , Conscious Sedation/methods , Emergency Medical Services/statistics & numerical data , Female , Humans , Hypnotics and Sedatives/administration & dosage , Male , Middle Aged , Monitoring, Intraoperative/methods , Phacoemulsification/adverse effects , Retrospective Studies , Risk Assessment , Syncope, Vasovagal/epidemiology , Syncope, Vasovagal/etiology
14.
Int Ophthalmol ; 35(2): 173-8, 2015 Apr.
Article in English | MEDLINE | ID: mdl-24728533

ABSTRACT

Primary angle closure occurs as a result of crowded anterior segment anatomy, causing appositional contact between the peripheral iris and trabecular meshwork, thereby obstructing aqueous outflow. Several studies highlight the role of the crystalline lens in its pathogenesis. The objective of this work is to compare the long-term efficacy of phacoemulsification versus laser peripheral iridotomy (LPI) in the management of chronic primary angle closure (CPAC). Prospective case-control study with 30 eyes of 30 patients randomly divided in two groups: 15 eyes in the LPI group and 15 eyes in the IOL group. Patients in the LPI group underwent LPI using argon and Nd:YAG laser. Patients in the IOL group underwent phacoemulsification with posterior chamber intraocular lens (IOL) implantation. Examinations before and after the procedure included gonioscopy, Goldmann applanation tonometry, and anterior chamber evaluation using the Pentacam rotating Scheimpflug camera. The mean follow-up time was 31.13 ± 4.97 months. There was a statistically significant reduction in the intraocular pressure (IOP) and number of anti-glaucoma medications (p < 0.01) only in the IOL group. Anterior chamber depth, angle, and volume were all higher in the IOL group (p < 0.01) at the end of the follow-up period. Phacoemulsification with posterior chamber IOL implantation results in a higher anterior chamber depth, angle, and volume, when compared to LPI. Consequently, phacoemulsification has greater efficacy in lowering IOP and preventing its long-term increase in patients with CPAC and cataract.


Subject(s)
Glaucoma, Angle-Closure/surgery , Iridectomy/standards , Phacoemulsification/standards , Adult , Aged , Chronic Disease , Female , Follow-Up Studies , Glaucoma, Angle-Closure/physiopathology , Humans , Intraocular Pressure/physiology , Iridectomy/methods , Laser Therapy/methods , Lens Implantation, Intraocular , Male , Middle Aged , Prospective Studies
15.
J Cataract Refract Surg ; 40(9): 1506-1513.e4, 2014 Sep.
Article in English | MEDLINE | ID: mdl-25135543

ABSTRACT

PURPOSE: To develop and assess the validity of an evaluation tool to assess quantitatively the hydrodissection and phacoemulsification portions of cataract surgery performed by residents. DESIGN: Case series. SETTING: Jules Stein Eye Institute, Olive View-UCLA Medical Center, and Veterans Administration Medical Center, Los Angeles, California, USA. METHODS: The UCLA ophthalmology faculty members were surveyed and the literature was reviewed to develop a grading tool consisting of 15 questions to evaluate surgical technique, including questions from the Global Rating Assessment of Skills in Intraocular Surgery and from the International Council of Ophthalmology's Ophthalmology Surgical Competency Assessment Rubric. Video clips of the hydrodissection and phacoemulsification portions of cataract surgery performed by 1 postgraduate year 2 (PGY2) resident, 1 PGY3 resident, 2 PGY4 residents, and an advanced surgeon were independently graded in a masked fashion by an 8-member faculty panel. RESULTS: Eleven of the 15 questions had a significant association with surgical experience level (P<.05, analysis of variance). Interobserver variability in grading yielded intraclass correlation coefficients between 0.28 and 0.72. The questions with the lowest interobserver variability were hydrodissection questions on instrument handling, flow of operation, and nucleus rotation. Nucleus cracking also had low variability. Less directly visible tasks, especially 3-dimensional tasks, had wider interobserver variability. CONCLUSIONS: Surgical performance can be validly measured using an evaluation tool. Improved videography and studies to identify the best questions for evaluating each step of cataract surgery may help ophthalmic educators more precisely measure training outcomes for improving teaching interventions. FINANCIAL DISCLOSURE: No author has a financial or proprietary interest in any material or method mentioned.


Subject(s)
Clinical Competence/standards , Education, Medical, Graduate , Educational Measurement/methods , Internship and Residency , Ophthalmology/education , Phacoemulsification/standards , Teaching/methods , Adult , Cataract Extraction/education , Cataract Extraction/standards , Humans , Observer Variation , Operative Time , Phacoemulsification/education , Reproducibility of Results , Surveys and Questionnaires , Video Recording
17.
Arch. Soc. Esp. Oftalmol ; 88(4): 139-144, abr. 2013. ilus, graf
Article in Spanish | IBECS | ID: ibc-111856

ABSTRACT

Objetivo: Estudiar la implicación de las características preoperatorias anatómicas (según el parámetro del grosor foveal central, determinado mediante tomografía de coherencia óptica) y funcionales (según el parámetro de la mejor agudeza visual corregida, [MAVC]) en la recuperación funcional tras la cirugía de las membranas epirretinianas maculares (MEM). Métodos: En este estudio prospectivo, longitudinal se incluyeron 88 ojos (de 86 pacientes), intervenidos mediante vitrectomía debido a MEM, en un período de 3 años. Se analizaron: etiología de la MEM, MAVC, existencia o no de metamorfopsia, estado del cristalino, y grosor foveal central. Asimismo se recogieron los datos relativos a la cirugía y las complicaciones derivadas de la misma, así como los cambios observados en la MAVC y en el grosor foveal a lo largo del período de seguimiento. Resultados: Se produjo mejoría de la MAVC en el 82% de los casos, así como una disminución del grosor foveal en el 79% de los casos intervenidos, ambos estadísticamente significativos (p<0,01). Sin embargo, la mayor parte de los pacientes exhibieron grados variables de edema y/o engrosamiento macular en el postoperatorio. Se halló correlación significativa entre la MAVC preoperatoria y postoperatoria (p=0,001), así como entre el grosor foveal central preoperatorio y postoperatorio (p=0,004), pero no entre la MAVC y el grosor foveal. Conclusiones: Se produce una recuperación funcional en términos de MAVC en más del 80% de los pacientes tras cirugía de MEM. La mayor parte de los ojos muestran persistencia del engrosamiento macular, si bien este no parece tener influencia en la agudeza visual final. El mejor determinante de recuperación funcional postoperatoria (agudeza visual postoperatoria) parece ser, en nuestra experiencia, la agudeza visual preoperatoria y no el grosor macular(AU)


Objective: To study the influence of anatomic preoperative characteristics (based on the parameter, foveal central thickness, measured by optical coherence tomography) and functional characteristics (based on the parameter, best corrected visual acuity, [BCVA]) on functional recovery after epiretinal membrane (ERM) surgery. Methods: A total of 88 eyes (of 86 patients), on whom a vitrectomy due to ERM was performed during a 3 years period were reviewed in this longitudinal, prospective study. An analysis was made of, ERM aetiology, BCVA, presence or absence of metamorphopsia, lens status, and central foveal thickness. Data relating to surgery and local complications, changes in BCVA, and changes in foveal central thickness were collected during the follow-up period. Results: An improvement was in observed in BCVA in 82%, as well as a decrease in foveal thickness in 79% of the eyes which underwent surgery, both of these being statistically significant (P<0.01). However, most of the patients showed different grades of oedema and/or macular thickening in the postoperative period. A significant correlation was found between preoperative and postoperative BCVA (P=0.001), and also between preoperative and postoperative central foveal thickness (P=0.004), but not between BCVA and foveal thickness. Conclusions: There is functional recovery in terms of BCVA in more than 80% of the patients after ERM surgery. Most of the eyes showed persistent macular thickening, but this did not seem to have influenced the final BCVA. The best determinant of postoperative functional recovery (postoperative visual acuity) is, in our experience, the preoperative BCVA, and not the macular thickness(AU)


Subject(s)
Humans , Male , Female , Middle Aged , Macular Edema/complications , Macular Edema/diagnosis , Macular Edema/surgery , Vitrectomy/methods , Vitrectomy , Visual Acuity/physiology , Phacoemulsification/standards , Phacoemulsification , Macular Edema/physiopathology , Macular Edema , Prospective Studies , Longitudinal Studies , Ophthalmoscopy/methods , Ophthalmoscopy , Tomography, Optical Coherence/methods , Tomography, Optical Coherence/trends , Tomography, Optical Coherence
18.
Graefes Arch Clin Exp Ophthalmol ; 251(4): 1157-61, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23280561

ABSTRACT

BACKGROUND: To measure the efficiency of phacoemulsification, we have developed a new experimental model for testing phaco-efficiency and analyzed re-aspiration of repulsed particles. METHODS: Using a Kitaro wetlab system, a piece of blood agar (BA) was placed in an artificial chamber and the phacoemulsifier was placed horizontally. The settings of the phacoemulsifier (Infiniti, Alcon Laboratories) were 26 cc/min for aspiration, 350 cc/min for vacuum, and 95 cm of bottle height. The time to remove BAs was measured using Ozil 100 %, Ozil 40 %, and longitudinal 40 % of phaco power. The angle between the re-aspirated BA particles and the axis of the phacoemulsifier (re-aspiration zone, degree) was analyzed. RESULTS: The average time (seconds) to remove BAs was lower in the Ozil 100 % and the Ozil 40 % mode than in the longitudinal mode (0.37 ± 0.39, 0.85 ± 0.57, and 2.22 ± 1.40 respectively, P value < 0.01). Repulsion exceeding 1 mm occurred more frequently in the longitudinal mode than in the Ozil 100 % mode (100 % vs 40 %, P value = 0.01, Fisher's exact test). The average of re-aspiration zone was 25.9 ± 14.5 in the longitudinal 40 % and 54.0 ± 23.0 in the Ozil 40 % (P value = 0.016). CONCLUSIONS: The Ozil mode was more efficient than the longitudinal mode. In addition, the Ozil mode provided less repulsion and wider aspiration zone.


Subject(s)
Anterior Chamber , Phacoemulsification/standards , Suction , Artificial Organs , Humans , Hydrodynamics , Phacoemulsification/methods , Vacuum
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