Refractive Changes Following Vitrectomy

Sponsor
Bursa Retina Eye Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04712786
Collaborator
(none)
47
1
26
55

Study Details

Study Description

Brief Summary

We aimed o compare the refractive changes associated with pars plana vitrectomy with or without intraocular gas tamponade in pseudophakic eyes. This retrospective study included pseudophakic patients with Nd:YAG laser posterior capsulotomy who underwent 23G PPV between February 2015 and March 2019. Group 1 consisted of patients with regmatogenous RD who underwent PPV and 12% perflouropropane (C3F8) gas tamponade whereas Group 2 consisted of patients who underwent PPV for epiretinal membrane or vitreous hemorrhage (VH). No tamponade was used in Group 2. Minimum follow-up was 12 months.

Condition or Disease Intervention/Treatment Phase
  • Other: pars plana vitrectomy

Detailed Description

This research was reviewed by an independent ethical review board and conforms with the principles and applicable guidelines for the protection of human subjects in biomedical research. This was a retrospective, comparative case series including pseudophakic patients who underwent PPV. Group 1 consisted of patients with pseudophakic RRD who underwent PPV and 12% perflouropropane (C3F8) gas tamponade whereas Group 2 consisted of patients with ERM or VH who underwent PPV without any tamponade between February 2015 and March 2019 at Bursa Retina Eye Hospital. Informed consent was obtained from all the participants. The study was in line with the ethical standarts of the Helsinki Declaration

Patient eligibility Patients who underwent uncomplicated cataract surgery with phacoemulsification and in-the-bag IOL implantation and subsequent neodymium:yttrium-aluminum-garnet (Nd:YAG) laser due to capsular opacification were included. Preoperative refractive data obtained after Nd:YAG laser and six months prior to vitrectomy surgery. Postoperative refractive data was obtained at 12 months after vitrectomy. Eyes with a preoperative spherical refractive error > ±6 D or cylindrical refractive error > ±3 D were excluded. Also eyes with corneal disorders were excluded.

Ocular parameters

All patients underwent complete ophtalmic examination including best corrected visual acuity (BCVA) in the logMAR scale, slit-lamp examination, intraocular pressure (IOP) assessment, fundus examination and autokeratorefractometry (auto kerato-refractometer KR-8800 from Topcon, Tokyo, Japan) at preoperative and postoperative month-12. Induced astigmatism values were calculated through vector analysis.

Surgical procedures

All surgeries were performed by the same surgeon (S.Y.). Retrobulbar block anesthesia (a mixture of 2 ml of lidocaine hydrochloride 2% and 2 ml of bupivacaine hydrochloride 0.5%) was used. Three port 23-gauge (G) transconjunctival PPV was performed using the vitrectomy system DORC (Dutch Ophthalmic Research Center, Zuidland, Netherlands) and Zeiss microscope with EIBOS 2 (Haag Streit, Mason, OH, USA) attachment for non-contact fundus viewing.

In group 1, all patients underwent a near-complete vitrectomy including base shaving, laser endo-photocoagulation and C3F8 gas tamponade. In group 2, patients with ERM received a limited vitrectomy including; core vitrectomy, induction of a posterior vitreous detachment if not present and peeling of the ERM and inner limiting membrane (ILM). Peripheral retina was examined with indentation to identify any retinal breaks. Neither laser endo-photocoagulation, nor gas tamponade and vitreous base shaving was performed. For patients with VH patients, a near-complete vitrectomy, including base shaving, laser endo-photocoagulation was performed except for gas tamponade. In both groups, the sclera is sutured with 8-0 polyglactin suture (Vicryl) in case of wound leakage.

Study Design

Study Type:
Observational
Actual Enrollment :
47 participants
Observational Model:
Other
Time Perspective:
Retrospective
Official Title:
Refractive Changes in Pseudophakic Eyes Following Vitrectomy With or Without Gas Tamponade
Actual Study Start Date :
Dec 1, 2020
Actual Primary Completion Date :
Dec 25, 2020
Actual Study Completion Date :
Dec 27, 2020

Arms and Interventions

Arm Intervention/Treatment
Group

27 patients, Group 1 consisted of patients with pseudophakic rhegmatogoneous retinal detachment who underwent pars plana vitrectomy and 12% perflouropropane (C3F8) gas tamponade and 20 patients Group 2 consisted of patients with epiretinal membrane or vitreous hemorrhage who underwent PPV without any tamponade

Other: pars plana vitrectomy
23 gauge pars plana vitrectomy was performed for retinal detachment, vitreous hemorrhage or epiretinal membrane

Outcome Measures

Primary Outcome Measures

  1. The rate of spherical and cylindrical refractive changes [12 months]

    Changes in spherical and cylindrical refractive error 12 months after pars plana vitrectomy

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

Inclusion Criteria

  • Patients aged ≥ 18 years

  • Pseudophakic patients who underwent pars plana vitrectomy

Exclusion Criteria

  • Patients aged 18 years >

  • Patients with a spherical refractive error > ±6 D

  • Patients with a cylindrical refractive error > ±3 D

Contacts and Locations

Locations

Site City State Country Postal Code
1 Retina Eye Hospital Bursa Turkey 16130

Sponsors and Collaborators

  • Bursa Retina Eye Hospital

Investigators

  • Principal Investigator: Sami Yılmaz, MD, Bursa Retina Eye Hospital
  • Study Director: Remzi Avcı, Professor, Bursa Retina Eye Hospital
  • Principal Investigator: Aysegul Mavi Yıldız, MD, Bursa Retina Eye Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
sami yilmaz, Medical doctor, ophthalmology specialist, Bursa Retina Eye Hospital
ClinicalTrials.gov Identifier:
NCT04712786
Other Study ID Numbers:
  • BursaRetinaEyeH
First Posted:
Jan 15, 2021
Last Update Posted:
Jan 15, 2021
Last Verified:
Jan 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by sami yilmaz, Medical doctor, ophthalmology specialist, Bursa Retina Eye Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 15, 2021