Eye Trauma
Conditions
Keywords
Corneal, penetrating injury, lamellar laceration, COVID, polyglactin, Vicryl
Brief summary
Vicryl (polyglactin) 10-0 resorbable suture is rarely used, little known to ophthalmologists but may offer therapeutic and practical advantages in eligible cases of corneal trauma, particularly during a COVID-19 pandemic. This has imposed new sanitary restrictions : limited access to the operating room in ophthalmology only for functional emergencies and a drastically reduced capacity for external consultations in favor of teleconsultation. The aim of this study is to evaluate the Vicryl 10-0 (polyglactin 910) resorbable monofilament suture in corneal trauma, rather than classic Nylon 10-0: structural and functional results, and adaptation of postoperative follow-up during a sanitary crisis period.
Interventions
OTHERdata collection
Collection of clinical and paraclinical data during preoperative consultation Collection of clinical and paraclinical data during post-operative consultations Tele-consultation to determine if criteria for good healing / adherence, treatment tolerance / response to questions Remote follow-up 6 and 12 months after the trauma
Sponsors
Centre Hospitalier Universitaire de Saint Etienne
Study design
Observational model
COHORT
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
* Corneal penetrating injury and/or lamellar laceration
Exclusion criteria
* Corneal Penetrating injury trauma requiring necessarily ONLY Nylon 10-0 * Traumatism requiring necessarily a cryopreserved human amniotic membrane (for example) * Traumatism eligible for biological glue (long-axis wound \< 2 mm)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| change visual acuity (Snellen scale) from baseline and 2, 6, 12 and 18 months after the intervention | Months: 0, 2, 6, 12, 18 | Collected in the medical record. |
| change Visual acuity (Parinaud scale) from baseline and 2, 6, 12 and 18 months after the intervention | Months: 0, 2, 6, 12, 18 | Collected in the medical record. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Astigmatism (diopter) | Months: 0, 2, 6, 12, 18 | Collected in the medical record. Measured by OCT-TOMEY-CASIA). |
| Number of postoperative external consultations | Months: 0, 2, 6, 12, 18 | Collected in the medical record. |
| Adverse events | Months: 0, 2, 6, 12, 18 | Collected in the medical record. All adverse events connecting to the eye surgery. |
Countries
France
Outcome results
None listed