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1.
Pediatr Emerg Care ; 37(9): 462-465, 2021 Sep 01.
Article in English | MEDLINE | ID: covidwho-1266235

ABSTRACT

OBJECTIVES: The objective of this study was to describe the incidence and severity of ocular exposure to alcohol-based hand rub (ABHR) in children presenting to a tertiary medical center during the severe acute respiratory syndrome coronavirus 2 pandemic. METHODS: A retrospective single-center observational study conducted from February 21, 2020, to October 11, 2020. Subjects 10 years or younger who presented with ABHR-induced ocular injury were included. The same period from 2019 was studied and a comparison was performed between the 2 years. Outcome measures included the number of subjects with ocular injury due to ABHR, extent of ocular epithelial defects, length of hospitalization and time to resolution. RESULTS: A total of 9 patients presented to the Pediatric Emergency Department after sustaining ocular chemical injuries from ABHR during this period. Treatment included immediate irrigation followed by topical antibiotics, steroids, and lubrication. Six children were discharged and followed as outpatients with no reported adverse ocular sequelae. Three patients exhibited epithelial defects involving 85% to 100% of the cornea, 30% to 75% of the conjunctiva and required inpatient treatment ranging from 4 to 11 days. All patients experienced a complete resolution of the ocular epithelial defects after 12 to 19 days. No long-term irreversible damage was observed and visual acuity returned to normal in all patients. CONCLUSIONS: The utilization of ABHR during the severe acute respiratory syndrome coronavirus 2 pandemic resulted in childhood ocular injury. Prompt treatment led to good visual outcomes. These products should be regarded as potentially toxic and stored out of the reach of young children.


Subject(s)
COVID-19 , Eye Injuries , Hand Sanitizers , Child , Child, Preschool , Humans , Retrospective Studies , SARS-CoV-2
2.
Cornea ; 40(8): 1070-1072, 2021 08 01.
Article in English | MEDLINE | ID: covidwho-1240939

ABSTRACT

PURPOSE: The aim of this report was to report 2 patients who presented with acute corneal graft rejection 2 weeks after receiving the BNT162b2 messenger RNA (mRNA) vaccine for severe acute respiratory syndrome coronavirus 2. METHODS: Case report. RESULTS: Two men, aged 73 and 56 years, with a history of penetrating keratoplasty due to keratoconus were noted to have acute corneal graft rejection 2 weeks after receiving a first dose of the BNT162b2 mRNA vaccine. Both patients were treated with hourly dexamethasone 0.1% and oral prednisone 60 mg per day with prompt resolution of keratoplasty rejection. CONCLUSIONS: The BNT162b2 mRNA vaccine may be have been associated with a low-risk corneal graft rejection that responded well to topical and systemic steroids. Treating physicians should be aware of this potential complication and patients should be advised to report any visual changes after vaccination.


Subject(s)
COVID-19 Vaccines/adverse effects , COVID-19/prevention & control , Graft Rejection/etiology , Keratoplasty, Penetrating , SARS-CoV-2 , Vaccines, Synthetic/adverse effects , Acute Disease , Administration, Ophthalmic , Administration, Oral , Aged , BNT162 Vaccine , COVID-19 Testing , Dexamethasone/therapeutic use , Graft Rejection/drug therapy , Humans , Male , Middle Aged , Prednisone/therapeutic use
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