Effect of 0.2% carbomer ophthalmic ointment on eye discomfort after general anesthesia: A non-randomized cohort study.

Anestesia general Eye discomfort Eye lesion Eye protection Gel oftálmico General anesthesia Lesión ocular Malestar ocular Ophthalmic ointment

Journal

Revista espanola de anestesiologia y reanimacion
ISSN: 2341-1929
Titre abrégé: Rev Esp Anestesiol Reanim (Engl Ed)
Pays: Spain
ID NLM: 101778594

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 12 08 2020
accepted: 17 06 2021
pubmed: 15 10 2022
medline: 15 12 2022
entrez: 14 10 2022
Statut: ppublish

Résumé

Eye lesions during surgery are rare. Its common causes include direct trauma, chemical damage, and corneal exposure. Eye discomfort may present after surgery in the absence of structural damage. In our hospital, every patient under general anesthesia receives eye protection with eye occlusion associated in most cases with ophthalmic ointment application. We aim to analyze the incidence of eye discomfort with 0.2% carbomer application. A cohort study was conducted. Patients who underwent surgery under general anesthesia lasting less than 4h between February and November 2017 were enrolled. We excluded patients with previous ophthalmologic pathology, those undergoing eye, otolaryngology, face or head surgery, and patients in which eye occlusion was not possible. For analysis, patients were divided into two groups: simple eyelid occlusion (Group 1) and eyelid occlusion plus ophthalmic ointment (Group 2). Primary outcome was the incidence of eye discomfort and secondary outcomes were to stablish associated risk factors. 400 patients were analyzed, 50% were exposed to 0.2% carbomer. There was no difference in patients' demographics. During the first 24h post-surgery 7.25% of patients showed visual symptoms, and at one-week postoperative no patient referred symptoms. Most frequent symptoms were blurry vision, pruritus, epiphora and red-eye. On multivariate analysis, the main risk factor associated with eye discomfort was 0.2% carbomer application (RR 13.5 CI 3.27-56.2). Emergent surgery and age were also found to be risk factors. 0.2% carbomer does not prevent ophthalmologic symptoms after surgery and it may even increase them in short procedures.

Sections du résumé

BACKGROUND AND OBJECTIVE OBJECTIVE
Eye lesions during surgery are rare. Its common causes include direct trauma, chemical damage, and corneal exposure. Eye discomfort may present after surgery in the absence of structural damage. In our hospital, every patient under general anesthesia receives eye protection with eye occlusion associated in most cases with ophthalmic ointment application. We aim to analyze the incidence of eye discomfort with 0.2% carbomer application.
METHODS METHODS
A cohort study was conducted. Patients who underwent surgery under general anesthesia lasting less than 4h between February and November 2017 were enrolled. We excluded patients with previous ophthalmologic pathology, those undergoing eye, otolaryngology, face or head surgery, and patients in which eye occlusion was not possible. For analysis, patients were divided into two groups: simple eyelid occlusion (Group 1) and eyelid occlusion plus ophthalmic ointment (Group 2). Primary outcome was the incidence of eye discomfort and secondary outcomes were to stablish associated risk factors.
RESULTS RESULTS
400 patients were analyzed, 50% were exposed to 0.2% carbomer. There was no difference in patients' demographics. During the first 24h post-surgery 7.25% of patients showed visual symptoms, and at one-week postoperative no patient referred symptoms. Most frequent symptoms were blurry vision, pruritus, epiphora and red-eye. On multivariate analysis, the main risk factor associated with eye discomfort was 0.2% carbomer application (RR 13.5 CI 3.27-56.2). Emergent surgery and age were also found to be risk factors.
CONCLUSION CONCLUSIONS
0.2% carbomer does not prevent ophthalmologic symptoms after surgery and it may even increase them in short procedures.

Identifiants

pubmed: 36241513
pii: S2341-1929(22)00175-5
doi: 10.1016/j.redare.2021.06.004
pii:
doi:

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

674-679

Informations de copyright

Copyright © 2021 Sociedad Española de Anestesiología, Reanimación y Terapéutica del Dolor. Publicado por Elsevier España, S.L.U. All rights reserved.

Auteurs

G Madrid Díaz (G)

Departamento de Anestesiología, Fundación Santa Fe de Bogotá, Bogotá D.C., Colombia. Electronic address: gamanesthesia@gmail.com.

A Pinilla (A)

Departamento de Anestesiología, Fundación Santa Fe de Bogotá, Bogotá D.C., Colombia; Escuela de Medicina, Universidad de los Andes, Bogotá D.C., Colombia; Escuela de Medicina, Universidad El Bosque, Bogotá D.C., Colombia.

E Arango (E)

Departamento de Anestesiología, Fundación Santa Fe de Bogotá, Bogotá D.C., Colombia; Escuela de Medicina, Universidad de los Andes, Bogotá D.C., Colombia; Escuela de Medicina, Universidad El Bosque, Bogotá D.C., Colombia.

O Amaya (O)

Departamento de Anestesiología, Fundación Santa Fe de Bogotá, Bogotá D.C., Colombia; Escuela de Medicina, Universidad de los Andes, Bogotá D.C., Colombia; Escuela de Medicina, Universidad El Bosque, Bogotá D.C., Colombia.

F Raffan (F)

Departamento de Anestesiología, Fundación Santa Fe de Bogotá, Bogotá D.C., Colombia; Escuela de Medicina, Universidad de los Andes, Bogotá D.C., Colombia; Escuela de Medicina, Universidad El Bosque, Bogotá D.C., Colombia.

L Ferrer (L)

Departamento de Anestesiología, Fundación Santa Fe de Bogotá, Bogotá D.C., Colombia; Escuela de Medicina, Universidad de los Andes, Bogotá D.C., Colombia; Escuela de Medicina, Universidad El Bosque, Bogotá D.C., Colombia.

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