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Twenty-four-hour intraocular pressure monitoring in normotensive patients undergoing chronic hemodialysis.
Panagiotou, Evangelia S; Liakopoulos, Vassilios; Giannopoulos, Theodoros; Voudouragkaki, Irini C; Demirtzi, Paraskevi; Paschalinou, Eleni; Nikitidou, Olga; Kapis, Paraskevas V; Konstas, Anastasios G P.
Afiliação
  • Panagiotou ES; Glaucoma Unit, 1 University Department of Ophthalmology, Aristotle University of Thessaloniki, Thessaloniki - Greece.
  • Liakopoulos V; Renal Unit, 1 University Department of Internal Medicine, Aristotle University of Thessaloniki, Thessaloniki - Greece.
  • Giannopoulos T; Glaucoma Unit, 1 University Department of Ophthalmology, Aristotle University of Thessaloniki, Thessaloniki - Greece.
  • Voudouragkaki IC; Glaucoma Unit, 1 University Department of Ophthalmology, Aristotle University of Thessaloniki, Thessaloniki - Greece.
  • Demirtzi P; Renal Unit, 1 University Department of Internal Medicine, Aristotle University of Thessaloniki, Thessaloniki - Greece.
  • Paschalinou E; Glaucoma Unit, 1 University Department of Ophthalmology, Aristotle University of Thessaloniki, Thessaloniki - Greece.
  • Nikitidou O; Renal Unit, 1 University Department of Internal Medicine, Aristotle University of Thessaloniki, Thessaloniki - Greece.
  • Kapis PV; Glaucoma Unit, 1 University Department of Ophthalmology, Aristotle University of Thessaloniki, Thessaloniki - Greece.
  • Konstas AG; Glaucoma Unit, 1 University Department of Ophthalmology, Aristotle University of Thessaloniki, Thessaloniki - Greece.
Eur J Ophthalmol ; 26(1): 24-9, 2016.
Article em En | MEDLINE | ID: mdl-26165324
ABSTRACT

PURPOSE:

To investigate 24-hour intraocular pressure (IOP) changes caused by hemodialysis (HD).

METHODS:

A prospective, observational, comparative 24-hour trial was performed on consecutive subjects with normal IOP undergoing maintenance HD 3 days a week between 1300 and 1700 hours in an academic setting. Following a comprehensive ocular assessment, those with conditions that may influence IOP were excluded and one eye was randomly selected. Twenty-four-hour IOP monitoring was performed on HD day 1 and then on a day without HD. The IOP was measured at 1000, 1300, 1500, 1700, 2200, 0200, and 0600 employing Goldmann and Perkins tonometry on habitual position. During the course of 1 year, 18 patients completed the study.

RESULTS:

Monitoring of IOP on HD day showed a significantly higher mean 24-hour IOP (15.4 ± 2.7 vs 14.1 ± 2.2 mm Hg; p = 0.025), higher mean peak 24-hour IOP (18.5 ± 3.5 vs 15.8 ± 2.5 mm Hg; p = 0.003), and wider 24-hour IOP fluctuation (6.2 ± 2.3 vs 4.0 ± 1.9 mm Hg; p = 0.001). When individual time points were compared, IOP was significantly higher at 1700 on HD day, reflecting a gradual IOP elevation during HD (p = 0.021). Further, during the HD procedure (1300-1700), the mean IOP was significantly higher on a HD day (16.4 ± 3.0 vs 14.7 ± 2.4 mm Hg; p = 0.004).

CONCLUSIONS:

This prospective, before/after trial suggests that HD significantly impacts 24-hour IOP characteristics in normotensive eyes. The long-term significance of these findings requires further elucidation in normotensive patients and, predominantly, in patients with glaucoma undergoing HD.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glaucoma de Ângulo Aberto / Diálise Renal / Ritmo Circadiano / Pressão Intraocular / Falência Renal Crônica Tipo de estudo: Diagnostic_studies / Observational_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glaucoma de Ângulo Aberto / Diálise Renal / Ritmo Circadiano / Pressão Intraocular / Falência Renal Crônica Tipo de estudo: Diagnostic_studies / Observational_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article