Atonic pupil after cataract surgery.

J Cataract Refract Surg

Department of Ophthalmology, Storm Eye Institute, Medical University of South Carolina, Charleston, USA.

Published: March 1995

We report and describe the clinical findings of three patients who developed atonic pupil after uncomplicated extracapsular cataract extraction with posterior chamber intraocular lens implantation. All patients had normally reactive pupils one day postoperatively, but after two weeks, the pupils were dilated and nonreactive to light, accommodation, and miotics. To estimate the incidence of atonic pupil after cataract surgery, we sent a survey on the frequency, clinical features, and possible etiologies of this syndrome to members of the American Society of Cataract and Refractive Surgery. Of the 567 respondents, 60% had seen at least one case of atonic pupil in the past five years; they reported a total of 1543 cases during that time. This is probably a conservative figure since many cases undoubtedly go unnoticed because of a lack of visual disturbance. We believe this condition occurs more frequently than previously reported. The atonic pupil should be recognized as a possible complication of cataract surgery that should be included in the preoperative consent form.

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0886-3350(13)80505-6DOI Listing

Publication Analysis

Top Keywords

atonic pupil
20
cataract surgery
12
pupil cataract
8
atonic
5
cataract
5
surgery
4
surgery report
4
report describe
4
describe clinical
4
clinical findings
4

Similar Publications

Aim: To observe the clinical outcomes of 30-gauge (G) needle-guided 10-0 prolene suture purse-string pupilloplasty for atonic pupil management.

Methods: Eight patients with atonic pupils who underwent suture purse-string pupilloplasty were retrospectively analyzed. Preoperative data and at least 6mo of postoperative data were collected from all the patients.

View Article and Find Full Text PDF

Bilateral acute iris transillumination (BAIT) is characterized by abundant pigment discharge into the anterior chamber. Atonic pupil and severe intraocular pressure (IOP) elevations may be observed. Generally, there is a viral upper respiratory tract infection or systemic fluoroquinolone usage before BAIT.

View Article and Find Full Text PDF

Warburg micro syndrome (WARBM) is a rare, autosomal recessive, neurodevelopmental disorder characterized by microcephaly, cortical dysplasia, corpus callosum hypoplasia, congenital hypotonia leading to subsequent spastic quadriplegia, severe developmental delay and hypogenitalism. Ophthalmologic findings that may affect any ocular segment including characteristic, small, atonic pupils. WARBM is known to be caused by biallelic, pathogenic variants in at least five genes although additional genetic loci may exist.

View Article and Find Full Text PDF
Article Synopsis
  • Bilateral acute iris transillumination (BAIT) syndrome is a rare and poorly understood eye condition marked by rapid pigment dispersion, iris depigmentation, and pigment accumulation in the eye's anterior chamber.
  • A case study describes a 46-year-old healthy woman who experienced BAIT in both eyes after using topical moxifloxacin/dexamethasone for bacterial conjunctivitis.
  • The case was further complicated by the development of nonarteritic anterior ischemic optic neuropathy in her left eye following the BAIT syndrome diagnosis.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!