Irvine-Gass Syndrome
Irvine-Gass syndrome (IGS) is pseudophakic cystoid macular edema (CME) that develops following cataract surgery, representing one of the most common causes of postoperative visual impairment. 1
Clinical Definition and Epidemiology
- IGS is characterized by cystoid macular edema occurring after cataract surgery, typically presenting with blurred or cloudy vision in the postoperative period 1, 2
- The condition remains one of the most common complications following uneventful cataract surgery, despite modern surgical techniques 1
- Most cases are benign and self-limiting, resolving spontaneously without permanent visual impairment 1
- However, persistent edema and refractory cases can occur, potentially causing deterioration of visual function 1
Typical Clinical Presentation
- Patients typically present with blurred or cloudy vision weeks to months after cataract surgery 2, 3
- The condition can occur bilaterally, even after uncomplicated phacoemulsification 3
- Acute bilateral presentation has been documented, with CME developing 25-32 days after surgery in sequential operations 3
- Visual acuity is typically reduced, with best corrected visual acuity commonly in the 6/12 to 6/18 range during active disease 2
Diagnostic Evaluation
- Optical coherence tomography (OCT) is the primary diagnostic tool, demonstrating characteristic cystoid spaces in the macula 1, 2, 4
- Spectral-domain OCT reveals intraretinal cystic fluid with increased central macular thickness (mean baseline thickness approximately 530 μm in documented cases) 4
- Fluorescein angiography shows characteristic petaloid pattern of fluorescein leakage in the macular region 5
- Photoreceptor inner segment/outer segment junction abnormalities on OCT correlate with incomplete visual recovery and serve as prognostic indicators 4
Natural History and Prognosis
- In most cases, macular edema resolves spontaneously within 3-6 months without intervention 1
- Complete resolution can occur by 6-12 months with appropriate treatment 2, 3, 4
- Eyes with interruption of the inner segment/outer segment junction at baseline (approximately 20% of cases) show persistent photoreceptor damage and incomplete visual recovery 4
- Macular thickness changes correlate positively with visual acuity changes (r = 0.75), making OCT useful for monitoring treatment response 4
Risk Factors and Recurrence
- Patients who develop CME following their first cataract operation have increased risk of developing the condition in the contralateral eye 3
- This risk persists despite prophylactic measures including topical NSAIDs and corticosteroids 3
- Bilateral presentation can occur even in healthy individuals without systemic comorbidities 2
Important Differential Diagnosis
- Central serous chorioretinopathy can occur simultaneously or sequentially with IGS, though this association is exceptional 5
- The presence of focal fluorescein leakage on angiography distinguishes central serous chorioretinopathy from pure IGS 5
- Posterior capsule opacity may initially be suspected but can be ruled out with OCT imaging 2
Common Clinical Pitfalls
- Failing to perform OCT imaging in patients with persistent visual complaints after cataract surgery delays diagnosis 2, 4
- Assuming all post-cataract visual complaints are due to posterior capsule opacity without macular imaging misses IGS 2
- Not counseling patients about contralateral eye risk before second-eye surgery in those who developed IGS after first-eye surgery 3
- Overlooking photoreceptor junction abnormalities on OCT that predict incomplete visual recovery 4