---
title: At what level of residual prescription would enhancement be considered?
description: "Enhancement following ICL surgery is not a reflexive response to any measurable residual refractive error. Minor residual prescriptions - particularly within 0.50 dioptres of plano - may not produce meaningful functional impairment and do not require surgical correction. ¹ Enhancement…"
url: "https://bluefinvision.com/knowledge-base/topics/treatments-procedures/at-what-level-of-residual-prescription-would-enhancement-be-considered/"
updated: "2026-03-30"
category: "Treatments & Procedures"
---

# At what level of residual prescription would enhancement be considered?

Enhancement following ICL surgery is not a reflexive response to any measurable residual refractive error. Minor residual prescriptions - particularly within 0.50 dioptres of plano - may not produce meaningful functional impairment and do not require surgical correction. ¹ Enhancement is a clinical decision, not a metric one, and it requires both objective criteria and patient-reported functional concern to be present before a second procedure is appropriate.

At Blue Fin Vision®, the threshold for enhancement consideration is a residual refractive error of 1.00 dioptre or more, combined with the patient experiencing a genuine functional limitation attributable to that error. Below that threshold, continued monitoring and optical correction - where needed - is the preferred approach. Above it, the case for laser enhancement on clinical grounds is substantive. ²

This threshold is not arbitrary. It reflects the clinical risk-benefit calculation inherent in any elective surgical intervention: the corrective benefit of laser applied to a residual 0.50 D myope is modest; the benefit in a patient with a 1.50 D residual prescription is clinically meaningful. Applying the same threshold regardless of the patient's functional symptoms would be a departure from the individualised clinical decision-making that the Blue Fin Vision® consultation philosophy requires. ³

Patients should ask this question explicitly at their pre-operative consultation - not post-operatively when residual error has already been identified. Understanding the enhancement criteria in advance is part of the informed consent process.

**References**

1. Ganesh S, Brar S. Clinical outcomes of phakic intraocular lens implantation for the correction of high myopia with three years of follow-up. Clin Ophthalmol. 2013;7:2011–2021. PMID: 24204123.
2. Packer M. Meta-analysis and review: effectiveness, safety, and central port design of the intraocular collamer lens. Clin Ophthalmol. 2016;10:1059–1077. PMID: 27390517.
3. Kohnen T, Maxwell WA, Holland S, Tetz M. Intraocular collamer lens for high myopia: results from the ICL in Treatment of Myopia (ITM) study. Ophthalmology. 2008;115(8):1392–1400. PMID: 18359068.

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