Fluocinolone acetonide intravitreal implant for treating chronic diabetic macular oedema

Section 7 of the National Institute for Health and Care Excellence (Constitution and Functions) and the Health and Social Care Information Centre (Functions) Regulations 2013 requires integrated care boards, NHS England and, with respect to their public health functions, local authorities to comply with the recommendations in this evaluation within 3 months of its date of publication. Because fluocinolone acetonide intravitreal implant has been recommended for people with phakic eyes through the cost-comparison process, NHS England and integrated care boards have agreed to provide funding to implement this guidance 30 days after publication.

The Welsh ministers have issued directions to the NHS in Wales on implementing NICE technology appraisal guidance. When a NICE technology appraisal guidance recommends the use of a drug or treatment, or other technology, the NHS in Wales must usually provide funding and resources for it within 2 months of the first publication of the final draft guidance.

When NICE recommends a treatment 'as an option', the NHS must make sure it is available within the period set out in the paragraphs above. This means that, if a patient has visual impairment caused by chronic diabetic macular oedema that has not responded well enough to available treatments, and the doctor responsible for their care thinks that fluocinolone acetonide intravitreal implant is the right treatment, it should be available for use, in line with NICE's recommendations.