An Overview and Brief History

Intravenous fluorescein angiography (IVFA) is a form of diagnostic imaging used to assess retinal and choroidal vasculature. This procedure involves the intravenous injection of fluorescein dye, which enhances the visualization of blood vessels as a series of high-resolution images are captured from both eyes.

The foundational concept of fluorescein angiography was introduced by medical students Herald Novotny and David Alvis. The technique gained widespread adoption in the 1960s, marking a significant advancement in retinal imaging and enhancing the ability to diagnose and manage various ocular conditions.

How Does Fluorescein Angiography Work?

Fluorescein dye is injected into the patient’s antecubital vein and quickly reaches retinal and choroidal vasculature.

Fluorescent dyes photoluminesce, which absorbs light in one wavelength and emit light at a different wavelength. Fluorescein molecules used in IVFA absorb light in the blue light range (465 nm to 490 nm) and emit light in the yellow-green range (520 nm to 530 nm). 

The fundus camera is equipped with two filters. The first filter is an excitation filter in the absorption range of 465-490 nm, allowing only blue light to pass from the camera flash and excite the fluorescein molecules. The second filter is a barrier in the 520 to 530 nm range, allowing only light emitted by the fluorescein molecules to pass through and be captured in the image.

In a healthy eye, the endothelium of retinal blood vessels does not allow fluorescein leakage due to tight junctions. This allows for high-quality imaging of the retinal vessels and the detection of any abnormal leakage.

How do I counsel a patient about the risks of this test?

“IVFA is a dye-based test and therefore, there are certain risks associated with the test, that I need to inform you about.”

Most patients can experience:

  • Yellowing of their skin 6 to 12 hours post-injection and yellowing of urine for up to 36 hours after the procedure.

  • Transient nausea and vomiting during the test (about 10% of patients, although it is a quick onset and resolution).

  • Extravasation of dye.

  • Transient discolouration at the site of injection.

Less likely adverse risks and events include:

  • Mild allergic reactions: Pruritus, dizziness urticaria (about 1% of patients).

  • Severe allergic reactions: One or two organ systems affected (0.01% of patients)

  • Anaphylaxis: Hypotension leading to shock (1 in 200,000 to 350,000 patients)

As this test is happening in a healthcare setting, with nursing present, we are able to monitor for these events and act promptly and accordingly. Do you wish to proceed?”

Download our consent form here!

Quiz Yourself: What are the steps to performing an IVFA?