Evidence map›Paper›PMID 42828611›Full record

ArticleJapanese journal of ophthalmology2026

Safety outcomes of half-dose fluorescein and indocyanine green angiography: a clinical assessment of adverse events.

Kouta Kawasaki, Koji Tanaka, Ryusaburo Mori, Hajime Goto, Takumi Kobayashi, Ayaka Nakai, Michiteru Kono, Yu Wakatsuki, Akiyuki Kawamura, Hiroyuki Nakashizuka

Abstract read
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Article in Japanese journal of ophthalmology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Kouta KawasakiDivision of Ophthalmology, Department of Visual Sciences, Nihon University School of Medicine, 1-6 Kandasurugadai, Chiyoda-ku, Tokyo, 101-8309, Japan.
Koji TanakaDivision of Ophthalmology, Department of Visual Sciences, Nihon University School of Medicine, 1-6 Kandasurugadai, Chiyoda-ku, Tokyo, 101-8309, Japan. Tanaka.koji@nihon-u.ac.jp.ORCID http://orcid.org/0000-0003-3323-4148
Ryusaburo MoriDivision of Ophthalmology, Department of Visual Sciences, Nihon University School of Medicine, 1-6 Kandasurugadai, Chiyoda-ku, Tokyo, 101-8309, Japan.
Hajime GotoDivision of Ophthalmology, Department of Visual Sciences, Nihon University School of Medicine, 1-6 Kandasurugadai, Chiyoda-ku, Tokyo, 101-8309, Japan.
Takumi KobayashiDivision of Ophthalmology, Department of Visual Sciences, Nihon University School of Medicine, 1-6 Kandasurugadai, Chiyoda-ku, Tokyo, 101-8309, Japan.
Ayaka NakaiDivision of Ophthalmology, Department of Visual Sciences, Nihon University School of Medicine, 1-6 Kandasurugadai, Chiyoda-ku, Tokyo, 101-8309, Japan.
Michiteru KonoDivision of Ophthalmology, Department of Visual Sciences, Nihon University School of Medicine, 1-6 Kandasurugadai, Chiyoda-ku, Tokyo, 101-8309, Japan.
Yu WakatsukiDivision of Ophthalmology, Department of Visual Sciences, Nihon University School of Medicine, 1-6 Kandasurugadai, Chiyoda-ku, Tokyo, 101-8309, Japan.
Akiyuki KawamuraDivision of Ophthalmology, Department of Visual Sciences, Nihon University School of Medicine, 1-6 Kandasurugadai, Chiyoda-ku, Tokyo, 101-8309, Japan.
Hiroyuki NakashizukaDivision of Ophthalmology, Department of Visual Sciences, Nihon University School of Medicine, 1-6 Kandasurugadai, Chiyoda-ku, Tokyo, 101-8309, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo evaluate whether half‑dose administration of fluorescein and indocyanine green is associated with the incidence of adverse events during fluorescein angiography (FA) and indocyanine green angiography (ICGA). STUDY

designRetrospective cohort study.

methodsWe analyzed 10,435 angiographic examinations in 10,435 unique patients performed using standard doses (fluorescein, 5 mL [500 mg]; indocyanine green, 2 mL [25 mg]) between April 2015 and March 2023, and half doses (fluorescein, 2.5 mL [250 mg]; indocyanine green, 1 mL [12.5 mg]) between April 2023 and March 2024. Explanatory variables included dye dose (half vs. standard), age, sex, diabetes, hypertension, asthma, history of drug allergy, vital signs at examination (systolic/diastolic blood pressure, pulse rate), and meteorological factors (temperature, atmospheric pressure). After univariable analyses, multivariable logistic regression was performed. P < 0.05 was considered statistically significant.

resultsAdverse events assessed in the main analyses included rash, nausea/vomiting during FA, ICGA, or combined FA+ICGA, and hypotension. The overall incidence of adverse events was significantly lower in the half‑dose group (6.21%) than in the standard‑dose group (10.65%; P < 0.001). Half-dose administration was associated with lower odds of rash (odds ratio [OR] = 0.46; P = 0.001), nausea/vomiting during FA (OR = 0.24; P < 0.001), and nausea/vomiting during combined FA+ICGA (OR = 0.58; P = 0.002). Younger age was an independent risk factor for several adverse events.

conclusionsHalf‑dose dye administration was associated with lower incidences of rash and nausea/vomiting. Dose reduction may contribute to improved safety in FA and ICGA.

Indexed as

Adverse eventFluoresceinHalf dose angiographyIndocyanine green

Identifiers

PMID42828611

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.