Evidence map›Paper›PMID 40206928›Full record

ArticleCureus2025

Dose Adjustment of Intravenous Immunoglobulin Therapy With Serum IgG Monitoring to Prevent Hyperviscosity in a 13-Year-Old Boy With Kawasaki Disease.

Shin Takeo, Shoichiro Kanda, Keiichi Takizawa, Yuko Kajiho, Akiko Kinumaki

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

5 authors.

Shin TakeoPediatrics, The University of Tokyo, Tokyo, JPN.
Shoichiro KandaPediatrics, The University of Tokyo, Tokyo, JPN.
Keiichi TakizawaPediatrics, The University of Tokyo, Tokyo, JPN.
Yuko KajihoPediatrics, The University of Tokyo, Tokyo, JPN.
Akiko KinumakiPediatrics, The University of Tokyo, Tokyo, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kawasaki disease (KD) primarily affects infants and young children, with cases in patients over 10 years of age being relatively rare. The standard treatment involves intravenous administration of high-dose intravenous immunoglobulin (IVIG) at 2 g/kg. In pediatric medicine, drug dosages are typically adjusted according to body size; however, in older children, body size-based dosing often results in excessively high doses, and adult dosages are frequently used as upper limits. Notably, no such upper limit exists for IVIG. Given that IVIG administration can cause severe cardiac and neurological complications due to hyperviscosity syndrome, careful dose management is essential. Here, we report the case of a 13-year-old KD patient weighing 53 kg who underwent repeated high-dose IVIG therapy. Serum IgG levels, total protein concentration, and hematocrit were monitored over time as an indicator of blood viscosity, allowing for dose adjustments. As a result, the patient successfully completed the treatment course without experiencing major adverse effects. Notably, the adjusted IVIG regimen effectively prevented the development of hyperviscosity syndrome. Furthermore, the patient did not develop coronary artery aneurysms, indicating that the treatment maintained both safety and therapeutic efficacy in managing Kawasaki disease. On the other hand, the increase in serum IgG levels following IVIG at a dose of 2 g/kg was greater in this patient compared to younger children receiving the same treatment. This case highlights the necessity of monitoring IgG levels to balance the efficacy and safety of IVIG therapy in older KD patients. However, there is no established threshold for IgG levels that would indicate a safe upper limit for IVIG administration, highlighting the need for further investigation.

Indexed as

adolescent medicineindividualisation of drug dosageintravenous immunoglobulin (ivig)kawasaki disease (kd)retropharyngeal edema

Identifiers

PMID40206928
PMCPMC11979441

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