Evidence map›Paper›PMID 36384904›Full record

ArticleInternal medicine (Tokyo, Japan)2023

Safe Introduction of Hydroxychloroquine Focusing on Early Intolerance Due to Adverse Drug Reactions in Patients with Systemic Lupus Erythematosus.

Yusuke Yoshida, Naoya Oka, Ai Yorishima, Sho Masuda, Michinori Ishitoku, Kei Araki, Hiroki Kohno, Hirofumi Watanabe, Tomohiro Sugimoto, Sho Mokuda and 1 more

Abstract read
In one paragraph

Article in Internal medicine (Tokyo, Japan), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Yusuke YoshidaDepartment of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Japan.
Naoya OkaDepartment of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Japan.
Ai YorishimaDepartment of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Japan.
Sho MasudaDepartment of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Japan.
Michinori IshitokuDepartment of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Japan.
Kei ArakiDepartment of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Japan.
Hiroki KohnoDepartment of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Japan.
Hirofumi WatanabeDepartment of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Japan.
Tomohiro SugimotoDepartment of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Japan.
Sho MokudaDepartment of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Japan.
Shintaro HirataDepartment of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective This study explored the predictors of hydroxychloroquine intolerance and propose appropriate methods to initiate hydroxychloroquine in patients with systemic lupus erythematosus. Methods This retrospective study registered consecutive patients who were diagnosed with systemic lupus erythematosus and started treatment with hydroxychloroquine between 2015 and 2021. Any adverse events that required dose reduction or cessation of hydroxychloroquine, indicating intolerance to the drug, were recorded for up to 26 weeks after initiation of hydroxychloroquine. Results A total of 130 patients were included. Hydroxychloroquine intolerance due to adverse drug reactions was observed in 28 patients (21.5%), including gastrointestinal symptoms in 15 (11.5%) and cutaneous reactions in 7 (5.4%). Furthermore, the intolerance was observed more frequently in the maintenance group (patients treated daily with <20 mg prednisolone) than in the induction group (7.1% vs. 25.5%, p=0.04), and none of the patients in the induction group developed cutaneous reactions. The initial dose of hydroxychloroquine per ideal body weight was associated with hydroxychloroquine intolerance in a dose-dependent manner. Multivariable analyses revealed that the hydroxychloroquine dose per ideal body weight and higher levels of C4 predicted hydroxychloroquine intolerance. In particular, C4 levels were positively correlated with cutaneous reactions, whereas the dose of prednisolone was negatively correlated with gastrointestinal reactions. Conclusion Low-dose hydroxychloroquine may be optimal for induction in patients with systemic lupus erythematosus who have high C4 levels or are taking low doses of steroids.

Indexed as

Drug-Related Side Effects and Adverse ReactionsLupus Erythematosus, SystemicHumansHydroxychloroquinePrednisoloneRetrospective StudiesHydroxychloroquinePrednisoloneadverse drug reactioncomplementglucocorticoidshydroxychloroquinesystemic lupus erythematosus

Identifiers

PMID36384904
PMCPMC10400396

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Registered trials

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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.