Evidence map›Paper›PMID 41553555›Full record

ArticleEuropean journal of pediatrics2025

Coronary artery abnormalities in Kawasaki disease with BCG site reactivation.

Rakesh Kumar Pilania, Abarna Thangaraj, Sathish Loganathan, Dev Desai, Aparna Kv, Vaishali Thakur, Manpreet Dhaliwal, Saniya Sharma, Ankur Kumar Jindal, Pandiarajan Vignesh and 4 more

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Article in European journal of pediatrics, 2025. 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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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Rakesh Kumar Pilania *Pediatric Allergy and Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India. kumarpilania007@gmail.com.
Abarna Thangaraj *Pediatric Allergy and Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Sathish LoganathanPediatric Allergy and Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Dev DesaiPediatric Allergy and Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Aparna KvPediatric Allergy and Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Vaishali ThakurPediatric Allergy and Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Manpreet DhaliwalPediatric Allergy and Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Saniya SharmaPediatric Allergy and Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Ankur Kumar JindalPediatric Allergy and Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Pandiarajan VigneshPediatric Allergy and Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Deepti SuriPediatric Allergy and Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Amit RawatPediatric Allergy and Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Manphool SinghalDepartment of Radiodiagnosis and Imaging, PGIMER, Chandigarh, India.
Surjit SinghPediatric Allergy and Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BCG site reactivation is reported in Kawasaki disease (KD). However, it is not a part of American Heart Association (AHA) guidelines. Records of all KD patients admitted between January 2009 and June 2024 were reviewed. Patients with BCG site reactivation were analysed. Among 1206 KD patients, 19 had BCG site reactivation (1.57%). Median age at diagnosis was 7 months. Twelve out of 19 patients (63.2%) were infants. Echocardiography showed coronary artery abnormalities (CAAs) in 11 (57.9%; aneurysms in 10, dilatation in 1) and myocarditis in 1. CAAs developed in 83.3% (10/12) of infants with KD and BCG site reactivation, compared to 37.2% (73/196) of infants who did not have BCG reactivation (p = 0.006; odds ratio: 8.4). All patients received intravenous immunoglobulin (IVIg) and aspirin. Infliximab was used for IVIg resistance in 4 (21.1%) and for primary intensification in 6 (31.6%). Cumulative follow-up was 386 patient-months. Seven patients with CAAs showed regression over 12 months.

conclusionBCG site reactivation is uncommon in children with KD at our centre. It primarily occurs in infants with KD. There is a eightfold higher risk of CAAs among infants with KD and BCG site reactivation, than in those without BCG reactivation. WHAT IS KNOWN: • BCG site reactivation is a recognised clinical feature of Kawasaki disease. • The role of BCG site reactivation as a predictor of coronary artery abnormalities (CAAs) has not been clearly established. WHAT IS NEW: • At our centre, BCG site reactivation was observed in 1.58% of KD patients, predominantly in infancy. • Infants with BCG site reactivation had an eightfold higher risk of CAAs (83.3% vs 37.2%). • BCG reactivation may serve as a simple bedside marker to identify infants at risk of severe KD who may require closer monitoring and timely/intensified therapy.

Indexed as

BCG VaccineCoronary Artery DiseaseCoronary Vessel AnomaliesMucocutaneous Lymph Node SyndromeChild, PreschoolEchocardiographyFemaleHumansImmunoglobulins, IntravenousInfantMaleRecurrenceRetrospective StudiesBCG VaccineImmunoglobulins, IntravenousAcquired heart diseaseBCGChildrenCoronary artery abnormalities (CAAs)InfantsKawasaki disease (KD)

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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.