Evidence map›Paper›PMID 36380069›Full record

ArticlePediatric research2023

Cardiovascular outcomes in children with Kawasaki disease: a population-based cohort study.

Cal Robinson, Rahul Chanchlani, Anastasia Gayowsky, Sandeep Brar, Elizabeth Darling, Catherine Demers, Tapas Mondal, Rulan Parekh, Hsien Seow, Michelle Batthish

Abstract read
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In one paragraph

Article in Pediatric research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% of its field
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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

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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 at 4 institutions in 2 countries.

Cal RobinsonDepartment of Pediatrics, McMaster University, Hamilton, ON, Canada.
Rahul ChanchlaniDivision of Nephrology, Department of Pediatrics, McMaster University, Hamilton, ON, Canada.
Anastasia GayowskyICES McMaster, Hamilton, ON, Canada.
Sandeep BrarDepartment of Epidemiology & Biostatistics, University of California, San Francisco, CA, USA.
Elizabeth DarlingMcMaster Midwifery Research Centre, McMaster University, Hamilton, ON, Canada.
Catherine DemersDivision of Cardiology, Department of Medicine, McMaster University, Hamilton, ON, Canada.
Tapas MondalDivision of Cardiology, Department of Pediatrics, McMaster University, Hamilton, ON, Canada.
Rulan ParekhDivision of Nephrology, Department of Pediatrics, University of Toronto, Toronto, ON, Canada.
Hsien SeowDepartment of Oncology, McMaster University, Hamilton, ON, Canada.
Michelle BatthishDivision of Rheumatology, Department of Pediatrics, McMaster University, Hamilton, ON, Canada. batthim@mcmaster.ca.ORCID http://orcid.org/0000-0001-6412-1029
McMaster University · CAUniversity of Toronto · CAImpact · CAUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe risk of cardiovascular events after Kawasaki disease (KD) remains uncertain. Our objective was to determine the risk of cardiovascular events and mortality after KD.

methodsPopulation-based retrospective cohort study using Ontario health administrative databases (0-18 years; 1995-2018). EXPOSURE: pediatric KD hospitalizations. Each case was matched to 100 non-exposed controls. PRIMARY OUTCOME: major adverse cardiac events (MACE; cardiovascular death, myocardial infarction, or stroke composite). SECONDARY OUTCOMES: composite cardiovascular events and mortality. We determined incidence rates and adjusted hazard ratios (aHR) using multivariable Cox models.

resultsAmong 4597 KD survivors, 79 (1.7%) experienced MACE, 632 (13.8%) composite cardiovascular events, and 9 (0.2%) died during 11-year median follow-up. The most frequent cardiovascular events among KD survivors were ischemic heart disease (4.6 events/1000 person-years) and arrhythmias (4.5/1000 person-years). KD survivors were at increased risk of MACE between 0-1 and 5-10 years, and composite cardiovascular events at all time periods post-discharge. KD survivors had a lower mortality risk throughout follow-up (aHR 0.36, 95% CI 0.19-0.70).

conclusionKD survivors are at increased risk of post-discharge cardiovascular events but have a lower risk of death, which justifies enhanced cardiovascular disease surveillance in these patients. IMPACT: Among 4597 Kawasaki disease (KD) survivors, 79 (1.7%) experienced major adverse cardiac events (MACE) and 632 (13.8%) had composite cardiovascular events during 11-year median follow-up. KD survivors had significantly higher risks of post-discharge MACE and cardiovascular events versus non-exposed children. Only nine KD survivors (0.2%) died during follow-up, and the risk of mortality was significantly lower among KD survivors versus non-exposed children. Childhood KD survivors should receive preventative counseling and cardiovascular surveillance, aiming to mitigate adult cardiovascular disease.

Indexed as

Cardiovascular DiseasesMucocutaneous Lymph Node SyndromeAdultAftercareChildCohort StudiesHumansPatient DischargeRetrospective StudiesRisk Factors

Identifiers

PMID36380069
OpenAlexW4309361283

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.