Evidence map›Paper›PMID 32623612›Full record

ArticlePediatric cardiology2020

Cost-Effectiveness of Implantable Cardioverter-Defibrillators in Children with Cardiac Conditions Associated with Risk for Sudden Cardiac Death.

Meredith B Haag, Alyssa R Hersh, David E Toffey, James A Sargent, Eric C Stecker, Stephen B Heitner, Aaron B Caughey, Seshadri Balaji

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric cardiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. A systematic literature review of economic evaluations and cost-of-illness studies of inherited cardiomyopathies.Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation · 2023
    Review
  3. [Congenital long QT syndrome].Archivos peruanos de cardiologia y cirugia cardiovascular
    Review
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

8 authors at 3 institutions in 1 country.

Meredith B HaagDivision of Pediatric Cardiology, Oregon Health and Science University, Doernbecher Children's Hospital, Portland, OR, USA.ORCID http://orcid.org/0000-0003-3893-3001
Alyssa R HershDepartment of Obstetrics and Gynecology, Oregon Health and Science University, Portland, OR, USA.ORCID http://orcid.org/0000-0003-0601-9346
David E ToffeyDepartment of Obstetrics and Gynecology, Beth Israel Deaconess Medical Center, Boston, MA, USA.ORCID http://orcid.org/0000-0003-3300-5943
James A SargentMcGovern Medical School at UTHealth, Houston, TX, USA.ORCID http://orcid.org/0000-0002-9895-8561
Eric C SteckerOregon Health and Science University, Knight Cardiovascular Institute, Portland, OR, USA.ORCID http://orcid.org/0000-0002-6162-9561
Stephen B HeitnerOregon Health and Science University, Knight Cardiovascular Institute, Portland, OR, USA.ORCID http://orcid.org/0000-0003-2189-1474
Aaron B CaugheyDepartment of Obstetrics and Gynecology, Oregon Health and Science University, Portland, OR, USA.ORCID http://orcid.org/0000-0002-1752-0972
Seshadri BalajiDivision of Pediatric Cardiology, Oregon Health and Science University, Doernbecher Children's Hospital, Portland, OR, USA. balajis@ohsu.edu.ORCID http://orcid.org/0000-0001-5864-5125
Oregon Health & Science University · USBeth Israel Deaconess Medical Center · USThe University of Texas Health Science Center at Houston · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Children at high risk for sudden cardiac death (SCD) receive implantable cardioverter-defibrillators (ICD) for prevention, but the cost effectiveness of ICDs in children at intermediate risk is unclear. Our objective was to create a cost-effectiveness model to compare costs and outcomes in children at risk of SCD, with and without ICD. Utilizing hypertrophic cardiomyopathy as the proxy disease, a theoretical cohort of 8150 children was followed for 69 years. Model inputs were derived from the literature, with an incremental cost-effectiveness ratio (ICER) willingness-to-pay threshold of $100,000/quality-adjusted life year (QALY) used to delineate cost effectiveness. Outcomes included prevalence of severe neurological morbidity (SNM), SCD, cost, and QALYs. In children at intermediate risk of SCD (4-6% over 5 years), ICD resulted in 56 fewer cases of SNM, 2686 fewer deaths. In children at high risk (> 6% over 5 years), ICD placement resulted in 74 fewer cases of SNM and 3663 fewer deaths from cardiac causes. The costs of ICD were higher, but placement was cost effective with an ICER of $3009 per QALY in intermediate risk children, but ICD therapy was a dominant strategy in high-risk children. Sensitivity analysis demonstrated ICD placement was cost-effective until the annual probability of SCD was < 0.22%. The model was robust over a wide range of values. For children at risk of SCD, prophylactic ICD implantation is cost effective, resulting in improved outcomes and increased QALYs, despite increased costs. These findings highlight the economic benefits of ICD utilization in this population.

Indexed as

Quality-Adjusted Life YearsCardiomyopathy, HypertrophicChildCost-Benefit AnalysisDeath, Sudden, CardiacDefibrillators, ImplantableHumansMarkov ChainsCost-effectiveness analysisHypertrophic cardiomyopathyImplantable cardioverter-defibrillatorSudden cardiac death

Identifiers

PMID32623612
OpenAlexW3039106019

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.