Evidence map›Paper›PMID 30221333›Full record

SynthesisPharmacoEconomics2019

Systematic Literature Review of the Economic Burden of Celiac Disease.

Elizabeth S Mearns, Aliki Taylor, Talia Boulanger, Kelly J Craig, Michele Gerber, Daniel A Leffler, Jennifer Drahos, David S Sanders, Benjamin Lebwohl

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in PharmacoEconomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
3.4field-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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Observational
  8. Article
  9. Article
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  11. Article
  12. The global burden of coeliac disease: opportunities and challenges.Nature reviews. Gastroenterology & hepatology · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
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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

9 authors at 6 institutions in 2 countries.

Elizabeth S MearnsZS Associates, 350 Fifth Avenue, Suite 5100, New York, NY, 10018, USA. Elizabeth.mearns@zs.com.ORCID 0000-0003-2293-6590
Aliki TaylorTakeda Development Centre Europe, London, UK.ORCID 0000-0002-4863-9810
Talia Boulanger, Boston, MA, USA.ORCID 0000-0003-4711-5369
Kelly J CraigTruven Health Analytics, An IBM Company, Cambridge, MA, USA.ORCID 0000-0002-9954-2795
Michele GerberTakeda Pharmaceuticals International Co, Cambridge, MA, USA.ORCID 0000-0001-7169-743X
Daniel A LefflerTakeda Pharmaceuticals International Co, Cambridge, MA, USA.ORCID 0000-0002-0750-3386
Jennifer DrahosTakeda Pharmaceuticals International Co, Cambridge, MA, USA.ORCID 0000-0002-8454-9863
David S SandersRoyal Hallamshire Hospital and University of Sheffield, Sheffield, UK.ORCID 0000-0002-3739-0124
Benjamin LebwohlDepartment of Medicine, Celiac Disease Center, Columbia University Medical Center, New York, NY, USA.ORCID 0000-0001-9422-4774
Takeda (United States) · USColumbia University Irving Medical Center · USRoyal Hallamshire Hospital · GBSt. Elizabeth's Medical Center · USTakeda (United Kingdom) · GBTruven Health Analytics (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prevalence of celiac disease (CD) has rapidly increased over recent decades, but costs related to CD remain poorly quantified.

objectiveThis systematic review assessed the economic burden of CD in North America and Europe.

methodsMEDLINE, EMBASE, EconLit, and the Cochrane Library databases were systematically searched to identify English-language literature from 2007 to 2018 that assessed costs, cost effectiveness, and health resource utilization for CD.

resultsForty-nine studies met the inclusion criteria, of which 28 (57.1%) addressed costs of testing and diagnosis; 33 (67.3%) were from Europe. The cost per positive CD diagnosis of testing patients already undergoing esophagogastroduodenoscopy for other indications ranged from 1300 Canadian dollars ($Can) in Canada (2016 value) to €44,712 in the Netherlands (2013 value). Adding the CD test was cost effective when it combined diagnostic modalities (e.g., serology and biopsy). Direct annual excess costs to a US payer per diagnosed CD patient totaled $US6000 (2013 value) more than for a person without CD, chiefly due to outpatient care. Hospitalizations, emergency visits, and medication use were more common with CD. After initiating a gluten-free diet (GFD), patients visited primary care providers less often, used more medications, and missed fewer days from school and work.

conclusionsMost of the few available economic studies of CD assess testing and diagnosis costs, especially in Europe. Methods of testing generally are considered cost effective when they combine diagnostic modalities in symptomatic patients. Most costs to a payer of managing CD derive from outpatient care. Following GFD initiation, patients lose fewer days from work and school than pretreatment.

Indexed as

Cost of IllnessAmbulatory CareCeliac DiseaseCost-Benefit AnalysisDiet, Gluten-FreeEuropeHumansNorth AmericaTreatment Adherence and Compliance

Identifiers

PMID30221333
OpenAlexW2892265069

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.