Evidence map›Paper›PMID 9799881›Full record

ArticleJournal of epidemiology and community health1998

Costs, effects, and savings of screening for cystic fibrosis gene carriers.

M F Wildhagen, H B Hilderink, J G Verzijl, J B Verheij, L Kooij, T Tijmstra, L P ten Kate, J D Habbema

Open access · bronzeAbstract read
In one paragraph

Article in Journal of epidemiology and community health, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
1.9field-weighted citation impact, top 15% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Evaluating Cost-effectiveness of Interventions That Affect Fertility and Childbearing: How Health Effects Are Measured Matters.Medical decision making : an international journal of the Society for Medical Decision Making · 2015
    Review
  5. Genetic testing in the European Union: does economic evaluation matter?The European journal of health economics : HEPAC : health economics in prevention and care · 2012
    Article
  6. Cost-effectiveness of a school-based Tay-Sachs and cystic fibrosis genetic carrier screening program.Genetics in medicine : official journal of the American College of Medical Genetics · 2005
    Article
  7. Review
  8. Article
  9. 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

8 authors at 1 institution in 1 country.

M F WildhagenDepartment of Public Health, Erasmus University Rotterdam, The Netherlands.
H B Hilderink
J G Verzijl
J B Verheij
L Kooij
T Tijmstra
L P ten Kate
J D Habbema
Erasmus University Rotterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

STUDY

objectiveEvaluating the costs, effects, and savings of several strategies for cystic fibrosis (CF) gene carrier screening.

designA general model for evaluating prenatal, preconceptional, school, and neonatal carrier screening was constructed. For prenatal and preconceptional screening, two strategies were evaluated: single entry and double entry two step couple screening. Firstly, the Dutch situation was evaluated prospectively; subsequently the results were generalised to other carrier frequencies.

settingProspective simulation model. MAIN

resultsOf all screening strategies, neonatal carrier screening gives most carrier couples an informed choice concerning reproduction. If the parents of carrier newborns would not be tested however, prenatal screening detects most carrier couples. Prenatal and single entry preconceptional screening programmes have a favourable cost-savings balance in the Netherlands under a wide range of assumptions. For double entry preconceptional screening and neonatal screening, high enough values of uptake of screening, prenatal diagnosis, and induced abortion are necessary. School carrier screening does not have a favourable cost-savings balance.

conclusionsIf a CF screening programme is judged to be useful on individual and social grounds, costs considerations are no obstacle for prenatal and single entry preconceptional screening.

Indexed as

Decision Support TechniquesModels, EconomicChildCost-Benefit AnalysisCosts and Cost AnalysisCystic FibrosisFemaleGenetic Carrier ScreeningGenetic CounselingGenetic TestingHumansInfant, NewbornMalePrenatal DiagnosisProspective Studies

Identifiers

PMID9799881
PMCPMC1756730
OpenAlexW2111500387

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.