SYSTEMATIC REVIEW OF COST-EFFECTIVENESS ANALYSIS (CEA) OF THE CELL FREE DNA (CFDNA) / NON-INVASIVE PRENATAL TEST (NIPT) FOR TRISOMY 21 (T21) SCREENING

Author(s)

Bourdoncle M1, Li J2, Berthelot A2, Cognet M3, Sambuc C3, Scemama O3, Rumeau-Pichon C3
1CHU Toulouse, Toulouse, France, 2Assistance Publique des Hôpitaux de Paris (AP-HP), Paris, France, 3Haute Autorité de Santé (HAS), Saint-Denis La Plaine, France

OBJECTIVES:  The cfDNA test detects T21 with a higher accuracy than conventional prenatal screening. Cost-effectiveness, as well as other domains (e.g. ethics, preferences, organisation), must be assessed in order to recommend its use in France. Our aims were to systematically review cost-effectiveness analyses on the cfDNA test for T21 screening and to summarize the evidence. METHODS:  An update of the systematic review of the Belgian Health Care Knowledge Center, published in 2009, was performed by the French National Authority for Health up to April 2016. Inclusion was performed independently by two researchers; a third researcher resolved discrepancies. The following data was extracted: study type, perspective

Conference/Value in Health Info

2016-10, ISPOR Europe 2016, Vienna, Austria

Value in Health, Vol. 19, No. 7 (November 2016)

Code

PMD63

Topic

Economic Evaluation

Topic Subcategory

Cost-comparison, Effectiveness, Utility, Benefit Analysis

Disease

Rare and Orphan Diseases

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