Evidence map›Paper›PMID 36823598›Full record

ArticleOrphanet journal of rare diseases2023

Strategic discussion on funding and access to therapies targeting rare diseases in Spain: an expert consensus paper.

N Zozaya, J Villaseca, F Abdalla, A Ancochea, I Málaga, M Trapero-Bertran, N Martín-Sobrino, O Delgado, P Ferré, A Hidalgo-Vega

Abstract readConsensus Statement
In one paragraph

Article in Orphanet journal of rare diseases, 2023. 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
–field-weighted citation impact
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.

  1. Nurses' Knowledge of Rare Diseases: A Systematic Review.Nursing reports (Pavia, Italy) · 2025
    Review
  2. Review
  3. 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

10 authors.

N ZozayaHealth Economics Department, Weber, C/ Moreto 17, 5D, 28014, Madrid, Spain. neboa.zozaya@weber.org.es.ORCID 0000-0003-4618-6894
J VillasecaHealth Economics Department, Weber, C/ Moreto 17, 5D, 28014, Madrid, Spain.
F AbdallaHealth Economics Department, Weber, C/ Moreto 17, 5D, 28014, Madrid, Spain.
A AncocheaFederación Española de Enfermedades Raras (FEDER), Madrid, Spain.
I MálagaHead of the Neuropediatrics Unit, Asturias Central University Hospital, Asturias, Spain.
M Trapero-BertranDepartment of Basic Sciences, Universitat Internacional de Catalunya (UIC Barcelona), Barcelona, Spain.
N Martín-SobrinoCastilla y León Health Management Department, Technical Director of Pharmacy, Valladolid, Spain.
O DelgadoPharmacy Service, Son Espases University Hospital, Palma, Balearic, Spain.
P FerréTechnical Advisor On Temporal Leave, Ministry of Health, Madrid, Spain.
A Hidalgo-VegaPresident of Weber Foundation, Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn recent years, significant advances have been made in the field of rare diseases (RDs). However, there is a large number of RDs without specific treatment and half of these treatments have public funding in Spain. The aim of the FINEERR project was to carry out a multidisciplinary strategic discussion on the challenge of funding and access to RD-targeted drugs in Spain, in order to agree on specific proposals for medium-term improvement and hence support decision-making in the Spanish National Healthcare System (SNHS).

resultsThe FINEERR Project was organized around a CORE Advisory Committee, which provided an overview, agreed on the design and scope of the project, and selected the members within each of four working groups (WG). Overall, 40 experts discussed and reached a consensus on different relevant aspects, such as conditioning factors for initial funding and access, evaluation and access to RD-targeted therapies, funding of these therapies, and implementation of a new funding and access model. From these meetings, 50 proposals were defined and classified by their level of relevance according to the experts. A descriptive analysis of responses was performed for each proposal. Thereafter, experts completed another questionnaire where they ranked the 25 most relevant proposals according to their level of feasibility of being implemented in the SNHS. The most relevant and feasible proposals were to improve: process of referral of patients with RDs, control over monitoring mechanisms, and communication between healthcare professionals and patients.

conclusionsThe FINEERR project may provide a starting point for stakeholders involved in the process of funding and access to RD-targeted therapies in Spain to provide the necessary resources and implement measures to improve both the quality of life and life expectancy of patients with RDs.

Indexed as

Quality of LifeRare DiseasesHealth Services AccessibilityHumansSpainAccessFundingMeasuresOrphan drugsRare diseasesReflectionRegulatory scienceReimbursementSpain

Identifiers

PMID36823598
PMCPMC9950008

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Registered trials

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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.