Evidence map›Paper›PMID 38175253›Full record

Observational studyAnnals of hematology2024

A multicentre ambispective observational study into the incidence and clinical management of aplastic anaemia in Spain (IMAS study).

Carlos Vallejo, Ana Rosell, Blanca Xicoy, Carmen García, Carmen Albo, Marta Polo, Isidro Jarque, Brígida Esteban, M Lorena Codesido

Abstract readObservational StudyMulticenter Study
PubMed Publisher
In one paragraph

Observational study in Annals of hematology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

9 authors at 8 institutions in 1 country.

Carlos VallejoComplejo Asistencial Universitario de Salamanca, Salamanca, Spain. cvallejo@um.es.ORCID http://orcid.org/0000-0002-8484-8097
Ana RosellHospital Universitario Virgen de La Victoria, Málaga, Spain.
Blanca XicoyInstitut Català d'Oncologia, Hospital Universitari Germans Trias i Pujol, Josep Carreras Leukemia Research Institute, Universitat Autònoma de Barcelona, Badalona, Spain.
Carmen GarcíaHospital General Universitario de Alicante, Alicante, Spain.
Carmen AlboHospital Universitario Álvaro Cunqueiro, Vigo, Spain.
Marta PoloHospital Clínico Universitario San Carlos, Madrid, Spain.
Isidro JarqueHospital Universitario La Fe, Valencia, Spain.
Brígida EstebanInstituto de Investigación Sanitaria Biodonostia, Donostia-San Sebastián, Spain.
M Lorena CodesidoInstituto de Investigación Sanitaria Biodonostia, Donostia-San Sebastián, Spain.
Biogipuzkoa Health Research Institute · ESFundación Pethema · ESHospital Clínico San Carlos · ESHospital Clínico Universitario Virgen de la Victoria · ESHospital General Universitario de Alicante Doctor Balmis · ESHospital Universitari i Politècnic La Fe · ESUniversitat Autònoma de Barcelona · ESUniversity Hospital Complex Of Vigo · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aplastic anemia (AA) is a rare, life-threatening hematological disease, with a poorly defined incidence. As the data available on AA varies substantially worldwide, a multicenter, ambispective, observational study was carried out between 2010 and 2019 to assess the incidence, clinical management and survival of AA at seven Spanish hospitals. The incidence of AA was 2.83 per million inhabitants per year, consistent with that reported previously in Europe, with a median age at diagnosis of 61 years-old (range 12-86), and a similar number of males and females. The initial diagnosis was severe or very severe AA in 55.8% of cases and 93.7% required transfusion. The most frequent first line therapy was anti-thymocyte globulin (ATG) plus cyclosporin A (CsA, 44.2%), followed by other CsA-based regimes (46.3%), with hematopoietic stem cell transplantation an infrequent 1st line therapy. The 6-month response rate was 68.2%, which then increased over a median follow-up of 3.9 years. The 5-year overall survival (5OS) was 73.6%, similar in severe (78.6%) and very severe AA patients (74.6%) but lower in moderate AA (MAA) patients (68.4%). The 5OS was 100% in 0-25 year-old patients but dropping to 58.3% in patients ≥ 60 years-old. At the last contact, 75.8% of the patients were alive. In conclusion, the incidence, characteristics and management of AA in our study are consistent with that reported previously. In terms of survival, although the global long-term OS rate was good, there is room for improvement, particularly in older patients. Finally, what appears to be a worse long-term survival of MAA patients, as reported previously, reinforces the importance of not underestimating this condition when diagnosed as MAA.

Indexed as

Anemia, AplasticHematopoietic Stem Cell TransplantationAdolescentAdultAgedAged, 80 and overAntilymphocyte SerumChildChild, PreschoolCyclosporineFemaleHumansImmunosuppressive AgentsIncidenceInfantInfant, NewbornAntilymphocyte SerumCyclosporineImmunosuppressive AgentsAplastic anaemiaClinical managementIncidenceResponse to treatmentSurvival and fatality rate

Identifiers

PMID38175253
OpenAlexW4390588482

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.