Evidence map›Paper›PMID 39756394›Full record

Observational studyBritish journal of haematology2025

Avatrombopag in adults with immune thrombocytopenia: A multicentre real-life observational study in Madrid, Spain (AVAMAD study).

Cristina Pascual-Izquierdo, Mª Jose Llacer-Ferrandis, Almudena de-la-Iglesia, Silvia Monsalvo-Saornil, María Menor-Gómez, Juan Jose Gil-Fernández, Esther Chica-Gullon, María Teresa Álvarez-Román, Gloria Perez-Segura, Denis Zafra and 6 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in British journal of haematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Observational
  2. Article
  3. Article
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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

16 authors.

Cristina Pascual-IzquierdoHematología, Hospital General Universitario Gregorio Marañon, Instituto de Investigación Gregorio Marañon, Madrid, Spain.ORCID https://orcid.org/0000-0001-5442-4886
Mª Jose Llacer-FerrandisHematología, Hospital General Universitario Gregorio Marañon, Instituto de Investigación Gregorio Marañon, Madrid, Spain.
Almudena de-la-IglesiaHematología, Hospital Universitario Puerta de Hierro, Madrid, Spain.
Silvia Monsalvo-SaornilHematología, Hospital Universitario Puerta de Hierro, Madrid, Spain.
María Menor-GómezHematología, Hospital Universitario Principe de Asturias, Madrid, Spain.
Juan Jose Gil-FernándezHematología, Hospital Universitario Principe de Asturias, Madrid, Spain.
Esther Chica-GullonHospital Universitario Getafe, Madrid, Spain.
María Teresa Álvarez-RománHematología, Hospital Universitario La Paz, Madrid, Spain.
Gloria Perez-SeguraHematología, Hospital Universitario 12 de Octubre, Madrid, Spain.
Denis ZafraHematología, Hospital Universitario 12 de Octubre, Madrid, Spain.
Ariana Ortuzar-PasalodosHematología, Hospital Universitario Rey Juan Carlos, Madrid, Spain.
Isabel Teresa González-Gascón-Y-MarínHematología, Hospital Universitario Infanta Leonor, Madrid, Spain.
Gemma MorenoHematología, Hospital Universitario Ramón y Cajal, Madrid, Spain.
Teresa Arquero-PorteroHematología, Hospital Universitario Fundación Jimenez Díaz, Instituto de Investigación Fundación Jiménez Díaz (IIS-FJD), Madrid, Spain.
Marta Moreno-CarbonellHematología, Hospital General Universitario Gregorio Marañon, Instituto de Investigación Gregorio Marañon, Madrid, Spain.
Nuria RevillaHematología, Hospital Universitario Fundación Jimenez Díaz, Instituto de Investigación Fundación Jiménez Díaz (IIS-FJD), Madrid, Spain.ORCID https://orcid.org/0000-0002-0995-1043

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune thrombocytopenia (ITP) is a rare acquired disorder where thrombopoietin-receptor agonists have become mainstays of ITP treatment. With the recent approval of avatrombopag (AVA), real-world studies are essential to evaluate its efficacy and safety. Our study of 66 adult ITP patients treated with AVA showed a high response rate. After starting AVA, 74.2% did not require rescue medications, with minimal adverse effects. Additionally, 56.0% of patients reduced other ITP medications, and all patients aged ≥65 years responded to AVA. Results should be confirmed in larger studies, but AVA appears to be an effective and safe treatment for ITP patients.

Indexed as

ArgininePurpura, Thrombocytopenic, IdiopathicThiazolesThiophenesAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedReceptors, ThrombopoietinSpainTreatment OutcomeArginineavatrombopagReceptors, ThrombopoietinThiazolesThiophenesavatrombopagimmune thrombocytopeniaITPTPO‐RA

Identifiers

PMID39756394
PMCPMC11829131

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.