Evidence map›Paper›PMID 41158433›Full record

ArticleEJHaem2025

Common Themes and Uncertainties in Management of Secondary Polycythaemia: An International Clinician Survey of Practice.

Phillip Lr Nicolson, Midhat Asif, Richard J Buka, Peter Dyer, Eman Hassan, Claire N Harrison, Bernard D Maybury, Andrew J Doyle

Abstract read
In one paragraph

Article in EJHaem, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Phillip Lr NicolsonDepartment of Cardiovascular Sciences College of Medicine and Health University of Birmingham Birmingham UK.ORCID https://orcid.org/0000-0002-4843-2975
Midhat AsifDepartment of Clinical Haematology Queen Elizabeth Hospital Birmingham UK.
Richard J BukaDepartment of Cardiovascular Sciences College of Medicine and Health University of Birmingham Birmingham UK.ORCID https://orcid.org/0000-0002-2738-6236
Peter DyerDepartment of Clinical Haematology Royal Stoke Hospital Stoke-on-Trent UK.
Eman HassanDepartment of Cardiovascular Sciences College of Medicine and Health University of Birmingham Birmingham UK.ORCID https://orcid.org/0000-0002-0696-6848
Claire N HarrisonDepartment of Clinical Haematology Guy's and St Thomas' NHS Foundation Trust London UK.
Bernard D MayburyDepartment of Clinical Haematology Queen Elizabeth Hospital Birmingham UK.ORCID https://orcid.org/0000-0001-7064-8900

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Secondary and idiopathic polycythaemia is far more common than polycythaemia vera. Whilst venesection for polycythaemia vera has a robust evidence base, the data supporting this treatment for secondary and/or idiopathic polycythaemia are limited to small single-arm studies showing transient improvement in symptoms or physiologic endpoints. As a result the British Society for Haematology Guideline for the management of specific situations in polycythaemia vera and secondary erythrocytosis suggests Methods: To assess attitudes and practice in the treatment of secondary and idiopathic polycythaemia we designed an international clinician survey to evaluate current practice and define the point of clinical equipoise at which clinicians would be content to enter patients into a randomised venesection study. This survey was distributed using the wide-reaching HaemSTAR research network. Results: A total of 123 clinicians responded, of which 90 were experienced senior clinicians. 62% reported not routinely offering regular venesection whereas 38% of respondents did. Those considering venesection rose to ∼2/3 of respondents in specific circumstances such as polycythaemia-related symptoms, previous arterial or unprovoked venous thrombosis. Respondents were more likely to offer venesection to patients with idiopathic- compared to androgen- or hypoxia-driven polycythaemia. Of those who would venesect, most would use a threshold Hct ≥ 0.55, with a target Hct < 0.55 but there was significant variability. Conclusions: Our survey showed considerable variability in venesection practice for patients with secondary or idiopathic polycythaemia, probably reflecting the paucity of the evidence base. There was widespread support for a trial of venesection vs observation in secondary polycythaemia and this survey has helped to define the threshold Hct at which clinical equipoise exists.

Identifiers

PMID41158433
PMCPMC12558438

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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.