ArticleAmerican journal of hematology2018
Community counts: Evolution of a national surveillance system for bleeding disorders.
Article in American journal of hematology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
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.
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.
Who cites it
17 citing papers in PubMed.
- Risk factors for joint bleeding in severe hemophilia A and B: analysis of the Community Counts longitudinal surveillance cohort.Blood vessels, thrombosis & hemostasis · 2025Article
- Inhibitor development and clinical characteristics in children with severe hemophilia A in the ATHN 8 US cohort study.Blood vessels, thrombosis & hemostasis · 2025Article
- Contemporary approaches to treat people with hemophilia: what's new and what's not?Research and practice in thrombosis and haemostasis · 2025Review
- The role of public health in rare diseases: hemophilia as an example.Frontiers in public health · 2025Review
- Importance of Inhibitor Surveillance During Emicizumab Prophylaxis in Young Children With Hemophilia: An Illustrative Case Series.Case reports in hematology · 2025Article
- Clinical and treatment characteristics of infants and toddlers less than 2 years of age with hemophilia.Blood advances · 2024Article
- Prevalence of comorbid conditions among older males with haemophilia receiving care in haemophilia treatment centers in the United States.Haemophilia : the official journal of the World Federation of Hemophilia · 2022Article
- Occurrence rates of inherited bleeding disorders other than haemophilia and von Willebrand disease among people receiving care in specialized treatment centres in the United States.Haemophilia : the official journal of the World Federation of Hemophilia · 2022Article
- Bleeding Disorders in Women and Girls: State of the Science and CDC Collaborative Programs.Journal of women's health (2002) · 2022Review
- Women and girls with haemophilia receiving care at specialized haemophilia treatment centres in the United States.Haemophilia : the official journal of the World Federation of Hemophilia · 2021Article
- Occurrence rates of von Willebrand disease among people receiving care in specialized treatment centres in the United States.Haemophilia : the official journal of the World Federation of Hemophilia · 2021Article
- Validation of the chromogenic Bethesda assay for factor VIII inhibitors in hemophilia a patients receiving Emicizumab.International journal of laboratory hematology · 2021Article
- Genetic causes of haemophilia in women and girls.Haemophilia : the official journal of the World Federation of Hemophilia · 2021Review
- Evaluation of anti-factor VIII antibody levels in patients with haemophilia A receiving immune tolerance induction therapy or bypassing agents.Haemophilia : the official journal of the World Federation of Hemophilia · 2021Article
- Evaluation of CDC's Hemophilia Surveillance Program - Universal Data Collection (1998-2011) and Community Counts (2011-2019), United States.Morbidity and mortality weekly report. Surveillance summaries (Washington, D.C. : 2002) · 2020Article
- Occurrence rates of haemophilia among males in the United States based on surveillance conducted in specialized haemophilia treatment centres.Haemophilia : the official journal of the World Federation of Hemophilia · 2020Article
- Potential of the Community Counts registry to characterize rare bleeding disorders.Haemophilia : the official journal of the World Federation of Hemophilia · 2019Article
Corrections and comments
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Authors and funding
13 authors.
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Abstract
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What OpenQuestion holds
Registered trials
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.