Evidence map›Paper›PMID 40600700›Full record

ArticleAmerican journal of hematology2025

Characterizing the Healthcare Utilization and Costs of Hereditary Hemorrhagic Telangiectasia.

Hanny Al-Samkari, Tracy J Mayne, Misty Troutt, Hemant Patle, Marianne Clancy, Eric Duhaime

Abstract read
In one paragraph

Article in American journal of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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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

6 authors.

Hanny Al-SamkariDivision of Hematology Oncology, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID 0000-0001-6175-1383
Tracy J MayneSlipstream IT, Blue Bell, Pennsylvania, USA.
Misty TrouttSlipstream IT, Blue Bell, Pennsylvania, USA.
Hemant PatleSlipstream IT, Blue Bell, Pennsylvania, USA.
Marianne ClancyCure HHT, Monkton, Maryland, USA.
Eric DuhaimeDiagonal Therapeutics, Watertown, Massachusetts, USA.

Funding

Diagonal Therapeutics
6 · The paper itself

Abstract

Hereditary hemorrhagic telangiectasia (HHT) is the second-most common inherited bleeding disorder worldwide, afflicting one in 4000-5000 people, and is the most morbid inherited bleeding disorder of women. HHT causes recurrent severe epistaxis, chronic gastrointestinal bleeding, heavy menstrual bleeding, and arteriovenous malformations in the lung, liver, and brain that cause serious bleeding and nonbleeding complications. There are no approved treatments worldwide, and the direct medical costs of HHT have not been well-characterized. We utilized the Komodo Healthcare Map claims database to create a large sample of US patients diagnosed with HHT, including a subgroup with anemia and a subgroup receiving hematologic support (iron infusions and/or red cell transfusions). We quantified mean per patient per year (PPPY) and total population inpatient, outpatient, and pharmacy costs in 2022 and 2023. The mean PPPY costs for all HHT patients (n = 24 407; n = 23 524), those with anemia (n = 13 856; n = 13 192) and those receiving hematologic support (n = 6191; n = 5818) were approximately $19 000, $27 000, and $40 000, respectively, across years, representing > $450 000 000 in annual healthcare costs in the sample. The leading cost drivers were related to treatment for bleeding and its consequences. While accounting for nearly 60% of HHT patients, those with anemia accounted for ~80% of direct medical costs. Across the majority of leading inpatient, outpatient, and pharmacy cost drivers, patients with anemia and anemia treatment accounted for 75%-100% of cost. The PPPY costs of HHT are comparable to, or exceed, those of other rare, resource-intensive serious diseases, including sickle cell disease, muscular dystrophy, and cystic fibrosis.

Indexed as

Health Care CostsPatient Acceptance of Health CareTelangiectasia, Hereditary HemorrhagicAdolescentAdultAgedAnemiaChildDatabases, FactualFemaleHumansMaleMiddle AgedUnited StatesYoung Adultanemiableedingcostepistaxisgastrointestinal bleedinghereditary hemorrhagic telangiectasiairon deficiencyOsler‐Weber‐Rendu

Identifiers

PMID40600700
PMCPMC12417757

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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.