Hereditary Hemorrhagic Telangiectasia in Uruguay: Epidemiologic and clinical features of the evaluated population.

Criscuolo, Zelika - Chiesa, Camila - Losada, Germán - Marsiglia, Bruno - Matta, Leandro - Nogara, Renata - Pereira, Hernán - Rodriguez, Sebastián - Mezzano, Rossana - Ruiz, Santiago

Resumen:

Background Hereditary Hemorrhagic Telangiectasia (HHT) is a rare autosomal dominant vascular dysplasia, characterized by mucocutaneous telangiectasias and visceral arteriovenous malformations (AVMs). Despite an estimated global prevalence of 1 in 5,000, HHT remains underdiagnosed in many regions. Prior to this study, no epidemiologic data were available for Uruguay. Objective To describe the epidemiologic and clinical characteristics of HHT patients in Uruguay, estimate the national prevalence of the disease, assess adherence to international screening guidelines, and diagnostic delays. Methods A cross-sectional observational study was conducted in Uruguay using data from the national HHT reference registry. Patients who met the Curaçao criteria or had a confirmed pathogenic genetic variant were included. Data were obtained through a standardized telephone survey and medical record review. Variables included demographic data, clinical manifestations, diagnostic workup, and treatment. Descriptive and bivariate analyses were performed using SPSS software. Results The registry included 134 patients, of whom 90 were surveyed. Estimated HHT prevalence in Uruguay was 3.83 per 100,000 inhabitants (95% CI, 3.26 - 4.61). The mean age was 48.2 years (SD ± 18.3), with a female-to-male ratio of 1.73:1. Epistaxis affected 88.9% of adults, with more than 50% classified as moderate-to-severe and had anemia. Common treatments included oral (60.7%) and intravenous (41.6%) iron, tranexamic acid (24.7%), and propranolol (11.2%). Pulmonary, cerebral, hepatic and digestive arteriovenous malformations were present in 20%, 15%,19% and 50% of patients, respectively. The mean diagnostic delay was 5.7 years (SD ± 10.6). Only 22% of patients completed the recommended screening. Conclusion HHT remains underdiagnosed and undertreated in Uruguay, with significant diagnostic delays and low adherence to international screening guidelines. This first national epidemiological study underscores the urgent need for a formally recognized national referral center to ensure high-quality, multidisciplinary care and to raise disease awareness, with the aim of reducing preventable complications.

Detalles Bibliográficos
2025
Programa de Desarrollo de la Ciencia Básica
Agencia Nacional de Investigación e Innovación, Fondo María Viñas
Brain Vascular Malformation Consortium
Hereditary Hemorrhagic Telangiectasia
Epistaxis
Arteriovenous Malformation
Rare Diseases
Epidemiology
Ciencias Médicas y de la Salud
Medicina Clínica
Sistemas Cardíaco y Cardiovascular
Inglés
Institut Pasteur de Montevideo
IPMON en REDI
https://hdl.handle.net/20.500.12381/5571
https://doi.org/10.1101/2025.08.18.25333772;
Acceso abierto
Reconocimiento-NoComercial-SinObraDerivada 4.0 Internacional. (CC BY-NC-ND)
_version_ 1880371521442021376
author Criscuolo, Zelika
author2 Chiesa, Camila
Losada, Germán
Marsiglia, Bruno
Matta, Leandro
Nogara, Renata
Pereira, Hernán
Rodriguez, Sebastián
Mezzano, Rossana
Ruiz, Santiago
author2_role author
author
author
author
author
author
author
author
author
author_facet Criscuolo, Zelika
Chiesa, Camila
Losada, Germán
Marsiglia, Bruno
Matta, Leandro
Nogara, Renata
Pereira, Hernán
Rodriguez, Sebastián
Mezzano, Rossana
Ruiz, Santiago
author_role author
bitstream.checksum.fl_str_mv 710ccfef5cb01d54b75d1d847d6b6b7b
2f81d0e45f5e3874d55582bda48e63ad
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
bitstream.url.fl_str_mv https://redi.anii.org.uy/jspui/bitstream/20.500.12381/5571/2/license.txt
https://redi.anii.org.uy/jspui/bitstream/20.500.12381/5571/1/2025.08.18.25333772v1.full.pdf
collection IPMON en REDI
dc.creator.none.fl_str_mv Criscuolo, Zelika
Chiesa, Camila
Losada, Germán
Marsiglia, Bruno
Matta, Leandro
Nogara, Renata
Pereira, Hernán
Rodriguez, Sebastián
Mezzano, Rossana
Ruiz, Santiago
dc.date.accessioned.none.fl_str_mv 2026-06-08T15:43:45Z
dc.date.available.none.fl_str_mv 2026-06-08T15:43:45Z
dc.date.issued.none.fl_str_mv 2025-08-21
dc.description.abstract.none.fl_txt_mv Background Hereditary Hemorrhagic Telangiectasia (HHT) is a rare autosomal dominant vascular dysplasia, characterized by mucocutaneous telangiectasias and visceral arteriovenous malformations (AVMs). Despite an estimated global prevalence of 1 in 5,000, HHT remains underdiagnosed in many regions. Prior to this study, no epidemiologic data were available for Uruguay. Objective To describe the epidemiologic and clinical characteristics of HHT patients in Uruguay, estimate the national prevalence of the disease, assess adherence to international screening guidelines, and diagnostic delays. Methods A cross-sectional observational study was conducted in Uruguay using data from the national HHT reference registry. Patients who met the Curaçao criteria or had a confirmed pathogenic genetic variant were included. Data were obtained through a standardized telephone survey and medical record review. Variables included demographic data, clinical manifestations, diagnostic workup, and treatment. Descriptive and bivariate analyses were performed using SPSS software. Results The registry included 134 patients, of whom 90 were surveyed. Estimated HHT prevalence in Uruguay was 3.83 per 100,000 inhabitants (95% CI, 3.26 - 4.61). The mean age was 48.2 years (SD ± 18.3), with a female-to-male ratio of 1.73:1. Epistaxis affected 88.9% of adults, with more than 50% classified as moderate-to-severe and had anemia. Common treatments included oral (60.7%) and intravenous (41.6%) iron, tranexamic acid (24.7%), and propranolol (11.2%). Pulmonary, cerebral, hepatic and digestive arteriovenous malformations were present in 20%, 15%,19% and 50% of patients, respectively. The mean diagnostic delay was 5.7 years (SD ± 10.6). Only 22% of patients completed the recommended screening. Conclusion HHT remains underdiagnosed and undertreated in Uruguay, with significant diagnostic delays and low adherence to international screening guidelines. This first national epidemiological study underscores the urgent need for a formally recognized national referral center to ensure high-quality, multidisciplinary care and to raise disease awareness, with the aim of reducing preventable complications.
dc.description.sponsorship.none.fl_txt_mv Programa de Desarrollo de la Ciencia Básica
Agencia Nacional de Investigación e Innovación, Fondo María Viñas
Brain Vascular Malformation Consortium
dc.identifier.anii.es.fl_str_mv FMV_1_2021_1_166595
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1101/2025.08.18.25333772;
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/20.500.12381/5571
dc.language.iso.none.fl_str_mv eng
dc.rights.*.fl_str_mv Acceso abierto
dc.rights.license.none.fl_str_mv Reconocimiento-NoComercial-SinObraDerivada 4.0 Internacional. (CC BY-NC-ND)
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
dc.source.none.fl_str_mv reponame:IPMON en REDI
instname:Institut Pasteur de Montevideo
instacron:Institut Pasteur de Montevideo
dc.subject.anii.none.fl_str_mv Ciencias Médicas y de la Salud
Medicina Clínica
Sistemas Cardíaco y Cardiovascular
dc.subject.es.fl_str_mv Hereditary Hemorrhagic Telangiectasia
Epistaxis
Arteriovenous Malformation
Rare Diseases
Epidemiology
dc.title.none.fl_str_mv Hereditary Hemorrhagic Telangiectasia in Uruguay: Epidemiologic and clinical features of the evaluated population.
dc.type.es.fl_str_mv Preprint
dc.type.none.fl_str_mv info:eu-repo/semantics/preprint
description Background Hereditary Hemorrhagic Telangiectasia (HHT) is a rare autosomal dominant vascular dysplasia, characterized by mucocutaneous telangiectasias and visceral arteriovenous malformations (AVMs). Despite an estimated global prevalence of 1 in 5,000, HHT remains underdiagnosed in many regions. Prior to this study, no epidemiologic data were available for Uruguay. Objective To describe the epidemiologic and clinical characteristics of HHT patients in Uruguay, estimate the national prevalence of the disease, assess adherence to international screening guidelines, and diagnostic delays. Methods A cross-sectional observational study was conducted in Uruguay using data from the national HHT reference registry. Patients who met the Curaçao criteria or had a confirmed pathogenic genetic variant were included. Data were obtained through a standardized telephone survey and medical record review. Variables included demographic data, clinical manifestations, diagnostic workup, and treatment. Descriptive and bivariate analyses were performed using SPSS software. Results The registry included 134 patients, of whom 90 were surveyed. Estimated HHT prevalence in Uruguay was 3.83 per 100,000 inhabitants (95% CI, 3.26 - 4.61). The mean age was 48.2 years (SD ± 18.3), with a female-to-male ratio of 1.73:1. Epistaxis affected 88.9% of adults, with more than 50% classified as moderate-to-severe and had anemia. Common treatments included oral (60.7%) and intravenous (41.6%) iron, tranexamic acid (24.7%), and propranolol (11.2%). Pulmonary, cerebral, hepatic and digestive arteriovenous malformations were present in 20%, 15%,19% and 50% of patients, respectively. The mean diagnostic delay was 5.7 years (SD ± 10.6). Only 22% of patients completed the recommended screening. Conclusion HHT remains underdiagnosed and undertreated in Uruguay, with significant diagnostic delays and low adherence to international screening guidelines. This first national epidemiological study underscores the urgent need for a formally recognized national referral center to ensure high-quality, multidisciplinary care and to raise disease awareness, with the aim of reducing preventable complications.
eu_rights_str_mv openAccess
format preprint
id IPMON_791b2ca65b7818fb6761d0d6a0efc883
identifier_str_mv FMV_1_2021_1_166595
instacron_str Institut Pasteur de Montevideo
institution Institut Pasteur de Montevideo
instname_str Institut Pasteur de Montevideo
language eng
network_acronym_str IPMON
network_name_str IPMON en REDI
oai_identifier_str oai:redi.anii.org.uy:20.500.12381/5571
publishDate 2025
reponame_str IPMON en REDI
repository.mail.fl_str_mv msarroca@pasteur.edu.uy
repository.name.fl_str_mv IPMON en REDI - Institut Pasteur de Montevideo
repository_id_str 9421_2
rights_invalid_str_mv Reconocimiento-NoComercial-SinObraDerivada 4.0 Internacional. (CC BY-NC-ND)
Acceso abierto
spelling Reconocimiento-NoComercial-SinObraDerivada 4.0 Internacional. (CC BY-NC-ND)Acceso abiertoinfo:eu-repo/semantics/openAccess2026-06-08T15:43:45Z2026-06-08T15:43:45Z2025-08-21https://hdl.handle.net/20.500.12381/5571FMV_1_2021_1_166595https://doi.org/10.1101/2025.08.18.25333772;Background Hereditary Hemorrhagic Telangiectasia (HHT) is a rare autosomal dominant vascular dysplasia, characterized by mucocutaneous telangiectasias and visceral arteriovenous malformations (AVMs). Despite an estimated global prevalence of 1 in 5,000, HHT remains underdiagnosed in many regions. Prior to this study, no epidemiologic data were available for Uruguay. Objective To describe the epidemiologic and clinical characteristics of HHT patients in Uruguay, estimate the national prevalence of the disease, assess adherence to international screening guidelines, and diagnostic delays. Methods A cross-sectional observational study was conducted in Uruguay using data from the national HHT reference registry. Patients who met the Curaçao criteria or had a confirmed pathogenic genetic variant were included. Data were obtained through a standardized telephone survey and medical record review. Variables included demographic data, clinical manifestations, diagnostic workup, and treatment. Descriptive and bivariate analyses were performed using SPSS software. Results The registry included 134 patients, of whom 90 were surveyed. Estimated HHT prevalence in Uruguay was 3.83 per 100,000 inhabitants (95% CI, 3.26 - 4.61). The mean age was 48.2 years (SD ± 18.3), with a female-to-male ratio of 1.73:1. Epistaxis affected 88.9% of adults, with more than 50% classified as moderate-to-severe and had anemia. Common treatments included oral (60.7%) and intravenous (41.6%) iron, tranexamic acid (24.7%), and propranolol (11.2%). Pulmonary, cerebral, hepatic and digestive arteriovenous malformations were present in 20%, 15%,19% and 50% of patients, respectively. The mean diagnostic delay was 5.7 years (SD ± 10.6). Only 22% of patients completed the recommended screening. Conclusion HHT remains underdiagnosed and undertreated in Uruguay, with significant diagnostic delays and low adherence to international screening guidelines. This first national epidemiological study underscores the urgent need for a formally recognized national referral center to ensure high-quality, multidisciplinary care and to raise disease awareness, with the aim of reducing preventable complications.Programa de Desarrollo de la Ciencia BásicaAgencia Nacional de Investigación e Innovación, Fondo María ViñasBrain Vascular Malformation ConsortiumengHereditary Hemorrhagic TelangiectasiaEpistaxisArteriovenous MalformationRare DiseasesEpidemiologyCiencias Médicas y de la SaludMedicina ClínicaSistemas Cardíaco y CardiovascularHereditary Hemorrhagic Telangiectasia in Uruguay: Epidemiologic and clinical features of the evaluated population.Preprintinfo:eu-repo/semantics/preprintMetabolic Diseases and Aging Laboratory, Institut Pasteur de Montevideo. Mataojo 2020, Montevideo, Uruguay.Unidad Académica Médica 1, Hospital Maciel. 25 de Mayo 174, Montevideo, Uruguay.Facultad de Medicina, Universidad de la República Oriental del Uruguay.Departamento de Medicina Transfusional, Centro Hospitalario Pereira Rossell. Lord Ponsonby 2410, Montevideo, Uruguay.//Ciencias Médicas y de la Salud/Medicina Clínica/Sistemas Cardíaco y Cardiovascularreponame:IPMON en REDIinstname:Institut Pasteur de Montevideoinstacron:Institut Pasteur de MontevideoCriscuolo, ZelikaChiesa, CamilaLosada, GermánMarsiglia, BrunoMatta, LeandroNogara, RenataPereira, HernánRodriguez, SebastiánMezzano, RossanaRuiz, SantiagoLICENSElicense.txtlicense.txttext/plain; charset=utf-85124https://redi.anii.org.uy/jspui/bitstream/20.500.12381/5571/2/license.txt710ccfef5cb01d54b75d1d847d6b6b7bMD52ORIGINAL2025.08.18.25333772v1.full.pdf2025.08.18.25333772v1.full.pdfCriscuolo et al. preprintapplication/pdf317929https://redi.anii.org.uy/jspui/bitstream/20.500.12381/5571/1/2025.08.18.25333772v1.full.pdf2f81d0e45f5e3874d55582bda48e63adMD5120.500.12381/55712026-06-08 12:43:46.197oai:redi.anii.org.uy:20.500.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://hdl.handle.net/20.500.12381/575Organismo científico-tecnológicohttps://pasteur.uy/https://redi.anii.org.uy/oai/requestmsarroca@pasteur.edu.uyUruguayopendoar:9421_22026-06-08T15:43:46IPMON en REDI - Institut Pasteur de Montevideofalse
spellingShingle Hereditary Hemorrhagic Telangiectasia in Uruguay: Epidemiologic and clinical features of the evaluated population.
Criscuolo, Zelika
Hereditary Hemorrhagic Telangiectasia
Epistaxis
Arteriovenous Malformation
Rare Diseases
Epidemiology
Ciencias Médicas y de la Salud
Medicina Clínica
Sistemas Cardíaco y Cardiovascular
title Hereditary Hemorrhagic Telangiectasia in Uruguay: Epidemiologic and clinical features of the evaluated population.
title_full Hereditary Hemorrhagic Telangiectasia in Uruguay: Epidemiologic and clinical features of the evaluated population.
title_fullStr Hereditary Hemorrhagic Telangiectasia in Uruguay: Epidemiologic and clinical features of the evaluated population.
title_full_unstemmed Hereditary Hemorrhagic Telangiectasia in Uruguay: Epidemiologic and clinical features of the evaluated population.
title_short Hereditary Hemorrhagic Telangiectasia in Uruguay: Epidemiologic and clinical features of the evaluated population.
title_sort Hereditary Hemorrhagic Telangiectasia in Uruguay: Epidemiologic and clinical features of the evaluated population.
topic Hereditary Hemorrhagic Telangiectasia
Epistaxis
Arteriovenous Malformation
Rare Diseases
Epidemiology
Ciencias Médicas y de la Salud
Medicina Clínica
Sistemas Cardíaco y Cardiovascular
url https://hdl.handle.net/20.500.12381/5571
https://doi.org/10.1101/2025.08.18.25333772;