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  1. Article ; Online: Plastic Bronchitis and Protein-Losing Enteropathy in the Fontan Patient: Evolving Understanding and Emerging Therapies.

    Mackie, Andrew S / Veldtman, Gruschen R / Thorup, Lene / Hjortdal, Vibeke E / Dori, Yoav

    The Canadian journal of cardiology

    2022  Volume 38, Issue 7, Page(s) 988–1001

    Abstract: Plastic bronchitis (PB) and protein-losing enteropathy (PLE) are rare but potentially devastating complications of the Fontan circulation. PB occurs in ∼4% of Fontan patients, typically presents within 2 to 3 years of Fontan completion with chronic cough, ...

    Abstract Plastic bronchitis (PB) and protein-losing enteropathy (PLE) are rare but potentially devastating complications of the Fontan circulation. PB occurs in ∼4% of Fontan patients, typically presents within 2 to 3 years of Fontan completion with chronic cough, wheezing, fever, or acute asphyxiation, and is characterised by proteinaceous airway casts that are expectorated or found on bronchoscopy. PLE develops in 4% to 13% of patients, usually within 5 to 10 years post Fontan, and manifests with edema, ascites, hypoalbuminemia, lymphopenia, hypogammaglobulinemia, and elevated fecal alpha-1 antitrypsin 1. These disorders have similar pathophysiology involving disruption of the lymphatic system resulting from elevated central venous pressure combined with elevated lymphatic production and inflammation, resulting in lymphatic drainage into low-pressure circuits such as the airways (PB) and duodenum (PLE). Our understanding of these disorders has greatly improved over the past decade as a result of advances in imaging of the lymphatic system through magnetic resonance lymphangiography and early success with lymphatic interventions including lymphatic embolisation, thoracic duct embolisation, and percutaneous thoracic duct decompression. Both PB and PLE require a multidisciplinary approach that addresses and optimises residual hemodynamic lesions through catheter-based intervention, lowers central venous pressure through medical therapy, minimises symptoms, and targets abnormal lymphatic perfusion when symptoms persist. This review summarises the pathophysiology of these disorders and the current evidence base regarding management, proposes treatment algorithms, and identifies future research opportunities. Key considerations regarding the development of a lymphatic intervention program are also highlighted.
    MeSH term(s) Bronchitis/diagnosis ; Bronchitis/etiology ; Bronchitis/therapy ; Fontan Procedure/adverse effects ; Heart Defects, Congenital/complications ; Heart Defects, Congenital/surgery ; Humans ; Plastics ; Protein-Losing Enteropathies/diagnosis ; Protein-Losing Enteropathies/etiology ; Protein-Losing Enteropathies/therapy
    Chemical Substances Plastics
    Language English
    Publishing date 2022-03-18
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 632813-1
    ISSN 1916-7075 ; 0828-282X
    ISSN (online) 1916-7075
    ISSN 0828-282X
    DOI 10.1016/j.cjca.2022.03.011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Echocardiography in adults with congenital heart disease: Combining the best of both worlds.

    Tretter, Justin T / Oechslin, Erwin N / Veldtman, Gruschen R

    International journal of cardiology

    2018  Volume 272, Page(s) 84–85

    MeSH term(s) Adult ; Consensus ; Echocardiography ; Heart Defects, Congenital ; Humans
    Language English
    Publishing date 2018-08-29
    Publishing country Netherlands
    Document type Editorial ; Comment
    ZDB-ID 779519-1
    ISSN 1874-1754 ; 0167-5273
    ISSN (online) 1874-1754
    ISSN 0167-5273
    DOI 10.1016/j.ijcard.2018.04.008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Bridging the psychological issues of living with the Fontan circulation.

    Brida, Margarita / Grbcic, Stefania / Holbein, Christina / Veldtman, Gruschen R

    International journal of cardiology

    2018  Volume 260, Page(s) 72–73

    MeSH term(s) Fontan Procedure ; Heart Defects, Congenital
    Language English
    Publishing date 2018--01
    Publishing country Netherlands
    Document type Editorial ; Comment
    ZDB-ID 779519-1
    ISSN 1874-1754 ; 0167-5273
    ISSN (online) 1874-1754
    ISSN 0167-5273
    DOI 10.1016/j.ijcard.2018.02.105
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Effect of Sodium-Glucose Cotransporter 2 Inhibitors in Adults With Congenital Heart Disease.

    Neijenhuis, Ralph M L / MacDonald, Simon T / Zemrak, Filip / Mertens, Bart J A / Dinsdale, Anna / Hunter, Amanda / Walker, Niki L / Swan, Lorna / Reddy, Sushma / Rotmans, Joris I / Jukema, J Wouter / Jongbloed, Monique R M / Veldtman, Gruschen R / Egorova, Anastasia D

    Journal of the American College of Cardiology

    2024  Volume 83, Issue 15, Page(s) 1403–1414

    Abstract: Background: Heart failure (HF) is the principal cause of morbidity and mortality in adults with congenital heart disease (ACHD). Robust evidence-based treatment options are lacking.: Objectives: This study aims to evaluate the safety, tolerability, ... ...

    Abstract Background: Heart failure (HF) is the principal cause of morbidity and mortality in adults with congenital heart disease (ACHD). Robust evidence-based treatment options are lacking.
    Objectives: This study aims to evaluate the safety, tolerability, and short-term HF-related effects of sodium-glucose cotransporter 2 inhibitors (SGLT2i) in a real-world ACHD population.
    Methods: All patients with ACHD treated with SGLT2i in 4 European ACHD centers were included in this retrospective study. Data were collected from 1 year before starting SGLT2i to the most recent follow-up. Data on side effects, discontinuation, mortality, and hospitalizations were collected.
    Results: In total, 174 patients with ACHD were treated with SGLT2i from April 2016 to July 2023. The mean age was 48.7 ± 15.3 years, 72 (41.4%) were female, and 29 (16.7%) had type 2 diabetes mellitus. Ten (5.7%) patients had mild, 75 (43.1%) moderate, and 89 (51.1%) severe congenital heart disease. HF was the most frequent starting indication (n = 162, 93.1%), followed by type 2 diabetes (n = 11, 6.3%) and chronic kidney disease (n = 1, 0.6%). At median follow-up of 7.7 months (Q1-Q3: 3.9-13.2 months), 18 patients (10.3%) reported side effects, 12 (6.9%) permanently discontinued SGLT2i, and 4 (2.3%) died of SGLT2i-unrelated causes. A significant reduction in the HF hospitalization rate was observed from 6 months before to 6 months after starting SGLT2i (relative rate = 0.30; 95% CI: 0.14-0.62; P = 0.001).
    Conclusions: SGLT2i generally seem safe, well-tolerated, and potentially beneficial in patients with ACHD. SGLT2i was associated with a 3-fold reduction in the 6-month HF hospitalization rate. These results warrant prospective randomized investigation of the potential benefits of SGLT2i for patients with ACHD.
    MeSH term(s) Adult ; Female ; Humans ; Male ; Middle Aged ; Diabetes Mellitus, Type 2/drug therapy ; Heart Defects, Congenital/drug therapy ; Heart Failure/drug therapy ; Retrospective Studies
    Language English
    Publishing date 2024-03-25
    Publishing country United States
    Document type Journal Article
    ZDB-ID 605507-2
    ISSN 1558-3597 ; 0735-1097
    ISSN (online) 1558-3597
    ISSN 0735-1097
    DOI 10.1016/j.jacc.2024.02.017
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Improved survival in Fontan-associated protein-losing enteropathy.

    Veldtman, Gruschen R / Webb, Gary D

    Journal of the American College of Cardiology

    2014  Volume 64, Issue 1, Page(s) 63–65

    MeSH term(s) Female ; Fontan Procedure/mortality ; Fontan Procedure/trends ; Humans ; Male ; Protein-Losing Enteropathies/mortality ; Protein-Losing Enteropathies/surgery
    Language English
    Publishing date 2014-07-08
    Publishing country United States
    Document type Comment ; Editorial
    ZDB-ID 605507-2
    ISSN 1558-3597 ; 0735-1097
    ISSN (online) 1558-3597
    ISSN 0735-1097
    DOI 10.1016/j.jacc.2014.05.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Genotype-phenotype correlations in Marfan syndrome.

    Landis, Benjamin J / Veldtman, Gruschen R / Ware, Stephanie M

    Heart (British Cardiac Society)

    2017  Volume 103, Issue 22, Page(s) 1750–1752

    MeSH term(s) Aneurysm, Dissecting ; Aortic Aneurysm ; Fibrillin-1/genetics ; Fibrillins/genetics ; Genetic Association Studies ; Humans ; Marfan Syndrome/genetics ; Microfilament Proteins/genetics
    Chemical Substances Fibrillin-1 ; Fibrillins ; Microfilament Proteins
    Language English
    Publishing date 2017-06-08
    Publishing country England
    Document type Editorial ; Comment
    ZDB-ID 1303417-0
    ISSN 1468-201X ; 1355-6037
    ISSN (online) 1468-201X
    ISSN 1355-6037
    DOI 10.1136/heartjnl-2017-311513
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Hepatic Venous Pressure Gradient in Fontan Physiology Has Limited Diagnostic and Prognostic Significance.

    Egbe, Alexander C / Miranda, William R / Veldtman, Gruschen R / Graham, Rondell P / Kamath, Patrick S

    CJC open

    2020  Volume 2, Issue 5, Page(s) 360–364

    Abstract: Background: Hepatic venous pressure gradient (HVPG) is measure of portal pressure and a prognostic tool in patients with viral and alcoholic cirrhosis; its utility is unknown in patients with Fontan-associated liver disease (FALD). Limited data suggest ... ...

    Abstract Background: Hepatic venous pressure gradient (HVPG) is measure of portal pressure and a prognostic tool in patients with viral and alcoholic cirrhosis; its utility is unknown in patients with Fontan-associated liver disease (FALD). Limited data suggest that patients with FALD have normal HVPG. On the basis of the available data, we hypothesized that there would be no association between HVPG, liver disease severity, and transplant-free survival in FALD.
    Methods: A retrospective study of Fontan patients who had liver biopsy and HVPG assessment at Mayo Clinic was performed. HVPG was calculated as wedged HVP minus free HVP; liver disease severity was measured by histologic assessment of fibrosis and standard clinical liver disease risk scores.
    Results: Of 56 patients (aged 28 ± 7 years), the mean Fontan pressure was 16 ± 4 and the mean HVPG was 1.4 ± 0.3 mm Hg (range, 0-3). Perisinusoidal fibrosis and periportal fibrosis were present in 56 (100%) and 54 (94%) patients, respectively; 18 (32%) met criteria for cirrhosis. There was no correlation between HVPG and degree of hepatic fibrosis. Similarly, there was no correlation between HVPG and any clinical liver disease risk score. Six (11%) patients died and 2 (4%) underwent heart transplantation during follow-up; HVPG was not associated with transplant-free survival.
    Conclusions: HVPG is not elevated in FALD even in the setting of cirrhosis and does not correlate with liver disease severity or clinical outcomes. These results suggest the limited diagnostic and prognostic role of HVPG in the management of FALD and highlight the potential pitfalls of using HVPG in this population.
    Language English
    Publishing date 2020-05-04
    Publishing country United States
    Document type Journal Article
    ISSN 2589-790X
    ISSN (online) 2589-790X
    DOI 10.1016/j.cjco.2020.04.011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: The pulmonary vascular bed in patients with functionally univentricular physiology and a Fontan circulation.

    Krimly, Ahmed / Jain, C Charles / Egbe, Alexander / Alzahrani, Ahmed / Al Najashi, Khalid / Albert-Brotons, Dimpna / Veldtman, Gruschen R

    Cardiology in the young

    2021  Volume 31, Issue 8, Page(s) 1241–1250

    Abstract: Fontan palliation represents one of the most remarkable surgical advances in the management of individuals born with functionally univentricular physiology. The operation secures adult survival for all but a few with unfavourable anatomy and/or ... ...

    Abstract Fontan palliation represents one of the most remarkable surgical advances in the management of individuals born with functionally univentricular physiology. The operation secures adult survival for all but a few with unfavourable anatomy and/or physiology. Inherent to the physiology is passive transpulmonary blood flow, which produces a vulnerability to adequate filling of the systemic ventricle at rest and during exertion. Similarly, the upstream effects of passive flow in the lungs are venous congestion and venous hypertension, especially marked during physical activity. The pulmonary vascular bed has emerged as a defining character on the stage of Fontan circulatory behaviour and clinical outcomes. Its pharmacologic regulation and anatomic rehabilitation therefore seem important strategic therapeutic targets. This review seeks to delineate the important aspects of pulmonary artery development and maturation in functionally univentricular physiology patients, pulmonary artery biology, pulmonary vascular reserve with exercise, and pulmonary artery morphologic and pharmacologic rehabilitation.
    MeSH term(s) Fontan Procedure ; Heart Defects, Congenital/surgery ; Heart Ventricles/surgery ; Hemodynamics ; Humans ; Lung ; Pulmonary Artery/surgery ; Pulmonary Circulation
    Language English
    Publishing date 2021-08-11
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 1078466-4
    ISSN 1467-1107 ; 1047-9511
    ISSN (online) 1467-1107
    ISSN 1047-9511
    DOI 10.1017/S104795112100192X
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Overcoming the challenges of anticoagulation in adults with congenital heart disease.

    Faircloth, Jenna M / Palumbo, Joseph S / Veldtman, Gruschen R

    Heart (British Cardiac Society)

    2015  Volume 101, Issue 6, Page(s) 418–420

    MeSH term(s) Humans
    Language English
    Publishing date 2015-03
    Publishing country England
    Document type Comment ; Editorial
    ZDB-ID 1303417-0
    ISSN 1468-201X ; 1355-6037
    ISSN (online) 1468-201X
    ISSN 1355-6037
    DOI 10.1136/heartjnl-2014-306805
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Fontan Liver Lesions: Not Always HCC.

    Haeffele, Christiane / Aggarwal, Avin / Lutchman, Glen / Veldtman, Gruschen R / Wu, Fred M / Lui, George K

    JACC. Case reports

    2019  Volume 1, Issue 2, Page(s) 175–178

    Abstract: A 24-year-old Fontan procedure patient underwent surveillance liver cardiac magnetic resonance imaging. Findings were suggestive of hepatocellular carcinoma (HCC). Currently, HCC is diagnosed based on imaging alone. Given her otherwise reassuring ... ...

    Abstract A 24-year-old Fontan procedure patient underwent surveillance liver cardiac magnetic resonance imaging. Findings were suggestive of hepatocellular carcinoma (HCC). Currently, HCC is diagnosed based on imaging alone. Given her otherwise reassuring clinical profile, she underwent liver biopsy. Pathology demonstrated focal nodular hyperplasia. This raises concern for overdiagnosis of HCC in Fontan patients without tissue confirmation. (
    Language English
    Publishing date 2019-08-21
    Publishing country Netherlands
    Document type Case Reports
    ISSN 2666-0849
    ISSN (online) 2666-0849
    DOI 10.1016/j.jaccas.2019.05.031
    Database MEDical Literature Analysis and Retrieval System OnLINE

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