Heart transplantation: a treatment approach for cardiomyopathy

    Authors

    Keywords

    heart transplantion, monozygotic twins, cardiomyopathy

    DOI

    https://doi.org/10.15836/ccar2024.617

    Full Text

    Heart transplantation is a treatment method reserved for patients in the final stage of heart failure for whom all other treatment options have been exhausted. The aim of the paper is to describe the cases of two patients who underwent a heart transplant with a satisfactory result, and to highlight the role of the nurse in preoperative and postoperative care. The patients were 11-year-old twins admitted with symptoms of heart failure. They were diagnosed with dilated cardiomyopathy, with an ejection fraction (EF) of less than 30%. An extensive clinical, laboratory, targeted genetic, imaging and microbiological examination for cardiotropic viruses were performed, but did not reveal the etiology of the disease. Both patients had severe dilated cardiomyopathy, primarily affecting the left ventricle, with markedly weakened systolic function. Cardiac MRI and invasive cardiology procedures, including left and right heart catheterization, were also conducted. Laboratory findings indicated an extremely high level of NT-proBNP, a marker of heart failure, and both twins presented with deep hypomagnesemia resistant to compensation methods. Until the transplant, patients were dependent on magnesium supplementation. Despite ongoing medical treatment, their general condition severely deteriorated, prompting referral to the heart transplant team within Eurotransplant five months after diagnosis. Heart transplantation was successfully performed in both patients within six weeks of each other, six months after the diagnosis of cardiomyopathy. Transplantation enables optimal medical, personal and social rehabilitation of the patient. The nurse’s role includes educating the patient about the procedures involved in treatment, which encompasses laboratory and diagnostic methods for all organ systems, notifying the physican of any deviations, maintaining a protocol for tests administration and ensuring that the patient consents to the possibility of transplantation. Only patients with meticulously managed medical documentation can remain on the Eurotransplant list, as any deviations lead to automatic removal. (1-3)

    Literature

    1. Malčić I, Šmalcelj A, Anić D, Planinc D i sur. Prirođene srčane greške od dječje do odrasle dobi - smjernice za liječenje odraslih s prirođenim srčanim greškama (OPSG). Zagreb, Medicinska naklada, str. 271-303.
    2. Malčić I, Jelusić M, Kniewald H, Barisić N, Jelasić D, Bozikov J. Epidemiology of cardiomyopathies in children and adolescents: a retrospective study over the last 10 years. Cardiol Young. 2002 May;12(3):253–9. https://doi.org/10.1017/S1047951102000550
    3. Nugent AW, Daubeney PE, Chondros P, Carlin JB, Cheung M, Wilkinson LC, et al. National Australian Childhood Cardiomyopathy Study. The epidemiology of childhood cardiomyopathy in Australia. N Engl J Med. 2003 April 24;348(17):1639–46. https://doi.org/10.1056/NEJMoa021737
    Cardiologia Croatica
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    Heart transplantation: a treatment approach for cardiomyopathy

    Extended Abstract
    Issue11-12
    Published
    Pages617
    PDF via DOIhttps://doi.org/10.15836/ccar2024.617
    heart transplantion
    monozygotic twins
    cardiomyopathy

    Authors

    Marina Petrinić*ORCIDUniversity Hospital Centre Zagreb, Zagreb, Croatia
    Vesna StrelarORCIDUniversity Hospital Centre Zagreb, Zagreb, Croatia

    *Correspondence email: marina.petrinic@gmail.com

    Full Text

    Heart transplantation is a treatment method reserved for patients in the final stage of heart failure for whom all other treatment options have been exhausted. The aim of the paper is to describe the cases of two patients who underwent a heart transplant with a satisfactory result, and to highlight the role of the nurse in preoperative and postoperative care. The patients were 11-year-old twins admitted with symptoms of heart failure. They were diagnosed with dilated cardiomyopathy, with an ejection fraction (EF) of less than 30%. An extensive clinical, laboratory, targeted genetic, imaging and microbiological examination for cardiotropic viruses were performed, but did not reveal the etiology of the disease. Both patients had severe dilated cardiomyopathy, primarily affecting the left ventricle, with markedly weakened systolic function. Cardiac MRI and invasive cardiology procedures, including left and right heart catheterization, were also conducted. Laboratory findings indicated an extremely high level of NT-proBNP, a marker of heart failure, and both twins presented with deep hypomagnesemia resistant to compensation methods. Until the transplant, patients were dependent on magnesium supplementation. Despite ongoing medical treatment, their general condition severely deteriorated, prompting referral to the heart transplant team within Eurotransplant five months after diagnosis. Heart transplantation was successfully performed in both patients within six weeks of each other, six months after the diagnosis of cardiomyopathy. Transplantation enables optimal medical, personal and social rehabilitation of the patient. The nurse’s role includes educating the patient about the procedures involved in treatment, which encompasses laboratory and diagnostic methods for all organ systems, notifying the physican of any deviations, maintaining a protocol for tests administration and ensuring that the patient consents to the possibility of transplantation. Only patients with meticulously managed medical documentation can remain on the Eurotransplant list, as any deviations lead to automatic removal. (1–3)

    Literature

    1. 1.
      Malčić I, Šmalcelj A, Anić D, Planinc D i sur. Prirođene srčane greške od dječje do odrasle dobi - smjernice za liječenje odraslih s prirođenim srčanim greškama (OPSG). Zagreb, Medicinska naklada, str. 271-303.
    2. 2.
      Malčić I, Jelusić M, Kniewald H, Barisić N, Jelasić D, Bozikov J. Epidemiology of cardiomyopathies in children and adolescents: a retrospective study over the last 10 years. Cardiol Young. 2002 May;12(3):253–9.DOI
    3. 3.
      Nugent AW, Daubeney PE, Chondros P, Carlin JB, Cheung M, Wilkinson LC, et al. National Australian Childhood Cardiomyopathy Study. The epidemiology of childhood cardiomyopathy in Australia. N Engl J Med. 2003 April 24;348(17):1639–46.DOI