Evidence map›Paper›PMID 32738034›Full record

ArticleESC heart failure2020

Is heart transplantation a real option in patients with Duchenne syndrome? Inferences from a case report.

Antonio Piperata, Tomaso Bottio, Giuseppe Toscano, Martina Avesani, Andrea Vianello, Gino Gerosa

Abstract readCase Reports
In one paragraph

Article in ESC heart failure, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Advanced Heart Failure Therapies in Neuromuscular Diseases.Current treatment options in cardiovascular medicine · 2024
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
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.

Antonio PiperataCardiac Surgery Unit, Department of Cardiology, Thoracic, Vascular, and Public Health Sciences, University of Padua, Via N. Giustiniani, 2, Padua, 35128, Italy.
Tomaso BottioCardiac Surgery Unit, Department of Cardiology, Thoracic, Vascular, and Public Health Sciences, University of Padua, Via N. Giustiniani, 2, Padua, 35128, Italy.ORCID 0000-0001-7299-2983
Giuseppe ToscanoCardiac Surgery Unit, Department of Cardiology, Thoracic, Vascular, and Public Health Sciences, University of Padua, Via N. Giustiniani, 2, Padua, 35128, Italy.
Martina AvesaniPediatric and Congenital Cardiology Unit, Department of Woman and Child's Health, University of Padua, Padua, Italy.
Andrea VianelloRespiratory Pathophysiology Unit, Cardiology, Thoracic, Vascular, and Public Health Sciences, University of Padua, Via N. Giustiniani, 2, Padua, 35128, Italy.
Gino GerosaCardiac Surgery Unit, Department of Cardiology, Thoracic, Vascular, and Public Health Sciences, University of Padua, Via N. Giustiniani, 2, Padua, 35128, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Duchenne muscular dystrophy (DMD) is the most frequent and severe form of MD. It firstly affects the skeletal muscles, causing severe disability, and subsequently the myocardium. The only two options to treat end-stage heart failure in these patients are either a left ventricular assist device (LVAD) implantation as destination therapy or a heart transplant. These hypotheses are still controversial, and data are very limited. We describe the case of an 18-year-old male patient, affected by DMD and in a wheelchair from the age of 11. He progressively developed dilated cardiomyopathy, and in 2016, at the age of 14 years, he underwent HeartWare LVAD implantation, as destination therapy, without post-operative complications. He has been followed up for 47 consecutive months; and 30 months after LVAD implantation, he developed an infection of the exit site, treated by antibiotics and surgical toilette. Following this event, on the basis of patient's good general conditions and willingness, we started to consider heart transplant as an option. Before the patient was listed, he underwent accurate workup, and we found higher values of forced vital capacity, forced expiratory volume in 1 s, and peak expiratory flow, compared with the predicted values of same-age DMD patients. The patient have neither scoliosis nor need for non-invasive mechanical ventilation, and finally, he was always treated with steroids with stable thoraco-abdominal function over the years. According to these considerations, the patient was listed for heart transplant. In 12 February 2020, at the age of 18 years, the patient underwent heart transplant with no post-operative complications. Cardiac transplantation is not considered a valid option for DMD patients, because of the shortage of donor availability and the systemic nature of DMD disease. Considering that this patient had already experienced an LVAD-related complication and he had better general condition than his DMD peers, we listed him for a heart transplant. We described the case of a DMD patient who underwent successful heart transplantation after 47 months of HeartWare LVAD assistance. Three months' follow-up is uneventful.

Indexed as

Cardiomyopathy, DilatedHeart-Assist DevicesHeart FailureHeart TransplantationMuscular Dystrophy, DuchenneAdolescentHumansMaleDuchenne syndromeHeart transplantLVAD device

Identifiers

PMID32738034
PMCPMC7524121

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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.