Heart Transplantation Requiring Permanent Pacemaker: Risk Factors and Outcomes

Michael Keller1, Ye In Christopher Kwon1, Yashar Haghighi1

  • 1Division of Cardiothoracic Surgery, Department of Surgery, Pauley Heart Center, Virginia Commonwealth University School of Medicine, Richmond, VA 23298, USA.

Insights

Permanent pacemaker (PPM) implantation after heart transplantation (HT) is not linked to increased mortality. Early PPM showed lower graft failure and primary graft dysfunction, while late PPM had short-term survival impacts but not long-term.

Area of Science:

  • Cardiology
  • Transplantation Medicine
  • Medical Devices

Background:

  • A subset of heart transplant recipients require permanent pacemakers (PPM).
  • Understanding risk factors and outcomes for PPM implantation post-heart transplantation (HT) is crucial.

Purpose of the Study:

  • To explore risk factors and outcomes associated with early (pre-discharge) and late (>6 months post-transplant) PPM implantation in adult HT recipients.
  • To assess the impact of PPM implantation on recipient survival and graft function.

Main Methods:

  • Utilized the United Network for Organ Sharing (UNOS) database (2013-2023) for adult HT patients receiving early or late PPM.
  • Employed propensity score matching (PSM) for control cohorts.
  • Analyzed recipient survival, graft failure, primary graft dysfunction (PGD), and mortality using Cox and logistic regression, and Kaplan-Meier curves.

Main Results:

  • Early PPM recipients (n=354) demonstrated similar survival but lower graft failure and PGD rates compared to controls.
  • Late PPM recipients (n=554) showed reduced short-term survival (30 days, 1 year) but not at 5 years.
  • Neither early nor late PPM independently increased mortality risk post-HT; Donation after Circulatory Death (DCD) organs correlated with lower early PPM risk.

Conclusions:

  • Permanent pacemaker implantation, whether early or late, is not an independent predictor of mortality following heart transplantation.
  • Distinct short-term morbidity and mortality profiles exist between early and late PPM implantation groups.
  • Further investigation into the specific mechanisms driving these observed differences is warranted.

Related Concept Videos

Cardiomyopathy V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

Managing cardiomyopathy involves addressing underlying or precipitating causes, treating heart failure with medications, and implementing dietary changes and a balanced exercise and rest regimen.Lifestyle ModificationsCardiomyopathy patients should adopt a low-sodium diet to reduce fluid retention and manage heart failure. A personalized exercise and rest plan helps maintain physical fitness without overstraining the heart. Avoiding alcohol and tobacco is essential to prevent further damage to...
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...