PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
September 1, 1999Pacing and Clinical Electrophysiology310 citations

Altered Cardiac Histology Following Apical Right Ventricular Pacing in Patients with Congenital Atrioventricular Block

View Full Paper
PKPeter P. KarpawichRRRaja RabahJHJoel E. Haas

Key Result

Chronic apical right ventricular pacing caused significant histopathological alterations in patients, including myofiber size variation and fibrosis (P < 0.05).

Key Points

  • To determine whether chronic right ventricular apical pacing leads to histopathological cellular and subcellular abnormalities in patients with congenital complete atrioventricular block.
  • Analyzed 16 endomyocardial biopsies from 14 age-matched patients with congenital complete atrioventricular block and otherwise normal cardiac anatomy.
  • Compared 8 biopsies from pre-pacemaker implant patients (median age 15.5 years) with 8 biopsies from patients following 3 to 12 years (median 5.5 years) of chronic apical ventricular pacing, including one paired longitudinal case.
  • Biopsies obtained after chronic pacing showed a significant increase in histopathological abnormalities compared to unpaced samples (P < 0.05).
  • Pacing-associated myocardial damage included myofiber size variation, fibrosis, fat deposition, sclerosis, and mitochondrial morphological changes.

Structured PICO

Does chronic apical right ventricular pacing cause adverse histopathological alterations in patients with congenital complete atrioventricular block?

P
Population
Patients with congenital complete atrioventricular block (CCAVB) and otherwise normal anatomy
I
Intervention
Chronic apical right ventricular pacing
C
Comparator
Prior to pacemaker implant (unpaced state)
O
Outcome
Histopathological alterations (myofiber size variation, fibrosis, fat deposition, sclerosis, and mitochondrial morphological changes)surrogate

Chronic apical right ventricular pacing in young patients with congenital AV block is associated with adverse histopathological changes, such as fibrosis and mitochondrial alterations, which may contribute to clinical ventricular dysfunction.

Abstract

Previous studies have demonstrated that right ventricular apical pacing inherently alters ventricular contraction, regional blood flow, wall stress, and predisposes to diminished function. However, histological consequences of chronic apical pacing potentially contributing to the observed ventricular dysfunction remain conjectural. Previous canine studies have demonstrated histopathological cellular abnormalities with apically initiated ventricular pacing that may result in the observed diminished ventricular function. To determine if comparable adverse changes also occur in the clinical setting, 16 endomyocardial biopsies were obtained from 14 age‐matched patients with congenital complete atrioventricular block (CCAVB) and otherwise normal anatomy, divided into two groups: eight biopsies (median patient age 15.5 years) from patients prior to pacemaker implant and another eight biopsies (median patient age 16 years) from patients following 3–12 years (median 5.5) of chronic ventricular pacing. In one patient, biopsy samples were obtained before and after pacing. Results demonstrated a significant (P < 0.05) increase in histopathological alterations among the patient biopsy samples following pacing, consisting of myofiber size variation, fibrosis, fat deposition, sclerosis, and mitochondrial morphological changes. These findings indicate that chronic apical right heart ventricular pacing may adversely alter myocellular growth, epecially among the young, on the cellular and subcellular level, potentially contributing to the diminished function observed clincially.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Karpawich et al. (1999) studied this question. Chronic apical right ventricular pacing caused significant histopathological alterations in patients, including myofiber size variation and fibrosis (P < 0.05).

synapsesocial.com/papers/6970eb032d1b404414ca79behttps://doi.org/10.1111/j.1540-8159.1999.tb00631.x
Ask AI
Helpful
Bookmark
Share
View Full Paper