Marc Silver

Dr. Marc Silver

orcid

Research Focus & Metrics

Academic Career Length

2Years (2025-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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12 February 2025 in JACC: Case Reports
Verified
Journal Article
Open access
MAMousab Al Abbas
Mousab Al Abbas
SSSmitha Sagaram
Smitha Sagaram
MSMarc Silver
Marc Silver
Intravascular hypervolemia with polycythemia is a blood volume phenotype in patients with heart failure that portends additional risks including thrombotic events. This paper presents 4 patients with heart failure with this blood volume phenotype and focuses on its identification and the role of therapeutic phlebotomy including patient selection and outcomes.

16 November 2025
Verified
Book Chapter
Closed access
PDF file
KVKonstantinos Voudris
Konstantinos Voudris
RTRoderick Tung
Roderick Tung
MSMarc Silver
Marc Silver
SNSrihari S. Naidu
Srihari S. Naidu
SNSherif Nagueh
Sherif Nagueh
PSPaul Sorajja
Paul Sorajja

Verified
Journal Article
Open access
PDF file
Radha GopalanRadha Gopalan
Radha Gopalan
MEMahmoud Elbsiony
Mahmoud Elbsiony
JMJamal Mahar
Jamal Mahar
ASAnusha Sunkara
Anusha Sunkara
AKAnantharam Kalya
Anantharam Kalya
MSMarc Silver
Marc Silver
This narrative review synthesizes the available evidence on pregnancy-associated heart failure with preserved ejection fraction (HFpEF) and presents an operational definition and hypothesis-generating conceptual framework for this underrecognized cardio-obstetric phenotype that extends the traditional reduced-ejection-fraction framework of pregnancy-associated heart failure. Pregnancy-associated HFpEF refers to heart failure occurring during pregnancy or postpartum in patients with preserved left ventricular ejection fraction and objective evidence of congestion, elevated cardiac filling pressures, or impaired diastolic function, after consideration of alternative causes. Although peripartum cardiomyopathy has historically shaped the understanding of pregnancy-associated heart failure, limited observational studies and case reports have described heart-failure presentations during pregnancy or postpartum despite preserved left ventricular systolic function. Whether these presentations represent a distinct pregnancy-associated HFpEF phenotype after exclusion of alternative causes remains uncertain. This phenotype is closely linked to hypertensive disorders of pregnancy, obesity, diabetes, renal dysfunction, advanced maternal age, and social vulnerability, and may overlap mechanistically with preeclampsia through shared pathways of endothelial dysfunction, increased afterload, elevated filling pressures, and pulmonary congestion. Diagnosis remains challenging because normal pregnancy can mimic HFpEF symptoms and alter biomarkers and echocardiographic parameters, while existing HFpEF algorithms have not been validated in pregnant populations. Recognition requires integration of clinical evidence of congestion, natriuretic peptide levels, echocardiographic evidence of diastolic dysfunction or elevated filling pressures, assessment of pulmonary hypertension and right ventricular involvement, and the postpartum clinical trajectory. Given the heterogeneity of this phenotype, a personalized-medicine approach may be particularly relevant, integrating maternal risk factors, obstetric context, biomarkers, and cardiac imaging rather than relying on preserved LVEF alone. Although hypertensive disorders of pregnancy are associated with increased long-term cardiovascular and HFpEF risk, whether pregnancy-associated HFpEF itself independently predicts future heart failure remains unknown. The operational definition, conceptual framework, and postpartum considerations presented in this narrative review are intended to organize the available evidence and generate hypotheses rather than serve as a formal diagnostic or management protocol, and they require prospective validation before routine clinical adoption.