Neha Bansal

Dr. Neha Bansal

orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

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14 June 2024 in The Journal of Heart and Lung Transplantation
Verified
Journal Article
Closed access
IHIan B. Hollis
Ian B. Hollis
DJDouglas L. Jennings
Douglas L. Jennings
SKSelim Krim
Selim Krim
VTVan-Khue Ton
Van-Khue Ton
ADAnique Ducharme
Anique Ducharme
RRRavi K. Ratnagiri
Ravi K. Ratnagiri

2 June 2021 in Pediatric Cardiology
Verified
Journal Article
Closed access
PDF file
NBNeha Bansal
Neha Bansal
EAEstela Azeka
Estela Azeka
CNCindy Neunert
Cindy Neunert
JKJohn S. Kim
John S. Kim
JMJenna Murray
Jenna Murray
CVChristina VanderPluym
Christina VanderPluym

17 May 2022 in Journal of the American Heart Association
Verified
Journal Article
Open access
PDF file
JGJustin Godown
Justin Godown
DFDarlene Fountain
Darlene Fountain
NBNeha Bansal
Neha Bansal
RARebecca Ameduri
Rebecca Ameduri
SASusan Anderson
Susan Anderson
SHSeth A. Hollander
Seth A. Hollander
Background: Children with Down syndrome (DS) have a high risk of cardiac disease that may prompt consideration for heart transplantation (HTx). However, transplantation in patients with DS is rarely reported. This project aimed to collect and describe waitlist and post– HTx outcomes in children with DS. Methods and Results: This is a retrospective case series of children with DS listed for HTx. Pediatric HTx centers were identified by their participation in 2 international registries with centers reporting HTx in a patient with DS providing detailed demographic, medical, surgical, and posttransplant outcome data for analysis. A total of 26 patients with DS were listed for HTx from 1992 to 2020 (median age, 8.5 years; 46% male). High‐risk or failed repair of congenital heart disease was the most common indication for transplant (N=18, 69%). A total of 23 (88%) patients survived to transplant. All transplanted patients survived to hospital discharge with a median posttransplant length of stay of 22 days. At a median posttransplant follow‐up of 2.8 years, 20 (87%) patients were alive, 2 (9%) developed posttransplant lymphoproliferative disorder, and 8 (35%) were hospitalized for infection within the first year. Waitlist and posttransplant outcomes were similar in patients with and without DS ( P =non‐significant for all). Conclusions: Waitlist and post‐HTx outcomes in children with DS selected for transplant listing are comparable to pediatric HTx recipients overall. Given acceptable outcomes, the presence of DS alone should not be considered an absolute contraindication to HTx.

8 December 2022 in The Journal of Heart and Lung Transplantation
Verified
Journal Article
Closed access
NBNeha Bansal
Neha Bansal
ALAshwin K. Lal
Ashwin K. Lal
DKDevin Koehl
Devin Koehl
RCRyan S. Cantor
Ryan S. Cantor
JKJames K. Kirklin
James K. Kirklin
SUSimon Urschel
Simon Urschel

11 October 2021 in Pediatric Transplantation
Verified
Journal Article
Open access
PDF file
NBNeha Bansal
Neha Bansal
NONadia Ovchinsky
Nadia Ovchinsky
MFMarc Foca
Marc Foca
JLJacqueline M. Lamour
Jacqueline M. Lamour
DKDebora Kogan‐Liberman
Debora Kogan‐Liberman
NHNicole Hayde
Nicole Hayde
Background: Adult SOT recipients with COVID‐19 have higher mortality rates when compared to general population. There is paucity of data on outcomes in pediatric SOT recipients.Methods: This is a cross‐sectional study investigating the prevalence of COVID‐19 infection and outcomes in pediatric SOT (heart, liver, and kidney) recipients. We extracted demographic and clinical characteristics and COVID‐19 testing (PCR or [Ab] test) results from medical records. Clinical characteristics were compared between patients who were positive for COVID‐19 (PCR or Ab) and those who did not, using Mann‐Whitney, Student's t test, or chi‐square test. p value <.05 was statistically significant.Results: A total of 108 SOT recipients with a median age of 13.1 (8.4, 17.8) years and median 4.2 (2.7, 7.9) years from transplant were checked for COVID‐19 via a PCR or Ab test. A positive PCR was confirmed in 10 patients (9.3%), while 12 patients (11.1%) were positive for COVID‐19 Ab. The patients who tested positive in our cohort were 9/50 (18%) heart, 6/68 (8.8%) kidney, and 7/50 (14%) liver transplant recipients. There were no differences in the clinical characteristics between patients with and without COVID‐19 infection. All patients were either asymptomatic (50%) or had self‐limiting symptoms. No changes were made to the immunosuppressive regimen. Only one patient was hospitalized and none had an oxygen requirement.Conclusions: In our cohort of pediatric SOT recipients, COVID‐19 infection was asymptomatic or mild. This data may aid clinicians in counseling patients and families in this increased‐risk population.

25 January 2021 in Pediatric Cardiology
Verified
Journal Article
Closed access
PDF file
NBNeha Bansal
Neha Bansal
AMAmrit Misra
Amrit Misra
TFThomas J. Forbes
Thomas J. Forbes
DKDaisuke Kobayashi
Daisuke Kobayashi