Zeba Nauroz
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Zeba Nauroz has a total of 64 co-authors. Here are the top co-authors by number of shared publications:
- Christine M. Durand
Department of Medicine, Johns Hopkins University School of Medicine , Baltimore, Maryland
4 shared publications - Dorry Lidor Segev
Department of Surgery New York University New York New York USA
4 shared publications - Mary Grace Bowring
Johns Hopkins University School of Medicine, Baltimore, MD
4 shared publications - Allan B. Massie
Department of Surgery, New York University Langone Transplant Institute, New York, USA
3 shared publications - Aaron A. R. Tobian
Department of Pathology Johns Hopkins University School of Medicine Baltimore Maryland USA
2 shared publications Allan Massie
2 shared publications
Latest Publications
- Open Access
- 20 October 2025
- Published by Elsevier in The Journal of Heart and Lung Transplantation
- Vol. 45 (3) , 460-467
Potential pool of cardiothoracic organs from donors with HIV
- 20 October 2025
- Published by Elsevier in The Journal of Heart and Lung Transplantation
- Vol. 45 (3) , 460-467
Open AccessPotential pool of cardiothoracic organs from donors with HIV
- Open Access
- 24 September 2025
- Published by Elsevier in American Journal of Transplantation
- Vol. 26 (2) , 383-392
Increased rate of deceased donor liver transplantation for candidates willing to receive organs from donors with human immunodeficiency virus
- 24 September 2025
- Published by Elsevier in American Journal of Transplantation
- Vol. 26 (2) , 383-392
Open AccessIncreased rate of deceased donor liver transplantation for candidates willing to receive organs from donors with human immunodeficiency virus
- Open Access
- 8 August 2025
- Published by Wiley in Transplant Infectious Disease
- Vol. 27 (5) , e70090
Trends over Time in Practice and Outcomes of Lung Transplantation in Recipients With Human Immunodeficiency Virus
Background: People with human immunodeficiency virus (HIV) are at an increased risk for end‐stage lung disease, for which lung transplantation (LT) may be necessary. Methods: We aimed to characterize the national practice patterns of LT in recipients with HIV (HIV R+) and post‐LT outcomes, including rejection in the US over time. Using the Scientific Registry of Transplant Recipients data (from January 1, 2004, to December 1, 2024, for practice patterns and from January 1, 2016, to December 1, 2024, for outcomes), we compared 96 adult HIV R+ to 42 341 LT recipients without HIV (HIV R‐). We examined the association between HIV and outcomes using Gini coefficients, Cox regression, and modified Poisson regression before and after 2020. Results: HIV R+ LTs increased from 0.1% in 2004 to 0.4% of LTs in 2024 ( p = 0.07). Pre‐2020, 18 centers performed 80% of HIV R+ LTs (Gini = 0.78); post‐2020, 14 centers performed 80% of HIV R+ LTs (Gini = 0.76), indicating no expansion of the practice across centers. HIV R+ did not have an increased risk of mortality (adjusted hazard ratio pre‐2020: 0.91 [95% confidence interval 0.41–1.62], p = 0.7 and post‐2020: 1.05 [0.49–3.25], p = 0.8), or increased risk of 1‐year rejection rate (adjusted relative risk pre‐2020: 0.60 [0.20–1.77], p = 0.3, and post‐2020: 0.77 [0.26–2.2], p = 0.6). Conclusions: Increasing numbers of HIV R+ LTs and comparable outcomes to those without HIV are encouraging, yet few centers perform these transplants. image
- 8 August 2025
- Published by Wiley in Transplant Infectious Disease
- Vol. 27 (5) , e70090
Open AccessTrends over Time in Practice and Outcomes of Lung Transplantation in Recipients With Human Immunodeficiency Virus
Background: People with human immunodeficiency virus (HIV) are at an increased risk for end‐stage lung disease, for which lung transplantation (LT) may be necessary. Methods: We aimed to characterize the national practice patterns of LT in recipients with HIV (HIV R+) and post‐LT outcomes, including rejection in the US over time. Using the Scientific Registry of Transplant Recipients data (from January 1, 2004, to December 1, 2024, for practice patterns and from January 1, 2016, to December 1, 2024, for outcomes), we compared 96 adult HIV R+ to 42 341 LT recipients without HIV (HIV R‐). We examined the association between HIV and outcomes using Gini coefficients, Cox regression, and modified Poisson regression before and after 2020. Results: HIV R+ LTs increased from 0.1% in 2004 to 0.4% of LTs in 2024 ( p = 0.07). Pre‐2020, 18 centers performed 80% of HIV R+ LTs (Gini = 0.78); post‐2020, 14 centers performed 80% of HIV R+ LTs (Gini = 0.76), indicating no expansion of the practice across centers. HIV R+ did not have an increased risk of mortality (adjusted hazard ratio pre‐2020: 0.91 [95% confidence interval 0.41–1.62], p = 0.7 and post‐2020: 1.05 [0.49–3.25], p = 0.8), or increased risk of 1‐year rejection rate (adjusted relative risk pre‐2020: 0.60 [0.20–1.77], p = 0.3, and post‐2020: 0.77 [0.26–2.2], p = 0.6). Conclusions: Increasing numbers of HIV R+ LTs and comparable outcomes to those without HIV are encouraging, yet few centers perform these transplants. image
- Open Access
- 19 January 2024
- Published by Wiley in Clinical Transplantation
- Vol. 38 (1) , e15233
Letter to the editor: Poor sensitivity of anti‐nucleocapsid antibody in detecting prior COVID‐19 in vaccinated solid organ transplant recipients
- 19 January 2024
- Published by Wiley in Clinical Transplantation
- Vol. 38 (1) , e15233
Open AccessLetter to the editor: Poor sensitivity of anti‐nucleocapsid antibody in detecting prior COVID‐19 in vaccinated solid organ transplant recipients
- 6 December 2023
- Published by Elsevier in The Journal of Heart and Lung Transplantation
- Vol. 43 (4) , 615-625
Impact of recipient age on mortality among Cytomegalovirus (CMV)-seronegative lung transplant recipients with CMV-seropositive donors
- 6 December 2023
- Published by Elsevier in The Journal of Heart and Lung Transplantation
- Vol. 43 (4) , 615-625
Impact of recipient age on mortality among Cytomegalovirus (CMV)-seronegative lung transplant recipients with CMV-seropositive donors