Allan B. Massie
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Allan B. Massie has a total of 44 co-authors. Here are the top co-authors by number of shared publications:
- Dorry Lidor Segev
Department of Surgery New York University New York New York USA
6 shared publications - Sommer E. Gentry
Department of Surgery, NYU Langone Health, New York, New York
3 shared publications - Abu Ahmed Shamim
The JiVitA Project, Gaibandha, Bangladesh
2 shared publications - Alain Bernard Labrique
Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland
2 shared publications - Eric K. H. Chow
Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD
2 shared publications - Keith West
Center for Human Nutrition, Department of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA
2 shared publications
Latest Publications
- Open Access
- 27 May 2015
- Published by Elsevier in American Journal of Transplantation
- Vol. 15 (12) , 3215-3223
Landscape of Deceased Donors Labeled Increased Risk for Disease Transmission Under New Guidelines
- 27 May 2015
- Published by Elsevier in American Journal of Transplantation
- Vol. 15 (12) , 3215-3223
Open AccessLandscape of Deceased Donors Labeled Increased Risk for Disease Transmission Under New Guidelines
- Open Access
- 19 May 2015
- Published by Wolters Kluwer Health in Liver Transplantation
- Vol. 21 (8) , 1031-1039
Liver sharing and organ procurement organization performance under redistricted allocation
Concerns have been raised that optimized redistricting of liver allocation areas might have the unintended result of shifting livers from better‐performing to poorer‐performing organ procurement organizations (OPOs). We used liver simulated allocation modeling to simulate a 5‐year period of liver sharing within either 4 or 8 optimized districts. We investigated whether each OPO's net liver import under redistricting would be correlated with 2 OPO performance metrics (observed to expected liver yield and liver donor conversion ratio), along with 2 other potential correlates (eligible deaths and incident listings above a Model for End‐Stage Liver Disease score of 15). We found no evidence that livers would flow from better‐performing OPOs to poorer‐performing OPOs in either redistricting scenario. Instead, under these optimized redistricting plans, our simulations suggest that livers would flow from OPOs with more‐than‐expected eligible deaths toward those with fewer‐than‐expected eligible deaths and that livers would flow from OPOs with fewer‐than‐expected incident listings to those with more‐than‐expected incident listings; the latter is a pattern that is already established in the current allocation system. Redistricting liver distribution to reduce geographic inequity is expected to align liver allocation across the country with the distribution of supply and demand rather than transferring livers from better‐performing OPOs to poorer‐performing OPOs. Liver Transpl 21:1031‐1039, 2015. © 2015 AASLD.
- 19 May 2015
- Published by Wolters Kluwer Health in Liver Transplantation
- Vol. 21 (8) , 1031-1039
Open AccessLiver sharing and organ procurement organization performance under redistricted allocation
Concerns have been raised that optimized redistricting of liver allocation areas might have the unintended result of shifting livers from better‐performing to poorer‐performing organ procurement organizations (OPOs). We used liver simulated allocation modeling to simulate a 5‐year period of liver sharing within either 4 or 8 optimized districts. We investigated whether each OPO's net liver import under redistricting would be correlated with 2 OPO performance metrics (observed to expected liver yield and liver donor conversion ratio), along with 2 other potential correlates (eligible deaths and incident listings above a Model for End‐Stage Liver Disease score of 15). We found no evidence that livers would flow from better‐performing OPOs to poorer‐performing OPOs in either redistricting scenario. Instead, under these optimized redistricting plans, our simulations suggest that livers would flow from OPOs with more‐than‐expected eligible deaths toward those with fewer‐than‐expected eligible deaths and that livers would flow from OPOs with fewer‐than‐expected incident listings to those with more‐than‐expected incident listings; the latter is a pattern that is already established in the current allocation system. Redistricting liver distribution to reduce geographic inequity is expected to align liver allocation across the country with the distribution of supply and demand rather than transferring livers from better‐performing OPOs to poorer‐performing OPOs. Liver Transpl 21:1031‐1039, 2015. © 2015 AASLD.
- 1 April 2015
- Published by Wolters Kluwer Health in Obstetrical & Gynecological Survey
- Vol. 70 (4) , 244-246
Effect of Maternal Multiple Micronutrient vs Iron–Folic Acid Supplementation on Infant Mortality and Adverse Birth Outcomes in Rural Bangladesh
- 1 April 2015
- Published by Wolters Kluwer Health in Obstetrical & Gynecological Survey
- Vol. 70 (4) , 244-246
Effect of Maternal Multiple Micronutrient vs Iron–Folic Acid Supplementation on Infant Mortality and Adverse Birth Outcomes in Rural Bangladesh
- Top Cited PapersOpen Access
- 7 July 2014
- Published by Elsevier in American Journal of Transplantation
- Vol. 14 (8) , 1723-1730
Big Data in Organ Transplantation: Registries and Administrative Claims
- 7 July 2014
- Published by Elsevier in American Journal of Transplantation
- Vol. 14 (8) , 1723-1730
Top Cited PapersOpen AccessBig Data in Organ Transplantation: Registries and Administrative Claims
- Open Access
- 27 June 2014
- Published by Wolters Kluwer Health in Liver Transplantation
- Vol. 20 (10) , 1237-1243
Impact of Broader Sharing on the Transport Time for Deceased Donor Livers
Recent allocation policy changes have increased the sharing of deceased donor livers across local boundaries, and sharing even broader than this has been proposed as a remedy for persistent geographic disparities in liver transplantation. It is possible that broader sharing may increase cold ischemia times (CITs) and thus harm recipients. We constructed a detailed model of transport modes (car, helicopter, and fixed-wing aircraft) and transport times between all hospitals, and we investigated the relationship between the transport time and the CIT for deceased donor liver transplants. The median estimated transport time was 2.0 hours for regionally shared livers and 1.0 hour for locally allocated livers. The model-predicted transport mode was flying for 90% of regionally shared livers but for only 22% of locally allocated livers. The median CIT was 7.0 hours for regionally shared livers and 6.0 hours for locally allocated livers. Variation in the transport time accounted for only 14.7% of the variation in the CIT, and the transport time on average composed only 21% of the CIT. In conclusion, nontransport factors play a substantially larger role in the CIT than the transport time. Broader sharing will have only a marginal impact on the CIT but will significantly increase the fraction of transplants that are transported by flying rather than driving. Liver Transpl 20:1237-1243, 2014. © 2014 AASLD.
- 27 June 2014
- Published by Wolters Kluwer Health in Liver Transplantation
- Vol. 20 (10) , 1237-1243
Open AccessImpact of Broader Sharing on the Transport Time for Deceased Donor Livers
Recent allocation policy changes have increased the sharing of deceased donor livers across local boundaries, and sharing even broader than this has been proposed as a remedy for persistent geographic disparities in liver transplantation. It is possible that broader sharing may increase cold ischemia times (CITs) and thus harm recipients. We constructed a detailed model of transport modes (car, helicopter, and fixed-wing aircraft) and transport times between all hospitals, and we investigated the relationship between the transport time and the CIT for deceased donor liver transplants. The median estimated transport time was 2.0 hours for regionally shared livers and 1.0 hour for locally allocated livers. The model-predicted transport mode was flying for 90% of regionally shared livers but for only 22% of locally allocated livers. The median CIT was 7.0 hours for regionally shared livers and 6.0 hours for locally allocated livers. Variation in the transport time accounted for only 14.7% of the variation in the CIT, and the transport time on average composed only 21% of the CIT. In conclusion, nontransport factors play a substantially larger role in the CIT than the transport time. Broader sharing will have only a marginal impact on the CIT but will significantly increase the fraction of transplants that are transported by flying rather than driving. Liver Transpl 20:1237-1243, 2014. © 2014 AASLD.
- Open Access
- 6 March 2013
- Published by Elsevier in American Journal of Transplantation
- Vol. 13 (5) , 1317-1322
Center-Level Utilization of Kidney Paired Donation
- 6 March 2013
- Published by Elsevier in American Journal of Transplantation
- Vol. 13 (5) , 1317-1322
Open AccessCenter-Level Utilization of Kidney Paired Donation
- Open Access
- 15 September 2011
- Published by Elsevier in American Journal of Transplantation
- Vol. 11 (11) , 2362-2371
MELD Exceptions and Rates of Waiting List Outcomes
- 15 September 2011
- Published by Elsevier in American Journal of Transplantation
- Vol. 11 (11) , 2362-2371
Open AccessMELD Exceptions and Rates of Waiting List Outcomes
- Open Access
- 21 April 2011
- Published by Springer Nature in Trials
- Vol. 12 (1) , 102
A cluster-randomized, placebo-controlled, maternal vitamin a or beta-carotene supplementation trial in bangladesh: design and methods
We present the design, methods and population characteristics of a large community trial that assessed the efficacy of a weekly supplement containing vitamin A or beta-carotene, at recommended dietary levels, in reducing maternal mortality from early gestation through 12 weeks postpartum. We identify challenges faced and report solutions in implementing an intervention trial under low-resource, rural conditions, including the importance of population choice in promoting generalizability, maintaining rigorous data quality control to reduce inter- and intra- worker variation, and optimizing efficiencies in information and resources flow from and to the field.
- 21 April 2011
- Published by Springer Nature in Trials
- Vol. 12 (1) , 102
Open AccessA cluster-randomized, placebo-controlled, maternal vitamin a or beta-carotene supplementation trial in bangladesh: design and methods
We present the design, methods and population characteristics of a large community trial that assessed the efficacy of a weekly supplement containing vitamin A or beta-carotene, at recommended dietary levels, in reducing maternal mortality from early gestation through 12 weeks postpartum. We identify challenges faced and report solutions in implementing an intervention trial under low-resource, rural conditions, including the importance of population choice in promoting generalizability, maintaining rigorous data quality control to reduce inter- and intra- worker variation, and optimizing efficiencies in information and resources flow from and to the field.