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Early Development and Durability of SARS-CoV-2 Antibodies Among Solid Organ Transplant Recipients: A Pilot Study
Boyarsky, Brian J; Ou, Michael T; Werbel, William A; Avery, Robin K; Clarke, William A; Tobian, Aaron A R; Massie, Allan B; Segev, Dorry L; Garonzik Wang, Jacqueline M
PMCID:8085060
PMID: 33617174
ISSN: 1534-6080
CID: 5126982
Safety of the First Dose of SARS-CoV-2 Vaccination in Solid Organ Transplant Recipients [Letter]
Boyarsky, Brian J; Ou, Michael T; Greenberg, Ross S; Teles, Aura T; Werbel, William A; Avery, Robin K; Massie, Allan B; Segev, Dorry L; Garonzik-Wang, Jacqueline M
PMCID:8084895
PMID: 33560728
ISSN: 1534-6080
CID: 5126962
Response to "COVID-19 in SOT versus non-SOT" [Comment]
Avery, Robin K; Chiang, Teresa P-Y; Marr, Kieren A; Garonzik-Wang, Jacqueline; Segev, Dorry L; Massie, Allan B
PMID: 33560556
ISSN: 1600-6143
CID: 5126952
Better Understanding the Disparity Associated With Black Race in Heart Transplant Outcomes: A National Registry Analysis
Maredia, Hasina; Bowring, Mary Grace; Massie, Allan B; Bae, Sunjae; Kernodle, Amber; Oyetunji, Shakirat; Merlo, Christian; Higgins, Robert S D; Segev, Dorry L; Bush, Errol L
BACKGROUND:Black heart transplant recipients have higher risk of mortality than White recipients. Better understanding of this disparity, including subgroups most affected and timing of the highest risk, is necessary to improve care of Black recipients. We hypothesize that this disparity may be most pronounced among young recipients, as barriers to care like socioeconomic factors may be particularly salient in a younger population and lead to higher early risk of mortality. METHODS:We studied 22 997 adult heart transplant recipients using the Scientific Registry of Transplant Recipients data from January 2005 to 2017 using Cox regression models adjusted for recipient, donor, and transplant characteristics. RESULTS:=0.1). CONCLUSIONS:Young Black recipients have a high risk of mortality in the first year after heart transplant, which has been masked in decades of research looking at disparities in aggregate. To reduce overall racial disparities, clinical research moving forward should focus on targeted interventions for young Black recipients during this period.
PMID: 33525893
ISSN: 1941-3297
CID: 5126932
Rising Cost of Thyroid Surgery in Adult Patients
Sahli, Zeyad T; Zhou, Sheng; Sharma, Ashwyn K; Segev, Dorry L; Massie, Allan; Zeiger, Martha A; Mathur, Aarti
BACKGROUND:The aim of this study is to describe the economic trends in adults who underwent elective thyroidectomy. METHODS:We performed a population-based study utilizing the Premier Healthcare Database to examine adult patients who underwent elective thyroidectomy between January 2006 and December 2014. Time was divided into three equal time periods (2006-2008, 2009-2011, and 2012-2014). To examine trend in patient charges, we modeled patient charges using generalized linear regressions adjusting for key covariates with standard errors clustered at the hospital level. RESULTS:Our study cohort consisted of 52,012 adult patients who underwent a thyroid operation. During the study period, the most common procedure changed from a thyroid lobectomy to bilateral thyroidectomy. Over the study period, there was an increase in the proportion of completion thyroidectomies from 1.1% to 1.6% (PÂ <Â 0.001), malignant diagnoses from 21.7% to 26.8% (PÂ <Â 0.001), procedures performed at teaching hospitals from 27.7% to 32.9% (PÂ <Â 0.001), and procedures performed on an outpatient basis from 93.85% to 97.55% (PÂ <Â 0.001). The annual increase in median patient charge adjusted for inflation was $895 or 4.3% resulting in an increase of 38.8% over 9Â y. Higher thyroidectomy charges were associated with male patients, malignant surgical pathology, patients undergoing limited or radical neck dissection, experiencing complications, those with managed health care insurance, and a prolonged length of stay. CONCLUSIONS:Despite recent changes in thyroid surgery practices to decrease the economic burden of hospitals, costs continue to rise 4.3% annually. Additional prospective studies are needed to identify factors associated with this increasing cost.
PMCID:7946711
PMID: 33316757
ISSN: 1095-8673
CID: 5126872
Decreased incidence of acute rejection without increased incidence of cytomegalovirus (CMV) infection in kidney transplant recipients receiving rabbit anti-thymocyte globulin without CMV prophylaxis - a cohort single-center study
de Paula, Mayara Ivani; Bowring, Mary Grace; Shaffer, Ashton A; Garonzik-Wang, Jacqueline; Bessa, Adrieli Barros; Felipe, Claudia Rosso; Cristelli, Marina Pontello; Massie, Allan B; Medina-Pestana, Jose; Segev, Dorry L; Tedesco-Silva, Helio
Induction therapy with rabbit anti-thymocyte globulin (rATG) in low-risk kidney transplant recipients (KTR) remains controversial, given the associated increased risk of cytomegalovirus (CMV) infection. This natural experiment compared 12-month clinical outcomes in low-risk KTR without CMV prophylaxis (January/3/13-September/16/15) receiving no induction or a single 3Â mg/kg dose of rATG. We used logistic regression to characterize delayed graft function (DGF), negative binomial to characterize length of hospital stay (LOS), and Cox regression to characterize acute rejection (AR), CMV infection, graft loss, death, and hospital readmissions. Recipients receiving 3Â mg/kg rATG had an 81% lower risk of AR (aHR 0.14 0.190.25 , PÂ <Â 0.001) but no increased rate of hospital readmissions because of infections (0.68 0.911.21 , PÂ =Â 0.5). There was no association between 3Â mg/kg rATG and CMV infection/disease (aHR 0.86 1.101.40 , PÂ =Â 0.5), even when the analysis was stratified according to recipient CMV serostatus positive (aHR 0.94 1.251.65 , PÂ =Â 0.1) and negative (aHR 0.28 0.571.16 , PÂ =Â 0.1). There was no association between 3Â mg/kg rATG and mortality (aHR 0.51 1.253.08 , PÂ =Â 0.6), and graft loss (aHR 0.34 0.731.55 , PÂ =Â 0.4). Among low-risk KTR receiving no CMV pharmacological prophylaxis, 3Â mg/kg rATG induction was associated with a significant reduction in the incidence of AR without an increased risk of CMV infection, regardless of recipient pretransplant CMV serostatus.
PMCID:8573716
PMID: 33314321
ISSN: 1432-2277
CID: 5126862
LIMITED IMMUNOGENICITY OF A SINGLE DOSE OF SARS-CoV-2 MRNA VACCINE IN SOLID ORGAN TRANSPLANT RECIPIENTS [Meeting Abstract]
Boyarsky, Brian; Ou, Michael; Greenberg, Ross; Teles, Aura; Werbel, William; Avery, Robin K.; Tobian, Aaron; Massie, Allan; Segev, Dorry; Garonzik-Wang, Jacqueline
ISI:000689725500551
ISSN: 0934-0874
CID: 5133232
Characterizing the landscape and impact of infections following kidney transplantation
Jackson, Kyle R; Motter, Jennifer D; Bae, Sunjae; Kernodle, Amber; Long, Jane J; Werbel, William; Avery, Robin; Durand, Christine; Massie, Allan B; Desai, Niraj; Garonzik-Wang, Jacqueline; Segev, Dorry L
Infections remain a major threat to successful kidney transplantation (KT). To characterize the landscape and impact of post-KT infections in the modern era, we used United States Renal Data System (USRDS) data linked to the Scientific Registry of Transplant Recipients (SRTR) to study 141Â 661 Medicare-primary kidney transplant recipients from January 1, 1999 to December 31, 2014. Infection diagnoses were ascertained by International Classification of Diseases, Ninth Revision (ICD-9) codes. The cumulative incidence of a post-KT infection was 36.9% at 3Â months, 53.7% at 1Â year, and 78.0% at 5Â years. The most common infections were urinary tract infection (UTI; 46.8%) and pneumonia (28.2%). Five-year mortality for kidney transplant recipients who developed an infection was 24.9% vs 7.9% for those who did not, and 5-year death-censored graft failure (DCGF) was 20.6% vs 10.1% (PÂ <Â .001). This translated to a 2.22-fold higher mortality risk (adjusted hazard ratio [aHR]: 2.15 2.222.29 , PÂ <Â .001) and 1.92-fold higher DCGF risk (aHR: 1.84 1.911.98 , PÂ <Â .001) for kidney transplant recipients who developed an infection, although the magnitude of this higher risk varied across infection types (for example, 3.11-fold higher mortality risk for sepsis vs 1.62-fold for a UTI). Post-KT infections are common and substantially impact mortality and DCGF, even in the modern era. Kidney transplant recipients at high risk for infections might benefit from enhanced surveillance or follow-up to mitigate these risks.
PMID: 32506639
ISSN: 1600-6143
CID: 5126422
Effects of COVID-19 pandemic on pediatric kidney transplant in the United States
Charnaya, Olga; Chiang, Teresa Po-Yu; Wang, Richard; Motter, Jennifer D; Boyarsky, Brian J; King, Elizabeth A; Werbel, William A; Durand, Christine M; Avery, Robin K; Segev, Dorry L; Massie, Allan B; Garonzik-Wang, Jacqueline M
BACKGROUND:In March 2020, COVID-19 infections began to rise exponentially in the USA, placing substantial burden on the healthcare system. As a result, there was a rapid change in transplant practices and policies, with cessation of most procedures. Our goal was to understand changes to pediatric kidney transplantation (KT) at the national level during the COVID-19 epidemic. METHODS:Using SRTR data, we examined changes in pediatric waitlist registration, waitlist removal or inactivation, and deceased donor and living donor (DDKT/LDKT) events during the start of the disease transmission in the USA compared with the same time the previous year. RESULTS:) in states with high vs. low COVID activity. Transplant recipients during the pandemic were more likely to have received a DDKT, but had similar calculated panel-reactive antibody (cPRA) values, waitlist time, and cause of kidney failure as before the pandemic. CONCLUSIONS:The COVID-19 pandemic initially reduced access to kidney transplantation among pediatric patients in the USA but has not had a sustained effect.
PMID: 32980942
ISSN: 1432-198x
CID: 5126712
EARLY SAFETY OF SARS-CoV-2 MRNA VACCINES IN SOLID ORGAN TRANSPLANT RECIPIENTS [Meeting Abstract]
Ou, Michael; Boyarsky, Brian; Motter, Jennifer; Greenberg, Ross; Teles, Aura; Ruddy, Jake; Krach, Michelle; Werbel, William; Avery, Robin K.; Massie, Allan; Segev, Dorry; Garonzik-Wang, Jacqueline
ISI:000689725500549
ISSN: 0934-0874
CID: 5133222