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Short Report: Evaluating the Effects of Automated Donor Referral Technology on Deceased Donor Referrals
Levan, Macey L; Trahan, Chad; Klitenic, Samantha B; Hewlett, Jonathan; Strout, Tyler; Levan, Michael A; Vanterpool, Karen B; Segev, Dorry L; Adams, Bradley L; Massie, Allan B; Niles, Patricia
UNLABELLED:Automation of deceased donor referrals with standardized clinical triggers allows organ procurement organizations to be rapidly aware of medically eligible potential donors without the need for manual reporting and subjective decision-making of otherwise very busy hospital staff. In October 2018, 3 Texas hospitals (pilot hospitals) began using an automated referral system; our goal was to evaluate the impact of this system on eligible donor referral. METHODS/UNASSIGNED:We studied ventilated referrals (n = 28 034) in a single organ procurement organization from January 2015 to March 2021. We estimated the change in referral rate in the 3 pilot hospitals due to the automated referral system using a difference-in-differences analysis with Poisson regression. RESULTS/UNASSIGNED:). CONCLUSIONS/UNASSIGNED:Following deployment of an automated referral system that did not require any actions by the referring hospital, referrals, authorizations, and organ donors increased substantially in the 3 pilot hospitals. Broader deployment of automated referral systems may lead to increases in the deceased donor pool.
PMCID:10109458
PMID: 37077729
ISSN: 2373-8731
CID: 5466242
Severe acute respiratory syndrome coronavirus 2 antibody response to a third dose of homologous messenger RNA vaccination in liver transplantation recipients
Strauss, Alexandra T; Chang, Amy; Alejo, Jennifer L; Chiang, Teresa P-Y; Hernandez, Nicole F; Zeiser, Laura B; Boyarsky, Brian J; Avery, Robin K; Tobian, Aaron A R; Levan, Macey L; Warren, Daniel S; Massie, Allan B; Garonzik-Wang, Jacqueline M; Segev, Dorry L; Werbel, William A
PMID: 35389558
ISSN: 1527-6473
CID: 5480292
Quantifying excess deaths among solid organ transplant recipients in the COVID-19 era
Massie, Allan B; Werbel, William A; Avery, Robin K; Po-Yu Chiang, Teresa; Snyder, Jon J; Segev, Dorry L
Estimating the total coronavirus disease 2019 (COVID-19) mortality burden of solid organ transplant recipients (SOTRs), both directly through COVID-19 infection and indirectly through other impacts on the healthcare system and society, is critical for understanding the disease's impact on the SOTR population. Using SRTR data, we modeled expected mortality risk per month pre-COVID (January 2015-February 2020) for kidney/liver/heart/lung SOTRs, and compared monthly COVID-era deaths (March 2020-March 2021) to expected rates, overall and among subgroups. Deaths above expected rates were designated "excess deaths." Between March 2020 and March 2021, there were 3739/827/265/252 excess deaths among kidney/liver/heart/lung SOTRs, respectively, representing a 41.2%/27.4%/18.5%/15.0% increase above expected deaths. 93.0% of excess deaths occurred in patients age≥50. The observed:expected ratio was highest among Hispanic SOTRs (1.82) and lowest among White SOTRs (1.20); 56.0% of excess deaths occurred among Black or Hispanic SOTRs. 64.7% of excess deaths occurred among patients who had survived ≥5 years post-transplant. Excess deaths peaked in January 2021; geographic distribution of excess deaths broadly mirrored COVID-19 incidence. COVID-19 likely caused over 5000 excess deaths among SOTRs in the US in a 13-month period, representing 1 in 75 SOTRs and a substantial proportion of all deaths among SOTRs during this time. SOTRs will remain at elevated mortality risk until the COVID-19 pandemic can be controlled.
PMID: 35294799
ISSN: 1600-6143
CID: 5200282
Questions of accountability and transparency in the US organ donation and transplantation system [Letter]
Levan, Macey L; Klitenic, Samantha; Massie, Allan; Parent, Brendan; Caplan, Arthur; Gentry, Sommer; Segev, Dorry
PMID: 35710989
ISSN: 1546-170x
CID: 5282752
Hurricanes and Mortality among Patients Receiving Dialysis
Blum, Matthew F; Feng, Yijing; Anderson, G Brooke; Segev, Dorry L; McAdams-DeMarco, Mara; Grams, Morgan E
BACKGROUND:Hurricanes are severe weather events that can disrupt power, water, and transportation systems. These disruptions may be deadly for patients requiring maintenance dialysis. We hypothesized that the mortality risk among patients requiring maintenance dialysis would be increased in the 30 days after a hurricane. METHODS:Patients registered as requiring maintenance dialysis in the United States Renal Data System who initiated treatment between January 1, 1997 and December 31, 2017 in one of 108 hurricane-afflicted counties were followed from dialysis initiation until transplantation, dialysis discontinuation, a move to a nonafflicted county, or death. Hurricane exposure was determined as a tropical cyclone event with peak local wind speeds ≥64 knots in the county of a patient's residence. The risk of death after the hurricane was estimated using time-varying Cox proportional hazards models. RESULTS:The median age of the 187,388 patients was 65 years (IQR, 53-75) and 43.7% were female. There were 27 hurricanes and 105,398 deaths in 529,339 person-years of follow-up on dialysis. In total, 29,849 patients were exposed to at least one hurricane. Hurricane exposure was associated with a significantly higher mortality after adjusting for demographic and socioeconomic covariates (hazard ratio, 1.13; 95% confidence interval, 1.05-1.22). The association persisted when adjusting for seasonality. CONCLUSIONS:Patients requiring maintenance dialysis have a higher mortality risk in the 30 days after a hurricane.
PMID: 35835459
ISSN: 1533-3450
CID: 5279972
Immunogenicity of Ad26.COV2.S prime and two subsequent doses of mRNA SARS-CoV-2 vaccines in solid organ transplant recipients: A case series [Letter]
Chang, Amy; Mitchell, Jonathan; Alejo, Jennifer L; Chiang, Teresa P Y; Abedon, Aura T; Kim, Jake D; Avery, Robin K; Tobian, Aaron A R; Levan, Macey L; Warren, Daniel S; Garonzik-Wang, Jacqueline M; Massie, Allan B; Segev, Dorry L; Werbel, William A
PMID: 35822545
ISSN: 1399-0012
CID: 5279872
Clinical Protection During the First Omicron Wave in Unvaccinated, Convalescent US Adults-Reply [Comment]
Alejo, Jennifer L; Makary, Martin A; Segev, Dorry L
PMID: 35819425
ISSN: 1538-3598
CID: 5279852
Defining the ethical considerations surrounding kidney transplantation for frail and cognitively impaired patients: a Delphi study of geriatric transplant experts
Shrestha, Prakriti; Van Pilsum Rasmussen, Sarah E; King, Elizabeth A; Gordon, Elisa J; Faden, Ruth R; Segev, Dorry L; Humbyrd, Casey Jo; McAdams-DeMarco, Mara
BACKGROUND:Among adult kidney transplant (KT) candidates, 21% are frail and 55% have cognitive impairment, increasing the risk of pre- and post-KT mortality. Centers often assess frailty status and cognitive function during transplant evaluation to help identify appropriate candidate. Yet, there are no ethical guidelines regarding the use of frailty and cognitive function during this evaluation. We seek to develop a clinical consensus on balancing utility and justice in access to KT for frail and cognitively impaired patients. METHODS:Twenty-seven experts caring for ESRD patients completed a two-round Delphi panel designed to facilitate consensus (> 80% agreement). RESULTS:Experts believed that denying patients transplantation based solely on expected patient survival was inequitable to frail or cognitively impaired candidates; 100% agreed that frailty and cognitive impairment are important factors to consider during KT evaluation. There was consensus that health related quality of life and social support are important to consider before waitlisting frail or cognitively impaired patients. Experts identified important factors to consider before waitlisting frail (likely to benefit from KT, frailty reversibility, age, and medical contraindications) and cognitively impaired (degree of impairment and medication adherence) patients. CONCLUSIONS:Clinical experts believed it was ethically unacceptable to allocate organs solely based on patients' expected survival; frailty and cognitive impairment should be measured at evaluation when weighed against other clinical factors. Ethical guidelines regarding the use of frailty and cognitive function during KT evaluation ought to be developed.
PMCID:9264705
PMID: 35804289
ISSN: 1471-2318
CID: 5267972
Antibody Response to a Fourth Dose of SARS-CoV-2 Vaccine in Solid Organ Transplant Recipients: An Update
Mitchell, Jonathan; Alejo, Jennifer L; Chiang, Teresa P Y; Kim, Jake; Chang, Amy; Abedon, Aura T; Avery, Robin K; Tobian, Aaron A R; Massie, Allan B; Levan, Macey L; Warren, Daniel S; Garonzik-Wang, Jacqueline M; Segev, Dorry L; Werbel, William A
PMID: 35426888
ISSN: 1534-6080
CID: 5204472
A Fourth Dose of COVID-19 Vaccine Does Not Induce Neutralization of the Omicron Variant Among Solid Organ Transplant Recipients With Suboptimal Vaccine Response
Karaba, Andrew H; Johnston, Trevor S; Aytenfisu, Tihitina Y; Akinde, Olivia; Eby, Yolanda; Ruff, Jessica E; Abedon, Aura T; Alejo, Jennifer L; Blankson, Joel N; Cox, Andrea L; Bailey, Justin R; Klein, Sabra L; Pekosz, Andrew; Segev, Dorry L; Tobian, Aaron A R; Werbel, William A
Background:Humoral responses to coronavirus disease 2019 (COVID-19) vaccines are attenuated in solid organ transplant recipients (SOTRs), necessitating additional booster vaccinations. The Omicron variant demonstrates substantial immune evasion, and it is unknown whether additional vaccine doses increase neutralizing capacity versus this variant of concern (VOC) among SOTRs. Methods:Within an observational cohort, 25 SOTRs with low seroresponse underwent anti-severe acute respiratory syndrome coronavirus 2 spike and receptor-binding domain immunoglobulin (Ig)G testing using a commercially available multiplex ELISA before and after a fourth COVID-19 vaccine dose (D4). Surrogate neutralization (percent angiotensin-converting enzyme 2 inhibition [%ACE2i], range 0%-100% with >20% correlating with live virus neutralization) was measured against full-length spike proteins of the vaccine strain and 5 VOCs including Delta and Omicron. Changes in IgG level and %ACE2i were compared using the paired Wilcoxon signed-rank test. Results:Anti-receptor-binding domain and anti-spike seropositivity increased post-D4 from 56% to 84% and 68% to 88%, respectively. Median (interquartile range) anti-spike antibody significantly increased post-D4 from 42.3 (4.9-134.2) to 228.9 (1115.4-655.8) World Health Organization binding antibody units. %ACE2i (median [interquartile range]) also significantly increased against the vaccine strain (5.8% [0%-16.8%] to 20.6% [5.8%-45.9%]) and the Delta variant (9.1% [4.9%-12.8%] to 17.1% [10.3%-31.7%]), yet neutralization versus Omicron was poor, did not increase post-D4 (4.1% [0%-6.9%] to 0.5% [0%-5.7%]), and was significantly lower than boosted healthy controls. Conclusions:Although a fourth vaccine dose increases anti-spike IgG and neutralizing capacity against many VOCs, some SOTRs may remain at high risk for Omicron infection despite boosting. Thus, additional protective interventions or alternative vaccination strategies should be urgently explored.
PMID: 35417115
ISSN: 1534-6080
CID: 5219052