Reactivation of Chagas disease among heart transplant recipients in the United States, 2012‐2016

Background Heart transplantation has been shown to be a safe and effective intervention for progressive cardiomyopathy from chronic Chagas disease. However, in the presence of the immunosuppression required for heart transplantation, the likelihood of Chagas disease reactivation is significant. Reac...

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Published inTransplant infectious disease Vol. 20; no. 6; pp. e12996 - n/a
Main Authors Gray, Elizabeth B., La Hoz, Ricardo M., Green, Jaime S., Vikram, Holenarasipur R., Benedict, Theresa, Rivera, Hilda, Montgomery, Susan P.
Format Journal Article
LanguageEnglish
Published Denmark Wiley Subscription Services, Inc 01.12.2018
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Abstract Background Heart transplantation has been shown to be a safe and effective intervention for progressive cardiomyopathy from chronic Chagas disease. However, in the presence of the immunosuppression required for heart transplantation, the likelihood of Chagas disease reactivation is significant. Reactivation may cause myocarditis resulting in allograft dysfunction and the rapid onset of congestive heart failure. Reactivation rates have been well documented in Latin America; however, there is a paucity of data regarding the risk in non‐endemic countries. Methods We present our experience with 31 patients with chronic Chagas disease who underwent orthotopic heart transplantation in the United States from 2012 to 2016. Patients were monitored following a standard schedule. Results Of the 31 patients, 19 (61%) developed evidence of reactivation. Among the 19 patients, a majority (95%) were identified by laboratory monitoring using polymerase chain reaction testing. One patient was identified after the onset of clinical symptoms of reactivation. All subjects with evidence of reactivation were alive at follow‐up (median: 60 weeks). Conclusions Transplant programs in the United States are encouraged to implement a monitoring program for heart transplant recipients with Chagas disease. Our experience using a preemptive approach of monitoring for Chagas disease reactivation was effective at identifying reactivation before symptoms developed.
AbstractList Heart transplantation has been shown to be a safe and effective intervention for progressive cardiomyopathy from chronic Chagas disease. However, in the presence of the immunosuppression required for heart transplantation, the likelihood of Chagas disease reactivation is significant. Reactivation may cause myocarditis resulting in allograft dysfunction and the rapid onset of congestive heart failure. Reactivation rates have been well documented in Latin America; however, there is a paucity of data regarding the risk in non-endemic countries.BACKGROUNDHeart transplantation has been shown to be a safe and effective intervention for progressive cardiomyopathy from chronic Chagas disease. However, in the presence of the immunosuppression required for heart transplantation, the likelihood of Chagas disease reactivation is significant. Reactivation may cause myocarditis resulting in allograft dysfunction and the rapid onset of congestive heart failure. Reactivation rates have been well documented in Latin America; however, there is a paucity of data regarding the risk in non-endemic countries.We present our experience with 31 patients with chronic Chagas disease who underwent orthotopic heart transplantation in the United States from 2012 to 2016. Patients were monitored following a standard schedule.METHODSWe present our experience with 31 patients with chronic Chagas disease who underwent orthotopic heart transplantation in the United States from 2012 to 2016. Patients were monitored following a standard schedule.Of the 31 patients, 19 (61%) developed evidence of reactivation. Among the 19 patients, a majority (95%) were identified by laboratory monitoring using polymerase chain reaction testing. One patient was identified after the onset of clinical symptoms of reactivation. All subjects with evidence of reactivation were alive at follow-up (median: 60 weeks).RESULTSOf the 31 patients, 19 (61%) developed evidence of reactivation. Among the 19 patients, a majority (95%) were identified by laboratory monitoring using polymerase chain reaction testing. One patient was identified after the onset of clinical symptoms of reactivation. All subjects with evidence of reactivation were alive at follow-up (median: 60 weeks).Transplant programs in the United States are encouraged to implement a monitoring program for heart transplant recipients with Chagas disease. Our experience using a preemptive approach of monitoring for Chagas disease reactivation was effective at identifying reactivation before symptoms developed.CONCLUSIONSTransplant programs in the United States are encouraged to implement a monitoring program for heart transplant recipients with Chagas disease. Our experience using a preemptive approach of monitoring for Chagas disease reactivation was effective at identifying reactivation before symptoms developed.
Background Heart transplantation has been shown to be a safe and effective intervention for progressive cardiomyopathy from chronic Chagas disease. However, in the presence of the immunosuppression required for heart transplantation, the likelihood of Chagas disease reactivation is significant. Reactivation may cause myocarditis resulting in allograft dysfunction and the rapid onset of congestive heart failure. Reactivation rates have been well documented in Latin America; however, there is a paucity of data regarding the risk in non‐endemic countries. Methods We present our experience with 31 patients with chronic Chagas disease who underwent orthotopic heart transplantation in the United States from 2012 to 2016. Patients were monitored following a standard schedule. Results Of the 31 patients, 19 (61%) developed evidence of reactivation. Among the 19 patients, a majority (95%) were identified by laboratory monitoring using polymerase chain reaction testing. One patient was identified after the onset of clinical symptoms of reactivation. All subjects with evidence of reactivation were alive at follow‐up (median: 60 weeks). Conclusions Transplant programs in the United States are encouraged to implement a monitoring program for heart transplant recipients with Chagas disease. Our experience using a preemptive approach of monitoring for Chagas disease reactivation was effective at identifying reactivation before symptoms developed.
BackgroundHeart transplantation has been shown to be a safe and effective intervention for progressive cardiomyopathy from chronic Chagas disease. However, in the presence of the immunosuppression required for heart transplantation, the likelihood of Chagas disease reactivation is significant. Reactivation may cause myocarditis resulting in allograft dysfunction and the rapid onset of congestive heart failure. Reactivation rates have been well documented in Latin America; however, there is a paucity of data regarding the risk in non‐endemic countries.MethodsWe present our experience with 31 patients with chronic Chagas disease who underwent orthotopic heart transplantation in the United States from 2012 to 2016. Patients were monitored following a standard schedule.ResultsOf the 31 patients, 19 (61%) developed evidence of reactivation. Among the 19 patients, a majority (95%) were identified by laboratory monitoring using polymerase chain reaction testing. One patient was identified after the onset of clinical symptoms of reactivation. All subjects with evidence of reactivation were alive at follow‐up (median: 60 weeks).ConclusionsTransplant programs in the United States are encouraged to implement a monitoring program for heart transplant recipients with Chagas disease. Our experience using a preemptive approach of monitoring for Chagas disease reactivation was effective at identifying reactivation before symptoms developed.
Heart transplantation has been shown to be a safe and effective intervention for progressive cardiomyopathy from chronic Chagas disease. However, in the presence of the immunosuppression required for heart transplantation, the likelihood of Chagas disease reactivation is significant. Reactivation may cause myocarditis resulting in allograft dysfunction and the rapid onset of congestive heart failure. Reactivation rates have been well documented in Latin America; however, there is a paucity of data regarding the risk in non-endemic countries. We present our experience with 31 patients with chronic Chagas disease who underwent orthotopic heart transplantation in the United States from 2012 to 2016. Patients were monitored following a standard schedule. Of the 31 patients, 19 (61%) developed evidence of reactivation. Among the 19 patients, a majority (95%) were identified by laboratory monitoring using polymerase chain reaction testing. One patient was identified after the onset of clinical symptoms of reactivation. All subjects with evidence of reactivation were alive at follow-up (median: 60 weeks). Transplant programs in the United States are encouraged to implement a monitoring program for heart transplant recipients with Chagas disease. Our experience using a preemptive approach of monitoring for Chagas disease reactivation was effective at identifying reactivation before symptoms developed.
Author Vikram, Holenarasipur R.
Rivera, Hilda
La Hoz, Ricardo M.
Benedict, Theresa
Gray, Elizabeth B.
Green, Jaime S.
Montgomery, Susan P.
AuthorAffiliation 4 Division of Infectious Diseases, Mayo Clinic, Phoenix, Arizona
2 Division of Infectious Diseases and Geographic Medicine, University of Texas Southwestern Medical Center, Dallas, Texas
1 Parasitic Diseases Branch, Centers for Disease Control and Prevention, Atlanta, Georgia
3 Division of Infectious Disease and International Medicine, University of Minnesota Medical Center, Minneapolis, Minnesota
AuthorAffiliation_xml – name: 1 Parasitic Diseases Branch, Centers for Disease Control and Prevention, Atlanta, Georgia
– name: 3 Division of Infectious Disease and International Medicine, University of Minnesota Medical Center, Minneapolis, Minnesota
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Keywords Chagas disease
heart transplant
reactivation
Trypanosoma cruzi
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AUTHORS’ CONTRIBUTIONS
EBG and SPM participated in the conception and design of the project; RML, JSG, and VRH contributed patient summaries for the case series; TB and HR performed serologic and PCR laboratory testing; EBG analyzed data; EBG wrote the manuscript; and RML, JSG, VRH, TB, HR, and SPM critically revised the manuscript.
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PublicationTitle Transplant infectious disease
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Snippet Background Heart transplantation has been shown to be a safe and effective intervention for progressive cardiomyopathy from chronic Chagas disease. However, in...
Heart transplantation has been shown to be a safe and effective intervention for progressive cardiomyopathy from chronic Chagas disease. However, in the...
BackgroundHeart transplantation has been shown to be a safe and effective intervention for progressive cardiomyopathy from chronic Chagas disease. However, in...
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SourceType Open Access Repository
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StartPage e12996
SubjectTerms Activation
Adult
Aged
Allografts - parasitology
Allografts - pathology
Cardiomyopathy
Chagas Cardiomyopathy - epidemiology
Chagas Cardiomyopathy - parasitology
Chagas Cardiomyopathy - pathology
Chagas Cardiomyopathy - surgery
Chagas disease
Congestive heart failure
Coronary artery disease
Female
Follow-Up Studies
Heart
Heart - parasitology
Heart Failure - epidemiology
Heart Failure - parasitology
Heart Failure - pathology
Heart Failure - surgery
heart transplant
Heart transplantation
Heart Transplantation - adverse effects
Humans
Immunosuppression
Immunosuppression Therapy - adverse effects
Immunosuppression Therapy - methods
Male
Middle Aged
Monitoring
Myocarditis
Myocardium - pathology
Patients
Polymerase chain reaction
Preempting
reactivation
Recurrence
Risk Factors
Transplantation
Transplants & implants
Trypanosoma cruzi
Trypanosoma cruzi - isolation & purification
United States - epidemiology
Vector-borne diseases
Title Reactivation of Chagas disease among heart transplant recipients in the United States, 2012‐2016
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Ftid.12996
https://www.ncbi.nlm.nih.gov/pubmed/30204269
https://www.proquest.com/docview/2140792928
https://www.proquest.com/docview/2102334129
https://pubmed.ncbi.nlm.nih.gov/PMC6289649
Volume 20
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