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2707. Complications of Babesiosis in Immunocompromised and Asplenic/Hyposplenic Patients
BACKGROUND: Babesiosis is a tick-borne disease frequently encountered in the region of New England in the US, with increasing incidence and complications ranging from hemolysis to end-organ damage and death. Immunocompromised (IC) patients and patients with impaired splenic function are at increased...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678342/ http://dx.doi.org/10.1093/ofid/ofad500.2318 |
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author | Harris, Courtney E Kakoullis, Loukas Aleissa, Muneerah M Haddad, Esther Arbona Kim, Andy J Rooks, Rebecca Yates, Bridget Kanwal, Urwah Izaguirre, Natalie E Little, Jessica S Hammond, Sarah P Montgomery, Mary W Sherman, Amy C Maguire, James Woolley, Ann E Baden, Lindsey R Issa, Nicolas C |
author_facet | Harris, Courtney E Kakoullis, Loukas Aleissa, Muneerah M Haddad, Esther Arbona Kim, Andy J Rooks, Rebecca Yates, Bridget Kanwal, Urwah Izaguirre, Natalie E Little, Jessica S Hammond, Sarah P Montgomery, Mary W Sherman, Amy C Maguire, James Woolley, Ann E Baden, Lindsey R Issa, Nicolas C |
author_sort | Harris, Courtney E |
collection | PubMed |
description | BACKGROUND: Babesiosis is a tick-borne disease frequently encountered in the region of New England in the US, with increasing incidence and complications ranging from hemolysis to end-organ damage and death. Immunocompromised (IC) patients and patients with impaired splenic function are at increased risk of complications and relapse. METHODS: This was a multicenter, retrospective study cohort of adult patients diagnosed with babesiosis from 03/2015 – 03/2023 at two institutions. Patient demographics, diagnostic testing, treatment, and outcomes were obtained from the electronic medical record. We aimed to investigate how patient risk factors, complications, length of therapy, and frequency of relapse inform clinical decisions in IC patients. RESULTS: We identified 57 IC or asplenic/hyposplenic patients with babesiosis. Median age was 66 (IQR 60–76) and 40 (70%) were male. 45 patients (79%) were IC, 21 (37%) were asplenic, and 9 (16%) were both. The initial diagnostic test was a peripheral blood smear in 38 (67%). 25 (35%) were also co-infected with Borrelia spp. 54 patients (95%) received initial treatment with combinations of azithromycin (53, 98%), atovaquone (52, 96%), clindamycin (12, 22%), and quinine (2, 7%) with a median duration of 24.5 days [IQR 11-46]). Median treatment duration was shorter in those who were asplenic only (12 days, IQR 9-25.8) compared to those IC with splenic function (27.5 days, IQR 14-46.8) and those who were IC and asplenic (48 days, IQR 17.8-135.8). 3 patients did not receive treatment against Babesia. Prior to therapy discontinuation, 37 (65%) of patients had a documented negative smear, and 12 (21%) were PCR negative. 3 cases (5%) experienced a relapse, with 1 patient remaining PCR positive before treatment discontinuation. 4 patients (7%) died within 90 days of babesia diagnosis, with 1 death (2%) secondary to babesiosis [Table 1]. [Figure: see text] [Figure: see text] [Figure: see text] CONCLUSION: Our analysis demonstrates a low relapse and babesiosis-related mortality rate in this cohort, where IC patients typically receive a prolonged treatment course. Parasitemia detection by blood smear continues to be the initial test to determine disease severity and clearance of parasitemia. Further studies are warranted to determine the optimal length of therapy and criteria for therapy cessation, including the role of PCR. DISCLOSURES: Courtney E. Harris, MD, Dynamed: Advisor/Consultant Sarah P. Hammond, MD, F2G: Advisor/Consultant|F2G: Grant/Research Support|GSK: Grant/Research Support|Pfizer: Advisor/Consultant|Scynexis: Grant/Research Support|Seres therapeutics: Advisor/Consultant Nicolas C. Issa, MD, AiCuris: Grant/Research Support|Astellas: Grant/Research Support|Boehringer Ingelheim: Advisor/Consultant|Fujifilm: Grant/Research Support|GSK: Grant/Research Support|Merck: Grant/Research Support|Moderna: Grant/Research Support |
format | Online Article Text |
id | pubmed-10678342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106783422023-11-27 2707. Complications of Babesiosis in Immunocompromised and Asplenic/Hyposplenic Patients Harris, Courtney E Kakoullis, Loukas Aleissa, Muneerah M Haddad, Esther Arbona Kim, Andy J Rooks, Rebecca Yates, Bridget Kanwal, Urwah Izaguirre, Natalie E Little, Jessica S Hammond, Sarah P Montgomery, Mary W Sherman, Amy C Maguire, James Woolley, Ann E Baden, Lindsey R Issa, Nicolas C Open Forum Infect Dis Abstract BACKGROUND: Babesiosis is a tick-borne disease frequently encountered in the region of New England in the US, with increasing incidence and complications ranging from hemolysis to end-organ damage and death. Immunocompromised (IC) patients and patients with impaired splenic function are at increased risk of complications and relapse. METHODS: This was a multicenter, retrospective study cohort of adult patients diagnosed with babesiosis from 03/2015 – 03/2023 at two institutions. Patient demographics, diagnostic testing, treatment, and outcomes were obtained from the electronic medical record. We aimed to investigate how patient risk factors, complications, length of therapy, and frequency of relapse inform clinical decisions in IC patients. RESULTS: We identified 57 IC or asplenic/hyposplenic patients with babesiosis. Median age was 66 (IQR 60–76) and 40 (70%) were male. 45 patients (79%) were IC, 21 (37%) were asplenic, and 9 (16%) were both. The initial diagnostic test was a peripheral blood smear in 38 (67%). 25 (35%) were also co-infected with Borrelia spp. 54 patients (95%) received initial treatment with combinations of azithromycin (53, 98%), atovaquone (52, 96%), clindamycin (12, 22%), and quinine (2, 7%) with a median duration of 24.5 days [IQR 11-46]). Median treatment duration was shorter in those who were asplenic only (12 days, IQR 9-25.8) compared to those IC with splenic function (27.5 days, IQR 14-46.8) and those who were IC and asplenic (48 days, IQR 17.8-135.8). 3 patients did not receive treatment against Babesia. Prior to therapy discontinuation, 37 (65%) of patients had a documented negative smear, and 12 (21%) were PCR negative. 3 cases (5%) experienced a relapse, with 1 patient remaining PCR positive before treatment discontinuation. 4 patients (7%) died within 90 days of babesia diagnosis, with 1 death (2%) secondary to babesiosis [Table 1]. [Figure: see text] [Figure: see text] [Figure: see text] CONCLUSION: Our analysis demonstrates a low relapse and babesiosis-related mortality rate in this cohort, where IC patients typically receive a prolonged treatment course. Parasitemia detection by blood smear continues to be the initial test to determine disease severity and clearance of parasitemia. Further studies are warranted to determine the optimal length of therapy and criteria for therapy cessation, including the role of PCR. DISCLOSURES: Courtney E. Harris, MD, Dynamed: Advisor/Consultant Sarah P. Hammond, MD, F2G: Advisor/Consultant|F2G: Grant/Research Support|GSK: Grant/Research Support|Pfizer: Advisor/Consultant|Scynexis: Grant/Research Support|Seres therapeutics: Advisor/Consultant Nicolas C. Issa, MD, AiCuris: Grant/Research Support|Astellas: Grant/Research Support|Boehringer Ingelheim: Advisor/Consultant|Fujifilm: Grant/Research Support|GSK: Grant/Research Support|Merck: Grant/Research Support|Moderna: Grant/Research Support Oxford University Press 2023-11-27 /pmc/articles/PMC10678342/ http://dx.doi.org/10.1093/ofid/ofad500.2318 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstract Harris, Courtney E Kakoullis, Loukas Aleissa, Muneerah M Haddad, Esther Arbona Kim, Andy J Rooks, Rebecca Yates, Bridget Kanwal, Urwah Izaguirre, Natalie E Little, Jessica S Hammond, Sarah P Montgomery, Mary W Sherman, Amy C Maguire, James Woolley, Ann E Baden, Lindsey R Issa, Nicolas C 2707. Complications of Babesiosis in Immunocompromised and Asplenic/Hyposplenic Patients |
title | 2707. Complications of Babesiosis in Immunocompromised and Asplenic/Hyposplenic Patients |
title_full | 2707. Complications of Babesiosis in Immunocompromised and Asplenic/Hyposplenic Patients |
title_fullStr | 2707. Complications of Babesiosis in Immunocompromised and Asplenic/Hyposplenic Patients |
title_full_unstemmed | 2707. Complications of Babesiosis in Immunocompromised and Asplenic/Hyposplenic Patients |
title_short | 2707. Complications of Babesiosis in Immunocompromised and Asplenic/Hyposplenic Patients |
title_sort | 2707. complications of babesiosis in immunocompromised and asplenic/hyposplenic patients |
topic | Abstract |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678342/ http://dx.doi.org/10.1093/ofid/ofad500.2318 |
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