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Pregnancies in kidney transplant recipients with complement gene variant-mediated thrombotic microangiopathy

BACKGROUND: Pregnancies in patients with complement gene variant-mediated thrombotic microangiopathy (cTMA) are challenging, and pregnancies in such patients after kidney transplantation (KTX) are even more so. METHODS: We identified nine pregnancies following KTX of three genetically high-risk cTMA...

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Autores principales: Haninger-Vacariu, Natalja, Aigner, Christof, Gaggl, Martina, Kain, Renate, Prohászka, Zoltán, Böhmig, Georg A, Sunder-Plassmann, Raute, Sunder-Plassmann, Gere, Schmidt, Alice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8023217/
https://www.ncbi.nlm.nih.gov/pubmed/33841869
http://dx.doi.org/10.1093/ckj/sfaa113
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author Haninger-Vacariu, Natalja
Aigner, Christof
Gaggl, Martina
Kain, Renate
Prohászka, Zoltán
Böhmig, Georg A
Sunder-Plassmann, Raute
Sunder-Plassmann, Gere
Schmidt, Alice
author_facet Haninger-Vacariu, Natalja
Aigner, Christof
Gaggl, Martina
Kain, Renate
Prohászka, Zoltán
Böhmig, Georg A
Sunder-Plassmann, Raute
Sunder-Plassmann, Gere
Schmidt, Alice
author_sort Haninger-Vacariu, Natalja
collection PubMed
description BACKGROUND: Pregnancies in patients with complement gene variant-mediated thrombotic microangiopathy (cTMA) are challenging, and pregnancies in such patients after kidney transplantation (KTX) are even more so. METHODS: We identified nine pregnancies following KTX of three genetically high-risk cTMA patients enrolled in the Vienna thrombotic microangiopathy cohort. Preventive plasma therapy was used in three pregnancies, and one patient had ongoing eculizumab (ECU) therapy during two pregnancies. RESULTS: Seven out of nine pregnancies (78%) resulted in the delivery of healthy children. The other two included one early abortion at gestational Week 12 during ongoing ECU therapy and one late foetal death at gestational Week 33 + 3, most likely not related to complement dysregulation. Kidney transplant function after delivery remained stable in all but one pregnancy. In the aforementioned case, a severe cTMA flare occurred after delivery despite use of preventive plasma infusions. Kidney graft function could be rescued in this patient by ECU. As such, successful pregnancies can be accomplished in kidney transplant recipients (KTRs) with a history of cTMA. We used preemptive plasma therapy or ongoing ECU treatment in selected cases. CONCLUSIONS: Thus, becoming pregnant can be encouraged in KTRs with native kidney cTMA. Extensive preconception counselling, however, is mandatory in such cases.
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spelling pubmed-80232172021-04-09 Pregnancies in kidney transplant recipients with complement gene variant-mediated thrombotic microangiopathy Haninger-Vacariu, Natalja Aigner, Christof Gaggl, Martina Kain, Renate Prohászka, Zoltán Böhmig, Georg A Sunder-Plassmann, Raute Sunder-Plassmann, Gere Schmidt, Alice Clin Kidney J Original Articles BACKGROUND: Pregnancies in patients with complement gene variant-mediated thrombotic microangiopathy (cTMA) are challenging, and pregnancies in such patients after kidney transplantation (KTX) are even more so. METHODS: We identified nine pregnancies following KTX of three genetically high-risk cTMA patients enrolled in the Vienna thrombotic microangiopathy cohort. Preventive plasma therapy was used in three pregnancies, and one patient had ongoing eculizumab (ECU) therapy during two pregnancies. RESULTS: Seven out of nine pregnancies (78%) resulted in the delivery of healthy children. The other two included one early abortion at gestational Week 12 during ongoing ECU therapy and one late foetal death at gestational Week 33 + 3, most likely not related to complement dysregulation. Kidney transplant function after delivery remained stable in all but one pregnancy. In the aforementioned case, a severe cTMA flare occurred after delivery despite use of preventive plasma infusions. Kidney graft function could be rescued in this patient by ECU. As such, successful pregnancies can be accomplished in kidney transplant recipients (KTRs) with a history of cTMA. We used preemptive plasma therapy or ongoing ECU treatment in selected cases. CONCLUSIONS: Thus, becoming pregnant can be encouraged in KTRs with native kidney cTMA. Extensive preconception counselling, however, is mandatory in such cases. Oxford University Press 2020-08-20 /pmc/articles/PMC8023217/ /pubmed/33841869 http://dx.doi.org/10.1093/ckj/sfaa113 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of ERA-EDTA. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Articles
Haninger-Vacariu, Natalja
Aigner, Christof
Gaggl, Martina
Kain, Renate
Prohászka, Zoltán
Böhmig, Georg A
Sunder-Plassmann, Raute
Sunder-Plassmann, Gere
Schmidt, Alice
Pregnancies in kidney transplant recipients with complement gene variant-mediated thrombotic microangiopathy
title Pregnancies in kidney transplant recipients with complement gene variant-mediated thrombotic microangiopathy
title_full Pregnancies in kidney transplant recipients with complement gene variant-mediated thrombotic microangiopathy
title_fullStr Pregnancies in kidney transplant recipients with complement gene variant-mediated thrombotic microangiopathy
title_full_unstemmed Pregnancies in kidney transplant recipients with complement gene variant-mediated thrombotic microangiopathy
title_short Pregnancies in kidney transplant recipients with complement gene variant-mediated thrombotic microangiopathy
title_sort pregnancies in kidney transplant recipients with complement gene variant-mediated thrombotic microangiopathy
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8023217/
https://www.ncbi.nlm.nih.gov/pubmed/33841869
http://dx.doi.org/10.1093/ckj/sfaa113
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