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Successful Pregnancies During Ongoing Eculizumab Therapy in Two Patients With Complement-Mediated Thrombotic Microangiopathy

In patients with pregnancy-associated complement gene variant–mediated thrombotic microangiopathy (cTMA), terminal complement blockade is used for treatment of cTMA flares during pregnancy or following delivery. We report pregnancy and delivery outcomes of 2 genetically high-risk patients with cTMA,...

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Autores principales: Haninger-Vacariu, Natalja, Aigner, Christof, Kain, Renate, Prohászka, Zoltán, Gaggl, Martina, Böhmig, Georg A., Piggott, Leah Charlotte, Sunder-Plassmann, Raute, Sunder-Plassmann, Gere, Schmidt, Alice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7380370/
https://www.ncbi.nlm.nih.gov/pubmed/32734241
http://dx.doi.org/10.1016/j.xkme.2019.12.004
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author Haninger-Vacariu, Natalja
Aigner, Christof
Kain, Renate
Prohászka, Zoltán
Gaggl, Martina
Böhmig, Georg A.
Piggott, Leah Charlotte
Sunder-Plassmann, Raute
Sunder-Plassmann, Gere
Schmidt, Alice
author_facet Haninger-Vacariu, Natalja
Aigner, Christof
Kain, Renate
Prohászka, Zoltán
Gaggl, Martina
Böhmig, Georg A.
Piggott, Leah Charlotte
Sunder-Plassmann, Raute
Sunder-Plassmann, Gere
Schmidt, Alice
author_sort Haninger-Vacariu, Natalja
collection PubMed
description In patients with pregnancy-associated complement gene variant–mediated thrombotic microangiopathy (cTMA), terminal complement blockade is used for treatment of cTMA flares during pregnancy or following delivery. We report pregnancy and delivery outcomes of 2 genetically high-risk patients with cTMA, including 1 kidney transplant recipient, during ongoing eculizumab therapy. In both patients, the first manifestation of cTMA occurred independent from pregnancy. One patient has a history of 2 uneventful pregnancies with prophylactic plasma infusions, and the other has a history of early abortion during long-term eculizumab therapy following kidney transplantation. Overall, pregnancy and delivery outcomes under ongoing eculizumab therapy in our 2 patients with preserved kidney function were excellent as compared with other patients reported in the literature. Eculizumab plasma concentrations were maintained in the therapeutic range during pregnancy and were also detectable in cord blood. Results of cord blood analysis showed deficient complement activity, with low factor and regulator levels, most likely reflecting the age of the neonates and presence of eculizumab in cord blood. In conclusion, pregnancy during ongoing eculizumab treatment appeared to be safe in 2 women with a history of high-risk genetic cTMA and excellent kidney function, even following kidney transplantation.
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spelling pubmed-73803702020-07-29 Successful Pregnancies During Ongoing Eculizumab Therapy in Two Patients With Complement-Mediated Thrombotic Microangiopathy Haninger-Vacariu, Natalja Aigner, Christof Kain, Renate Prohászka, Zoltán Gaggl, Martina Böhmig, Georg A. Piggott, Leah Charlotte Sunder-Plassmann, Raute Sunder-Plassmann, Gere Schmidt, Alice Kidney Med Case Report In patients with pregnancy-associated complement gene variant–mediated thrombotic microangiopathy (cTMA), terminal complement blockade is used for treatment of cTMA flares during pregnancy or following delivery. We report pregnancy and delivery outcomes of 2 genetically high-risk patients with cTMA, including 1 kidney transplant recipient, during ongoing eculizumab therapy. In both patients, the first manifestation of cTMA occurred independent from pregnancy. One patient has a history of 2 uneventful pregnancies with prophylactic plasma infusions, and the other has a history of early abortion during long-term eculizumab therapy following kidney transplantation. Overall, pregnancy and delivery outcomes under ongoing eculizumab therapy in our 2 patients with preserved kidney function were excellent as compared with other patients reported in the literature. Eculizumab plasma concentrations were maintained in the therapeutic range during pregnancy and were also detectable in cord blood. Results of cord blood analysis showed deficient complement activity, with low factor and regulator levels, most likely reflecting the age of the neonates and presence of eculizumab in cord blood. In conclusion, pregnancy during ongoing eculizumab treatment appeared to be safe in 2 women with a history of high-risk genetic cTMA and excellent kidney function, even following kidney transplantation. Elsevier 2020-02-22 /pmc/articles/PMC7380370/ /pubmed/32734241 http://dx.doi.org/10.1016/j.xkme.2019.12.004 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Haninger-Vacariu, Natalja
Aigner, Christof
Kain, Renate
Prohászka, Zoltán
Gaggl, Martina
Böhmig, Georg A.
Piggott, Leah Charlotte
Sunder-Plassmann, Raute
Sunder-Plassmann, Gere
Schmidt, Alice
Successful Pregnancies During Ongoing Eculizumab Therapy in Two Patients With Complement-Mediated Thrombotic Microangiopathy
title Successful Pregnancies During Ongoing Eculizumab Therapy in Two Patients With Complement-Mediated Thrombotic Microangiopathy
title_full Successful Pregnancies During Ongoing Eculizumab Therapy in Two Patients With Complement-Mediated Thrombotic Microangiopathy
title_fullStr Successful Pregnancies During Ongoing Eculizumab Therapy in Two Patients With Complement-Mediated Thrombotic Microangiopathy
title_full_unstemmed Successful Pregnancies During Ongoing Eculizumab Therapy in Two Patients With Complement-Mediated Thrombotic Microangiopathy
title_short Successful Pregnancies During Ongoing Eculizumab Therapy in Two Patients With Complement-Mediated Thrombotic Microangiopathy
title_sort successful pregnancies during ongoing eculizumab therapy in two patients with complement-mediated thrombotic microangiopathy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7380370/
https://www.ncbi.nlm.nih.gov/pubmed/32734241
http://dx.doi.org/10.1016/j.xkme.2019.12.004
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