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Clinical features of women with thrombotic microangiopathy in pregnancy: A case series from a single Japanese tertiary perinatal care center

Aim Although perinatal thrombotic microangiopathy has become increasingly understood, the racial characteristics of patients with this condition remain unclear. Herein, we report the characteristics of patients with perinatal thrombotic microangiopathy at a single institution in Japan. Methods We co...

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Published in:The journal of obstetrics and gynaecology research 2023-12, Vol.49 (12), p.2804-2810
Main Authors: Nagaoka, Kanako, Kaneko, Kayoko, Miyagawa, Eiko, Abe, Sawako, Kohno, Chie, Tsurane, Kotoyi, Mito, Asako, Ozawa, Nobuaki, Sago, Haruhiko, Arata, Naoko, Murashima, Atsuko
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container_end_page 2810
container_issue 12
container_start_page 2804
container_title The journal of obstetrics and gynaecology research
container_volume 49
creator Nagaoka, Kanako
Kaneko, Kayoko
Miyagawa, Eiko
Abe, Sawako
Kohno, Chie
Tsurane, Kotoyi
Mito, Asako
Ozawa, Nobuaki
Sago, Haruhiko
Arata, Naoko
Murashima, Atsuko
description Aim Although perinatal thrombotic microangiopathy has become increasingly understood, the racial characteristics of patients with this condition remain unclear. Herein, we report the characteristics of patients with perinatal thrombotic microangiopathy at a single institution in Japan. Methods We conducted a retrospective study over a 5‐year period from January 1, 2017, to December 31, 2021, using the electronic medical records of pregnant women who delivered at the perinatal center of our hospital. We extracted the data of those who developed perinatal thrombotic microangiopathy and evaluated their characteristics at the time of disease onset, final diagnosis, and maternal and fetal outcomes. Results Of the 10 224 deliveries that occurred during the 5‐year period, only seven patients (0.06%) had perinatal thrombotic microangiopathy. The median pre‐pregnant body mass index was 18.65 kg/m2 (minimum 17.3 kg/m2, maximum 20.7 kg/m2). More than half of the patients were conceived by in‐vitro fertilization, and 42% these had twin deliveries. Four patients had a history of rheumatic disease. The other three patients without underlying diseases developed thrombotic microangiopathy with HELLP syndrome, and one patient transitioned to atypical hemolytic uremic syndrome. Conclusions Based on low body mass index and in‐vitro fertilization, which are characteristic of Japanese women, medical complications and twin pregnancies may be a risk for thrombotic microangiopathy. Additionally, depending on the cause of thrombotic microangiopathy, its timing and onset differed.
doi_str_mv 10.1111/jog.15790
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Herein, we report the characteristics of patients with perinatal thrombotic microangiopathy at a single institution in Japan. Methods We conducted a retrospective study over a 5‐year period from January 1, 2017, to December 31, 2021, using the electronic medical records of pregnant women who delivered at the perinatal center of our hospital. We extracted the data of those who developed perinatal thrombotic microangiopathy and evaluated their characteristics at the time of disease onset, final diagnosis, and maternal and fetal outcomes. Results Of the 10 224 deliveries that occurred during the 5‐year period, only seven patients (0.06%) had perinatal thrombotic microangiopathy. The median pre‐pregnant body mass index was 18.65 kg/m2 (minimum 17.3 kg/m2, maximum 20.7 kg/m2). More than half of the patients were conceived by in‐vitro fertilization, and 42% these had twin deliveries. Four patients had a history of rheumatic disease. The other three patients without underlying diseases developed thrombotic microangiopathy with HELLP syndrome, and one patient transitioned to atypical hemolytic uremic syndrome. Conclusions Based on low body mass index and in‐vitro fertilization, which are characteristic of Japanese women, medical complications and twin pregnancies may be a risk for thrombotic microangiopathy. Additionally, depending on the cause of thrombotic microangiopathy, its timing and onset differed.</description><identifier>ISSN: 1341-8076</identifier><identifier>EISSN: 1447-0756</identifier><identifier>DOI: 10.1111/jog.15790</identifier><language>eng</language><publisher>Kyoto, Japan: John Wiley &amp; Sons Australia, Ltd</publisher><subject>antiphospholipid syndrome ; Body mass index ; Electronic medical records ; Fertilization ; Fetuses ; Hemolytic uremic syndrome ; hypertension ; Patients ; pregnancy ; Pregnancy complications ; systemic lupus erythematosus ; thrombotic microangiopathies ; Thrombotic microangiopathy ; Womens health</subject><ispartof>The journal of obstetrics and gynaecology research, 2023-12, Vol.49 (12), p.2804-2810</ispartof><rights>2023 Japan Society of Obstetrics and Gynecology.</rights><rights>2023 Japan Society of Obstetrics and Gynecology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3250-72ef28e29cdaf32126811b0d4cf5344354c41c039bfd081929634eee155bfb6d3</cites><orcidid>0000-0002-1748-1635 ; 0000-0003-3411-5896</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Nagaoka, Kanako</creatorcontrib><creatorcontrib>Kaneko, Kayoko</creatorcontrib><creatorcontrib>Miyagawa, Eiko</creatorcontrib><creatorcontrib>Abe, Sawako</creatorcontrib><creatorcontrib>Kohno, Chie</creatorcontrib><creatorcontrib>Tsurane, Kotoyi</creatorcontrib><creatorcontrib>Mito, Asako</creatorcontrib><creatorcontrib>Ozawa, Nobuaki</creatorcontrib><creatorcontrib>Sago, Haruhiko</creatorcontrib><creatorcontrib>Arata, Naoko</creatorcontrib><creatorcontrib>Murashima, Atsuko</creatorcontrib><title>Clinical features of women with thrombotic microangiopathy in pregnancy: A case series from a single Japanese tertiary perinatal care center</title><title>The journal of obstetrics and gynaecology research</title><description>Aim Although perinatal thrombotic microangiopathy has become increasingly understood, the racial characteristics of patients with this condition remain unclear. Herein, we report the characteristics of patients with perinatal thrombotic microangiopathy at a single institution in Japan. Methods We conducted a retrospective study over a 5‐year period from January 1, 2017, to December 31, 2021, using the electronic medical records of pregnant women who delivered at the perinatal center of our hospital. We extracted the data of those who developed perinatal thrombotic microangiopathy and evaluated their characteristics at the time of disease onset, final diagnosis, and maternal and fetal outcomes. Results Of the 10 224 deliveries that occurred during the 5‐year period, only seven patients (0.06%) had perinatal thrombotic microangiopathy. The median pre‐pregnant body mass index was 18.65 kg/m2 (minimum 17.3 kg/m2, maximum 20.7 kg/m2). More than half of the patients were conceived by in‐vitro fertilization, and 42% these had twin deliveries. Four patients had a history of rheumatic disease. The other three patients without underlying diseases developed thrombotic microangiopathy with HELLP syndrome, and one patient transitioned to atypical hemolytic uremic syndrome. Conclusions Based on low body mass index and in‐vitro fertilization, which are characteristic of Japanese women, medical complications and twin pregnancies may be a risk for thrombotic microangiopathy. 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Herein, we report the characteristics of patients with perinatal thrombotic microangiopathy at a single institution in Japan. Methods We conducted a retrospective study over a 5‐year period from January 1, 2017, to December 31, 2021, using the electronic medical records of pregnant women who delivered at the perinatal center of our hospital. We extracted the data of those who developed perinatal thrombotic microangiopathy and evaluated their characteristics at the time of disease onset, final diagnosis, and maternal and fetal outcomes. Results Of the 10 224 deliveries that occurred during the 5‐year period, only seven patients (0.06%) had perinatal thrombotic microangiopathy. The median pre‐pregnant body mass index was 18.65 kg/m2 (minimum 17.3 kg/m2, maximum 20.7 kg/m2). More than half of the patients were conceived by in‐vitro fertilization, and 42% these had twin deliveries. Four patients had a history of rheumatic disease. The other three patients without underlying diseases developed thrombotic microangiopathy with HELLP syndrome, and one patient transitioned to atypical hemolytic uremic syndrome. Conclusions Based on low body mass index and in‐vitro fertilization, which are characteristic of Japanese women, medical complications and twin pregnancies may be a risk for thrombotic microangiopathy. Additionally, depending on the cause of thrombotic microangiopathy, its timing and onset differed.</abstract><cop>Kyoto, Japan</cop><pub>John Wiley &amp; Sons Australia, Ltd</pub><doi>10.1111/jog.15790</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-1748-1635</orcidid><orcidid>https://orcid.org/0000-0003-3411-5896</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1341-8076
ispartof The journal of obstetrics and gynaecology research, 2023-12, Vol.49 (12), p.2804-2810
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source Wiley-Blackwell Read & Publish Collection
subjects antiphospholipid syndrome
Body mass index
Electronic medical records
Fertilization
Fetuses
Hemolytic uremic syndrome
hypertension
Patients
pregnancy
Pregnancy complications
systemic lupus erythematosus
thrombotic microangiopathies
Thrombotic microangiopathy
Womens health
title Clinical features of women with thrombotic microangiopathy in pregnancy: A case series from a single Japanese tertiary perinatal care center
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