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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 |
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container_title | The journal of obstetrics and gynaecology research |
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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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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.</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 & 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. Additionally, depending on the cause of thrombotic microangiopathy, its timing and onset differed.</description><subject>antiphospholipid syndrome</subject><subject>Body mass index</subject><subject>Electronic medical records</subject><subject>Fertilization</subject><subject>Fetuses</subject><subject>Hemolytic uremic syndrome</subject><subject>hypertension</subject><subject>Patients</subject><subject>pregnancy</subject><subject>Pregnancy complications</subject><subject>systemic lupus erythematosus</subject><subject>thrombotic microangiopathies</subject><subject>Thrombotic microangiopathy</subject><subject>Womens health</subject><issn>1341-8076</issn><issn>1447-0756</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1kU1OwzAQhSMEEqWw4AaW2MAirZ04f-yqCgpVpW5gHTnuOHWV2MF2VfUOHJqBskLCG1t633sz44miW0YnDM90Z9sJy4qKnkUjxnkR0yLLz_GdchaXtMgvoyvvd5SyomLlKPqcd9poKTqiQIS9A0-sIgfbgyEHHbYkbJ3tGxu0JL2WzgrTajuIsD0SbcjgoDXCyOMjmREpPBAPTmOIQhcRxGvTdkCWYhAGUA3gghbuSAbEjAhYVwoHRIJB6Tq6UKLzcPN7j6P356e3-Uu8Wi9e57NVLNMko3GRgEpKSCq5ESpNWJKXjDV0w6XKUs7TjEvOJE2rRm1oyaqkylMOACzLGtXkm3Qc3Z9yB2c_9uBD3WsvoeuwSbv3dVLmLOe84iWid3_Qnd07g90hhblVmeUcqYcThR_kvQNVD073OGfNaP29F3S19c9ekJ2e2IPu4Pg_WC_Xi5PjCwjAkK8</recordid><startdate>202312</startdate><enddate>202312</enddate><creator>Nagaoka, Kanako</creator><creator>Kaneko, Kayoko</creator><creator>Miyagawa, Eiko</creator><creator>Abe, Sawako</creator><creator>Kohno, Chie</creator><creator>Tsurane, Kotoyi</creator><creator>Mito, Asako</creator><creator>Ozawa, Nobuaki</creator><creator>Sago, Haruhiko</creator><creator>Arata, Naoko</creator><creator>Murashima, Atsuko</creator><general>John Wiley & Sons Australia, Ltd</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TO</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1748-1635</orcidid><orcidid>https://orcid.org/0000-0003-3411-5896</orcidid></search><sort><creationdate>202312</creationdate><title>Clinical features of women with thrombotic microangiopathy in pregnancy: A case series from a single Japanese tertiary perinatal care center</title><author>Nagaoka, Kanako ; Kaneko, Kayoko ; Miyagawa, Eiko ; Abe, Sawako ; Kohno, Chie ; Tsurane, Kotoyi ; Mito, Asako ; Ozawa, Nobuaki ; Sago, Haruhiko ; Arata, Naoko ; Murashima, Atsuko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3250-72ef28e29cdaf32126811b0d4cf5344354c41c039bfd081929634eee155bfb6d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>antiphospholipid syndrome</topic><topic>Body mass index</topic><topic>Electronic medical records</topic><topic>Fertilization</topic><topic>Fetuses</topic><topic>Hemolytic uremic syndrome</topic><topic>hypertension</topic><topic>Patients</topic><topic>pregnancy</topic><topic>Pregnancy complications</topic><topic>systemic lupus erythematosus</topic><topic>thrombotic microangiopathies</topic><topic>Thrombotic microangiopathy</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>The journal of obstetrics and gynaecology research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nagaoka, Kanako</au><au>Kaneko, Kayoko</au><au>Miyagawa, Eiko</au><au>Abe, Sawako</au><au>Kohno, Chie</au><au>Tsurane, Kotoyi</au><au>Mito, Asako</au><au>Ozawa, Nobuaki</au><au>Sago, Haruhiko</au><au>Arata, Naoko</au><au>Murashima, Atsuko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical features of women with thrombotic microangiopathy in pregnancy: A case series from a single Japanese tertiary perinatal care center</atitle><jtitle>The journal of obstetrics and gynaecology research</jtitle><date>2023-12</date><risdate>2023</risdate><volume>49</volume><issue>12</issue><spage>2804</spage><epage>2810</epage><pages>2804-2810</pages><issn>1341-8076</issn><eissn>1447-0756</eissn><abstract>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.</abstract><cop>Kyoto, Japan</cop><pub>John Wiley & 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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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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