Follow-Up Duration of Echocardiography in Patients with Kawasaki Disease with No Initial Coronary Aneurysms

To evaluate the optimal duration of echocardiographic follow-up in patients with Kawasaki disease without an initial coronary aneurysm. In this single-center, retrospective, observational study, we reviewed the results of follow-up echocardiography in children with Kawasaki disease enrolled in the P...

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Veröffentlicht in:The Journal of pediatrics 2022-05, Vol.244, p.133-138.e1
Hauptverfasser: Wang, Qianzhi, Morikawa, Yoshihiko, Akahoshi, Shogo, Miyata, Koichi, Sakakibara, Hiroshi, Matsushima, Takahiro, Koyama, Yutaro, Obonai, Toshimasa, Kaneko, Tetsuji, Miura, Masaru
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container_end_page 138.e1
container_issue
container_start_page 133
container_title The Journal of pediatrics
container_volume 244
creator Wang, Qianzhi
Morikawa, Yoshihiko
Akahoshi, Shogo
Miyata, Koichi
Sakakibara, Hiroshi
Matsushima, Takahiro
Koyama, Yutaro
Obonai, Toshimasa
Kaneko, Tetsuji
Miura, Masaru
description To evaluate the optimal duration of echocardiographic follow-up in patients with Kawasaki disease without an initial coronary aneurysm. In this single-center, retrospective, observational study, we reviewed the results of follow-up echocardiography in children with Kawasaki disease enrolled in the Prospective Observational Study on Stratified Treatment with Immunoglobulin Plus Steroid Efficacy for Kawasaki Disease from a children's hospital. The main enrollment criterion was the absence of coronary aneurysms, defined as a maximum z-score (Zmax) ≥2.5, in the proximal right coronary artery and the proximal left anterior descending artery within 9 days from treatment initiation. The primary outcome was Zmax on follow-up echocardiography at up to 5 years. Among 386 patients, 106 (27.5%) received prednisolone with intravenous immunoglobulin for first-line therapy, and 57 (14.8%) showed a poor response. Echocardiography at 1 month detected 9 patients with a Zmax ≥2, including 3 (0.8%) with coronary aneurysms requiring additional antithrombotic treatment and observation. Of 7 patients (1.8%) with normal echocardiographic findings at 1 month but a Zmax ≥2 later, 2 were lost to follow-up and 5 experienced spontaneous resolution, but none of the 7 patients required any change in management. The optimal duration of echocardiographic follow-up may be 1 month in patients with no initial coronary aneurysms and a Zmax
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In this single-center, retrospective, observational study, we reviewed the results of follow-up echocardiography in children with Kawasaki disease enrolled in the Prospective Observational Study on Stratified Treatment with Immunoglobulin Plus Steroid Efficacy for Kawasaki Disease from a children's hospital. The main enrollment criterion was the absence of coronary aneurysms, defined as a maximum z-score (Zmax) ≥2.5, in the proximal right coronary artery and the proximal left anterior descending artery within 9 days from treatment initiation. The primary outcome was Zmax on follow-up echocardiography at up to 5 years. Among 386 patients, 106 (27.5%) received prednisolone with intravenous immunoglobulin for first-line therapy, and 57 (14.8%) showed a poor response. Echocardiography at 1 month detected 9 patients with a Zmax ≥2, including 3 (0.8%) with coronary aneurysms requiring additional antithrombotic treatment and observation. Of 7 patients (1.8%) with normal echocardiographic findings at 1 month but a Zmax ≥2 later, 2 were lost to follow-up and 5 experienced spontaneous resolution, but none of the 7 patients required any change in management. The optimal duration of echocardiographic follow-up may be 1 month in patients with no initial coronary aneurysms and a Zmax &lt;2 at 1 month. 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Of 7 patients (1.8%) with normal echocardiographic findings at 1 month but a Zmax ≥2 later, 2 were lost to follow-up and 5 experienced spontaneous resolution, but none of the 7 patients required any change in management. The optimal duration of echocardiographic follow-up may be 1 month in patients with no initial coronary aneurysms and a Zmax &lt;2 at 1 month. 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Morikawa, Yoshihiko ; Akahoshi, Shogo ; Miyata, Koichi ; Sakakibara, Hiroshi ; Matsushima, Takahiro ; Koyama, Yutaro ; Obonai, Toshimasa ; Kaneko, Tetsuji ; Miura, Masaru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-38c42801d68d38d59c19aa0a4ea7f59b69ce0597a4102c63afd792e4383eda593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>American Heart Association</topic><topic>Child</topic><topic>Coronary Aneurysm - diagnostic imaging</topic><topic>Coronary Aneurysm - etiology</topic><topic>coronary artery lesion</topic><topic>Coronary Vessels - diagnostic imaging</topic><topic>Echocardiography</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Immunoglobulins, Intravenous - therapeutic use</topic><topic>Infant</topic><topic>Mucocutaneous Lymph Node Syndrome - complications</topic><topic>Mucocutaneous Lymph Node Syndrome - diagnostic imaging</topic><topic>Mucocutaneous Lymph Node Syndrome - drug therapy</topic><topic>Retrospective Studies</topic><topic>z-score</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Qianzhi</creatorcontrib><creatorcontrib>Morikawa, Yoshihiko</creatorcontrib><creatorcontrib>Akahoshi, Shogo</creatorcontrib><creatorcontrib>Miyata, Koichi</creatorcontrib><creatorcontrib>Sakakibara, Hiroshi</creatorcontrib><creatorcontrib>Matsushima, Takahiro</creatorcontrib><creatorcontrib>Koyama, Yutaro</creatorcontrib><creatorcontrib>Obonai, Toshimasa</creatorcontrib><creatorcontrib>Kaneko, Tetsuji</creatorcontrib><creatorcontrib>Miura, Masaru</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of pediatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Qianzhi</au><au>Morikawa, Yoshihiko</au><au>Akahoshi, Shogo</au><au>Miyata, Koichi</au><au>Sakakibara, Hiroshi</au><au>Matsushima, Takahiro</au><au>Koyama, Yutaro</au><au>Obonai, Toshimasa</au><au>Kaneko, Tetsuji</au><au>Miura, Masaru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Follow-Up Duration of Echocardiography in Patients with Kawasaki Disease with No Initial Coronary Aneurysms</atitle><jtitle>The Journal of pediatrics</jtitle><addtitle>J Pediatr</addtitle><date>2022-05-01</date><risdate>2022</risdate><volume>244</volume><spage>133</spage><epage>138.e1</epage><pages>133-138.e1</pages><issn>0022-3476</issn><eissn>1097-6833</eissn><abstract>To evaluate the optimal duration of echocardiographic follow-up in patients with Kawasaki disease without an initial coronary aneurysm. 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subjects American Heart Association
Child
Coronary Aneurysm - diagnostic imaging
Coronary Aneurysm - etiology
coronary artery lesion
Coronary Vessels - diagnostic imaging
Echocardiography
Follow-Up Studies
Humans
Immunoglobulins, Intravenous - therapeutic use
Infant
Mucocutaneous Lymph Node Syndrome - complications
Mucocutaneous Lymph Node Syndrome - diagnostic imaging
Mucocutaneous Lymph Node Syndrome - drug therapy
Retrospective Studies
z-score
title Follow-Up Duration of Echocardiography in Patients with Kawasaki Disease with No Initial Coronary Aneurysms
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