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Nationwide survey of late‐onset hemolysis in very low birthweight infants
BACKGROUND: In Japan, some cases of late‐onset acute hemolysis in very low birthweight (VLBW) infants have been reported. These cases had common features but the cause of hemolysis was unknown. The incidence and prognosis of this disease are also unknown. However, there are only few reports of such...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986906/ https://www.ncbi.nlm.nih.gov/pubmed/33012035 http://dx.doi.org/10.1111/ped.14493 |
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author | Miyazono, Yayoi Arai, Junichi Kanai, Yu Hitaka, Daisuke Kajikawa, Daigo Takeuchi, Shusuke Nagafuji, Motomichi Fujiyama, Satoshi Saito, Makoto Takada, Hidetoshi |
author_facet | Miyazono, Yayoi Arai, Junichi Kanai, Yu Hitaka, Daisuke Kajikawa, Daigo Takeuchi, Shusuke Nagafuji, Motomichi Fujiyama, Satoshi Saito, Makoto Takada, Hidetoshi |
author_sort | Miyazono, Yayoi |
collection | PubMed |
description | BACKGROUND: In Japan, some cases of late‐onset acute hemolysis in very low birthweight (VLBW) infants have been reported. These cases had common features but the cause of hemolysis was unknown. The incidence and prognosis of this disease are also unknown. However, there are only few reports of such hemolytic episodes in countries other than Japan. Thus, this study aimed to examine the incidence and clinical course of late‐onset acute hemolysis and to establish it as a new disease concept. METHODS: A nationwide prospective survey was conducted from 2011 to 2015 as a rare disease surveillance project of the Japan Society for Neonatal Health and Development. RESULTS: Twenty‐four cases were confirmed. The median (range) gestational age, birthweight, and onset of hemolytic episodes were 26 weeks and 2 days (23 weeks and 4 days–31 weeks and 2 days), 898 g (627–1,416 g), and 19 days after birth (9–33 days), respectively. Phototherapy, blood transfusion, and exchange transfusion were required in 22 (96%), 24 (100%), and 7 (29%) cases, respectively. During the observation period, no recurrence of the hemolytic episode occurred. All patients survived; however, one case developed kernicterus and suffered severe neurological sequelae. CONCLUSIONS: In this study, at least 1 out of 1,259 VLBW infants developed hemolysis at 9–33 days after birth in Japan. Owing to the risk of kernicterus, this disease should be recognized as among the important pathological conditions of VLBW infants, suggesting the need to manage jaundice and anemia until 5 weeks after birth. |
format | Online Article Text |
id | pubmed-7986906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79869062021-03-25 Nationwide survey of late‐onset hemolysis in very low birthweight infants Miyazono, Yayoi Arai, Junichi Kanai, Yu Hitaka, Daisuke Kajikawa, Daigo Takeuchi, Shusuke Nagafuji, Motomichi Fujiyama, Satoshi Saito, Makoto Takada, Hidetoshi Pediatr Int Original Articles BACKGROUND: In Japan, some cases of late‐onset acute hemolysis in very low birthweight (VLBW) infants have been reported. These cases had common features but the cause of hemolysis was unknown. The incidence and prognosis of this disease are also unknown. However, there are only few reports of such hemolytic episodes in countries other than Japan. Thus, this study aimed to examine the incidence and clinical course of late‐onset acute hemolysis and to establish it as a new disease concept. METHODS: A nationwide prospective survey was conducted from 2011 to 2015 as a rare disease surveillance project of the Japan Society for Neonatal Health and Development. RESULTS: Twenty‐four cases were confirmed. The median (range) gestational age, birthweight, and onset of hemolytic episodes were 26 weeks and 2 days (23 weeks and 4 days–31 weeks and 2 days), 898 g (627–1,416 g), and 19 days after birth (9–33 days), respectively. Phototherapy, blood transfusion, and exchange transfusion were required in 22 (96%), 24 (100%), and 7 (29%) cases, respectively. During the observation period, no recurrence of the hemolytic episode occurred. All patients survived; however, one case developed kernicterus and suffered severe neurological sequelae. CONCLUSIONS: In this study, at least 1 out of 1,259 VLBW infants developed hemolysis at 9–33 days after birth in Japan. Owing to the risk of kernicterus, this disease should be recognized as among the important pathological conditions of VLBW infants, suggesting the need to manage jaundice and anemia until 5 weeks after birth. John Wiley and Sons Inc. 2021-02-06 2021-02 /pmc/articles/PMC7986906/ /pubmed/33012035 http://dx.doi.org/10.1111/ped.14493 Text en © 2020 The Authors. Pediatrics International published by John Wiley & Sons Australia, Ltd on behalf of Japan Pediatric Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Miyazono, Yayoi Arai, Junichi Kanai, Yu Hitaka, Daisuke Kajikawa, Daigo Takeuchi, Shusuke Nagafuji, Motomichi Fujiyama, Satoshi Saito, Makoto Takada, Hidetoshi Nationwide survey of late‐onset hemolysis in very low birthweight infants |
title | Nationwide survey of late‐onset hemolysis in very low birthweight infants |
title_full | Nationwide survey of late‐onset hemolysis in very low birthweight infants |
title_fullStr | Nationwide survey of late‐onset hemolysis in very low birthweight infants |
title_full_unstemmed | Nationwide survey of late‐onset hemolysis in very low birthweight infants |
title_short | Nationwide survey of late‐onset hemolysis in very low birthweight infants |
title_sort | nationwide survey of late‐onset hemolysis in very low birthweight infants |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986906/ https://www.ncbi.nlm.nih.gov/pubmed/33012035 http://dx.doi.org/10.1111/ped.14493 |
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