儿童急性淋巴细胞白血病诱导化疗期间临床缓解时间和外周血计数恢复情况

Q4 Medicine
Mst Arafatara Khatun, C. Jamal, A. A. Rahman, M. Karim, Farzana Alam Mou, Sabina Karim
{"title":"儿童急性淋巴细胞白血病诱导化疗期间临床缓解时间和外周血计数恢复情况","authors":"Mst Arafatara Khatun, C. Jamal, A. A. Rahman, M. Karim, Farzana Alam Mou, Sabina Karim","doi":"10.3329/bmrcb.v49i3.67959","DOIUrl":null,"url":null,"abstract":"Background: Acute lymphoblastic leukemia(ALL) is the most common pediatric malignancy. Infection and bleeding are the leading cause of death during induction chemotherapy in childhood ALL. So, proper knowledge about anticipated infection and bleeding are very important during this period. But the duration of clinical remission and recovery of peripheral blood count during induction chemotherapy is not well reported in literature.\nObjective: The aim of the study was to determine the time of attainment of clinical remission and recovery of peripheral blood count after initiation of induction chemotherapy and to determine if the duration of clinical remission and peripheral blood count recovery differs between therapeutic risk groups.\n Methods: This prospective observational study was conducted from January 2021 to December 2021 in the Department of Paediatric Haematology and Oncology, BSMMU. Newly diagnosed admitted Eighty-Six ALL of both sexes aged 1 to 17.9 years were included. After commencing chemotherapy, physical examination was recorded every day until clinical remission and complete blood count (CBC) was recorded one to two days interval until peripheral blood count recovery. The number of  packed red blood cell (PRBC) and platelet transfusions and the number of days of  intravenous antibiotics were recorded.\nResults: Mean duration of clinical remission, complete Hemoglobin (Hb), Absolute neutrophil count(ANC) and platelet recovery was 8.4 ± 4.5 days, 25±7.9 days, 23.3±5.6 days and 21.8±6.4 days respectively (p<0.01). Time to attain partial recovery of platelet was 14.0±4.9 days in high risk and 19.2±5.3 days in standard risk group. PRBC transfusion requirement was 2.2±1.2 units in high risk group and  1.7±0.8 units  in standard risk group (p<0.05). Time to attain partial recovery of ANC, number of days with I/V antibiotics and duration of treatment interruption were higher in high risk group.\n Conclusion: Time of clinical remission was similar between risk group. Platelet recovery occurred earlier than Hemoglobin (Hb) and absolute neutrophil count (ANC) recovery. Transfusion and supportive care requirement were more in high risk group during induction chemotherapy. So, more supportive care should be arranged up to three weeks of induction period to increase survival of high risk childhood ALL.\nBangladesh Med Res Counc Bull 2023; 49: 177-182","PeriodicalId":8704,"journal":{"name":"Bangladesh Medical Research Council Bulletin","volume":"64 s295","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Time of Attainment of Clinical Remission and Peripheral Blood Count Recovery during Induction Chemotherapy for Childhood Acute Lymphoblastic Leukemia\",\"authors\":\"Mst Arafatara Khatun, C. Jamal, A. A. Rahman, M. Karim, Farzana Alam Mou, Sabina Karim\",\"doi\":\"10.3329/bmrcb.v49i3.67959\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Acute lymphoblastic leukemia(ALL) is the most common pediatric malignancy. Infection and bleeding are the leading cause of death during induction chemotherapy in childhood ALL. So, proper knowledge about anticipated infection and bleeding are very important during this period. But the duration of clinical remission and recovery of peripheral blood count during induction chemotherapy is not well reported in literature.\\nObjective: The aim of the study was to determine the time of attainment of clinical remission and recovery of peripheral blood count after initiation of induction chemotherapy and to determine if the duration of clinical remission and peripheral blood count recovery differs between therapeutic risk groups.\\n Methods: This prospective observational study was conducted from January 2021 to December 2021 in the Department of Paediatric Haematology and Oncology, BSMMU. Newly diagnosed admitted Eighty-Six ALL of both sexes aged 1 to 17.9 years were included. After commencing chemotherapy, physical examination was recorded every day until clinical remission and complete blood count (CBC) was recorded one to two days interval until peripheral blood count recovery. The number of  packed red blood cell (PRBC) and platelet transfusions and the number of days of  intravenous antibiotics were recorded.\\nResults: Mean duration of clinical remission, complete Hemoglobin (Hb), Absolute neutrophil count(ANC) and platelet recovery was 8.4 ± 4.5 days, 25±7.9 days, 23.3±5.6 days and 21.8±6.4 days respectively (p<0.01). Time to attain partial recovery of platelet was 14.0±4.9 days in high risk and 19.2±5.3 days in standard risk group. PRBC transfusion requirement was 2.2±1.2 units in high risk group and  1.7±0.8 units  in standard risk group (p<0.05). Time to attain partial recovery of ANC, number of days with I/V antibiotics and duration of treatment interruption were higher in high risk group.\\n Conclusion: Time of clinical remission was similar between risk group. Platelet recovery occurred earlier than Hemoglobin (Hb) and absolute neutrophil count (ANC) recovery. Transfusion and supportive care requirement were more in high risk group during induction chemotherapy. So, more supportive care should be arranged up to three weeks of induction period to increase survival of high risk childhood ALL.\\nBangladesh Med Res Counc Bull 2023; 49: 177-182\",\"PeriodicalId\":8704,\"journal\":{\"name\":\"Bangladesh Medical Research Council Bulletin\",\"volume\":\"64 s295\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bangladesh Medical Research Council Bulletin\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3329/bmrcb.v49i3.67959\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bangladesh Medical Research Council Bulletin","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3329/bmrcb.v49i3.67959","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

摘要

背景:急性淋巴细胞白血病(Acute lymphoblastic leukemia, ALL)是儿童最常见的恶性肿瘤。感染和出血是儿童ALL诱导化疗期间死亡的主要原因。因此,在此期间,正确了解可能发生的感染和出血是非常重要的。但诱导化疗期间临床缓解的持续时间和外周血计数的恢复,文献报道较少。目的:本研究的目的是确定诱导化疗开始后临床缓解和外周血计数恢复的时间,并确定临床缓解和外周血计数恢复的持续时间在治疗风险组之间是否存在差异。方法:这项前瞻性观察性研究于2021年1月至2021年12月在BSMMU儿科血液学和肿瘤科进行。新诊断入院86例,年龄1 ~ 17.9岁,男女均有。化疗开始后,每天进行体检直至临床缓解,每隔1 ~ 2天记录全血细胞计数(CBC),直至外周血计数恢复。记录红细胞和血小板输注次数及静脉注射抗生素天数。结果:临床缓解、全血红蛋白(Hb)、绝对中性粒细胞计数(ANC)和血小板恢复的平均时间分别为8.4±4.5 d、25±7.9 d、23.3±5.6 d和21.8±6.4 d (p<0.01)。血小板部分恢复时间:高危组14.0±4.9 d,标准危组19.2±5.3 d。高危组PRBC需要量为2.2±1.2单位,标准危险组为1.7±0.8单位(p<0.05)。高危组ANC达到部分恢复的时间、I/V抗生素使用天数和治疗中断时间更长。结论:两组患者临床缓解时间相近。血小板恢复早于血红蛋白(Hb)和绝对中性粒细胞计数(ANC)恢复。高危组诱导化疗期间输血及支持护理需求较多。因此,更多的支持性护理应安排在长达三周的诱导期,以提高高危儿童ALL的生存率。孟加拉国医疗理事会2023年公报;49: 177 - 182
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Time of Attainment of Clinical Remission and Peripheral Blood Count Recovery during Induction Chemotherapy for Childhood Acute Lymphoblastic Leukemia
Background: Acute lymphoblastic leukemia(ALL) is the most common pediatric malignancy. Infection and bleeding are the leading cause of death during induction chemotherapy in childhood ALL. So, proper knowledge about anticipated infection and bleeding are very important during this period. But the duration of clinical remission and recovery of peripheral blood count during induction chemotherapy is not well reported in literature. Objective: The aim of the study was to determine the time of attainment of clinical remission and recovery of peripheral blood count after initiation of induction chemotherapy and to determine if the duration of clinical remission and peripheral blood count recovery differs between therapeutic risk groups.  Methods: This prospective observational study was conducted from January 2021 to December 2021 in the Department of Paediatric Haematology and Oncology, BSMMU. Newly diagnosed admitted Eighty-Six ALL of both sexes aged 1 to 17.9 years were included. After commencing chemotherapy, physical examination was recorded every day until clinical remission and complete blood count (CBC) was recorded one to two days interval until peripheral blood count recovery. The number of  packed red blood cell (PRBC) and platelet transfusions and the number of days of  intravenous antibiotics were recorded. Results: Mean duration of clinical remission, complete Hemoglobin (Hb), Absolute neutrophil count(ANC) and platelet recovery was 8.4 ± 4.5 days, 25±7.9 days, 23.3±5.6 days and 21.8±6.4 days respectively (p<0.01). Time to attain partial recovery of platelet was 14.0±4.9 days in high risk and 19.2±5.3 days in standard risk group. PRBC transfusion requirement was 2.2±1.2 units in high risk group and  1.7±0.8 units  in standard risk group (p<0.05). Time to attain partial recovery of ANC, number of days with I/V antibiotics and duration of treatment interruption were higher in high risk group.  Conclusion: Time of clinical remission was similar between risk group. Platelet recovery occurred earlier than Hemoglobin (Hb) and absolute neutrophil count (ANC) recovery. Transfusion and supportive care requirement were more in high risk group during induction chemotherapy. So, more supportive care should be arranged up to three weeks of induction period to increase survival of high risk childhood ALL. Bangladesh Med Res Counc Bull 2023; 49: 177-182
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
0.30
自引率
0.00%
发文量
48
期刊介绍: The official publication of the Bangladesh Medical Research Council.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信