Muhammad Matloob Alam , Mohamed Bayoumy , Areej Ali , Muayad Alali , Bayanah Al-enezi , Ibraheem Abosoudah
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Majority of patients had hematological disorder/malignancy (<em>n</em> <!-->=<!--> <span>101; 77%) followed by solid tumors (</span><em>n</em> <!-->=<!--> <!-->30; 23%). Most of them received allogeneic transplant (<em>n</em> <!-->=<!--> <!-->92; 70.2%). CMV reactivation was observed in 38 (29%) patients; out of them, only (<em>n</em> <!-->=<!--> <!-->3; 2.3%) had clinical manifestation/organ involvement and most cases of CMV were resolved (<em>n</em> <!-->=<!--> <span><span>35; 26.7%). Benign hematological disorder, conditioning regimen containing ATG, allogeneic BMT, graft-versus-host disease (GVHD) prophylaxis used and development of GVHD were identifiable risk factors in all patients, and </span>lymphopenia <300/mm</span><sup>3</sup> (<em>p</em> <!-->=<!--> <!-->0.047) was the only identifiable risk factors in allogeneic BMT patients associated with development CMV reactivation. Patients, who had CMV reactivation had significantly higher rate of GVHD (31.6% vs 15.1%; <em>p</em> <!-->=<!--> <span>0.031), however relapse rate (21% vs 25.8%) and mortality rate (22.5% vs 33.3%) in patients with CMV reactivation vs no CMV reactivation respectively were not statistically significant. Overall survival and event free survival of patients with and without CMV antigenemia were also comparable.</span></p></div><div><h3>Conclusions</h3><p>Antigenemia-guided pre-emptive strategy with ganciclovir<span> was very affective and CMV reactivation tended not to affect the outcome in our study cohort.</span></p></div>","PeriodicalId":19984,"journal":{"name":"Pediatric Infectious Disease","volume":"8 1","pages":"Pages 1-7"},"PeriodicalIF":0.0000,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.pid.2016.03.004","citationCount":"2","resultStr":"{\"title\":\"Cytomegalovirus infection in children after bone marrow transplantation: Risk factors, clinical aspects and outcomes\",\"authors\":\"Muhammad Matloob Alam , Mohamed Bayoumy , Areej Ali , Muayad Alali , Bayanah Al-enezi , Ibraheem Abosoudah\",\"doi\":\"10.1016/j.pid.2016.03.004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background and objectives</h3><p><span>Cytomegalovirus (CMV) infection remains the most common and potentially severe viral complication in patients<span> given hematopoietic stem cell transplantation. The aim of this study was to determine the incidence, risk factors and outcomes of </span></span>CMV<span> infection in pediatric BMT unit.</span></p></div><div><h3>Material and methods</h3><p>This study was a retrospective analysis of clinical, laboratory and outcome data of 131 pediatric patients who underwent BMT.</p></div><div><h3>Results</h3><p>The mean age of the study population was 6.5<!--> <!-->±<!--> <!-->4 years. Out of 131 pediatric patients, 85 were males (64.9%). Majority of patients had hematological disorder/malignancy (<em>n</em> <!-->=<!--> <span>101; 77%) followed by solid tumors (</span><em>n</em> <!-->=<!--> <!-->30; 23%). Most of them received allogeneic transplant (<em>n</em> <!-->=<!--> <!-->92; 70.2%). CMV reactivation was observed in 38 (29%) patients; out of them, only (<em>n</em> <!-->=<!--> <!-->3; 2.3%) had clinical manifestation/organ involvement and most cases of CMV were resolved (<em>n</em> <!-->=<!--> <span><span>35; 26.7%). Benign hematological disorder, conditioning regimen containing ATG, allogeneic BMT, graft-versus-host disease (GVHD) prophylaxis used and development of GVHD were identifiable risk factors in all patients, and </span>lymphopenia <300/mm</span><sup>3</sup> (<em>p</em> <!-->=<!--> <!-->0.047) was the only identifiable risk factors in allogeneic BMT patients associated with development CMV reactivation. Patients, who had CMV reactivation had significantly higher rate of GVHD (31.6% vs 15.1%; <em>p</em> <!-->=<!--> <span>0.031), however relapse rate (21% vs 25.8%) and mortality rate (22.5% vs 33.3%) in patients with CMV reactivation vs no CMV reactivation respectively were not statistically significant. 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引用次数: 2
摘要
背景与目的巨细胞病毒(CMV)感染仍然是造血干细胞移植患者中最常见和潜在严重的病毒并发症。本研究的目的是确定CMV感染在儿科BMT单元的发生率、危险因素和结局。材料和方法本研究回顾性分析了131例行BMT的儿科患者的临床、实验室和结局资料。结果研究人群平均年龄为6.5±4岁。131例儿童患者中,男性85例(64.9%)。大多数患者有血液系统疾病/恶性肿瘤(n = 101;77%),其次是实体瘤(n = 30;23%)。大多数患者接受同种异体移植(n = 92;70.2%)。38例(29%)患者观察到巨细胞病毒再激活;其中,只有(n = 3;2.3%)有临床表现/器官受累,大多数CMV病例得到解决(n = 35;26.7%)。良性血液学疾病、含ATG的调节方案、同种异体BMT、移植物抗宿主病(GVHD)预防措施的使用和GVHD的发展是所有患者可识别的危险因素,淋巴细胞减少<300/mm3 (p = 0.047)是同种异体BMT患者中与CMV再激活相关的唯一可识别的危险因素。CMV再激活患者的GVHD发生率显著高于CMV再激活患者(31.6% vs 15.1%;p = 0.031),但CMV再激活与未CMV再激活患者的复发率(21% vs 25.8%)和死亡率(22.5% vs 33.3%)分别无统计学意义。CMV抗原血症患者和非CMV抗原血症患者的总生存期和无事件生存期也具有可比性。结论在我们的研究队列中,更昔洛韦指导下的更昔洛韦先发制人策略非常有效,CMV再激活倾向于不影响结果。
Cytomegalovirus infection in children after bone marrow transplantation: Risk factors, clinical aspects and outcomes
Background and objectives
Cytomegalovirus (CMV) infection remains the most common and potentially severe viral complication in patients given hematopoietic stem cell transplantation. The aim of this study was to determine the incidence, risk factors and outcomes of CMV infection in pediatric BMT unit.
Material and methods
This study was a retrospective analysis of clinical, laboratory and outcome data of 131 pediatric patients who underwent BMT.
Results
The mean age of the study population was 6.5 ± 4 years. Out of 131 pediatric patients, 85 were males (64.9%). Majority of patients had hematological disorder/malignancy (n = 101; 77%) followed by solid tumors (n = 30; 23%). Most of them received allogeneic transplant (n = 92; 70.2%). CMV reactivation was observed in 38 (29%) patients; out of them, only (n = 3; 2.3%) had clinical manifestation/organ involvement and most cases of CMV were resolved (n = 35; 26.7%). Benign hematological disorder, conditioning regimen containing ATG, allogeneic BMT, graft-versus-host disease (GVHD) prophylaxis used and development of GVHD were identifiable risk factors in all patients, and lymphopenia <300/mm3 (p = 0.047) was the only identifiable risk factors in allogeneic BMT patients associated with development CMV reactivation. Patients, who had CMV reactivation had significantly higher rate of GVHD (31.6% vs 15.1%; p = 0.031), however relapse rate (21% vs 25.8%) and mortality rate (22.5% vs 33.3%) in patients with CMV reactivation vs no CMV reactivation respectively were not statistically significant. Overall survival and event free survival of patients with and without CMV antigenemia were also comparable.
Conclusions
Antigenemia-guided pre-emptive strategy with ganciclovir was very affective and CMV reactivation tended not to affect the outcome in our study cohort.