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儿童急性淋巴细胞白血病的死亡率模式:来自印度北部一个单一中心的经验。

Pattern of mortality in childhood acute lymphoblastic leukemia: experience from a single center in northern India.

作者信息

Marwaha Ram Kumar, Kulkarni Ketan Prasad, Bansal Deepak, Trehan Amita

机构信息

Division of Pediatric Hematology-Oncology, Department of Pediatrics, Advanced Pediatric Center, PGIMER, Chandigarh, India.

出版信息

J Pediatr Hematol Oncol. 2010 Jul;32(5):366-9. doi: 10.1097/MPH.0b013e3181e0d036.

Abstract

The outcome of acute lymphoblastic leukemia (ALL) in developing countries is inferior compared with the resource-rich nations. This descriptive study was designed to determine the pattern of deaths in children with ALL treated at a single center and identify the problem areas in management. Case records of 532 patients with ALL were analyzed. Information regarding the clinical-demographic profile, therapy, and course of illness were recorded. One hundred twenty-eight (24.0%) deaths were recorded. Sepsis (53.3%) and bleeding (15.7%) were the most common causes of mortality. The mortality rate fell significantly during the induction and remission phases of the therapy in 2 consecutive time periods between 1990 to 1997 and 1998 to 2006. The factors associated with an increased risk of death were longer symptom diagnosis interval (P=0.049), bulk disease (P=0.008), mediastinal adenopathy (P=0.001), higher total leukocyte count (P=0.001), and lower platelet count (P=0.007) at presentation as compared with the survivors. Multivariate analysis showed that longer symptom diagnosis interval (P=0.001), mediastinal adenopathy (P=0.006), lower platelet count (P=0.001), and higher total leukocyte count significantly influenced death. The estimated median time to death for the induction and remission deaths were 0.5 and 17 months, respectively. A high mortality rate necessitates the reappraisal of our treatment protocols. Many deaths should be avoidable by the provision of adequate supportive care, close supervision during and after chemotherapy, and appropriate antibiotic and antifungal therapy.

摘要

与资源丰富的国家相比,发展中国家急性淋巴细胞白血病(ALL)的治疗结果较差。本描述性研究旨在确定在单一中心接受治疗的ALL患儿的死亡模式,并找出管理中的问题领域。分析了532例ALL患者的病例记录。记录了有关临床人口统计学特征、治疗和病程的信息。记录了128例(24.0%)死亡病例。败血症(53.3%)和出血(15.7%)是最常见的死亡原因。在1990年至1997年以及1998年至2006年这两个连续时间段内,治疗的诱导期和缓解期死亡率显著下降。与幸存者相比,与死亡风险增加相关的因素包括症状诊断间隔时间较长(P=0.049)、肿块性疾病(P=0.008)、纵隔淋巴结肿大(P=0.001)、就诊时白细胞总数较高(P=0.001)以及血小板计数较低(P=0.007)。多变量分析显示,症状诊断间隔时间较长(P=0.001)、纵隔淋巴结肿大(P=0.006)、血小板计数较低(P=0.001)以及白细胞总数较高对死亡有显著影响。诱导期和缓解期死亡的估计中位死亡时间分别为0.5个月和17个月。高死亡率需要重新评估我们的治疗方案。通过提供充分的支持性护理、化疗期间及之后的密切监测以及适当的抗生素和抗真菌治疗,许多死亡是可以避免的。

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