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镰状细胞病患儿的死亡率:一项人群研究。

Mortality of children with sickle cell disease: a population study.

机构信息

Núcleo de Ações e Pesquisa em Apoio Diagnóstico, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.

出版信息

J Pediatr (Rio J). 2010 Jul-Aug;86(4):279-84. doi: 10.2223/JPED.2005. Epub 2010 May 27.

Abstract

OBJECTIVE

To describe the deaths of children with sickle cell disease (SCD) in Minas Gerais, Brazil, and followed up at the Fundação Hemominas.

METHODS

Cohort of children diagnosed by the Neonatal Screening Program in Minas Gerais (March/1998 - February/2005). Deaths were identified by searching for children who did not attend scheduled consultations at hemocenters. Clinical and epidemiological data were abstracted from death certificates, the newborn screening database, individual medical records, and from interviews with families.

RESULTS

During the period, 1,833,030 newborns were screened; 1,396 had SCD (1:1,300). There were 78 deaths: 63 with SS genotype, 12 with SC genotype, and three with Sbeta+thalassemia genotype. Fifty-six children (71.8%) died before 2 years of age; 59 died in hospitals and 18 at home or during transportation. Causes of death according to certificates (n = 78): infections, 38.5%; acute splenic sequestration, 16.6%; other causes, 9%; did not receive medical care, 15.4%; and not identified on certificates, 20.5%. According to interviews (n = 52) acute splenic sequestration was responsible for one third of deaths, in contrast with 14% recorded on death certificates. Survival probabilities at 5y (SEM) for children with SS, SC, and Sbeta+thalassemia were 89.4 (1.4), 97.7 (0.7), and 94.7% (3.0), respectively (SS vs. SC, p < 0.0001).

CONCLUSIONS

Even with a carefully controlled newborn screening program, the probability of SS children dying was still found to be high. Causes not identified on death certificates may indicate difficulties recognizing SCD and its complications. Educational campaigns directed at health professionals and SCD patients' families should be boosted in order to decrease SCD mortality.

摘要

目的

描述巴西米纳斯吉拉斯州接受 Fundação Hemominas 随访的镰状细胞病(SCD)患儿的死亡情况。

方法

该队列纳入了米纳斯吉拉斯州新生儿筛查计划(1998 年 3 月至 2005 年 2 月)诊断为 SCD 的患儿。通过搜索未在血液中心预约定期就诊的患儿来确定死亡情况。从死亡证明、新生儿筛查数据库、个人病历和对家属的访谈中提取临床和流行病学数据。

结果

在此期间,共有 1833030 名新生儿接受了筛查;其中 1396 名患有 SCD(1:1300)。共有 78 例死亡:63 例为 SS 基因型,12 例为 SC 基因型,3 例为 Sβ+地中海贫血基因型。56 名儿童(71.8%)在 2 岁前死亡;59 名死于医院,18 名死于家中或在转运途中。根据死亡证明(n=78)的死因:感染,38.5%;急性脾梗塞,16.6%;其他原因,9%;未接受医疗护理,15.4%;死亡证明上未注明,20.5%。根据访谈(n=52),急性脾梗塞导致三分之一的患儿死亡,而死亡证明上仅记录了 14%。SS、SC 和 Sβ+地中海贫血基因型患儿的 5 年生存率(SEM)分别为 89.4(1.4)、97.7(0.7)和 94.7%(3.0)(SS 与 SC,p<0.0001)。

结论

即使有精心控制的新生儿筛查计划,SS 患儿的死亡率仍很高。死亡证明上未注明的死因可能表明难以识别 SCD 及其并发症。应加强针对卫生专业人员和 SCD 患儿家属的教育宣传活动,以降低 SCD 的死亡率。

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