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资源有限环境下重症新生儿高胆红素血症的临床评估:尼日利亚东南部的一项4年纵向研究

Clinical evaluation of severe neonatal Hyperbilirubinaemia in a resource-limited setting: a 4-year longitudinal study in south-East Nigeria.

作者信息

Osuorah Chidiebere D I, Ekwochi Uchenna, Asinobi Isaac N

机构信息

Child Survival Unit, Medical Research Council UK, The Gambia Unit, Fajara, Banjul, Gambia.

Department of Paediatrics, Enugu State University of Science and Technology, Enugu, Enugu State, Nigeria.

出版信息

BMC Pediatr. 2018 Jun 23;18(1):202. doi: 10.1186/s12887-018-1174-z.

Abstract

BACKGROUND

Neonatal hyperbilirubinaemia is one of the commonest causes of hospital visit in the neonatal period. When severe, it is a leading cause of irreversible neurological and musculoskeletal disability. Prompt recognition and timely interventions are imperative for a drastic reduction in complications associated with severe hyperbilirubinaemia in newborns.

METHODS

We report a 4-year descriptive and longitudinal study to determine the causes, clinical presentations and long-term outcomes in newborns admitted for severe neonatal jaundice.

METHODS

Newborns admitted and managed for severe neonatal jaundice at the Enugu State University Teaching Hospital during a 4-year period were enrolled and followed up for 2 years.

RESULTS

A total of 1920 newborns were admitted during the study period and 48 were managed for severe hyperbilirubinaemia giving an in-hospital incidence rate of 25 (95% CI 18-32) per 1000 admitted newborns. The mean age of onset was 3.4 ± 0.5 days (range 1-8 days) and hospital presentation from time of first notice was 4.3 ± 0.4 days (range 1-9 days). The total and unconjugated admission serum bilirubin ranged from 7.1 to 71.1 (mean 26 ± 2.5 mg/dl) and 4.2 to 46.3 mg/dl (mean 18.3 ± 9.2) respectively. Earliest sign of severe hyperbilirubinaemia in newborns were: refusal to suck (15.2%) and depressed primitive reflexes (24.5%) while the commonest signs included high pitch cry (11.9%), convulsion and stiffness (6.9%) and vomiting (6.3%) in addition to the former signs. The major causes of severe hyperbilirubinaemia were idiopathic (33.3%), sepsis (35.3%), ABO incompatibility (17.6%) and glucose-6-phosphate dehydrogenase (G6PD) deficiency (11.8%). Long-term sequelae on follow-up included delayed developmental milestone attainment, postural deformities, visual and seizure disorders.

CONCLUSIONS

There is urgent need for continued education for mothers, families and healthcare workers on the danger newborns with jaundice could face if not brought early to the hospital for timely diagnosis and management.

摘要

背景

新生儿高胆红素血症是新生儿期最常见的就诊原因之一。严重时,它是不可逆的神经和肌肉骨骼残疾的主要原因。迅速识别和及时干预对于大幅减少与新生儿严重高胆红素血症相关的并发症至关重要。

方法

我们报告一项为期4年的描述性纵向研究,以确定因严重新生儿黄疸入院的新生儿的病因、临床表现和长期预后。

方法

对在4年期间于埃努古州立大学教学医院因严重新生儿黄疸入院并接受治疗的新生儿进行登记,并随访2年。

结果

研究期间共收治1920例新生儿,其中48例因严重高胆红素血症接受治疗,每1000例入院新生儿的院内发病率为25例(95%可信区间18 - 32)。发病的平均年龄为3.4±0.5天(范围1 - 8天),从首次发现到入院的时间为4.3±0.4天(范围1 - 9天)。入院时总血清胆红素和未结合胆红素范围分别为7.1至71.1(平均26±2.5mg/dl)和4.2至46.3mg/dl(平均18.3±9.2)。新生儿严重高胆红素血症最早的体征为:拒乳(15.2%)和原始反射减弱(24.5%),而最常见的体征除上述体征外还包括高音调哭声(11.9%)、惊厥和强直(6.9%)以及呕吐(6.3%)。严重高胆红素血症的主要病因是特发性(33.3%)、败血症(35.3%)、ABO血型不合(17.6%)和葡萄糖-6-磷酸脱氢酶(G6PD)缺乏(11.8%)。随访的长期后遗症包括发育里程碑延迟达成、姿势畸形、视觉和癫痫障碍。

结论

迫切需要对母亲、家庭和医护人员进行持续教育,使其了解黄疸新生儿若不及早送医进行及时诊断和治疗可能面临的危险。

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