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首页> 外文期刊>BMC Pediatrics >Clinical evaluation of severe neonatal Hyperbilirubinaemia in a resource-limited setting: a 4-year longitudinal study in south-East Nigeria
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Clinical evaluation of severe neonatal Hyperbilirubinaemia in a resource-limited setting: a 4-year longitudinal study in south-East Nigeria

机译:严重新生儿血红蛋白在资源有限的环境中的临床评价:东南尼日利亚的4年纵向研究

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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. 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. 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. 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. 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.
机译:新生儿高胆管血症是新生儿期间最常见的医院访问原因之一。当严重时,它是不可逆神经系统和肌肉骨骼残疾的主要原因。及时识别和及时干预均急剧减少与新生儿中严重的血红蛋白血症相关的并发症。我们报告了4年的描述性和纵向研究,以确定为严重新生儿批准的新生儿的原因,临床介绍和长期成果。新生儿在4年期间在伊古州立大学教学医院进行严重新生儿黄疸的新生儿被注册,并进行了2年。在研究期间共提供了1920年的新生儿,48例用于治疗严重的高胆管血症,每1000人入院的新生儿的医院发生率为25(95%CI 18-32)。起初的平均年龄是3.4?±0.5?0.5?天(范围1-8?天)和医院呈现从第一通知时的呈现为4.3?±0.4天(范围1-9?天)。总和未缀合的入院血清胆红素分别为7.1至71.1(平均26Ω·α≤2.5?mg / dl)和4.2至46.3×mg / dl(平均18.3?±9.2)。新生儿中严重的血红蛋白血症的最早标志是:拒绝吸吮(15.2%)和抑郁的原始反射(24.5%),而最常见的迹象包括高间距哭(11.9%),抽搐和僵硬(6.9%)和呕吐(6.3%)除了前一个标志。严重的高胆碱的主要原因是特发性(33.3%),败血症(35.3%),abo不相容(17.6%)和葡萄糖-6-磷酸脱氢酶(G6PD)缺乏(11.8%)。随访中的长期后遗症包括延迟发育里程碑达到,姿势畸形,视觉和癫痫发作。迫切需要对母亲,家庭和医疗保健工人继续教育,危险的新生儿与黄疸可能会面临,如果没有提前到医院,以便及时诊断和管理。

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