Bilgin K, Yaramiş A, Haspolat K, Taş M A, Günbey S, Derman O
Department of Pediatrics, Dicle Medical School, Diyarbakir, Turkey.
Pediatrics. 2001 Jan;107(1):36-41. doi: 10.1542/peds.107.1.36.
To determine whether adjunctive therapy with recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF) could reverse sepsis-associated neonatal neutropenia and improve neonatal survival and to assess its safety compared with conventional therapy in a control group.
This prospective, randomized, controlled trial was performed in 60 infants with neutropenia and clinical signs of sepsis. A subcutaneous injection of rhGM-CSF (5 microgram/kg/day) was administered to 30 of the patients for 7 consecutive days. Hematologic parameters (absolute neutrophil, eosinophil, monocyte, lymphocyte counts, and platelet number) and outcome were compared with 30 conventionally treated (control) patients.
Twenty-five patients from the GM-CSF-treated group and 24 from the conventionally treated group had early-onset sepsis (</=3 days' postnatal age), and the other 11 patients had late-onset sepsis (>3 days' postnatal age). There was no difference between groups in terms of birth weight; gestational age; gender; maturity; maternal age; and incidence of prolonged rupture of membranes, maternal hypertension, or severity of sepsis. All neonates tolerated GM-CSF well with no adverse reactions. The absolute neutrophil count on day 7 was significantly increased in the GM-CSF-treated group compared with the conventionally treated group: 8088 +/- 2822/mm(3) versus 2757 +/- 823/mm(3). The mean platelet count was significantly higher on days 14 in the GM-CSF-treated group compared with conventionally treated group: 266 867 +/- 55 102/mm(3) versus 229 200 +/- 52 317/mm(3). Hematologic parameters were otherwise similar between groups before treatment and on day 28. Twenty-seven neonates in the rh-GMCSF group and 21 in the control group survived to hospital discharge. The mortality rate in the rhGM-CSF group (10%) was significantly lower than in the conventionally treated group (30%).
Treatment with rhGM-CSF is associated with an increase in absolute neutrophil, eosinophil, monocyte, lymphocyte, and platelet counts and decreased mortality in critically ill septic neutropenic neonates. These results suggest that rhGM-CSF may be effective in the treatment of neonatal sepsis with neutropenia, and further randomized trials are needed to confirm its beneficial effects.
确定重组人粒细胞巨噬细胞集落刺激因子(rhGM-CSF)辅助治疗能否逆转脓毒症相关的新生儿中性粒细胞减少症并提高新生儿存活率,并与对照组的传统治疗方法相比评估其安全性。
这项前瞻性、随机、对照试验在60例患有中性粒细胞减少症且有脓毒症临床体征的婴儿中进行。30例患者连续7天皮下注射rhGM-CSF(5微克/千克/天)。将血液学参数(绝对中性粒细胞、嗜酸性粒细胞、单核细胞、淋巴细胞计数及血小板数量)和结果与30例接受传统治疗(对照)的患者进行比较。
GM-CSF治疗组的25例患者和传统治疗组的24例患者患有早发型脓毒症(出生后年龄≤3天),另外11例患者患有晚发型脓毒症(出生后年龄>3天)。两组在出生体重、胎龄、性别、成熟度、母亲年龄以及胎膜早破、母亲高血压发生率或脓毒症严重程度方面无差异。所有新生儿对GM-CSF耐受性良好,无不良反应。与传统治疗组相比,GM-CSF治疗组第7天的绝对中性粒细胞计数显著增加:8088±2822/立方毫米对2757±823/立方毫米。与传统治疗组相比,GM-CSF治疗组第14天的平均血小板计数显著更高:266867±55102/立方毫米对229200±52317/立方毫米。两组在治疗前和第28天的其他血液学参数相似。rh-GMCSF组的27例新生儿和对照组的21例新生儿存活至出院。rhGM-CSF组的死亡率(10%)显著低于传统治疗组(30%)。
rhGM-CSF治疗与绝对中性粒细胞、嗜酸性粒细胞、单核细胞、淋巴细胞和血小板计数增加以及重症脓毒症中性粒细胞减少新生儿死亡率降低相关。这些结果表明,rhGM-CSF可能对治疗伴有中性粒细胞减少症的新生儿脓毒症有效,需要进一步的随机试验来证实其有益效果。