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血小板和不成熟中性粒细胞与早产儿喂养不耐受。

Platelets and Immature Neutrophils in Preterm Infants with Feeding Intolerance.

机构信息

Division of Neonatology, Department of Pediatrics, Sidra Medicine, Doha, Qatar.

Department of Internal Medicine, Morsani College of Medicine, University of South Florida, Tampa, Florida.

出版信息

Am J Perinatol. 2021 Sep;38(11):1150-1157. doi: 10.1055/s-0040-1710555. Epub 2020 May 23.

Abstract

OBJECTIVE

Feeding intolerance (FI) is a common presentation of necrotizing enterocolitis (NEC) and sepsis. NEC and sepsis are associated with hematological changes, but these changes alone are not reliable biomarkers for early diagnosis. This study examined whether the combination of hematological indices and FI can be used as an early diagnostic tool for NEC or sepsis.

STUDY DESIGN

This retrospective cohort study included infants born at <1,500 g or <30 weeks who had symptoms of FI. The exclusion criteria were congenital or chromosomal disorders, thrombocytopenia or platelet transfusion before the onset of FI, and history of bowel resection. We compared the hematological indices from infants with pathologic FI (due to NEC or sepsis) to infants with benign FI.

RESULTS

During the study period, 211 infants developed FI; 185 met the inclusion criteria. Infants with pathologic FI ( = 90, 37 cases with NEC and 53 with sepsis) had lower birth gestational age and weight compared with 95 infants with benign FI ( = 95). Pathologic FI was associated with lower platelet count (median 152 × 10/μL vs. 285 × 10/μL,  < 0.001) and higher immature-to-total neutrophil (I/T) ratio (median 0.23 vs. 0.04,  < 0.001) at the onset of FI. Pathologic FI was also associated with a decrease in baseline platelets compared with an increase in benign FI. For diagnosis of pathologic FI, a decrease ≥10% in platelets from baseline had a sensitivity and specificity of 0.64 and 0.73, respectively, I/T ratio ≥0.1 had a sensitivity and specificity of 0.71 and 0.78, respectively, and the combination of both parameters had a sensitivity and specificity of 0.50 and 0.97, respectively.

CONCLUSION

FI caused by NEC or sepsis was associated with a decrease in platelets from baseline, and a lower platelet level and higher I/T ratio at the onset of FI. These findings can help clinicians in the management of preterm infants with FI.

KEY POINTS

· FI is a common presentation of NEC and sepsis in preterm infants.. · FI due to NEC or sepsis is associated with changes in platelets and I/T ratio.. · These changes could be useful as early markers for diagnosis..

摘要

目的

喂养不耐受(FI)是坏死性小肠结肠炎(NEC)和败血症的常见表现。NEC 和败血症与血液学变化有关,但这些变化本身并不能作为早期诊断的可靠生物标志物。本研究探讨了血液学指标与 FI 的联合应用是否可作为 NEC 或败血症的早期诊断工具。

研究设计

本回顾性队列研究纳入了出生体重<1500g 或<30 周且出现 FI 症状的婴儿。排除标准为先天性或染色体疾病、FI 发病前血小板减少或血小板输注、以及肠切除术病史。我们比较了有病理 FI(由 NEC 或败血症引起)和良性 FI 的婴儿的血液学指标。

结果

在研究期间,有 211 名婴儿出现 FI;185 名符合纳入标准。与 95 名良性 FI(95 例)相比,有病理 FI(90 例,37 例 NEC,53 例败血症)的婴儿出生胎龄和体重更小。病理 FI 与血小板计数降低(中位数 152×10/μL 比 285×10/μL,<0.001)和 FI 发病时未成熟中性粒细胞与总中性粒细胞(I/T)比值升高(中位数 0.23 比 0.04,<0.001)有关。与良性 FI 相比,病理 FI 还与基线血小板减少有关,而与血小板增加无关。对于病理 FI 的诊断,血小板从基线下降≥10%的敏感性和特异性分别为 0.64 和 0.73,I/T 比值≥0.1 的敏感性和特异性分别为 0.71 和 0.78,两者联合的敏感性和特异性分别为 0.50 和 0.97。

结论

NEC 或败血症引起的 FI 与基线血小板减少以及 FI 发病时较低的血小板水平和较高的 I/T 比值有关。这些发现有助于临床医生管理有 FI 的早产儿。

关键点

·FI 是早产儿 NEC 和败血症的常见表现。·NEC 或败血症引起的 FI 与血小板和 I/T 比值变化有关。·这些变化可能作为早期诊断标志物有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0fe/9536080/da8128002878/nihms-1837166-f0001.jpg

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