Pediatric Department, Minia University, Al Minya, Egypt.
Radiology Department, Minia University, Al Minya, Egypt.
Ann Hematol. 2024 Nov;103(11):4749-4757. doi: 10.1007/s00277-024-06002-5. Epub 2024 Oct 1.
In neonates admitted to the neonatal intensive care unit (NICU), arterial and venous thromboembolism is a major cause of morbidity and death which could be attributed to multiple risk factors exposure. This study aimed to evaluate the clinical characteristics, laboratory and radiological assessments, predisposing risk factors, and outcomes of thrombosis in neonates admitted to NICU. This prospective cohort study was conducted at NICU, Minia, and Alexandria University Children's Hospital. Screening of 886 patients admitted to NICU over one year with different clinical presentations, patients were classified into the thrombotic and non-thrombotic groups based on the presence or absence of thrombosis. Thrombosis was diagnosed based on clinical, laboratory and different radiologic assessments. Genetic testing for factor V Leiden mutations G1691A, prothrombin mutation G20210A, protein C, protein S, and antithrombin III gene mutations were performed for patients with a family history of thrombosis. Out of a total of 886 neonatal admissions, 36 patients were diagnosed with evident thrombosis (40 per 1000 NICU admissions). The sites of venous thrombosis detection were Portal vein thrombosis in 11 patients (30.6%), superior vena cava thrombosis in 7 patients (19.4%), deep venous thrombosis in 5 patients (13.9%), central venous thrombosis in 5 patients (13.9%), intra-cardiac thrombosis in 3 patients (8.3%) and necrotic skin patches in one patient (2.8%). Only 69% of enrolled thrombosis patients showed genetic mutations the most common of which was factor V Leiden mutation (52.3%). Sepsis, central venous line (CVL) insertion, C reactive protein (CRP), and duration of NICU admission were significantly more common in the thrombotic group (p < 0.001) and were associated with a higher risk of thrombosis (ORs: 1.02, 7.7, and 1.11, respectively) (p < 0.001). Higher mortality occurred in thrombosis neonates compared with a non-thrombotic group (52.8% versus 17.4%) (p < 0.001). NICU-admitted neonates are exposed to multiple overlapped risk factors, the detection of which is important for preventing potential thrombosis and improving the patient's outcomes. The complexity of sepsis pathogenesis and management could potentiate multiple acquired risk factors. inherited thrombophilia detection is required for prevention of further morbidities.
在入住新生儿重症监护病房(NICU)的新生儿中,动静脉血栓栓塞是导致发病率和死亡率的主要原因,这可能归因于多种危险因素的暴露。本研究旨在评估入住 NICU 的新生儿血栓形成的临床特征、实验室和影像学评估、易患危险因素和结局。这项前瞻性队列研究在米尼亚的 NICU 和亚历山大大学儿童医院进行。对一年内因不同临床表现而入住 NICU 的 886 名患者进行筛查,根据是否存在血栓形成将患者分为血栓形成组和非血栓形成组。基于临床、实验室和不同影像学评估来诊断血栓形成。对有血栓形成家族史的患者进行因子 V 莱登突变 G1691A、凝血酶原突变 G20210A、蛋白 C、蛋白 S 和抗凝血酶 III 基因突变的基因检测。在总共 886 例新生儿入院中,36 例患者被诊断为明显血栓形成(40/1000 例 NICU 入院)。静脉血栓形成的部位有 11 例(30.6%)为门静脉血栓形成,7 例(19.4%)为上腔静脉血栓形成,5 例(13.9%)为深静脉血栓形成,5 例(13.9%)为中心静脉血栓形成,3 例(8.3%)为心脏内血栓形成,1 例(2.8%)为坏死皮肤斑块。仅 69%的入组血栓形成患者显示出基因突变,最常见的是因子 V 莱登突变(52.3%)。败血症、中央静脉导管(CVL)置入、C 反应蛋白(CRP)和 NICU 住院时间在血栓形成组中明显更为常见(p<0.001),与血栓形成风险增加相关(ORs:1.02、7.7 和 1.11,分别)(p<0.001)。与非血栓形成组相比,血栓形成的新生儿死亡率更高(52.8% 对 17.4%)(p<0.001)。入住 NICU 的新生儿易受多种重叠危险因素的影响,检测这些危险因素对预防潜在血栓形成和改善患者结局非常重要。败血症发病机制和治疗的复杂性可能会增加多种获得性危险因素。需要进行遗传性血栓形成易感性检测,以预防进一步的发病。