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首页> 外文期刊>The Journal of pediatrics >Patent ductus arteriosus, low platelets, cyclooxygenase inhibitors, and intraventricular hemorrhage in very low birth weight preterm infants
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Patent ductus arteriosus, low platelets, cyclooxygenase inhibitors, and intraventricular hemorrhage in very low birth weight preterm infants

机译:极低出生体重早产儿的动脉导管未闭,低血小板,环氧合酶抑制剂和脑室内出血

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Objective: To assess the risk for intraventricular hemorrhage (IVH) in very low birth weight preterm infants with patent ductus arteriosus (PDA) and low platelet count with treatment with cyclooxygenase (COX) inhibitors. Study design: Diagnosis and treatment of PDA, as well as risk factors for IVH, were assessed using prospectively collected data of all infants born at a gestational age 32 weeks and with a birth weight ≤1500 g at Innsbruck University Hospital (January 2003-December 2009). Infants with severe thrombocytopenia (50 × 109/L) were excluded from analysis. Results: Sixty-five (20%) of the 325 infants had IVH, and 149 (45.9%) of the 325 were treated with COX inhibitors. Treatment of PDA with COX inhibitors was not an independent risk predictor for IVH in preterm infants with platelets ≥100 × 109/L. However, COX inhibitors amplified the risk of bleeding in the presence of moderately decreased platelets (50-99 × 10 9/L) on days of life 2-7. Multivariable OR for IVH were 0.89 [95% CI 0.43-1.87] for patients with platelets ≥100 × 109/L and treatment with COX inhibitors, 3.40 [95% CI 1.13-10.29] for those with moderately decreased platelets without treatment, and 53.3 [95% CI 5.9-484] for patients with both moderately decreased platelets and COX inhibitor treatment compared with those with platelets ≥100 × 109/L and no treatment (reference group) (P .001). Conclusion: In very low birth weight infants with moderate thrombocytopenia treatment with COX inhibitors increased the risk for intracerebral bleeding. Any benefits of this therapy should be carefully balanced against this potential hazard.
机译:目的:评估使用环加氧酶(COX)抑制剂治疗的出生体重很低的极低早产儿动脉导管未闭(PDA)和血小板计数低的早产儿发生脑室内出血(IVH)的风险。研究设计:使用因斯布鲁克大学医院于2003年1月出生在孕年龄<32周且出生体重≤1500 g的所有婴儿的前瞻性数据,评估了PDA的诊断和治疗以及IVH的危险因素。 2009年12月)。严重血小板减少症(<50×109 / L)的婴儿被排除在分析之外。结果:325名婴儿中有65名(20%)患有IVH,而325名婴儿中有149名(45.9%)用了COX抑制剂治疗。在血小板≥100×109 / L的早产儿中,用COX抑制剂治疗PDA并不是IVH的独立危险因素。但是,COX抑制剂会在2-7天的生命中在血小板适度减少(50-99×10 9 / L)的情况下增加出血的风险。血小板≥100×109 / L并接受COX抑制剂治疗的患者,IVH的多变量OR为0.89 [95%CI 0.43-1.87],未经治疗的血小板中度降低者IVP的多变量为3.40 [95%CI 1.13-10.29],和53.3与血小板≥100×109 / L且未治疗的血小板相比,血小板中度降低和COX抑制剂治疗的患者[95%CI 5.9-484](P <.001)。结论:在极低出生体重的婴儿中,使用COX抑制剂进行中度血小板减少症治疗会增加脑出血的风险。应谨慎权衡此疗法的任何益处与这种潜在危害。

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