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首页> 外文期刊>Italian journal of pediatrics >Efficacy of pentoxifylline treatment for neonatal sepsis: a meta-analysis of randomized controlled studies
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Efficacy of pentoxifylline treatment for neonatal sepsis: a meta-analysis of randomized controlled studies

机译:己酮可可碱治疗新生儿败血症的疗效:一项随机对照研究的荟萃分析

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Pentoxifylline may be an important approach to treat neonatal sepsis. However, its use has not been well established. We conduct a systematic review and meta-analysis to evaluate the efficacy of pentoxifylline treatment for neonatal sepsis. PubMed, Embase, and the Cochrane Central Register of Controlled Trials are searched. Randomized controlled trials (RCTs) assessing the influence of pentoxifylline treatment on neonatal sepsis are included. Two investigators independently have searched articles, extracted data, and assessed the quality of included studies. This meta-analysis is performed using the random-effect model. Seven RCTs involving 439 patients are included in the meta-analysis. Compared with control intervention for neonatal sepsis, pentoxifylline treatment is associated with reduced hospital stay (Std. MD?=?-0.61; 95% CI?=?-0.93 to ??0.29; P?=?0.0002) and metabolic acidosis (RR?=?0.38; 95% CI?=?0.22 to 0.66; P?=?0.0006), but has no remarkable impact on mortality (RR?=?0.59; 95% CI?=?0.30 to 1.16; P?=?0.13), serum TNF-α (Std. MD?=?-0.38; 95% CI?=?-1.29 to 0.52; P?=?0.41), serum CRP (Std. MD?=?-0.25; 95% CI?=?-0.92 to 0.42; P?=?0.47), plasma IL-6 (Std. MD?=?-0.13; 95% CI?=?-0.41 to 0.15; P?=?0.37), disseminated intravascular coagulopathy (RR?=?0.55; 95% CI?=?0.25 to 1.21; P?=?0.14), and oliguria/anuria (RR?=?0.77; 95% CI?=?0.28 to 2.16; P?=?0.62). In addition, pentoxifylline treatment can significantly reduce mortality (RR?=?0.50; 95% CI?=?0.29 to 0.88; P?=?0.02) after excluding the study conducted by Akdag during the sensivity analysis. Pentoxifylline treatment may be associated with reduced mortality and hospital stay in neonatal sepsis.
机译:己酮可可碱可能是治疗新生儿败血症的重要方法。但是,尚未很好地确定其用途。我们进行了系统的审查和荟萃分析,以评估己酮可可碱治疗新生儿败血症的疗效。搜索PubMed,Embase和Cochrane对照试验中央注册簿。包括评估己酮可可碱治疗对新生儿败血症影响的随机对照试验(RCT)。两名研究人员独立地搜索了文章,提取了数据并评估了纳入研究的质量。使用随机效应模型执行该荟萃分析。荟萃分析包括七个涉及439例患者的RCT。与新生儿败血症的对照干预相比,己酮可可碱治疗可减少住院时间(标准MD≥=-0.61; 95%CI≥= -0.93至≤0.29; P≥0.0002)和代谢性酸中毒(RR) λ= 0.38; 95%CI = 0.22〜0.66; P = 0.0006;但对死亡率没有显着影响(RR = 0.59; 95%CI = 0.30〜1.16; P = 0.36。 0.13),血清TNF-α(标准MD?=?-0.38; 95%CI?=?-1.29至0.52; P?=?0.41),血清CRP(标准MD?=?-0.25; 95%CI α=β-0.92至0.42;Pα=α0.47),血浆IL-6(标准MDα=α-0.13; 95%CIβ=α-0.41至0.15;Pα=α0.37),弥散性血管内凝血病。 (RR = 0.55; 95%CI = 0.25至1.21; P = 0.14)和少尿/无尿(RR = 0.77; 95%CI = 0.28至2.16; P = 0.62。 )。此外,己酮可可碱治疗在敏感性分析中排除了Akdag进行的研究后,可显着降低死亡率(RR≥0.50; 95%CI≥0.29至0.88;P≥0.02)。己酮可可碱治疗可降低新生儿败血症的死亡率和住院时间。

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