Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Department of Health Sciences, San Paolo Hospital Medical School, University of Milan, Milan, Italy.
Intern Emerg Med. 2021 Aug;16(5):1357-1367. doi: 10.1007/s11739-020-02609-4. Epub 2021 Jan 21.
Women with criteria and non-criteria obstetric antiphospholipid syndrome (APS) carry an increased risk of pregnancy complications, including fetal growth restriction (FGR). The management of obstetric APS traditionally involves clinicians, obstetricians and gynaecologists; however, the most appropriate prophylactic treatment strategy for FGR prevention in APS is still debated. We performed a systematic review and network meta-analysis (NetMA) to summarize current evidence on pharmacological treatments for the prevention of FGR in APS. We searched PubMed and Embase from inception until July 2020, for randomized controlled trials and prospective studies on pregnant women with criteria or non-criteria obstetric APS. NetMA using a frequentist framework were conducted for the primary outcome (FGR) and for secondary outcomes (fetal or neonatal death and preterm birth). Adverse events were narratively summarised. Out of 1124 citations, we included eight studies on 395 pregnant patients with obstetric APS treated with low-dose aspirin (LDA) + unfractionated heparin (UFH) (n = 132 patients), LDA (n = 115), LDA + low molecular weight heparin (n = 100), LDA + corticosteroids (n = 29), LDA + UFH + intravenous immunoglobulin (n = 7), or untreated (n = 12). No difference among treatments emerged in terms of FGR prevention, but estimates were largely imprecise, and most studies were at high/unclear risk of bias. An increased risk of fetal or neonatal death was found for LDA monotherapy as compared to LDA + heparin, and for no treatment as compared to LDA + corticosteroids. The risk of preterm birth was higher for LDA + UFH + IVIg as compared to LDA or LDA + heparin, and for LDA + corticosteroids as compared to LDA or LDA + LMWH. No treatment was associated with an increased risk of bleeding, thrombocytopenia or osteopenia.
患有标准和非标准产科抗磷脂综合征(APS)的女性妊娠并发症风险增加,包括胎儿生长受限(FGR)。产科 APS 的传统管理涉及临床医生、产科医生和妇科医生;然而,APS 预防 FGR 的最合适预防治疗策略仍存在争议。我们进行了系统评价和网络荟萃分析(NetMA),以总结目前关于药物治疗预防 APS 中 FGR 的证据。我们从成立到 2020 年 7 月,在 PubMed 和 Embase 上搜索了关于患有标准或非标准产科 APS 的孕妇的随机对照试验和前瞻性研究。使用似然框架进行 NetMA 是针对主要结局(FGR)和次要结局(胎儿或新生儿死亡和早产)进行的。不良事件以叙述性方式进行总结。在 1124 条引文中外,我们纳入了 8 项研究,涉及 395 名患有产科 APS 的孕妇,这些孕妇接受了低剂量阿司匹林(LDA)+未分级肝素(UFH)治疗(n=132 名患者)、LDA(n=115 名)、LDA+低分子肝素(n=100 名)、LDA+皮质类固醇(n=29 名)、LDA+UFH+静脉注射免疫球蛋白(n=7 名)或未治疗(n=12 名)。在预防 FGR 方面,各种治疗方法之间没有差异,但估计结果很大程度上不精确,并且大多数研究存在高/不明确的偏倚风险。与 LDA+肝素相比,LDA 单药治疗与胎儿或新生儿死亡风险增加相关,与 LDA+皮质类固醇相比,与不治疗相关。与 LDA 或 LDA+肝素相比,LDA+UFH+IVIg 治疗与早产风险增加相关,与 LDA 或 LDA+LMWH 相比,LDA+皮质类固醇与早产风险增加相关。不治疗与出血、血小板减少或骨质疏松症风险增加无关。