Bonavina Giulia, Bonitta Gianluca, Aiolfi Alberto, Salmeri Noemi, Candiani Massimo, Cavoretto Paolo Ivo, Bonavina Luigi, Bulfoni Alessandro
Department of Obstetrics and Gynecology, IRCCS Multimedica, Milan, Italy.
IRCCS Ospedale Galeazzi - Sant'Ambrogio, Division of General Surgery, Department of Biomedical Science for Health, University of Milan, Milan, Italy.
World J Emerg Surg. 2025 May 24;20(1):43. doi: 10.1186/s13017-025-00602-w.
Preventing postpartum haemorrhage remains a high priority worldwide. We aimed to provide all available evidence comparing maternal and neonatal outcomes of different prophylactic endovascular procedures in patients with abnormal placentation.
Pubmed, Embase and ClinicalTrials.gov databases were searched from inception to Nov, 2024, using relevant key words. Studies comparing outcomes of women undergoing or not prophylactic endovascular procedures in planned cesarean delivery in patients with antenatally suspected or confirmed PAS, placenta previa or both were included. An arm-based random effect frequentist network meta-analysis was performed. All available maternal and neonatal outcomes were evaluated.
Three randomized controlled trials and 59 observational studies were eligible reporting on 6973 women (42.9% did not undergo any endovascular procedure, 26.7% underwent aortic balloon occlusion, REBOA, 16.6%, internal iliac balloon occlusion, PBO-IIA, 5.8%, common iliac artery occlusion, PBO-CIA, placement, and 7.8% underwent uterine artery embolization, UAE). The pooled network analysis showed that all prophylactic endovascular procedures were associated with reduced perioperative blood loss, with proximal balloon occlusion (REBOA) having the strongest effect (SMD -1.80 L, 95%CI -2.38;-1.21; I = 97.2%). Also, peripartum hysterectomy rates were significantly lower in women undergoing prophylactic UAE and REBOA compared to the control group; moreover, patients with placenta previa without any prophylactic endovascular procedure had a 4 to fivefold increased risk of peripartum hysterectomy compared to the REBOA group (I = 20.6%). REBOA was associated with a significant decrease in massive transfusion rates (I = 0%), surgery-related complications (I = 0%), ICU admissions (I = 40.3%), and units of red blood cells transfused (I = 92.8%), compared to PBO-IIA and control groups. The control group versus women undergoing prophylactic UAE showed a significant increase in total operative time (I = 96.5%) and Clavien-Dindo grade IV post-operative complications (I = 26%), compared to REBOA. All prophylactic endovascular procedures had a comparable risk ratio in terms of units of platelets transfused, maternal mortality, and use of additional post-operative bilateral uterine artery embolization among the treatment groups. As for neonatal outcomes, no significant differences were detected.
Although the preponderance of observational studies suggests caution in interpreting the results of this meta-analysis, our findings suggest that prophylactic endovascular interventional procedures, particularly aortic balloon occlusion, may substantially improve clinical outcomes in women with PAS, placenta previa or both.
CRD4202457398.
预防产后出血在全球范围内仍然是一项高度优先事项。我们旨在提供所有现有证据,比较不同预防性血管内手术在胎盘植入异常患者中的母婴结局。
从数据库建立至2024年11月,使用相关关键词检索PubMed、Embase和ClinicalTrials.gov数据库。纳入比较产前怀疑或确诊为胎盘植入异常(PAS)、前置胎盘或两者皆有的患者在计划剖宫产时接受或未接受预防性血管内手术的女性结局的研究。进行基于臂的随机效应频率网络荟萃分析。评估所有可用的母婴结局。
三项随机对照试验和59项观察性研究符合条件,报告了6973名女性(42.9%未接受任何血管内手术,26.7%接受主动脉球囊阻断术(REBOA),16.6%接受髂内动脉球囊阻断术(PBO-IIA),5.8%接受髂总动脉阻断术(PBO-CIA)置入,7.8%接受子宫动脉栓塞术(UAE))。汇总网络分析表明,所有预防性血管内手术均与围手术期失血减少相关,近端球囊阻断术(REBOA)效果最强(标准化均数差-1.80L,95%置信区间-2.38;-1.21;I²=97.2%)。此外,与对照组相比,接受预防性UAE和REBOA的女性围产期子宫切除术发生率显著更低;此外,与REBOA组相比,未接受任何预防性血管内手术的前置胎盘患者围产期子宫切除术风险增加4至5倍(I²=20.6%)。与PBO-IIA组和对照组相比,REBOA与大量输血率(I²=0%)、手术相关并发症(I²=0%)、重症监护病房(ICU)入住率(I²=40.3%)和红细胞输注单位数(I²=92.8%)显著降低相关。与REBOA相比,对照组与接受预防性UAE的女性相比,总手术时间显著增加(I²=96.5%),Clavien-Dindo IV级术后并发症显著增加(I²=26%)。在治疗组之间,所有预防性血管内手术在血小板输注单位数、孕产妇死亡率和术后额外双侧子宫动脉栓塞术的使用方面具有可比的风险比。至于新生儿结局,未检测到显著差异。
尽管观察性研究占多数表明在解释本荟萃分析结果时需谨慎,但我们的研究结果表明,预防性血管内介入手术,尤其是主动脉球囊阻断术,可能会显著改善患有PAS、前置胎盘或两者皆有的女性的临床结局。
PROSPERO注册号:CRD4202457398。