Pelvic artery embolization versus vaginal packing for controlling vaginal bleeding in locally advanced cervical cancer: a retrospective cohort study from a tertiary cancer center in Xinjiang, China

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Authors: Hong Yang, Fenglin Xu, Yuhan Liu, Qiuyu Chen, Yonghui Song, Yu Wu, Wei Zhong, Tingchuan Xiong, Lina You, Wukui Huang
Cited by: 1
References: 21

Abstract

Introduction: Vaginal bleeding is a frequent and potentially life-threatening complication in locally advanced cervical cancer. Pelvic artery embolization (PAE) directly occludes the bleeding arteries and allows targeted hemostasis, whereas vaginal packing (VP) relies on temporary mechanical compression. Theoretically, PAE may achieve faster and more durable bleeding control. However, few studies have compared the efficacy and safety of these two methods, limiting the early application of PAE. This study aimed to compare the effectiveness and safety of PAE versus VP, and to identify factors influencing hemostatic efficacy. Methods: This retrospective cohort study was conducted at a single tertiary cancer center in Xinjiang, China, and included patients with locally advanced cervical cancer presenting with vaginal bleeding between January 2010 and December 2024. Patients were categorized into the VP group (135 cases) and the PAE group (150 cases) based on the hemostatic intervention received. Next, we compared the hemostatic efficacy, adverse reactions, and recurrence of bleeding between the two groups. Multivariate logistic regression analysis was subsequently employed for identify the factors influencing hemostatic efficacy. Results: A total of 285 patients were included in this study. Compared with the VP group, the PAE group achieved significantly higher overall hemostatic efficacy (94.0% vs. 57.8%, P

Fields of Study & Subjects

Uterine Myomas and Treatments Maternal and fetal healthcare Endometrial and Cervical Cancer Treatments

Publication details

Journal / source
Frontiers in Oncology
Publisher
Frontiers Media SA
Volume
15
Pages
1711701–1711701
Publication date
6 January 2026
Language
EN