Trzesniowski Ania, Lakhanpal Gaurav, Sulakvelidze Levan, Kennedy Richard, Lakhanpal Sanjiv, Pappas Peter J
Center for Vascular Medicine, Glen Burnie, MD.
Center for Vascular Medicine, Glen Burnie, MD; Center for Vein Restoration, Greenbelt, MD.
J Vasc Surg Venous Lymphat Disord. 2025 Jan;13(1):101990. doi: 10.1016/j.jvsv.2024.101990. Epub 2024 Oct 17.
We previously reported that in women with symptomatic pelvic venous insufficiency secondary to combined iliac vein stenosis (IVS) and ovarian vein reflux (OVR), treated with iliac vein stenting alone that 78% reported complete symptom resolution up to 6 months. The purpose of this investigation was to determine the long-term effectiveness of this treatment strategy, the poststent reintervention rate and the incidence of poststent ovarian vein embolization (OVE) for residual symptoms.
A retrospective review of prospectively collected data at the Center for Vascular Medicine was performed. We investigated women with pelvic pain or dyspareunia secondary to combined IVS and OVR who were treated with stenting alone. Patients whose primary complaint was dysmenorrhea and/or leg symptoms were excluded from the analysis. Assessments and interventions consisted of an evaluation for other causes of pelvic venous disorder by a gynecologist, documentation of preintervention and 3-, 6-, 12-, 24-, and 36-month visual analog scale pain scores; transabdominal duplex ultrasound examination; stent type, diameter, and length; vein territory covered; and reintervention rates. All patients underwent diagnostic venography of their pelvic, left ovarian veins, and pelvic reservoirs, and intravascular ultrasound examination of their iliac veins.
From February 2018 to January 2023, 141 women with a pelvic venous disorder secondary to IVS and OVR were identified. The average age was 44.7 ± 10.5 years with 3.18 ± 1.82 pregnancies. The average follow-up time for the entire cohort was 12.0 ± 12.1 months (median, 10.65 months). Types of stents were Venovo 48 (34%), Wallstent 14 (10%), and Abre 79 (56%). The most common diameter and stent lengths used were 14 and 16 mm and 140 and 150 mm, respectively. The most common vein territories covered were the inferior vena cava to the left external iliac vein in 83% and inferior vena cava to right external iliac vein in 13%. Pelvic and dyspareunia VAS scores before the intervention and at 3, 6, 12, 24, and 36 months after the intervention were as follows: 6.4 ± 73 (n = 141), 2.6 ± 3.3 (n = 98), 1.71 ± 2.83 (n = 77), 2.04 ± 3.5 (n = 76), 2.4 ± 3.7 (n = 30), and 1.15 ± 3 (n = 13) (P ≤ .001). Of the entire cohort no patients required OVE and pelvic reservoir embolization. Pelvic reservoirs were present in 113 of 141 patients (83%). Stent reinterventions were required in 19 of 141 patients (13%).
The majority of women with pelvic pain secondary to combined IVS and OVR achieved near complete symptom resolution with iliac vein stenting alone, despite the presence of a pelvic reservoir in 83% of patients. Although most women complained of some minimal residual pelvic pain or dyspareunia, the majority were satisfied with their outcomes and did not require further intervention. In this patient population, iliac vein stenting should be considered the primary treatment modality. OVE should be reserved for patients with persistent or recurrent pelvic pain unresolved with stenting.
我们之前报道过,对于因髂静脉狭窄(IVS)合并卵巢静脉反流(OVR)导致有症状的盆腔静脉功能不全的女性,仅接受髂静脉支架置入治疗后,78%的患者报告在6个月内症状完全缓解。本研究的目的是确定该治疗策略的长期有效性、支架置入术后再干预率以及支架置入术后卵巢静脉栓塞(OVE)治疗残余症状的发生率。
对血管医学中心前瞻性收集的数据进行回顾性分析。我们调查了因IVS合并OVR导致盆腔疼痛或性交困难且仅接受支架置入治疗的女性。主要诉求为痛经和/或腿部症状的患者被排除在分析之外。评估和干预包括由妇科医生评估盆腔静脉疾病的其他病因、记录干预前以及干预后3个月、6个月、12个月、24个月和36个月的视觉模拟评分疼痛分数;经腹双功超声检查;支架类型、直径和长度;覆盖的静脉区域;以及再干预率。所有患者均接受盆腔、左卵巢静脉和盆腔贮器的诊断性静脉造影,以及髂静脉的血管内超声检查。
2018年2月至2023年1月,共确定141例因IVS合并OVR导致盆腔静脉疾病的女性。平均年龄为44.7±10.5岁,平均妊娠次数为3.18±1.82次。整个队列的平均随访时间为12.0±12.1个月(中位数为10.65个月)。支架类型包括Venovo 48例(34%)、Wallstent 14例(10%)和Abre 79例(56%)。最常用的直径和支架长度分别为14和16mm以及140和150mm。最常见的覆盖静脉区域为下腔静脉至左髂外静脉,占83%,下腔静脉至右髂外静脉,占13%。干预前及干预后3个月、6个月、12个月、24个月和36个月的盆腔疼痛和性交困难视觉模拟评分如下:6.4±73(n = 141)、2.6±3.3(n = 98)、1.71±2.83(n = 77)、2.04±3.5(n = 76)、2.4±3.7(n = 30)和1.15±3(n = 13)(P≤0.001)。整个队列中,无患者需要OVE和盆腔贮器栓塞。141例患者中有113例(83%)存在盆腔贮器。141例患者中有19例(13%)需要进行支架再干预。
大多数因IVS合并OVR导致盆腔疼痛的女性仅通过髂静脉支架置入术就实现了症状几乎完全缓解,尽管83%的患者存在盆腔贮器。虽然大多数女性仍抱怨有一些轻微的残余盆腔疼痛或性交困难,但大多数患者对治疗结果满意,不需要进一步干预。在这类患者中,髂静脉支架置入术应被视为主要治疗方式。OVE应仅用于支架置入术后仍有持续性或复发性盆腔疼痛无法缓解的患者。