Clinical UM Guideline |
Subject: Transcatheter Uterine Artery Embolization | |
Guideline #: CG-SURG-28 | Publish Date: 10/01/2024 |
Status: Reviewed | Last Review Date: 08/08/2024 |
Description |
This document addresses the use of transcatheter uterine artery embolization (UAE) as a treatment for fibroid tumors. UAE is a pelvic angiographic procedure used to decrease the symptoms of heavy bleeding and pelvic pain associated with fibroid tumors. Using hemostatic particles, selected vasculature providing the blood supply to the fibroids are occluded. When the blood supply is occluded, the fibroids decrease in size, thereby reducing the symptoms.
Transcatheter UAE has also been used for treatment of other acute pelvic hemorrhagic conditions such as uterine hemorrhage and ectopic pregnancy. Transcatheter uterine artery embolization is a technique performed by an interventional radiologist.
Note: Please see the following related document for additional information:
Clinical Indications |
Medically Necessary:
Not Medically Necessary:
Coding |
The following codes for treatments and procedures applicable to this document are included below for informational purposes. Inclusion or exclusion of a procedure, diagnosis or device code(s) does not constitute or imply member coverage or provider reimbursement policy. Please refer to the member's contract benefits in effect at the time of service to determine coverage or non-coverage of these services as it applies to an individual member.
When services may be Medically Necessary when criteria are met:
CPT |
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37243 | Vascular embolization or occlusion, inclusive of all radiological supervision and interpretation, intraprocedural roadmapping, and imaging guidance necessary to complete the intervention; for tumors, organ ischemia, or infarction [when specified as embolization of uterine artery] |
37244 | Vascular embolization or occlusion, inclusive of all radiological supervision and interpretation, intraprocedural roadmapping, and imaging guidance necessary to complete the intervention; for arterial or venous hemorrhage or lymphatic extravasation [when specified as embolization of uterine artery] |
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ICD-10 Procedure |
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04LE3DT | Occlusion of right uterine artery with intraluminal device, percutaneous approach |
04LE3ZT | Occlusion of right uterine artery, percutaneous approach |
04LF3DU | Occlusion of left uterine artery with intraluminal device, percutaneous approach |
04LF3ZU | Occlusion of left uterine artery, percutaneous approach |
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ICD-10 Diagnosis |
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D25.0-D25.9 | Leiomyoma of uterus (fibroids) |
N92.0-N92.6 | Excessive, frequent and irregular menstruation |
N93.8-N93.9 | Abnormal uterine or vaginal bleeding, other specified or unspecified |
N99.820-N99.821 | Postprocedural hemorrhage of a genitourinary system organ or structure following a procedure |
O00.0-O00.91 | Ectopic pregnancy |
O03.6 | Delayed or excessive hemorrhage following complete or unspecified abortion |
O04.6 | Delayed or excessive hemorrhage following (induced) termination of pregnancy |
O07.1 | Delayed or excessive hemorrhage following failed attempted termination of pregnancy |
O08.1 | Delayed or excessive hemorrhage following ectopic and molar pregnancy |
O72.0-O72.2 | Postpartum hemorrhage |
R10.2 | Pelvic and perineal pain |
R10.30-R10.32 | Pain localized to other parts of lower abdomen |
When services are Not Medically Necessary:
For the procedure codes listed above when criteria are not met, for the diagnosis listed below; or when the code describes a procedure or situation designated in the Clinical Indications section as not medically necessary.
ICD-10 Diagnosis |
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N80.03 | Adenomyosis of the uterus |
Discussion/General Information |
Transcatheter UAE deprives blood flow to uterine fibroids by embolizing the blood supply to the fibroids using a catheter placed into an artery (usually the femoral or radial artery) which is directed to the vessels that supply the fibroids. Once localized, the blood supply is blocked (a process called embolization) by injecting one of several substances which cause arterial occlusion, resulting in atrophy and death of the target tissue (fibroid) over a period of weeks or months. UAE has been reported to have a success rate of 81-100% (American College of Radiology [ACR], 2017). Indications for UAE include bulk symptoms and heavy menstrual bleeding. Side effects of the procedure are pelvic pain, vaginal expulsion of submucosal fibroids, and postembolization syndrome, a flu-like syndrome that presents with pain, nausea, fevers, and leukocytosis. UAE has been shown to cause persistent decreases in pain, heavy menstrual bleeding, and an average decrease in uterine fibroid size of >50% at 5 years (ACR, 2023).
UAE for Uterine Fibroids
Randomized controlled trials and meta-analyses provided early outcomes comparing the outcomes of UAE to surgical intervention and characterizing the complications following UAE (Bruijn, 2016; Martin, 2013; Moss, 2011; Torr, 2012). Overall, no significant differences in quality of life (QOL) were observed between UAE and surgery, though reintervention was significantly more likely following UAE. The most frequent adverse effects of UAE included pain, fever, amenorrhea, passage of fibrous tissue and post-embolization syndrome.
The National Institute for Health and Care Excellence (NICE) published interventional procedure guidance for uterine artery embolization for fibroids (2010). The recommendations include the following:
1.1 Current evidence on UAE for fibroids shows that the procedure is efficacious for symptom relief in the short and medium term for a substantial proportion of patients. There are no major safety concerns. Therefore this procedure may be used provided that normal arrangements are in place for clinical governance and audit.
1.2 During the consent process patients should be informed, in particular, that symptom relief may not be achieved in some women, that symptoms may return and that further procedures may therefore be required. Patients contemplating pregnancy should be informed that the effects of the procedure on fertility and on pregnancy are uncertain.
1.3 Patient selection should be carried out by a multidisciplinary team, including a gynecologist and an interventional radiologist.
1.4 NICE encourages further research into the effects of UAE compared with other procedures to treat fibroids, particularly for women wishing to maintain or improve their fertility.
In 2017, the Agency for Healthcare Research and Quality (AHRQ) published a comparative effectiveness review entitled “Management of uterine fibroids.” The purpose of the review was to evaluate treatment effectiveness and the risk of leiomyosarcoma in individuals with fibroids. In regard to UAE, AHRQ concluded:
There was high strength of evidence that UAE is effective for reducing fibroid volume. The strength of evidence supporting improvements in bleeding and quality of life is moderate for UAE. Five-year follow-up data were available from two large, good quality trials in which well over half the women who received an embolization did not need a subsequent intervention (including hysterectomy). The effect of UAE on reproductive outcomes is not well studied and evidence is insufficient to guide care or determine safety.
Laughlin-Tommaso and colleagues (2019) reported on The Fibroid Interventions: Reducing Symptoms Today and Tomorrow (FIRSTT) randomized controlled trial. The trial’s primary aim was to compare treatment effectiveness between UAE versus magnetic resonance imaging (MRI)-guided ultrasound surgery, and the secondary aim was to compare QOL, pain, fibroid symptom scores, and ovarian function between the two treatments for uterine leiomyomas. A total of 83 individuals were treated with 43 individuals in the MRI-guided ultrasound surgery group and 40 individuals in the UAE group. Of those in the MRI-guided ultrasound group, 16 (37%) individuals accepted enrollment in the study, but declined randomization, and of those in the UAE group, 18 (45%) individuals accepted enrollment in the study, but declined randomization. The results showed the rate of secondary procedure was higher in the MRI-guided ultrasound surgery group (30%) than the UAE group (13%) (hazard ratio, 2.81; 95% Confidence Interval [CI], 1.01-7.79). Secondary procedures included hysterectomy, myomectomy, and UAE. Ovarian function was evaluated by measuring serum anti-Müllerian hormone (AMH). At 24 months, the median interquartile range absolute change in AMH was significantly larger in the UAE group (-0.6 units [-1.2-0.4]) than the MRI-guided ultrasound surgery group (-0.2 units [-0.4-0.4]; p=0.03). Overall, QOL, pain, and fibroid symptom scores improved in both groups with a higher improvement in the UAE group; however, there was incomplete follow-up in both groups with only 44% follow-up in the MRI-guided ultrasound surgery group and 55% follow-up in the UAE group. This study shows positive results for UAE, however, limitations noted are the small sample size, partial randomization, and incomplete follow-up assessments of QOL, pain, and fibroid symptom scores.
In 2020, Manyonda and colleagues published the results of a multicenter, randomized, open-label trial which enrolled 254 premenopausal women, 18 or older, to evaluate myomectomy (n=105) compared to UAE (n=98), in those with symptomatic uterine fibroids who wanted to avoid hysterectomy. The study’s primary outcome of interest was fibroid-related QOL. Secondary measures included menstrual blood loss estimation by self-report, occurrence of pregnancy and pregnancy outcomes, and overall satisfaction with the procedure. A total of 206 individuals (81%) were available for evaluation of the primary outcome. At 2 years, the mean score on the health-related QOL domain of the UFS-QOL questionnaire was 84.6 (standard deviation [SD] 21.5) in the myomectomy group and 80.0 (SD 22.0) in the UAE group (p=0.01). Perioperative and postoperative complications occurred in 29% of the individuals in the myomectomy group and in 24% of the individuals in the UAE group (relative risk, 1.2; 95% CI, 0.8 to 1.9; p=0.40). At 2-year follow-up, additional fibroid-related procedures were performed in 16% of the UAE group and 7% of the myomectomy group. The median length of hospital stay was 2 days for the UAE group and 4 days for the myomectomy group. There were too few pregnancies during the trial to compare differences, if any, in fertility-sparing outcomes following the procedures. With respect to the study’s primary outcome, authors conclude that, among individuals with symptomatic uterine fibroids, treatment with myomectomy resulted in better fibroid-related QOL at 2 years compared to treatment with UAE. Both UAE and myomectomy remain reasonable options for individuals seeking uterine-sparing treatment of symptomatic uterine fibroids.
In 2023 the ACR revised the Appropriateness Criteria for Management of Uterine Fibroids. The criteria include the following:
Another Cochrane review by Gupta and colleagues (2024) compared the benefits and risk of UAE versus other medical or surgical interventions for symptomatic uterine fibroids, 7 RCTs with 793 individuals were included in the review. Three trials compared UAE with abdominal hysterectomy, 2 compared UAE with myomectomy, and 2 compared UAE with either hysterectomies (n=53) or myomectomies (n= 62). The primary outcomes measured were participant satisfaction and live birth rate. The participant satisfaction rates were up to 41% lower or up to 48% higher with UAE compared to surgery within 2 years of the procedure, findings on satisfaction rates were also inconclusive at 5 years. The UAE group had shorter hospital stays and more rapid recoveries. The evidence on major complications was inconclusive and inconsistent from either intervention, however, the risk of minor complications was increased after UAE, there was also a higher likelihood of needing another surgery after UAE at 2 and 5 year follow‐up. There was very low quality evidence to suggest that fertility outcomes may be better after myomectomy than after UAE, but this evidence was based on a small, selected subgroup and should be regarded cautiously. The authors concluded that UAE is a safe option with an earlier initial recovery but it does carry an elevated risk of minor complications and the need for subsequent surgeries later on. The quality of the evidence varied from very low for live birth, to moderate for satisfaction ratings and for most safety outcomes. The main study limitations were failure to clearly report methods, and lack of blinding for subjective outcomes.
Based on evaluation of the existing peer-reviewed medical literature, there is adequate evidence to support the use of UAE for the treatment of acute pelvic and obstetric hemorrhage, ectopic pregnancy, and symptomatic uterine fibroids (including pedunculated fibroids [Katsumori, 2005; Kim, 2018; Smeets, 2009; Zhang, 2022]). For the treatment of pelvic and obstetric hemorrhage, UAE has been shown to be a safe and effective method to control bleeding when compared with alternative methods, such as surgical intervention. For ectopic pregnancy, it has been illustrated that UAE is a safe and effective adjunct to methotrexate treatment, decreasing the need for surgical interventions following drug-only treatment methods that are often unsuccessful.
UAE for non-ectopic pregnancies
A 2020 Cochrane review by Long and colleagues evaluated the clinical effectiveness and safety of surgery, medical treatment, and expectant management of non‐tubal ectopic pregnancy on fertility outcomes and complications. The review included 5 RCTs (n=303) all reporting on Caesarean scar pregnancy. Two of the studies compared UAE or uterine arterial chemoembolization (UACE) plus methotrexate versus systemic methotrexate and subsequent dilation and suction curettage; 1 compared UACE plus methotrexate versus ultrasonography‐guided local methotrexate injection; and 2 compared suction curettage under hysteroscopy versus suction curettage under ultrasonography after UAE/UACE. The quality of evidence ranged from moderate to very low. Limitations were small sample sizes, wide confidence intervals for most analyses, multiple comparisons with a small number of trials, and insufficient data to assess heterogeneity. Therefore the authors concluded that it is uncertain whether there is a difference in success rates, complications, or adverse events between UAE/UACE and administration of systemic methotrexate before suction curettage (low‐quality evidence). However, blood loss was lower if suction curettage was completed after UAE/UACE than after administration of systemic methotrexate alone (moderate‐quality evidence). There are no studies of non‐tubal ectopic pregnancy other than CSP and RCTs for these types of pregnancy are unlikely.
Repeat UAE for Uterine Fibroids
Due to a paucity of data, the current literature evaluating clinical outcomes following repeat UAE for treatment of persistent symptoms of uterine fibroids after an initial UAE is insufficient to establish efficacy (McLucas, 2009; Yousefi, 2006).
Contraindications to UAE
Andrews and colleagues (2004) cite contraindications for uterine artery embolization to include pregnancy, infection, malignancy, coagulopathy and prior pelvic irradiation. The Society of Obstetricians and Gynecologists of Canada stated in a guideline entitled “The management of uterine leiomyomas” the following recommendations regarding UAE:
Uterine artery occlusion by embolization or surgical methods may be offered to selected women with symptomatic uterine fibroids who wish to preserve their uterus. Women choosing uterine artery occlusion for the treatment of fibroids should be counselled regarding possible risks, including the likelihood that fecundity and pregnancy may be impacted.
An increase in uterine size due to fibroid volume is a consideration prior to UAE. A study by Choi (2013) evaluated the safety, effectiveness, and rate of complications of UAE in individuals with large uterine fibroids. A total of 323 individuals without adenomyosis underwent UAE for symptomatic uterine fibroids. The individuals were divided into 2 groups: group 1 (treatment group) included 63 individuals with a large tumor of at least 10 cm in size or a uterine volume of at least 700 cm and group 2 (260 women) was the control group. Group 1 demonstrated a 46.5% tumor volume reduction compared with 52% in group 2. Group 1 had a 40.7% uterine volume reduction compared with 36.3% in group 2. There were no reported significant differences in satisfaction or the presence of procedure-related complications.
Other therapies for symptomatic uterine fibroids include hysterectomy, myomectomy, hormonal therapy with gonadotropin-releasing hormone (GnRH) analogues and luteinizing-hormone releasing hormone (LHRH) analogues, and endurance until menopause when fibroids often regress.
UAE for Adenomyosis
The current published literature does not support the use of UAE for adenomyosis. A review by Popovic (2011) evaluated 15 studies in which 511 individuals received UAE for adenomyosis. Although 387 of the 511 individuals reported symptomatic relief, the authors of the review concluded that the evidence is insufficient to establish UAE as a potential first-line treatment for adenomyosis. Larger, randomized trials with sufficient follow-up periods are necessary to determine true value of UAE. In 2012, the ACR revised its Appropriateness Criteria® for the Radiologic Management of Uterine Leiomyomas and concluded that “UAE has shown early success in controlling the symptoms of bleeding with adenomyosis.” However, there is a recurrence rate of approximately 40%-50% at 2 years and the long-term durability of UAE is questionable. This was reaffirmed in 2023.
A retrospective study by Smeets (2012) reported on 40 individuals with adenomyosis who were treated with UAE. Mean clinical follow-up was 65 months. A total of 8 individuals required additional therapy due to insufficient symptom relief (7 hysterectomies and 1 repeat UAE). Follow-up consisted of the use of uterine fibroid symptom relief and QOL questionnaires. Of the 33 individuals with a preserved uterus who responded to QOL questionnaires, 29 had scores indicating they were asymptomatic, and 4 individuals had scores indicating substantial clinical symptoms despite embolization. This study is limited by its small sample size and retrospective design.
In 2013 NICE published a uterine artery embolization for treating adenomyosis interventional procedures guidance. The recommended indications include the following:
2.2 Treatment for symptomatic adenomyosis includes anti-inflammatory medications, hormone therapy and endometrial ablation. For severe symptoms that do not respond adequately, hysterectomy has been the conventional surgical treatment. Uterine artery embolization may be an alternative option for patients who do not wish to have hysterectomy and/or who wish to preserve their fertility.
In 2017, de Bruijn and colleagues published a systematic review and meta-analysis with the aim to evaluate UAE for the treatment of adenomyosis. The study selection process yielded 30 studies, which were mainly comprised of retrospective studies with small sample sizes and unclear methodologies. While the authors found an improvement of symptoms in 872 individuals (83.1%) and a reduction of uterine volume in all individuals at 3 months, there were complications in 615 individuals (59%). The authors concluded that UAE could be a treatment alternative to hysterectomy; however, randomized controlled trials are needed to confirm this conclusion. Other study limitations include possible selection bias and lack of comparison to other treatments in the included studies.
Evidence from prospective cohort studies supports the use of UAE for individuals with adenomyosis and fibroids who fail conservative measures and desire uterus-preserving therapy. Prospective cohort studies of individuals with adenomyosis and fibroids demonstrate improvement in quality of life and symptom scores, especially when fibroids predominate (Froeling et al. 2012) In individuals with adenomyosis with or without fibroids, UAE improved symptom scores and quality of life at up to 7 years follow-up. Eighteen percent of individuals underwent hysterectomy for persistent symptoms (Smeets 2012, de Brujin 2017).
Definitions |
Adenomyosis: A benign uterine disease in which the endometrium invades the myometrium resulting in enlargement of the uterus, menorrhagia and dysmenorrhea.
Cesarean scar pregnancy: A pregnancy that is implanted on or in a scar from a prior cesarean birth.
Ectopic pregnancy: A pregnancy which occurs when a fertilized egg becomes implanted outside the uterus in locations such as the fallopian tubes, cervix, ovaries or in the pelvic or abdominal space.
Embolization: The insertion of a substance through a catheter into a blood vessel to prevent the flow of blood.
Fibroid ablation – A surgical procedure that uses energy to destroy fibroid tissue while avoiding damage to the normal uterine tissue. The fibroids are not removed, but shrink in size.
Hysterectomy – Surgery to remove the entire uterus.
Myomectomy: Procedure in which uterine fibroids are surgically removed from the uterus.
Pedunculated fibroid: Benign (noncancerous) growths in the uterus (fibroids) attached to the uterine wall by a stalk-like growth called a peduncle.
Post-embolization syndrome: A frequent occurrence following uterine artery embolization which peaks about 48 hours post-procedure and is characterized by low-grade fever, pain, fatigue, nausea and vomiting.
Uterine fibroids: Common and benign (non-cancerous) tumors of the uterus (also known as leiomyomata).
References |
Peer Reviewed Publications:
Government Agency, Medical Society, and Other Authoritative Publications:
Index |
Embolization of Uterine Artery for Treatment of Fibroid TumorsUterine
Embolization for Treatment of Fibroid Tumors
History |
Status | Date | Action |
Reviewed | 08/08/2024 | Medical Policy & Technology Assessment Committee (MPTAC) review. Updated Definitions, Discussion, References and Website sections. |
Reviewed | 08/10/2023 | MPTAC review. Updated Discussion/General Information and References sections. |
Reviewed | 08/11/2022 | Medical Policy & Technology Assessment Committee (MPTAC) review. Updated References section. Updated Coding section with 10/01/2022 ICD-10-CM changes; added N80.03 replacing N80.0. |
Reviewed | 08/12/2021 | MPTAC review. Updated References section. |
Reviewed | 08/13/2020 | MPTAC review. Updated Background/Overview, Definitions and References sections. Reformatted Coding section; updated with additional diagnosis codes. |
Reviewed | 08/22/2019 | MPTAC review. Updated Discussion/General Information and References sections. |
Reviewed | 09/13/2018 | MPTAC review. Updated Discussion/General Information and References sections. |
Reviewed | 11/02/2017 | MPTAC review. Updated header language from “Current Effective Date” to “Publish Date.” Updated Discussion/General Information and References sections. |
Reviewed | 11/03/2016 | MPTAC review. Updated Discussion/General Information, References and Coding sections. |
Revised | 11/05/2015 | MPTAC review. Updated formatting in Criteria. Updated Discussion/General Information and References sections. Removed ICD-9 codes from Coding section. |
Reviewed | 11/13/2014 | MPTAC review. Updated Discussion/General Information and References sections. |
Revised | 11/14/2013 | MPTAC review. Removed list of contraindications from Not Medically Necessary statement and clarified Not Medically Necessary statement. Updated Discussion/General Information, Definitions, and References. Updated Coding section with 01/01/2014 CPT changes; removed CPT 37204, 37210 deleted 12/31/2013, and 75894 (no longer applicable). |
Revised | 11/08/2012 | MPTAC review. Added adenomyosis to Not Medically Necessary Clinical Indications. Updated Discussion/General Information and References. |
Reviewed | 02/16/2012 | MPTAC review. Updated Discussion/General Information, Definitions, and References. |
| 10/01/2011 | Updated Coding section with 10/01/2011 ICD-9 changes. |
Reviewed | 02/17/2011 | MPTAC review. Updated References. |
Reviewed | 02/25/2010 | MPTAC review. Discussion and References updated. |
Reviewed | 02/26/2009 | MPTAC review. Place of Service removed. References updated. |
Revised | 02/21/2008 | MPTAC review. Medically necessary criteria clarified. Discussion and References updated. |
| 08/03/2007 | References updated. |
New | 03/08/2007 | MPTAC review. Initial guideline development. SURG.00018 Transcatheter Uterine Artery Embolization transferred to CG-SURG- 28 Transcatheter Uterine Artery Embolization. References updated. |
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