Uterine artery embolization for uterine fibroids
Institute for Clinical Systems Improvement
Record ID 32003000572
English
Authors' objectives:
This review aims to assess the available evidence on the effectiveness of uterine artery embolization for uterine fibroids.
Authors' recommendations:
With regard to uterine artery embolization (UAE) for uterine fibroids, the ICSI Technology Assessment Committee finds:
UAE is generally safe in appropriately selected patients. Patients must be aware of the potential for premature menopause following UAE. Hysterectomy was performed in 1.6% to 4.5% of patients following UAE (although not always attributable to failure of UAE).
The goal of UAE is amelioration of symptoms. In case series completed to date, 85% to 96% of UAE patients interviewed reported a reduction in bleeding at up to 12 months following UAE and 61% to 93% have reported a reduction in bulk-related symptoms. (Conclusion Grade III).
A reduction in fibroid size of 17% to 58% has been reported. Since the fibroids are still present, pain and pressure symptoms may persist.
Uterine volume decreased by 13% to 52% at up to 1 year following UAE.
There are limited long-term follow-up data. A patient registry has been established.
There are insufficient data on the safety of pregnancy following UAE; based on current evidence the procedure should be performed only for women not desiring future pregnancy.
Authors' methods:
Review
Details
Project Status:
Completed
URL for project:
http://www.icsi.org/index.asp
Year Published:
2003
English language abstract:
An English language summary is available
Publication Type:
Not Assigned
Country:
United States
MeSH Terms
- Arteries
- Embolization, Therapeutic
- Leiomyoma
- Uterus
Contact
Organisation Name:
Institute for Clinical Systems Improvement
Contact Address:
8009 34th Avenue South, Suite 1200, Bloomington, MN, USA. Tel: +1 952 814 7060; Fax: +1 952 858 9675
Contact Name:
icsi.info@icsi.org
Contact Email:
icsi.info@icsi.org
Copyright:
Institute for Clinical Systems Improvement (ICSI)
This is a bibliographic record of a published health technology assessment from a member of INAHTA or other HTA producer. No evaluation of the quality of this assessment has been made for the HTA database.