Utility of Intraoperative Fluorescence Imaging in Gynecologic Surgery: Systematic Review and Consensus Statement.


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
Jun 2021
Historique:
received: 24 05 2020
accepted: 15 09 2020
pubmed: 24 10 2020
medline: 18 5 2021
entrez: 23 10 2020
Statut: ppublish

Résumé

This study aimed to review the current knowledge on the utility of intraoperative fluorescence imaging in gynecologic surgery and to give evidence-based recommendations to improve the quality of care for women who undergo gynecologic surgery. A computer-based systematic review of the MEDLINE, CENTRAL, Pubmed, EMBASE, and SciSearch databases as well as institutional guidelines was performed. The time limit was set at 2000-2019. For the literature search, PRISMA guidelines were followed. A modified-Delphi method was performed in three rounds by a panel of experts to reach a consensus of conclusions and recommendations. Indocyanine green (ICG) is used primarily in gynecology for sentinel node-mapping. In endometrial and cervical cancer, ICG is a feasible, safe, time-efficient, and reliable method for lymphatic mapping, with better bilateral detection rates. Experience in vulvar cancer is more limited, with ICG used together with Tc-99 m as a dual tracer and alone in video endoscopic inguinal lymphadenectomy. In early ovarian cancer, results are still preliminary but promising. Indocyanine green fluorescence imaging also is used for ureteral assessment, allowing intraoperative ureteral visualization, to reduce the risk of ureteral injury during gynecologic surgery. For most gynecologic cancers, ICG fluorescence imaging is considered the tracer of choice for lymphatic mapping. The use of this new technology expands to a better ureteral assessment.

Sections du résumé

BACKGROUND BACKGROUND
This study aimed to review the current knowledge on the utility of intraoperative fluorescence imaging in gynecologic surgery and to give evidence-based recommendations to improve the quality of care for women who undergo gynecologic surgery.
METHODS METHODS
A computer-based systematic review of the MEDLINE, CENTRAL, Pubmed, EMBASE, and SciSearch databases as well as institutional guidelines was performed. The time limit was set at 2000-2019. For the literature search, PRISMA guidelines were followed. A modified-Delphi method was performed in three rounds by a panel of experts to reach a consensus of conclusions and recommendations.
RESULTS RESULTS
Indocyanine green (ICG) is used primarily in gynecology for sentinel node-mapping. In endometrial and cervical cancer, ICG is a feasible, safe, time-efficient, and reliable method for lymphatic mapping, with better bilateral detection rates. Experience in vulvar cancer is more limited, with ICG used together with Tc-99 m as a dual tracer and alone in video endoscopic inguinal lymphadenectomy. In early ovarian cancer, results are still preliminary but promising. Indocyanine green fluorescence imaging also is used for ureteral assessment, allowing intraoperative ureteral visualization, to reduce the risk of ureteral injury during gynecologic surgery.
CONCLUSIONS CONCLUSIONS
For most gynecologic cancers, ICG fluorescence imaging is considered the tracer of choice for lymphatic mapping. The use of this new technology expands to a better ureteral assessment.

Identifiants

pubmed: 33095359
doi: 10.1245/s10434-020-09222-x
pii: 10.1245/s10434-020-09222-x
doi:

Substances chimiques

Coloring Agents 0
Indocyanine Green IX6J1063HV

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

3266-3278

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Auteurs

Ignacio Zapardiel (I)

Gynecologic Oncology Unit, La Paz University Hospital-IdiPAZ, Madrid, Spain.

Julio Alvarez (J)

Obstetrics and Gynecology Department, Infanta Sofia University Hospital, Madrid, Spain.

Manel Barahona (M)

Gynecology Department, Puerto Real University Hospital, Cádiz, Spain.

Pere Barri (P)

Gynecologic Surgery Unit, Hospital Quiron Dexeus, Barcelona, Spain.

Ana Boldo (A)

Obstetrics and Gynecology Department, Hospital de la Plana, Castellón, Spain.

Pera Bresco (P)

Gynecology Department, Hospital de Igualada, Barcelona, Spain.

Isabel Gasca (I)

Gynecology Department, Hospital de Valme, Seville, Spain.

Ibon Jaunarena (I)

Gynecologic Unit, Donostia University Hospital-Biodonostia Health Research Institute, Basque Country University, San Sebastián, Spain.

Ali Kucukmetin (A)

Northern Gynaecological Oncology Centre, Queen Elizabeth Hospital, Gateshead, UK.

Gloria Mancebo (G)

Gynecologic Oncology Unit, Hospital Universitario del Mar, Barcelona, Spain.

Borja Otero (B)

Gynecology Department, Hospital Universitario de Cruces, Bilbao, Spain.

Fernando Roldan (F)

Gynecology Department, Hospital Clinico Universitario Lozano Blesa, Saragossa, Spain.

Ramón Rovira (R)

Gynecology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Enma Suarez (E)

Gynecology Department, Hospital Universitario Vall d´Hebron, Barcelona, Spain.

Alvaro Tejerizo (A)

Gynecologic Oncology Unit, 12 de Octubre Universitary Hospital, Madrid, Spain.

Anna Torrent (A)

Gynecology Department, Hospital Universitario Son Espases, Majorca, Spain.

Mikel Gorostidi (M)

Gynecologic Unit, Donostia University Hospital-Biodonostia Health Research Institute, Basque Country University, San Sebastián, Spain. mikelgorostidi@icloud.com.

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