Ovarian Cancer Surgery

Author(s):  
Amer K. Karam ◽  
Christine Walsh ◽  
Beth Y. Karlan
2021 ◽  
Vol 160 (1) ◽  
pp. 182-186
Author(s):  
Emma L. Barber ◽  
Ravi Garg ◽  
Christianne Persenaire ◽  
Melissa Simon

2020 ◽  
Vol 74 (3) ◽  
pp. 7403205140p1 ◽  
Author(s):  
Mackenzi Pergolotti ◽  
Antoine Bailliard ◽  
Lauren McCarthy ◽  
Erica Farley ◽  
Kelley R. Covington ◽  
...  

2020 ◽  
Vol 18 (1) ◽  
Author(s):  
Antoni Llueca ◽  
◽  
Anna Serra ◽  
Maria Teresa Climent ◽  
Blanca Segarra ◽  
...  

An amendment to this paper has been published and can be accessed via the original article.


BMJ Open ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. e024108 ◽  
Author(s):  
Khadra Galaal ◽  
Alberto Lopes ◽  
Colin Pritchard ◽  
Andrew Barton ◽  
Jennifer Wingham ◽  
...  

IntroductionOvarian cancer is the leading cause of death from gynaecological cancer, with more than 7000 new cases registered in the UK in 2014. In patients suitable for surgery, the National Institute of Health and Care Excellence guidance for treatment recommends surgical resection of all macroscopic tumour, followed by chemotherapy. The surgical procedure can be extensive and associated with substantial blood loss which is conventionally replaced with a donor blood transfusion. While often necessary and lifesaving, the use of donor blood is associated with increased risks of complications and adverse surgical outcomes. Intraoperative cell salvage (ICS) is a blood conservation strategy in which red cells collected from blood lost during surgery are returned to the patient thus minimising the use of donor blood. This is the protocol for a feasibility randomised controlled trial with an embedded qualitative study and feasibility economic evaluation. If feasible, a later definitive trial will test the effectiveness and cost-effectiveness of ICS reinfusion versus donor blood transfusion in ovarian cancer surgery.Methods and analysisSixty adult women scheduled for primary or interval ovarian cancer surgery at participating UK National Health Service Trusts will be recruited and individually randomised in a 1:1 ratio to receive ICS reinfusion or donor blood (as required) during surgery. Participants will be followed up by telephone at 30 days postoperatively for adverse events monitoring and by postal questionnaire at 6 weeks and 3 monthly thereafter, to capture quality of life and resource use data. Qualitative interviews will capture participants’ and clinicians’ experiences of the study.Ethics and disseminationThis study has been granted ethical approval by the South West–Exeter Research Ethics Committee (ref: 16/SW/0256). Results will be disseminated via peer-reviewed publications and will inform the design of a larger trial.Trial registration numberISRCTN19517317.


2020 ◽  
Vol 135 ◽  
pp. 90S
Author(s):  
Sarah E. Rudasill ◽  
Rachel Budker ◽  
Alexandra L. Mardock ◽  
Nikhil Bellamkonda ◽  
Joshua G. Cohen

2017 ◽  
Vol 145 ◽  
pp. 4-5 ◽  
Author(s):  
S. Uppal ◽  
R. Spencer ◽  
M.G. del Carmen ◽  
L.W. Rice ◽  
J. Griggs

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