Postby WarriorSpouse » Sat Feb 25, 2017 11:03 am
I am sorry to hear of your diagnosis. The titanium staple is a standard medical device that is used during the resection procedure. I have not read or heard of any issues specifically related to the titanium item (device) itself. Like most items approved for use in the U.S., the FDA has approved it for its intended purpose and there have been medical trials prior to its use... They also monitor (via regulation) any adverse effects from the use of drugs and devices that can be researched on the FDA's website.
My guess is that any chance of infection exists in any surgery and not specific to this device alone. All surgeons will provide proper follow-up to the surgery to ensure proper healing and use of the device post surgery. They monitor things very closely and will probably have you on an antibiotic as a prophylactic measure for infection following the surgery.
As in all cases, seek advice from a major cancer center to confirm what many of us encounter on this journey. You will find that the search bar under the top left "Quick Links" link will allow you to see what others have said about this subject in the past and a major cancer center will give you comfort in the process and journey ahead.
Best wishes and thoughts as you move forward.
WS
D/H 47 years old, 10/2014, Stage IV M/CRC, nodes 12/15, para-aortic, 5 cm sigmoid resection, positive Virchow. KRAS mut, MSS, Highly Differentiated, Lynch Neg, 5FU/LV and Avastin 1 YR (Oxi for 5 months), Zeloda/Bev since 01/2016. 02/2019 recurrence para-nodes, back to 5FU/LV Oxy/Bev. It is working again. "...Perseverance is not a long race; it is many short races one after the other."-Walter Elliot