First off is to remember to breathe. For every one of us that ruptured or had an incidental find and had their aneurysm repaired endovascularly, I believe we all get the 6 month follow up angiogram to ensure the repair has worked. As @oct20 mentions, make sure you stay hydrated before and after the procedure, it’s not only extremely important for the medical team to put in the IVs, it’s important for your brain. After the procedure, hydration and protein is the key to a faster recovery. The hydration helps flush out the dye, hydration and protein helps your brain recover.
I learned about surgeons going through the radial (wrist) artery from members here. I remember when my Neurosurgeon was talking about the change from femoral (groin) artery to radial. My last angiogram to check the stent placement was the radial artery. I prefer it, leaps and bounds!
I have to pre-medicate due to my allergic reaction to the dye. The last pills are taken about two or three hours prior, I’m only allowed a small sip of water to take them. When I get to the hospital and have checked in, a RN takes me back to pre-op and preps me. Like @oct20 mentions, wear comfortable loose clothes, I wear sweat pants and if it’s warmer, a t-shirt with something funny or positive on it. You’ll have to remove your clothing and put on a hospital gown. I also take my tablet or a book. The person who comes with you will be given your bag of clothes, so be kind to them.
The pre-op RN takes your vitals and will ask you questions. They want to make sure you haven’t had anything to eat or drink. An Anesthesiologist will come in and talk to you briefly about the risks of anesthesia. The Nurse Anesthetist (RNA) will come in and put an IV in, sometimes it’s the pre-op RN. Either the surgeon or a Resident will come in and talk to you about the possible risks of the angiogram. There’ll be papers to sign saying you understand them. You’ll get a urinary catheter but you’ll already have medication in you so it’s not even uncomfortable when the RN puts it in. Once pre-op is completed, they’ll take you to the room where the procedure will take place.
There’s a bunch of folks in the procedure room, all busy doing what they do. You’ll be moved from the gurney to the table and the RNA will do some more things. For all of mine, the RNA stayed to my left side to watch the machine and me of course. Most times the team played music and they let me pick what I wanted to listen to which was nice. My Neurosurgeon stays to my left with her Resident. In the procedure room, there’s also another room with a big glass window for observation that holds various folks, Residents, Med Students and my Neurosurgeon’s NP that get to watch the procedure on the big tv. They don’t let me watch it which is sad to me. The Resident or someone always checks the pulse in my feet and marks them. When they were doing the radial access, they used a small handheld machine that finds the artery and ensures that it can be used, which also gets marked.
The surgeon comes in and either the surgeon or the Resident inserts the catheter. For me, my Neurosurgeon checks both sides of my brain once she’s in there, it’s to not only check my aneurysm but to make sure there are no others that decided to develop. If they use your radial artery, a cuff is placed after the closure device has been put in. The cuff is controlled by air, it’s a pretty cool little device. It slowly releases the pressure over the closure device and beats laying flat with a weight on your groin.
You’ll be moved from the table back to a gurney. They wheel you to the post surgery arena, where you’ll hang out for a while with yet another RN. Then they’ll move you to another room and another RN will monitor you and your cuff or the weighted bag if it’s the femoral artery. The RNs pass information to the next and they are really a vital part of the whole process.
Once the cuff is off and you’ve urinated and ate, you get discharged. The discharge will give you your rules on what to do when you get home. The rules aren’t as many for the radial vs the femoral in my opinion and recovery was much faster. I had to stay a couple of hours longer because Dr, Q-W was pushing out the dye with saline solution I think it was due to my allergic reaction. It’s very important that you follow the rules.
You have to have a driver because they give you anesthesia and your brain can be a bit wonky. I recall one person that was sent back home because they didn’t have a driver. Hopefully one of your daughters can take you. Your surgeon will tell the adult you take how the procedure went and that you’ve been moved so they can be with you. You also have to have an adult stay with you for 24 hours I think it is. I think your aunt will cover that need. BH says that was the rule except when Dr. Q-W went in through my wrist and it was just the rest of the day. You’ll have a rule on weight limit, BH thinks it was a week before I was allowed to pick up a half gallon of milk with my right wrist so don’t pick up your grandbaby.
I have photophobia due to my rupture and always wear sunglasses. I also wear a ball cap in the car as a passenger and we have one of those window shades for the passenger window I can put up if needed to help block the sun. I love when it’s overcast on my angiogram days.
The contrast will be similar I imagine to when they checked your kidneys, it was similar to when a Cardiologist checked my heart, the type of dye was just different as they used iodine back then I think it was. My Neurosurgeon uses gadolinium for my brain.
You’ll do fine, you’ve got this!