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All TopicsForum: Chemotherapy - Before, During and After → Topic: PORT PLACEMENT - Detailed description of process

Topic: PORT PLACEMENT - Detailed description of process

Forum: Chemotherapy - Before, During and After — Regimens, side effects, and support from others going through chemo.

Posted on: Sep 27, 2008 01:55 PM

tbird57 wrote:

Hi everyone

I just got my port placed yesterday and I had such a hard time finding a detailed description of the procedure, so I thought I would share this for anyone who is apprehensive or likes to know exactly what they are going to do to you:

1.  I arrived at the hospital and registered.  I was then taken back to the outpatient surgery/recovery area, got undressed from the waist up and took off my shoes, IV started, EKG hooked up, blood pressure and blood oxygen meter hooked up, and paperwork completed.  A small bag of Levaquin antibiotic was hooked up to my IV.

2.  I was taken back to a holding area outside the OR where they were going to place the port and the procedure was explained to me.  It takes about 1/2 hour to actually place the port.  They don't completely put you under for this procedure - they give you a sedative of morphine and fentanyl so that you "don't care" what they're doing, but you are awake and able to respond if they speak to you.  The sedative is the reason why you have to stop eating 6-12 hours before the procedure, and the reason why you have to wait an hour after the procedure before you can leave.   In addition to this sedative, they give you several local numbing injections in the areas where they are working in your upper chest below the collarbone and the base of your neck.

3.  I rejected the sedative and did this procedure with locals only.  Being able to go home quickly appealed to me, and I'm just the kind of person who feels like I'm not in control when I am sedated but not completely under - either put me completely under or nothing!  So this worked well for me.  (I asked the nurse if every man they worked on today had the "happy juice" and she emphatically stated, "you got THAT right!" - LOL)

4.  They transferred me to the operating table from my gurney bed; actually, I transferred myself by sliding over.  They gave me a warm blanket, took my right arm out of my hospital gown and gave me a small pillow for my head.  They also pulled and taped my skin down on the right side to simulate where the skin would be when sitting up for chemotherapy.  I was reconnected to the EKG, blood pressure and oxygen monitors too, and my hair covered with a surgical cap.  An imaging device was placed over my chest so they could check the final position of the catheter above my heart to be sure it was correctly placed.  They cleaned my skin in the surgical area with a strong blue solution and then draped my entire body and head in a blue surgical blanket.  They had a frame under the blanket where my head was and made a "window" on the side so I could look out.  A lovely nurse stood right by my head to soothe and talk to me throughout the procedure.  I was awake and alert, and curious and continued to talk to the surgical team, asking questions about the process.

5.  When I was prepped and ready, the surgeon came in.  The first local injections were in the base of my neck on the lower right side, where they begin the process by threading the catheter into a large vein, and pushing it in until it rests just above your heart.  The local injections sting and burn just like at the dentist, but once they take effect you are numb.  Any discomfort comes from the pushing sensation in your neck and you can feel pressure in the side of your throat, but it's not painful, just uncomfortable and strange.  The team kept me informed about what they were doing throughout and I kept them laughing with a funny story about a recent visit to the dentist which involved injections to the roof of my mouth - which was WAY more painful than this, I might add!

6.  When they finished with the neck part, the doctor gave me several more numbing injections in the chest for the actually port placement part of this procedure.  More stings and burns, but totally tolerable.  In this part of the procedure, they make an incision in your chest for the port which is about the size of a quarter, placing it under the skin below your collarbone, and then they make a tunnel for the catheter sticking out of your neck (at this point), push it under the skin down to the port, and connect the two.  There is a fair amount of pulling, pushing and tugging in this part of the process but it wasn't painful - again, just strange and uncomfortable.  It doesn't last long, and then they begin to stitch you up.  The subdermal layers are stitched with dissolving stitches and the top layer is glued with steristrips placed over the incisions.  You will have one tegaderm dressing over a small gauze pad a the base of your neck, and another on your chest below your collarbone.

7.  I was instructed to change the dressings every 2 or 3 days, and to keep the dressing on the neck wound for 5--7 days, and the chest wound for 10-14 days.  I was given supplies for 3 rounds of dressing changes. I was told it was okay to shower by wrapping the site in saran wrap but no soaking baths and ensure the area is kept dry.  The port can be used immediately, and does not need to heal before it can be accessed.

8.  Because I didn't have the happy juice cocktail, I was able to get dressed and leave right away!  A big plus to me.  Last night, the surgical areas were numb, and really didn't completely wear off until the wee hours of the morning - about 10 hours later.  There is very little pain involved, but it is uncomfortable to turn your head too much, and I am definitely favoring the area.  I also could not sleep on my right side last night, but was able to sleep on my left side just fine.  I don't plan on doing any housework today, but I'm able to do light cooking, work on the computer, etc. 

9.  There are very good pictures of what the placed port and scars look like on this site:  diehlmartin.com/infusion/ ... .

I hope this is helpful.  I was searching high and low for this kind of detail prior to the procedure, but couldn't find it.  I wish us all the very best of health,

Teena


Dx 5/14/2008, IDC, <1cm, Stage Ib, Grade 3, 0/2 nodes, ER-/PR-, HER2+
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Jan 15, 2012 11:42 PM exbrnxgrl wrote:

VR, ugh, sounds awful. My first chest tube literally fell out when I leaned over the side of the bed. I couldn't believe it and was in tears because I knew this meant they'd have to put another one in.
Tina, happy to say my port works perfectly now and I'm glad I have it.
Caryn

Bilateral mx 9/7/11 with one step ns reconstruction. As of 11/21/11, 2cm met to left hip
Diagnosis: 7/8/2011, IDC, 4cm, Stage IV, Grade 1, 1/15 nodes, mets, ER+/PR+, HER2-
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Jan 16, 2012 09:23 AM Marple wrote:

Bump for bethen.

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Jan 16, 2012 09:50 AM CharB22 wrote:

I had my port put in last Wed and then my 1st treatment the next day. My BS did the port and warned me about the lung puncture, so I was aware, and thankfully it didn't occur. You are all troopers!!! Wow...I can't imagine going through all that.

My only complaint, other than having to sleep on my back, is that the area around the port feels tight - is this common?

I am not battling breast cancer, I am surviving it.
Diagnosis: 12/1/2011, IDC, 1cm, Stage I, Grade 3, 0/2 nodes, ER-/PR-, HER2-
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Jan 16, 2012 10:38 AM exbrnxgrl wrote:

Char,
You had your port placed so very recently. It is still healing. Be patient and eventually you barely notice it's there.
As to lung punctures, I want to say again how rare they are. Everyone should know about the possibility because it is mentioned in the surgical consent form. Most people do recognize it when it happens. I was the rarity among rarities. As one doctor put it " You had a very unusual presentation".
Caryn

Bilateral mx 9/7/11 with one step ns reconstruction. As of 11/21/11, 2cm met to left hip
Diagnosis: 7/8/2011, IDC, 4cm, Stage IV, Grade 1, 1/15 nodes, mets, ER+/PR+, HER2-
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Jan 18, 2012 10:55 AM bethen wrote:

Hi

I just had my port placement yesterday, it went alot smoother than I thought that it would.  Today I do feel like I have been hit by a truck, more like a constant achy bruise.  How long does this take to heal?  I was told not to shower for a week, my first chemo is next week so I am hopeful that it does not ache at that time.  No problems with lungs thank goodness.  And the description at the beginning of this topic was spot on,so thanks so much for posting it, I personally like to know ahead of time what I am going to experience.  

Betsy

Betsy
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Jan 19, 2012 01:01 AM Cowgirl13 wrote:

Betsy, i too felt like i'd been hit by a truck and it was extremely painful getting out of bed for the first week.  I would say that you will be feeling fine in a week.  I was really glad to have my port.  I was just so surprised at how painful the first week was.

Good luck with your first chemo and let us know how it goes. 


Diagnosis: 5/28/2009, IDC, 2cm, Stage IIa, Grade 3, 0/4 nodes, ER+/PR+, HER2+
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Jan 19, 2012 04:31 AM sas-schatzi wrote:

To all- each port experience is different. Several keys.

Emergency stuff-----shortness of breath, unusual feelings of breathing, impending sense of doom, change in breathing pattern,-----------you feel something is wrong call EMS------forget calling doc ...When you get EMS bill ----state it was a medical emergency and it's covered by your taxes---------They are just trying to recover some costs------

Ports shouldn't have unusual pain-----if so---ask for evaluation.

Going into a facility that doesn't want to access your port---------bitch-------ask for a port certified person -------even if it's the middle of the night. ------of course if you are a trauma victim - duh .

Get a bracelet that identifies no access to the AND/LE side

My husbands last admission , I asked for his "no draw pink armband be put on his left arm. The respiratory therapasist that came to do a blood draw went for his left arm."I asked do you not see the band on his arm" Her response was "I will get the blood where I will get it."-------I said "no you won't'  She said"I'll try the other arm and if I can't get it , I will get it from this arm"---------I said like hell you will, do you not know what this hospitals policies are b/c I do."----------Took it to the CEO----------------I hate people that don't follow policy---------they should be fired-------no council-------fired-------they believe themselves above policy-------cluck'em

SAS
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Jan 19, 2012 07:56 PM llilly wrote:

I also had my chemo port put in today. 1/19/12. However, the only instructions I received were not to shower to get the area wet for 48 hours.  I did not receive any information on any dressing changes and my first chemotherapy treatment (Taxotere and Cytoxan) is one week from today.  Did anyone receive any additional information on how long to leave the first dressing on and then how to change it going forward?  I really do not want another infection and am trying to be very careful.  Thank you so very much.  

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Jan 19, 2012 11:23 PM sas-schatzi wrote:

LLilly-best to call doc's office. It was responsibility to write instructions. he probably wrote them in your chart. Review your discharge papers again before calling him. Remember you had a drug that causes amnesia. They could have told you and you just don't remember.
SAS
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Jan 30, 2012 08:59 PM, edited Jan 31, 2012 01:06 PM by sas-schatzi

Anyone interested I wrote a new topic thread on constipation------ah the things we share-sheila

community.breastcancer.org/for...

SAS
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Jan 30, 2012 09:24 PM Kelly2011 wrote:

Thanks for the information. My port is being placed at 730 a tomorrow and it was great reading this info.

Kelly E.
Diagnosis: 11/23/2011, IDC, 2cm, Stage IIa, Grade 3, 0/11 nodes, ER+/PR+, HER2+
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Feb 5, 2012 12:40 AM sas-schatzi wrote:

Bump

SAS
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Feb 5, 2012 02:44 PM clarrissa wrote:

I was also told not to get the area wet (left the tape/bandage on) for several days. I didn't have to do any dressing changes or anything. I just took the tape off after about a week.


Diagnosis: 11/18/2011, IDC, 4cm, Stage IV, mets
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Feb 5, 2012 02:53 PM Myleftboob wrote:

I was told not to shower, sponge bath only for 5 days after the port placement.  There was minor discomfort really.  Although laughing made it ache a little LOL!  I took the bandage off shower day too and was told to just let the steri strips peel off on their own.  Kind of feels like a big bug bite size wise.  A little weird but I think it's best for the long run.  I had another woman tell me she was sorry she didn't have it done and she only had TC X 4 (same as me) but I have to have Herceptin for a year as well.  If it goes OK, I think I'll leave it in for a while until I decide about reconstruction, might as well save the veins in my good arm.


Diagnosis: 12/10/2011, IDC, 2cm, Stage II, Grade 3, 0/4 nodes, ER+/PR-, HER2+
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Feb 16, 2012 08:56 PM ketch wrote:

I got my port-a-cath today. Crap!! It hurt! I asked for some "happy juice" and the onco told me that after it was over, I would see that I did not need it. He ate his words. He had a tough time finding a vein, prodding and poking. He apologized for net being able to find it. He is an excellent doctor and has done thousands of these, so I am sure it was me. I am a hard stick anyway for blood draws, but he said that did not matter, he should have gotten it. He finally did, but I sure wish I'd had something other than lidocaine. Now, it is worn off!!

dx 12/11, 1 cm ILC, 0/9 nodes, BMX 1/12 er+/pr+ her-
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Feb 16, 2012 11:54 PM sas-schatzi wrote:

Ketch, I so wish your doc had listened to you. If there is ever another need for something to be done, refuse to have it done unless you get the Happy Juice

SAS
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Feb 17, 2012 01:20 AM Cowgirl13 wrote:

my port was put in in surgery--a special trip for surgery.  and am  so glad--i think its barbaric to do it any other way.   Especially after all we go through.  maybe it is a West Coast thing.  It was incredibly painful for about a week--i could hardly get out of bed.  anyone know what that could be?


Diagnosis: 5/28/2009, IDC, 2cm, Stage IIa, Grade 3, 0/4 nodes, ER+/PR+, HER2+
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Feb 18, 2012 12:02 AM ketch wrote:

I am fine today. A little bit sore, but manageable. I have not taken tylenol all day. the port is ok, but will be glad when the tenderness goes away in a few days.

dx 12/11, 1 cm ILC, 0/9 nodes, BMX 1/12 er+/pr+ her-
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Feb 21, 2012 01:27 AM, edited Mar 17, 2012 01:51 AM by sas-schatzi

Ketch and all -A chest port will always be put in the hospital setting b/c of the risk of collapsing a lung. The newer ports put in the brachial artery-----arm , not sure.

SAS
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Mar 7, 2012 08:58 PM blondiex46 wrote:

Port next Thursday!!! 3/15

Original 8/96 - 1cm, chemo, rads.recurr..10/09..Mets to lungs, lymph nodes, bones in neck , ribs & liver, Femera then Falsodex, now Xeloda and Zometa!! Xeloda changing now to, Gemzar..
Diagnosis: 10/15/2009, 3cm, Stage IV, ER+/PR-, HER2-
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Mar 9, 2012 09:23 AM OneToughCookie wrote:

Had a power port put in on Monday afternoon with "twilight sleep.". NO pain, didn't even take a Tylenol afterward. Got TCH the next morning. Still no discomfort or pain. Guess I am really lucky or the previous chemos have fried my nerve endings. :)


Diagnosis: 10/10/2011, IDC, 1cm, Stage I, Grade 3, 0/2 nodes, ER-/PR-, HER2+
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Mar 11, 2012 11:52 PM blondiex46 wrote:

thanks, am nervous!!

Original 8/96 - 1cm, chemo, rads.recurr..10/09..Mets to lungs, lymph nodes, bones in neck , ribs & liver, Femera then Falsodex, now Xeloda and Zometa!! Xeloda changing now to, Gemzar..
Diagnosis: 10/15/2009, 3cm, Stage IV, ER+/PR-, HER2-
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Mar 26, 2012 09:16 PM penny4cats wrote:

i have to have a port installed- any feedback on interventional radiology and bard x power port slim design?


Diagnosis: 12/1/2009, ILC, 5cm, Stage IV, Grade 1, 13/17 nodes, mets, ER+/PR+, HER2-
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Mar 30, 2012 10:05 PM maginutah wrote:

Just got my port this morning and went immediately (after a stop at the cafeteria for food on stomach) for my first TCH infusion.  Arrived hospital 6:30 and left 6:15.  Long day, but happy that the port is in, as my only good arm is hard for sticks (medical keeps resort to the hand, which is a hard place for a stick).  I'm feeling well, tired.  Going to bed. 

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Mar 31, 2012 12:23 AM Elizabeth1889 wrote:

maginutah, I am glad your port placement and first treatment went well.  Good luck for a pain free and SE free weekend.


Diagnosis: 1/31/2011, IDC, 1cm, Stage IIa, Grade 1, 1/9 nodes, ER+/PR+, HER2-
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Mar 31, 2012 04:56 PM Tangela wrote:

I had port put in Mar. 16th,  was supposed to have Chemo Mar,27, but there was a kink in the Port and it wouldn't draw blood.. So I went Friday for one day surgery and they revised the port ..  Hope it works I sure am tired of being Cut on..

Now supposed tto have Chemo Wed. Apr. 4.Embarassed


Diagnosis: 12/9/2011, 6cm+, ER-/PR-, HER2-
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Mar 31, 2012 05:14 PM Rose12 wrote:

Does anyone know if it is ok to get chemo the day after your port insertion? I am getting my port Wed and Thursday start chemo. T/C X4.


Diagnosis: 2/1/2012, IDC, <1cm, Stage Ia, Grade 3, 0/3 nodes, ER+/PR-, HER2-
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Apr 4, 2012 05:35 AM, edited Apr 4, 2012 05:39 AM by sas-schatzi

Tangela ---------so glad they were able to fix port-----Yeah

Florida 55--------Yes aport can be used the next day. It can be used the same day if need be----------Your good to go girl Cool            Sorry this answers a few days late, you have probably received several treatments by now. Suggest wearing sleeveless tees at night. Keeps your fingers from scratching site in your sleep. Keep nails short. I washed all tees in clorox, but if you find that too harsh use Dreft.

SAS
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Apr 11, 2012 10:44 AM sas-schatzi wrote:

Bump

SAS
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Apr 22, 2012 12:34 AM sas-schatzi wrote:

Bump----read thead from beginning, has much info from many giving people sheila

SAS

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