This information describes your posterior pelvic exenteration surgery at Memorial Sloan Kettering Cancer Center (MSKCC) and what to expect afterward.
This booklet describes a posterior pelvic exenteration. It is a treatment for cancer that involves the gynecologic organs, the colon, the rectum, and the anus. The booklet includes information on:
- Changes that will happen to your body
- What will happen while you are in the hospital
- Preparing to go home
- Questions about changes in your life resulting from this surgery
- Resources to help.
The OperationThis operation is called a posterior exenteration because it removes organs toward the back of the pelvic cavity. The gastrointestinal system includes your mouth, esophagus, small and large intestines, rectum, and anus (see Figure 1). During the operation, part of your large intestine (colon) will be removed. Your rectum and anus will also be taken out. This means you will need a new place for stool to leave your body. The end of the remaining large intestine will be brought outside on your abdomen. This creates an ostomy or a new place for stool to leave your body. It is called a colostomy. The opening itself is called a stoma. A pouch will cover the stoma to collect stool. You will be taught how to care for the stoma as you recover. You will also get another booklet that answers questions you may have about living with an ostomy.
The gynecology system includes your ovaries, fallopian tubes, uterus, and vagina. Your ovaries, fallopian tubes, and uterus will be removed (see Figure 2). All or part of your vagina might also be removed. Your doctor will discuss this with you if it is necessary. In some cases, the vagina can be reconstructed. Ask your doctor if this is an option for you. A plastic surgeon will do it after the rest of the operation is done. A new vaginal canal is created from muscles and skin in other areas of your body. Your nurse will tell you about the care of your new vagina. If you do not want reconstruction, the area can be closed or covered with a flap of skin.
If your vagina is left, you should be able to have intercourse. If you can have reconstruction, you should be able to resume having intercourse when the area heals. If you cannot have reconstruction, remember that sex can include other forms of intimacy. Ask if your clitoris will be removed. Ask how much feeling you will retain in the vaginal area. Your doctor and nurse will tell you what to expect. For example, sensations may not be the same as they were before your surgery. You might like a referral to our Sexual Health Program. A therapist can assist you regarding these concerns.Back to top
You will likely see many doctors and nurses before the operation. Each specialist will describe his or her role in your care and answer your questions. You may see surgeons from other services who will work with your surgeon to complete the operation. You may see a psychologist who works with women having this operation. You may also see the wound, ostomy, and continence nurse, also known as a CWOCN. The CWOCN will talk to you about the ostomy you will have. It might help you to write down questions as you think of them. Take your list with you when you have appointments. You might also ask to speak with someone who has had the operation. Your social worker might be able to arrange that.
Your intestines, also called bowels, must be clean before surgery. The cleaning lowers the level of bacteria in your intestine. You will also be given antibiotics to take by mouth. The bowel cleaning and antibiotics help to prevent infections after surgery. You will get a fact card on your bowel preparation. The nurse will review it with you and answer any questions you have.Back to top
After SurgeryWhen you wake up, you will be in the Post-Anesthesia Care Unit (PACU). You will have many tubes, drains, pouches, and bandages on your abdomen. (see Figure 3). They may include:
- A Jackson Pratt drain or “JP” to drain fluid from around an incision or wound. The drain is taken out when the incision stops draining.
- A pouch on your stoma to collect stool.
You will have tubes, drains, pouches, and bandages on your abdomen. Please don’t be alarmed when you first see them. Your abdomen will become more swollen over the next few days and then the swelling will go down. Most of the drains and tubes will be removed over the next days to weeks. The stoma is covered with a pouch to collect the stool (see Figure 4). The stoma is swollen after surgery, but the swelling goes down over time over time. The CWOCN along with the nursing staff will teach you how to care for the stoma as you recover.
You will also have:
- Bandages and drains on your upper inside thighs if you had reconstruction of your vagina
- An intravenous (IV) to give you fluids
- A PCA (patient controlled analgesia) to give you pain medicine
- Compression boots on your calves to help blood circulate. These will stay on whenever you are in bed until you are discharged
You will need to cough, deep breathe, and use the incentive spirometer every hour while you are awake. You will be taught how to do these before your operation. Practice before your operation. That will make it easier for you to do them. The nurses will ask you to begin doing them when you arrive in the PACU.
Most women stay overnight in the PACU. You will be transferred to an inpatient room the next day. You will have pain at your incision site and your abdomen. Your pain will be managed with the PCA. A PCA is a pump that you control yourself; it gives you pain medicine through your IV. Your nurse will show you how to use it.
You will not be able to eat or drink for a few days after the surgery. Your doctor will first allow you to drink clear liquids such as tea, broth, and Jell-O®. Your diet will slowly be advanced to solid food.
You will get out of bed soon after you arrive in your inpatient room and will begin walking in the hall. Someone from the nursing staff will help you until you are able to walk on your own. You will be taught how to get out of bed in a way that lessens the pain to your incision. You may feel very tired and may not want to walk. However, walking will help you recover from the operation. If you take pain medicine before getting out of bed, your incision will hurt less. If you had vaginal reconstruction, you will not be able to sit for 6 to 8 weeks. You can lie on your back or side or you can stand.
You can expect bleeding from almost any of the incisions or around the drains. You may also have some discharge and tenderness for a few days. Your nurse will show and tell you what is normal and expected as he or she cares for you. You will also begin to learn how to care for the ostomy and incision lines. Most patients are in the hospital for 7 to 10 days.
Some of the tubes and drains may be removed before you are discharged from the hospital. If you have a stapled incision, the staples are usually taken out before you leave the hospital. Some women will have them removed at the first follow-up visit. If you go home with the drains, your nurses will teach you how to care for them.Back to top
When you are discharged from the hospital, you will be given supplies you need to care for yourself for the first month. You will then order your supplies from an outside source. Your discharge nurse case manager will arrange to have a visiting nurse see you at home. You may still have drains in when you go home. Ask your nurse or doctor when they will be removed. This nurse will help you while you are learning to care for your incision and ostomy. The changes will not be visible under most of your clothes.
As time goes on, you will get stronger. You will be more confident in caring for your incision and ostomy. Your appetite and energy will improve. Before too long, you will be able to resume most of your normal activities.Back to top
This is a major operation, which will change your body, and it will probably take time for you to adjust to these changes. You may feel frightened, angry, or worried. You may have questions or fears about how this surgery will impact your sexuality. These feelings are normal and occur in most patients.
Each person adjusts in her own way. For some, coming to terms with a changed body image will happen over several months. For others, it may take longer. Please know that we have many resources to help you. Your doctors and nurses will answer your questions. We also have social workers, psychologists, psychiatrists, and CWOCNs who have helped many women through this adjustment. You might like to see someone from our Sexual Health Program who deals with issues like these. We also have clergy available for spiritual support. We may be able to arrange for you to meet with another woman who has had this surgery, and who can talk with you and answer questions.
Just as your body will heal, and you will be able to resume your normal activities, you will also learn to adapt to the changes that at first seemed overwhelming. Every new situation requires time to adjust. Loss of a body part, external or internal, often triggers a time of grieving. Remember that we have many resources to guide you to recovery.
If you would like more support or information about intimacy after cancer, please speak with your nurse or doctor. You can also call The Female Sexual Medicine and Women’s Health Program for more information and an appointment.
Sexual Medicine and Women’s Health Program 646-888-5076
The Sexual Medicine and Women’s Health Program provides services at:
- 160 East 53rd Street - Rockefeller Outpatient Pavilion
- 300 East 66th Street - Evelyn H. Lauder Breast Center and MSKCC Imaging Center
If you are having persistent pain or incontinence call your nurse or doctor. He or she can give you a referral to Physical Therapy for an evaluation.
To make an appointment with a psychiatrist or psychologist, call 646-888-0200.
To speak with a social worker, call 212-639-7020.
To see a CWOCN, ask your doctor or nurse to contact that nurse and arrange a visit.
Bladder Support Group at MSKCC
- Second Thursday of each month
- To register call 646-888-8106
Women’s Cancer Network: Gynecological Cancer Foundation (GCF)
401 N. Michigan Avenue
Chicago, IL 60611
Abdomen: The part of the body below the ribs and above the pelvis
Antibiotics: Medicine used to treat infections
Catheter: A small tube that can be used to drain fluid from an area such as the bladder
Colostomy: A surgical procedure that brings one end of the colon outside the abdomen, creating a new exit for stool
Compression boots: Boots that wrap around the lower legs and gently boots: squeeze and relax to aid circulation
CWOCN: A nurse who manages wounds, ostomies, and continence problems
Discharge: The release of fluid from a wound or opening
Fallopian tubes: Slender tubes between the ovaries and the uterus through which eggs travel to the uterus
Gastrointestinal system: The system that includes the stomach and intestines
Gynecologic system: The system that includes the female reproductive organs
Ileostomy: A surgical procedure that brings one end of the ileum outside the abdomen, creating a new exit for stool
Ileum: A last section of the small intestine
Incentive spirometer: A device that measures the amount of air breathed into the lungs
Intravenous (IV): Through a blood vein
Jackson Pratt: A type of drain used after surgery to let fluid drain escape
Ostomy: A new opening such as a colostomy or ileostomy
Ovaries: The female organ that produces ova (eggs) and the hormones estrogen and progesterone
PACU: Post-anesthesia care unit; a recovery room
Patient-controlled analgesia : A method that lets a patient control the amount analgesia of pain medicine that goes into the body
Pelvic exenteration: An operation that removes many organs in the pelvis
Pelvis: The part of the body that is surrounded on three sides by the hip bones and spine
Post-Anesthesia Care Unit: Recovery room
Stoma: An opening from within the body to the outside
Urethra: The tube that carries urine from the bladder to the outside of the body
Visiting nurse: A nurse who travels to patients’ homesBack to top