Dr. Himesh Gandhi

Robotic Uro-Onco Surgeon

Robotic-assisted laparoscopic cystectomy

Robotic-assisted laparoscopic cystectomy

Cystectomy is the medical term for removing the entire bladder. It is sometimes referred to as radical cystectomy, a cystoprostatectomy or a cysto-prostato-urethrectomy, depending on which organs are removed.

The operation is performed under a general anaesthetic. This means that you will be asleep for the whole operation, so you will not feel any pain. The anaesthetic is given through a small injection into the back of your hand. For more information on having an anaesthetic, ask your nurse for a leaflet.
The type of cystectomy you will have will depend on your individual circumstances. Usually the surgeon will remove your bladder, prostate, seminal vesicles (where semen is stored) and lymph glands within the pelvis. In some cases, your surgeon will also remove your urethra (tube that urine passes down from the bladder before leaving the body). Our surgeon will discuss the operation with you in detail. It is important that you understand what is going to happen, so please ask questions if you are uncertain.

Laparoscopic surgery is also often called keyhole surgery. It is carried out using several small incisions (also called keyholes or port holes) rather than the one large incision used for traditional surgery. For this operation, your surgeon will make six small incisions or cuts (about 1cm) to your abdomen (tummy) and one slightly longer incision (5cm) to remove the bladder. Traditional open surgery would involve a single 15cm-18cm long incision.
Robotic-assisted surgery is a laparoscopic technique that uses a robotic console (the daVinci® Si system) to help your surgeon during the operation. Your surgeon is in the same room, but away from you and controls the robotic arms to perform the operation. It is important to understand that the robot is not performing the surgery.
The surgeon still carries out the procedure, but the robotic console allows more controlled and precise movements during the operation. The robotic console has three arms; one holds a high magnification 3D camera, which is inserted into your abdomen through one of the keyholes. This allows your surgeon to see inside your abdomen. The other robotic arms can hold various instruments, which your surgeon will use to carry out the operation. The instruments are smaller than those used for traditional open surgery. Robotic-assisted surgery has a number of advantages over traditional open surgery:

The benefits of this operation will be discussed with you in more detail, but your doctor may be recommending surgery for you because:

  • You have cancer in your bladder, which would be best managed by complete removal of the bladder 
  • Your bladder may be damaged from radiation treatment 
  • Your bladder may be bleeding after chemotherapy or radiotherapy 
  • Your bladder may be damaged or may be bleeding uncontrollably from other causes or treatments. 

Possible alternative treatments will depend on the reason you are being recommended a cystectomy. However, examples include:

  • Having radiation therapy with or without chemotherapy, or other forms of cancer treatment if you have cancer 
  • Choosing not to have treatment while recognising the risks of your condition. 

Your doctor or nurse will explain your choices and any alternative treatments to you in more detail. 

This is a major operation, which permanently changes your body in several ways. It affects how you pass urine, your ability to have children, to have sex and to some extent, your bowel function.

  • Passing urine: During the operation, your surgeon will carry out a procedure called a urinary diversion. The tubes that connect your kidneys to your bladder (the ureters) are disconnected from the bladder. They are joined to a short segment of your bowel that is isolated from the rest of your intestines. This is then brought to the skin surface, usually on the right hand side of your abdomen. This is known as an ileal conduit. The part of your bowel that opens on to your abdomen is known as a stoma or a urostomy. Your urine then empties through this stoma into a small bag, which you need to empty and change regularly. These are all major changes for you. It is important to us that you are able to return to as active a lifestyle as possible after this operation. This depends on how you feel mentally as well as physically. There are people you can talk to at the hospital. Some patients who have had this type of surgery are also willing to answer questions that you might have. Please ask your doctor or nurse specialist for more details. In some cases, an artificial bladder can be created from a section of your bowel, removing the need for a stoma. This is only suitable for a small proportion of patients – your consultant will discuss this with you if it is suitable for you. 
  • Ability to get an erection: The organs, nerves and blood vessels all lie close together within the pelvis. Therefore, when a cystectomy is carried out, the nerves that supply your penis are affected. This means that you may not be able to achieve an erection after your operation without additional treatment. You should also be aware that if you are able to get an erection, you will not ejaculate any semen, so you will be infertile. If you want to have a family, please discuss this with your doctor before your surgery as you will need to have semen stored. Some men find that treatments to restore erections, such as tablets, injections or vacuum devices are helpful, but not all do. If you would like further information about this, please speak to a member of staff looking after you before you come into hospital for your surgery. 
  • Bowel function: As a small portion of the bowel is used to make the urostomy, your bowel may also be affected by the operation. The remaining part of your bowel left for digestion and absorption of your food will be slightly shorter. This means that you may find that you go to the toilet more frequently or notice that your bowel movements are more ‘loose’ than before. Alternatively, you may experience some constipation for which you may require laxatives to help you open your bowels. This may last for up to a year. Your doctor can discuss this in more detail with you if this applies to you. 

Your surgeon will discuss the possible risks of this operation with you in more detail before asking you to sign a consent form. Please ask questions if you are uncertain about anything.
Possible early complications of any major operation
Problems that can occur while you are in hospital recovering are similar to those for any major operation. These include:

  • Damage to structures inside your abdomen or to your rectum. This risk is higher when the instruments are inserted, so the telescopic instrument (the high magnification 3D camera) is inserted first and then used to help insert the other instruments. 

  • Leakage from, or narrowing of, your intestine where the section of bowel was removed, which may need surgery. 

  • Urine could leak out where the ureters are joined to the section of your intestine. 

  • Blockage of the ureters, preventing urine from passing to your urostomy. This may require treatment in the future. 

  • Carbon dioxide (used during surgery) could become trapped in your abdomen. This can cause pain in one or both shoulders but disappears as the gas is reabsorbed by your body. 

  • The need to convert to traditional open surgery. 

  • Nerve compression, where the pressure from the positioning of your body during the operation can reduce the blood flow supplying your nerves and cause damage. This may require further treatment. 

  • The operation may not remove all of your cancer or it may become apparent once surgery has begun, that the cancer is not operable (if cancer was the reason for your surgery) 

  • Your sexual function (ability to get an erection) may be affected. 

  • There is a small risk of dying from this surgery (one to two in a hundred men). This is no higher than for traditional open surgery. 

You will have a pre-operative assessment or an appointment with the Proactive Care of Older People undergoing Surgery (POPS) team before your surgery.It is important that you come to this appointment, as this is when we will assess your suitability for surgery and the anaesthetic. We will also make sure you have had the relevant tests and examinations. If you do not come to this appointment, we may have to cancel your surgery.
The urology department currently runs an Enhanced Recovery After Surgery Programme (ERAS) for patients undergoing cystectomy. This programme aims to help you recover from your surgery and regain your independence as quickly as possible. There is researched evidence that eating, drinking, moving around soon after your operation and having good control of your pain helps with, and speeds up, your recovery. Therefore, the programme emphasises these aspects of your recovery and focuses on how you can help yourself after your surgery.
As part of the ERAS you will also come to a pre-cystectomy preparation clinic where you will meet one of the clinical nurse specialists (CNS) for bladder cancer, the dietician, the physiotherapist and the stoma nurse specialist.
The CNS will prepare you for your surgery and your hospital stay, answering any questions you may have and talking you through the ERP pathway.
The dietician will give you instructions on what you are allowed to eat and drink prior to your admission for surgery. He/she will also give you some nutritional supplement drinks to have at home prior to your admission.
The physiotherapist will focus on two elements. The first will be your physical function before your operation and the second will be what to expect physically after it. He/she will provide you with advice on your physical preparation for surgery and will explain their role in helping your recovery after your surgery. He/she will also discuss what is available after your surgery to help in your recovery.
The stoma nurse specialist will help prepare you for the formation of your urostomy/stoma and will teach you how to manage your stoma and change your urostomy bags. He/she will also make a mark on your tummy to help guide the surgeon as to the most suitable place for your stoma to be sited. This is usually away from skin creases when you sit, away from previous operation scars and somewhere that you can see easily. He/she will answer any questions you have regarding the stoma and stoma care and will provide you with some written information.
If you smoke, you should try to stop smoking, as this increases the risk of developing a chest infection or deep vein thrombosis (DVT), explained in the risks section. Smoking can also delay wound healing.
If you take any medicines that thin your blood, such as aspirin, warfarin, clopidogrel or rivaroxaban please tell your doctor or the nurse in pre-assessment/POPS. They will give you special instructions. If you take any of these medicines, you may need to come into the hospital earlier. This will be arranged at your pre-admission clinic appointment if it is needed. Please continue to take all your medicines unless you are told otherwise and remember to bring them into the hospital with you.

Generally you will come into hospital on the day of your operation and will be admitted via the Surgical Admissions Lounge (SAL). On admission you will be asked for a urine sample. Some patients will need to be admitted via a ward the day before. We will let you know if this is the case for you. You should expect to stay in hospital for seven to 10 days after your surgery.

We want to involve you in decisions about your care and treatment. If you decide to go ahead, you will be asked to sign a consent form. This states that you agree to have the treatment and you understand what it involves.
If you would like more information about our consent process, please speak to a member of staff caring for you.

You will not be able to eat or drink anything for six hours before you go to theatre. If you have prescription medicines, you can take these with a small sip of water. The anaesthetist will discuss with you exactly which tablets you are able to take.
On the morning of your surgery you should have a shower either at home if admitted on day of surgery, or on the ward if admitted the day before surgery. You will be given a clean gown and anti-thrombus stockings to put on. These help to prevent blood clots forming in your legs during surgery. You may take them off to shower during your hospital stay, but you must keep them on at all other times to help reduce the risk of blood clots. You should continue to wear them for two weeks after you leave hospital.
From the Surgical Admissions Lounge or ward you will be taken to the anaesthetic room where you will be seen by the anaesthetic nurse and doctors. Once anaesthetised, you will be taken through to the operating theatre.

After the surgery is finished, we will transfer you to the Intensive Critical Care Unit (ICCU) on the 1st floor of Main Tower Wing. In ICCU we will monitor your blood pressure, heart rate and fluid levels using very accurate equipment. You will usually stay there for 24 hours until you are ready to return to your ward. In exceptional circumstances you may need to stay on ICCU a little longer (24–48 hours).
On the day of your surgery, friends and family members can visit you afterwards but you should try to limit your visitors on the first night as you will still feel tired from the anaesthetic. Your urologist will come to see you following your surgery.
To reduce the pain post-operatively, the anaesthetist will discuss pain control with you before your surgery. You will usually have:

  • An injection into your back (directly into your spinal nerve system) of painkillers and local anaesthetic. The injection is given in theatre whilst you are still under anaesthetic and the pain relief lasts for about half a day. 
  • A device that you control, that releases painkillers into your blood stream via a drip in your arm (patient-controlled analgesia, PCA). 

After two to four days you should not usually need this level of pain relief and the ward staff will give you tablets or injections instead. Please tell the staff looking after you if you are still in pain or discomfort.
After your operation you will also have:

  • A drip running into a vein in your arm or neck to give you fluids until you are able to drink normally. This will be removed about three to five days after your operation). Soon after you are able to drink normally, you will be able to start eating again. 
  • A fine plastic tube from your nose through to your stomach to stop you from being sick. This is rarely needed and will be inserted while you are in theatre and is usually removed before you wake up. 
  • Dressings over your wounds on your abdomen and a stoma bag collecting urine from your new urostomy. 
  • One small plastic tube (drain) from your abdomen to drain away excess fluid. We will remove this five to seven days after your operation, but sometimes it will stay in a little longer if it continues to drain fluid. 
  • A tube (catheter) from your penis, also draining excess fluid. We will remove this one to two days after your operation. 
  • You will also have two thin tubes (stents) coming through the urostomy. The stoma nurse specialist will remove these about 10 -14 days after you leave hospital. Sometimes they may be removed before you leave hospital. These tubes are inserted to make sure the join between the ureters and the piece of bowel forming the ileal conduit has healed and will not leak if urine passes over this join. 

The doctors will check your stomach with a stethoscope every day, listening for any bowel sounds or ‘gurgling’. They may also ask you whether you have passed any wind. Please do not be embarrassed – these are both signs that your bowel is recovering from the surgery and that you will be able to start drinking again. If you start to eat or drink before this, you will feel nauseous and may be sick.
You may notice some swelling around your eyelids and face. This is because of the position you were in during surgery (head down). This usually disappears within 48 hours.

The ward staff will help you to get out of bed on the first or second day after your operation and to start walking soon after this. Usually, people are independently up and about around four to five days after surgery. A physiotherapist will help you with this.
For the first few days whilst you are recovering from your surgery, the ward staff and stoma nurses will provide stoma care for you. As you improve you will be able to start caring for your own urostomy and the ward staff and stoma nurses will teach you how to do this. The stoma nurse will make sure that you have everything you need for your urostomy before you leave hospital and will explain how to get further supplies. He/she will also ensure that you have follow-up arranged with the stoma team on discharge.
We will arrange a date for you to leave hospital (your discharge date) when you, and the team looking after you, feel that you are fit for discharge and are able to look after your urostomy yourself. This is usually about seven to 10 days after your surgery.
We will give you a date for your follow-up appointment, which is usually made for about two weeks after you leave hospital.

 

  • In the first few weeks after your surgery, you might experience blood-stained urine, bruising around your incision sites and/or red or sore areas around your stoma site. 
  • Recovery time after abdominal surgery varies but you should generally start to feel back to normal about six to 12 weeks after your surgery. 
  • Do not attempt to drive a car during the first six weeks after your surgery. Before you start driving again, make sure you feel able to do an emergency stop and check with your insurance provider that you are covered. 
  • Do not attempt to lift or move heavy objects, start digging the garden or do housework for the first six weeks after your surgery. Build up your activities slowly and only do as much as you feel able to. 
  • To help aid your recovery you should slowly increase your activity levels back to normal. Within the first six weeks this will be through slowly increasing the amount of walking you do or your activities around the house. 
  • During your stay on the ward you will see a physiotherapist who may discuss coming to an exercise class following your first six weeks of recovery. This is an eight week course aimed at increasing your strength and ability to do more. If you would like to attend this class please discuss with your physiotherapist or CNS.
  • When you can return to work will depend on the type of job you do. Please ask your surgeon if you are unsure how much time off you will need. 

Your follow-up appointment
You will have a follow-up appointment in the outpatient clinic two to three weeks after leaving hospital. Three and six months after your surgery you may have further follow-up appointments. These may involve blood tests or scans. Follow-up after that will be every six to twelve months depending on your final results. Your follow-up may be different to this if you need more treatment.

Robotic-assisted laparoscopic cystectomy

Cystectomy is the medical term for removing the entire bladder. It is sometimes referred to as radical cystectomy, a cystoprostatectomy or a cysto-prostato-urethrectomy, depending on which organs are removed.

The operation is performed under a general anaesthetic. This means that you will be asleep for the whole operation, so you will not feel any pain. The anaesthetic is given through a small injection into the back of your hand. For more information on having an anaesthetic, ask your nurse for a leaflet.
The type of cystectomy you will have will depend on your individual circumstances. Usually the surgeon will remove your bladder, prostate, seminal vesicles (where semen is stored) and lymph glands within the pelvis. In some cases, your surgeon will also remove your urethra (tube that urine passes down from the bladder before leaving the body). Our surgeon will discuss the operation with you in detail. It is important that you understand what is going to happen, so please ask questions if you are uncertain.

What is robotic-assisted laparoscopic surgery?

Laparoscopic surgery is also often called keyhole surgery. It is carried out using several small incisions (also called keyholes or port holes) rather than the one large incision used for traditional surgery. For this operation, your surgeon will make six small incisions or cuts (about 1cm) to your abdomen (tummy) and one slightly longer incision (5cm) to remove the bladder. Traditional open surgery would involve a single 15cm-18cm long incision.
Robotic-assisted surgery is a laparoscopic technique that uses a robotic console (the daVinci® Si system) to help your surgeon during the operation. Your surgeon is in the same room, but away from you and controls the robotic arms to perform the operation. It is important to understand that the robot is not performing the surgery.
The surgeon still carries out the procedure, but the robotic console allows more controlled and precise movements during the operation. The robotic console has three arms; one holds a high magnification 3D camera, which is inserted into your abdomen through one of the keyholes. This allows your surgeon to see inside your abdomen. The other robotic arms can hold various instruments, which your surgeon will use to carry out the operation. The instruments are smaller than those used for traditional open surgery. Robotic-assisted surgery has a number of advantages over traditional open surgery:

  • Average blood loss is around 200ml to 500ml compared to 500ml to 1,500ml for traditional open surgery. 
  • You are generally able to start eating and drinking more quickly after robotic assisted surgery. 
  • You are often able to leave hospital a day or two sooner than if you have traditional open surgery. 

Why should I have a cystectomy?
The benefits of this operation will be discussed with you in more detail, but your doctor may be recommending surgery for you because:

  • You have cancer in your bladder, which would be best managed by complete removal of the bladder 
  • Your bladder may be damaged from radiation treatment 
  • Your bladder may be bleeding after chemotherapy or radiotherapy 
  • Your bladder may be damaged or may be bleeding uncontrollably from other causes or treatments. 

What are the alternatives?
Possible alternative treatments will depend on the reason you are being recommended a cystectomy. However, examples include:

  • Having radiation therapy with or without chemotherapy, or other forms of cancer treatment if you have cancer 
  • Choosing not to have treatment while recognising the risks of your condition. 

Your doctor or nurse will explain your choices and any alternative treatments to you in more detail. 

How will the surgery affect me?
This is a major operation, which permanently changes your body in several ways. It affects how you pass urine, your ability to have children, to have sex and to some extent, your bowel function.

  • Passing urine: During the operation, your surgeon will carry out a procedure called a urinary diversion. The tubes that connect your kidneys to your bladder (the ureters) are disconnected from the bladder. They are joined to a short segment of your bowel that is isolated from the rest of your intestines. This is then brought to the skin surface, usually on the right hand side of your abdomen. This is known as an ileal conduit. The part of your bowel that opens on to your abdomen is known as a stoma or a urostomy. Your urine then empties through this stoma into a small bag, which you need to empty and change regularly. These are all major changes for you. It is important to us that you are able to return to as active a lifestyle as possible after this operation. This depends on how you feel mentally as well as physically. There are people you can talk to at the hospital. Some patients who have had this type of surgery are also willing to answer questions that you might have. Please ask your doctor or nurse specialist for more details. In some cases, an artificial bladder can be created from a section of your bowel, removing the need for a stoma. This is only suitable for a small proportion of patients – your consultant will discuss this with you if it is suitable for you. 
  • Ability to get an erection: The organs, nerves and blood vessels all lie close together within the pelvis. Therefore, when a cystectomy is carried out, the nerves that supply your penis are affected. This means that you may not be able to achieve an erection after your operation without additional treatment. You should also be aware that if you are able to get an erection, you will not ejaculate any semen, so you will be infertile. If you want to have a family, please discuss this with your doctor before your surgery as you will need to have semen stored. Some men find that treatments to restore erections, such as tablets, injections or vacuum devices are helpful, but not all do. If you would like further information about this, please speak to a member of staff looking after you before you come into hospital for your surgery. 
  • Bowel function: As a small portion of the bowel is used to make the urostomy, your bowel may also be affected by the operation. The remaining part of your bowel left for digestion and absorption of your food will be slightly shorter. This means that you may find that you go to the toilet more frequently or notice that your bowel movements are more ‘loose’ than before. Alternatively, you may experience some constipation for which you may require laxatives to help you open your bowels. This may last for up to a year. Your doctor can discuss this in more detail with you if this applies to you. 

What are the risks of a cystectomy?
Your surgeon will discuss the possible risks of this operation with you in more detail before asking you to sign a consent form. Please ask questions if you are uncertain about anything.
Possible early complications of any major operation
Problems that can occur while you are in hospital recovering are similar to those for any major operation. These include:

  • Bleeding requiring the need for a blood transfusion or re-operation 
  • Injury to nearby nerves or tissues 
  • A chest infection 
  • Blood clots in your lower leg (deep vein thrombosis or DVT), which could pass to your lung 
  • Wound infection 
  • Bruising around your wounds, poor wound healing or weakness at the wound sites. 

Specific risks for a robotic-assisted cystectomy

  • Damage to structures inside your abdomen or to your rectum. This risk is higher when the instruments are inserted, so the telescopic instrument (the high magnification 3D camera) is inserted first and then used to help insert the other instruments. 
  • Leakage from, or narrowing of, your intestine where the section of bowel was removed, which may need surgery. 
  • Urine could leak out where the ureters are joined to the section of your intestine. 
  • Blockage of the ureters, preventing urine from passing to your urostomy. This may require treatment in the future. 
  • Carbon dioxide (used during surgery) could become trapped in your abdomen. This can cause pain in one or both shoulders but disappears as the gas is reabsorbed by your body. 
  • The need to convert to traditional open surgery. 
  • Nerve compression, where the pressure from the positioning of your body during the operation can reduce the blood flow supplying your nerves and cause damage. This may require further treatment. 
  • The operation may not remove all of your cancer or it may become apparent once surgery has begun, that the cancer is not operable (if cancer was the reason for your surgery) 
  • Your sexual function (ability to get an erection) may be affected. 
  • There is a small risk of dying from this surgery (one to two in a hundred men). This is no higher than for traditional open surgery. 

Preparing for your surgery
You will have a pre-operative assessment or an appointment with the Proactive Care of Older People undergoing Surgery (POPS) team before your surgery.It is important that you come to this appointment, as this is when we will assess your suitability for surgery and the anaesthetic. We will also make sure you have had the relevant tests and examinations. If you do not come to this appointment, we may have to cancel your surgery.
The urology department currently runs an Enhanced Recovery After Surgery Programme (ERAS) for patients undergoing cystectomy. This programme aims to help you recover from your surgery and regain your independence as quickly as possible. There is researched evidence that eating, drinking, moving around soon after your operation and having good control of your pain helps with, and speeds up, your recovery. Therefore, the programme emphasises these aspects of your recovery and focuses on how you can help yourself after your surgery.
As part of the ERAS you will also come to a pre-cystectomy preparation clinic where you will meet one of the clinical nurse specialists (CNS) for bladder cancer, the dietician, the physiotherapist and the stoma nurse specialist.
The CNS will prepare you for your surgery and your hospital stay, answering any questions you may have and talking you through the ERP pathway.
The dietician will give you instructions on what you are allowed to eat and drink prior to your admission for surgery. He/she will also give you some nutritional supplement drinks to have at home prior to your admission.
The physiotherapist will focus on two elements. The first will be your physical function before your operation and the second will be what to expect physically after it. He/she will provide you with advice on your physical preparation for surgery and will explain their role in helping your recovery after your surgery. He/she will also discuss what is available after your surgery to help in your recovery.
The stoma nurse specialist will help prepare you for the formation of your urostomy/stoma and will teach you how to manage your stoma and change your urostomy bags. He/she will also make a mark on your tummy to help guide the surgeon as to the most suitable place for your stoma to be sited. This is usually away from skin creases when you sit, away from previous operation scars and somewhere that you can see easily. He/she will answer any questions you have regarding the stoma and stoma care and will provide you with some written information.
If you smoke, you should try to stop smoking, as this increases the risk of developing a chest infection or deep vein thrombosis (DVT), explained in the risks section. Smoking can also delay wound healing.
If you take any medicines that thin your blood, such as aspirin, warfarin, clopidogrel or rivaroxaban please tell your doctor or the nurse in pre-assessment/POPS. They will give you special instructions. If you take any of these medicines, you may need to come into the hospital earlier. This will be arranged at your pre-admission clinic appointment if it is needed. Please continue to take all your medicines unless you are told otherwise and remember to bring them into the hospital with you.

Coming into hospital
Generally you will come into hospital on the day of your operation and will be admitted via the Surgical Admissions Lounge (SAL). On admission you will be asked for a urine sample. Some patients will need to be admitted via a ward the day before. We will let you know if this is the case for you. You should expect to stay in hospital for seven to 10 days after your surgery.

Giving my consent (permission)
We want to involve you in decisions about your care and treatment. If you decide to go ahead, you will be asked to sign a consent form. This states that you agree to have the treatment and you understand what it involves.
If you would like more information about our consent process, please speak to a member of staff caring for you.

The day of your operation
You will not be able to eat or drink anything for six hours before you go to theatre. If you have prescription medicines, you can take these with a small sip of water. The anaesthetist will discuss with you exactly which tablets you are able to take.
On the morning of your surgery you should have a shower either at home if admitted on day of surgery, or on the ward if admitted the day before surgery. You will be given a clean gown and anti-thrombus stockings to put on. These help to prevent blood clots forming in your legs during surgery. You may take them off to shower during your hospital stay, but you must keep them on at all other times to help reduce the risk of blood clots. You should continue to wear them for two weeks after you leave hospital.
From the Surgical Admissions Lounge or ward you will be taken to the anaesthetic room where you will be seen by the anaesthetic nurse and doctors. Once anaesthetised, you will be taken through to the operating theatre.

After your operation
After the surgery is finished, we will transfer you to the Intensive Critical Care Unit (ICCU) on the 1st floor of Main Tower Wing. In ICCU we will monitor your blood pressure, heart rate and fluid levels using very accurate equipment. You will usually stay there for 24 hours until you are ready to return to your ward. In exceptional circumstances you may need to stay on ICCU a little longer (24–48 hours).
On the day of your surgery, friends and family members can visit you afterwards but you should try to limit your visitors on the first night as you will still feel tired from the anaesthetic. Your urologist will come to see you following your surgery.
To reduce the pain post-operatively, the anaesthetist will discuss pain control with you before your surgery. You will usually have:

  • An injection into your back (directly into your spinal nerve system) of painkillers and local anaesthetic. The injection is given in theatre whilst you are still under anaesthetic and the pain relief lasts for about half a day. 
  • A device that you control, that releases painkillers into your blood stream via a drip in your arm (patient-controlled analgesia, PCA). 

After two to four days you should not usually need this level of pain relief and the ward staff will give you tablets or injections instead. Please tell the staff looking after you if you are still in pain or discomfort.
After your operation you will also have:

  • A drip running into a vein in your arm or neck to give you fluids until you are able to drink normally. This will be removed about three to five days after your operation). Soon after you are able to drink normally, you will be able to start eating again. 
  • A fine plastic tube from your nose through to your stomach to stop you from being sick. This is rarely needed and will be inserted while you are in theatre and is usually removed before you wake up. 
  • Dressings over your wounds on your abdomen and a stoma bag collecting urine from your new urostomy. 
  • One small plastic tube (drain) from your abdomen to drain away excess fluid. We will remove this five to seven days after your operation, but sometimes it will stay in a little longer if it continues to drain fluid. 
  • A tube (catheter) from your penis, also draining excess fluid. We will remove this one to two days after your operation. 
  • You will also have two thin tubes (stents) coming through the urostomy. The stoma nurse specialist will remove these about 10 -14 days after you leave hospital. Sometimes they may be removed before you leave hospital. These tubes are inserted to make sure the join between the ureters and the piece of bowel forming the ileal conduit has healed and will not leak if urine passes over this join. 

The doctors will check your stomach with a stethoscope every day, listening for any bowel sounds or ‘gurgling’. They may also ask you whether you have passed any wind. Please do not be embarrassed – these are both signs that your bowel is recovering from the surgery and that you will be able to start drinking again. If you start to eat or drink before this, you will feel nauseous and may be sick.
You may notice some swelling around your eyelids and face. This is because of the position you were in during surgery (head down). This usually disappears within 48 hours.

Your recovery
The ward staff will help you to get out of bed on the first or second day after your operation and to start walking soon after this. Usually, people are independently up and about around four to five days after surgery. A physiotherapist will help you with this.
For the first few days whilst you are recovering from your surgery, the ward staff and stoma nurses will provide stoma care for you. As you improve you will be able to start caring for your own urostomy and the ward staff and stoma nurses will teach you how to do this. The stoma nurse will make sure that you have everything you need for your urostomy before you leave hospital and will explain how to get further supplies. He/she will also ensure that you have follow-up arranged with the stoma team on discharge.
We will arrange a date for you to leave hospital (your discharge date) when you, and the team looking after you, feel that you are fit for discharge and are able to look after your urostomy yourself. This is usually about seven to 10 days after your surgery.
We will give you a date for your follow-up appointment, which is usually made for about two weeks after you leave hospital.

Getting back to normal

  • In the first few weeks after your surgery, you might experience blood-stained urine, bruising around your incision sites and/or red or sore areas around your stoma site. 
  • Recovery time after abdominal surgery varies but you should generally start to feel back to normal about six to 12 weeks after your surgery. 
  • Do not attempt to drive a car during the first six weeks after your surgery. Before you start driving again, make sure you feel able to do an emergency stop and check with your insurance provider that you are covered. 
  • Do not attempt to lift or move heavy objects, start digging the garden or do housework for the first six weeks after your surgery. Build up your activities slowly and only do as much as you feel able to. 
  • To help aid your recovery you should slowly increase your activity levels back to normal. Within the first six weeks this will be through slowly increasing the amount of walking you do or your activities around the house. 
  • During your stay on the ward you will see a physiotherapist who may discuss coming to an exercise class following your first six weeks of recovery. This is an eight week course aimed at increasing your strength and ability to do more. If you would like to attend this class please discuss with your physiotherapist or CNS.
  • When you can return to work will depend on the type of job you do. Please ask your surgeon if you are unsure how much time off you will need. 

Your follow-up appointment
You will have a follow-up appointment in the outpatient clinic two to three weeks after leaving hospital. Three and six months after your surgery you may have further follow-up appointments. These may involve blood tests or scans. Follow-up after that will be every six to twelve months depending on your final results. Your follow-up may be different to this if you need more treatment.

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