It all depends on the surgery. Both EPP and pleurectomy are very serious and complicated procedures. However, surgeons who specialize in doing these procedures have learned to make them much safer, between selection of patients and meticulous technique that gets the surgery done as quickly as possible. Both procedures require a large incision in the chest. In EPP, one lung is removed plus all the pleura on that side of the chest. Artificial patches need to be put in place over the heart and diaphragm where the pleura has been removed. For a pleurectomy/decortication, the pleura on one side of the chest is removed, to get rid of the cancer and also free up the lung.
When you wake up after surgery, you will have drains, which are tubes coming out of your chest to remove any fluid or air that accumulates. You will probably have a tube coming out of your bladder, so that the doctors can monitor your output of urine, making sure you have enough fluids and that your kidneys are working. You will need oxygen especially if you have had a lung removed. Pain control is usually achieved with epidural anesthesia. That means a thin catheter has been placed going into the layers around your spinal cord and delivering medication, which can completely relieve your pain. As many as 60% of patients experience one complication or another after an EPP. There are many less complications with pleurectomy. Your surgeon will do everything to minimize complications, and treat them if they occur. This includes adequate pain control so you can be up and around, which lowers the risk of many complications. While this procedure offers a chance for better long-term survival, even in the best of hands, between 3 and 7% of patients die from complications after an EPP.
General complications from any serious surgery include infection at the surgical site, bleeding from the area, pneumonia, blood clots in the legs, urinary tract infection, and generalized infection (sepsis), among others.
With a pleurectomy, there will be many chest tubes in place to drain any liquid or air. These will remain in place for as long as 10 days. They are removed more quickly with an EPP. The complications of a pleurectomy, aside from those common to all surgeries, include infection inside the chest, and hemorrhage inside the chest. Both of these require surgery to correct.
With an EPP, a very dangerous complication happens if the tube which led to the removed lung, which has been closed off surgically, reopens. This requires surgery to repair. The most unusual complication has to do with the fact that the linings outside the heart have been removed, so the heart has been handled during surgery. That can lead to an irregular heartbeat, also known as an arrhythmia. This is treated with medication at the time it occurs and for about a month after surgery. After an EPP, patients can have a blood clot travel to the remaining lung, which is more dangerous since there is only one lung. They can also have heart attacks.
Other complications have to do with infections or openings in reconstructed areas such as the diaphragm.
For the first few days, the epidural or other significant pain control medication will allow you take deep breaths, get up and move around. This will help you recover more quickly. Eventually you will be getting pain medicine by mouth. You will be more comfortable breathing. Various tubes and drains will be removed.
You may stay in the hospital between a week and two weeks, unless you have had a major complication. You will not really feel recovered for six to eight weeks after such major procedures. Hopefully, once you are healing, the pain from your tumor will be decreased and your breathing will be easier.
- Exactly what is meant by the term mesothelioma?
- How do I get copies of my medical records?
- Help Issues
- What does my family need to know?
- How can friends find out what to do?
- Hospice
- Discussing Difficult Issues: Talking to your family about your wishes
- Wills and Advance Directives
- Are their different types of mesothelioma? What are the differences?
- What does the word pleura mean?
- Who is at risk for developing mesothelioma?
- Is there a specific cause for mesothelioma? If so, what is it?
- How can mesothelioma be prevented?
- What actually is asbestos?
- What kinds of symptoms might I experience from mesothelioma?
- My doctor suspects mesothelioma. If that’s what I have, how will the doctor diagnose it?
- Are there any blood tests that might indicate that I have mesothelioma?
- What kinds of tests might the doctor order to see if I have mesothelioma?
- What is a biopsy? How is it done? What kind of biopsy should I have done?
- Who will tell me the results of my biopsy? Can I be sure that the diagnosis of mesothelioma is correct?
- How do you know if your doctor has experience treating mesothelioma?
- Do I need another (second) opinion?
- How will I find a doctor to give me a second opinion?
- What kinds of doctors treat mesothelioma?
- How do I know where I should receive treatment?
- What can I do to make the most possible out of my doctor visits?
- What can I expect at a mesothelioma treatment center?
- Why does my cancer need to be “staged?” How is it done?
- What are the specifics of staging? How is the information put together to find a stage?
- Are there other staging systems?
- In what ways can mesothelioma spread?
- What are lymph glands, also called lymph nodes?
- What does prognosis mean?
- Is mesothelioma always fatal?
- What is the outlook in my case? How long do I have to live?
- What are some of the survival statistics for mesothelioma?
- What do statistics tell me?
- What is supportive care in mesothelioma?
- What are the ways mesothelioma is treated?
- How do the doctors decide if I am healthy enough to have surgery?
- Are there specific tests that will be done in order to decide if I can have surgery?
- What kind of surgery might I have for pleural mesothelioma?
- What kind of surgery might I have for peritoneal mesothelioma?
- What about other mesotheliomas?
- What determines which surgical procedure I will have?
- What will be done to prepare me for surgery? What can I do myself?
- What will I feel like after abdominal surgery for mesothelioma? Will I have complications?
- What if I need chemotherapy? What does that mean, and how will it help me?
- What will chemotherapy be like? How often will I be treated, and how many times?
- What side effects might I experience during chemotherapy?
- What blood tests are checked during chemotherapy, and why are they checked?
- How can radiation be a therapy for cancer?
- How will the course of my treatment be arranged? How many treatments will I need?
- What equipment is used to deliver radiation?
- What actually happens during a radiation procedure? How long does it take? Will it be painful?
- What side effects can I expect from radiation treatment?
- What are my most likely treatment options?
- What is a clinical trial?
- If I want to participate in a clinical trial, how do I find out what to do? Where is there information on clinical trials for mesothelioma?
- Will I know if treatment is working? With the side effects from chemotherapy, how will I be able to tell? What if my tumor “remains stable?”
- Will I have a number of choices? What if I don’t qualify for the trial I want to participate in?
- Are there new, experimental treatments being investigated to treat mesothelioma?
- What is complementary therapy? What is alternative therapy? What is the difference? Should I consider either or both of these?
- When faced with the decision of which treatment to choose, how will I know what to do?
- Will the fatigue ever go away (like after treatment is over)?
- I am tired all the time. Why am I tired, and what can I do about it?
- I know I feel sad, which seems normal considering the situation. How would I know if I am depressed? Can that be treated?
- What can I do about my shortness of breath, which is really preventing me from doing a lot of things?
- I am very worried about my pain. What if nothing can be done to help me? What if I take narcotics and get addicted?
- Constipation is an issue, partly because of my pain medicine but also just in general. What can I do about constipation?
- What is a deep venous thrombosis? Why is it dangerous? Could it happen to me? How can I try and prevent it?
- I know people have horrible nausea and vomiting during chemotherapy. What can be done to help me with that?
- Will chemotherapy make all my hair fall out? What can I do about it?
- Will radiation therapy make all my hair fall out?
- How do I know why I am coughing or whether I need to do something about it?
- I have lost my appetite. What can I do?
- Will the side effects of my treatment be permanent? Will I have more side effects later on?
- How should I eat after being diagnosed with mesothelioma? Should I change my diet? Do I need supplements, and if so, which supplements? Is there any relationship between diet and survival in patients with mesothelioma?
- What are the benefits of exercise for mesothelioma patients?
- Should I return to work, and when?
- How often will I be seeing the doctor?
- What about vaccinations?
- Will my insurance pay for my treatment? How much will I have to pay?
- What about other kinds of insurance?
- If my mesothelioma comes back, where is it likely to recur?
- How is recurrence treated?
- What if my mesothelioma doesn’t respond to treatment?
- What other documents to I need?
- How will I know if I should stop treatment?
- Do I have any legal rights, having been diagnosed with mesothelioma? What if I was exposed to asbestos while working?
- How do I find a lawyer?
- What if my mesothelioma is the result of doing my job?
- What records does my lawyer need?
- Can I wait and take care of this later?
- Where can I go to get help in dealing with my own stress?
- How can I keep in touch with everyone and try to keep the family together when things are difficult?
- What do I do when something goes wrong in the middle of the night?
- How can I get help with the day-to-day demands?


