heart problems

rory
rory Member Posts: 30
Does anyone have heart problems resulting from radiation or chemo?

Comments

  • gdpawel
    gdpawel Member Posts: 523 Member
    Radiation Therapy Side Effects

    The side effects of Radiation Therapy can be classified as Acute, Subacute
    and Delayed.

    Acute reactions occur during the course of treatment and are temporary.
    They are manifested as signs of increased inter-cranal pressure or
    worsening of neurological deficits. They results from an increase in cerebral
    edema(abnormal accumulation of fluid). The administration of
    corticosteroids usually decreases or alleviates symptoms. Steroids are
    generally administered during the course of therapy to prevent this
    occurrence. Other acute reactions are nausea, vomiting, anorexia(loss of
    apetite), fatigue, alopecia(loss of hair) and skin irritation.

    Subacute reactions generally develop one to three months after completion
    of therapy. These are temporary in nature. Symptoms include anorexia(loss
    of apetite), sleepiness, lethargy(drowsiness) and an increase in neurological
    deficits. These effects result from the temporary disruption of myelin
    formation, which helps speed the relay of nerve signals. It takes
    approximately six weeks for myelin to repair.

    Delayed reactions usally occur 6-24 months after completion of therapy.
    These effects are irreversible and often progressive. They result from direct
    injury to brain tissue and blood vessels. These reactions are due to changes
    in the white matter and death of brain tissue caused by radiation-damaged
    blood vessels. Symptoms vary from mild to severe decreased intellect,
    memory impairment, confusion, personality changes and alteration of the
    normal function of the area irradiated. Leukoencephalopathy(degeneration
    of the white matter) occurs at the tumor site and surrounding irradiated brain.
    The clinical manifestations range from mild cognitive neurological
    impairment to dementia to death. Those at increased risk for long-term
    radiation effects are children less than 2 and adults over 50 years of age.
    Long-term effects can be initially managed to some degree with
    corticosteroids and surgery to remove necrotic tissue. Other long-term
    reactions include loss of vision, development of secondary
    malignancies(oncogenesis) and pituitary-hypothalamic dysfunction(changes
    in normal hormone levels)leading to problems with your thyroid, sugar
    metabolism, fertility or ability to process water.


    Subacute and late effects of radiation on different organs.

    In the months and years following exposure to large doses of
    radiation, subacute and finally late effects of radiation injury
    are seen. Cytologic atypia, which is likely to become less
    prominent as the cells undergo successive divisions but
    occasionally may lead to cancer, may be present along with
    atrophy, infarction, ulceration, hemorrhage, inflammation, edema,
    and scarring due in part to progressive stenosis of radiation
    injured vessels, which become sclerotic and may accumulate foam
    cells deep to the intima (considered almost pathognomonic of
    radiation injury in the case of irradiated small vessels). To a
    large extent, late effects of radiation on an organ may be
    likened to diabetes, in which there also is progressive tissue
    degeneration due to progressive ischemia from slowly degenerating
    vessels, except that in the case of diabetes the injury is
    systemic and not localized to the irradiated area. Epithelium in
    irradiated tissue may vary from atrophic to hyperplastic over a
    short distance. Telangiectatic vessels are frequently
    encountered. Persistent round cell infiltration with a prominent
    plasma cell component is very common. The slow destruction of an
    irradiated organ may lead to death years after completion of the
    therapy. These problems essentially place the radiation
    therapist between a rock and a hard place, wishing to give
    neither too little radiation and thus impair the chances for
    curing a cancer, nor too much radiation with the risk of such
    complications as pulmonary fibrosis, bowel wall injury, and
    cerebral radionecrosis.

    Neuropathy, a problem that sometimes occurs with chemotherapy treatment. It is damage to the nerves. It can occur from some chemotherapy drugs used in conventional cancer treatment.

    There are three major goups of nerves in the human body, the peripheral nerves that carry information to and from the limbs, the nerves that supply the bowels and other internal organs, and the nerves of the head which connect to the ears, eyes, taste buds, etc. Nerves in any or all of these major groups can be affected by certain chemotherapy drugs.

    Nerves are vulnerable to many kinds of damage. They can be damaged by certain cancers. This may be caused by the cancer cells producing a particular kind of biological agent that interferes with the function of the nerves. Sometimes, they can be damged by drugs used in chemotherapy treatment. The chemotherapy drugs that most likely cause nerve damage are the vinca alkaloids(vincristine, vindesine and vinblastine), platinum drugs(cisplatinum, carboplatinum) and the taxanes(taxol, taxotere). These drugs have the potential of interfering with nerve function.

    You may notice symptoms in different areas of your body depending on which groups of nerves are affected. Symptoms in the hands and feet happen when peripheral nerve damage happens and are not rare with vinca alkaloids. The first sign of nerve damage is usually a feeling of tingling and numbness like what you experience when your foot goes to sleep after you've been sitting for a long time in an uncomfortable position. If the problem progresses further, it often produces weakness of the muscles, resulting in loss of strength at the wrist or the ankle. You will notice difficulty in doing up buttons and picking up coins. You may notice that you will tend to trip while walking up stairs or dragging your feet and tend to have a wide-based gait. In severe cases, the weakness may be so severe that you will need a wheelchair.

    When the nerves in the bowel are affected, constipation is the earliest sign. In a few people, the abdomen becomes bloated with a distended bowel that is basically paralyzed. Some of the nerves in the head can also be affected. Platinum drugs can affect the auditory nerve and cause loss of hearing and tinnitus(ringing in the ears). Vision can very occasionally be affected.

    A lot depends on how quickly your cancer treatment can be stopped. Sometimes the need for treatment is more urgent then the residual nerve damage. Sometimes, the balance between benefit from the drug and the side effect of nerve damage is more finely balanced.

    Once treatment has been stopped, recovery is usually slow. It may take months to get even partial improvement and often there will be some residual impairment, either a motor weakness or a sensory numbness or both. Recovery is slower in the feet and legs than in the hands and arms.

    There is no specific treatment that enhances nerve recovery. There are no drugs that will directly stimulate nerve regeneration or recovery. If you have severe and prolonged pain, then the pain may require narcotics often combined with antidepressants. In some cases, certain types of anticonvulsants would be helpful. Treatment options are subjects that you should discuss with your doctor, so you have accurate expectations of potential benefits and side effects.
  • gdpawel
    gdpawel Member Posts: 523 Member
    gdpawel said:

    Radiation Therapy Side Effects

    The side effects of Radiation Therapy can be classified as Acute, Subacute
    and Delayed.

    Acute reactions occur during the course of treatment and are temporary.
    They are manifested as signs of increased inter-cranal pressure or
    worsening of neurological deficits. They results from an increase in cerebral
    edema(abnormal accumulation of fluid). The administration of
    corticosteroids usually decreases or alleviates symptoms. Steroids are
    generally administered during the course of therapy to prevent this
    occurrence. Other acute reactions are nausea, vomiting, anorexia(loss of
    apetite), fatigue, alopecia(loss of hair) and skin irritation.

    Subacute reactions generally develop one to three months after completion
    of therapy. These are temporary in nature. Symptoms include anorexia(loss
    of apetite), sleepiness, lethargy(drowsiness) and an increase in neurological
    deficits. These effects result from the temporary disruption of myelin
    formation, which helps speed the relay of nerve signals. It takes
    approximately six weeks for myelin to repair.

    Delayed reactions usally occur 6-24 months after completion of therapy.
    These effects are irreversible and often progressive. They result from direct
    injury to brain tissue and blood vessels. These reactions are due to changes
    in the white matter and death of brain tissue caused by radiation-damaged
    blood vessels. Symptoms vary from mild to severe decreased intellect,
    memory impairment, confusion, personality changes and alteration of the
    normal function of the area irradiated. Leukoencephalopathy(degeneration
    of the white matter) occurs at the tumor site and surrounding irradiated brain.
    The clinical manifestations range from mild cognitive neurological
    impairment to dementia to death. Those at increased risk for long-term
    radiation effects are children less than 2 and adults over 50 years of age.
    Long-term effects can be initially managed to some degree with
    corticosteroids and surgery to remove necrotic tissue. Other long-term
    reactions include loss of vision, development of secondary
    malignancies(oncogenesis) and pituitary-hypothalamic dysfunction(changes
    in normal hormone levels)leading to problems with your thyroid, sugar
    metabolism, fertility or ability to process water.


    Subacute and late effects of radiation on different organs.

    In the months and years following exposure to large doses of
    radiation, subacute and finally late effects of radiation injury
    are seen. Cytologic atypia, which is likely to become less
    prominent as the cells undergo successive divisions but
    occasionally may lead to cancer, may be present along with
    atrophy, infarction, ulceration, hemorrhage, inflammation, edema,
    and scarring due in part to progressive stenosis of radiation
    injured vessels, which become sclerotic and may accumulate foam
    cells deep to the intima (considered almost pathognomonic of
    radiation injury in the case of irradiated small vessels). To a
    large extent, late effects of radiation on an organ may be
    likened to diabetes, in which there also is progressive tissue
    degeneration due to progressive ischemia from slowly degenerating
    vessels, except that in the case of diabetes the injury is
    systemic and not localized to the irradiated area. Epithelium in
    irradiated tissue may vary from atrophic to hyperplastic over a
    short distance. Telangiectatic vessels are frequently
    encountered. Persistent round cell infiltration with a prominent
    plasma cell component is very common. The slow destruction of an
    irradiated organ may lead to death years after completion of the
    therapy. These problems essentially place the radiation
    therapist between a rock and a hard place, wishing to give
    neither too little radiation and thus impair the chances for
    curing a cancer, nor too much radiation with the risk of such
    complications as pulmonary fibrosis, bowel wall injury, and
    cerebral radionecrosis.

    Neuropathy, a problem that sometimes occurs with chemotherapy treatment. It is damage to the nerves. It can occur from some chemotherapy drugs used in conventional cancer treatment.

    There are three major goups of nerves in the human body, the peripheral nerves that carry information to and from the limbs, the nerves that supply the bowels and other internal organs, and the nerves of the head which connect to the ears, eyes, taste buds, etc. Nerves in any or all of these major groups can be affected by certain chemotherapy drugs.

    Nerves are vulnerable to many kinds of damage. They can be damaged by certain cancers. This may be caused by the cancer cells producing a particular kind of biological agent that interferes with the function of the nerves. Sometimes, they can be damged by drugs used in chemotherapy treatment. The chemotherapy drugs that most likely cause nerve damage are the vinca alkaloids(vincristine, vindesine and vinblastine), platinum drugs(cisplatinum, carboplatinum) and the taxanes(taxol, taxotere). These drugs have the potential of interfering with nerve function.

    You may notice symptoms in different areas of your body depending on which groups of nerves are affected. Symptoms in the hands and feet happen when peripheral nerve damage happens and are not rare with vinca alkaloids. The first sign of nerve damage is usually a feeling of tingling and numbness like what you experience when your foot goes to sleep after you've been sitting for a long time in an uncomfortable position. If the problem progresses further, it often produces weakness of the muscles, resulting in loss of strength at the wrist or the ankle. You will notice difficulty in doing up buttons and picking up coins. You may notice that you will tend to trip while walking up stairs or dragging your feet and tend to have a wide-based gait. In severe cases, the weakness may be so severe that you will need a wheelchair.

    When the nerves in the bowel are affected, constipation is the earliest sign. In a few people, the abdomen becomes bloated with a distended bowel that is basically paralyzed. Some of the nerves in the head can also be affected. Platinum drugs can affect the auditory nerve and cause loss of hearing and tinnitus(ringing in the ears). Vision can very occasionally be affected.

    A lot depends on how quickly your cancer treatment can be stopped. Sometimes the need for treatment is more urgent then the residual nerve damage. Sometimes, the balance between benefit from the drug and the side effect of nerve damage is more finely balanced.

    Once treatment has been stopped, recovery is usually slow. It may take months to get even partial improvement and often there will be some residual impairment, either a motor weakness or a sensory numbness or both. Recovery is slower in the feet and legs than in the hands and arms.

    There is no specific treatment that enhances nerve recovery. There are no drugs that will directly stimulate nerve regeneration or recovery. If you have severe and prolonged pain, then the pain may require narcotics often combined with antidepressants. In some cases, certain types of anticonvulsants would be helpful. Treatment options are subjects that you should discuss with your doctor, so you have accurate expectations of potential benefits and side effects.

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  • rteq2000
    rteq2000 Member Posts: 4
    No heart problems yet, but after 10 years have passed since I did chemo, my white blood count has never improved. I also became hypothyroid. Anyone else?
  • ladonna
    ladonna Member Posts: 1
    Yes, I have CHF from as the result of chemotherapy. I was treated for lympnoma in 1980, and was fine for 17 years. In 1997, I was diagnosed with CHF. Are you experiencing this problem?
  • lindazame
    lindazame Member Posts: 46
    Yes, me and most of the HD survivors I know who were treated in the 70's and early 80's. you can reach me at zame@earthlink.net
    Linda
  • brmanning
    brmanning Member Posts: 3
    I have heart problems from taking chemotherapy. I took it in 2000. I was just diagnosed with cardiac myopathy. My heart is functioning only at 35 to 40%.
  • brian50
    brian50 Member Posts: 27 Member
    brmanning said:

    I have heart problems from taking chemotherapy. I took it in 2000. I was just diagnosed with cardiac myopathy. My heart is functioning only at 35 to 40%.

    Heart Problems
    Recently joined the 25 year survivor club.Been in good health, work and keep myself fit.
    At the start of the year had some bad heart pains when walking briskly,pain became more frequent so went to Doctor ,he did some tests and found my cholestrol to be very high,have to go into hospital next month for more tests.Now taking daily atenolol,simvastatin and aspirin.

    No idea if related to my Leuakaemia treatment 25 years ago,had a bonemarrow transplant from my sister as well.