Pain in mnd - final script


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Pain in mnd - final script

  1. 1. Jacqui, Louise, Shay & Brendon Motor Neurone Disease - Pain and Associated Psychological Perspectives in Terminal IllnessThe following presentation will focus on the management of pain and its psychological effects on MND sufferers in the last 6-months (as determined clinically) before death.
  2. 2. Section 1 - Defining Terminal IllnessTerminal illness is not a medical diagnosis, but is a term made popular in the 20 th century to describea disease that has no known cure and is expected to result in the eventual death of the sufferer.Typically an illness will be classed as terminal if death is expected to occur within 6-months of thediagnosis of the illness. There is therefore no particular ailment that can be classed as terminal, butrather certain diseases may be considered terminal at a particular point in its progression within thesufferer. Once a disease has been diagnosed as terminal, treatment efforts are usually halted andmulti-disciplinary palliative care is put in place. This provides pain relief and other appropriatemeasures to ensure as much comfort and well-being in the end stages of life. Many (if not most?)terminal illnesses result in a degree of associated pain that may be progressive as the patient entersthe final stages of the illness. This creates a distinct and special relationship between the patient’sphysical symptoms and psychological well-being as the individual attempts to deal with pain whilstknowing that death is inevitable.Section 2 - Definition of PainWhat is pain? - Pain is an unpleasant sensory and emotional experience associated with actual orpotential tissue damage or described in terms of such damage. It implies a monistic view of theexperience of pain and is inappropriate to encumber it with concepts of pain behaviour. Physiciansrecognise the individuals report because pain is subjective and it varies both with the physical stateof the individual and his/her state of mind (Merskey, 1991).Types of pain include: Acute Pain: Commonly associated with a specific injury that signifies injury or damage has occurred. This pain type can last from seconds to six months (Smeltzer & Brunner, 2010). Chronic Pain: Constant pain that persists beyond expected healing time and can seldom be attributed to a specific cause or injury. This pain lasts for six months or longer (Marcus, 2009). Referred: Pain that occurs from deep structures such as joints, muscles, ligaments, tendons, viscera and is difficult to locate as opposed to superficial pain. (Lautenbacher & Fillingim, 2004). Radiating: Radiating pain “moves” from its point of origin to other parts of the body meaning that tissue injury at one site can produce pain in a region separate and distinct from that involved in the injury (Knight & Draper,2008)Sensation thresholds appear to be universal in that despite cultural/ethical differences inbackground, sensation is reported at the same level cross-culturally. However, pain perception maydiffer across cultures with pain tolerance often notably different depending on cultural background.This indicates that pain is a highly personalised experience within individuals with variationsreported across cultures, (Zatzick & Dimsdale, 1990).
  3. 3. Section 3 - Defining Motor Neurone DiseaseMotor Neurone Disease (MND), a progressive neurodegenerative disease, is a group ofneurobiological disorders that afflict the upper and lower motor neurones, leading to the attrition ofmuscles. Damage and death of the motor neurones is the underlying cause of the disease. Whenmotor neurons fail to give out signals, muscles cease to respond and the process of muscle wastingbegins, (atrophy). The result is a loss of limb movement and difficulties with speech, swallowing andbreathing. There is no known cure or cause. The disease was first characterised in 1874 by Jean-Martin Charcot who named the illness Amyotrophic Lateral Sclerosis (ALS), a term which classifiesthe most common form of the illness and is often used synonymously with MND (McLeod & Clark,2007). It is relatively rare with approximately 5000 cases in the UK at any one time (Moore,McDermott & Shaw, 2008).Only 5% of known cases of MND have been traced back to family history, with the other 95% beingsporadic, meaning that no genetic evidence exists for the onset of the disease. Length of life fromfirst diagnosis is typically 2 – 5 years; however there are many well known deviations from this.Stephen Hawking, perhaps the most well-known case, has lived with the disease for over 40-years.The most important risk factor for MND is age with the peak incidence between 50 – 70 years ofage. Men are more likely to develop MND than women with a ratio of 3:2, (Ng, Khan & Mathers,2009).The disease is associated with varying degrees of pain in sufferers, and as with any terminal illness,may impact heavily on the psychological well-being of patients.
  4. 4. Section 4 - Pain associated with MND - Physical and PsychologicalNon-motor disturbances (NMDs) affect most patients with MND. These include a range of difficulties(e.g. fatigue, sleep disorders, constipation) with pain, anxiety and depression featuring prominently.In one survey, palliative care staff members ranked pain as the number one physical problem inpatients with a variety of terminal illnesses. Anxiety and depression were ranked first and second inthe list of psychological difficulties, (Stiel, et al. 2011).PhysicalPhysical pain in MND can be subdivided into a number of specific pain areas. These pain categoriesinclude muscle cramps, spasticity, constipation, spasms, skin pressure and musculo-skeletal pain.Each of these categories presents different challenges for the sufferers of MND and their carers.Common issues and treatments are shown in the diagram below:Management of Physical Pain in MNDAccording to the Motor Neurone Disease Association, the only available treatment for MND isRiluzole (Rilutek). In a trial by Miller, Mitchell, Lyon & Moore (2007), Riluzole taken 100mg daily, was
  5. 5. found to be a reasonably safe form of treatment and almost certainly prolongs median survival of anMND/ALS patient by approximately 2 – 3 months. There are a number of specific drug trials that arecurrently underway, however much of the previous clinical trials that have been carried out haveproved to be largely disappointing.Pharmacological management of pain in MND can incorporate the use of medication that is non-steroidal anti-inflammatory (NSAID), especially if an active inflammatory process like arthritis ortenosynovitis is evident. Taking prescribed amounts of acetaminophen, about 1000mg every 6hours, along with NSAID or by itself if NSAIDs are intolerable may help. For pain alleviation, tricyclicantidepressants and anti-epileptic drugs such as Neurontin or Gabapentin can be useful. Neurontinmay also help with relief of spasms (DeLisa, Gans & Walsh, 2005). Some reports have suggestedhowever, that Gabapentin can be ineffective in the control of pain and may also produce side effectssuch as memory and attention impairments along with diminished cognitive ability. Earlier researchsuggested that Gabapentin was well tolerated in most patients with possible side effects beingmainly transient and occurring during the titration phase, (Serpell, 2002). However, more recentresearch reported that the adverse effects of gabapentin were more prevalent, suggesting thatadverse effects may be dose dependent with motor/ambulatory effects recorded even in doses toolow to produce significant therapeutic effects on pain, (30 mg/kg). Doses of gabapentin needed toproduce significant therapeutic effects (100 mg/kg) also significantly increased deficits in cognitivefunctions. Although it was noted that adverse side effects may subside after about ten days in somepatients, for others the adverse reactions to the medication became greater with repeated dosing,(Lindner, Bourin, Chen, McElroy, Leet, Hogan, Stock & Machet, 2006). The side effects often noted incurrent medications result in much trial-and-error treatment of pain which in turn may lead tonegative thinking and depression.Another method of managing pain associated with MND is through the use of Marijuana (Cannabis).It has been noted to aid in muscle relaxation, stimulation of appetite, bronchodilation, sleepinduction, saliva reduction and analgesia. Several cannabinoids have been shown to have strongantioxidative and neuroprotective effects that lengthen the endurance of the neuronal cell. Specialcare must be taken by physicians with regards to medicinal usage of marijuana for MND patients,and they must also have an understanding and follow local and state laws concerning its use (Delisaet. al., 2005).Physical disability in patients leads to activity limitations, this can be characterised by utilisingphysical performance measures. One such measure is the Physical Functioning Scale (PFS) of the 36item short form health survey (SF-36) (Bohannon & DePasquale, 2010).The physical aspects of MND frequently receive the majority of attention with psychosocial aspectsafforded secondary important (McLeod & Clarke, 2007).PsychologicalPhysicians and others involved in the care of patients with MND need to be aware that depressionassociated with pain is a significant problem irrespective of the level of physical disability (Tedman,Young & Williams, 1997).In terminal illness depression may be a reaction to pain and other symptoms of the illness. Howeverit may also be a comorbidity of the condition. Distinguishing between a reactive feeling of sadnessand a treatable depressive illness remains a dilemma (Lloyd-Williams & Riddleston, 2002). This issuecauses difficulties with diagnosing depression in terminal illness and as a result, under-diagnosesand under-treatment have been noted, (Stiel, et al. 2011).
  6. 6. Further issues of cultural restraint and relative levels of care also make psychological pain moredifficult to determine than physical pain, and therefore treat. The diagram below shows the impactsof individual differences on levels of psychological pain and associated treatments:Measurement of Depression associated with painBeck Depression Index BDI) – a widely used scale that measures the severity of depression – a shortform of the BDI (BDI-SF) consists of 13 items – has been used in a study of terminally ill patients.Self-Rating Depression Scale – 20 item self-administered instrument – used in a study which lookedat depression in chronic medical diseasesManagement of Psychological Pain in MND
  7. 7. Section 5 - Comorbidity Factors (Desire for Death & Suicidal Thoughts)Hope and hopelessness are important issues for MND patients, with hopelessness contributingsignificantly to suffering and for some a desire for hastened death (McLeod & Clarke, 2007).Both physical pain and feelings of hopelessness have been noted as predictors of patient interest inassisted suicide Ganzini, Silveira & Johnston, 2002). To assess the severity of ALS at various stages ofprogression, the ALS Functional Rating Scale (ALSFRS-R) is available. This assessment covers fourdomains: bulbar functions, fine motor skills, gross motor skills and respiratory status. In assessingsymptoms of depression, patients may be administered the Patient Health Questionnaire (PHQ)which assesses depressive disorders based on criteria in the DSM – IV, (Albert, Whitaker. Rabkin, delBene, Tider, O’Sullivan & Mitsumoto, 2009).There are few options for MND patients with regard to treatment and they eventually have to dealwith decisions to either accept or forgo life-sustaining therapies. The concerns of patients andcaregivers bring about fears of pain and suffocation that may manifest as both helplessness andhopelessness. It should be noted however, that feelings of hopelessness may be influenced byreligious beliefs and/or cultural factors. For example, if the patient believes in life after death,feelings of hopelessness may be diminished.With increasing levels of physical pain and comorbidity with psychological factors in dealing with aterminal illness, the risk of suicidal thoughts is a concern.The desire for escape from intolerable pain is considered to be one of the most frequently reportedincentives for suicidal behaviour. For a number of patients, pain may become so severe that it isintolerable and patients consider that their future will be ‘an eternity of suffering, ‘pill after pill afterpill’. It has been suggested that the feelings of defeat and entrapment play a vital role in thedecision that patients make when the yearning to escape the pain results in the consideration ofsuicide (Tang and Crane, 2006).Suicide vulnerability factors (Ganzini, Silveira & Johnston, 2002) - Fear of losing autonomy - Loss of autonomy - Fear of losing independence - Loss of independence - Perception of being a burden on their families - Depression with a feeling of hopelessness as a consequence of the clinical conditions - Hopelessness in dealing with pain when death is inevitableSuicide Facts (Maytal and Stern, 2006) - Suicide act is committed in only a minority of terminally ill patients - Statistically significant association between clinical depression and the desire for hastened death - 59% of patients who expressed a desire for hastened death had clinical depression - 8% of patients without a desire for hastened death were depressed - Terminally ill patients with a history of depression had vulnerability for a desire for hastened death even if they did not have active symptoms of mood disorder - Statistically significant association between a history of depression and a desire for a hastened death
  8. 8. Section 6 - ConclusionSummaryMotor Neurone disease is the terminal illness reported within this presentation and can be definedas a progressive neurodegenerative disease that results in the loss of limb movement and leads todifficulties when speaking, swallowing and breathing. The statistics of MND have been notedrevealing that 95% of cases have no genetic evidence. MND has no known cure with statistics ofsurvival for more than 10 years following diagnosis being extremely uncommon – with exception!Stephen Hawking is a theoretical physicist and cosmologist who was diagnosed with MND when hewas 21 and is chronically disabled, but still alive at the age of 69.Initial reactions on discovering one’s fate can result in significant emotional trauma. The diagnosisof a terminal illness affects not only the patient, who may express a number of different emotions,including disbelief, anger and grief but also those who are close to them, who may feel helplessness,a sense of inadequacy, sorrow and anger that they are going to be parted.The presentation has also outlined the definition of pain and given consideration to the types ofpain that are commonly associated with, not only specific injuries, but also pain that can beexperienced whilst enduring the chronic effects of the terminal illness identified within thispresentation. Chronic pain can be long lasting and indeed present often through the final stages ofterminal illness and can be particularly associated with degenerative conditions, such as thedegeneration of the motor neurones. Chronic pain in terminal illness can result in an increasedfocus on emotions such as sadness and thoughts associated with the pain. There is an increasingrecognition of the cognitive and affective dimensions of pain.(new slide)The measurement and management of the physical pain associated with MND has also beenconsidered. The physical symptoms of MND often begin very gradually, with clumsy fingers and aweak grip often being the first symptoms of muscular problems associated with MND. As thedisease progresses so do the physical disabilities. The presentation reported the use of Physicalperformance measures such as the SF36, a short form health survey which can help identify whereinput is required. A multi-disciplinary approach is usually adopted, with physiotherapy and dietaryinput as well as pharmacological intervention to target the management of pain.The measurement and management of the psychological pain associated with MND was alsodiscussed and reported depression associated with pain as being a significant problem of MND.Measurement of depression via the Beck Depression Index (BDI) for severity of depression and theSelf Rating Depression Scale used for depression in chronic medical diseases has been able tohighlight the requirement of not only a range of pharmacological interventions for depression butalso a range of psychological methods of coping with pain.The presentation then focussed on the co-morbidity factors associated with pain in MND anddiscussed the possibility of a desire for death and suicidal thoughts as a last resort to be freed fromthe pointless pain. There is a strong link between physical pain and psychological well-being interminally ill patients. Coping with pain, whilst knowing that death is inevitable, is often associatedwith powerful feelings of depression and hopelessness. When an illness is not terminal, fighting thepain, coping and managing, may actually bring about positive feelings of gaining control and puttingup a fight, however, for those with a terminal illness it may seem that there is nothing to fight for.This hopelessness and despair may lead to ideas of suicide and the desire for hastened death.
  9. 9. Evaluation & SuggestionsManaging pain in terminally ill patients requires a multi-disciplinary approach. Pharmacologicalintervention by medical staff is needed but, just as important, are the psychologists, counsellors andcaregivers who try to relieve the psychological distress and provide support for the emotional andpsychological symptoms associated with terminal illness. It is important to remember that themanagement of pain in terminal illness is not restricted to physical pain but also includespsychological pain. This comorbidity is the key factor on why it is considered “pain in specialcircumstances”Although previous research has failed to understand the causes of MND, current research of stemcells to develop new motor neurons and the identification of faulty genes in the development ofMND are underway. A referral to a neurologist is the common pathway for patients diagnosed withMND, future consideration could be given to the pain associated with MND at an earlier stageensuring that not only pharmacological input for management of pain is prescribed but earlyintervention of the psychological management of pain should be made available to ensure thatpatients have engagement in controlling their management of such a debilitating terminal illness.Final ThoughtsCoping with and managing pain can obviously be regarded as challenging in any situation. However,the feelings of depression and hopelessness associated with terminal illness create a uniquecircumstance under which individuals need to cope with and manage pain without the positiveeffects of hope and whilst battling with related negative emotions.
  10. 10. Section 7 - ReferencesAlbert, S. M., Whitaker, A., Rabkin, J. G., del Bene, M., Tider, T., O’Sullivan, & Mitsumoto, H. (2009). Medicaland Supportive Care among People with ALS in the Months before Death or Tracheostomy. Journal of Painand Symptom Management. Vol. 38, No.4, 546 – 553.Anand, K.J.S., Craig, K.D. (1996). New Perspectives on the definition of pain. Pain. Vol. 67, Issue 1. P.3-6Bohannon, R.W., DePasquale, L. (2010). Physical Functioning Scale of the Short-Form (SF)36: InternalConsistency and Validity with Older Adults. Journal of Geriatric Physical Therapy. Vol.33, Issue1, p.16-18Brunner, L., S. & Smeltzer, S., C., O. (2010). Brunner & Suddarth’s textbook of medical-surgical nursing. WoltersKluwer Health/Lippincott Williams & Wilkins: Philadelphia.DeLisa, J. A. Gans, B. M. & Walsh, N. E. (2005). Physical medicine and rehabilitation: principles and practice.Lippincott Williams & Wilkins: Philadelphia.Dobratz, M.C. (1990). The Life Closure Scale: a measure of psychological adaptation in death and dying. Hosp.J; Vol. 6. Issue 3. P. 1-15Ganzini, L., Silveira, M. J. & Johnston, W.S. (2002). Predictors and Correlates of Interest in Assisted Suicide inthe Final Month of Life Among ALS Patients in Oregon and Washington. Journal of Pain and SymptomManagement. Vol. 24, No.3, 312 – 317.Knight, K., L. & Draper, D., O. (2008). Therapeutic modalities: the art and the science. Lippincott Williams &Wilkins: Baltimore, MD.Lautenbacher, S. & Filingim, R., B. (2004). Pathophysiology of pain perception. Kluwer Academic /Plenum: NewYork.Lindner, M. D., Bourin, C., Chen, P., McElroy, J. F., Leet, J. E., Hogan, J. B., Stock, D. A. & Machet, F. (2006).Adverse Effects of Gabapentin and Lack of Anti-Allodynic Efficacy of Amitriptyline in the Streptozotocin Modelof Painful Diabetic Neuropathy. Experimental and Clinical Psychopharmacology. Vol. 14, No. 1, 42 – 51.Lloyd-Williams, M. & Riddleston, H. (2002). The Stability of Depression Scores in Patients Who Are ReceivingPalliative Care. Journal of Pain and Symptom Management. Vol. 24, No. 6, 593 – 597.Mancini, R., L. (2008). Motor neuron disease research progress. Nova Biomedical Books:New York.Marcus, D., A. (2009). Chronic pain: a primary care guide to practical management. Humana Press, cop.: NewYork, NY.Maytal, G., Stern, T.A. 2006. The Desire for death in the setting of terminal illness: A case discussion. PrimaryCare Companion Journal of Psychiatry. Vol. 8. Issue 5.McLeod, J.E. & Clarke, D.M. (2007). A review of psychosocial aspects of motor neurone disease. Journal ofNeurological Science, 258 (1-2) 4-10Merskey, H. (1991). The Definition of Pain. European Psychiatry. Vol. 6, Issue 4. p.153-159Miller, R.G., Mitchell, J.D., Lyon, M., Moore, D.H. (2007). Riluzole for Amyotrophic Lateral Sclerosis(ALS)/Motor Neurone Disease (MND). Cochrane Database System Review. 2007 Jan 24; (1); CD1001447
  11. 11. Mitsumoto, H. (2009). Amyotrophic lateral sclerosis: a guide for patients and families. New York : DemosHealth.Moore, C., McDermott, C.J., Shaw, P.J. (2008). Clinical aspects of Motor Neurone Disease. Medicine. Vol. 36,Issue 12. P.640-645McLeod, J.E., Clark, D.M. (2007). A Review of psychosocial aspects of Motor Neurone Disease. Journal of theNeurological Sciences. Vol. 258 p.4-10Ng, L., Khan, F. & Mathers, S. (2009). Multidisciplinary Care for Adults with Amyotrophic Lateral Sclerosis orMotor Neuron Disease. Cochrane Database of Systematic Reviews: Issue 4, Art No. CD007425. The CochraneCollaboration. Pub by John Wiley & Sons, LtdSerpell, M. G. (2002). Gabapentin in Neuropathic Pain Syndromes: A Randomized, Double-Blind, Placebo-Controlled Trial. Pain. 99, 557 – 566.Stiel, S., Hollberg, C., Pestinger, M., Ostgathe, C., Friedemann, N., Lindena, G., Elsner, F., Radbruch, L. and theMembers of the HOPE Steering Group. (2011). Subjective Definitions of Problems and Symptoms in PalliativeCare. Palliative Care: Research and Treatment. 5, 1 – 7.Tang, N.K.Y., & Crane, C. (2006). Suicidality in chronic pain: a review of the prevalence, risk factors andpsychological links. Psychological Medicine. Vol. 36. P. 575-586Tedman, B.M., Young, C.A. & Williams, I.R. (1997). Assessment of depression in patients with motor neuronedisease and other neurologically disabiling illness. Journal of Neurological Sciences. 152. Supp 1:S75-9Terminal Illness Law & Legal Definition (2011). Retrieved on 13 th May 2011 from, D. F. & Dimsdale, J. E. (1990). Cultural Variations in Response to Painful Stimuli. PsychosomaticMedicine. 52: 544 – 557.