Delirium (PDQ®): Supportive care - Health Professional Information [NCI]

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Delirium

Definition

Delirium is a neuropsychiatric complication that can occur in patients with cancer, particularly in those with advanced disease. The prevention of delirium in the patient with cancer has not been systematically examined, but studies in hospitalized elderly patients suggest that early identification of risk factors reduces the occurrence rate of delirium and the duration of episodes.[1]

Delirium has been defined as a disorder of global cerebral dysfunction characterized by disordered awareness, attention, and cognition.[2] In addition, delirium is associated with behavioral manifestations. The text revision of the fourth edition of the Diagnostic and Statistical Manual for Mental Disorders (DSM-IV-TR) cites the core clinical criteria for diagnosis as follows:[3]

  • A disturbance of consciousness with reduced clarity of awareness and attention deficit.
  • Other cognitive or perceptual disturbances.
  • Acuity of onset (hours to days) and fluctuation over the course of the day.
  • The presence of an underlying cause such as a general medical condition (e.g., hypoxia or electrolyte disturbance), medication, a combination of etiologies, or indeterminate etiology.

Other associated noncore clinical criteria features include sleep-wake cycle disturbance, delusions, emotional lability, and disturbance of psychomotor activity. The latter forms the basis of classifying delirium into three different subtypes:[4,5]

1. Hypoactive.
2. Hyperactive.
3. Mixed, with both hypoactive and hyperactive features.

In this summary, unless otherwise stated, evidence and practice issues as they relate to adults are discussed. The evidence and application to practice related to children may differ significantly from information related to adults. When specific information about the care of children is available, it is summarized under its own heading.

References:

1. Inouye SK, Bogardus ST Jr, Charpentier PA, et al.: A multicomponent intervention to prevent delirium in hospitalized older patients. N Engl J Med 340 (9): 669-76, 1999.
2. Lipowski ZJ: Delirium in the elderly patient. N Engl J Med 320 (9): 578-82, 1989.
3. American Psychiatric Association.: Delirium, dementia, and amnestic and other cognitive disorders. In: American Psychiatric Association.: Diagnostic and Statistical Manual of Mental Disorders: DSM-IV-TR. 4th rev. ed. Washington, DC: American Psychiatric Association, 2000, pp 135-80.
4. Clinical features, course, and outcome. In: Lipowski ZJ: Delirium: Acute Confusional States. New York, NY: Oxford University Press, 1990, pp 54-70.
5. Camus V, Burtin B, Simeone I, et al.: Factor analysis supports the evidence of existing hyperactive and hypoactive subtypes of delirium. Int J Geriatr Psychiatry 15 (4): 313-6, 2000.

Impact of Delirium on Patient, Family, and Health Care Personnel

The clinical presentation of delirium is associated with a high level of distress in patients, family members, and health care personnel.[1,2,3] Delirium is associated with a high burden of symptom distress, particularly in relation to delusions, perceptual disturbances, and psychomotor agitation. Incontinence, falls, failure to maintain adequate hydration, a prolonged hospital stay, and death are more likely to occur in the patient with delirium.[4,5,6,7,8,9,10]

Dysfunctional cognition in the delirious patient hinders communication between patient and family and between patient and health care personnel. As a result, reliable symptom assessment, counseling, and active patient participation in the therapeutic decision-making process are all compromised.[11] Psychomotor agitation and emotional lability in the delirious patient may be misinterpreted as a presentation of increased pain expression.[12] Consequently, conflict over the needed level of analgesia can arise among the patient, family, and staff. A potentially destructive triangle can develop when the patient's family misinterprets agitation as increased pain and advocates for inappropriate escalation of opioid dosing.[13]

A psychosocial intervention for family caregivers of patients with advanced cancer may be beneficial in providing knowledge of delirium and detection rates and in increasing family caregiver self-confidence in decision making.[14]

References:

1. Breitbart W, Gibson C, Tremblay A: The delirium experience: delirium recall and delirium-related distress in hospitalized patients with cancer, their spouses/caregivers, and their nurses. Psychosomatics 43 (3): 183-94, 2002 May-Jun.
2. Morita T, Hirai K, Sakaguchi Y, et al.: Family-perceived distress from delirium-related symptoms of terminally ill cancer patients. Psychosomatics 45 (2): 107-13, 2004 Mar-Apr.
3. Cohen MZ, Pace EA, Kaur G, et al.: Delirium in advanced cancer leading to distress in patients and family caregivers. J Palliat Care 25 (3): 164-71, 2009.
4. Lawlor PG, Gagnon B, Mancini IL, et al.: Occurrence, causes, and outcome of delirium in patients with advanced cancer: a prospective study. Arch Intern Med 160 (6): 786-94, 2000.
5. Bruera E, Miller L, McCallion J, et al.: Cognitive failure in patients with terminal cancer: a prospective study. J Pain Symptom Manage 7 (4): 192-5, 1992.
6. Hogan DB: Revisiting the O complex: urinary incontinence, delirium and polypharmacy in elderly patients. CMAJ 157 (8): 1071-7, 1997.
7. O'Keeffe ST, Lavan JN: Clinical significance of delirium subtypes in older people. Age Ageing 28 (2): 115-9, 1999.
8. Lawlor PG: Delirium and dehydration: some fluid for thought? Support Care Cancer 10 (6): 445-54, 2002.
9. O'Keeffe S, Lavan J: The prognostic significance of delirium in older hospital patients. J Am Geriatr Soc 45 (2): 174-8, 1997.
10. Caraceni A, Nanni O, Maltoni M, et al.: Impact of delirium on the short term prognosis of advanced cancer patients. Italian Multicenter Study Group on Palliative Care. Cancer 89 (5): 1145-9, 2000.
11. Lawlor PG, Fainsinger RL, Bruera ED: Delirium at the end of life: critical issues in clinical practice and research. JAMA 284 (19): 2427-9, 2000.
12. Gagnon B, Lawlor PG, Mancini IL, et al.: The impact of delirium on the circadian distribution of breakthrough analgesia in advanced cancer patients. J Pain Symptom Manage 22 (4): 826-33, 2001.
13. Fainsinger RL, Tapper M, Bruera E: A perspective on the management of delirium in terminally ill patients on a palliative care unit. J Palliat Care 9 (3): 4-8, 1993 Autumn.
14. Gagnon P, Charbonneau C, Allard P, et al.: Delirium in advanced cancer: a psychoeducational intervention for family caregivers. J Palliat Care 18 (4): 253-61, 2002 Winter.

Incidence and Prevalence

Occurrence rates range from 28% to 48% in patients with advanced cancer on admission to hospital or hospice,[1,2,3] and approximately 85% to 90% of these patients will experience delirium in the hours to days before death.[3,4,5,6] The term acute confusional state has also been used to describe this syndrome; in the last days of life, the condition sometimes referred to as terminal restlessness probably represents a terminal delirium.[7]

Although delirium clearly has a recognized association with the dying phase, many episodes of delirium are reversible; therapeutic intervention can result in delirium reversal, or at least improvement, in 30% to 75% of episodes.[3,5,8,9,10,11] Variability in reported occurrence rates and clinical outcomes most likely reflects sampling from different clinical settings or different stages in the clinical trajectory of cancer, in addition to inconsistency in diagnostic terminology.[12]

References:

1. Minagawa H, Uchitomi Y, Yamawaki S, et al.: Psychiatric morbidity in terminally ill cancer patients. A prospective study. Cancer 78 (5): 1131-7, 1996.
2. Pereira J, Hanson J, Bruera E: The frequency and clinical course of cognitive impairment in patients with terminal cancer. Cancer 79 (4): 835-42, 1997.
3. Lawlor PG, Gagnon B, Mancini IL, et al.: Occurrence, causes, and outcome of delirium in patients with advanced cancer: a prospective study. Arch Intern Med 160 (6): 786-94, 2000.
4. Massie MJ, Holland J, Glass E: Delirium in terminally ill cancer patients. Am J Psychiatry 140 (8): 1048-50, 1983.
5. Bruera E, Miller L, McCallion J, et al.: Cognitive failure in patients with terminal cancer: a prospective study. J Pain Symptom Manage 7 (4): 192-5, 1992.
6. Breitbart W, Alici Y: Agitation and delirium at the end of life: "We couldn't manage him". JAMA 300 (24): 2898-910, E1, 2008.
7. Travis SS, Conway J, Daly M, et al.: Terminal restlessness in the nursing facility: assessment, palliation, and symptom management. Geriatr Nurs 22 (6): 308-12, 2001 Nov-Dec.
8. Gagnon P, Allard P, Mâsse B, et al.: Delirium in terminal cancer: a prospective study using daily screening, early diagnosis, and continuous monitoring. J Pain Symptom Manage 19 (6): 412-26, 2000.
9. Maddocks I, Somogyi A, Abbott F, et al.: Attenuation of morphine-induced delirium in palliative care by substitution with infusion of oxycodone. J Pain Symptom Manage 12 (3): 182-9, 1996.
10. Tuma R, DeAngelis LM: Altered mental status in patients with cancer. Arch Neurol 57 (12): 1727-31, 2000.
11. Breitbart W, Gibson C, Tremblay A: The delirium experience: delirium recall and delirium-related distress in hospitalized patients with cancer, their spouses/caregivers, and their nurses. Psychosomatics 43 (3): 183-94, 2002 May-Jun.
12. Lawlor PG: The panorama of opioid-related cognitive dysfunction in patients with cancer: a critical literature appraisal. Cancer 94 (6): 1836-53, 2002.

Etiology of Delirium

Delirium is often multifactorial, especially in the setting of advanced cancer. General etiologic factors include the following:[1,2,3,4,5,6,7,8,9,10]

  • Indirect central nervous system effects related to systemic complications of cancer such as organ failure (e.g., hepatic or renal failure), metabolic or electrolyte disturbance (e.g., hypoglycemia, hypercalcemia, hyponatremia, or dehydration), infection, and paraneoplastic syndromes (e.g., bulbar encephalitis).[11]
  • Exogenous substances such as the wide variety of medications and treatments used in these patients, including most of the commonly used chemotherapeutic agents,[12,13,14,15,16,17,18,19] bone marrow or stem cell transplantation, biological response modifiers (e.g., interleukin and interferon), glucocorticoids, and especially psychoactive agents such as opioid analgesics, antidepressants, benzodiazepines, antihistamines, and other sedating agents.
  • Withdrawal phenomena associated with substances such as alcohol and benzodiazepines.

Despite the very limited systematic study of risk factors for delirium in patients with cancer, risk factors have been identified in hospitalized elderly patients (some of them with cancer) and include the following:[20,21,22]

  • Severe illness.
  • Level of comorbidity.
  • Advanced age.
  • Prior dementia.
  • Hypoalbuminemia.
  • Infection.
  • Azotemia.
  • Psychoactive medications.

Studies of hospitalized elderly patients suggest that the level of risk is proportionate to the number of risk factors present.[23] Cancer is particularly prevalent in the elderly population. Many patients with cancer, particularly those with advanced disease, are likely to have a high level of baseline vulnerability. Such vulnerability leaves them predisposed to precipitants such as psychoactive medications.[24] It is also likely that the predictors of poor pain control in cancer patients (neuropathic pain, incidental pain, opioid tolerance, somatization, and a history of drug or alcohol abuse) result in higher opioid doses and thereby increase the risk of delirium.[25]

Distinct from delirium, older (65 years or older), long-term (>5 years) cancer survivors are also at increased risk of cognitive deficits and possibly dementia, as noted in a co-twin control design study of 702 Swedish cancer survivors.[10]

References:

1. Lawlor PG, Gagnon B, Mancini IL, et al.: Occurrence, causes, and outcome of delirium in patients with advanced cancer: a prospective study. Arch Intern Med 160 (6): 786-94, 2000.
2. Agostini JV, Leo-Summers LS, Inouye SK: Cognitive and other adverse effects of diphenhydramine use in hospitalized older patients. Arch Intern Med 161 (17): 2091-7, 2001 Sep 24.
3. Fann JR, Roth-Roemer S, Burington BE, et al.: Delirium in patients undergoing hematopoietic stem cell transplantation. Cancer 95 (9): 1971-81, 2002.
4. Prieto JM, Blanch J, Atala J, et al.: Psychiatric morbidity and impact on hospital length of stay among hematologic cancer patients receiving stem-cell transplantation. J Clin Oncol 20 (7): 1907-17, 2002.
5. Morita T, Tei Y, Tsunoda J, et al.: Underlying pathologies and their associations with clinical features in terminal delirium of cancer patients. J Pain Symptom Manage 22 (6): 997-1006, 2001.
6. Morita T, Tei Y, Tsunoda J, et al.: Increased plasma morphine metabolites in terminally ill cancer patients with delirium: an intra-individual comparison. J Pain Symptom Manage 23 (2): 107-13, 2002.
7. van Steijn JH, Nieboer P, Hospers GA, et al.: Delirium after interleukin-2 and alpha-interferon therapy for renal cell carcinoma. Anticancer Res 21 (5): 3699-700, 2001 Sep-Oct.
8. Walker LG, Walker MB, Heys SD, et al.: The psychological and psychiatric effects of rIL-2 therapy: a controlled clinical trial. Psychooncology 6 (4): 290-301, 1997.
9. Meyers CA, Albitar M, Estey E: Cognitive impairment, fatigue, and cytokine levels in patients with acute myelogenous leukemia or myelodysplastic syndrome. Cancer 104 (4): 788-93, 2005.
10. Heflin LH, Meyerowitz BE, Hall P, et al.: Cancer as a risk factor for long-term cognitive deficits and dementia. J Natl Cancer Inst 97 (11): 854-6, 2005.
11. Paraneoplastic syndromes. In: Posner JB: Neurologic Complications of Cancer. Philadelphia, Pa: FA Davis, 1995, pp 353-85.
12. Eberhardt B, Dilger S, Musial F, et al.: Short-term monitoring of cognitive functions before and during the first course of treatment. J Cancer Res Clin Oncol 132 (4): 234-40, 2006.
13. Hermelink K, Untch M, Lux MP, et al.: Cognitive function during neoadjuvant chemotherapy for breast cancer: results of a prospective, multicenter, longitudinal study. Cancer 109 (9): 1905-13, 2007.
14. Nelson CJ, Nandy N, Roth AJ: Chemotherapy and cognitive deficits: mechanisms, findings, and potential interventions. Palliat Support Care 5 (3): 273-80, 2007.
15. Taillibert S, Voillery D, Bernard-Marty C: Chemobrain: is systemic chemotherapy neurotoxic? Curr Opin Oncol 19 (6): 623-7, 2007.
16. Bender CM, Sereika SM, Brufsky AM, et al.: Memory impairments with adjuvant anastrozole versus tamoxifen in women with early-stage breast cancer. Menopause 14 (6): 995-8, 2007 Nov-Dec.
17. Stewart A, Collins B, Mackenzie J, et al.: The cognitive effects of adjuvant chemotherapy in early stage breast cancer: a prospective study. Psychooncology 17 (2): 122-30, 2008.
18. Chang EL, Wefel JS, Hess KR, et al.: Neurocognition in patients with brain metastases treated with radiosurgery or radiosurgery plus whole-brain irradiation: a randomised controlled trial. Lancet Oncol 10 (11): 1037-44, 2009.
19. Ahles TA, Saykin AJ, McDonald BC, et al.: Longitudinal assessment of cognitive changes associated with adjuvant treatment for breast cancer: impact of age and cognitive reserve. J Clin Oncol 28 (29): 4434-40, 2010.
20. Schor JD, Levkoff SE, Lipsitz LA, et al.: Risk factors for delirium in hospitalized elderly. JAMA 267 (6): 827-31, 1992.
21. O'Keeffe ST, Lavan JN: Predicting delirium in elderly patients: development and validation of a risk-stratification model. Age Ageing 25 (4): 317-21, 1996.
22. Elie M, Cole MG, Primeau FJ, et al.: Delirium risk factors in elderly hospitalized patients. J Gen Intern Med 13 (3): 204-12, 1998.
23. Inouye SK, Charpentier PA: Precipitating factors for delirium in hospitalized elderly persons. Predictive model and interrelationship with baseline vulnerability. JAMA 275 (11): 852-7, 1996.
24. Casarett DJ, Inouye SK; American College of Physicians-American Society of Internal Medicine End-of-Life Care Consensus Panel.: Diagnosis and management of delirium near the end of life. Ann Intern Med 135 (1): 32-40, 2001.
25. Fainsinger RL, Nekolaichuk CL, Lawlor PG, et al.: A multicenter study of the revised Edmonton Staging System for classifying cancer pain in advanced cancer patients. J Pain Symptom Manage 29 (3): 224-37, 2005.

Assessment, Diagnosis, and Monitoring

The diagnosis of delirium should be considered for any patient with cancer demonstrating an acute onset of agitation or uncooperative behavior, personality change, impaired cognitive functioning, altered attention span, fluctuating level of consciousness, or uncharacteristic anxiety or depression. However, the diagnoses of delirium and cognitive impairment are frequently missed and poorly documented.[1,2,3,4,5]

Medical and nursing staff, as well as family members, may attribute a functional cause to some of the early, prodromal, and more subtle signs of delirium such as increased anxiety, restlessness, and emotional lability.[6] Failure to recognize delirium is particularly likely if the patient is encountered in a transient lucid phase, which can commonly occur as part of the fluctuating nature of delirium.[7] Delirium is most frequently misdiagnosed as depression or dementia.[7,8,9,10] The hypoactive subtype is considered especially likely to be misdiagnosed as depression.[7]

Differentiating delirium from dementia or recognizing delirium superimposed on dementia can be difficult because of some shared clinical features such as disorientation and impairment of memory, thinking, and judgment.[11,12,13] However, dementia typically appears in relatively alert individuals; disturbance of consciousness is not a common feature. The temporal onset of symptoms of delirium is acute (hours to days), not insidious (months to years) as in dementia.[14] In elderly patients with cancer, delirium is often superimposed on dementia, giving rise to a particularly difficult diagnostic challenge. In this situation, the diagnosis may become more apparent when delirium fails to reverse or when some features of delirium, especially cognitive impairment, persist. Dementia is often then the most likely explanation for a persistent or residual cognitive deficit.[14]

Vigilance on the part of nursing staff and a systematic approach to recording serial observations assist in the detection of delirium. Regular cognitive screening facilitates the diagnosis of delirium in cancer patients.[15] Instruments such as the Mini-Mental State Examination (MMSE), Blessed Orientation Memory and Concentration Test (BOMC), and Confusion Assessment Method (CAM) have favorable psychometric properties and are brief enough to allow repeated administration in cancer patients.[16,17,18] The BOMC and MMSE screen for cognitive impairment and require active patient participation in assessment. The Bedside Confusion Scale also requires active patient participation; however, it is remarkably brief, and its psychometric potential as a screening instrument compares favorably with the CAM.[19] The CAM does not require formal patient participation. The Memorial Delirium Assessment Scale (MDAS) and Delirium Rating Scale-Revised-98 have been validated as having diagnostic and severity rating potential.[20,21] The MDAS allows prorating of scores when a patient cannot actively participate in testing for reasons such as dyspnea or fatigue.

References:

1. McCartney JR, Palmateer LM: Assessment of cognitive deficit in geriatric patients. A study of physician behavior. J Am Geriatr Soc 33 (7): 467-71, 1985.
2. Harwood DM, Hope T, Jacoby R: Cognitive impairment in medical inpatients. II: Do physicians miss cognitive impairment? Age Ageing 26 (1): 37-9, 1997.
3. Hustey FM, Meldon SW: The prevalence and documentation of impaired mental status in elderly emergency department patients. Ann Emerg Med 39 (3): 248-53, 2002.
4. Rincon HG, Granados M, Unutzer J, et al.: Prevalence, detection and treatment of anxiety, depression, and delirium in the adult critical care unit. Psychosomatics 42 (5): 391-6, 2001 Sep-Oct.
5. Inouye SK, Foreman MD, Mion LC, et al.: Nurses' recognition of delirium and its symptoms: comparison of nurse and researcher ratings. Arch Intern Med 161 (20): 2467-73, 2001.
6. Breitbart W, Chochinov HM, Passik S: Psychiatric aspects of palliative care. In: Doyle D, Hanks GW, MacDonald N, eds.: Oxford Textbook of Palliative Medicine. 2nd ed. New York, NY: Oxford University Press, 1998, pp 933-56.
7. Inouye SK: The dilemma of delirium: clinical and research controversies regarding diagnosis and evaluation of delirium in hospitalized elderly medical patients. Am J Med 97 (3): 278-88, 1994.
8. Nicholas LM, Lindsey BA: Delirium presenting with symptoms of depression. Psychosomatics 36 (5): 471-9, 1995 Sep-Oct.
9. Farrell KR, Ganzini L: Misdiagnosing delirium as depression in medically ill elderly patients. Arch Intern Med 155 (22): 2459-64, 1995 Dec 11-25.
10. Armstrong SC, Cozza KL, Watanabe KS: The misdiagnosis of delirium. Psychosomatics 38 (5): 433-9, 1997 Sep-Oct.
11. Fick D, Foreman M: Consequences of not recognizing delirium superimposed on dementia in hospitalized elderly individuals. J Gerontol Nurs 26 (1): 30-40, 2000.
12. Johnson J, Sims R, Gottlieb G: Differential diagnosis of dementia, delirium and depression. Implications for drug therapy. Drugs Aging 5 (6): 431-45, 1994.
13. Cole MG, McCusker J, Dendukuri N, et al.: Symptoms of delirium among elderly medical inpatients with or without dementia. J Neuropsychiatry Clin Neurosci 14 (2): 167-75, 2002 Spring.
14. Lipowski ZJ: Delirium in the elderly patient. N Engl J Med 320 (9): 578-82, 1989.
15. Bruera E, Miller L, McCallion J, et al.: Cognitive failure in patients with terminal cancer: a prospective study. J Pain Symptom Manage 7 (4): 192-5, 1992.
16. Folstein MF, Folstein SE, McHugh PR: "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res 12 (3): 189-98, 1975.
17. Inouye SK, van Dyck CH, Alessi CA, et al.: Clarifying confusion: the confusion assessment method. A new method for detection of delirium. Ann Intern Med 113 (12): 941-8, 1990.
18. Katzman R, Brown T, Fuld P, et al.: Validation of a short Orientation-Memory-Concentration Test of cognitive impairment. Am J Psychiatry 140 (6): 734-9, 1983.
19. Stillman MJ, Rybicki LA: The bedside confusion scale: development of a portable bedside test for confusion and its application to the palliative medicine population. J Palliat Med 3 (4): 449-56, 2000.
20. Trzepacz PT, Mittal D, Torres R, et al.: Validation of the Delirium Rating Scale-revised-98: comparison with the delirium rating scale and the cognitive test for delirium. J Neuropsychiatry Clin Neurosci 13 (2): 229-42, 2001 Spring.
21. Breitbart W, Rosenfeld B, Roth A, et al.: The Memorial Delirium Assessment Scale. J Pain Symptom Manage 13 (3): 128-37, 1997.

General Management Approach to Delirium

An integrated approach to management involves educating family members about the nature of the delirium syndrome and its potential treatment.[1,2,3] Family concerns, particularly the misinterpretation of symptoms such as agitation, emotional lability, and disinhibition, must be addressed. Depending on the clinical circumstances, guarded optimism regarding reversibility can be expressed. On the basis of discussion with family members, a consensus is then reached on the goals of care; this, in turn, will determine the desired and appropriate level of assessment and therapeutic intervention, which could be directed at identifying and treating underlying precipitants to reverse or improve delirium.[2] The extent of assessment will likely be influenced by the clinical setting, disease variables, and level of distress. It may therefore be appropriate in some situations to forego further assessment and focus solely on symptomatic treatment.

Regardless of the level of investigational or therapeutic aggression, symptomatic treatment is usually required for most patients. Monitoring and reassessment should be ongoing, particularly when pharmacological sedation is required to initially control symptoms.[4]

Nonpharmacologic Aspects of Symptom Management

Various environmental strategies have been proposed to reduce the symptomatic distress associated with delirium. These strategies include discrete efforts at reorientation such as a well-lit room with familiar objects, a visible clock or calendar, limited staff changes (and possibly one-on-one nursing care), reduced noise stimulation, and the presence of family.[5,6,7] Although some controversy surrounds the use of physical restraints, their judicious use may sometimes be necessary to prevent self-harm or physical aggression directed at caregivers.

Identification of Underlying Causes and Their Treatment

Delirium reversal is consistent with the goals of care; therefore, the standard management approach in patients with cancer is to search for and treat the reversible precipitants of delirium.[1,2] Although patients with cancer generally have a high level of baseline vulnerability to the development of delirium (owing to factors such as cachexia, hypoalbuminemia, advanced age, and prior dementia), the greatest therapeutic benefit is more likely to be derived from identifying and treating superimposed precipitants with relatively low-burden interventions such as discontinuation or dose reduction of psychoactive medications,[8] subcutaneous fluid administration via hypodermoclysis to treat dehydration, intravenous or subcutaneous bisphosphonate treatment of hypercalcemia, and possibly oral or intravenous antibiotics to treat infection.[9,10] This process typically involves a careful history and physical examination in addition to basic laboratory tests and imaging.[7] If no obvious precipitant is identified in preliminary searching, the decision to proceed with more invasive or elaborate tests is mainly determined by the goals of care.

Opioid analgesics, required for most patients with advanced disease, are among the psychoactive agents that precipitate delirium most frequently.[9,11] A prospective cohort study in an oncology inpatient population (n = 114) demonstrated that patients exposed to daily oral opioid doses higher than 90 mg of morphine or morphine equivalents were at significantly higher risk of developing delirium. These results are still significant when controlling for the effects of corticosteroids, benzodiazepines, and other psychotropic medications. However, this study did not provide enough data (on comorbidities, laboratory values, etc.) to determine which patients specifically were at risk for delirium when exposed to more than 90 mg of opioids per day.[12]

Patients with delirium should be assessed for other symptoms that suggest opioid neurotoxicity, for example, tactile hallucinations, agitation, myoclonus, allodynia, hyperalgesia, and possibly seizures. It is postulated that this toxic state relates to the accumulation of the parent opioid compound or its metabolites.[11,13] Intervention in the form of dose reduction or opioid switching in association with assisted hydration typically allows for clearing of the offending opioid or its metabolites.

On identifying opioid toxicity, therefore, it is important to search for other precipitants such as dehydration or infection.[14] A common clinical scenario consists of a patient with infection who may become drowsy, take less fluid, become dehydrated, and then exhibit signs of opioid toxicity, including delirium. Therapeutic intervention should target the triad of precipitants in this scenario. (Refer to the Opioid switching (Opioid rotation) section in the PDQ summary on Pain for more information.)

Symptomatic Management: The Role of Pharmacologic Agents

No pharmacological treatment has been approved by the U.S. Food and Drug Administration (FDA) for the treatment of delirium. Evidence and clinical experience suggest that antipsychotics play a major role in the treatment of delirium; however, only a few of these studies were conducted in patients with cancer. Antipsychotics are antidopaminergic agents and include typical antipsychotics such as haloperidol [7] and the newer atypical antipsychotic agents such as olanzapine, risperidone, and quetiapine.[15,16];[17][Level of evidence: I]

All antipsychotics presumably work by blocking the postsynaptic dopamine receptors, primarily in the mesolimbic region. However, simultaneous blockade of striatal dopamine receptors by these agents can cause extrapyramidal side effects (EPS) such as abnormal involuntary movements, akathisia, parkinsonian symptoms, and cogwheeling. The typical antipsychotics such as haloperidol carry a higher risk of EPS. The newer atypical antipsychotics have additional effects on the serotonin system that help reduce the EPS.

Antipsychotics have a complex mechanism of action with effects on several other neurotransmitter systems. Atypical antipsychotics have been associated with higher risk of weight gain and metabolic issues because of these effects on other neurotransmitter systems. All antipsychotics have been associated with anticholinergic side effects and negative effects on the cardiovascular and cerebrovascular systems, depending on the medication and dosing used.

Haloperidol, a neuroleptic agent with potent antidopaminergic properties, is still considered the drug of choice for the treatment of delirium in the patient with cancer;[1,7] however, the evidence remains limited. A double-blind trial of haloperidol, chlorpromazine, and lorazepam in the treatment of hospitalized patients with delirium and acquired immunodeficiency syndrome suggested that haloperidol and chlorpromazine were equivalent in efficacy, and both were associated with a low prevalence of EPS. Lorazepam, however, was ineffective and associated with adverse effects, resulting in early closure of this arm of the protocol.[18][Level of evidence: I] The optimal dose range of haloperidol for patients with delirium has not been determined. Consensus guidelines recommended initial doses in the range of 1 to 2 mg every 2 to 4 hours as needed and lower starting doses, such as 0.5 mg every 4 hours as needed, in elderly patients.[7]

Haloperidol can be administered orally, intravenously, subcutaneously, or intramuscularly. Parenteral doses are roughly twice as potent as oral doses. Peak plasma concentrations are achieved 2 to 4 hours after an oral dose, and measurable plasma concentrations occur 15 to 30 minutes after intramuscular administration. Haloperidol may cause fewer EPS when administered intravenously. The EPS can be treated with agents such as benztropine in doses of 1 to 2 mg once or twice a day. Neuroleptic malignant syndrome, a rare complication with haloperidol use, is characterized by hyperthermia, increased mental confusion, leukocytosis, muscular rigidity, myoglobinuria, and high serum creatinine phosphokinase. Injectable haloperidol is approved by the FDA only for intramuscular administration. However, it is frequently administered intravenously to treat agitated delirium.

Intravenous administration and higher doses of haloperidol have been associated with risk of sudden death due to Torsades de Pointes (TdP) and QTc prolongation. In this context, an FDA alert raised concerns about intravenous use of haloperidol.[19] The updated labeling of haloperidol includes a strong warning about the TdP and QTc prolongation issues, especially in patients with specific cardiovascular risk factors, and recommends consideration of alternative agents. The FDA alert also recommends extreme caution and close electrocardiogram monitoring if haloperidol is administered intravenously. The FDA alert is based on case reports and small case-control studies. There are no randomized studies investigating this issue, and the data from case reports and case-control studies are confounded by multiple factors (e.g., comorbid conditions and other agents known to cause QTc prolongation).[20]

Evidence suggests that QTc prolongation and TdP might be primarily associated with higher haloperidol doses (6 mg or higher). No cases of QTc prolongation or TdP have been reported with a cumulative intravenous dose smaller than 2 mg. The presence of certain risk factors might increase the risk of QTc prolongation and TdP. Major risk factors include the following:

  • Pre-existing heart disease.
  • Electrolyte imbalance.
  • Concomitant pro-arrhythmic agents and other agents affecting cardiac function.
  • Mechanical ventilation.
  • High baseline QTc (>450 msec).

Elderly patients, female patients, and patients with endocrine disorders (e.g., diabetes) may carry a higher risk of QTc and TdP. In patients with cancer, special attention should be paid to past or concomitant use of cardiotoxic chemotherapy regimens such as anthracycline-based regimens. Baseline and continuous ECG monitoring is recommended in patients receiving high doses of haloperidol and/or with known risk factors for developing QTc prolongation. Many of the alternatives (i.e., currently available typical and atypical antipsychotics) are also associated with QTc prolongation and TdP.[20]

In select cases, the risk-benefit equation might favor intravenous use of haloperidol, especially in patients with established intravenous access; in addition, no other currently available antipsychotics can be delivered intravenously. Before the newer atypical antipsychotics became available, chlorpromazine was considered an alternative to haloperidol, although it is associated with orthostatic hypotension and a greater level of sedation.

Among the atypical antipsychotics, olanzapine has been studied more extensively. In an open trial of 79 hospitalized cancer patients with delirium,[17] an oral formulation was used, with an initial dose range of 2.5 to 10 mg and a mean of 3 mg per dose in two daily doses. Seventy-six percent of patients had complete resolution of their delirium while taking olanzapine. No patients experienced EPS, but 30% experienced sedation, which was usually not severe enough to discontinue treatment. Predictors of a poor response included age older than 70 years, history of dementia, central nervous system involvement with cancer, hypoxia, hypoactive subtype, and delirium of severe intensity. Olanzapine is also reported to have antiemetic and possibly analgesic properties, although it is not used primarily for these indications.[21][Level of evidence: II]

Risperidone, another atypical antipsychotic, is also used extensively to treat delirium in clinical practice. In a single-blind randomized trial, the effectiveness of risperidone (n = 17) was compared with that of olanzapine (n = 15) for the treatment of delirium in patients with cancer. Both groups showed significant improvement in delirium as assessed by the Delirium Rating Scale. The response rates for improvement did not differ between the two groups. At the last observation, the mean dose of risperidone was 0.9 mg per day and that of olanzapine was 2.4 mg per day.[22] Risperidone is available in oral tablet and liquid formulations; dosing begins at 0.5 to 1 mg per day in two divided daily doses that are titrated, if necessary, to a total daily dose of 4 to 6 mg per day.

Other atypical antipsychotics—specifically, quetiapine [23] and aripiprazole [24]—have limited evidence in the treatment of delirium. The lack of an available parenteral formulation for any of the atypical antipsychotics is a disadvantage, especially in the context of agitated delirium.

Except for lorazepam and midazolam in selected situations, benzodiazepines are generally not recommended for the treatment of delirium.[7] Lorazepam is a short-acting agent, and its use is largely reserved for the treatment of alcohol or benzodiazepine withdrawal. Lorazepam (0.5–1 mg orally or parenterally, every 1–2 hours) has also been used along with haloperidol in patients with delirium who are particularly sensitive to EPS. Another exception is midazolam, a very short-acting benzodiazepine, which is given by continuous subcutaneous or intravenous infusion in doses ranging from 30 to 100 mg over 24 hours. Midazolam is used to achieve deep sedation, especially in a terminal hyperactive or mixed delirium when agitation is refractory to other treatments, for example, doses of haloperidol in the region of 20 mg per day.

The decision to use a deep level of pharmacologically induced sedation in the treatment of agitated delirium often raises ethical concerns, fueled by the marked variability in the reported frequency (ranging from 10% to 52%) for this practice in patients dying from advanced cancer. Consistent with the goals of care, it is important that appropriate efforts are made to assess the reversibility of delirium, clarify the intent of sedation (the relief of refractory symptoms), and maintain clear communication with family members and health care team members regarding rationale and process.[2,4] (Refer to the Sedation for Refractory Delirium and Other Intractable Symptoms section of this summary for more information.)

Some preliminary evidence suggests that the hypoactive subtype of delirium is less responsive to neuroleptic treatment.[17] Although psychostimulants have been proposed for the treatment of hypoactive delirium,[25][Level of evidence: III];[26][Level of evidence: II] little empirical evidence attests to their benefit. In a prospective clinical study of 14 patients with advanced cancer and hypoactive delirium, patients demonstrated improvement in cognitive function after receiving 20 to 50 mg of methylphenidate hydrochloride per day.[27][Level of evidence: III] Relatively higher doses of stimulants (>10 mg of methylphenidate) should be used with caution in delirious patients because such doses can contribute to the unmasking of paranoia and confusion and can lead to agitation. Clinical experience suggests that psychostimulants should be avoided in the presence of hallucinations or delusions.[2]

Sedation for Refractory Delirium and Other Intractable Symptoms

Delirium at the end of life often requires a pharmacological sedative approach. This issue cannot be considered in isolation from the ethical dilemma that it evokes. The need to sedate terminally ill patients for poorly controlled symptoms that include delirium, pain, dyspnea, and psychological effects has been reported frequently.[28,29,30,31];[32,33][Level of evidence: III] Although clinical experience suggests that good palliative care can effectively manage the symptoms of most cancer patients, patients may experience symptoms that can be termed "refractory."[34] Although sedative drugs are a therapeutic option, the incidence of these refractory situations in advanced cancer patients is controversial. This highlights the need to distinguish between "difficult" and "refractory" symptoms. A clear understanding of the terminology describing sedation and sedative medications is necessary; however, the extent to which sedation has been used for managing agitated delirium is difficult to clarify because of inconsistent definitions and confusing terminology.[35,36] Nevertheless, agitated behavior requiring sedation that is variously described as delirium, terminal restlessness, mental anguish, and agitation is a recurring theme in the literature.[37]

A systematic review of the definitions of sedation for symptom relief noted a marked variation in the literature.[36] A sedation definition was proposed to include two core factors:

  • Presence of severe suffering refractory to standard palliative management.
  • Use of sedative medications with the primary aim of relieving distress.

This review defined palliative sedation as "the use of sedative medications to relieve intolerable and refractory distress by the reduction in patient consciousness." The identified inconsistencies in the definition of sedation (i.e., primary versus secondary, light versus deep, and intermittent versus continuous sedation) should be subcategories of palliative sedation.[36]

The use of palliative sedation for psychosocial and existential symptoms can be particularly controversial. Many ethical and clinical questions can arise for the clinician—questions that are more easily resolved in the case of palliative sedation for pain and physical symptoms.

For example, the ethical basis for the use of terminal sedation (double effect) is less clearly applicable in the case of psychiatric symptoms. Under this principle, the intended effect (relieving psychological suffering) would be considered allowable as long as any risks or negative effects (i.e., shortened survival) are unintended by the professional. Difficulty arises here because the principle discusses only the professional's intention, when it is the patient's intention that can be unclear and potentially problematic. Is the depressed patient who no longer wants to suffer depressive symptoms asking only for that relief, or is it also the patient's intent to ask the professional to shorten his or her life? Clinicians who feel uncomfortable in such situations might want to seek guidance from their ethics committees.

Other difficult questions can arise from the potentially negative value that is culturally assigned to "zoning out" as a lower form of coping. Should the anxious patient who no longer wants to face the anxiety associated with the end of life and desires sedation be encouraged to work through such issues? Or is it allowable for the anxiety of such patients to be handled with sedation? How many alternatives should be tried before anxiety is considered unacceptable? When dealing with such requests, professionals should consider their own cultural and religious biases and the cultural and/or religious backgrounds of patients and their families.

Few studies detail the use of terminal sedation for psychiatric symptoms. Four palliative care programs in Israel, South Africa, and Spain participated in one survey.[38][Level of evidence: III] One unique study has described the Japanese palliative care experience around these issues.[39,40][Level of evidence: II]

Noting the limitations of surveys and retrospective chart reviews,[41,42] researchers have completed prospective studies to determine the use of sedation for uncontrolled symptoms in terminally ill patients. Four palliative care programs with inpatient units in Israel, South Africa, and Spain reported that 97 out of 387 patients (25%) required sedation.[38] In 59 of the 97 patients (60%), sedation was used for refractory delirium, with midazolam being the most common medication prescribed. A study of similar design in Canada reported that 80% of 150 patients developed delirium prior to death.[43] Of the 150 patients, 9 required sedation for refractory delirium. A retrospective study at the MD Anderson Cancer Center in Houston included 1,207 patients admitted to the palliative care unit. Palliative sedation was used in 15% of admissions. The most common indications were delirium (82%) and dyspnea (6%). Sedation in these circumstances is often used on a temporary basis and was reversible in 23% of this group of patients.[44] An Italian study of 2,033 patients showed that 83 patients required palliative sedation, most frequently for dyspnea (37%) and delirium (31%).[45][Level of evidence: III]

The relatively short period between onset of sedation and death has been consistently reported as 1 to 6 days.[37] It has been noted, however, that palliative care patients who have delirium and appear extremely ill may still have treatable, reversible complications.[46,47,48,49]

Various medications have been utilized for palliative sedation.[50,51] These include benzodiazepines (midazolam), phenothiazines (chlorpromazine), butyrophenones (haloperidol), anaesthetic agents (propofol), and barbiturates. Midazolam is the drug most frequently reported as useful because of its rapid onset and ease of titration. Choice of medication is often determined by clinician preference and/or institutional policy.

Given the common association between delirium and sedation, it is important to have some understanding of the extensive literature on the ethical validity of using sedation management.[37] Numerous articles have addressed the importance of the double-effect argument as applied to the practice of sedation in palliative care. The concept of the double effect distinguishes between the compelling primary intent to relieve suffering and the unavoidable consequence of potentially accelerating death.[37] Legal opinions tend to support the doctrine of double effect as a major ethical foundation for the distinction between palliative care and euthanasia.[52] One study proposed physician intent, proportionality, and autonomy as the ethical principles relevant to palliative sedation therapy. A prospective study of 102 palliative care patients in 21 (out of 56) palliative care units in Japan found that these principles were generally followed when continuous deep palliative sedation therapy was used, supporting the ethical validity of these decisions.[39] The following principles have been recommended as a decision-making guide for sedation for refractory delirium:[37,53,54]

1. The designation of a refractory problem should follow repeat assessments by skilled clinicians familiar with palliative care. Appropriate assessment and management should be completed in the context of a relationship with the patient and family. Other palliative care clinicians should be consulted if necessary.
2. The need for a sedative management approach should ideally be evaluated during a team conference to avoid individual clinician bias or burnout.
3. If sedation is considered appropriate and reasonable, temporary sedation should be considered.
4. A multidisciplinary assessment of the family should ensure that their views are adequately assessed and understood.

Some families may need continuous information and professional guidance when palliative sedation is used, and this need increases with the duration of the sedation. Individuals or groups outside the family and health care team may have strong opinions about palliative sedation and may offer unsolicited guidance that conflicts with what the patient desires. Concerns identified in a study conducted in The Netherlands relate to the following:[55]

  • Aim of continuous sedation.
  • Patient well-being.
  • Family well-being.

Current Clinical Trials

Check NCI's list of cancer clinical trials for U.S. supportive and palliative care trials about cognitive/functional effects that are now accepting participants. The list of trials can be further narrowed by location, drug, intervention, and other criteria.

General information about clinical trials is also available from the NCI Web site.

References:

1. Breitbart W, Chochinov HM, Passik S: Psychiatric aspects of palliative care. In: Doyle D, Hanks GW, MacDonald N, eds.: Oxford Textbook of Palliative Medicine. 2nd ed. New York, NY: Oxford University Press, 1998, pp 933-56.
2. Lawlor PG, Fainsinger RL, Bruera ED: Delirium at the end of life: critical issues in clinical practice and research. JAMA 284 (19): 2427-9, 2000.
3. Gagnon P, Charbonneau C, Allard P, et al.: Delirium in advanced cancer: a psychoeducational intervention for family caregivers. J Palliat Care 18 (4): 253-61, 2002 Winter.
4. Lawlor PG, Bruera ED: Delirium in patients with advanced cancer. Hematol Oncol Clin North Am 16 (3): 701-14, 2002.
5. McCusker J, Cole M, Abrahamowicz M, et al.: Environmental risk factors for delirium in hospitalized older people. J Am Geriatr Soc 49 (10): 1327-34, 2001.
6. Meagher DJ, O'Hanlon D, O'Mahony E, et al.: The use of environmental strategies and psychotropic medication in the management of delirium. Br J Psychiatry 168 (4): 512-5, 1996.
7. Practice guideline for the treatment of patients with delirium. American Psychiatric Association. Am J Psychiatry 156 (5 Suppl): 1-20, 1999.
8. Gaudreau JD, Gagnon P, Harel F, et al.: Psychoactive medications and risk of delirium in hospitalized cancer patients. J Clin Oncol 23 (27): 6712-8, 2005.
9. Lawlor PG, Gagnon B, Mancini IL, et al.: Occurrence, causes, and outcome of delirium in patients with advanced cancer: a prospective study. Arch Intern Med 160 (6): 786-94, 2000.
10. Sagawa R, Akechi T, Okuyama T, et al.: Etiologies of delirium and their relationship to reversibility and motor subtype in cancer patients. Jpn J Clin Oncol 39 (3): 175-82, 2009.
11. Lawlor PG: The panorama of opioid-related cognitive dysfunction in patients with cancer: a critical literature appraisal. Cancer 94 (6): 1836-53, 2002.
12. Gaudreau JD, Gagnon P, Roy MA, et al.: Opioid medications and longitudinal risk of delirium in hospitalized cancer patients. Cancer 109 (11): 2365-73, 2007.
13. Morita T, Tei Y, Tsunoda J, et al.: Increased plasma morphine metabolites in terminally ill cancer patients with delirium: an intra-individual comparison. J Pain Symptom Manage 23 (2): 107-13, 2002.
14. Lawlor PG: Delirium and dehydration: some fluid for thought? Support Care Cancer 10 (6): 445-54, 2002.
15. Adityanjee, Schulz SC: Clinical use of quetiapine in disease states other than schizophrenia. J Clin Psychiatry 63 (Suppl 13): 32-8, 2002.
16. Tune L: The role of antipsychotics in treating delirium. Curr Psychiatry Rep 4 (3): 209-12, 2002.
17. Breitbart W, Tremblay A, Gibson C: An open trial of olanzapine for the treatment of delirium in hospitalized cancer patients. Psychosomatics 43 (3): 175-82, 2002 May-Jun.
18. Breitbart W, Marotta R, Platt MM, et al.: A double-blind trial of haloperidol, chlorpromazine, and lorazepam in the treatment of delirium in hospitalized AIDS patients. Am J Psychiatry 153 (2): 231-7, 1996.
19. US Food and Drug Administration.: FDA Alert (September 17, 2007): Information for Healthcare Professionals: Haloperidol (marketed as Haldol, Haldol Decanoate and Haldol Lactate). Rockville, Md: Food and Drug Administration, Center for Drug Evaluation and Research, 2007. Available online. Last accessed October 8, 2013.
20. Hassaballa HA, Balk RA: Torsade de pointes associated with the administration of intravenous haloperidol. Am J Ther 10 (1): 58-60, 2003 Jan-Feb.
21. Khojainova N, Santiago-Palma J, Kornick C, et al.: Olanzapine in the management of cancer pain. J Pain Symptom Manage 23 (4): 346-50, 2002.
22. Kim SW, Yoo JA, Lee SY, et al.: Risperidone versus olanzapine for the treatment of delirium. Hum Psychopharmacol 25 (4): 298-302, 2010.
23. Kim KY, Bader GM, Kotlyar V, et al.: Treatment of delirium in older adults with quetiapine. J Geriatr Psychiatry Neurol 16 (1): 29-31, 2003.
24. Boettger S, Friedlander M, Breitbart W, et al.: Aripiprazole and haloperidol in the treatment of delirium. Aust N Z J Psychiatry 45 (6): 477-82, 2011.
25. Morita T, Otani H, Tsunoda J, et al.: Successful palliation of hypoactive delirium due to multi-organ failure by oral methylphenidate. Support Care Cancer 8 (2): 134-7, 2000.
26. Platt MM, Breitbart W, Smith M, et al.: Efficacy of neuroleptics for hypoactive delirium. J Neuropsychiatry Clin Neurosci 6 (1): 66-7, 1994 Winter.
27. Gagnon B, Low G, Schreier G: Methylphenidate hydrochloride improves cognitive function in patients with advanced cancer and hypoactive delirium: a prospective clinical study. J Psychiatry Neurosci 30 (2): 100-7, 2005.
28. Fainsinger RL, Tapper M, Bruera E: A perspective on the management of delirium in terminally ill patients on a palliative care unit. J Palliat Care 9 (3): 4-8, 1993 Autumn.
29. Caraceni A: Delirium in palliative medicine. European Journal of Palliative Care 2 (2): 62-7, 1995.
30. MacLeod AD: The management of delirium in hospice practice. European Journal of Palliative Care 4 (4): 116-20, 1997.
31. Bergevin P, Bergevin RM: Recognizing delirium in terminal patients. Am J Hosp Palliat Care 13 (2): 28-9, 1996 Mar-Apr.
32. Twycross RG: Symptom control: The problem areas. Palliat Med 7 (Suppl 1): 1-8, 1993.
33. Rietjens JA, van Zuylen L, van Veluw H, et al.: Palliative sedation in a specialized unit for acute palliative care in a cancer hospital: comparing patients dying with and without palliative sedation. J Pain Symptom Manage 36 (3): 228-34, 2008.
34. Cherny NI, Portenoy RK: Sedation in the management of refractory symptoms: guidelines for evaluation and treatment. J Palliat Care 10 (2): 31-8, 1994 Summer.
35. Macleod AD: Use of sedatives in palliative medicine. Palliat Med 11 (6): 493-4, 1997.
36. Morita T, Tsuneto S, Shima Y: Definition of sedation for symptom relief: a systematic literature review and a proposal of operational criteria. J Pain Symptom Manage 24 (4): 447-53, 2002.
37. Fainsinger RL: Treatment of delirium at the end of life: Medical and ethical issues. In: Portenoy RK, Bruera E, eds.: Topics in Palliative Care. Volume 4. New York, NY: Oxford University Press, 2000, pp 261-77.
38. Fainsinger RL, Waller A, Bercovici M, et al.: A multicentre international study of sedation for uncontrolled symptoms in terminally ill patients. Palliat Med 14 (4): 257-65, 2000.
39. Morita T, Chinone Y, Ikenaga M, et al.: Ethical validity of palliative sedation therapy: a multicenter, prospective, observational study conducted on specialized palliative care units in Japan. J Pain Symptom Manage 30 (4): 308-19, 2005.
40. Morita T, Chinone Y, Ikenaga M, et al.: Efficacy and safety of palliative sedation therapy: a multicenter, prospective, observational study conducted on specialized palliative care units in Japan. J Pain Symptom Manage 30 (4): 320-8, 2005.
41. Chater S, Viola R, Paterson J, et al.: Sedation for intractable distress in the dying--a survey of experts. Palliat Med 12 (4): 255-69, 1998.
42. Fainsinger RL, Landman W, Hoskings M, et al.: Sedation for uncontrolled symptoms in a South African hospice. J Pain Symptom Manage 16 (3): 145-52, 1998.
43. Fainsinger RL, De Moissac D, Mancini I, et al.: Sedation for delirium and other symptoms in terminally ill patients in Edmonton. J Palliat Care 16 (2): 5-10, 2000 Summer.
44. Elsayem A, Curry Iii E, Boohene J, et al.: Use of palliative sedation for intractable symptoms in the palliative care unit of a comprehensive cancer center. Support Care Cancer 17 (1): 53-9, 2009.
45. Caraceni A, Zecca E, Martini C, et al.: Palliative sedation at the end of life at a tertiary cancer center. Support Care Cancer 20 (6): 1299-307, 2012.
46. Fainsinger RL, Bruera E: Is this opioid analgesic tolerance? J Pain Symptom Manage 10 (7): 573-7, 1995.
47. Fainsinger RL: Use of sedation by a hospital palliative care support team. J Palliat Care 14 (1): 51-4, 1998 Spring.
48. de Stoutz ND, Tapper M, Fainsinger RL: Reversible delirium in terminally ill patients. J Pain Symptom Manage 10 (3): 249-53, 1995.
49. Dunlop RJ: Is terminal restlessness sometimes drug induced? Palliat Med 3: 65-6, 1989.
50. Rousseau PC: Palliative sedation. Am J Hosp Palliat Care 19 (5): 295-7, 2002 Sep-Oct.
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Changes to This Summary (01 / 09 / 2013)

The PDQ cancer information summaries are reviewed regularly and updated as new information becomes available. This section describes the latest changes made to this summary as of the date above.

This summary was extensively revised and renamed from Cognitive Disorders and Delirium.

This summary is written and maintained by the PDQ Supportive and Palliative Care Editorial Board, which is editorially independent of NCI. The summary reflects an independent review of the literature and does not represent a policy statement of NCI or NIH. More information about summary policies and the role of the PDQ Editorial Boards in maintaining the PDQ summaries can be found on the About This PDQ Summary and PDQ NCI's Comprehensive Cancer Database pages.

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Purpose of This Summary

This PDQ cancer information summary for health professionals provides comprehensive, peer-reviewed, evidence-based information about the pathophysiology and treatment of delirium. It is intended as a resource to inform and assist clinicians who care for cancer patients. It does not provide formal guidelines or recommendations for making health care decisions.

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This summary is reviewed regularly and updated as necessary by the PDQ Supportive and Palliative Care Editorial Board, which is editorially independent of the National Cancer Institute (NCI). The summary reflects an independent review of the literature and does not represent a policy statement of NCI or the National Institutes of Health (NIH).

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The lead reviewers for Delirium are:

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