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Brief Summary

GUIDELINE TITLE

Control of pain in adults with cancer. A national clinical guideline.

BIBLIOGRAPHIC SOURCE(S)

  • Scottish Intercollegiate Guidelines Network (SIGN). Control of pain in adults with cancer. A national clinical guideline. Edinburgh (Scotland): Scottish Intercollegiate Guidelines Network (SIGN); 2008 Nov. 71 p. (SIGN publication; no. 106). [264 references]

GUIDELINE STATUS

** REGULATORY ALERT **

FDA WARNING/REGULATORY ALERT

Note from the National Guideline Clearinghouse: This guideline references a drug(s) for which important revised regulatory and/or warning information has been released.

  • December 16, 2008 - Antiepileptic drugs: The U.S. Food and Drug Administration (FDA) has completed its analysis of reports of suicidality (suicidal behavior or ideation [thoughts]) from placebo-controlled clinical trials of drugs used to treat epilepsy, psychiatric disorders, and other conditions. Based on the outcome of this review, FDA is requiring that all manufacturers of drugs in this class include a Warning in their labeling and develop a Medication Guide to be provided to patients prescribed these drugs to inform them of the risks of suicidal thoughts or actions. FDA expects that the increased risk of suicidality is shared by all antiepileptic drugs and anticipates that the class labeling change will be applied broadly.

BRIEF SUMMARY CONTENT

 ** REGULATORY ALERT **
 RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Note from the Scottish Intercollegiate Guidelines Network (SIGN) and National Guideline Clearinghouse (NGC): In addition to these evidence-based recommendations, the guideline development group also identifies points of best clinical practice in the full-text guideline document.

The grades of recommendations (A–D) and levels of evidence (1++, 1+, 1-, 2++, 2+, 2-, 3, 4) are defined at the end of the "Major Recommendations" field.

Psychosocial Issues

Psychological Distress

B - Comprehensive chronic pain assessment should include routine screening for psychological distress.

A - Cognitive behaviour therapy should be considered as part of a comprehensive treatment programme for those with cancer related pain and resulting distress and disability.

Psychological Factors and Adherence to Treatment

D - Patient beliefs concerning pain should be assessed and discussed as part of a comprehensive, biopsychosocial cancer pain assessment.

C - Patients should receive education about the range of pain control interventions available to them.

Assessment of Pain

What is Pain?

For the purposes of this guideline, pain has been defined as "an unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage."

A comprehensive assessment of pain should consider the following domains:

  • Physical effects/manifestations of pain
  • Functional effects (interference with activities of daily living)
  • Psychological factors (level of anxiety, cultural influences, fears, effects on interpersonal relationships, factors affecting pain tolerance, (see Table below)
  • Spiritual aspects

Table. Factors Affecting Pain Tolerance

Aspects That Lower Pain Tolerance Aspects That Raise Pain Tolerance

Discomfort

Insomnia

Fatigue

Anxiety

Fear

Anger

Boredom

Sadness

Depression

Introversion

Social abandonment

Mental isolation

Relief of symptoms

Sleep

Rest, or paradoxically, physiotherapy

Relaxation therapy

Explanation/support

Understanding/empathy

Diversional activity

Companionship/listening

Elevation of mood

Understanding of the meaning and significance of the pain

Social inclusion

Encouragement to express emotions

Adapted from Twycross R, Lack S. Symptom control in far advanced cancer: pain relief London: Pitman; 1983.

Why Assess Pain?

D - Prior to treatment an accurate assessment should be performed to determine the cause, type and severity of pain, and its effect on the patient.

Who Should Assess Pain?

D - The patient should be the prime assessor of his or her pain.

How Should Pain Be Assessed?

D - Patients with cancer pain should have treatment outcomes monitored regularly using visual analogue scales, numerical rating scales or verbal rating scales.

C - Self assessment pain scales should be used in patients with cognitive impairment, where feasible.

C - Observational pain rating scales should be used in patients who cannot complete a self assessment scale.

Principles of Pain Management

B - Patients should be given information and instruction about pain and pain management and be encouraged to take an active role in their pain management.

World Health Organization (WHO) Cancer Pain Relief Programme

D - The principles of treatment outlined in the WHO cancer pain relief programme should be followed when treating pain in patients with cancer.

Using the WHO Analgesic Ladder

B - A patient's treatment should start at the step of the WHO analgesic ladder appropriate for the severity of the pain.

B - Prescribing of analgesia should always be adjusted as the pain severity alters.

D - Analgesia for continuous pain should be prescribed on a regular basis, not 'as required'.

D - Appropriate analgesia for breakthrough pain must be prescribed.

Treatment with Non-Opioid Drugs

Paracetamol and Non-Steroidal Anti-Inflammatory Drugs

A - Patients at all stages of the WHO analgesic ladder should be prescribed paracetamol and/or a non-steroidal anti-inflammatory drug unless contraindicated.

A - Patients taking non-steroidal anti-inflammatory drugs who are at high risk of gastrointestinal complications should be prescribed either misoprostol 800 mcg/day, standard dose proton pump inhibitors or double dose histamine-2 receptor antagonists as pharmacological prophylaxis.

Bisphosphonates

B - Bisphosphonates should be considered as part of the therapeutic regimen for the treatment of pain in patients with metastatic bone disease.

Antidepressants and Anticonvulsants

A - Patients with neuropathic pain should be given either a tricyclic antidepressant (e.g., amitriptyline or imipramine) or anticonvulsant (e.g., gabapentin, carbamazepine or phenytoin) with careful monitoring of side effects.

Cannabinoids

A - Cannabinoids are not recommended for the treatment of cancer pain.

Treatment with Opioid Drugs

Choice of Opioid

Mild to Moderate Pain (Step 2 of the WHO Ladder)

D - For mild to moderate pain, (score 3-6 out of 10 on a visual analogue scale or a numerical rating scale) weak opioids such as codeine should be given in combination with a non-opioid analgesic.

Moderate to Severe Pain (Step 3 of the WHO Ladder)

D - Oral morphine is recommended as first line therapy to treat severe pain in patients with cancer.

D - Diamorphine is recommended as first line subcutaneous therapy to treat severe pain in patients with cancer.

Breakthrough Pain

D - Patients with moderate or severe breakthrough pain should receive breakthrough analgesia.

D - When using oral morphine for breakthrough pain the dose should be one sixth of the around the clock morphine dose and should be increased appropriately whenever the around the clock dose is increased.

Patients with Renal Impairment

C - In the presence of reduced kidney function all opioids should be used with caution and at reduced doses and/or frequency.

Administration of Opioids

D - Continuous subcutaneous infusion of opioids is simpler to administer and equally as effective as continuous intravenous infusion and should be considered for patients unable to take opioids orally.

D - Advice on stability of commonly used drug combinations for continuous subcutaneous infusion should be available to staff who prepare these infusions.

D - Advice on the use of other combinations should be taken from palliative care specialists.

D - Patients with stable pain on oral morphine should be prescribed a once or twice daily modified release preparation.

D - Patients with stable pain on oral oxycodone should be prescribed a twice daily modified release preparation.

Non-Pharmacological Treatment

Radiotherapy for Relieving Pain in Patients with Bone Metastases

B - All patients with pain from bone metastases which is proving difficult to control by pharmacological means should be referred to a clinical oncologist for consideration of external beam radiotherapy or radioisotope treatment.

Cementoplasty

D - Patients with bone pain from malignant vertebral collapse proving difficult to control by pharmacological means should be referred for consideration of vertebroplasty where this technique is available.

D - Patients with bone pain from pelvic bone metastases proving difficult to control by pharmacological means and reduced mobility should be considered for percutaneous cementoplasty.

Anaesthetic Interventions

B - Interventions such as coeliac plexus block and neuraxial opioids should be considered to improve pain control and quality of life in patients with difficult to control cancer pain.

Definitions:

Levels of Evidence

1++: High quality meta-analyses, systematic reviews of randomised controlled trials (RCTs), or RCTs with a very low risk of bias

1+: Well-conducted meta-analyses, systematic reviews, or RCTs with a low risk of bias

1-: Meta-analyses, systematic reviews, or RCTs with a high risk of bias

2++: High quality systematic reviews of case control or cohort studies

High quality case control or cohort studies with a very low risk of confounding or bias and a high probability that the relationship is causal

2+: Well-conducted case control or cohort studies with a low risk of confounding or bias and a moderate probability that the relationship is causal

2-: Case control or cohort studies with a high risk of confounding or bias and a significant risk that the relationship is not causal

3: Non-analytic studies (e.g., case reports, case series)

4: Expert opinion

Grades of Recommendation

Note: The grade of recommendation relates to the strength of the evidence on which the recommendation is based. It does not reflect the clinical importance of the recommendation.

A: At least one meta-analysis, systematic review, or RCT rated as 1++ and directly applicable to the target population; or

A body of evidence consisting principally of studies rated as 1+, directly applicable to the target population, and demonstrating overall consistency of results

B: A body of evidence including studies rated as 2++, directly applicable to the target population, and demonstrating overall consistency of results; or

Extrapolated evidence from studies rated as 1++ or 1+

C: A body of evidence including studies rated as 2+, directly applicable to the target population and demonstrating overall consistency of results; or

Extrapolated evidence from studies rated as 2++

D: Evidence level 3 or 4; or

Extrapolated evidence from studies rated as 2+

Good Practice Points: Recommended best practice based on the clinical experience of the guideline development group

CLINICAL ALGORITHM(S)

None provided

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The specific type of supporting evidence is explicitly identified in each section of the guideline.

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • Scottish Intercollegiate Guidelines Network (SIGN). Control of pain in adults with cancer. A national clinical guideline. Edinburgh (Scotland): Scottish Intercollegiate Guidelines Network (SIGN); 2008 Nov. 71 p. (SIGN publication; no. 106). [264 references]

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

2000 Jun (revised 2008 Nov)

GUIDELINE DEVELOPER(S)

Scottish Intercollegiate Guidelines Network - National Government Agency [Non-U.S.]

SOURCE(S) OF FUNDING

Scottish Executive Health Department

GUIDELINE COMMITTEE

Not stated

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Guideline Development Group: Professor John Welsh, Professor of Palliative Medicine, (Chair) Beatson Oncology Centre, Glasgow; Dr Esther Murray, Consultant Clinical Psychologist in Psychosocial Oncology, Ayrshire Central Hospital; Dr Lesley Colvin, Consultant Anaesthetist, Western General Hospital, Edinburgh; Ms Marguerite Connolly, District Nursing Sister, NHS Grampian; Dr Paul Cormie, MacMillan Lead General Practitioner (Cancer and Palliative Care), NHS Borders; Dr David Craig, Consultant Clinical Psychologist, Southern General Hospital, Glasgow; Dr John Currie, Consultant Anaesthetist, Royal Hospital for Sick Children, Glasgow; Professor Marie Fallon, St Columba's Hospice Chair of Palliative Medicine, Institute of Genetics and Molecular Medicine, Edinburgh Cancer Research Centre, Western General Hospital, Edinburgh; Dr Graeme Giles, Consultant in Palliative Medicine, Strathcarron Hospice, Denny; Mr Adam Gillespie, Lay Representative, Glasgow; Reverend Tom Gordon, Chaplain, Marie Curie Hospice, Edinburgh; Mr Robin Harbour, Quality and Information Director, SIGN; Dr Derek Jones, Lecturer in Occupational Therapy, Queen Margaret University, Edinburgh; Ms Linda Kerr, Clinical Nurse Specialist in Palliative Care, Ayr Hospital; Ms Alison MacRobbie, Palliative/Community Care Pharmacist, NHS Highland; Ms Jane Mair, Community Cancer Support Nurse, Inverurie; Dr Moray Nairn, Programme Manager, SIGN; Dr Kathleen Sherry, Consultant in Palliative Medicine, The Ayrshire Hospice, Ayr; Ms Janet Trundle, Macmillan Specialist Pharmacist in Palliative Care, NHS Greater Glasgow and Clyde; Ms Gillian Wilson, Lay Representative, Dunbar

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

All members of the guideline development group made declarations of interest and further details of these are available on request from the Scottish Intercollegiate Guidelines Network (SIGN) Executive.

GUIDELINE STATUS

GUIDELINE AVAILABILITY

AVAILABILITY OF COMPANION DOCUMENTS

The following are available:

PATIENT RESOURCES

The following is available:

Please note: This patient information is intended to provide health professionals with information to share with their patients to help them better understand their health and their diagnosed disorders. By providing access to this patient information, it is not the intention of NGC to provide specific medical advice for particular patients. Rather we urge patients and their representatives to review this material and then to consult with a licensed health professional for evaluation of treatment options suitable for them as well as for diagnosis and answers to their personal medical questions. This patient information has been derived and prepared from a guideline for health care professionals included on NGC by the authors or publishers of that original guideline. The patient information is not reviewed by NGC to establish whether or not it accurately reflects the original guideline's content.

NGC STATUS

This summary was completed by ECRI on January 3, 2002. The information was verified by the guideline developer as of February 4, 2002. This summary was updated on May 3, 2005 following the withdrawal of Bextra (valdecoxib) from the market and the release of heightened warnings for Celebrex (celecoxib) and other nonselective nonsteroidal anti-inflammatory drugs (NSAIDs). This summary was updated by ECRI on May 20, 2005, following the U.S. Food and Drug Administration advisory on Aredia (pamidronate disodium) and Zometa (zoledronic acid). This summary was updated by ECRI on June 16, 2005, following the U.S. Food and Drug Administration advisory on COX-2 selective and non-selective non-steroidal anti-inflammatory drugs (NSAIDs). This summary was updated by ECRI Institute on January 29, 2009. The updated information was verified by the guideline developer on February 4, 2009. This summary was updated by ECRI Institute on May 1, 2009 following the U.S. Food and Drug Administration advisory on antiepileptic drugs.

COPYRIGHT STATEMENT

DISCLAIMER

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