Table 1
Screening and Initial Assessment
Recommendation |
Commentary/Details |
Standardized screening |
- How much bodily pain have you had during the last week (none, very mild, mild, moderate, severe, very severe)
- Do you have bodily pain that has lasted for >3 months?
- A response of moderate pain or more during last week plus bodily pain for >3 months can be considered a positive screen result
|
If patient screens positive on initial assessment |
- Use biopsychosocial approach that includes:
- An evaluation of the pain’s —
- Onset and duration
- Intensity and character
- Exacerbating and alleviating factors
- Past and current treatments
- Underlying or co-occurring disorders and conditions
- The effect of pain on psychological function
- Physical examination
- Psychosocial evaluation
- Diagnostic workup
- Pain assessment tools can include
- Brief Pain Inventory (BPI)
- 3-item pain health questionnaire (PEG)
|
Monitoring patients |
- Periodically assess progress on achieving functional goals
- Documentation of pain intensity, quality of life, adverse events, and adherent vs aberrant behaviors
- Conduct assessments at regular intervals and after each change/initiation of therapy after an adequate amount of time
|
Table 2
Nonpharmacologic Approaches for PLWH
Modality |
Features, Rationale |
CBT |
- Acceptance of responsibility for change
- Development of adaptive behaviors (eg. exercise)
- Addressing maladaptive behaviors (eg, avoidance of exercise due to fear of pain)
|
Yoga |
- Treatment of chronic neck/back pain, headache, rheumatoid arthritis, general musculoskeletal pain
|
Physical/occupational therapy |
|
Hypnosis |
|
Acupuncture |
- A trial might be considered for chronic pain
|
CBT=cognitive behavioral therapy
Table 3
Pharmacologic Treatments for Chronic Neuropathic Pain in PLWH
Treatment |
Recommendations |
Antiretroviral therapy |
- Early initiation recommend for preventing/treating HIV-associated distal symmetric polyneuropathy
|
Gabapentin |
- First-line oral pharmacologic treatment
- Typical adult regimen titrates to 2400mg/day in 2 divided doses
- Improves sleep scores, somnolence
- Patients with inadequate response might receive
- Trial of SNRIs
- Trial of TCAs
- Trial of pregabalin for patients with post-herpetic neuralgia
|
Medical cannabis |
- May be effective in appropriate patients
- Relatively high value placed on symptoms reduction, relatively low value placed on legal implication of medical cannabis possession
- May be more effective for patients with prior cannabis use
- Balance potential benefits against potential risks of neuropsychiatric adverse effects
- Balance potential benefit against harmful effects of smoked forms in patients with preexisting severe lung disease
- Balance risks of addiction in patients with cannabis use disorder
|
Alpha lipoic acid |
- For peripheral difficult-to-treat neuropathic pain
- May be helpful for patients with diabetic neuropathy
|
Lamotrigine |
- Not recommended
- May cause lamotrigine-related rash
|
Opioid analgesics |
- Do not use as first-line agents
- Potential risk of pronociception, cognitive impairment, respiratory depression, endocrine/immunological changes, misuse/addiction
- Consider time-limited trial for patients who do not respond to first-line therapies and report moderate-to-severe pain
- Use smallest effective dose
- Combine short- and long-acting opioids
|
HIV=human immunodeficiency virus; SNRI-serotonin-norepinephrine reuptake inhibitors; TCS=tricyclic antidepressant
Table 4
Opioid Analgesics for PLWH
Agent |
Comments/Rationale |
Opioids as a class |
- Balance potential benefits with potential risks of adverse events, misuse, diversion, and addiction
- As second- or third-line treatment, typical adult regimen should start with lowest effective dose and combine short- and long-acting opioids
|
Tramadol |
- Up to 3 months of use
- May decrease pain and improve stiffness, function, overall well-being in patients with osteoarthritis
- Use 37.5mg combined with 325mg of acetaminophen once/day to 400mg in divided doses
|
Table 5
Safeguarding Against Opioid-Related Harm
Recommendation |
Comments/Rationale |
Routine monitoring |
- Consists of several components
- Urine drug testing
- Pill counts
- Prescription drug monitoring programs
|
Opioid patient-provider agreement (PPA) |
- Tool for shared decision-making
- Consists of 2 components
- Informed consent
- Plan of care
- Consider broad differential diagnosis when patient’s behavior is inconsistent with PPA
|
Urine drug testing |
- Understand clinical uses/limitations
- Understand test characteristics
- Understand differential diagnosis of abnormal results
|
Table 6
Recommended Methods to Minimize Adverse Opioid-Related Events in PLWH
Recommendation |
Comments/Details |
Safe storage |
- Store safely away from individuals at risk of misuse/overdose
|
Patient/family education |
- Educate family members about overdose signs
- Have poison control number readily visible
- Teach patients/caregivers about use of naloxone to reverse overdose and have naloxone rescue kit available
- Educate patients/caregivers about adverse effects related to drug-drug interactions
|
Be knowledgeable about drug-drug interactions |
- Be prepared to identify/manage these interactions
- Follow patients closely when interactions are likely
|
Table 7
Pharmacologic Management of Chronic Pain in PLWH Who Are Taking Methadone
Recommendation |
Comments/Details |
Collaboration with opioid treatment program |
- Obtain signed release
- Maintain ongoing communication with program for assessment/periodic monitoring
|
Initial screening |
- Electrocardiogram to identify QTc interval prolongation
- Helpful if patient is taking other medications that may additively prolong QTc interval
|
Splitting methadone doses |
- Divide into 6- to 8-hour doses
- Some programs may offer split-dose regimen, alternatively medical provider may need to prescribe remaining doses
|
If additional methadone not possible |
- Additional medication alternatives
- Gabapentin for neuropathic pain
- NSAIDs for musculoskeletal pain
- Additional opioid
|
Acute exacerbations of pain (“breakthrough”) |
- Use small amount of short-acting opioids
|
Table 8
Treating PLWH and Chronic Pain Who Are Taking Buprenorphine
Recommendation |
Comments/Details |
Use adjuvant therapy for mild-to-moderate breakthrough pain |
- Includes nonpharmacologic treatments, steroids, nonopioid analgesics, and topical agents
|
Increase dosage of buprenorphine |
- Increase in divided doses as an initial step
|
If maximal dose of burprenorphine is reached |
- Add long-acting potent opiod (eg, fentanyl, morphine, hydromorphone)
|
If additional opioid is ineffective |
- Closely monitor trial of higher doses
|
If there is inadequate analgesia |
- Transition patient to methadone maintenance
|
Table 9
Recommended Instruments for Screening Common Mental Health Disorders in PLWH and Chronic Pain
Recommendation |
Comments/Details |
Review patient’s baseline mental status for modifiable risk factors |
- Self-esteem/coping skills
- Recent major loss/grief
- Unhealthy substance use
- History of violence/lack of safety in the home
- Mood disorders
- Serious mental illness/suicidal ideation
|
Screen patients for depression |
- 2-question screen
- During past 2 weeks have you been bothered by feeling down, depressed, hopeless?
- During past 2 weeks have you had little interest/pleasure in doing things?
- If affirmative, ask if patient would like help
|
Use screening tool |
- Patient Health Questionnaire-9 (PHQ-9) recommended
|
Screen for comorbid neurocognitive disorders |
- Includes frequent memory loss, slower reasoning, planning activities, or solving problems, difficulties paying attention
|
Neuropsychiatric evaluation |
- Recommended for all patients with chronic pain to establish baseline capacity
|
Reference
- Bruce RD, Merlin J, Lum PJ, Ahmed E, Alexander C, Corbett AH, Foley K, LeonardK, Treisman GJ, Selwyn P.2017 HIV Medicine Association of Infectious Diseases Society of America Clinical Practice Guideline for the Management of Chronic Pain in Patients Living With Human Immunodeficiency Virus. Clin Infect Dis. 2017 Oct 30;65(10):1601-1606.