Medical Management for Neuropathic Pain at Left L5 Level
First-line treatment for neuropathic pain at the left L5 level should begin with either pregabalin/gabapentin or a secondary amine tricyclic antidepressant (TCA) such as nortriptyline or desipramine. 1
First-Line Medications
Gabapentinoids
- Pregabalin is FDA-approved for neuropathic pain management, including pain associated with spinal cord injury 2
- Start pregabalin at 100-300 mg at night, gradually increasing to 900-3600 mg/day in 2-3 divided doses 1
- Pregabalin binds to the α-2-δ subunit of voltage-gated calcium channels, inhibiting the release of excitatory neurotransmitters 1
- Gabapentin is an alternative to pregabalin, with similar efficacy but different pharmacokinetics 1
Antidepressants
- Secondary amine TCAs (nortriptyline, desipramine) are preferred over tertiary amines due to fewer anticholinergic side effects 1
- Start TCAs at low doses (10 mg/day), especially in older adults, and titrate slowly to a maximum of 75 mg/day 1
- Obtain a screening ECG for patients over 40 years before starting TCAs due to potential cardiac risks 1
- Selective serotonin-norepinephrine reuptake inhibitors (SNRIs) like duloxetine (60-120 mg/day) and venlafaxine (150-225 mg/day) are effective alternatives with fewer anticholinergic effects 1
Topical Treatments for Localized Pain
- Consider 5% lidocaine patches for localized peripheral neuropathic pain, particularly with allodynia 1
- High-concentration capsaicin patches may be beneficial for localized neuropathic pain 1
- 1% menthol cream can be applied twice daily to the affected area and corresponding dermatomal region of the spine 1
Treatment Algorithm
- Start with either pregabalin/gabapentin OR a secondary amine TCA (nortriptyline/desipramine) 1
- Allow at least 2-4 weeks at therapeutic dose to properly assess efficacy 1
- If partial response is achieved, add another first-line agent from a different class 1
- If inadequate response to first-line agents, consider second-line treatments 1
Second-Line Medications
- Tramadol (200-400 mg in two or three doses) has a dual mechanism as a weak μ-opioid agonist and inhibits serotonin/norepinephrine reuptake 1
- Start tramadol at 50 mg once or twice daily, with a maximum dose of 400 mg/day, and use lower doses in older adults and those with renal/hepatic dysfunction 1
- Strong opioids should be used in the smallest effective dose and only when other options have failed 1
Special Considerations for L5 Neuropathic Pain
- Lumbosacral radiculopathy may be relatively refractory to existing first- and second-line medications compared to other neuropathic pain conditions 3
- Recent trials of nortriptyline, morphine, and their combination, as well as pregabalin showed limited efficacy in lumbosacral radiculopathy 3
- Patients with failed back surgery syndrome, many of whom have lumbosacral radiculopathy, may respond to spinal cord stimulation when medications are ineffective 1
Combination Therapy
- A fixed-dose combination of low-dose pregabalin and duloxetine has shown similar efficacy to high-dose pregabalin monotherapy with potentially fewer side effects 4
- The combination achieved similar analgesia with comparable rates of dizziness and somnolence, but less peripheral edema than high-dose pregabalin alone 4
Monitoring and Side Effects
- Most common side effects of pregabalin/gabapentin include dizziness, somnolence, and peripheral edema 4
- TCAs can cause anticholinergic adverse effects including dry mouth, orthostatic hypotension, constipation, and urinary retention 1
- SNRIs commonly cause nausea, which can be minimized by starting at a lower dose (e.g., duloxetine 30 mg daily) for one week 1
- Adjust gabapentinoid doses in patients with renal impairment 1
Treatment-Resistant Cases
- If trials of first-line medications alone and in combination fail, consider tramadol or opioid analgesics 1
- For refractory cases, especially with lumbosacral radiculopathy, referral for consideration of spinal cord stimulation may be appropriate 1
- Low-dose naltrexone (1.5-4.5 mg) has shown some efficacy in treatment-resistant neuropathic pain conditions 3