Chronic Pain

Treatment

Procedures for Chronic Back Pain | Dr. Martinez de la Maza | Neurosurgery

Advanced Interventional Solutions When Conservative Treatment Is Not Enough

Dr. Ernesto Martinez de la Maza
Neurosurgery • Spine Surgery

💚 Chronic Pain Does Not Have to Be Your New Normal

If you have lived with back pain for months or years, trying multiple treatments without meaningful relief, I deeply understand your frustration and exhaustion. Chronic pain does not only affect your body; it impacts your work, your relationships, your mood, and your ability to enjoy life.

However, there is a spectrum of modern interventional procedures that can offer significant and lasting relief without the need for major surgery. These procedures sit between conservative treatment (medications, physical therapy) and fusion surgery, offering a valuable intermediate option.

Do not resign yourself to pain. Let us explore together which options may be appropriate for your specific situation.

When Are Interventional Procedures Appropriate?

Procedures for chronic pain occupy an important space between conservative treatment and major surgery.

Interventional procedures for spinal pain are indicated when:

Many of these patients have herniated disc and spinal stenosis as the source of their pain.

✅ Ideal Candidates

  • Persistent pain: More than 3-6 months despite appropriate conservative treatment
  • Identifiable source: A specific anatomical source of the pain (facets, discs, compressed nerves)
  • No severe neurological deficit: No progressive weakness or loss of sphincter control
  • Alternative to surgery: The patient is not a candidate for, or wishes to avoid, major surgery
  • Failure of conservative care: Medications, physical therapy, and simple injections do not provide sufficient relief
  • Quality of life affected: Pain significantly limits daily activities and work

❌ When They Are Not Appropriate

  • Acute spinal cord compression: Requires urgent surgical decompression
  • Severe spinal instability: Requires surgical fusion
  • Progressive neurological deficit: Worsening weakness requires surgery
  • Predominantly psychogenic pain: Without a clear anatomical correlation
  • Unrealistic expectations: Procedures improve but rarely eliminate pain 100%
  • Active infection: A contraindication for invasive procedures

💡 The Spinal Pain Treatment Ladder

The modern approach to back pain follows a progressive therapeutic ladder:

Step 1: Conservative Treatment (6-12 weeks)

  • Anti-inflammatory medications and analgesics
  • Physical therapy and therapeutic exercise
  • Activity modification and ergonomics
  • Complementary therapies (acupuncture, massage)

Step 2: Diagnostic Procedures (If conservative care fails)

  • Selective blocks to identify the source of the pain
  • Diagnostic epidural injections
  • Provocative discography (in selected cases)

Step 3: Therapeutic Procedures (If diagnostics are positive)

  • Radiofrequency rhizotomy
  • Repeated therapeutic injections
  • Spinal cord stimulation
  • Intrathecal pumps for severe pain

Step 4: Minimally Invasive or Open Surgery

  • Neural decompression (if compression is present)
  • Spinal fusion (if instability is present)
  • Artificial disc replacement (selected cases)

When fusion surgery is required, there are surgical spine treatments appropriate for each case.

Interventional procedures sit at Steps 2 and 3, offering options before considering major surgery. The key is to select the correct procedure for each patient's specific problem.

Diagnostic vs. Therapeutic Procedures

A fundamental concept: some procedures are performed first to diagnose the source of the pain before definitive therapeutic procedures.

🔍 Diagnostic Procedures

Goal: To precisely identify the anatomical structure generating the pain.

Why are they necessary?

Imaging (MRI, CT) shows anatomy but does not always identify the source of the pain. Many degenerative changes are asymptomatic. Diagnostic blocks use a local anesthetic to temporarily "switch off" a specific structure.

Examples:

  • Medial branch block: For facet pain
  • Nerve root block: To identify the root causing radiculopathy
  • Sinuvertebral nerve block: For discogenic pain
  • Provocative discography: To confirm the disc as the source of pain

Interpretation:

If the block provides >50-75% temporary pain relief, it confirms that this structure is the source and justifies a therapeutic procedure at that location.

💊 Therapeutic Procedures

Goal: To provide lasting pain relief through the destruction of painful nerves, reduction of inflammation, or neuromodulation.

Characteristics:

They are performed after diagnostic procedures confirm the source of the pain. They seek long-term relief (months to years).

Examples:

  • Radiofrequency rhizotomy: After positive medial branch blocks
  • Epidural steroid injections: To reduce radicular inflammation
  • Spinal cord stimulation: For chronic radicular pain
  • Intrathecal pump: For severe refractory pain

Duration of effect:

Variable depending on the procedure: epidurals (weeks-months), rhizotomy (6-24 months), spinal cord stimulation (years), intrathecal pump (indefinite with refills).

⚠️ Why Not "Skip" Directly to Therapeutic Procedures

Some patients ask: "Why not perform the rhizotomy directly without diagnostic blocks?"

Important reasons:

  • Precision: Diagnostic blocks confirm that we are treating the correct source of the pain
  • Predicting response: Relief with blocks predicts the success of the therapeutic procedure
  • Avoiding unnecessary procedures: If blocks do not help, the therapeutic procedure probably will not help either
  • Ethically and medically appropriate: The established standard of care in pain medicine

In some cases (e.g., epidurals for acute radiculopathy), procedures can be diagnostic AND therapeutic at the same time.

Image-Guided Nerve Blocks and Injections

Precise procedures that use fluoroscopy (real-time X-ray) or ultrasound to deliver medications exactly where they are needed.

Main Types of Blocks and Injections

💉 Epidural Injections

What they are: Injection of local anesthetic + corticosteroid into the epidural space (around the spinal cord/nerve roots).

Indications:

  • Herniated disc with radiculopathy
  • Spinal stenosis
  • Post-surgical radicular pain

Approaches:

  • Interlaminar (between laminae)
  • Transforaminal (through the neural foramen)
  • Caudal (through the sacral hiatus)

Outpatient 30 minutes

🎯 Facet Joint Blocks

What they are: Injection into the facet joints (small joints between vertebrae).

Indications:

  • Mechanical axial low back pain
  • Pain that worsens with extension
  • Confirmed facet joint arthritis

Types:

  • Intra-articular: Inside the facet joint
  • Medial branch block: On the nerves that innervate the facets (diagnostic prior to rhizotomy)

Diagnostic Therapeutic

🧭 Selective Nerve Root Blocks

What they are: Injection targeted at a specific nerve root.

Goals:

  • Diagnostic: Identify which root is causing symptoms when there are multiple compressions
  • Therapeutic: Reduce inflammation of a specific root

Special value:

  • Before surgery: confirm the correct level
  • Multiple herniations: identify which one is symptomatic

Precision Fluoroscopy-guided

💡 How Are These Procedures Performed?

Preparation:

  • Outpatient procedure, generally no fasting required
  • Positioning on the fluoroscopy table (face down for lumbar, on the side for cervical)
  • Skin sterilization, sterile drapes
  • Local anesthetic in the skin

During the procedure:

  • Real-time fluoroscopy to guide the needle with millimeter precision
  • Contrast injection to confirm correct positioning
  • Administration of medications (typically anesthetic + corticosteroid)
  • Duration: 15-45 minutes depending on complexity

After the procedure:

  • Observation for 30-60 minutes
  • May go home the same day with a companion
  • Avoid driving for 24 hours
  • Normal activities the next day, generally

Expected Effects and Duration

Type of Procedure Immediate Relief (anesthetic) Lasting Relief (corticosteroid) Typical Duration Repetitions
Lumbar Epidural Hours 2-7 days later 6 weeks - 6 months Series of 3 max/year
Cervical Epidural Hours 3-7 days later 4-12 weeks Series of 3 max/year
Facet Joint Block Hours 1-2 weeks later 1-6 months 3-4 times/year
Medial Branch Block Hours (diagnostic) Not applicable (diagnostic) Diagnostic only 1-2 for confirmation
Nerve Root Block Hours 3-10 days later 4-12 weeks 2-3 times/year

⚠️ Risks of Blocks and Injections

Although generally safe, these procedures carry risks that should be considered:

Common Risks (Mild)

  • Temporary pain at the injection site (very common)
  • Transient worsening of pain (2-3 days)
  • Mild headache
  • Temporary nausea
  • Facial flushing (corticosteroid effect)

Rare Risks (Serious)

  • Infection (1 in 1000-5000)
  • Bleeding/epidural hematoma (very rare)
  • Dural puncture with persistent headache
  • Neurological damage (extremely rare)
  • Allergic reaction to medications

Minimizing risks: Sterile technique, fluoroscopy for precision, physician experience, pre-procedure evaluation of coagulation.

Radiofrequency Rhizotomy: Interrupting Pain Signals

A procedure that uses heat generated by radiofrequency waves to selectively lesion the nerves that transmit pain, providing lasting relief.

Radiofrequency rhizotomy (RFR), also called radiofrequency ablation or neurotomy, is one of the most effective procedures for chronic lumbar and cervical facet pain that does not respond to conservative treatment.

🎯 The Fundamental Concept of Rhizotomy

The facet joints of the spine are innervated by small nerves called medial branches. When these joints are the source of pain (facet joint arthritis), these nerves constantly transmit pain signals to the brain.

Rhizotomy interrupts this transmission by creating a small thermal lesion in the nerve, effectively "disconnecting" it. The nerve can eventually regenerate (which is why the procedure is not permanent), but this takes 6-24 months, providing a prolonged period of relief.

How Is Radiofrequency Rhizotomy Performed?

Step 1: Diagnostic Confirmation

CRITICAL: Before performing a rhizotomy, two separate diagnostic medial branch blocks must be performed, with at least 50-75% pain relief from each one. This confirms that the facets are the source of the pain.

  • First block: With a short-acting anesthetic (lidocaine)
  • Second block: With a long-acting anesthetic (bupivacaine)
  • A positive response to both: A predictor of rhizotomy success

Step 2: The Day of the Procedure

Preparation:

  • Outpatient procedure under conscious sedation (optional) or local anesthesia only
  • Positioning on the fluoroscopy table
  • Sterilization and sterile drapes

Technique:

  • Special radiofrequency needles are placed next to the medial branches under fluoroscopic guidance
  • Typically 4-6 nerves are treated (2-3 levels, bilateral)
  • Sensory stimulation to confirm correct positioning (the patient feels tingling)
  • Motor stimulation to ensure we are away from motor nerves
  • Local anesthetic at each site
  • Application of radiofrequency energy: 80-90°C for 60-90 seconds per nerve

Step 3: After the Procedure

Immediate recovery:

  • Observation for 30-60 minutes
  • Discharge home the same day
  • Pain at the injection sites (normal, may last 1-2 weeks)
  • Possible temporary worsening of back pain

Timeline of improvement:

  • Weeks 1-2: There may be more pain (inflammation from the thermal lesion)
  • Weeks 2-4: Gradual relief begins
  • Weeks 4-8: Maximum benefit generally reached
  • Months 6-24: Period of lasting relief

Expected Results

✅ Candidates with Good Results

  • Excellent response to blocks:>75% relief with diagnostics
  • Pure facet pain: No significant discogenic or radicular component
  • Confirmed facet joint arthritis: On imaging
  • Age >40 years: Statistically better response
  • Predominantly axial pain: In the back itself, not the legs
  • No prior surgery: Or fusion far from the treated level

⚠️ Factors for Suboptimal Response

  • Partial response to blocks: 25-50% relief
  • Mixed pain: Facet + discogenic component
  • Recent fusion surgery: At adjacent levels
  • Predominantly neuropathic pain: Burning, electric
  • Psychosocial factors: Severe depression, active litigation
  • Very high BMI: Makes precise localization difficult

📊 Success Statistics for Radiofrequency Rhizotomy

Based on rigorous scientific studies:

  • Positive response rate: 60-80% of well-selected patients
  • >50% relief: 70-80% at 3 months
  • >50% relief: 50-60% at 12 months
  • Average duration: 9-12 months (range 6-24 months)
  • Repeat procedures: Similar success rate if the first one worked

Important: Rhizotomy improves pain; it rarely eliminates it completely. A 50-70% reduction in pain is considered an excellent success that significantly restores quality of life.

⚠️ Potential Complications of Rhizotomy

Common and benign:

  • Pain at the injection site (nearly universal, 1-2 weeks)
  • Temporary worsening of back pain (30-40%, resolves in 2-4 weeks)
  • Temporary muscle spasm
  • Superficial hematoma at the puncture site

Rare but important:

  • Neuritis (nerve pain) persisting >4-6 weeks (2-5%)
  • Numbness in the nerve's distribution area
  • Transient muscle weakness (very rare with correct technique)
  • Infection (extremely rare, <0.1%)

Why might a rhizotomy fail?

  • The facets were not the true source of the pain
  • Anatomical variation of the nerve
  • Inadequate thermal lesion (technique)
  • Pain from multiple sources (only one was treated)

Spinal Cord Stimulation: Advanced Neuromodulation

A revolutionary technology that modifies pain signals before they reach the brain, offering relief for conditions that do not respond to other treatments.

Spinal cord stimulation (SCS) represents a paradigm shift in the treatment of chronic pain. Instead of trying to eliminate the source of the pain (surgery) or block its transmission (medications), SCS modifies how the brain perceives pain signals.

🧠 The Gate Control Theory of Pain

SCS is based on the theory proposed by Melzack and Wall in 1965: there is a "gate" in the spinal cord that controls which signals reach the brain. By stimulating the cord with gentle electrical pulses, we can "close the gate" to pain signals while allowing normal signals through.

It is like rubbing an area after bumping it - the tactile stimulation competes with and reduces the perception of pain.

Who Are Candidates for SCS?

Main Indications

  • Failed Back Surgery Syndrome (FBSS): Persistent or recurrent pain after spine surgery
  • Refractory pain: Includes cases of chronic pain without an evident structural cause.
  • Chronic radiculopathy: Leg pain that does not respond to treatment, without the need for decompressive surgery
  • Neuropathic limb pain: Diabetic neuropathy, CRPS (complex regional pain syndrome)
  • Peripheral artery disease: With ischemic limb pain
  • Refractory angina: Cardiac pain that does not respond to medical treatment

✅ Selection Criteria

To be a candidate for SCS, the patient must meet:

  • Chronic pain >6 months: Persistent despite appropriate treatment
  • Neuropathic predominance: Burning, electric, or tingling type pain
  • Appropriate anatomy: No need for urgent decompressive surgery
  • Favorable psychological evaluation: No untreated severe depression
  • Successful trial:>50% relief during the trial period
  • Realistic expectations: Understands that it improves pain, it does not eliminate it

❌ Contraindications

  • Active neural compression: Requires surgical decompression
  • Active infection: Systemic or local
  • Coagulation disorders: Uncorrected
  • Severe psychiatric illness: Untreated
  • Substance abuse: Active and untreated
  • Need for frequent MRIs: Some systems are not MRI-conditional
  • Pacemaker/defibrillator: Requires special evaluation

Spinal Cord Stimulation Technologies

📡 Traditional (Tonic) SCS

Characteristics:

  • Frequency: 40-60 Hz
  • Sensation: Paresthesias (tingling) in the painful area
  • First generation, well established
  • Relatively simple programming

Effective Traditional

⚡ High-Frequency SCS (HF10)

Characteristics:

  • Frequency: 10,000 Hz
  • Sensation: NO paresthesias (subthreshold)
  • Better for back and leg pain
  • Studies show superiority vs. traditional SCS

New Generation No Paresthesias

🔄 Burst SCS

Characteristics:

  • Bursts of pulses in a specific pattern
  • Sensation: Minimal or no paresthesias
  • Mimics natural neuronal patterns
  • Effective for the emotional component of pain

Innovative Selective

The SCS Implantation Process

Phase 1: Trial Period - 5-7 days

Goal: To determine whether the stimulation relieves your pain BEFORE implanting the permanent system.

Procedure:

  • Under conscious sedation or local anesthesia
  • 1-2 thin electrodes (leads) are placed in the epidural space under fluoroscopic guidance
  • Positioning is adjusted with patient feedback
  • The leads are connected to an external stimulator worn on a belt
  • Discharge home the same day

During the trial:

  • Keep a diary of pain and activities
  • Test different programs with the manufacturer's representative
  • Assess relief during activities of daily living

Success criterion:>50% reduction in pain and/or significant improvement in function.

Reversible No Commitment

Phase 2: Permanent Implantation (If trial is successful)

Procedure:

  • Generally under general anesthesia or deep sedation
  • Two small incisions: in the back (for the leads) and in the flank/buttock (for the generator)
  • Permanent leads are placed in the epidural space at the optimal position identified during the trial
  • The pulse generator (IPG) is implanted under the skin in the buttock or abdomen area
  • Extension cables connect the leads to the IPG under the skin
  • Duration: 1-2 hours
  • Hospitalization: typically 23 hours (day of surgery + the following morning)

Phase 3: Living with SCS

Recovery:

  • Activity restrictions for 4-6 weeks (to allow healing)
  • No lifting objects >5 kg
  • No extreme twisting or bending
  • Gradual return to normal activities

Programming and adjustments:

  • A remote control allows adjustment of intensity and program
  • Follow-ups with a representative for optimization
  • Regular consultations with the physician (initially frequent, then every 6-12 months)

Battery:

  • Rechargeable: Lasts 8-10 years, recharged daily (~1 hour)
  • Non-rechargeable: Lasts 2-5 years depending on use, requires surgical replacement

📊 SCS Results

Effectiveness for FBSS (Failed Back Surgery Syndrome):

  • 50% relief: 50-60% of patients long term
  • Medication reduction: 40-50% significantly reduce opioids
  • Functional improvement: 60-70% report improvement in daily activities
  • Patient satisfaction: 70-80% would recommend the procedure

Durability:

  • The response is maintained in most patients at 2-5 years
  • Some patients experience a loss of efficacy (requiring reprogramming or revision)

Important: SCS is more effective for neuropathic leg pain than for axial back pain, although newer technologies (HF10) have improved results for back pain.

⚠️ SCS Complications and Considerations

Technical complications:

  • Lead migration: 10-15%, may require revision
  • Lead fracture: 5-10% long term
  • Loss of efficacy: 20-30% require reprogramming or revision
  • Infection: 3-5% (most superficial, some require removal)
  • Dural puncture: 3-5% during placement, generally without consequences

Lifestyle considerations:

  • Some systems do not allow MRI (check with the manufacturer)
  • Metal detectors at airports: an identification card is necessary
  • Contact sports: generally not recommended
  • Future procedures: you must inform physicians about the SCS

Intrathecal Drug Infusion: Pain Pumps

For the most severe and refractory pain, continuous delivery of medications directly into the cerebrospinal fluid provides relief at doses up to 300 times lower than oral administration.

Intrathecal pumps represent an option for patients with severe chronic pain that does not respond to other treatments, including high doses of oral opioids with significant side effects.

💊 The Principle of Intrathecal Therapy

By delivering medications directly into the cerebrospinal fluid that bathes the spinal cord (the intrathecal space), these medications act immediately on the receptors in the cord, where pain signals are processed BEFORE reaching the brain.

Main advantage: Doses 100-300 times lower than the oral route → The same relief with minimal systemic side effects.

Who Are Candidates for an Intrathecal Pump?

Main Indications

  • Cancer pain: Cancer with severe refractory pain
  • Severe FBSS: After multiple failed surgeries
  • Severe neuropathic pain: That does not respond to neuromodulation
  • Severe spasticity: With associated pain (intrathecal baclofen)
  • Need for high opioid doses: With intolerable side effects from the oral route

Selection Criteria

  • Successful trial:>50% relief with a single intrathecal injection
  • Life expectancy:>3-6 months (generally)
  • Psychological evaluation: No contraindications
  • Family support: For managing refills
  • Appropriate anatomy: Accessible intrathecal space
  • No substance abuse: Active

Medications Used in Intrathecal Pumps

Medication Main Indication Advantages Considerations
Morphine Nociceptive and neuropathic pain Most studied, FDA-approved, potent Granuloma formation (rare), tolerance
Baclofen Severe spasticity Very effective for spasms, FDA-approved Not an analgesic, dangerous withdrawal syndrome
Ziconotide Severe pain (non-opioid) Does not develop tolerance, potent Neuropsychiatric side effects, slow titration
Bupivacaine Neuropathic pain, adjunct Local anesthetic, non-opioid Generally combined with others
Clonidine Neuropathic pain, adjunct Potentiates opioids, sympatholytic effect Hypotension, generally in combination

Note: Combinations of medications are frequently used (e.g., morphine + bupivacaine + clonidine) for a synergistic effect and to reduce the side effects of each one.

The Intrathecal Pump Implantation Process

Phase 1: Intrathecal Trial

Goal: To confirm that intrathecal administration provides significant relief.

Trial methods:

  • Single injection: One intrathecal dose, observation over several hours
  • External catheter: A temporary catheter for 1-3 days with continuous infusion

Evaluation:>50% pain relief during the medication's effect = a positive trial

Phase 2: Pump Implantation

Anesthesia: General or deep sedation

Procedure:

  • An intrathecal catheter is placed in the subarachnoid space (generally at the lumbar level)
  • The catheter tip is positioned at the optimal spinal level based on the pain distribution
  • The pump (a device about the size of a hockey puck) is implanted under the skin in the abdomen
  • The catheter is tunneled under the skin and connected to the pump
  • The pump is programmed with a conservative initial dose

Duration: 1-2 hours

Hospitalization: 1-2 nights typically

Phase 3: Long-Term Management

Regular refills:

  • Frequency: Every 1-6 months depending on the reservoir size and daily dose
  • Procedure: Percutaneous puncture of the pump port with a special needle
  • Duration: 15-20 minutes, outpatient
  • Residual medication is removed and refilled with fresh medication

Dose adjustments:

  • Wireless programming without the need for puncture
  • Gradual titration to find the optimal dose
  • Changes in concentration or medications when necessary

Battery:

  • Modern pumps: battery lasts 5-7 years
  • Pump replacement: minor surgery, the catheter remains in place

📊 Results of Intrathecal Pumps

For cancer pain:

  • Pain relief: 70-80% reduction on pain scales
  • Reduction of oral opioids: 50-90%
  • Improvement in quality of life: Significant in studies
  • Side effects: Markedly reduced vs. systemic opioids

For non-cancer pain (FBSS, neuropathic):

  • >50% relief: 50-70% of patients long term
  • Satisfaction: 60-80% would recommend the procedure
  • Function: Variable improvement, less dramatic than in cancer pain

⚠️ Complications of Intrathecal Pumps

Mechanical complications:

  • Catheter problem: Disconnection, obstruction, migration (10-15%)
  • Pump malfunction: Rare with modern devices
  • Infection: 5-10%, may require complete removal of the system

Medication-related complications:

  • Inflammatory granuloma: A mass at the catheter tip, more common with high-dose morphine
  • Respiratory depression: If the dose is excessive or there is a programming error
  • Withdrawal syndrome: If the pump empties or malfunctions (an emergency)
  • Tolerance: The need to increase the dose over time

Special considerations:

  • Regular refills are MANDATORY: They cannot be forgotten or delayed
  • Medical identification: A bracelet/card indicating an implanted pump
  • MRI: Most pumps are MRI-conditional (specific protocols)
  • Travel: Carry enough medication and the physician's contact information

Choosing the Right Procedure for Your Case

There is no single "best" procedure for everyone: the key is to identify the most appropriate option based on your anatomy, type of pain, and personal goals.

🎯 The Decision Algorithm for Pain Procedures

Selecting the correct procedure follows a logical process based on:

  • Anatomical source of the pain: Identified by history, physical examination, and imaging
  • Type of pain: Nociceptive (tissue) vs. neuropathic (nerve)
  • Distribution of the pain: Axial (back) vs. radicular (leg/arm)
  • Duration and severity: Acute vs. chronic, mild vs. severe
  • Response to previous treatments: What has worked, what has not
  • Patient goals: Pain reduction vs. functional improvement vs. medication reduction

Common Clinical Scenarios and Appropriate Procedures

Scenario 1: Lumbar Herniated Disc with Acute Sciatica

Presentation: Leg pain greater than back pain, recent onset (<6 weeks), herniation confirmed on MRI.

Recommended procedure: Transforaminal epidural injection

Rationale:

  • Reduces inflammation of the compressed nerve root
  • Allows time for the herniation to resolve spontaneously (many do)
  • Avoids or delays the need for surgery in 50-70% of cases
  • A series of 1-3 injections at 2-4 week intervals

If it fails: Consider decompressive surgery (microdiscectomy) if there is a neurological deficit or the pain persists >6-8 weeks.

Scenario 2: Chronic Axial Low Back Pain, Without Radiculopathy

Presentation: Lower back pain for >6 months, worse with extension/rotation, without significant leg pain, facet joint arthritis on imaging.

Recommended sequence:

  1. Diagnostic medial branch blocks(2 sessions with >50% relief each time)
  2. If diagnostics are positive → Radiofrequency rhizotomy

Expectations: 6-24 months of relief, a repeatable procedure if the pain returns

If it fails or relief is inadequate: Reassess the source of the pain (a discogenic component? instability?)

Scenario 3: Failed Back Surgery Syndrome (FBSS)

Presentation: Persistent or recurrent pain after 1-2 spine surgeries, predominantly neuropathic leg pain.

Recommended algorithm:

  1. Rule out a correctable surgical problem (residual compression, pseudarthrosis)
  2. If anatomy is stable → Spinal cord stimulation trial
  3. If the trial is successful (>50% relief) → Permanent SCS implantation
  4. If SCS fails or is contraindicated → Consider an intrathecal pump for severe cases

Importance: FBSS is one of the best indications for neuromodulation. Suboptimal results with simple injection procedures.

Scenario 4: Moderate Lumbar Spinal Stenosis

Presentation: Neurogenic claudication (pain/weakness in the legs when walking), relieved by rest or leaning forward, multilevel stenosis on MRI.

Procedure: Interlaminar epidural injections

Rationale:

  • Reduces inflammation of the compressed nerve roots
  • Improves tolerance for exercise and physical therapy
  • May provide enough relief to avoid/delay surgery

If it fails after a series of 3: Consider decompressive laminectomy if there is significant functional limitation.

Scenario 5: Severe Spinal Cancer Pain

Presentation: Vertebral metastases, severe pain requiring high-dose opioids with significant side effects.

Multimodal approach:

  1. Neurosurgical evaluation for spinal cord compression (urgent surgery if present)
  2. Radiotherapy/radiosurgery for local tumor control
  3. Intrathecal pump for pain control if refractory
  4. Vertebroplasty for painful compression fractures

Goal: To maximize quality of life with minimal treatment side effects.

Type of Pain First Line Second Line Refractory Cases
Acute radiculopathy Transforaminal epidural Series of 3 epidurals Decompressive surgery
Facet pain Diagnostic blocks RF rhizotomy Repeat rhizotomy
FBSS (leg predominance) SCS trial Permanent SCS Intrathecal pump
Multilevel stenosis Interlaminar epidurals Series of 3 epidurals Laminectomy
Severe cancer pain Systemic opioids Radiotherapy + pump Intrathecal pump
Discogenic pain Conservative therapy Epidurals/injections Surgery (fusion or ADR)

💚 The Right Procedure Can Change Your Life

I have seen patients who had lost hope reclaim their lives after the appropriate procedure. The key is not finding the "most advanced" or "newest" procedure, but the procedure that is most appropriate for your specific problem.

During your consultation:

  • We will review your medical history and previous treatments in detail
  • We will analyze your imaging together to identify the anatomical sources of the pain
  • We will honestly discuss which procedures are appropriate (and which are NOT) for your case
  • We will set realistic expectations about the anticipated results
  • We will create a progressive treatment plan, starting with the least invasive option

My commitment: I will never recommend a procedure that I would not perform on a member of my own family with the same condition.


Preguntas Frecuentes


  • He probado todo para mi dolor (terapia, medicamentos, infiltraciones) y nada funciona. ¿Existen otras opciones antes de considerar una gran cirugía de fusión?

    Sí. Para pacientes como usted, que sufren de dolor crónico intratable y que quizás no son candidatos para una cirugía correctiva mayor, existen terapias de neuromodulación avanzadas. Estas no "curan" la causa anatómica del dolor, sino que se enfocan en modificar o bloquear la señal de dolor antes de que llegue al cerebro.

    Los dos procedimientos principales que ofrecemos son:

    • Neuroestimulación Espinal: Utiliza impulsos eléctricos suaves para "enmascarar" la sensación de dolor.
    • Bombas de Infusión Intratecal: Administran medicación analgésica directamente en el espacio que rodea la médula espinal.

    Estas opciones representan un paso muy importante en el manejo del dolor cuando las terapias convencionales han fallado.

  • ¿Qué es un Neuroestimulador Espinal? ¿Cómo funciona un "marcapasos para el dolor"?

    Un neuroestimulador espinal es un dispositivo de alta tecnología que funciona, efectivamente, como un "marcapasos para el dolor". El sistema consiste en un pequeño generador de impulsos (similar a un marcapasos cardíaco) que se implanta bajo la piel y se conecta a unos cables delgados (electrodos) que se colocan con precisión en el espacio epidural, cerca de la médula espinal.

    Estos electrodos emiten impulsos eléctricos muy suaves que interrumpen las señales de dolor que viajan por la médula espinal hacia el cerebro. En lugar de sentir dolor, el paciente percibe una sensación diferente, como un ligero hormigueo (parestesia) o, con la tecnología más moderna, simplemente una reducción del dolor sin ninguna otra sensación. Es una forma de cambiar la percepción del dolor a nivel neurológico.

  • ¿En qué consiste la Bomba de Infusión de Medicamentos? ¿Por qué es mejor que tomar pastillas?

    Una bomba de infusión intratecal es un dispositivo que administra medicación (generalmente analgésicos potentes como la morfina o relajantes musculares como el baclofeno) directamente en el líquido cefalorraquídeo que rodea la médula espinal.

    La ventaja es la potencia y la reducción de efectos secundarios. Al entregar el medicamento directamente al sistema nervioso central, se necesitan dosis increíblemente pequeñas para lograr un alivio efectivo. Hablamos de una dosis que puede ser hasta 300 veces menor que la que se necesitaría por vía oral. Esto permite un control del dolor mucho más potente sin los efectos secundarios que limitan el uso de estos medicamentos en pastillas (somnolencia, estreñimiento, confusión, etc.)

  • ¿Cómo puedo saber si uno de estos dispositivos funcionará para mí antes de implantarlo permanentemente?

    Esta es la parte más importante y segura del proceso. Ninguno de estos dispositivos se implanta de forma permanente sin que usted tenga la oportunidad de probarlo primero. Realizamos una fase de prueba que dura aproximadamente una semana:

    • Para el Neuroestimulador: Se colocan los electrodos en la espalda a través de una aguja (un procedimiento mínimamente invasivo), pero se dejan conectados a un generador externo que usted lleva en un cinturón. Durante una semana, usted va a casa y evalúa en su vida diaria cuánto alivio del dolor experimenta.
    • Para la Bomba de Infusión: Se puede realizar una prueba con una inyección única o una infusión continua a través de un catéter externo.

    Solo si usted experimenta una reducción significativa de su dolor (generalmente más del 50%) durante esta fase de prueba, procedemos a implantar el dispositivo permanente. Usted tiene el control total de la decisión.

  • ¿Qué implica vivir con un neuroestimulador o una bomba de infusión? ¿Necesitan mantenimiento?

    Vivir con estos dispositivos le devuelve el control sobre su dolor. Usted tendrá un programador externo que le permitirá ajustar la intensidad de la estimulación o recibir dosis adicionales de medicación (siempre dentro de los límites seguros que establecemos).

    En cuanto al mantenimiento:

    • Neuroestimulador: La batería del generador implantado tiene una vida útil de varios años (dependiendo del uso). Cuando se agota, se reemplaza en un procedimiento quirúrgico menor. Los modelos más nuevos son recargables a través de la piel.
    • Bomba de Infusión: La bomba contiene un reservorio de medicamento que debe ser rellenado periódicamente (típicamente cada 1 a 3 meses). Esto se hace en el consultorio a través de una simple inyección en el puerto de la bomba, que se encuentra bajo la piel de su abdomen. Es un procedimiento rápido y sencillo.

    Ambos procedimientos son completamente reversibles. Si en algún momento ya no se necesita o desea el dispositivo, se puede retirar quirúrgicamente.