Neuromodulation · London
Spinal cord stimulation, by a named neuromodulation consultant.
A two-stage neuromodulation pathway for chronic neuropathic pain under NICE TA159. Percutaneous trial first, permanent implant only if pain falls by half or more. Full manufacturer choice: Medtronic, Abbott, Boston Scientific, Nevro and Saluda.
Why patients choose us
- 01
A named neuromodulation consultant, in a high-volume implant centre
Not a general pain list. A consultant pain physician or functional neurosurgeon with a high SCS implant volume, in a centre that meets NICE TA159 and NSUKI standards.
- 02
The right waveform for the pain pattern
Tonic, burst, HF10 kHz, DTM or closed-loop Evoke. We match the device to the pain phenotype rather than to the rep in the room.
- 03
Independent, and free
We are paid by no manufacturer and no clinic, so the recommendation is impartial and costs you nothing.
Indicative pricing
What a private SCS implant costs in London.
All-inclusive package prices across our partner centres: trial, permanent implant, hardware, hospital stay and programming. Send the pain history and we quote firm figures.
In short
A full SCS pathway in our network: £28,000 to £48,000, trial to permanent implant in 4 to 6 weeks.
| Procedure | Indicative range | Typical duration | Discharge |
|---|---|---|---|
| Neuromodulation consultation and case review | £350–£600 | 45–60 min | Same visit |
| Percutaneous SCS screening trial (5–14 days) | £6,500–£9,500 | 60–90 min | 2 weeks |
| Permanent SCS implant (tonic or burst, primary cell) | £28,000–£34,000 | 90–120 min | Same day |
| Permanent SCS implant (HF10, DTM or closed-loop, rechargeable) | £36,000–£48,000 | 90–150 min | Same day or overnight |
| DRG stimulation (focal CRPS, groin, foot pain) | £32,000–£42,000 | 120–180 min | Overnight |
| IPG replacement at end of battery life | £9,500–£14,000 | 45–60 min | Same day |
NHS SCS is commissioned under NICE TA159 in England through specialist neuromodulation centres, with long waits. Private packages cover the consultation, trial, permanent implant, hardware, hospital stay and programming visits.
The journey
From referral to long-term follow-up - what happens, in order.
One team from first message to annual review, including the trial, permanent implant, programming and IPG replacement years later.
- 01
Before
You send us the pain history and imaging
A short, confidential form. Distribution of pain (legs, arms, groin), duration, prior surgery, current medication, MRI or CT reports and psychological screening if done.
- 02
Before
We come back with a recommendation
Within one working day: whether SCS fits under NICE TA159, or whether DRG stimulation, intrathecal pump or medial branch RFA is the better call. Indicative price. An honest read either way.
- 03
Before
Screening trial booked
Percutaneous epidural leads placed under local anaesthetic and X-ray at T8 to T10 for leg pain, or cervical for arm pain. You go home with an external generator for 5 to 14 days.
- 04
Trial and implant
The trial period at home
You live normally, keep a pain and function diary, and try different programmes. A rep and nurse support you throughout. The bar for permanent implant is at least 50% pain reduction.
- 05
Trial and implant
Permanent implant
60 to 120 minutes under sedation or light general anaesthetic. New leads anchored to fascia and tunnelled to an IPG pocket in the flank or buttock. Same-day or one-night stay.
- 06
After
Programming and titration
First programming at 2 to 4 weeks once swelling settles. Multiple follow-ups to tune amplitude, frequency and pulse width. Remote programming via the manufacturer app.
- 07
After
Long-term follow-up
Annual review, MRI-conditional documentation and IPG replacement at 5 to 10 years for primary-cell systems, or recharging schedule for rechargeable units.
When it helps
When SCS is the right step - and when it is not.
The pain syndromes with the strongest evidence for SCS under NICE TA159, plus the situations where DRG, intrathecal pump or targeted RFA is a better fit.
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Failed back surgery syndrome (FBSS)
Persistent neuropathic leg pain after one or more lumbar operations, with radicular distribution and MRI showing epidural fibrosis rather than a fresh compressive lesion.
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Complex regional pain syndrome (CRPS)
Type I or II CRPS of a limb with allodynia, autonomic and trophic changes. DRG stimulation often outperforms conventional SCS for focal foot, hand or knee distributions.
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Painful diabetic neuropathy (PDN)
Symmetrical lower-limb burning neuropathic pain despite optimised glycaemic control and first-line pharmacotherapy. HF10 kHz has the strongest evidence in this group.
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Neuropathic pain after peripheral nerve injury
Post-traumatic or post-surgical mononeuropathy: ilioinguinal, genitofemoral, intercostal, brachial plexus injury with well-mapped neuropathic distribution.
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Post-herpetic neuralgia
Selected patients with truncal or limb post-herpetic pain unresponsive to gabapentinoids, tricyclics, topical lidocaine and interventional blocks.
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Refractory angina
Chronic refractory angina despite maximal medical therapy and revascularisation options exhausted. High-cervical leads for cardiac coverage.
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Ischaemic limb pain
Non-reconstructable peripheral vascular disease with rest pain, in selected patients where amputation is being considered.
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Red flag: untreated psychological comorbidity
Active untreated depression, somatisation or unrealistic expectations predict a poor SCS outcome. Screening and preparation come first, not the implant.
Waveforms and devices
SCS is a family of waveforms and devices, not one implant.
The evidence for each waveform, and the trial data (SENZA-RCT, SENZA-PDN, ACCURATE, EVOKE) behind them. We match the device to the pain phenotype.
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Tonic paraesthesia-based (traditional)
Low-frequency stimulation (40 to 60 Hz) that overlays the pain area with a tingling paraesthesia. The original waveform, still effective, but many patients dislike the sensation.
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Burst (DeRidder, Abbott)
Packets of high-frequency spikes delivered in bursts, sub-perception. Modulates the medial pain pathway and reduces the affective component of chronic pain.
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HF10 kHz (Nevro Senza)
Sub-perception 10 kHz stimulation. Level 1 evidence from SENZA-RCT (superior to tonic for back and leg pain) and SENZA-PDN (48% responders at 24 months in painful diabetic neuropathy).
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DTM (differential target multiplexed, Medtronic)
Multiplexed programmes that target glia as well as neurons. Randomised evidence of superiority to conventional SCS for chronic back and leg pain at 12 months.
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Closed-loop Evoke (Saluda)
Measures the evoked compound action potential (ECAP) and adjusts amplitude in real time, so dose stays constant with posture. AVALON and EVOKE trials show durable responder rates.
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Dorsal root ganglion (DRG) stimulation
Leads placed at a specific DRG rather than the epidural space. Superior to conventional SCS for focal CRPS, groin and foot pain in the ACCURATE trial.
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Percutaneous vs paddle leads
Percutaneous cylindrical leads via a Tuohy needle are the standard. Surgical paddle leads (via laminotomy) offer more contacts and less migration, used for revisions or specific coverage.
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Rechargeable vs primary cell IPG
Rechargeable systems (10-year life, smaller) require weekly charging. Primary cell systems (Abbott Proclaim XR, 10 years at low dose) need no charging but eventually a surgical swap.
Our London network
A small panel of neuromodulation consultants, we picked them.
Consultant pain physicians and functional neurosurgeons at King's College Hospital Private Pain, London Pain Clinic at Guy's, HCA The Wellington Pain Management, Cleveland Clinic London and Imperial Private at Chelsea and Westminster.
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Consultant pain physicians or functional neurosurgeons with high annual SCS implant volumes
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Centres meeting NICE TA159, NSUKI (Neuromodulation Society UK and Ireland) and BPS standards
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Full manufacturer choice: Medtronic, Abbott, Boston Scientific, Nevro and Saluda
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Access to DRG stimulation and intrathecal pump pathways for the cases where SCS is not the right call
Safety and recovery
What to expect afterwards - honestly.
SCS is a well-established neuromodulation technique. The things worth planning are lead migration, infection risk, MRI conditions and eventual IPG revision.
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Sedation and anaesthesia
Trial leads are placed awake under local anaesthesia and X-ray to confirm paraesthesia coverage. Permanent implant is done under conscious sedation or light general anaesthetic.
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Lead migration
The commonest hardware problem, in 3 to 10% of cases at 5 years. Programming can compensate for small shifts; larger migrations need a revision procedure.
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Infection
Pocket or lead infection in about 2 to 5% of implants. Managed with antibiotics and, in most cases, removal of the system followed by re-implant after a clear interval.
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Dural puncture and headache
Uncommon at the trial stage. Managed conservatively, with an epidural blood patch reserved for persistent postural headache.
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Loss of efficacy over time
A minority of patients lose benefit over months to years. Reprogramming, waveform switching or DRG conversion recovers response in many cases.
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MRI compatibility
All current systems are MRI-conditional under specific field strengths and body regions. We document the exact conditions and hand you a manufacturer card.
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IPG revision and replacement
Primary cell batteries last 5 to 10 years at typical settings; rechargeable IPGs last around 10 years before elective replacement under local anaesthetic.
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Explant
Around 10 to 15% of systems are eventually removed for loss of efficacy, infection or patient preference. Explant is a straightforward day-case procedure.
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Red flags after implant
Fever, spreading redness, wound discharge, new weakness or loss of bladder or bowel control need urgent contact with the implanting team or A&E the same day.
Reading your neuromodulation record
Your SCS record in four parts. Read the last one first.
Whichever manufacturer or waveform was chosen, the record the implanting team sends you keeps to the same shape.
- 01 Indication
Pain diagnosis and NICE TA159 fit
Which neuropathic pain syndrome, duration of at least 6 months, and confirmation that adequate trials of conventional medical and interventional therapy have failed.
- 02 Trial
Screening result and responder status
Percentage pain reduction on the numerical rating scale, function and mood changes, and preferred waveform during the 5 to 14 day trial.
- 03 Implant
Hardware, lead position and MRI conditions
Manufacturer, IPG model, lead type and vertebral level, rechargeable or primary cell, and the exact MRI field strength and region conditions that apply.
- 04 Plan
Programming, follow-up and battery review
Read this first: initial programme, planned follow-ups, expected battery life and when a replacement is anticipated.
Recognised by major UK insurers
Cover for SCS varies by insurer and by indication. Most major insurers fund SCS under NICE TA159 with prior authorisation. We confirm cover before booking.
Frequently asked
Everything we get asked about SCS.
Quick answers on waveforms, the trial, cost, MRI compatibility and NICE TA159 candidacy.
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What is spinal cord stimulation?
Spinal cord stimulation (SCS) delivers small electrical pulses through leads placed in the epidural space, usually at T8 to T10 for leg pain and in the cervical spine for arm pain. The leads connect to a battery (IPG) implanted in the flank or buttock. It modulates neuropathic pain signals and is offered under NICE TA159 for chronic neuropathic pain of at least 6 months duration when conventional therapy has failed.
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Who is a candidate for SCS in the UK?
NICE TA159 recommends SCS for adults with chronic neuropathic pain of at least 6 months duration who have tried standard medical management. The commonest indications are failed back surgery syndrome (FBSS), complex regional pain syndrome (CRPS), painful diabetic neuropathy (PDN) and neuropathic pain after nerve injury. A successful screening trial with at least 50% pain reduction is required before permanent implant.
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What is the difference between tonic, burst, HF10 and DTM?
Tonic delivers low-frequency pulses that create a tingling paraesthesia. Burst (Abbott) sends packets of spikes sub-perception and reduces the emotional component of pain. HF10 (Nevro) uses 10 kHz sub-perception stimulation with Level 1 evidence in the SENZA-RCT for back and leg pain and in SENZA-PDN for painful diabetic neuropathy. DTM (Medtronic) multiplexes programmes to target glia as well as neurons and showed superiority to conventional SCS at 12 months.
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What happens during the trial?
Percutaneous leads are placed under local anaesthetic and X-ray, exiting through the skin to an external generator you wear on a belt. You go home for 5 to 14 days, keep a pain and function diary, and try different programmes. If you achieve at least 50% pain reduction and functional improvement, we proceed to permanent implant. If not, the leads are removed at the bedside.
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How much does private SCS cost in the UK?
A permanent implant is £28,000 to £48,000 all-inclusive, depending on device (tonic, burst, HF10, DTM, closed-loop Evoke) and whether the IPG is rechargeable or primary cell. The screening trial is £6,500 to £9,500. DRG stimulation is £32,000 to £42,000. IPG replacement at end of battery life is £9,500 to £14,000.
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Can I have an MRI after an SCS implant?
All current SCS systems (Medtronic Intellis and Inceptiv, Abbott Proclaim XR, Boston WaveWriter Alpha, Nevro Senza Omnia, Saluda Evoke) are MRI-conditional. This means MRI is allowed under specific field strengths (usually 1.5T, some 3T) and body regions. We give you a manufacturer card documenting the exact conditions, which the radiographer follows before every scan.
Ready to talk it through?
A named neuromodulation consultant within one working day.
Send us the pain history and imaging. We come back with a NICE TA159 assessment, a device recommendation and a firm price across two or three options.
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Chronic pain
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Failed back surgery syndrome
Persistent neuropathic pain after lumbar surgery, and the options that follow.
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