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PERIPHERAL NERVE FIELD STIMULATION: MIRAGE OR REALITY?. Dr Paul Verrills Interventional Pain Physician MBBS FAFMM MPainMed FIPP Metro Spinal Clinic, Australia. Disclosures. Royalties: NIL Shareholder for Clinical Intelligence Pty Ltd Teaching – Consultant ( adhoc peer-peer)
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PERIPHERAL NERVE FIELD STIMULATION: MIRAGE OR REALITY? Dr Paul Verrills Interventional Pain PhysicianMBBS FAFMM MPainMed FIPP Metro Spinal Clinic, Australia
Disclosures • Royalties: NIL • Shareholder for Clinical Intelligence Pty Ltd • Teaching – Consultant (adhoc peer-peer) • Nevro Corporation • St. Jude Medical • Medtronic • Arthrocare • Mundipharma • Spinal Modulation • Boston Scientific
Peripheral Nerve field Stimulation • subcutaneous implantation of percutaneous leadsin the painful areas • electrical field around the activated bipoles • field of paresthesia within the peripheral distribution of pain
Peripheral Nerve field Stimulation Theory behind Neuromodulation: • stimulation of large myelinated fibres closes the gate (via spinal cord) • putative inhibitory neurotransmitters thought to be released during large myelinated nerve fibre stimulation include: • gamma-aminobutyricacid (GABA) • adenosine
Peripheral Nerve field Stimulation • Scientific challenges: • exact mechanism of producing pain relief is poorly understood • lack of prospective randomized clinical studies • no unifying protocol for implantation • confusion in regards to Indications for the PNfS • lack of scientific data on: • adequate lead depth of implant • adequate parameters for implant • stimulation modalities
Metro Spinal Clinic PNfS lead depth study (2011) • observational study (n = 28) • low-back, n = 19 (17 subcutaneous and 2 iliac crest nerve stimulation) • occipital nerve stimulation, n = 9 • influence of (1) electrode depth and (2) electrode configuration on sensation perception
Metro Spinal Clinic PNfS lead depth study (2011) References • Abejón D., Deer T., Verrills P. 2011. Subcutaneous Stimulation: How to Assess Optimal Implantation Depth. Neuromodulation 2011; e-pub ahead of print. DOI: 10.1111/j.1525-1403.2011.00357 • McRoberts WP., Cairns K. 2010. A Retrospective Study Evaluating the Effects of Electrode Depth and Spacing for Peripheral Nerve Field Stimulation in Patients with Back Pain. North American Neuromodulation Society Meeting, Las Vegas. Poster Presentation.
Metro Spinal Clinic PNfS lead depth study (2011) • Electrode depths were measured using the 'pin-drop- technique’.
Lead depth Correlates with Perception Threshold = data obtained from McRoberts et al. Similar trends were observed between the two studies. • Pearson Correlation = 0.348, p≤0.001 • n= 459 data points from 27 patients (head and low back subcutaneous) with 18 different stimulation configurations (27 points missing)
Lead depth studies Across three separate studies using three different depth measurement methods, low back subcutaneous paresthesia was observed at an average lead depth of 9.2 - 10.5mm.
Paresthesia Descriptions Paresthesia descriptions were classified into 5 groups based on cutaneous fibre type
Distribution of categorised sensations at maximum discomfort
Distributions of sensations at maximum discomfort amplitude • The LBP and ONS groups have similar distributions. Major sensations experienced are tingling, vibration, pinch, and stabbing.
Head (ONS) n = 8 Low back PNfS has higher perception thresholds than ONS Low Back n = 13
Study summary = • Implant depth of 10~12 mm from the surface can maximise the target sensation (Aβ_FA) of PNfS effective pain relief. • Cathodalthreshold is lower than anodal one (as in Spinal cord Stimulation (SCS)). • However, it is likely that anodes reach threshold within the normal usage range of current in PNfS. • In PNFS both cathodes and anodes may be used to target the stimulation location.
PNfS 200 cases study • IRB approved • Prospective observational study over 2 years + • 203 patients with intractable pain • Key pain regions: • Occipital / craniofacial • Thoracic • Abdominal / groin • Low back
PNfS 200 cases • Outcomes: • Average pain (11 - point NPRS / VAS scale) • Percentage pain relief (%) • Oswestry Disability Index (ODI) • Analgesic medication use • Changes to paid employment (if applicable) • Patient satisfaction with the treatment • Adverse events monitored
Results: occipital - craniofacial *** • n = 63 • an average pain reduction of 4.9 ± 0.32, on an 11-point scale was reported (***p≤0.0001, Wilcoxon Mann-Whitney U-test)
Results: thoracic *** • n = 17 • an average pain reduction of 5.3 ± 0.56, on an 11-point scale was reported (***p≤0.0001, Wilcoxon Mann-Whitney U-test)
Results: abdominal / groin *** • n = 15 • an average pain reduction of 5.8 ± 0.52, on an 11-point scale was reported (***p≤0.0001, Wilcoxon Mann-Whitney U-test)
Results: low back *** • n = 108 • an average pain reduction of 4.1 ± 0.26, on an 11-point scale was reported (***p≤0.0001, Wilcoxon Mann-Whitney U-test)
Results: occipital / craniofacial • 66% of patients reported good (>50%) to excellent (>75%) pain relief
Results: thoracic • 82% of patients reported good (>50%) to excellent (>75%) pain relief
Results: abdominal / groin • 87% of patients reported good (>50%) to excellent (>75%) pain relief
Results: low back • 68% of patients reported good (>50%) to excellent (>75%) pain relief
Results: combined areas ** • combined regions PNfS, n = 203 • an average pain reduction of 4.3 ± 2.5, on an 11-point scale was reported (**p≤0.00, Wilcoxon Mann-Whitney U-test)
Results: combined areas • 73% of patients reported good (>50%) to excellent (>75%) pain relief
Sustained pain relief: combined areas • Pain relief achieved shortly after implantation was sustained for greater than 12 months
Sustained pain relief: combined areas • Pain relief achieved shortly after implantation was sustained for greater than 12 months
Sustained pain relief: combined areas • Pain relief achieved shortly after implantation was sustained for greater than 12 months
Results: combined areas • 74% of patients reduced their analgesic use • reduction in analgesics correlated with improved pain relief (next slide)
Pain Relief correlates with Decreased Analgesic Use Results: combined areas Pearson’s Correlation, r = 0.704; p ≤ 0.0001
Results: combined areas * • Pre PNfS = 34.413.5 vs≥ 12 months Follow Up = 28.3 6.4 (n = 203) • Disability was reduced following PNFS; (*p ≤ 0.03, t-test )
Results: combined areas • 48% of patients below the age of 60 years increased their capacity for paid employment.
Complications and adverse events 26 patients total (12.8% of all cases)
Patient satisfaction (≥ 12 months) • Overall, 85% of patients were satisfied with their outcome
Summary • Science behind PNfS • Underlying Issues of PNfS therapy • Clinical data for key pain areas • Combined clinical data for 203 PNfS patients
Conclusions • PNFS therapy for intractable chronic pain conditions: • Safe • Effective • PNFS has the potential to fundamentally change the way we think about pain management
Conclusions Peripheral Nerve field Stimulation ? REALITY MIRAGE OR