Table 22.
Factor | Clinical trial | Clinical practice |
Patient selection | ||
History and physical examination of cervical facet joints | Inclusion criteria:
Exclusion criteria:
|
Inclusion criteria:
Exclusion criteria:
|
History and physical examination AA/AO joints | No recommendation | No recommendation |
Failure of conservative treatment | At least 3 months | Preferably 3 months, but may be less in certain circumstances (eg, incapacitating pain with strong suspicion of facetogenic origin, competitive athlete, deployment) |
Radiological findings for facet joint pain | No recommendation | No recommendation |
Patient reported outcomes | Follow IMMPACT and other relevant guidelines, more detailed than clinical practice | Dependent on patient’s goals |
Pain relief cut-off for positive MBB | >50% (consider higher cut-off for efficacy trials or subgroup analysis) | >50% |
Functional measures | Sole criterion not recommended for assessing MBB results (composite with pain relief should be considered for RFA effectiveness) | Sole criterion not recommended for assessing MBB results (composite with pain relief may be considered for RFA effectiveness) |
Repeat RFA | >30% for at least 3 months per IMMPACT and lumbar facet guidelines29 281 | >30% for at least 3 months per IMMPACT and lumbar facet guidelines29 281 |
Repeat diagnostic MBB for repeat RFA | No – previous RFA should be an exclusion criterion for studies not evaluating repeat RFA | No |
Injection technique | ||
AO and AA imaging | Pre-injection CT or MRI, fluoroscopy and real-time contrast injection with strong consideration of DSA or CT | Pre-injection CT or MRI, fluoroscopy and real-time contrast injection or DSA |
Approach | Posterior/posterior oblique | Posterior/posterior oblique |
Volume and prognostic test | ||
Medial branch block | < 0.3 mL | < 0.3 mL |
Diagnostic block (IA vs MBB) | MBB | MBB |
Diagnostic block (single vs dual) | Single block (consider dual blocks only for efficacy studies) | Single block (consider dual blocks in individuals with low index of suspicion) |
Imaging | Fluoroscopy or US | Fluoroscopy or US |
Approach | Lateral (TON, C3–C7) | Lateral (TON, C3–C7) |
Posterior oblique (C8) | Posterior oblique (C8) | |
Volume and steroid use for AA/AO injections | Non-particulate <1 mL | Non-particulate <1 mL |
Sedation | Avoid | Avoid |
RFA technique | ||
Stimulation | Motor for all levels | Motor for all levels |
Sensory for single lesions and C2–3 | Sensory for single lesions and C2–3 | |
Needle orientation | Parallel (preferable) or near-parallel | Parallel or near-parallel |
Posterior two-thirds of the articular pillar for C2–3 | Posterior two-thirds of the articular pillar for C2–3 | |
Lesion size | No recommendation due to unknown risk/benefit | No recommendation due to unknown risk/benefit |
Cannulae confirmation | PA/lateral and possibly contralateral oblique | PA/lateral and contralateral oblique if necessary |
Implanted devices | Exclude patients | Neurostimulators – deactivate |
Pacemakers – asynchronous mode if possible | ||
Defibrillators – deactivate if possible | ||
Grounding pad placement | Dry, hairless skin devoid of tattoos | Dry, hairless skin devoid of tattoos |
Spinal hardware | Exclude patients unless specifically addressing outcomes in this population | Avoid contact with hardware, adjust approach (eg, posterior oblique) as necessary |
Repeat RFA | No more than twice/year | No more than twice/year |
Post-lesion steroids | No steroids for efficacy study unless administered to all patients | Per physician judgment based on risk:benefit analysis |
Anticoagulation | Exclude subjects who cannot stop anticoagulants | Discontinue only after careful risk:benefit assessment |
AA, atlanto–axial; AO, atlanto–occipital; CT, computed tomography; DSA, digital subtraction angiography; IA, intra-articular; MBB, medial branch block; MRI, magnetic resonance imaging; PA, posteroanterior; RFA, radiofrequency ablation; TON, third occipital nerve; US, ultrasound.