| Literature DB >> 33329959 |
Sarah McNutt1, David R Hallan1, Elias Rizk1.
Abstract
Occipital neuralgia, a neuropathy of the occipital nerves, can cause significant pain and distress, resulting in a decrease in the patient's quality of life. Options for surgical treatment involve transection or decompression of the greater and lesser occipital nerves. Current evidence provides no clear consensus regarding one technique over the other. Here, we present a systematic review of the literature to potentially answer this question. Eligible studies compared neurolysis versus neurectomy for the treatment of occipital neuralgia after failure of conservative therapy. Our outcome of interest was resolution of symptoms. We performed a search of MEDLINE/PubMed and Ovid from inception to 2019. Eligible studies included the words "occipital neuralgia" and "surgery." All studies comparing neurolysis to neurectomy were included in the analysis. None of the studies identified were randomized control trials. Each study was evaluated by two independent researchers who assigned a level of evidence according to the American Association of Neurology (AAN) algorithm. Data extracted included mechanism of surgery (neurolysis or neurectomy), resolution of pain symptoms, and length of follow-up. Each study was level IV evidence. After reviewing the data, there was insufficient evidence to recommend one method of treatment over the other. This inconclusive result highlights the importance of a national registry to compare outcomes between the two treatment modalities.Entities:
Keywords: headache; neurectomy; neurolysis; occipital neuralgia; surgery
Year: 2020 PMID: 33329959 PMCID: PMC7733770 DOI: 10.7759/cureus.11461
Source DB: PubMed Journal: Cureus ISSN: 2168-8184
Figure 1PRISMA Flow Diagram
Level of evidence according to the American Association of Neurology algorithm. Table reproduction approved by Payne et al. [9].
AAN: American Association of Neurology.
| AAN level of evidence | AAN description |
| Class I | A cohort with prospective data collection. All relevant confounding characteristics are presented and substantially equivalent between comparison groups, or there is an appropriate statistical adjustment for differences. Outcome measurement is objective or determined without knowledge of risk factor status. Primary outcome(s) are defined, exclusion/inclusion criteria are defined, and dropouts are accounted for (dropout rate is less than 20%). |
| Class II | Cohort study with retrospective data collection or case-control study. All relevant confounding characteristics are presented and substantially equivalent among comparison groups, or there is an appropriate statistical adjustment for differences. There is masked or objective outcome assessment. Primary outcome(s) are defined, exclusion/inclusion criteria are defined, and dropouts are accounted for (dropout rate is less than 20%). |
| Class III | Cohort or case-control study. There is a description of major confounding differences between risk groups that could affect outcome. Outcome assessment is masked, objective, or performed by someone other than the investigator who measured the risk factor. |
| Class IV | Study did not include persons at risk for disease. Study did not include patients with and without the risk factor. There is an undefined or unaccepted measure of risk factor or outcome. No measure of association or statistical precision is presented or calculable. |
GRADE guidelines. Table reproduction approved by Payne et al. [9].
| Study design | Initial quality of evidence | Factors that decrease the quality level | Factors that increase the quality level |
| Randomized trials or double-upgraded observational studies | High | High likelihood of bias | Large effect |
| Downgraded randomized trials or upgraded observational studies | Moderate | Indirectness of evidence | All plausible confounding would reduce a demonstrated effect or suggest a spurious effect if no effect was observed |
| Double-downgraded randomized trials or observational studies | Low | Imprecision | Dose response gradient |
| Triple-downgraded randomized trials, downgraded observational studies, or case series/reports | Very low | High probability of publication bias | N/A |
Neurectomy vs Neurolysis.
AAN: American Association of Neurology.
| Author | Published in | Study type | Neurectomy or neurolysis | Number of patients | Outcome | Mean follow-up | AAN level of evidence | GRADE criteria |
| Andrychowski et al. [ | Folia Neuropathologica | Case Report | Neurolysis then neurectomy x2 | 1 | Relapse of symptoms within one month after neurolysis. No resolution after first neurectomy. Elimination of pain after second neurectomy. | 6 months | 4 | Very low |
| Ducic et al. [ | Plastic and Reconstructive Surgery | Retrospective Review | Neurolysis | 190 | 166 (80%) had greater than 50% relief of pain. 72 (43.4%) had complete relief. 40 (19.5%) had less than 50% relief of symptoms. | 12 months | 4 | Low |
| Neurectomy | 16 | |||||||
| Cornely et al. [ | Headache | Case Report | Neurolysis | 1 | Neuralgic pain remained absent. | 12 months | 4 | Very low |
| Jung et al. [ | Korean Journal of Pain | Case Report | Neurectomy | 1 | Headache disappeared gradually, despite the fact that he had discontinued all pain medications. | 5 months | 4 | Very low |
| Li et al. [ | Turkish Neurosurgery | Prospective Review | Neurolysis | 76 | Headache symptoms of 68 (89.5%) completely resolved; another five (6.6%) patients were significantly relieved without the need for any further medical treatments. Three (3.9%) experienced recurrence. All experienced hypoesthesia of the innervated area and recovered gradually within one to six months. | 20 months | 4 | Low |
| Pisapia et al. [ | World Neurosurgery | Retrospective Review | Neurolysis | 11 | 19 (66%) experienced a good or excellent outcome with no difference in mean pain reduction among the three cohorts. | 5.6 years | 4 | Low |
| Neurectomy | 10 | |||||||
| Neurolysis + Neurectomy | 8 | |||||||
| Ducic et al. [ | American Headache Society | Retrospective Review | Neurectomy | 7 | Six experienced pain reduction and improvement in quality of life of greater than 80%. | 32 months | 4 | Low |
| Ducic et al. [ | Annals of Plastic Surgery | Retrospective Review | Neurectomy | 71 | 41% of patients showed a 90% or greater decrease in symptoms. Bothersome numbness or hypersensitivity in the denervated area in 31%. | 33 months | 4 | Low |
| Choi et al. [ | Acta Neurochirurgica | Retrospective Review | Neurolysis | 68 | 47 (69.1%) achieved excellent or good results. | 5 years | 4 | Low |
| Ko et al. [ | Journal of Neurological Surgery | Case Report | Neurolysis | 1 | Resolution. | 12 months | 4 | Very low |
| Jose et al. [ | Journal of Craniofacial Surgery | Prospective Review | Neurolysis | 11 | Three reported complete elimination of pain, six reported significant relief. Two failed to notice any improvement. | 12.5 months | 4 | Low |
| Janjua et al. [ | Journal of Clinical Neuroscience | Case Report | Neurectomy | 1 | Pain free. | 2 months | 4 | Very low |