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Treatment of low back pain elicited by superior cluneal nerve entrapment neuropathy after lumbar fusion surgery
OBJECT: Low back pain (LBP) attributable to fusion failure, implant failure, infection, malalignment, or adjacent segment disease may persist after lumbar fusion surgery (LFS). Superior cluneal nerve (SCN) entrapment neuropathy (SCNEN) is a clinical entity that can produce LBP. We report that SCNEN...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society for Spine Surgery and Related Research
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698489/ https://www.ncbi.nlm.nih.gov/pubmed/31440627 http://dx.doi.org/10.22603/ssrr.1.2016-0027 |
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author | Iwamoto, Naotaka Isu, Toyohiko Kim, Kyongsong Chiba, Yasuhiro Morimoto, Daijiro Matsumoto, Juntaro Isobe, Masanori |
author_facet | Iwamoto, Naotaka Isu, Toyohiko Kim, Kyongsong Chiba, Yasuhiro Morimoto, Daijiro Matsumoto, Juntaro Isobe, Masanori |
author_sort | Iwamoto, Naotaka |
collection | PubMed |
description | OBJECT: Low back pain (LBP) attributable to fusion failure, implant failure, infection, malalignment, or adjacent segment disease may persist after lumbar fusion surgery (LFS). Superior cluneal nerve (SCN) entrapment neuropathy (SCNEN) is a clinical entity that can produce LBP. We report that SCNEN treatment improved LBP in patients who had undergone LFS. METHODS: Between April 2012 and August 2015, we treated 8 patients (4 men and 4 women ranging in age from 38 to 88 years; mean age, 69 years) with SCNEN for their LBP after LFS. Our criteria for the diagnosis of SCNEN included a trigger point over the posterior iliac crest 7 cm from the midline and numbness and radiating pain in the SCN area upon compression of the trigger point. Symptom relief was obtained in more than 75% of patients within 2 h of inducing a local nerve block at the trigger point in the buttocks. The mean postoperative follow-up period was 28 months (range, 9-54 months). RESULTS: LBP was unilateral in 3 and bilateral in 5 patients. The senior author (T.I.) operated all patients for SCNEN under local anesthesia because they reported recurrence of pain after the analgesic effect of repeat injections wore off. This led to a significant improvement of their LBP. CONCLUSIONS: SCNEN should be considered in patients reporting LBP after LFS. Treatment of SCNEN may be a useful option in patients with failed back surgery syndrome after LFS. |
format | Online Article Text |
id | pubmed-6698489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Japanese Society for Spine Surgery and Related Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-66984892019-08-22 Treatment of low back pain elicited by superior cluneal nerve entrapment neuropathy after lumbar fusion surgery Iwamoto, Naotaka Isu, Toyohiko Kim, Kyongsong Chiba, Yasuhiro Morimoto, Daijiro Matsumoto, Juntaro Isobe, Masanori Spine Surg Relat Res Technical Note OBJECT: Low back pain (LBP) attributable to fusion failure, implant failure, infection, malalignment, or adjacent segment disease may persist after lumbar fusion surgery (LFS). Superior cluneal nerve (SCN) entrapment neuropathy (SCNEN) is a clinical entity that can produce LBP. We report that SCNEN treatment improved LBP in patients who had undergone LFS. METHODS: Between April 2012 and August 2015, we treated 8 patients (4 men and 4 women ranging in age from 38 to 88 years; mean age, 69 years) with SCNEN for their LBP after LFS. Our criteria for the diagnosis of SCNEN included a trigger point over the posterior iliac crest 7 cm from the midline and numbness and radiating pain in the SCN area upon compression of the trigger point. Symptom relief was obtained in more than 75% of patients within 2 h of inducing a local nerve block at the trigger point in the buttocks. The mean postoperative follow-up period was 28 months (range, 9-54 months). RESULTS: LBP was unilateral in 3 and bilateral in 5 patients. The senior author (T.I.) operated all patients for SCNEN under local anesthesia because they reported recurrence of pain after the analgesic effect of repeat injections wore off. This led to a significant improvement of their LBP. CONCLUSIONS: SCNEN should be considered in patients reporting LBP after LFS. Treatment of SCNEN may be a useful option in patients with failed back surgery syndrome after LFS. The Japanese Society for Spine Surgery and Related Research 2017-12-20 /pmc/articles/PMC6698489/ /pubmed/31440627 http://dx.doi.org/10.22603/ssrr.1.2016-0027 Text en Copyright © 2017 by The Japanese Society for Spine Surgery and Related Research https://creativecommons.org/licenses/by-nc-nd/4.0/ Spine Surgery and Related Research is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Technical Note Iwamoto, Naotaka Isu, Toyohiko Kim, Kyongsong Chiba, Yasuhiro Morimoto, Daijiro Matsumoto, Juntaro Isobe, Masanori Treatment of low back pain elicited by superior cluneal nerve entrapment neuropathy after lumbar fusion surgery |
title | Treatment of low back pain elicited by superior cluneal nerve entrapment neuropathy after lumbar fusion surgery |
title_full | Treatment of low back pain elicited by superior cluneal nerve entrapment neuropathy after lumbar fusion surgery |
title_fullStr | Treatment of low back pain elicited by superior cluneal nerve entrapment neuropathy after lumbar fusion surgery |
title_full_unstemmed | Treatment of low back pain elicited by superior cluneal nerve entrapment neuropathy after lumbar fusion surgery |
title_short | Treatment of low back pain elicited by superior cluneal nerve entrapment neuropathy after lumbar fusion surgery |
title_sort | treatment of low back pain elicited by superior cluneal nerve entrapment neuropathy after lumbar fusion surgery |
topic | Technical Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698489/ https://www.ncbi.nlm.nih.gov/pubmed/31440627 http://dx.doi.org/10.22603/ssrr.1.2016-0027 |
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