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Effectiveness of continuous hypertonic saline infusion with an automated infusion pump for decompressive neuroplasty: a randomized clinical trial
DC Field | Value | Language |
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dc.contributor.author | Lee, HJ | - |
dc.contributor.author | Lee, J | - |
dc.contributor.author | Park, YW | - |
dc.contributor.author | Gil, HY | - |
dc.contributor.author | Choi, E | - |
dc.contributor.author | Nahm, FS | - |
dc.contributor.author | Lee, PB | - |
dc.date.accessioned | 2022-01-14T05:18:57Z | - |
dc.date.available | 2022-01-14T05:18:57Z | - |
dc.date.issued | 2019 | - |
dc.identifier.issn | 2005-9159 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/20089 | - |
dc.description.abstract | BACKGROUND: Hypertonic saline (HS) injections for decompressive neuroplasty (DN) can cause pain. We assessed whether a continuous infusion of HS through an infusion pump would reduce injection-related pain compared with repeated bolus administrations.
METHODS: Fifty patients scheduled for DN were randomized to either the bolus injection or the continuous infusion group. After appropriately placing the epidural catheter, 4 mL of 5% NaCl was injected as four boluses of 1 mL each at 15-minute intervals or infused over 1 hour using an infusion pump. The severity of pain induced by HS injection, as measured by the 11-point numerical rating scale (NRS), was the primary outcome. The severity of low back or lower extremity pain, as measured by the 11-point NRS and Oswestry Disability Index (ODI), 3 months following the procedure, was the secondary outcome. RESULTS: Data from 21 patients in the bolus group and 23 in the continuous infusion group were analyzed. No statistically significant difference in injection-related pain was identified between the two groups during the initial HS administration (P = 0.846). However, there was a statistically significant reduction in injection-related pain in the continuous infusion group compared to the bolus injection group from the second assessment onwards (P = 0.001, < 0.001, and < 0.001, respectively). No significant between-group differences in the NRS and ODI scores 3 months post-procedure were noted (P = 0.614 and 0.949, respectively). CONCLUSIONS: Our study suggests that administering HS through a continuous infusion is a useful modality for reducing HS injection-related pain during DN. | - |
dc.title | Effectiveness of continuous hypertonic saline infusion with an automated infusion pump for decompressive neuroplasty: a randomized clinical trial | - |
dc.type | Article | - |
dc.identifier.pmid | 31257828 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615446/ | - |
dc.subject.keyword | Chronic Pain | - |
dc.subject.keyword | Epidural | - |
dc.subject.keyword | Hypertonic | - |
dc.subject.keyword | Infusion Pumps | - |
dc.subject.keyword | Injections | - |
dc.subject.keyword | Low Back Pain | - |
dc.subject.keyword | Pain | - |
dc.subject.keyword | Procedural | - |
dc.subject.keyword | Radiculopathy | - |
dc.subject.keyword | Saline Solutions | - |
dc.subject.keyword | Spinal Stenosis | - |
dc.contributor.affiliatedAuthor | Gil, HY | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.3344/kjp.2019.32.3.196 | - |
dc.citation.title | The Korean journal of pain | - |
dc.citation.volume | 32 | - |
dc.citation.number | 3 | - |
dc.citation.date | 2019 | - |
dc.citation.startPage | 196 | - |
dc.citation.endPage | 205 | - |
dc.identifier.bibliographicCitation | The Korean journal of pain, 32(3). : 196-205, 2019 | - |
dc.identifier.eissn | 2093-0569 | - |
dc.relation.journalid | J020059159 | - |
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