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Effectiveness of continuous epidural analgesia on acute herpes zoster and postherpetic neuralgia A retrospective study

Authors
Seo, Young-GyunKim, Se HeeChoi, Sang SikLee, Mi KyoungLee, Chung HunKim, Jung Eun
Issue Date
2월-2018
Publisher
LIPPINCOTT WILLIAMS & WILKINS
Keywords
continuous epidural analgesia; epidural injection; herpes zoster; local anesthetics; postherpetic neuralgia
Citation
MEDICINE, v.97, no.5
Indexed
SCIE
SCOPUS
Journal Title
MEDICINE
Volume
97
Number
5
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/77812
DOI
10.1097/MD.0000000000009837
ISSN
0025-7974
Abstract
Despite early treatment of herpes zoster (HZ), postherpetic neuralgia (PHN) can persist. This study was designed to compare the therapeutic and pain relief effects of continuous epidural analgesia (CEA) on the chronic phase as well as the acute phase of HZ with standard medical treatment. Medical records of 227 patients with moderate to severe zoster-associated pain that had not responded to standard medications were retrospectively reviewed. Patients received standard treatment alone (medical group) or standard treatment plus concurrent CEA (epidural group). The acute and chronic groups were classified according to a 4-week cut-off with regard to time between the onset of the rash and the first treatment. Four groups were studied: Group A (acute/medical group); Group B (acute/epidural group); Group C (chronic/medical group); and Group D (chronic/epidural group). Pain was assessed using the visual analog scale (VAS) and measured every 2 weeks for 6 months. We compared the pain rating at 6 months after the first treatment with the initial pain rating. Response to treatment was defined as a >= 50% reduction in pain severity since the initial visit. Remission was considered complete for patients whose VAS pain score was <= 2 for >3 successive visits and who no longer needed medical support. Patients who received a combination of standard treatment plus CEA (Groups B and D) had significantly higher response to treatment (P=.001) than patients receiving standard treatment alone (Groups A and C). The adjusted odds ratio (OR) for response to treatment in the epidural group versus the medical group was 5.17 (95% confidence interval [CI]: 1.75-15.23) in the acute group and 5.37 (95% CI: 1.62-17.79) in the chronic groups. The adjusted OR for complete remission in the epidural group versus the medical group was 3.05 (95% CI: 1.20-7.73) in the acute group and 4.46 (95% CI: 1.20-16.54) in the chronic group. CEA can effectively relieve pain caused by PHN and acute HZ and increase remission rates. Combining CEA with standard medical treatment may offer a clinical advantage in the management of pain caused by PHN as well as acute HZ.
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