Evidence map›Paper›PMID 41926349›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2026

Effects of Esketamine Infusion by Patient-Controlled Intravenous Analgesia in Patients With Zoster-Associated Pain: A Retrospective Study.

Yingying Lou, Song Zhou, Yonggan Ying

Abstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Yingying LouDepartment of Pain, Ningbo Medical Center Lihuili Hospital, Ningbo, Zhejiang, China.
Song ZhouDepartment of Cardiothoracic Surgery, Ningbo Medical Center Lihuili Hospital, Ningbo, Zhejiang, China.
Yonggan YingDepartment of Pain, Ningbo Medical Center Lihuili Hospital, Ningbo, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Esketamine has been used for the management of acute and chronic pain. This study aimed to evaluate the effects of patient-controlled intravenous analgesia (PCIA) with esketamine on zoster-associated pain during the subacute stage. MATERIAL AND METHODS This retrospective study analyzed 86 patients treated at Ningbo Medical Center Lihuili Hospital between January 1, 2024, and September 1, 2024. Patients were divided into an esketamine group (group ES, n=44) and a control group (group C, n=42). Group ES received intravenous esketamine via PCIA for 5 days, whereas group C received 0.9% saline. Both groups underwent pulsed radiofrequency treatment. Numeric rating scale (NRS) scores, Pittsburgh Sleep Quality Index (PSQI) scores, postoperative analgesic consumption, incidence of postherpetic neuralgia, Central Sensitization Index (CSI) scores, and adverse events were assessed before and after treatment. RESULTS Group ES demonstrated significantly lower NRS and PSQI scores at 1 week (NRS: Z=2.075, P=0.038; PSQI: Z=4.224, P<0.001) and 4 weeks (NRS: Z=2.117, P=0.034; PSQI: Z=5.775, P<0.001). Tramadol and pregabalin consumption did not differ between groups at 1, 4, 12, or 24 weeks (P>0.01). The postherpetic neuralgia rate was 25.00% in group ES and 42.86% in group C (χ²=3.066, P=0.08). CSI scores differed at 12 weeks (t=2.591, P=0.011) and 24 weeks (t=2.135, P=0.036). Group ES had higher incidences of dizziness, nausea, and vomiting, but lower incidences of rebound pain and constipation. CONCLUSIONS Esketamine was associated with reduced pain intensity and improved sleep quality in patients with zoster-associated pain during the early posttreatment period.

Indexed as

Analgesia, Patient-ControlledHerpes ZosterKetamineAgedAnalgesicsFemaleHumansInfusions, IntravenousMaleMiddle AgedNeuralgia, PostherpeticPain ManagementPain MeasurementRetrospective StudiesTreatment OutcomeAnalgesicsEsketamineKetamine

Identifiers

PMID41926349
PMCPMC13055405

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.