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Intravenous Patient-Controlled Analgesia with Esketamine Improves Early Depressive Symptoms in Patients with Postherpetic Neuralgia: A Single-Center Retrospective Cohort Study

Ling Qiu, Xuhui Chen, Fu Jia, Xingqu Chen, Xiaobin Wang

preprint DOI: 10.21203/rs.3.rs-4102452/v1 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Retrospective study
Sample size 83
Population Patients with postherpetic neuralgia hospitalized at the affiliated hospital of Southwest Medical University
Interventions Esketamine Sufentanil
Duration Treatment from June 2021 to March 2023; assessments before treatment and at 3 days, 7 days, 1 month, 2 months, and 3 months post-treatment
Measures Numeric Rating Scale (NRS), Patient Health Questionnaire-9 (PHQ-9), Generalized Anxiety Disorder-7 (GAD-7)
Topics Esketamine
Key points Esketamine patient-controlled analgesia produced greater reductions in depression scores at 3 and 7 days and in anxiety scores at 3 days, 7 days, and 3 months compared with sufentanil, but no differences in depression at 1, 2, or 3 months or anxiety at 1 or 2 months. Pain reductions were significant and similar in both groups at all post-treatment time points.

Abstract

Abstract Objective Patients with Postherpetic Neuralgia (PHN) often exhibit depressive-like symptoms, significantly impacting their quality of life. Esketamine, known for its analgesic properties, has also been recognized for its rapid antidepressant effects. However, its efficacy in the treatment of PHN requires further exploration. This study aims to evaluate the impact of intravenous patient-controlled analgesia with esketamine on depressive mood in PHN patients.

Methods: This retrospective study analyzed PHN patients hospitalized and treated at the affiliated hospital of Southwest Medical University from June 2021 to March 2023. Patients were divided into the esketamine group (E group) and the sufentanil group (S group) based on their treatment regimens. Primary outcomes included pain NRS, depression PHQ-9, and anxiety GAD-7 scores measured before treatment, and at 3 days, 7 days, 1 month, 2 months, and 3 months post-treatment.

Results: A total of 83 patients were included in the analysis. Before treatment, there were no statistically significant differences in pain NRS, depression PHQ-9, and anxiety GAD-7 scores between the two groups (P > 0.05). Compared to before treatment, significant reductions in pain NRS scores were observed at all post-treatment time points in both groups (P < 0.05), with no differences between groups (P > 0.05). The E group exhibited significantly lower depression PHQ-9 scores than the S group at 3 days and 7 days post-treatment (P < 0.05), but no significant differences were observed at 1 month, 2 months, and 3 months (P > 0.05). Anxiety GAD-7 scores were significantly lower in the E group compared to the S group at 3 days, 7 days, and 3 months post-treatment (P < 0.05), with no statistical differences at 1 month or 2 months post-treatment (P > 0.05).

Conclusion: Intravenous patient-controlled analgesia with esketamine not only alleviates pain in PHN patients but also improves early symptoms of anxiety and depression.

Comparable studies

Other observational and cohort studies on esketamine, most cited first.

Study Year Design Participants
Treating bipolar depression with esketamine: Safety and effectiveness data from a naturalistic multicentric study on esketamine in bipolar versus unipolar treatment‐resistant depression Patients with treatment-resistant bipolar depression (B-TRD) and unipolar... 2023 Observational cohort n = 70
Comparative Effectiveness of Intravenous Ketamine and Intranasal Esketamine in Clinical Practice Among Patients With Treatment-Refractory Depression: An Observational Study. Adults with treatment-resistant depression 2023 Observational study n = 62
Predicting outcome with Intranasal Esketamine treatment: A machine-learning, three-month study in Treatment-Resistant Depression (ESK-LEARNING) Treatment-resistant depression patients 2023 Retrospective, multicentric, real-world study n = 149
Esketamine in treatment-resistant depression patients comorbid with substance-use disorder: A viewpoint on its safety and effectiveness in a subsample of patients from the REAL-ESK study Patients with treatment-resistant depression and a substance use disorder 2023 Observational, retrospective, multicentre study n = 26
Rapid infusion of esketamine for unipolar and bipolar depression: a retrospective chart review Patients with treatment-resistant depression and bipolar depression meeting DSM-IV-TR... 2017 Retrospective observational study n = 27

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