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Serotonin norepinephrine reuptake inhibitors in managing neuropathic pain following spinal and non-spinal surgery: A systematic review and meta-analysis of randomized controlled trials.
de Liyis, Bryan Gervais; Sutedja, Jane Carissa; Tjandra, David Christopher; Widha Putri, Ni Luh Putu Saswatasya; Gunawan, Made Favian Budi; Karuniamaya, Chrysanta Paramitha; Barus, Jimmy Fransisco Abadinta; Pinzon, Rizaldi Taslim; Widyadharma, I Putu Eka.
Afiliación
  • de Liyis BG; Faculty of Medicine, Universitas Udayana, Bali, Indonesia.
  • Sutedja JC; Faculty of Medicine, Universitas Udayana, Bali, Indonesia.
  • Tjandra DC; Faculty of Medicine, Universitas Udayana, Bali, Indonesia.
  • Widha Putri NLPS; Faculty of Medicine, Universitas Udayana, Bali, Indonesia.
  • Gunawan MFB; Faculty of Medicine, Universitas Udayana, Bali, Indonesia.
  • Karuniamaya CP; Faculty of Medicine, Universitas Udayana, Bali, Indonesia.
  • Barus JFA; Department of Neurology, School of Medicine and Health Science, Atma Jaya Catholic University of Indonesia, Jakarta, Indonesia.
  • Pinzon RT; Department of Neurology, Duta Wacana University School of Medicine, Yogyakarta, Indonesia.
  • Widyadharma IPE; Department of Neurology, Faculty of Medicine, Universitas Udayana, Bali, Indonesia. Electronic address: eka.widyadharma@unud.ac.id.
Clin Neurol Neurosurg ; 239: 108223, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38484604
ABSTRACT

BACKGROUND:

While serotonin norepinephrine reuptake inhibitors (SNRIs) offer promise in managing Post-surgical neuropathic pain (PSNP), uncertainties remain. This study aims to evaluate the effectiveness and adverse events of SNRIs in managing PSNP.

METHODS:

Systematic searches of PubMed, Embase, and Cochrane databases up to January 1st 2023 identified randomized controlled trials (RCTs) comparing SNRIs to placebo for PSNP. The primary outcome measures were pain at rest and adverse events post-surgery. Subgroup analyses were conducted based on surgical type and specific SNRIs.

RESULTS:

A total of 19 RCTs, encompassing 1440 participants (719 in the SNRI group vs 721 in the placebo group), met the inclusion criteria and were included. The pooled results demonstrated that pain scores were significantly lower in patients treated with SNRIs at 2 hours (MD-0.26; 95%CI -0.47 to -0.04; p=0.02), 6 hours (MD-0.68; 95%CI -1.01 to -0.34; p<0.0001), 24 hours (MD-0.54; 95%CI -0.99 to -0.09; p=0.02), and 48 hours (MD-0.66; 95%CI -1.23 to -0.10; p=0.02) post-surgery. In terms of adverse events, dizziness (OR2.53; 95%CI 1.34-4.78; p=0.004) and dry mouth (OR2.21; 95%CI 1.25-3.92; p=0.007) were significantly higher in the SNRIs group. Subgroup analysis showed that SNRI was found to significantly lower the 24-hour pain score after spinal surgery (MD-0.45; 95%CI -0.84 to -0.05; p=0.03). Duloxetine (MD-0.63; 95%CI -1.15 to -0.11; p=0.02) had a significant effect in lowering the 24-hour pain score at rest compared to placebo, whereas venlafaxine did not.

CONCLUSIONS:

SNRIs yielded considerable pain score reductions across multiple post-surgical intervals, although accompanied by an increased incidence of dizziness and dry mouth.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Dolor Postoperatorio / Ensayos Clínicos Controlados Aleatorios como Asunto / Inhibidores de Captación de Serotonina y Norepinefrina / Neuralgia Idioma: En Revista: Clin Neurol Neurosurg Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Dolor Postoperatorio / Ensayos Clínicos Controlados Aleatorios como Asunto / Inhibidores de Captación de Serotonina y Norepinefrina / Neuralgia Idioma: En Revista: Clin Neurol Neurosurg Año: 2024 Tipo del documento: Article