The effect of Neurokinin-1 receptor antagonists on postoperative pain: A meta-analysis of randomized controlled trials.

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Tác giả: Viviana Teresa Agosta, Silvia Ajello, Filippo D'Amico, Jacopo D'Andria Ursoleo, Eoin Kelleher, Giovanni Landoni, Stefano Turi, Andrey G Yavorovskiy, Sara Zaffaroni

Ngôn ngữ: eng

Ký hiệu phân loại: 633.14 *Rye

Thông tin xuất bản: United States : Journal of clinical anesthesia , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 737839

 STUDY OBJECTIVE: Substance P is a neuropeptide with a pivotal role in pain transmission and modulation. Preclinical studies suggest that targeting substance P and inhibiting its receptor, neurokinin 1 (NK-1), is a potential avenue for pain relief. When translated into clinical settings, these preliminary findings yielded mixed results. This meta-analysis of randomized controlled trials (RCTs) aims to investigate whether a preemptive administration of NK-1 antagonists may reduce postoperative pain. DESIGN: We searched PubMed, Cochrane and EMBASE from inception to January 3, 2025, for studies comparing NK-1 antagonists versus placebo or standard care that reported data on postoperative pain. The primary outcome was pain at two hours after surgery measured through a 0-10 numeric scale. Secondary outcomes were postoperative pain at 24 and at 48 h and postoperative morphine equivalent consumption. SETTING: Hospitals. MAIN RESULTS: The search strategies identified 13 RCTs with a total of 1959 patients. All studies reported a single preoperative administration of NK-1 antagonists. NK-1 antagonists reduced postoperative pain two hours (n = 8
  MD -0.62
  95 % CI: -0.91, -0.32
  P <
  0.002
  I2 = 0 %) and at 24 h (n = 9
  MD -0.65
  95 % CI: -1.22, -0.09
  P = 0.02
  I2 = 86 %) but not 48 h after surgery. Morphine equivalent consumption was similar in the two groups. CONCLUSIONS: Preoperative single-administration of NK-1 antagonists reduces postoperative pain. The observed pain reduction pattern is consistent with the pharmacokinetics (half-life 9-12 h) of these inhibitors and with data from preclinical studies.
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