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[Evaluation of the association of polymorphisms of the CYP2C8 gene with the efficacy and safety of ketorolac in patients with postoperative pain syndrome].
Muradian, A A; Sychev, D A; Blagovestnov, D A; Petrov, D I; Skukin, D S; Epifanova, I P; Sozaeva, Z A; Kachanova, A A; Denisenko, N P; Abdullaev, S P; Grishina, E A.
Afiliación
  • Muradian AA; Russian Medical Academy of Continuous Professional Education.
  • Sychev DA; Russian Medical Academy of Continuous Professional Education.
  • Blagovestnov DA; Russian Medical Academy of Continuous Professional Education.
  • Petrov DI; Russian Medical Academy of Continuous Professional Education.
  • Skukin DS; Sklifosovsky Research Institute of Emergency Medicine.
  • Epifanova IP; Russian Medical Academy of Continuous Professional Education.
  • Sozaeva ZA; Russian Medical Academy of Continuous Professional Education.
  • Kachanova AA; Russian Medical Academy of Continuous Professional Education.
  • Denisenko NP; Russian Medical Academy of Continuous Professional Education.
  • Abdullaev SP; Russian Medical Academy of Continuous Professional Education.
  • Grishina EA; Russian Medical Academy of Continuous Professional Education.
Ter Arkh ; 94(5): 610-615, 2022 Jun 17.
Article en Ru | MEDLINE | ID: mdl-36286958
AIM: To evaluate the possible association of CYP2C8 gene polymorphisms with the clinical efficacy and safety of ketorolac in relation to postoperative pain. MATERIALS AND METHODS: The study included 107 patients after video laparoscopic cholecystectomy, who received ketorolac (30 mg 2.0 w/m 3 r/d) as postoperative pain relief. All patients were genotyped for CYP2C8. The pain syndrome was assessed using the visual analog scale, the McGill pain questionnaire. The profile of adverse reactions was assessed by the dynamics of red blood counts, as a possible trigger for the development of gastrointestinal bleeding according to the method of global assessment of triggers (Global Trigger Tool GTT). RESULTS: According to visual analog scale data: in carriers of the genotype CYP2C8*3 (rs10509681) and CYP2C8*3 (rs11572080) after 12, 24, 36, 48 hours the intensity of pain syndrome is lower than in carriers of the wild type (p0.05). According to the McGill pain questionnaire, there were no statistically significant differences in pain intensity between the two groups. CONCLUSION: In carriers of the genotype CYP2C8*3 (rs10509681) and CYP2C8*3 (rs11572080), the effectiveness of anesthesia with ketorolac is higher than in carriers of the wild type. Carriage of the genotype CYP2C8*3 (rs10509681) and CYP2C8*3 (rs10509681) does not affect the risk of developing adverse reactions after ketorolac anesthesia.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Dolor Postoperatorio / Ketorolaco Tipo de estudio: Clinical_trials / Etiology_studies / Risk_factors_studies Límite: Humans Idioma: Ru Revista: Ter Arkh Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Dolor Postoperatorio / Ketorolaco Tipo de estudio: Clinical_trials / Etiology_studies / Risk_factors_studies Límite: Humans Idioma: Ru Revista: Ter Arkh Año: 2022 Tipo del documento: Article