Authors
Lukoyanychev E.E., Izmailov S.G., Evsyukov D.A., Bodrov A.A., Rotkov A.I., Panyushkin A.V.
City Clinical Hospital №7 of the Leninsky District of Nizhny Novgorod named after E.L. Berezova, Nizhny Novgorod
Abstract
Objective. Despite the spread of the laparoscopic method of hernia treatment, which provides a reduction in the duration of the hospital stage, a quick and comfortable rehabilitation period, the incidence of complications is estimated at 7–12%. One of the main causes of complications is an inadequate local and general reaction of the body to foreign material. The severity of the inflammatory reaction to the implant is determined by an imbalance in the system of pro-inflammatory and anti-inflammatory cytokines, which leads to a change in reactivity in the leukocyte cell system. Taken together, these disorders lead to a deviation from the norm of cytochemical and immunocytochemical parameters. Solving the problems of treatment and prevention of hernias of the anterior abdominal wall has a significant potential for increasing the working capacity of the population and reducing the financial costs of healthcare, improving the patient’s quality of life and cosmetic effect.
Material and methods. On the basis of SBIH NO «City Clinical Hospital №7 named after E.L. Berezov» of the city of Nizhny Novgorod prospectively analyzed the results of treatment of 74 patients aged 18 to 80 years, inclusive, who underwent prosthetic repair of an aponeurosis defect of an unstrapped hernia of the anterior abdominal wall with a standard polypropylene mesh implant. Patients of group I (groups of scientific control, n = 38) did not receive additional treatment. In group II (n = 36), patients from the first day after surgery received hydroxyethyldimethyldihydropyrimidine per os at a dose of 0.5 g 3 times a day before meals for 5–7 days. Blood sampling was performed before surgery and on days 3 and 5 after surgery. The study of the cytokine profile was performed using ELISA kits on the enzyme immunoassay analyzer “Lazurit” (Dynex, USA) by the Gemohelp laboratory (Nizhny Novgorod).
Results. The level of C-reactive protein is characterized by a significant rise on the 3rd day after surgery (p<0.001, Wilcoxon’s test) in both groups. By day 5, C-reactive protein continued to increase by 2 times in the control group (p<0.001, Wilcoxon test), and in the main group, the level decreased by 3 times, with a significant difference between the groups (p<0.0014, U-test). TNF-a in the main group after surgery decreased by 100% from the initial level (p<0.001, Wilcoxon test), in the control group, this indicator stably remained within the initial values. The level of IL-6 after surgery increased 3.4 times (p<0.001, Wilcoxon test) and 3.2 times (p = 0.022, Wilcoxon test) in groups I and II, respectively. In the control group on the 5th day its further growth was recorded, and in the main group it decreased, with a significant difference between the groups by 63% (p = 0.005, U-test). Interleukin 8 significantly differed between the groups on the 3rd and 5th day after surgery, significantly prevailing in group II by 96% (p = 0.016, U-test) and 94% (p = 0.048, U-test), by day, respectively. IL-10 on day 3 after surgery prevailed in group II by 103% (p<0.001, U-test), significantly exceeding the initial value by 56% (p = 0.030, Wilcoxon test). However, on day 5, its concentration was lower than in group I by 20% (p<0.049, U-test).
Conclusion. The pyrimidine drug hydroxyethyldimethyldihydropyrimidine has a significant effect on the concentration of C-reactive protein and cytokines (IL-4, IL-6, IL-10 and TNF-a) in the acute phase of inflammation as part of the pharmacological support of planned hernioplasty of the anterior abdominal wall, which may be associated with a decrease in the production of acute phase proteins, an increase in the processes of cell and tissue proliferation and angiogenesis.
Keywords: pharmacological support, hernioplasty of the anterior abdominal wall, regulation of inflammation, lymphocytes, C-reactive protein, hydroxyethyldimethyldihydropyrimidine.
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