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DOI 10.1186/s12879-024-09774-3

Медицинская библиотека · BMC infectious diseases · 2024

High adsorption capacity of hemoperfusion on imipenem in critically ill patients with septic shock: a case report.

Wang Chuhui, Li Chao, Yang Ping, Liu Kaixi, Xiong Xin, Liu Yangang, Li Xiaoxiao, Zhai Suodi

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Аннотация

BACKGROUND

Sepsis is a life-threatening organ dysfunction caused by an excessive host response to infection, manifested by elevated levels of inflammatory cytokines. At present, the use of hemoperfusion to remove inflammatory cytokines from the bloodstream has been expanding. Meanwhile, the pharmacokinetics and pharmacodynamics characteristics of antibiotics in critically ill patients may be impacted by hemoperfusion.

CASE PRESENTATION: The patient was a 69-year-old male with poorly controlled type 2 diabetes. When admitted to the ICU, Multiple Organ Dysfunction Syndrome (MODS) appeared within 48 h, and he was suspected of septic shock due to acute granulocytopenia and significantly increased procalcitonin. Broad-spectrum antibiotics imipenem was administered according to Sepsis 3.0 bundle and hemoperfusion lasting 4 h with a neutron-macroporous resin device (HA-380, Jafron, China) five times was conducted to lower the extremely high value of serum inflammatory factors. Blood samples were collected to measure imipenem plasma concentration to investigate the effect of hemoperfusion quantitatively. This study showed that 4 h of hemoperfusion had a good adsorption ability on inflammatory factors and could remove about 75.2% of imipenem.

CONCLUSIONS

This case demonstrated the high adsorption capacity of hemoperfusion on imipenem in critically ill patients. It implies a timely imipenem supplement is required, especially before hemoperfusion.

Для цитирования: Wang Chuhui, Li Chao, Yang Ping, Liu Kaixi, Xiong Xin, Liu Yangang, Li Xiaoxiao, Zhai Suodi. High adsorption capacity of hemoperfusion on imipenem in critically ill patients with septic shock: a case report.. BMC infectious diseases. 2024. DOI: 10.1186/s12879-024-09774-3.

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