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Chinese Journal of Experimental and Clinical Infectious Diseases(Electronic Edition) ›› 2023, Vol. 17 ›› Issue (02): 79-83. doi: 10.3877/cma.j.issn.1674-1358.2023.02.002

• Review • Previous Articles     Next Articles

Current situation and mechanism of liver function injury in patients with acquired immunodeficiency syndrome combined with pneumocystis pneumonia treated by Trimethoprim sulfamethoxazole

Tongtong Wang, Chunyu Zhu, Yingchu Liu, Guiju Gao()   

  1. Capital Medical University, Beijing 100069, China
    Clinical and Research Center of AIDS, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China
  • Received:2022-09-07 Online:2023-04-15 Published:2023-06-30
  • Contact: Guiju Gao

Abstract:

Pneumocystis pneumonia (PCP) is a life-threatening pulmonary infection that commonly occurs in immunocompromised patients and human immunodeficiency virus (HIV)-infected patients with low CD4+ T cell counts, which is one of the most common opportunistic infections (OIs) in patients with acquired immunodeficiency syndrome (AIDS). For a long time, Trimethoprim sulfamethoxazole (TMP-SMZ) remains the first-line recommended treatment for PCP. It kills pneumocystis by blocking folic acid synthesis. But it has many adverse reactions such as rash, fever, hepatotoxicity, thrombocytopenia and sometimes has to be discontinued, which affects clinical treatment outcome and patient’s prognosis. Hepatotoxicity caused by TMP-SMZ in patients with AIDS in our country is not rare. It can be manifested as elevated hepatic transaminases, jaundice and even acute liver injury. This review describes the epidemiology and treatment of HIV-associated PCP and the pathogenesis of hepatotoxicity caused by trimethoprim-sulfamethoxazole, in order to provide diagnosis and treatment ideas for clinical treatment of related diseases.

Key words: Acquired immunodeficiency syndrome, Pneumocystis pneumonia, Trimethoprim, Sulfamethoxazole drug combination, Chemical and drug induced liver injury

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