PMID- 36636370 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20230115 IS - 1178-6973 (Print) IS - 1178-6973 (Electronic) IS - 1178-6973 (Linking) VI - 16 DP - 2023 TI - Is Halving Maintenance of Voriconazole Safe and Efficient in Patients Suffering from Invasive Fungal Infections with Serious Hepatic Dysfunction? PG - 1-8 LID - 10.2147/IDR.S390026 [doi] AB - BACKGROUND: There is a wide debate about the efficacy and safety of voriconazole in patients with impaired hepatic function at Child-Pugh C level. OBJECTIVE: The purpose of this study was to investigate the safety and efficacy between the two groups treated with different dosages of voriconazole (400mg/day vs 200mg/day) in the treatment of invasive fungal infections (IFIs) in patients with hepatic dysfunction. METHODS: A retrospective study enrolling patients with hepatic dysfunction receiving intravenous voriconazole for IFIs from January 1st, 2017, to December 30th, 2021 was conducted. Patients were enrolled in the 400mg per day dose group and 200mg per day dose group. In patients with the same degree of hepatic impairment, factors affecting prognosis were screened and differences in steady-state blood trough concentrations (C(min)) of voriconazole, positive G/GM tests and adverse effects (AEs) were compared between the two groups described above. RESULTS: In total, 308 patients with IFIs were enrolled. For Child-Pugh C class, patients receiving the halved maintenance dose had a lower C(min) and AEs rate but higher recovered rate compared to those receiving maintenance dose, and significant predictors of recovery were dosage (OR, 5.131; 95% CI, 1.599-16.464; p = 0.006) and diabetes (OR, 0.111; 95% CI, 0.020-0.597; p = 0.010). For patients of Child-Pugh A & B class, chronic liver disease (OR, 0.334; 95% CI, 0.159-0.704; p = 0.004) was a prognosis-related factor. CONCLUSION: Halving maintenance dose ensure the efficacy and safety of voriconazole in patients suffering from invasive fungal infections with serious hepatic dysfunction. CI - (c) 2023 Cai et al. FAU - Cai, Xuezhou AU - Cai X AD - Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China. AD - Department of Pharmacy, Xianning Central Hospital, Hubei University of Science and Technology, Xianning, People's Republic of China. FAU - Li, Wei AU - Li W AD - Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China. FAU - Yang, Jian AU - Yang J AD - Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China. AD - Department of Pharmacy, General Hospital of Central Theater Command of Chinese People's Liberation Army, Wuhan, People's Republic of China. FAU - Wu, Guangjie AU - Wu G AD - Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China. FAU - Song, Jianxin AU - Song J AD - Department of Infectious Diseases, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China. FAU - Gong, Xuepeng AU - Gong X AD - Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China. FAU - Liu, Dong AU - Liu D AD - Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China. FAU - He, Yan AU - He Y AUID- ORCID: 0000-0003-2836-1767 AD - Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China. LA - eng PT - Journal Article DEP - 20230105 PL - New Zealand TA - Infect Drug Resist JT - Infection and drug resistance JID - 101550216 PMC - PMC9830075 OTO - NOTNLM OT - Child-Pugh OT - hepatic dysfunction OT - invasive fungal infections OT - through concentration OT - voriconazole COIS- The authors report no conflicts of interest in this work. EDAT- 2023/01/14 06:00 MHDA- 2023/01/14 06:01 PMCR- 2023/01/05 CRDT- 2023/01/13 02:01 PHST- 2022/10/13 00:00 [received] PHST- 2022/12/28 00:00 [accepted] PHST- 2023/01/13 02:01 [entrez] PHST- 2023/01/14 06:00 [pubmed] PHST- 2023/01/14 06:01 [medline] PHST- 2023/01/05 00:00 [pmc-release] AID - 390026 [pii] AID - 10.2147/IDR.S390026 [doi] PST - epublish SO - Infect Drug Resist. 2023 Jan 5;16:1-8. doi: 10.2147/IDR.S390026. eCollection 2023.