首页|不同日剂量美罗培南在肾功能亢进患者中的临床疗效

不同日剂量美罗培南在肾功能亢进患者中的临床疗效

Clinical efficies of different daily doses of meropenem in patients with hyperactive renal function

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目的 探讨不同日剂量美罗培南在肾功能亢进患者中的临床疗效.方法 回顾性分析东营市第二人民医院药学部在2021年1月至2022年12月期间纳入的144例使用美罗培南治疗的患者作为研究对象,按肌酐清除率(Ccr)分为肾功能亢进组(63例)和肾功能正常组(81例).其中亢进组男性37例,女性 26例,年龄 37~69(53.55±4.47)岁,体质量46~93(71.51±6.06)kg,病程 1~6(2.98± 0.93)年;正常组男性48例,女性33例,年龄41~73(53.50±4.42)岁,体质量49~89(71.56±6.01)kg,病程1~5(2.97±0.95)年.比较两组患者肾功能[Ccr、血清肌酐(Scr)、尿素氮(BUN)]、炎症指标[白细胞计数(WBC)、中性粒细胞百分比(NEUT%)、降钙素原(PCT)、C反应蛋白(CRP)]、用药情况及不同日剂量美罗培南的临床疗效.采用独立样本t检验和x2检验.结果 亢进组Ccr水平(126.14± 11.63)ml/min 高于正常组(116.25±10.51)ml/min,Scr(47.66±4.25)µmol/L和 BUN(3.10±0.33)mmol/L水平均低于正常组(58.62±5.62)μmol/L、(4.22±0.49)mmol/L,差异均有统计学意义(均P<0.05).亢进组WBC(15.55±1.23)×109/L、NEUT%(77.85±5.69)%、PCT(48.60±4.12)μg/L、CRP(16.17±3.55)mg/L 均高于正常组(9.44±1.56)×109/L、(68.52±5.52)%、(48.60±4.12)µg/L、(9.23±1.06)mg/L,差异均有统计学意义(均P<0.05).亢进组用药情况在0.5 g剂量(每6 h给药1次、每8h给药1次)、2.0 g剂量(每8 h给药1次)均高于正常组,在1.0 g剂量(每8 h给药1次、每12 h给药1次)均低于正常组,差异均有统计学意义(均P<0.05).亢进组在1/2日剂量、2/3日剂量的临床有效率均为0(0/15、0/17),均低于正常组的88.89%(8/9)、92.31%(24/26),差异均有统计学意义(均P<0.05);亢进组1倍日剂量的临床有效率50.00%(10/20)高于本组1/2及2/3日剂量,但仍然低于正常组1倍日剂量75.61%(31/41),差异均有统计学意义(均P<0.05).亢进组2倍日剂量的临床有效率81.82%(9/11)与正常组100.00%(5/5)比较,差异无统计学意义(P>0.05).结论 不同日剂量美罗培南影响肾功能亢进患者的临床疗效,用药剂量应≥2.0 g(日剂量),必要时可增加至3.0 g.
Objective To explore the clinical efficacies of different daily doses of meropenem in patients with hyperactive renal function.Methods A retrospective analysis was conducted on 144 patients treated with meropenem at Dongying Second People's Hospital from January 2021 to December 2022.Based on the creatinine clearance rate(CCr),the patients were divided into a hyperactive renal function group(63 cases)and a normal renal function group(81 cases).In the hyperactivity group,there were 37 males and 26 females,aged 37-69(53.55±4.47)years,with a body mass of 46-93(71.51±6.06)kg,with a disease course of 1-6(2.98±0.93)years.In the normal group,there were 48 males and 33 females,aged 41-73(53.50± 4.42)years,with a body weight of 49-89(71.56±6.01)kg,with a disease course of 1-5(2.97± 0.95)years.The renal function[Ccr,serum creatinine(Scr),and blood urea nitrogen(BUN)],inflammatory indicators[white blood cell count(WBC),neutrophil percentage(NEUT%),procalcitonin(PCT),and C-reactive protein(CRP)],medication status,and clinical efficacy of different daily doses of meropenem were compared between the two groups.Independent sample t test and x2 test were used.Results The Ccr level in the hyperactivity group was higher than that in the normal group[(126.14±11.63)ml/min vs.(116.25±10.51)ml/min],but the levels of Scr[(47.66± 4.25)μmol/L]and BUN[(3.10±0.33)mmol/L]were lower than those in the normal group[(58.62± 5.62)μmol/L and(4.22±0.49)mmol/L],with statistically significant differences(all P<0.05).The levels of WBC[(15.55±1.23)×109/L],NEUT%[(77.85±5.69)%],PCT[(48.60±4.12)μg/L],and CRP[(16.17±3.55)mg/L]in the hyperactivity group were higher than those in the normal group[(9.44± 1.56)×109/L,(68.52±5.52)%,(48.60±4.12)μg/L,and(9.23±1.06)mg/L],with statistically significant differences(all P<0.05).The drug use of the hyperactivity group was higher than that of the normal group at 0.5 g dose(administered every 6 h and every 8 h)and 2.0 g dose(administered every 8 h),but lower than that of the normal group at 1.0 g dose(administered every 8 h and every 12 h),with statistically significant differences(all P<0.05).The clinical effective rates of the hyperactivity group at 1/2 day dose and 2/3 day dose were 0(0/15 and 0/17),which were lower than those of the normal group[88.89%(8/9)and 92.31%(24/26)],with statistically significant differences(both P<0.05).The clinical effective rate of the hyperactivity group at 1 day dose[50.00%(10/20)]was higher than those at 1/2 day dose and 2/3 day dose,but still lower than that of the normal group[75.61%(31/41)],with statistically significant differences(all P<0.05).The clinical effective rate of the hyperactivity group at double daily dose was 81.82%(9/11),without statistically significant difference compared with 100.00%(5/5)of the normal group(P>0.05).Conclusions Different doses of meropenem affect the clinical efficacy in patients with hyperactive renal function.The dosage should be ≥ 2.0 g(daily dose),and can be increased to 3.0 g if necessary.

Hyperactive renal functionMeropenemDaily doseClinical efficacy

于菁菁、邵琛、曲朋、张老追

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东营市第二人民医院药学部,东营 257335

东营市第二人民医院内分泌肾内科,东营 257335

肾功能亢进 美罗培南 日剂量 临床疗效

山东省自然科学基金青年基金

ZR2020QH332

2024

国际医药卫生导报
中华医学会,国际医药卫生导报社

国际医药卫生导报

影响因子:0.781
ISSN:1007-1245
年,卷(期):2024.30(8)
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