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慢性丙型肝炎患者在临床实践中接受聚乙二醇干扰素联合利巴韦林治疗期间的细菌感染和中性粒细胞减少,无论基线是否存在中性粒细胞减少。

Bacterial infection and neutropenia during peginterferon plus ribavirin combination therapy in patients with chronic hepatitis C with and without baseline neutropenia in clinical practice.

作者信息

Yang J-F, Hsieh M-Y, Hou N-J, Dai C-Y, Huang J-F, Lin Z-Y, Chen S-C, Hsieh M-Y, Wang L-Y, Chuang W-L, Yu M-L

机构信息

Department of Preventive Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.

出版信息

Aliment Pharmacol Ther. 2009 May 1;29(9):1000-10. doi: 10.1111/j.1365-2036.2009.03957.x. Epub 2009 Feb 7.

Abstract

BACKGROUND

Peginterferon-alpha-based therapy frequently leads to neutropenia. It remains unclear whether neutropenia is associated with bacterial infection in chronic hepatitis C (CHC).

AIM

To evaluate the risk of bacterial infection and neutropenia in patients with CHC treated with peginterferon-alpha/ribavirin.

METHODS

In all, 207 patients with CHC with (group A, n = 30) and without (group B, n = 177) baseline neutropenia were treated with peginterferon-alpha/ribavirin.

RESULTS

Group A had significantly higher rates of moderate (<750 cells/microL) and severe (<500 cells/microL) neutropenia than group B (70.0% and 26.7% vs. 20.3% and 8.5% respectively, both P < 0.0001). The sustained virological response rate was similar between patients with and without neutropenia, at baseline or during treatment. Bacterial infection occurred in 4.3% of patients. Group A and patients with lower baseline neutrophil counts had substantially higher rates of bacterial infection. Patients with cirrhosis had significantly higher rates of infection during combination therapy than those without cirrhosis (15%, 3 of 20 vs. 3.2%, 6 of 187, P = 0.045). Nadir neutrophil counts were not correlated to infection episodes.

CONCLUSIONS

Bacterial infection during peginterferon-based therapy for CHC was associated with comorbidity of cirrhosis, but not with neutropenia, whether at baseline or during treatment. Neutropenic CHC patients might be treated safely with close monitoring.

摘要

背景

基于聚乙二醇干扰素-α的治疗常常导致中性粒细胞减少。慢性丙型肝炎(CHC)患者中性粒细胞减少是否与细菌感染相关尚不清楚。

目的

评估聚乙二醇干扰素-α/利巴韦林治疗的CHC患者发生细菌感染和中性粒细胞减少的风险。

方法

总共207例CHC患者接受聚乙二醇干扰素-α/利巴韦林治疗,其中有基线中性粒细胞减少的患者为A组(n = 30),无基线中性粒细胞减少的患者为B组(n = 177)。

结果

A组中度(<750个细胞/微升)和重度(<500个细胞/微升)中性粒细胞减少的发生率显著高于B组(分别为70.0%和26.7%,相比之下B组为20.3%和8.5%,P均<0.0001)。基线时或治疗期间,有或无中性粒细胞减少的患者持续病毒学应答率相似。4.3%的患者发生了细菌感染。A组和基线中性粒细胞计数较低的患者细菌感染发生率显著更高。肝硬化患者在联合治疗期间的感染发生率显著高于无肝硬化患者(15%,20例中有3例;相比之下3.2%,187例中有6例,P = 0.045)。中性粒细胞计数最低点与感染发作无关。

结论

基于聚乙二醇干扰素的CHC治疗期间的细菌感染与肝硬化合并症相关,但与基线时或治疗期间的中性粒细胞减少无关。中性粒细胞减少的CHC患者在密切监测下可能可安全治疗。

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