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1.
Chinese Journal of Primary Medicine and Pharmacy ; (12): 2097-2100, 2019.
Artigo em Chinês | WPRIM | ID: wpr-802895

RESUMO

Objective@#To observe the effects of linezolid on the levels of inflammatory factors and T lymphocytes in patients with severe tuberculosis.@*Methods@#Sixty patients with severe tuberculosis treated in Jinhua Guangfu Hospital from April 2016 to November 2017 were selected and divided into control group(n=30) and observation group(n=30) according to different treatment options.The control group was treated with personalized anti-tuberculosis regimen.The observation group was treated with linezolid on the basis of the control group, and both two groups were treated for 9 months.The changes of interleukin-1(IL-1), tumor necrosis factor alpha(TNF-α), IL-6, IL-10 and CD3+, CD4+, CD8+ and CD4+/CD8+ were observed before and after treatment.The incidence of liver injury, thrombocytopenia, myelosuppression, nausea and vomiting, diarrhea were observed.@*Results@#Before treatment, there were no statistically significant differences in IL-1, TNF-α, IL-6, IL-10, CD3+, CD4+, CD8+, CD4+/CD8+ between the two groups(all P>0.05). At 9 months after treatment, the levels of IL-1, TNF-α, IL-6 and IL-10 in the control group were (10.94±1.31)ng/L, (3.03±0.49)ng/L, (183.43±13.24)ng/L, (134.93±34.51)ng/L, respectively, which in the observation group were (6.89±1.29)ng/L, (2.49±0.45)ng/L, (129.48±10.74)ng/L, (189.35±43.27)ng/L, respectively, the differences between the two groups were statistically significant(t=12.195, 11.214, 8.414, 11.291, all P<0.05). The CD3+, CD4+, CD8+, CD4+/CD8+ in the control group were (47.61±7.16)%, (15.49±6.64)%, (20.58±5.61)%, (0.79±0.19) , respectively, which in the observation group were (65.46±8.31)%, (30.23±7.85)%, (34.59±7.41)%, (0.87±0.24) , respectively, the differences between the two groups were statistically significant(t=10.497, 7.865, 12.128, 10.291, all P<0.05). There were no statistically significant differences in the incidence of liver function impairment, thrombocytopenia, myelosuppression, nausea and vomiting, and diarrhea between the two groups(all P>0.05).@*Conclusion@#Linezolid in the treatment of severe tuberculosis can reduce the level of inflammatory factors, improve the cellular immune level of patients, and has a lower incidence of adverse effects.

2.
Chinese Journal of Primary Medicine and Pharmacy ; (12): 2097-2100, 2019.
Artigo em Chinês | WPRIM | ID: wpr-753743

RESUMO

Objective To observe the effects of linezolid on the levels of inflammatory factors and T lymphocytes in patients with severe tuberculosis.Methods Sixty patients with severe tuberculosis treated in Jinhua Guangfu Hospital from April 2016 to November 2017 were selected and divided into control group(n =30) and observation group(n =30) according to different treatment options.The control group was treated with personalized anti-tuberculosis regimen.The observation group was treated with linezolid on the basis of the control group,and both two groups were treated for 9 months.The changes of interleukin-1 (IL-1),tumor necrosis factor alpha (TNF-α),IL-6,IL-10 and CD3+,CD4+,CD8+ and CD4+/CD8+ were observed before and after treatment.The incidence of liver injury,thrombocytopenia,myelosuppression,nausea and vomiting,diarrhea were observed.Results Before treatment,there were no statistically significant differences in IL-1,TNF-α,IL-6,IL-10,CD4+,CD8+,CD8+,CD4+/CD8+ between the two groups(all P>0.05).At 9 months after treatment,the levels of IL-1,TNF-α,IL-6 and IL-10 in the control group were (10.94 ± 1.31) ng/L,(3.03 ± 0.49) ng/L,(183.43 ± 13.24) ng/L,(134.93 ± 34.51) ng/L,respectively,which in the observation group were (6.89 ± 1.29) ng/L,(2.49 ± 0.45) ng/L,(129.48 ± 10.74) ng/L,(189.35 ± 43.27)ng/L,respectively,the differences between the two groups were statistically significant(t =12.195,11.214,8.414,11.291,all P < 0.05).The CD3+,CD4+,CD8+,CD4+/CD8+ in the control group were (47.61 ± 7.16) %,(15.49 ± 6.64) %,(20.58 ± 5.61) %,(0.79 ± 0.19),respectively,which in the observation group were (65.46 ± 8.31) %,(30.23 ± 7.85) %,(34.59 ± 7.41) %,(0.87 ± 0.24),respectively,the differences between the two groups were statistically significant (t =10.497,7.865,12.128,10.291,all P < 0.05).There were no statistically significant differences in the incidence of liver function impairment,thrombocytopenia,myelosuppression,nausea and vomiting,and diarrhea between the two groups(all P > 0.05).Conclusion Linezolid in the treatment of severe tuberculosis can reduce the level of inflammatory factors,improve the cellular immune level of patients,and has a lower incidence of adverse effects.

3.
China Pharmacist ; (12): 464-466, 2015.
Artigo em Chinês | WPRIM | ID: wpr-460348

RESUMO

Objective:To evaluate the effect and safety of rifabutin combined with multi-drugs in the treatment of multi-drug resist-ant tuberculosis with long-term therapy. Methods:Totally 86 cases of patients with multi-drug resistant tuberculosis were divided into the control group and the treatment group with 43 ones in each according to a random number table method. The two groups were trea-ted with levofloxacin, pasiniazid, ethambutol, protionamide and amikacin etc. The control group was treated with rifapentine, and the treatment group was treated with rifabutin additionally. After 18-month treatment, the negative conversion ratio of sputum smear and sputum mycobacterium tuberculosis culture, lesion absorption rate and cavity closure rate of X-ray chest radiograph and adverse reac-tions in the two groups were compared. Results:The negative conversion ratio of sputum smear and sputum mycobacterium tuberculosis culture in the treatment group was 41. 86% and 32. 56%, respectively, which were similar with those in the control group ( P >0. 05). There were no significant differences in lesion absorption rate and cavity closure rate of X-ray chest radiograph and adverse re-actions between the two groups (P>0. 05). Conclusion:Rifapentine or rifabutin combined with multi-drugs in the treatment of multi-drug resistant tuberculosis can improve the negative conversion rate of sputum mycobacterium and lesion absorption and cavity closure with high safety.

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