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服用复方磺胺甲恶唑或单独服用甲氧苄啶患者粪便菌群的耐药性。

Resistance among fecal flora of patients taking sulfamethoxazole-trimethoprim or trimethoprim alone.

作者信息

Guerrant R L, Wood S J, Krongaard L, Reid R A, Hodge R H

出版信息

Antimicrob Agents Chemother. 1981 Jan;19(1):33-8. doi: 10.1128/AAC.19.1.33.

Abstract

Because of the widespread occurrence of resistance to sulfonamides among Enterobacteriaceae, some researchers have suggested using trimethoprim (TMP) alone instead of the combination sulfamethoxazole-trimethoprim (SMX-TMP) in treating infections with TMP-susceptible organisms. To answer whether SMX-TMP suppresses the emergence of resistant organisms compared with TMP alone, quantitative fecal cultures were made for total and TMP-resistant organisms before, during, and after SMX-TMP (800/160 mg twice a day) or TMP (200 or 100 mg twice a day) was given to 48 patients for 4 weeks in a prospective, randomized study. All three regimens left anaerobes intact and reduced the total aerobic coliform fecal flora by approximately 4 logs throughout the 4-week treatment period. In 11 of 19 (58%) patients taking TMP 200 mg twice daily, TMP-resistant organisms emerged or increased during therapy (P less than 0.01, compared with none of the 12 controls), whereas in only 4 of 18 (22%) patients on SMX-TMP did TMP-resistant organisms increase. These TMP-resistant organisms increased by less than 1 log and were predominantly Pseudomonas and Acinetobacter species. In only one instance did an SMX-TMP-resistant Escherichia coli strain emerge after 4 weeks of SMX-TMP therapy. The slight increase in Pseudomonas and Acinetobacter species seen with TMP alone in this study raises a potential risk of giving TMP alone in settings where these organisms may cause serious infections, as in immunosuppressed patients.

摘要

由于肠杆菌科细菌对磺胺类药物的耐药性广泛存在,一些研究人员建议在治疗对甲氧苄啶(TMP)敏感的微生物感染时,单独使用甲氧苄啶而非复方磺胺甲恶唑(SMX-TMP)。为了回答与单独使用TMP相比,SMX-TMP是否能抑制耐药菌的出现,在一项前瞻性随机研究中,对48例患者给予SMX-TMP(800/160mg,每日两次)或TMP(200或100mg,每日两次)治疗4周,在给药前、给药期间和给药后对总的和对TMP耐药的微生物进行定量粪便培养。在为期4周的治疗期间,所有三种治疗方案均未影响厌氧菌,并使需氧大肠菌群粪便菌群总数减少了约4个对数。在每日两次服用200mg TMP的19例患者中,有11例(58%)在治疗期间出现或增加了对TMP耐药的微生物(与12例对照组无一例出现相比,P<0.01),而在接受SMX-TMP治疗的18例患者中,只有4例(22%)出现了对TMP耐药的微生物增加。这些对TMP耐药的微生物增加不到1个对数,主要是假单胞菌属和不动杆菌属。在接受SMX-TMP治疗4周后,仅出现了1例对SMX-TMP耐药的大肠杆菌菌株。在本研究中,单独使用TMP时观察到的假单胞菌属和不动杆菌属的轻微增加,提示在这些微生物可能引起严重感染的情况下,如免疫抑制患者,单独使用TMP存在潜在风险。

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本文引用的文献

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Trimethoprim: laboratory and clinical studies.甲氧苄啶:实验室研究与临床研究
J Clin Pathol. 1968 Mar;21(2):202-9. doi: 10.1136/jcp.21.2.202.
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Trimethoprim-sulfamethoxazole: in vitro microbiological aspects.甲氧苄啶-磺胺甲恶唑:体外微生物学方面
J Infect Dis. 1973 Nov;128:Suppl:442-62 p. doi: 10.1093/infdis/128.supplement_3.s442.
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Trimethoprim-resistant coliforms.耐甲氧苄啶大肠菌群
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