1985
DOI: 10.1128/aac.27.4.652
|View full text |Cite
|
Sign up to set email alerts
|

Comparison of single-dose tetracycline hydrochloride to conventional therapy of urinary tract infections

Abstract: Sixty-two women with signs and symptoms compatible with lower urinary tract infections were randomized to receive single-dose tetracycline (2 g), multi-dose tetracycline (500 mg four times per day for 10 days), or single-dose amoxicillin (3 g). Urine cultures were obtained upon entry into the study and on days 4, 14, and 28 after therapy. Single-dose tetracycline cured 12 of 16 (75%) of women with documented urinary tract infections, compared with 15 of 16 (94%) in the multi-dose tetracycline group and 7 of 13… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
2
0

Year Published

1989
1989
2024
2024

Publication Types

Select...
5
1
1
1

Relationship

0
8

Authors

Journals

citations
Cited by 14 publications
(4 citation statements)
references
References 20 publications
0
2
0
Order By: Relevance
“…For example, a conventional treatment for mild urinary tract infections induced by catheters comprises the systemic use of 500 mg of TCL every 6 h for a duration of 10 days. [ 30 ] Typical TCL serum and crevicular fluid concentrations achieved with such systemic dosing are 3–4 and 5–12 µg mL −1 , respectively. [ 31 ] Already with a monolayer coating, we obtain a surface loading capacity of 4.5 µg mm −2 ; thus, for this simple coating, we can estimate a local concentration of liberated drug of ≈180 µg mL −1 within 6 h after exposure to a body fluid.…”
Section: Resultsmentioning
confidence: 99%
“…For example, a conventional treatment for mild urinary tract infections induced by catheters comprises the systemic use of 500 mg of TCL every 6 h for a duration of 10 days. [ 30 ] Typical TCL serum and crevicular fluid concentrations achieved with such systemic dosing are 3–4 and 5–12 µg mL −1 , respectively. [ 31 ] Already with a monolayer coating, we obtain a surface loading capacity of 4.5 µg mm −2 ; thus, for this simple coating, we can estimate a local concentration of liberated drug of ≈180 µg mL −1 within 6 h after exposure to a body fluid.…”
Section: Resultsmentioning
confidence: 99%
“…Because both tetracycline and nitroxoline are drugs commonly used in clinical practice for the treatment of bacterial infections, their combined use could improve the efficacy of tetracycline against gastrointestinal diseases caused by diarrhoeic bacteria, because nitroxoline would chelate cations (e.g., calcium, Mg 2+ ) which are reported to lower the absorption of this antibiotic in the gut [ 55 , 56 ]. In addition, as the above-mentioned antibacterial agents are used for the management of urinary tract infections (UTIs) [ 57 , 58 ], their combination could also be a potential treatment strategy against increased acquired resistance to orally administered antibiotics against UTI-causing E. coli [ 32 ], which has been a growing healthcare concern worldwide. Nitroxoline is an oral antibiotic used for the treatment of UTIs [ 59 ].…”
Section: Discussionmentioning
confidence: 99%
“…Because both tetracycline and nitroxoline are drugs commonly used in clinical practice for the treatment of bacterial infections, their combined use could improve the efficacy of tetracycline against gastrointestinal diseases caused by diarrheagenic bacteria, because nitroxoline would chelate cations (e.g., calcium, Mg 2+ ) which are reported to lower the absorption of this antibiotic in the gut [49,50]. In addition, as the above-mentioned antibacterial agents are used for the management of urinary tract infections (UTIs) [51,52], their combination could also be a potential treatment strategy against increased acquired resistance to orally administered antibiotics against E. coli caused UTIs [26], which has been a growing healthcare concern worldwide. The use of sanguinarine in pharmacological preparations is probably not feasible because it is slightly toxic when administered orally to rats, with a median lethal dose (LD50) value of 1,658 mg/kg [53].…”
Section: Discussionmentioning
confidence: 99%