Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1991-12-2
pubmed:abstractText
The subjects were 241 patients with lower respiratory tract infections treated at two medical centers in Austria; 161 of the patients were evaluated clinically and, of these, 69 were evaluated bacteriologically. The patients were randomly assigned to receive ofloxacin (n = 101) or a comparison drug (doxycycline [n = 27] or amoxicillin-clavulanate [n = 33]). The mean age of patients in the ofloxacin group was 61 years; that of patients in the comparison groups was 64 years. The mean duration of treatment was nine days; most patients received the study drug intravenously for three days and then orally for four to seven days. In most patients, the doses were 200 mg of ofloxacin twice daily; 100 mg of doxycycline twice daily; or 2,200 mg of amoxicillin-clavulanate intravenously two or three times daily, followed by 625 mg orally two to four times daily. The clinical response was rated satisfactory (all pretreatment symptoms disappeared) in 28% of the ofloxacin-treated patients and in 22% of the other two groups; improved (all except one symptom improved) in 70% and 65%, respectively; and unsatisfactory in 2% and 13%, respectively. The bacteriologic response was rated satisfactory in 59% of the 39 evaluable ofloxacin-treated patients and in 50% of the 30 patients in the other two groups. Most of the unsatisfactory responses were associated with persistent strains of Streptococcus pneumoniae. Transient side effects of mild to moderate severity were noted in nine of the 101 ofloxacin-treated patients and in seven of the 60 patients in the other two groups.(ABSTRACT TRUNCATED AT 250 WORDS)
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0149-2918
pubmed:author
pubmed:issnType
Print
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
460-6
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:1933997-Administration, Oral, pubmed-meshheading:1933997-Adolescent, pubmed-meshheading:1933997-Adult, pubmed-meshheading:1933997-Amoxicillin, pubmed-meshheading:1933997-Amoxicillin-Potassium Clavulanate Combination, pubmed-meshheading:1933997-Bronchitis, pubmed-meshheading:1933997-Chronic Disease, pubmed-meshheading:1933997-Clavulanic Acids, pubmed-meshheading:1933997-Doxycycline, pubmed-meshheading:1933997-Drug Administration Schedule, pubmed-meshheading:1933997-Drug Therapy, Combination, pubmed-meshheading:1933997-Humans, pubmed-meshheading:1933997-Injections, Intravenous, pubmed-meshheading:1933997-Middle Aged, pubmed-meshheading:1933997-Ofloxacin, pubmed-meshheading:1933997-Pneumococcal Infections, pubmed-meshheading:1933997-Pneumonia, pubmed-meshheading:1933997-Prospective Studies, pubmed-meshheading:1933997-Respiratory Tract Infections, pubmed-meshheading:1933997-Streptococcus pneumoniae
pubmed:articleTitle
Ofloxacin in the treatment of lower respiratory tract infections: report of a prospective, comparative trial.
pubmed:affiliation
Pulmonary Center, II. Department of Chest Medicine, Vienna, Austria.
pubmed:publicationType
Journal Article, Clinical Trial, Comparative Study, Randomized Controlled Trial