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1. |
A study on tissue concentrations of cephradine achieved in patiens with peripheral vascular disease |
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Current Medical Research and Opinion,
Volume 5,
Issue 6,
1978,
Page 427-432
MatharuS. S.,
RamsdenC. H.,
KesterR. C.,
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摘要:
SummaryThe levels of cephradine were measured in serum, voluntary muscle and subcutaneous fat samples collected from 30 patients during surgical operations for peripheral vascular disease. Cephradine 2 g was administered in two equal doses by intramuscular and intravenous routes before each operation. The mean levels found in the serum and muscle were well above the minimum inhibitory concentrations required for most important Gram-positive and Gram-negative pathogens, in contrast to the relatively low mean level found in subcutaneous fat.
ISSN:0300-7995
DOI:10.1185/03007997809111910
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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2. |
Oxaprozin versus aspirin in rheumatoid arthritis: a double-blind trial |
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Current Medical Research and Opinion,
Volume 5,
Issue 6,
1978,
Page 433-438
JamarR.,
DequekerJ.,
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摘要:
SummaryA parallel double-blind trial was carried out over a 3-month period in 40 patients suffering from active rheumatoid arthritis to compare the anti-inflammatory effectiveness and side-effects of treatment with oxaprozin and aspirin. The results showed that 1200 mg oxaprozin daily had similar anti-inflammatory properties to those of 3.9 g aspirin daily in rheumatoid arthritis. Better results were produced with 1200 mg oxaproxin daily than with a 600 mg dosage level, suggesting that there is a close dose-response relationship. The incidence of side-effects was similar with both drugs. Gastrointestinal intolerance was more frequent and severe in the aspirin group, whereas rash and headache were noted more often in patients receiving oxaprozin.
ISSN:0300-7995
DOI:10.1185/03007997809111911
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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3. |
Efficacy of co-trimoxazole in infantile gastro-enteritis |
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Current Medical Research and Opinion,
Volume 5,
Issue 6,
1978,
Page 439-443
Ghaffar BillooA.,
MalikAbdul,
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摘要:
SummaryA comparative, randomized trial was carried out in 105 children, aged between 2 months and 2 years and who were suffering from acute gastro-enteritis, to assess the effectiveness of co-trimoxazole with that of streptomycin and neomycin. Patients were treated in hospital for 5 days or longer and received daily doses either of 50 mg/kg streptomycin or neomycin, or of 6 mg trimethoprim plus 30 mg sulphamethoxazole/kg. Clinical and bacteriological assessments of response to treatment showed that better results were achieved in the co-trimoxazole group, and the duration of illness was also shorter in this group. In the 3 patients on neomycin and the 12 on streptomycin who did not respond clinically, symptoms were controlled in all of them within 2 to 3 days of being changed over to co-trimoxazole treatment.
ISSN:0300-7995
DOI:10.1185/03007997809111912
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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4. |
The contraceptive effects of a new low-dose combination type oral contraceptive |
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Current Medical Research and Opinion,
Volume 5,
Issue 6,
1978,
Page 444-449
KallioH.,
RhenK.,
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摘要:
SummaryA study was carried out in 9 women volunteers to investigate the central and peripheral effects of a low-dosage oral contraceptive combination of 0.75 mg lynestrenol plus 0.0375 mg ethinyl oestradiol given for 22 days per cycle over a period of 6 cycles. The results of assessments of a number of hormonal, vaginal and cervical parameters showed that this combination has a two-fold effect: a central effect on the pituitary and a peripheral effect on the ovaries and on endometrial development. The findings of an effect on cervical mucus, as with higher dose combinations, were not sufficiently consistent to warrant a claim for a cervical barrier. The preparation appeared to be well tolerated but there was a high incidence of irregular bleeding in the first treatment cycle. In most of the women, however, this had corrected itself by the second cycle.
ISSN:0300-7995
DOI:10.1185/03007997809111913
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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5. |
Comparative study of salsalate and aspirin in osteoarthrosis of the hip or knee |
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Current Medical Research and Opinion,
Volume 5,
Issue 6,
1978,
Page 450-453
LiyanageSunil P.,
TambarP. K.,
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摘要:
SummaryA short-term, double-blind controlled crossover study was carried out in 20 patients with osteoarthrosis of the hip or knee to compare the effectiveness and tolerance of salsalate and aspirin. After a 1-week placebo washout period, patients received either 3 g salsalate per day or 3.6 g soluble aspirin per day for 2 weeks before being crossed over to the alternative treatment. Paracetamol was used as a rescue analgesic. The results of clinical assessments of pain, stiffness and sleep disturbance, using visual analogue scales, showed that salsalate produced a comparable clinical improvement to that with aspirin, and similar serum salicylate levels. Salsalate, however, was significantly superior to aspirin with regard to side-effects and faecal occult blood loss.
ISSN:0300-7995
DOI:10.1185/03007997809111914
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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6. |
The use of salsalate for control of long-term musculoskeletal pain: an open, non-comparative assessment |
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Current Medical Research and Opinion,
Volume 5,
Issue 6,
1978,
Page 454-460
RegaladoR. G.,
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摘要:
SummaryAn open study was carried out in general practice to assess the analgesic effectiveness, tolerance and side-effects of salsalate when given at a dosage of 3 gper day for 6 weeks. Sixty-six patients who were known long-term analgesic users were treated: they included 16 with active inflammatory disease of rheumatoid type, 20 with degenerative joint disease, and 27 with other musculo-skeletal conditions. Three patients were withdrawn during the study because of gastro-intestinal upset. Assessments, using rating scale scores, were made pre-trial and at 2-weekly intervals of joint pain, other musculoskeletal pain, and duration of morning stiffness. The results showed that there was marked improvement in joint pain and morning stiffness, particularly in those patients with inflammatory joint disease. Improvement in musculo-skeletal discomfort was less evident. Side-effects were reported on 24 occasions, the most frequent being dyspepsia. Faecal occult blood tests showed that there were 7 patients with probable blood loss during treatment, 4 of them, however, had no other clinical signs or symptoms of gastrointestinal intolerance.
ISSN:0300-7995
DOI:10.1185/03007997809111915
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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7. |
Clinical therapeutic evaluation of methylcysteine hydrochloride in patients with chronic obstructive bronchitis: a balanced double-blind trial with placebo control |
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Current Medical Research and Opinion,
Volume 5,
Issue 6,
1978,
Page 461-471
AylwardMansel,
BaterP. A.,
DaviesD. E.,
HutchingsL. A.,
LewisP. A.,
MaddockJ.,
ProtheroeD. A.,
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摘要:
SummaryA double-blind, between-patient, placebo controlled trial was carried out to investigate the effects of methylcysteine hydrochloride in patients with chronic obstructive bronchitis. After a 2-week washout period on placebo, 30 patients were allocated at random to treatment for 6 weeks with either methylcysteine (1200 mg daily in Week 1, 800 mg daily in Week 2, then 600 mg daily) or with identical placebo tablets on the same regimen. During the post-treatment period, all patients returned to a single-blind placebo regimen (6 tablets daily) for a further 14 days. Assessments were made at the start, at regular intervals during the trial, and at the end of the post-treatment period, of subjective and objective measures of clinical response, and measurements of pulmonary function and certain physico-chemical properties of sputum. The results showed that methylcysteine increased sputum volume, reduced the viscidity of sputum, and significantly improved the subjective assessments of ease of expectoration and severity and frequency of cough, leading to a definite improvement in the patients' clinical state. No side-effects of clinical significance were reported and no abnormalities were found in any of the haematological, hepatic and renal function tests carried out.
ISSN:0300-7995
DOI:10.1185/03007997809111916
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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8. |
Night medication in rheumatoid arthritis. III. The use of sulindac |
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Current Medical Research and Opinion,
Volume 5,
Issue 6,
1978,
Page 472-475
SharmaB. K.,
HaslockIan,
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摘要:
SummaryA double-blind controlled trial was carried out in 18 in-patients with classical or definite rheumatoid arthritis to assess the effectiveness of night-time medication with 100 mg indomethacin plus 10 mg diazepam, 200 mg sulindac, and 200 mg sulindac plus 10 mg diazepam in improving sleep and reducing night pain and the duration of morning stiffness. Patients received each treatment regimen for 1 night. The results from the 17 patients completing the full trial protocol indicated that indomethacin plus diazepam was the most effective of the three regimens, although the differences did not reach conventional statistical significance. It is suggested that in further such studies with sulindac a larger dose and a longer duration of treatment should be used.
ISSN:0300-7995
DOI:10.1185/03007997809111917
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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9. |
The effectiveness of temazepam as a hypnotic: an open, multicentre assessment in 804 patients with sleep disorders |
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Current Medical Research and Opinion,
Volume 5,
Issue 6,
1978,
Page 476-483
HarryT. V. A.,
JohnsonP. A.,
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摘要:
SummaryAn open, multi-centre study was carried out in 804 patients complaining of sleep disorders to assess the effectiveness and acceptance of temazepam as a hypnotic. Patients received between 10 mg and 30 mg (mean 16.4 mg) temazepam each night for a week. Subjective assessments using a self-administered questionnaire were made daily of the quality and quantity of sleep. The results showed that sleep induction was rapid and most patients enjoyed a relatively uninterrupted night's sleep, and awakened feeling refreshed. Patient acceptance was good and there was a low incidence of residual or other adverse effects of treatment.
ISSN:0300-7995
DOI:10.1185/03007997809111918
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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10. |
A comparative trial of ketoprofen and ibuprofen in patients with rheumatic disease |
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Current Medical Research and Opinion,
Volume 5,
Issue 6,
1978,
Page 484-488
SaxenaR. P.,
SaxenaU.,
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摘要:
SummaryA comparative controlled study was carried out in 40 patients suffering from rheumatoid arthritis, osteoarthrosis or ankylosing spondylitis to assess the efficacy of ketoprofen and ibuprofen. Patients were allocated at random to receive either 100 mg ketoprofen twice daily or 400 mg ibuprofen 3-times daily over a period of 3 months. Subjective overall assessments of symptoms, based on rating scale scores for pain, duration of morning stiffness and inflammation, showed that there was a greater, more rapid and more sustained improvement in those patients treated with ketoprofen. Measurements of inflamed joint size and of grip strength also improved more with ketoprofen than with ibuprofen. Side-effects, notably nausea, epigastric discomfort and abdominal pain, were more frequent and severe with ketoprofen, leading to the withdrawal of 2 patients in the early stage of the trial, and were probably related to the high dosage used. Three patients receiving ibuprofen needed 7 injections of ACTH to control their symptoms.
ISSN:0300-7995
DOI:10.1185/03007997809111919
出版商:Taylor&Francis
年代:1978
数据来源: Taylor
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