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[Acetylsalicylic acid after iliac-femoro-popliteal interventions?].

To determine whether acetyl salicylic acid (ASA) in a daily dose of 1500 mg versus untreated controls is effective in patients with peripheral arterial disease a prospective randomized but not placebo-controlled one single centre trial was undertaken. Patients were assigned to one of two groups by means of multi-dimensional contingency tables whereas the risk factors age, sex, height, body weight, diabetic metabolic state, hypertension, history of myocardial infarction, smoking habits and preoperative clinical status according to the Fontaine classification where found in the state of balance. 298 patients with arterial occlusions in the iliaco-femoro-popliteal level were recruited during 1971-1974, the primary end points were probability of patency and probability of survival. In regard as well as to the probability of patency (p less than 0.56 Breslow, p less than 0.66 Mantel) as to the probability of survival (p less than 0.10 Breslow, p less than 0.70 Mantel) no statistical significant difference was detected. In conclusion ASA, in the doses administered here, was unable to improve patency or prolong patient survival, an outcome, which is at variance with results obtained by others.

Arterial Occlusive Diseases↗

[Treatment with rectal diazepam or acetylsalicylic acid in effervescing tablets in ambulatory cervical curettage and biopsy. A double-blind randomized study].

A double-blind randomised investigation with placebo control was undertaken to investigate the effect of 10 mg diazepam rectally or 1 g acetyl salicylic acid as effervescing tablets on pain and nervousness during and after outpatient cervical curettage and biopsy from the vaginal cervix or the cervical endothelium. A total of 97 women participated and were subdivided at random. Three patients were, however, excluded as they did not participate as planned. No differences were found between the three groups as regards pain and nervousness during the intervention and fatigue and drowsiness after the intervention. No statistically significant difference was found in the degree of satisfaction with the treatment in the various therapeutic groups.

Administration, Rectal↗

[Bronchoconstrictive and bronchodilating effects of acetylsalicylic acid in patients with bronchial asthma].

An aspirin test has been performed in 100 asthma patients. The response of the bronchi appeared contradictory: aspirin asthma on the one hand, and bronchodilatation on the other occurred in 31 and 28 patients, respectively; 41 patients appeared nonresponders. Maximum effect of the drug was noted in the small bronchi. Desensitization to aspirin and hemosorption reduced asthma patients sensitivity to nonsteroid antiinflammatory drugs.

Adolescent↗

[Experiences from general practice: use of acetylsalicylic acid and anticoagulants in patients following acute myocardial infarct].

An effective therapy with coumarin derivatives within the secondary prevention after acute myocardial infarction makes great demands on the dispensary care. The risk of serious complications is relatively high. The risk of therapy with acetyl salicylic acid (ASS) in low dosage is significantly smaller. A significant decrease of the rate of reinfarctions and lethality by acetyl salicylic acid was made evident. The retrospective evaluation of the duration of treatment and effectiveness of the therapy with anticoagulants in postinfarction patients (n = 260) had the following result: reduction of the anticoagulant therapy from 75% in the year 1985 to 35% in the year 1989. Increase of the acetyl salicylic acid therapy (250 mg/day) from 23% to 60% in the same period. Up to 1987 the average duration of treatment with anticoagulants was 61.2 +/- 33.6 months, since 1988 only 9.6 +/- 2.6 months. 80% of the patients had a temporary ineffective therapy with anticoagulants, 50% were transitorily in the therapeutic risk region. At present only patients with an increased thromboembolic risk received an obligatory anticoagulant therapy.

Aged↗

[Interpretation of reactions to acetylsalicylic acid and glaphenine].

Challenge test puts in evidence the responsibility of a drug. The biological checking by plasmatic histamine leads to distinguish between a specific histamine-release reaction and a non-specific one. Thus, glafenine has proved to be a non specific histamine release where as in some cases, acetyl-salicylic-acid (A.S.A.) behaves like a specific histamine release.

Adult↗