Literature DB >> 6134609

Rational use of anxiolytic/sedative drugs.

M Lader, H Petursson.   

Abstract

The benzodiazepines are the most effective, safest, and most widely used antianxiety drugs. As a class of drugs, there are few major differences between the various benzodiazepine derivatives. The main distinguishing features are different plasma half-lives and the presence or absence of pharmacologically active metabolites. Plasma half-lives vary considerably, from 2 to 3 hours to more than 100 hours. All benzodiazepines are equally effective in the short term management of anxiety and insomnia, and their classification into 'anxiolytics' and 'hypnotics' is not justified. There are numerous other indications for benzodiazepine use, such as muscle spasm in osteoarthritic conditions, and acute alcohol withdrawal, but the benzodiazepines have no antidepressive or analgesic effects. While there is no good evidence for their long term efficacy in the treatment of anxiety and insomnia, the benzodiazepines are more effective and safer than their main predecessors, the barbiturates. Some of the benzodiazepines, particularly those with long plasma half-lives which are commonly used as hypnotics, have a prolonged duration of action and cause marked 'hang-over' effects. Alcohol enhances the effects of these drugs, and thus can also increase their side effects. Adversely effects such as oversedation, tremor, ataxia and confusion are much more common in elderly patients. Ever since the benzodiazepines were first marketed 20 years ago their use has increased rapidly, and it is now estimated that between 12 and 16% of the adult population in developed countries use tranquillisers at some time each year. However, their overall use has probably diminished somewhat in the last few years. Although their indications are very common, it is possible that some of this extensive usage may be the result of dependence. Until recently, published reports of such dependence were comparatively few. However, withdrawal symptoms have now been demonstrated in a substantial proportion of patients on long term, normal dose benzodiazepine treatment. The abstinence syndrome usually lasts for 8 to 10 days, and is characterised by insomnia, anxiety, loss of appetite and bodyweight, tremor, perspiration, and a host of perceptual disturbances. More serious developments such as epileptic fits and psychosis are probably infrequent during withdrawal from therapeutic doses. The overall incidence of benzodiazepine dependence remains unknown.

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Year:  1983        PMID: 6134609     DOI: 10.2165/00003495-198325050-00004

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  27 in total

1.  The role of benzodiazepines in nonpsychiatric medical practice.

Authors:  L Lasagna
Journal:  Am J Psychiatry       Date:  1977-06       Impact factor: 18.112

2.  The similarities and differences between meprobamate and barbiturates.

Authors:  F M BERGER
Journal:  Clin Pharmacol Ther       Date:  1963 Mar-Apr       Impact factor: 6.875

3.  Withdrawal psychosis: a study of 30 consecutive cases.

Authors:  K Fruensgaard
Journal:  Acta Psychiatr Scand       Date:  1976-02       Impact factor: 6.392

4.  Cross-national study of the extent of anti-anxiety-sedative drug use.

Authors:  M B Balter; J Levine; D I Manheimer
Journal:  N Engl J Med       Date:  1974-04-04       Impact factor: 91.245

5.  Tolerance development with chlordiazepoxide in relation to the plasma levels of the parent compound and its main metabolites in mice.

Authors:  J D Christensen
Journal:  Acta Pharmacol Toxicol (Copenh)       Date:  1973

6.  Use of beta-blocking drugs in psychiatry and neurology.

Authors:  P J Tyrer
Journal:  Drugs       Date:  1980-10       Impact factor: 9.546

7.  Clinical implications of benzodiazepine pharmacokinetics.

Authors:  R I Shader; D J Greenblatt
Journal:  Am J Psychiatry       Date:  1977-06       Impact factor: 18.112

8.  Withdrawal from long-term benzodiazepine treatment.

Authors:  H Petursson; M H Lader
Journal:  Br Med J (Clin Res Ed)       Date:  1981-09-05

Review 9.  Clinical pharmacokinetics of diazepam.

Authors:  M Mandelli; G Tognoni; S Garattini
Journal:  Clin Pharmacokinet       Date:  1978 Jan-Feb       Impact factor: 6.447

Review 10.  Drug interactions with alcohol.

Authors:  M Linnoila; M J Mattila; B S Kitchell
Journal:  Drugs       Date:  1979-10       Impact factor: 9.546

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  7 in total

1.  Initial benzodiazepine use and improved health-related quality of life.

Authors:  Rolf van Hulten; Bart Teeuw; Albert Bakker; Hubert G Leufkens
Journal:  Pharm World Sci       Date:  2005-02

2.  Patients, prescribing, and benzodiazepines.

Authors:  L Nolan; K O'Malley
Journal:  Eur J Clin Pharmacol       Date:  1988       Impact factor: 2.953

3.  Benzodiazepines: dependence and a therapeutic approach to gradual withdrawal.

Authors:  D Blais; L Petit
Journal:  Can Fam Physician       Date:  1990-10       Impact factor: 3.275

Review 4.  Problems and pitfalls in the use of benzodiazepines in the elderly.

Authors:  W H Kruse
Journal:  Drug Saf       Date:  1990 Sep-Oct       Impact factor: 5.606

5.  Benzodiazépines: dépendance et approche thérapeutique pour un retrait graduel.

Authors:  D Blais; B Pharm; L P Pharm
Journal:  Can Fam Physician       Date:  1987-11       Impact factor: 3.275

6.  Sedatives and hypnotics in Stockholm: social factors and kinds of use.

Authors:  G Blennow; A Romelsjö; H Leifman; A Leifman; G Karlsson
Journal:  Am J Public Health       Date:  1994-02       Impact factor: 9.308

7.  Initial study of methylclonazepam in generalized anxiety disorder. Evidence for greater power in the cross-over design.

Authors:  M Ansseau; A Doumont; D Thiry; R von Frenckell; J Collard
Journal:  Psychopharmacology (Berl)       Date:  1985       Impact factor: 4.530

  7 in total

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