Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2001 Jan-Feb;27(1):83-91.

[Determinants of compliance with antidepressive drugs]

[Article in French]
Affiliations
  • PMID: 11294043

[Determinants of compliance with antidepressive drugs]

[Article in French]
I Gasquet et al. Encephale. 2001 Jan-Feb.

Abstract

A national survey was conducted in a representative sample of the general French population in order to assess antidepressant non compliance frequency and the factors that influence it. Two types of noncompliance were taken into account: 1) the premature interruption of the treatment; 2) the omission of doses. Data were collected by phone interview. Results show that 36.9% of the 423 included subjects (who represent 4.3% of the sample) were noncompliants (15.4% by treatment interruption and 21.5% by dosage modification). The two types of noncompliance have different risk factors. Treatment interruption was more frequent for patients with high level of schooling (OR = 2.5), in case of multiple take regimens (OR = 3), when the physician did not informed the patient about treatment (OR = 3.3) and when the patients' sources of information were exclusively non medical ones (OR = 3.7). Dosage modification was more frequent in female (OR = 2.1), when the treatment duration exceeded six months (OR = 2.5) and when the prescriber did not communicate with the patient relatives (OR = 1.8). The information delivered by the physician about the duration of the treatment was associated with the two types of compliance but with an opposite effect. This information has a protective effect on treatment interruption (OR = 0.5) but increases the risk of dosage modification (OR = 1.1).

PubMed Disclaimer

Publication types

Substances

LinkOut - more resources