Relationship between daily dose frequency and adherence to antihypertensive pharmacotherapy: Evidence from a meta-analysis
Background: Rates of patient adherence (compliance) to pharmacotherapy range from 90%. Negative determinants include multiple daily dosing (MDD), chronic duration, and asymptomatic disease. Reports suggest that once-daily (QD) dosing may improve adherence, but their findings are inconclusive. Object...
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Veröffentlicht in: | Clinical therapeutics 2002-02, Vol.24 (2), p.302-316 |
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Sprache: | eng |
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Zusammenfassung: | Background:
Rates of patient adherence (compliance) to pharmacotherapy range from 90%. Negative determinants include multiple daily dosing (MDD), chronic duration, and asymptomatic disease. Reports suggest that once-daily (QD) dosing may improve adherence, but their findings are inconclusive.
Objective:
The purpose of this study was to compare the rates of adherence with QD, twice-daily (BID), and MDD antihypertensive drug regimens.
Methods:
MEDLINE, Embase, and International Pharmaceutical Abstracts databases were searched to identify comparative trials of patient adherence to antihypertensive medication in solid, oral formulations. Data were combined using a random-effects meta-analytic model.
Results:
Eight studies involving a total of 11,485 observations were included (1830 for QD dosing, 4405 for BID dosing, 4147 for dosing >2 times daily [>BID], and 9655 for MDD), in which the primary objective was to assess adherence. The average adherence rate for QD dosing (91.4%, SD = 2.2%) was significantly higher (Z = 4.46,
P < 0.001) than for MDD (83.2%, SD = 3.5%). This rate was also significantly higher (Z = 2.22,
P = 0.026) than for BID dosing (92.7% [SD = 2.3%] vs 87.1% [SD = 2.9%]). The difference in adherence rates between BID dosing (90.8%, SD = 4.7%) and >BID dosing (86.3%, SD = 6.7%) was not significant (Z = 1.82,
P = 0.069).
Conclusions:
The results of this meta-analysis demonstrate that with antihypertensive medications, QD dosing regimens are associated with higher rates of adherence than either BID or MDD regimens. |
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ISSN: | 0149-2918 1879-114X |
DOI: | 10.1016/S0149-2918(02)85026-3 |