Sammendrag
Background
The purpose of our study was to evaluate the effects of a new reimbursement rule for
antihypertensive medication that made thiazides mandatory first-line drugs for newly treated,
uncomplicated hypertension. The objective of the new regulation was to reduce drug
expenditures.
Methods and Findings
We conducted an interrupted time-series analysis on prescribing data before and after the
new reimbursement rule for antihypertensive medication was put into effect. All patients
started on antihypertensive medication in 61 general practices in Norway were included in the
analysis. The new rule was put forward by the Ministry of Health and was approved by
parliament. Adherence to the rule was monitored only minimally, and there were no penalties
for non-adherence. Our primary outcome was the proportion of thiazide prescriptions among
all prescriptions made for persons started on antihypertensive medication. Secondary
outcomes included the proportion of patients who, within 4 mo, reached recommended
blood-pressure goals and the proportion of patients who, within 4 mo, were not started on a
second antihypertensive drug. We also compared drug costs before and after the intervention.
During the baseline period, 10% of patients started on antihypertensive medication were given
a thiazide prescription. This proportion rose steadily during the transition period, after which it
remained stable at 25%. For other outcomes, no statistically significant differences were
demonstrated. Achievement of treatment goals was slightly higher (56.6% versus 58.4%) after
the new rule was introduced, and the prescribing of a second drug was slightly lower (24.0%
versus 21.8%). Drug costs were reduced by an estimated Norwegian kroner 4.8 million (E0.58
million, US$0.72 million) in the first year, which is equivalent to Norwegian kroner 1.06 per
inhabitant (E0.13, US$0.16).
Conclusions
Prescribing of thiazides in Norway for uncomplicated hypertension more than doubled after
a reimbursement rule requiring the use of thiazides as the first-choice therapy was put into
effect. However, the resulting savings on drug expenditures were modest. There were no
significant changes in the achievement of treatment goals or in the prescribing of a second
antihypertensive drug.
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