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Table 2 Weekly number of defined daily doses of medicines per 1000 resident-days during the study period and summary of trends in individuals who did and did not receive an RMMR in the 6–12 months after RACF entry

From: Medicines use before and after comprehensive medicines review among residents of long-term care facilities: a retrospective cohort study

Medicine class

RMMR exposure status

Weekly DDDs/1000 resident-days

Summary of trends

17-weeks before index date

Week of index date

17-weeks after index date

Antidepressantsa

RMMR

459.3

491.7

488.0

• During the pre-intervention period and washout periods, antidepressant use was increasing at a similar rate in both groups

• During follow-up, use plateaued in the RMMR group, but continued to slowly increase in those without an RMMR (-0.34 vs. 0.66 DDDs/1000 days per week, p < 0.001)

No RMMR

434.5

460.5

468.7

Antipsychotics

RMMR

67.0

67.4

67.0

• Differences in weekly trends between groups during the pre-intervention and follow-up periods were negligible (≤ 0.1 DDDs/1000 days per week)

No RMMR

64.1

65.8

66.6

Benzodiazepines or zopiclone

RMMR

102.2

106.0

99.9

• During the pre-intervention period, benzodiazepine/zopiclone use increased at a similar rate in both groups (p = 0.524)

• Use declined more quickly in the RMMR group during the washout and follow-up periods, but the differences in trends were negligible (0.4 DDDs/1000 days per week, p = 0.001)

No RMMR

96.7

100.1

99.6

Opioids

RMMR

87.5

101.0

101.5

• During the pre-intervention period, opioid use increased in those with and without an RMMR, with only a negligible difference between groups of 0.1 DDDs/1000 days per week

• Opioid use plateaued after the index date with no difference in trends between the two groups (p > 0.05)

No RMMR

86.6

96.9

97.3

Medicines for cognitive symptoms of dementia

RMMR

119.0

113.8

112.4

• There were no significant differences in use between the two groups during the pre-intevention and washout periods (all p > 0.05)

• A small difference in weekly use between groups during the follow-up period (-0.7 vs. -0.4 DDDs/1000 days per week, p = 0.03) was observed. Cautious interpretation is advised due to considerable variation in use (weekly differences of up to 10 DDDs/1000 days) observed in the RMMR group during follow-up

No RMMR

116.2

112.6

111.4

Proton pump inhibitorsa

RMMR

489.0

499.5

466.2

• During the pre-intervention period, PPI use was increasing at a similar rate in both groups (p = 0.596)

• During the washout period, PPI use declined faster in the RMMR group (-2.6 vs. -1.5 DDDs/1000 days per week, p = 0.001)

• At the start of the follow-up period, the rate of PPI use in the RMMR group dropped below the rate among those without an RMMR (-14.0 vs. -2.8 DDDs/1000 days, p < 0.001) and continued to decline at the same rate in both groups thereafter (p = 0.334)

No RMMR

477.9

488.7

474.3

Osteoporosis medicines

RMMR

151.1

152.9

151.6

• There were no significant differences in use between the two groups during the pre-intevention, washout and follow-up periods (all p > 0.05)

• In the first week of the follow-up period, a significant drop in use was observed in the RMMR group (-3.0 vs. 0.04 DDDs/1000 days, p = 0.001). However, this was influenced by an outlier observation at the end of the follow-up period

No RMMR

150.6

147.1

145.8

Glucose lowering medicines

RMMR

282.2

262.4

249.7

• Use decreased at a similar rate in both groups during the pre-intervention, washout and follow-up periods (all p > 0.05)

No RMMR

292.9

261.5

251.3

Statinsa

RMMR

502.1

483.1

433.6

• Significant decrease in statin use in the RMMR group post-index date; refer to Table 3 and description in “Results“ section

No RMMR

492.2

476.7

451.8

ACE inhibitors or sartans

RMMR

636.4

628.4

608.2

• ACE inhibitor/sartan use decreased at a similar rate in both groups during the pre-intervention and follow-up periods (p > 0.05)

• There was a slightly faster rate of decline in the RMMR group during the washout period (-3.7 vs -1.6 DDDs/1000 days per week, p = 0.01). However, this was influenced by an outlier observation in the first week of the washout period

No RMMR

609.2

601.7

597.5

Beta blockers

RMMR

137.8

131.8

125.0

• Differences in weekly trends between groups during the pre-intervention, washout and follow-up periods were negligible (≤ 0.4 DDDs/1000 days per week)

No RMMR

130.3

132.5

124.8

Calcium channel blockers (CCBs)a

RMMR

241.6

243.3

228.0

• CCB use decreased at a similar rate in both groups during the pre-intervention and washout periods (p = 0.435)

• At the start of the follow-up period, CCB in the RMMR group dropped below the rate in the group without an RMMR (-4.2 versus 2.1 DDDs/1000 days, p < 0.001), but declined more quickly among those without an RMMR during follow-up (-0.12 vs. -0.62 DDDs/1000 days per week, p < 0.001)

No RMMR

241.2

240.6

232.3

Loop diuretics

RMMR

376.4

395.8

385.2

• During the pre-intervention period, use was increasing at a slightly faster rate among individuals RMMR (0.92 vs. 1.8 DDDs/1000 days per week, p = 0.015). However, use declined during the washout and follow-up periods, with no differences in trends observed between the two groups (p > 0.05)

No RMMR

355.9

386.7

366.6

Oral anticoagulants

RMMR

74.8

74.1

68.0

• Use was stable during the pre-intervention period, with only a negligible difference between groups (< 0.1 DDDs/1000 days per week)

• Oral anticoagulant use declined at a similar rate in both groups after the index date (p > 0.05)

No RMMR

72.0

71.9

65.6

  1. ACE Angiotensin converting enzyme, CCB calcium channel blocker, DDD Defined daily dose, RACF Residential aged care facility, RMMR Residential Medication Management Review
  2. a Medicine classess with significant changes in weekly DDDs/1000 resident-days after the index date in the RMMR group compared to those without an RMMR