| Literature DB >> 35885734 |
Srujitha Marupuru1, Alexis Roether1, A J Guimond1, Chris Stanley1, Tyler Pesqueira1, David R Axon1.
Abstract
This study aimed to compare the clinical outcomes of pharmacist-provided medication therapy management (MTM) services as compared to no MTM services (i.e., standard of care) on outpatient clinical outcomes for patients with diabetes, hypertension, or dyslipidemia. A systematic literature review of PubMed, EMBASE, Cochrane library, International Pharmaceutical Abstracts, PsycINFO, Scopus, CINAHL electronic databases, grey literature, websites, and journals, was conducted from 1 January 2005-20 July 2021. The search field contained a combination of keywords and MeSH terms such as: "medication therapy management", "pharmacist", "treatment outcomes". Studies published in United States, included adults ≥18 years old who received at least one pharmacist-provided MTM consultation and at least one group who received no MTM, and reported pre-specified clinical outcomes for diabetes mellitus, hypertension, or dyslipidemia were included. Of 849 studies identified, eight were included (cohort studies = 6, randomized controlled trials = 2). Clinical outcomes improved with MTM interventions, as evidenced by statistically significant changes in at least one of the three chronic conditions in most studies. Improvements were observed for diabetes outcomes (n = 4 studies), hypertension outcomes (n = 4 studies), and dyslipidemia outcomes (n = 3 studies). Overall, this study indicated that pharmacist delivered MTM services (versus no MTM services) can improve clinical outcomes for patients with diabetes, hypertension, and dyslipidemia.Entities:
Keywords: Medication therapy management; clinical outcomes; pharmacist
Year: 2022 PMID: 35885734 PMCID: PMC9318817 DOI: 10.3390/healthcare10071207
Source DB: PubMed Journal: Healthcare (Basel) ISSN: 2227-9032
Figure 1Medline/PubMed search strategy.
Figure 2PRISMA flowchart.
Characteristics of included studies.
| Author, Year | Study Design | Settings | Insurance Status | Eligible | Mode of | Team | Frequency of Follow Up/Year | Total | Mean Age Patients | % Male Patients |
|---|---|---|---|---|---|---|---|---|---|---|
| Hirsch, | RCT | University-based | All plans | DM, HTN | Face to face | Collaborative pharmacist–primary care provider | ≥4 | 667 | 67.5 | 42.6 |
| Planas, | RCT | Community pharmacy | Insured | DM, HTN | Face to face | Pharmacist | 12 | 52 | 64.7 | 37.2 |
| Brummel, | Cohort | Comprehensive provider of pharmacy service | Medicare, | DM | Face to face | Pharmacist | Any | 224 | 58.3 | 48.2 |
| Fox, | Cohort | Managed care organization | Medicare D | DM | Telephone | Collaborative pharmacist–primary care provider | ≥3 | 2114 | 69.2 | 50.1 |
| Pindolia, | Cohort | Health Alliance Plan | Health | 26 possible chronic conditions * | Telephone | Collaborative pharmacist–primary care provider | N/A | 2681 | 73.7 | 39.8 |
| Prudencio, | Cohort | Patient-Centered | N/A | DM | Face to face | Pharmacist | ≥1 | 811 | 63.0 | 49.0 |
| Skinner, | Cohort | Community health center | N/A | DM | Face to face | Pharmacist | ≥4 | 58 | 53.7 | 42.0 |
| Tilton, | Cohort | Academic health center | Low income | DM, HTN | Face to face | Pharmacist | ≥3 | 316 | 69.6 | 40.5 |
RCT = randomized controlled trial; N/A = data not available; DM = diabetes mellitus; HTN = hypertension. * 26 possible chronic diseases included Alzheimer’s disease, ankylosing spondylitis, arthritis, asthma, Benign prostatic hyperplasia, Coronary artery disease, Congestive heart failure, cancer, chronic obstructive pulmonary disease, depression, diabetes, epilepsy, erectile dysfunction, Fabry’s disease, hepatitis B/C, HIV/AIDS, hypertension, insomnia, multiple sclerosis, obesity, osteoporosis, Parkinson’s disease, plaque psoriasis, stress/urge incontinence, stroke/transient ischemic attack.
Clinical outcomes reported in included studies.
| Author, Year | N Analyzed | Follow-Up Period | Outcomes Reported | Intervention | Control | |
|---|---|---|---|---|---|---|
| Hirsch, | I-75 | Baseline, | Mean ± SD change | 6 months: | 6 months: | 0.21 |
| 9 months: | 9 months: | 0.95 | ||||
| Mean ± SD change | 6 months: | 6 months: | 0.54 | |||
| 9 months: | 9 months: | 0.67 | ||||
| Mean ± SD change | 6 months: | 6 months: |
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| 9 months: | 9 months: | 0.22 | ||||
| Mean ± SD change | 6 months: | 6 months: |
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| 9 months: | 9 months: | 0.27 | ||||
| Planas, | I-32 | Monthly within study period of 9 months | % With BP <130/80 mmHg at 9 months | 48.00 | 6.67 |
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| Mean SBP (mmHg) | 124.44 | 148.13 |
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| Brummel, | I-121 | 2006, 2007, 2008 | % With HbA1c <7% | 2006: 43.80 | 2006: 63.11 |
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| 2007: 73.55 | 2007: 72.82 | 0.90 | ||||
| 2008: 42.15 | 2008: 59.22 |
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| % With LDL <100 mg/dL | 2006: 63.64 | 2006: 65.05 | 0.82 | |||
| 2007: 83.47 | 2007: 73.79 | 0.07 | ||||
| 2008: 79.34 | 2008: 73.79 | 0.32 | ||||
| % With BP <130/80 mmHg | 2006: 66.12 | 2006: 61.17 | 0.44 | |||
| 2007: 71.07 | 2007: 72.82 | 0.77 | ||||
| 2008: 76.03 | 2008: 69.90 | 0.30 | ||||
| Fox, | I-255 | 1 January 2006– | % With LDL <100 mg/dL | 69.00 | 50.00 |
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| Mean ± SD LDL (mg/dL) | 83.4 ± 31.2 | 90.8 ± 31.0 |
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| Pindolia, | I-520 | 2006, 2007 | % Change in people with HbA1c <7% | 3 | 7 | N/A |
| % Change in people with LDL <100 mg/dL | −5 | 7 | N/A | |||
| Prudencio, | I-95 | 1 October 2014– | % With HbA1c <8% | 54 | 36 |
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| % With BP <140/90 mmHg | 93 | 77 |
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| % With statin prescription | 79 | 63 |
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| Skinner, | I-50 | 12-month | Mean ± SD HbA1c (%) | 7.5 ± 0.38 | 10.8 ± 2.0 |
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| Mean ± SD LDL (mg/dL) | 92.7 ± 36.4 | 110.8 ± 65.7 | 0.17 | |||
| Mean ± SD HDL (mg/dL) | 48.2 ± 10.3 | 45.2 ± 12.9 | 0.16 | |||
| Mean ± SD SBP (mmHg) | 136.5 ± 19.8 | 145.4 ± 17.8 | 0.12 | |||
| Mean ± SD DBP (mmHg) | 72.7 ± 10.3 | 73.8 ± 14.7 | 0.63 | |||
| Tilton, | I-158 | 2001–2011 | Mean ± SD HbA1c (%) | 6 months: | 6 months: |
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| 12 months: 7.49 | 12 months: 7.75 |
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| Mean ± SD SBP (mmHg) | 6 months: 135.3 | 6 months: 135.2 |
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| 12 months: 133.0 | 12 months: 134.6 |
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| Mean ± SD DBP (mmHg) | 6 months: 72.8 | 6 months: 76.3 |
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| 12 months: 72.2 | 12 months: 73.6 | 0.269 |
I = intervention; C = comparator; SD = standard deviation; LDL = low density lipoprotein; mg/dL = milligrams per deciliter; HDL = high density lipoprotein; SBP = systolic blood pressure; mmHg = millimeters of mercury; DBP = diastolic blood pressure; BP = blood pressure; HbA1c = hemoglobin A1c; DM = diabetes mellitus; N/A = data not available. Bold indicates significant p-value. The “negative sign” in front of lab values indicate the change in the clinical outcome. Tilton, 2019 study has missing standard deviations in their clinical outcomes reported.
Risk of bias assessment in included studies.
| Randomized Controlled Trials | ||||||||
|---|---|---|---|---|---|---|---|---|
| Author, Year | Randomization | Deviations from | Missing | Measurement of Outcome | Selection of | Overall | ||
| Hirsch, | Low | Low | Some Concerns | Low | Low | Moderate | ||
| Planas, | Low | Low | Low | Low | Low | Low | ||
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| Brummel, | Moderate | Low | Low | Moderate | Moderate | Moderate | Low | Moderate |
| Fox, | Moderate | Low | Low | Low | Moderate | Low | Low | Moderate |
| Pindolia, | Moderate | Moderate | Moderate | Low | Low | Low | Low | Moderate |
| Prudencio, | Moderate | Low | Low | Low | Low | Low | Low | Moderate |
| Skinner, | Moderate | Moderate | Low | Moderate | Low | Low | Low | Moderate |
| Tilton, | Moderate | Low | Low | Low | Low | Low | Low | Moderate |
Risk of bias in randomized controlled trials assessed using Cochrane risk-of-bias tool for randomized trials (RoB2) [19]. Risk of bias in cohort studies assessed using Cochrane Risk of Bias in Non-Randomized Studies—of Interventions (ROBINS-I) [20].